DIAGNOSIS OF SEPSIS

Abstract

Methods for predicting the development of sepsis in a subject at risk for developing sepsis are provided. In one method, features in a biomarker profile of the subject are evaluated. The subject is likely to develop sepsis if these features satisfy a particular value set. Methods for predicting the development of a stage of sepsis in a subject at risk for developing a stage of sepsis are provided. In one method, a plurality of features in a biomarker profile of the subject is evaluated. The subject is likely to have the stage of sepsis if these feature values satisfy a particular value set. Methods of diagnosing sepsis in a subject are provided. In one such method, a plurality of features in a biomarker profile of the subject is evaluated. The subject is likely to develop sepsis when the plurality of features satisfies a particular value set.

Description

1. FIELD OF THE INVENTION

The present invention relates to methods and compositions for diagnosing or predicting sepsis and/or its stages of progression in a subject. The present invention also relates to methods and compositions for diagnosing systemic inflammatory response syndrome in a subject.

2. BACKGROUND OF THE INVENTION

Early detection of a disease condition typically allows for a more effective therapeutic treatment with a correspondingly more favorable clinical outcome. In many cases, however, early detection of disease symptoms is problematic due to the complexity of the disease; hence, a disease may become relatively advanced before diagnosis is possible. Systemic inflammatory conditions represent one such class of diseases. These conditions, particularly sepsis, typically, but not always, result from an interaction between a pathogenic microorganism and the host's defense system that triggers an excessive and dysregulated inflammatory response in the host. The complexity of the host's response during the systemic inflammatory response has complicated efforts towards understanding disease pathogenesis (reviewed in Healy, 2002, Annul. Pharmacother. 36:648-54). An incomplete understanding of the disease pathogenesis, in turn, contributes to the difficulty in finding useful diagnostic biomarkers. Early and reliable diagnosis is imperative, however, because of the remarkably rapid progression of sepsis into a life-threatening condition.

The development of sepsis in a subject follows a well-described course, progressing from systemic inflammatory response syndrome (“SIRS”)-negative, to SIRS-positive, and then to sepsis, which may then progress to severe sepsis, septic shock, multiple organ dysfunction (“MOD”), and ultimately death. Sepsis may also arise in an infected subject when the subject subsequently develops SIRS. “Sepsis” is commonly defined as the systemic host response to infection with SIRS plus a documented infection. “Severe sepsis” is associated with MOD, hypotension, disseminated intravascular coagulation (“DIC”) or hypoperfusion abnormalities, including lactic acidosis, oliguria, and changes in mental status. “Septic shock” is commonly defined as sepsis-induced hypotension that is resistant to fluid resuscitation with the additional presence of hypoperfusion abnormalities.

Documenting the presence of the pathogenic microorganisms that are clinically significant to sepsis has proven difficult. Causative microorganisms typically are detected by culturing a subject's blood, sputum, urine, wound secretion, in-dwelling line catheter surfaces, etc. Causative microorganisms, however, may reside only in certain body microenvironments such that the particular material that is cultured may not contain the contaminating microorganisms. Detection may be complicated further by low numbers of microorganisms at the site of infection. Low numbers of pathogens in blood present a particular problem for diagnosing sepsis by culturing blood. In one study, for example, positive culture results were obtained in only 17% of subjects presenting clinical manifestations of sepsis (Rangel-Frausto et al., 1995, JAMA 273:117-123). Diagnosis can be further complicated by contamination of samples by non-pathogenic microorganisms. For example, only 12.4% of detected microorganisms were clinically significant in a study of 707 subjects with septicemia (Weinstein et al., 1997, Clinical Infectious Diseases 24:584-602).

The difficulty in early diagnosis of sepsis is reflected by the high morbidity and mortality associated with the disease. Sepsis currently is the tenth leading cause of death in the United States and is especially prevalent among hospitalized patients in non-coronary intensive care units (ICUs), where it is the most common cause of death. The overall rate of mortality is as high as 35%, with an estimated 750,000 cases per year occurring in the United States alone. The annual cost to treat sepsis in the United States alone is on the order of billions of dollars.

A need, therefore, exists for a method of diagnosing sepsis, using techniques that have satisfactory specificity and sensitivity performance, sufficiently early to allow effective intervention and prevention.

3. SUMMARY OF THE INVENTION

The present invention relates to methods and compositions for diagnosing sepsis, including the onset of sepsis, in a test subject. The present invention also relates to methods and compositions for predicting sepsis in a test subject.

The present invention further relates to methods and compositions for diagnosing or predicting stages of sepsis progression in a test subject. The present invention still further relates to methods and compositions for diagnosing systemic inflammatory response syndrome (SIRS) in a test subject.

In one aspect, the present invention provides a method of predicting the development of sepsis in a test subject at risk for developing sepsis. This method comprises evaluating whether a plurality of features in a biomarker profile of the test subject satisfies a value set, wherein satisfying the value set means that the test subject will develop sepsis with a likelihood that is determined by the accuracy of the decision rule to which the plurality of features are applied in order to determine whether they satisfy the value set. In some embodiments, the accuracy of the decision rule is at least 60%. Therefore, correspondingly, the likelihood that the test subject will develop sepsis when the plurality of features satisfies the value set is at least 60%.

Yet another aspect of the invention comprises a method of diagnosing sepsis in a test subject. These methods comprise evaluating whether a plurality of features in a biomarker profile of the test subject satisfies a value set, wherein satisfying the value set predicts that the test subject has sepsis with a likelihood that is determined by the accuracy of the decision rule to which the plurality of features are applied in order to determine whether they satisfy the value set. In some embodiments, the accuracy of the decision rule is at least 60%. Therefore, correspondingly, the likelihood that the test subject has sepsis when the plurality of features satisfies the value set is at least 60%.

In a particular embodiment, the biomarker profile comprises at least two features, each feature representing a feature of a corresponding biomarker listed in column four or five of Table 30. In one embodiment, the biomarker profile comprises at least two different biomarkers listed in column four or five of Table 30. In such an embodiment, the biomarker profile can comprise a respective corresponding feature for the at least two biomarkers. Generally, the at least two biomarkers are derived from at least two different genes. In the case where a biomarker in the at least two different biomarkers is listed in column four of Table 30, the biomarker can be, for example, a transcript made by the listed gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein listed in column five of Table 30, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In accordance with this embodiment, the biomarker profiles of the present invention can be obtained using any standard assay known to those skilled in the art, or in an assay described herein, to detect a biomarker. Such assays are capable, for example, of detecting the products of expression (e.g., nucleic acids and/or proteins) of a particular gene or allele of a gene of interest (e.g., a gene disclosed in Table 30). In one embodiment, such an assay utilizes a nucleic acid microarray. In some embodiments, the biomarker profile comprises at least two different biomarkers from column four or five of Table 32. In some embodiments, the biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, or 50 different biomarkers from Table 30.

In a particular embodiment, the biomarker profile comprises at least two different biomarkers that each contain one of the probesets listed in column 2 of Table 30, biomarkers that contain the complement of one of the probesets of Table 30, or biomarkers that contain an amino acid sequence encoded by a gene that either contains one of the probesets of Table 30 or the complement of one of the probesets of Table 30. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example amplified nucleic acid, or proteins. The biomarker profile further comprises a respective corresponding feature for the at least two biomarkers. Generally, the at least two biomarkers are derived from at least two different genes. In the case where a biomarker is based upon a gene that includes the sequence of a probeset listed in Table 30, the biomarker can be, for example, a transcript made by the gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein encoded by a gene that includes a probeset sequence described in Table 30, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In some embodiments, the biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 different biomarkers from any one of Table 31, 32, 33, 34, or 36.

In a particular embodiment, the biomarker profile comprises at least two different biomarkers listed in column three of Table 31. The biomarker profile further comprises a respective corresponding feature for the at least two biomarkers. Generally, the at least two biomarkers are derived from at least two different genes. The biomarker can be, for example, a transcript made by gene listed in Table 31, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein encoded by a gened listed in column three of Table 31, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In accordance with this embodiment, the biomarker profiles of the present invention can be obtained using any standard assay known to those skilled in the art, or in an assay described herein, to detect a biomarker. Such assays are capable, for example, of detecting the products of expression (e.g., nucleic acids and/or proteins) of a particular gene or allele of a gene of interest (e.g., a gene disclosed in Table 31). In one embodiment, such an assay utilizes a nucleic acid microarray.

In a particular embodiment, the biomarker profile comprises at least two different biomarkers that each contain one of the probesets listed in column 2 of Table 31. biomarkers that contain the complement of one of the probesets of Table 31, or biomarkers that contain an amino acid sequence encoded by a gene that either contains one of the probesets of Table 31 or the complement of one of the probesets of Table 31. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example amplified nucleic acid, or proteins. The biomarker profile further comprises a respective corresponding feature for the at least two biomarkers. Generally, the at least two biomarkers are derived from at least two different genes. In the case where a biomarker is based upon a gene that includes the sequence of a probeset listed in Table 31, the biomarker can be, for example, a transcript made by the gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still. the biomarker can be, for example, a protein encoded by a gene that includes a probeset sequence described in Table 31, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In some embodiments, the biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, or 50 different biomarkers from Table 31.

In a particular embodiment, the biomarker profile comprises at least three features, each feature representing a feature of a corresponding biomarker listed in column 3 or four of Table I. In one embodiment, the biomarker profile comprises at least three different biomarkers listed in column three or four of Table I. In such an embodiment, the biomarker profile can comprise a respective corresponding feature for the at least three biomarkers. Generally, the at least three biomarkers are derived from at least three different genes listed in Table I. In the case where a biomarker in the at least three different biomarkers is listed in column three of Table I, the biomarker can be, for example, a transcript made by the listed gene, a complement thereof, a splice variant thereof, a complement of a splice variant thereof, or a discriminating fragment or complement of any of the foregoing, a cDNA of any of the forgoing, a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein listed in column four of Table I, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, splice-variant thereof or protein. In accordance with this embodiment, the biomarker profiles of the present invention can be obtained using any standard assay known to those skilled in the art, or in an assay described herein, to detect a biomarker. Such assays are capable, for example, of detecting the products of expression (e.g., nucleic acids and/or proteins) of a particular gene or allele of a gene of interest (e.g., a gene disclosed in Table I). In one embodiment, such an assay utilizes a nucleic acid microarray. In some embodiments, the biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, or 50 different biomarkers from Table 1.

In a particular embodiment, the biomarker profile comprises at least three features, each feature representing a feature of a corresponding biomarker listed in column 3 or four of Table J. In one embodiment, the biomarker profile comprises at least three different biomarkers listed in column three or four of Table J. In such an embodiment, the biomarker profile can comprise a respective corresponding feature for the at least three biomarkers. Generally, the at least three biomarkers are derived from at least three different genes. In the case where a biomarker in the at least three different biomarkers is listed in column three of Table J, the biomarker can be, for example, a transcript made by the listed gene, a complement thereof, a splice variant thereof, a complement of a splice variant thereof, or a discriminating fragment or complement of any of the foregoing, a cDNA of any of the forgoing, a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein listed in column four of Table J, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, splice-variant thereof or protein. In accordance with this embodiment, the biomarker profiles of the present invention can be obtained using any standard assay known to those skilled in the art, or in an assay described herein, to detect a biomarker. Such assays are capable, for example, of detecting the products of expression (e.g., nucleic acids and/or proteins) of a particular gene or allele of a gene of interest (e.g., a gene disclosed in Table J). In one embodiment, such an assay utilizes a nucleic acid microarray. In some embodiments, the biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40 different biomarkers from Table J.

In a particular embodiment, the biomarker profile comprises at least three features, each feature representing a feature of a corresponding biomarker listed in column 3 or four of Table K. In one embodiment, the biomarker profile comprises at least three different biomarkers listed in column three or four of Table K. In such an embodiment, the biomarker profile can comprise a respective corresponding feature for the at least three biomarkers. Generally, the at least two or three biomarkers are derived from at least two or three different genes, respectively. In the case where a biomarker in the at least two or three different biomarkers is listed in column three of Table K, the biomarker can be, for example, a transcript made by the listed gene, a complement thereof, a splice variant thereof, a complement of a splice variant thereof, or a discriminating fragment or complement of any of the foregoing, a cDNA of any of the forgoing, a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein listed in column four of Table K. or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, splice-variant thereof or protein. In accordance with this embodiment, the biomarker profiles of the present invention can be obtained using any standard assay known to those skilled in the art, or in an assay described herein, to detect a biomarker. Such assays are capable, for example, of detecting the products of expression (e.g., nucleic acids and/or proteins) of a particular gene or allele of a gene of interest (e.g., a gene disclosed in Table K). In one embodiment, such an assay utilizes a nucleic acid microarray. In some embodiments, the biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10 different biomarkers from Table K.

Although the methods of the present invention are particularly useful for detecting or predicting the onset of sepsis in SIRS subjects, one of skill in the art will understand that the present methods may be used for any subject: including, but not limited to, subjects suspected of having SIRS or of being at any stage of sepsis. For example, a biological sample can be taken from a subject, and a profile of biomarkers in the sample can be evaluated in light of biomarker profiles obtained from several different types of training populations. Representative training populations variously include, for example, populations that include subjects who are SIRS-negative, populations that include subjects who are SIRS-positive, and/or populations that include subjects at a particular stage of sepsis. Evaluation of the biomarker profile in light of each of these different training populations can be used to determine whether the test subject is SIRS-negative, SIRS-positive, is likely to become septic, or has a particular stage of sepsis. Based on the diagnosis resulting from the methods of the present invention, an appropriate treatment regimen can then be initiated.

In particular embodiments, the invention also provides kits that are useful in diagnosing or predicting the development of sepsis or SIRS in a subject (see Section 5.3, infra). The kits of the present invention comprise at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150, 155, 160, 165, 170, 175, 180, 185, 190, 195 or 200 or more biomarkers and/or reagents used to detect the presence or abundance of such biomarkers. In some embodiments, each of these biomarkers is from Table 30. In some embodiments, each of these biomarkers is from Table 31. In some embodiments, each of these biomarkers is from Table 32. In some embodiments, each of these biomarkers is from Table 33. In some embodiments, each of these biomarkers is from Table 36. In some embodiments, each of these biomarkers is from FIG. 39, FIG. 43, FIG. 52, FIG. 53, or FIG. 56. In another embodiment, the kits of the present invention comprise at least two, but as many as several hundred or more biomarkers and/or reagents used to detect the presence or abundance of such biomarkers.

In a specific embodiment, the kits of the present invention comprise at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150, 155, 160, 165, 170, 175, 180, 185, 190, 195 or 200 or more reagents that specifically bind the biomarkers of the present invention. For example, such kits can comprise nucleic acid molecules and/or antibody molecules that specifically bind to biomarkers of the present invention.

Specific exemplary biomarkers that are useful in the present invention are set forth in Section 5.6, Section 5.11, as well as Tables 30, 31, 32, 34 and 36 of Section 6. The biomarkers of the kit can be used to generate biomarker profiles according to the present invention. Examples of types of biomarkers and/or reagents within such kits include, but are not limited to, proteins and fragments thereof, peptides, polypeptides, antibodies, proteoglycans, glycoproteins, lipoproteins, carbohydrates, lipids, nucleic acids (mRNA, DNA, cDNA), organic and inorganic chemicals, and natural and synthetic polymers or a discriminating molecule or fragment thereof.

In particular embodiments, the invention also provides still other kits that are useful in diagnosing or predicting the development of sepsis or SIRS in a subject (see Section 5.3, infra). The kits of the present invention comprise at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50 or more biomarkers. In some embodiments, each of these biomarkers is from Table I. In some embodiments, each of these biomarkers is from Table J. In some embodiments, each of these biomarkers is from Table K. In some embodiments, each of these biomarkers is found in Table I or Table 30. In some embodiments, each of these biomarkers is found in Table 1 or Table 31. In some embodiments, each of these biomarkers is from FIG. 39, FIG. 43, FIG. 52, FIG. 53, or FIG. 56. In another embodiment, the kits of the present invention comprise at least two, but as many as 50 or more biomarkers. In a specific embodiment, the kits of the present invention comprise at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150, 155, 160, 165, 170, 175, 180, 185, 190, 195 or 200 or more reagents that specifically bind the biomarkers of the present invention. Specific biomarkers that are useful in the present invention are set forth in Section 5.6, Section 5.11, as well as Tables I, J, K, L, M, N, and O. The biomarkers of the kits can be used to generate biomarker profiles according to the present invention. Examples of classes of compounds of the kits include, but are not limited to, proteins and fragments thereof, peptides, polypeptides, proteoglycans, glycoproteins, lipoproteins, carbohydrates, lipids, nucleic acids (mRNA, DNA, cDNA), organic and inorganic chemicals, and natural and synthetic polymers or a discriminating molecule or fragment thereof.

Still another aspect of the present invention comprises computers and computer readable media for evaluating whether a test subject is likely to develop sepsis or SIRS. For instance, one embodiment of the present invention provides a computer program product for use in conjunction with a computer system. The computer program product comprises a computer readable storage medium and a computer program mechanism embedded therein. The computer program mechanism comprises instructions for evaluating whether a plurality of features in a biomarker profile of a test subject at risk for developing sepsis satisfies a first value set. Satisfaction of the first value set predicts that the test subject is likely to develop sepsis. The features are measurable aspects of a plurality of biomarkers comprising at least three biomarkers listed in Table 1. In some embodiments, the computer program product further comprises instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a second value set. Satisfaction of the second value set predicts that the test subject is not likely to develop sepsis. In some embodiments, the biomarker profile has between 3 and 50 biomarkers listed in Table I, between 3 and 40 biomarkers listed in Table I, at least four biomarkers listed in Table I, or at least six biomarkers listed in Table I.

Another computer embodiment of the present invention comprises a central processing unit and a memory coupled to the central processing unit. The memory stores instructions for evaluating whether a plurality of features in a biomarker profile of a test subject at risk for developing sepsis satisfies a first value set. Satisfaction of the first value set predicts that the test subject is likely to develop sepsis. The features are measurable aspects of a plurality of biomarkers. This plurality of biomarkers comprises at least three biomarkers from Table I. In some embodiments, the memory further stores instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a second value set, wherein satisfying the second value set predicts that the test subject is not likely to develop sepsis. In some embodiments, the biomarker profile consists of between 3 and 50 biomarkers listed in Table I, between 3 and 40 biomarkers listed in Table I, at least four biomarkers listed in Table I, or at least eight biomarkers listed in Table I.

Another computer embodiment in accordance with the present invention comprises a computer system for determining whether a subject is likely to develop sepsis. The computer system comprises a central processing unit and a memory, coupled to the central processing unit. The memory stores instructions for obtaining a biomarker profile of a test subject. The biomarker profile comprises a plurality of features. The plurality of biomarkers comprises at least three biomarkers listed in Table I. The memory further comprises instructions for transmitting the biomarker profile to a remote computer. The remote computer includes instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a first value set. Satisfaction of the first value set predicts that the test subject is likely to develop sepsis. The memory further comprises instructions for receiving a determination, from the remote computer, as to whether the plurality of features in the biomarker profile of the test subject satisfies the first value set. The memory also comprises instructions for reporting whether the plurality of features in the biomarker profile of the test subject satisfies the first value set. In some embodiments, the remote computer further comprises instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a second value set. Satisfaction of the second value set predicts that the test subject is not likely to develop sepsis. In such embodiments, the memory further comprises instructions for receiving a determination. from the remote computer, as to whether the plurality of features in the biomarker profile of the test subject satisfies the second set as well as instructions for reporting whether the plurality of features in the biomarker profile of the test subject satisfies the second value set. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least six biomarkers listed in Table 1.

Still another embodiment of the present invention comprises a digital signal embodied on a carrier wave comprising a respective value for each of a plurality of features in a biomarker profile. The features are measurable aspects of a plurality of biomarkers. The plurality of biomarkers comprises at least three biomarkers listed in Table 1. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table 1. In some embodiments, the plurality of biomarkers comprises at least eight biomarkers listed in Table I.

Still another aspect of the present invention provides a digital signal embodied on a carrier wave comprising a determination as to whether a plurality of features in a biomarker profile of a test subject satisfies a value set. The features are measurable aspects of a plurality of biomarkers. This plurality of biomarkers comprises at least three biomarkers listed in Table I. Satisfying the value set predicts that the test subject is likely to develop sepsis. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least eight biomarkers listed in Table I.

Still another embodiment provides a digital signal embodied on a carrier wave comprising a determination as to whether a plurality of features in a biomarker profile of a test subject satisfies a value set. The features are measurable aspects of a plurality of biomarkers. The plurality of biomarkers comprises at least three biomarkers listed in Table 1. Satisfaction of the value set predicts that the test subject is not likely to develop sepsis. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least eight biomarkers listed in Table I.

Still another embodiment of the present invention provides a graphical user interface for determining whether a subject is likely to develop sepsis. The graphical user interface comprises a display field for a displaying a result encoded in a digital signal embodied on a carrier wave received from a remote computer. The features are measurable aspects of a plurality of biomarkers. The plurality of biomarkers comprises at least three biomarkers listed in Table I. The result has a first value when a plurality of features in a biomarker profile of a test subject satisfies a first value set. The result has a second value when a plurality of features in a biomarker profile of a test subject satisfies a second value set. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least eight biomarkers listed in Table I.

Yet another aspect of the present invention provides a computer system for determining whether a subject is likely to develop sepsis. The computer system comprises a central processing unit and a memory, coupled to the central processing unit. The memory stores instructions for obtaining a biomarker profile of a test subject. The biomarker profile comprises a plurality of features. The features are measurable aspects of a plurality of biomarkers. The plurality of biomarkers comprise at least three biomarkers listed in Table 1. The memory further stores instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a first value set. Satisfying the first value set predicts that the test subject is likely to develop sepsis. The memory also stores instructions for reporting whether the plurality of features in the biomarker profile of the test subject satisfies the first value set. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least eight biomarkers listed in Table I.

4. BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 illustrates a classification and regression tree for discriminating between a SIRS phenotypic state characterized by the onset of sepsis and a SIRS phenotypic state characterized by the absence of sepsis using T₋₃₆ static data obtained from a training population in accordance with an embodiment of the present invention.

FIG. 2 shows the distribution of feature values for five biomarkers used in the decision tree of FIG. 1 across T₋₃₆ static data obtained from a training population in accordance with an embodiment of the present invention. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 3 illustrates the overall accuracy, sensitivity, and specificity of 500 trees used to train a decision tree using the Random Forests method based upon T₋₃₆ static data obtained from a training population in accordance with an embodiment of the present invention.

FIG. 4 illustrates the biomarker importance in the decision rule trained using the trees of FIG. 3.

FIG. 5 illustrates the overall accuracy, with 95% confidence interval bars, specificity, and sensitivity of a decision rule developed with predictive analysis of microarrays (PAM) using the biomarkers of the present invention across T₋₃₆ static data obtained from a training population.

FIG. 6 is a list of biomarkers, rank-ordered by their respective degrees of discriminatory power, identified by PAM using T₋₃₆ static data obtained from a training population. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 7 illustrates CART, PAM, and random forests classification algorithm performance data, and associated 95% confidence intervals, for T₋₃₆ static data obtained from a training population.

FIG. 8 illustrates the number of times that common biomarkers were found to be important across the decision rules developed using (i) CART, (ii) PAM, (iii) random forests, and (iv) the Wilcoxon (adjusted) test, for T₋₃₆ static data obtained from a training population.

FIG. 9 illustrates an overall ranking of biomarkers for T₋₃₆ static data obtained from a training population. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 10 illustrates a classification and regression tree for discriminating between a SIRS phenotypic state characterized by the onset of sepsis and a SIRS phenotypic state characterized by the absence of sepsis using data using T₋₁₂ static data obtained from a training population in accordance with an embodiment of the present invention.

FIG. 11 shows the distribution of feature values for four biomarkers used in the decision tree of FIG. 10 using T₋₁₂ static data obtained from a training population in accordance with an embodiment of the present invention. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 12 illustrates the overall accuracy, sensitivity, and specificity of 500 trees used to train a decision tree using the Random Forests method based upon T₋₁₂ static data obtained from a training population in accordance with an embodiment of the present invention.

FIG. 13 illustrates the biomarker importance in the decision rule trained using the trees of FIG. 12. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 14 illustrates a calculation of biomarker importance, summing to 100%, determined by a multiple additive regression tree (MART) approach using T₋₂ static data obtained from a training population. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 15 illustrates the distribution of feature values of the biomarkers selected by the MART approach illustrated in FIG. 14 between the Sepsis and SIRS groups using T₋₁₂ static data obtained from a training population. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 16 illustrates the overall accuracy, with 95% confidence interval bars, specificity, and sensitivity of a decision rule developed with predictive analysis of microarrays (PAM) using the biomarkers of the present invention using T₋₂ static data obtained from a training population.

FIG. 17 is a list of biomarkers, rank-ordered by their respective degrees of discriminatory power, identified by PAM using T₋₂ static data obtained from a training population. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 18 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals using T₋₂ static data obtained from a training population.

FIG. 19 illustrates the number of times that common biomarkers were found to be important across the decision rules developed using (i) CART, (ii) MART, (iii) PAM, (iv) random forests, and (v) the Wilcoxon (adjusted) test using T₋₁₂ static data obtained from a training population. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 20 illustrates an overall ranking of biomarkers using T₁, static data obtained from a training population.

FIG. 21 illustrates a classification and regression tree for discriminating between a SIRS phenotypic state characterized by the onset of sepsis and a SIRS phenotypic state characterized by the absence of sepsis using T₋₁₂ baseline data obtained from a training population in accordance with an embodiment of the present invention.

FIG. 22 shows the distribution of the feature values of five biomarkers used in the decision tree of FIG. 21 using T₋₁₂ baseline data obtained from a training population in accordance with an embodiment of the present invention. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 23 illustrates the overall accuracy, sensitivity, and specificity of 500 trees used to train a decision tree using the Random Forests method using T₋₁₂ baseline data obtained from a training population in accordance with an embodiment of the present invention.

FIG. 24 illustrates the biomarker importance in the decision rule trained using the trees of FIG. 23. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 25 illustrates the overall accuracy, with 95% confidence interval bars, specificity, and sensitivity of a decision rule developed with predictive analysis of microarrays (PAM) using select biomarkers of the present invention and T₋₁₂ baseline data obtained from a training population.

FIG. 26 is a list of biomarkers, rank-ordered by their respective degrees of discriminatory power, identified by PAM using T₋₁₂ baseline data obtained from a training population. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 27 illustrates CART, PAM, and random forests classification algorithm (decision rule) performance data, and associated 95% confidence intervals, using T₋₁₂ baseline data obtained from a training population in accordance with an embodiment of the present invention.

FIG. 28 illustrates the number of times that common biomarkers were found to be important across the decision rules developed using (i) CART, (ii) PAM, (iii) random forests, and (iv) the Wilcoxon (adjusted) test using T₋₁₂ baseline data obtained from a training population.

FIG. 29 illustrates an overall ranking of biomarkers for data obtained using T₋₁₂ baseline data obtained from a training population. The biomarkers are referenced by their corresponding Affymetrix U133 plus 2.0 probeset names given in Table 30.

FIG. 30 illustrates the filters applied to identify biomarkers that discriminate between subjects that will get sepsis during a defined time period and subjects that will not get sepsis during the defined time period using data obtained from a training population, in accordance with an embodiment of the present invention. Other combinations of biomarkers are disclosed herein including, for example, in Section 5.3 and in Section 6.

FIG. 31 shows the correlation between IL18R1 expression, as determined by RT-PCR, and the intensity of the X206618_at probeset, as determined using Affymetrix U133 plus 2.0 microarray measurements, across a training population.

FIG. 32 shows the correlation between FCGR1A expression, as determined by RT-PCR, and the intensity of the X214511_x_at, X216950_s_at and X216951_at probesets, as determined using Affymetrix U133 plus 2.0 microarray measurements, across a training population.

FIG. 33 shows the correlation between MMP9 expression, as determined by RT-PCR, and the intensity of the X203936_s_at probeset, as determined using Affymetrix U133 plus 2.0 microarray measurements, across a training population.

FIG. 34 shows the correlation between CD86 expression, as determined by RT-PCR, and the intensity of the X205685_at, X205686_s_at, and X210895_s_at probesets, as determined using Affymetrix U133 plus 2.0 microarray measurements, across a training population.

FIG. 35 shows a computer system in accordance with the present invention.

FIG. 36 illustrates a classification and regression tree for discriminating between a SIRS phenotypic state characterized by the onset of sepsis and a SIRS phenotypic state characterized by the absence of sepsis using T₋₁₂ static data obtained from an RT-PCR discovery training population in accordance with an embodiment of the present invention.

FIG. 37 shows the distribution of feature values for seven biomarkers used in the decision tree of FIG. 36 across T₋₁₂ static data obtained from an RT-PCR discovery training population in accordance with an embodiment of the present invention.

FIG. 38 illustrates the overall accuracy, sensitivity, and specificity of 462 trees used to train a decision tree using the Random Forests method based upon T₋₂ static data obtained from an RT-PCR discovery training population in accordance with an embodiment of the present invention.

FIG. 39 illustrates the biomarker importance in the decision rule trained using the trees of FIG. 38.

FIG. 40 illustrates a calculation of biomarker importance, summing to 100%, determined by a multiple additive regression tree (MART) approach using T₋₁₂ static data obtained from an RT-PCR discovery training population.

FIG. 41 illustrates the distribution of feature values of the biomarkers selected by the MART approach illustrated in FIG. 40 between the Sepsis and SIRS groups using T-i static data obtained from an RT-PCR discovery training population.

FIG. 42 illustrates the overall accuracy, with 95% confidence interval bars, specificity, and sensitivity of a decision rule developed with predictive analysis of microarrays (PAM) using the biomarkers of the present invention using T₋₁₂ static data obtained from an RT-PCR discovery training population.

FIG. 43 is a list of biomarkers, rank-ordered by their respective degrees of discriminatory power, identified by PAM using T₋₂ static data obtained from an RT-PCR discovery training population.

FIG. 44 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals using T₋₁₂ static data obtained from an RT-PCR discovery training population.

FIG. 45 identified fifty selected biomarkers selected based on the decision rule performance summarized in FIG. 44.

FIG. 46 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals using T₋₁₂ static data obtained from an Affymetrix gene chip discovery training population.

FIG. 47 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals using T₋₁₂ static data obtained from an RT-PCR confirmatory training population.

FIG. 48 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals using T₋₁₂ static data obtained from a combined pool of a Affymetrix gene chip confirmatory training population and an RT-PCR confirmatory training population.

FIG. 49 illustrates a classification and regression tree for discriminating between a SIRS phenotypic state characterized by the onset of sepsis and a SIRS phenotypic state characterized by the absence of sepsis using T₋₁₂ static data obtained from a bead-based protein discovery training population in accordance with an embodiment of the present invention.

FIGS. 50A, 50B and 50C shows the distribution of feature values for ten biomarkers: (A) MIP1beta, thrombopoietin; (B) ICAM1, IL-10, adiponectin, alpha fetoprotein; and (C) IL-16, IL-6, beta-2 microglobulin, and C reactive protein; used in the decision tree of FIG. 49 across T₋₁₂ static data obtained from a bead-based protein discovery training population in accordance with an embodiment of the present invention.

FIG. 51 illustrates the overall accuracy, sensitivity, and specificity of 64 trees used to train a decision tree using the Random Forests method based upon T₋₁₂ static data obtained from a bead-based protein discovery training population in accordance with an embodiment of the present invention.

FIG. 52 illustrates the biomarker importance in the decision rule trained using the trees of FIG. 51.

FIG. 53 illustrates a calculation of biomarker importance, summing to 100%, determined by a multiple additive regression tree (MART) approach using T₋₁₂ static data obtained from a bead-based protein discovery training population in accordance with an embodiment of the present invention.

FIG. 54 illustrates the distribution of feature values of the biomarkers selected by the MART approach illustrated in FIG. 53 between the Sepsis and SIRS groups using T₋₁₂ static data obtained from a bead-based protein discovery training population in accordance with an embodiment of the present invention.

FIG. 55 illustrates the overall accuracy, with 95% confidence interval bars, specificity, and sensitivity of a decision rule developed with predictive analysis of microarrays (PAM) using the biomarkers of the present invention using T₋₁₂ static data obtained from a bead-based protein discovery training population in accordance with an embodiment of the present invention.

FIG. 56 is a list of biomarkers, rank-ordered by their respective degrees of discriminatory power, identified by PAM using T₋₁₂ static data obtained from a bead-based protein discovery training population in accordance with an embodiment of the present invention.

FIG. 57 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals using T₋₁ static data obtained from a bead-based protein discovery training population in accordance with an embodiment of the present invention.

FIG. 58 illustrates the number of times that common biomarkers were found to be important across the decision rules developed using (i) CART, (ii) MART, (iii) PAM, (iv) random forests, and (v) the Wilcoxon (adjusted) test using T₁₂ static data obtained from a bead-based protein discovery training population in accordance with an embodiment of the present invention.

FIG. 59 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals using T₋₁₂ static data obtained from a bead-based protein confirmation training population in accordance with an embodiment of the present invention.

FIGS. 60A and 60B plot the sepsis predicting accuracy of each of 24 families of subcombinations from Table J, using T₁₂ nucleic acid data, in a bar graph fashion, in accordance with an embodiment of the present invention: (A) 17-25 nucleotides; (B) 2-16 nucleotides.

FIGS. 61A and 61B plot the sepsis predicting performance (accuracy) of each individual subcombination in each of 24 families of subcombinations, for a total of 4800 subcombinations from Table J, using T₋₁₂ nucleic acid data, in accordance with an embodiment of the present invention: (A) 17-25 nucleotides; (B) 2-16 nucleotides.

FIGS. 62A and 62B plot the sepsis predicting accuracy of each of 8 families of subcombinations from Table K, using T₁₂ protein data, in a bar graph fashion, in accordance with an embodiment of the present invention: (A) 9-10 proteins; (B) 3-8 proteins.

FIGS. 63A and 63B plot the sepsis predicting performance (accuracy) of each individual subcombination in each of 8 families of subcombinations, for a total of 1600 subcombinations from Table K, using T₋₁₂ protein data, in accordance with an embodiment of the present invention: (A) 9-10 proteins; (B) 3-8 proteins.

FIGS. 64A and 64B plot the sepsis predicting accuracy of each of 8 families of subcombinations from Table K, using T₋₃ protein data, in a bar graph fashion, in accordance with an embodiment of the present invention: (A) 9-10 proteins; (B) 3-8 proteins.

FIGS. 65A and 65B plot the sepsis predicting performance (accuracy) of each individual subcombination in each of 8 families of subcombinations, for a total of 1600 subcombinations from Table K, using T₋₃ protein data, in accordance with an embodiment of the present invention: (A) 9-10 proteins; (B) 3-8 proteins.

FIGS. 66A and 66B plot the sepsis predicting accuracy of each of 23 families of subcombinations from Table J, using T₋₃₆ nucleic acid data, in a bar graph fashion, in accordance with an embodiment of the present invention: (A) 18-25 nucleotides; (B) 3-17 nucleotides.

FIGS. 67A and 67B plot the sepsis predicting performance (accuracy) of each individual subcombination in each of 23 families of subcombinations, for a total of 4600 subcombinations from Table J, using T₋₃₆ nucleic acid data, in accordance with an embodiment of the present invention: (A) 18-25 nucleotides; (B) 3-17 nucleotides.

FIGS. 68A and 68B plot the sepsis predicting accuracy of each of 23 families of subcombinations from Table I, using T₋₂ combined protein and nucleic acid data, in a bar graph fashion, in accordance with an embodiment of the present invention: (A) 18-25 gene expression and proteins; (B) 3-17 gene expression and proteins.

FIGS. 69A and 69B plot the sepsis predicting performance (accuracy) of each individual subcombination in each of 23 families of subcombinations, for a total of 4600 subcombinations from Table I, using T₋₁₂ combined protein and nucleic acid data, in accordance with an embodiment of the present invention: (A) 18-25 gene expression and proteins; (B) 3-17 gene expression and proteins.

FIGS. 70A and 70B plot the sepsis predicting accuracy of each of 23 families of subcombinations from Table I, using T₋₃₆ combined protein and nucleic acid data, in a bar graph fashion, in accordance with an embodiment of the present invention: (A) 18-25 gene expression and proteins; (B) 3-17 gene expression and proteins.

FIGS. 71A and 71B plot the sepsis predicting performance (accuracy) of each individual subcombination in each of 23 families of subcombinations, for a total of 4600 subcombinations from Table I, using T₋₃₆ combined protein and nucleic acid data, in accordance with an embodiment of the present invention: (A) 18-25 gene expression and proteins; (B) 3-17 gene expression and proteins.

5. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention allows for the rapid and accurate diagnosis or prediction of sepsis by evaluating biomarker features in biomarker profiles. These biomarker profiles can be constructed from one or more biological samples of subjects at a single time point (“snapshot”), or multiple such time points, during the course of time the subject is at risk for developing sepsis. Advantageously, sepsis can be diagnosed or predicted prior to the onset of conventional clinical sepsis symptoms, thereby allowing for more effective therapeutic intervention.

5.1 DEFINITIONS

“Systemic inflammatory response syndrome,” or “SIRS,” refers to a clinical response to a variety of severe clinical insults, as manifested by two or more of the following conditions within a 24-hour period:

• • body temperature greater than 38° C. (100.4° F.) or less than 36° C. (96.8° F.);
  • heart rate (HR) greater than 90 beats/minute;
  • respiratory rate (RR) greater than 20 breaths/minute, or P_CO2 less than 32 mmHg, or requiring mechanical ventilation; and
  • white blood cell count (WBC) either greater than 12.0×10⁹/L or less than 4.0×10⁹/L.

These symptoms of SIRS represent a consensus definition of SIRS that can be modified or supplanted by other definitions in the future. The present definition is used to clarify current clinical practice and does not represent a critical aspect of the invention (see, e.g., American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference: Definitions for Sepsis and Organ Failure and Guidelines for the Use of Innovative Therapies in Sepsis, 1992, Crit. Care. Med. 20, 864-874, the entire contents of which are herein incorporated by reference).

A subject with SIRS has a clinical presentation that is classified as SIRS, as defined above, but is not clinically deemed to be septic. Methods for determining which subjects are at risk of developing sepsis are well known to those in the art. Such subjects include, for example, those in an ICU and those who have otherwise suffered from a physiological trauma, such as a burn, surgery or other insult. A hallmark of SIRS is the creation of a proinflammatory state that can be marked by tachycardia, tachypnea or hyperpnea, hypotension, hypoperfusion, oliguria, leukocytosis or leukopenia, pyrexia or hypothermia and the need for volume infusion. SIRS characteristically does not include a documented source of infection (e.g., bacteremia).

“Sepsis” refers to a systemic host response to infection with SIRS plus a documented infection (e.g., a subsequent laboratory confirmation of a clinically significant infection such as a positive culture for an organism). Thus, sepsis refers to the systemic inflammatory response to a documented infection (see, e.g., American College of Chest Physicians Society of Critical Care Medicine, Chest, 1997, 101:1644-1655, the entire contents of which are herein incorporated by reference). As used herein, “sepsis” includes all stages of sepsis including, but not limited to, the onset of sepsis, severe sepsis, septic shock and multiple organ dysfunction (“MOD”) associated with the end stages of sepsis.

The “onset of sepsis” refers to an early stage of sepsis, e.g., prior to a stage when conventional clinical manifestations are sufficient to support a clinical suspicion of sepsis. Because the methods of the present invention are used to detect sepsis prior to a time that sepsis would be suspected using conventional techniques, the subject's disease status at early sepsis can only be confirmed retrospectively, when the manifestation of sepsis is more clinically obvious. The exact mechanism by which a subject becomes septic is not a critical aspect of the invention. The methods of the present invention can detect the onset of sepsis independent of the origin of the infectious process.

“Severe sepsis” refers to sepsis associated with organ dysfunction, hypoperfusion abnormalities, or sepsis-induced hypotension. Hypoperfusion abnormalities include, but are not limited to, lactic acidosis, oliguria, or an acute alteration in mental status.

“Septic shock” refers to sepsis-induced hypotension that is not responsive to adequate intravenous fluid challenge and with manifestations of peripheral hypoperfusion.

A “converter” or “converter subject” refers to a SIRS-positive subject who progresses to clinical suspicion of sepsis during the period the subject is monitored. typically during an ICU stay.

A “non-converter” or “non-converter subject” refers to a SIRS-positive subject who does not progress to clinical suspicion of sepsis during the period the subject is monitored, typically during an ICU stay.

A “biomarker” is virtually any detectable compound, such as a protein, a peptide, a proteoglycan, a glycoprotein, a lipoprotein, a carbohydrate, a lipid, a nucleic acid (e.g., DNA, such as cDNA or amplified DNA, or RNA, such as mRNA), an organic or inorganic chemical, a natural or synthetic polymer, a small molecule (e.g., a metabolite), or a discriminating molecule or discriminating fragment of any of the foregoing, that is present in or derived from a biological sample. “Derived from” as used in this context refers to a compound that, when detected, is indicative of a particular molecule being present in the biological sample. For example, detection of a particular cDNA can be indicative of the presence of a particular RNA transcript in the biological sample. As another example, detection of or binding to a particular antibody can be indicative of the presence of a particular antigen (e.g., protein) in the biological sample. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of an above-identified compound.

A biomarker can, for example, be isolated from the biological sample, directly measured in the biological sample, or detected in or determined to be in the biological sample. A biomarker can, for example, be functional, partially functional, or non-functional. In one embodiment of the present invention, a biomarker is isolated and used, for example, to raise a specifically-binding antibody that can facilitate biomarker detection in a variety of diagnostic assays. Any immunoassay may use any antibodies, antibody fragment or derivative thereof capable of binding the biomarker molecules (e.g., Fab, F(ab′)₂, Fv, or scFv fragments). Such immunoassays are well-known in the art. In addition, if the biomarker is a protein or fragment thereof, it can be sequenced and its encoding gene can be cloned using well-established techniques.

As used herein, the term “a species of a biomarker” refers to any discriminating portion or discriminating fragment of a biomarker described herein, such as a splice variant of a particular gene described herein (e.g., a gene listed in Table 30, or Table I, or Table J, or Table K, infra). Here, a discriminating portion or discriminating fragment is a portion or fragment of a molecule that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein.

As used herein, the terms “protein”, “peptide”, and “polypeptide” are, unless otherwise indicated, interchangeable.

A “biomarker profile” comprises a plurality of one or more types of biomarkers (e.g., an mRNA molecule, a cDNA molecule, a protein and/or a carbohydrate, etc.), or an indication thereof, together with a feature, such as a measurable aspect (e.g., abundance) of the biomarkers. A biomarker profile comprises at least two such biomarkers or indications thereof, where the biomarkers can be in the same or different classes, such as, for example, a nucleic acid and a carbohydrate. A biomarker profile may also comprise at least 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 100 or more biomarkers or indications thereof. In one embodiment, a biomarker profile comprises hundreds, or even thousands, of biomarkers or indications thereof. A biomarker profile can further comprise one or more controls or internal standards. In one embodiment, the biomarker profile comprises at least one biomarker, or indication thereof, that serves as an internal standard. In another embodiment, a biomarker profile comprises an indication of one or more types of biomarkers. The term “indication” as used herein in this context merely refers to a situation where the biomarker profile contains symbols, data, abbreviations or other similar indicia for a biomarker, rather than the biomarker molecular entity itself. For instance, consider an exemplary biomarker profile of the present invention that comprises the Affymetrix (Santa Clara, California) U133 plus 2.0 205013_s_at and 209369_at probesets. Another exemplary biomarker profile of the present invention comprises the name of genes used to derive the Affymetrix (Santa Clara, California) U133 plus 2.0 205013_s_at and 209369_at probesets. In still another exemplary biomarker profile of the present invention, the biomarker profile comprises a physical quantity of a transcript of a gene from which the 205013_s_at probeset was derived, and a physical quantity of a transcript of a gene from which the 209369_at probeset was derived. In another embodiment, the biomarker profile comprises a nominal indication of the quantity of a transcript of a gene from which the 205013_s_at probeset was derived and a nominal indication of the quantity of transcript of a gene from which the 209369_at probeset was derived. Still another exemplary biomarker profile of the present invention comprises a microarray to which a physical quantity of a gene transcript from which the 205013_s_at probeset was derived is bound at a first probe spot on the microarray and an abundance of a gene transcript from which the 209369_at probeset was derived is bound to a second probe spot on the microarray. In this last exemplary biomarker profile, at least twenty percent, forty percent, or more than forty percent of the probes spots are based on sequences in the probesets given in Table 30. In another exemplary biomarker profile, at least twenty percent, forty percent, or more than forty percent of the probes spots are based on sequences in the probesets given in Table 31.

Each biomarker in a biomarker profile includes a corresponding “feature.” A “feature”, as used herein, refers to a measurable aspect of a biomarker. A feature can include, for example, the presence or absence of biomarkers in the biological sample from the subject as illustrated in exemplary biomarker profile 1: Exemplary biomarker profile 1.

                     Feature
Biomarker            Presence in sample
transcript of gene A Present
transcript of gene B Absent

In exemplary biomarker profile 1, the feature value for the transcript of gene A is “presence” and the feature value for the transcript of gene B is “absence.”

A feature can include, for example, the abundance of a biomarker in the biological sample from a subject as illustrated in exemplary biomarker profile 2:

Exemplary Biomarker Profile 2.

                     Feature
                     Abundance in sample
Biomarker            in relative units
transcript of gene A 300
transcript of gene B 400

In exemplary biomarker profile 2, the feature value for the transcript of gene A is 300 units and the feature value for the transcript of gene B is 400 units.

A feature can also be a ratio of two or more measurable aspects of a biomarker as illustrated in exemplary biomarker profile 3: Exemplary biomarker profile 3.

                     Feature
                     Ratio of abundance of transcript of
Biomarker            gene A/transcript of gene B
transcript of gene A 300/400
transcript of gene B

In exemplary biomarker profile 3, the feature value for the transcript of gene A and the feature value for the transcript of gene B is 0.75 (300/400).

A feature may also be the difference between a measurable aspect of the corresponding biomarker that is taken from two samples, where the two samples are collected from a subject at two different time points. For example, consider the case where the biomarker is a transcript of a gene A and the “measurable aspect” is abundance of the transcript, in samples obtained from a test subject as determined by, e.g., RT-PCR or microarray analysis. In this example, the abundance of the transcript of gene A is measured in a first sample as well as a second sample. The first sample is taken from the test subject a number of hours before the second sample. To compute the feature for gene A, the abundance of the transcript of gene A in one sample is subtracted from the abundance of the transcript of gene A in the second sample. A feature can also be an indication as to whether an abundance of a biomarker is increasing in biological samples obtained from a subject over time and/or an indication as to whether an abundance of a biomarker is decreasing in biological samples obtained from a subject over time.

In some embodiments, there is a one-to-one correspondence between features and biomarkers in a biomarker profile as illustrated in exemplary biomarker profile 1, above. In some embodiments, the relationship between features and biomarkers in a biomarker profile of the present invention is more complex, as illustrated in Exemplary biomarker profile 3, above.

Those of skill in the art will appreciate that other methods of computation of a feature can be devised and all such methods are within the scope of the present invention. For example, a feature can represent the average of an abundance of a biomarker across biological samples collected from a subject at two or more time points. Furthermore, a feature can be the difference or ratio of the abundance of two or more biomarkers from a biological sample obtained from a subject in a single time point. A biomarker profile may also comprise at least three, four, five, 10, 20, 30 or more features. In one embodiment, a biomarker profile comprises hundreds, or even thousands, of features.

In some embodiments, features of biomarkers are measured using microarrays. The construction of microarrays and the techniques used to process microarrays in order to obtain abundance data is well known, and is described, for example, by Draghici, 2003, Data Analysis Tools for DNA Microarrays, Chapman & Hall/CRC, and international publication number WO 03/061564, each of which is hereby incorporated by reference in its entirety. A microarray comprises a plurality of probes. In some instances, each probe recognizes, e.g., binds to, a different biomarker. In some instances, two or more different probes on a microarray recognize, e.g., bind to, the same biomarker. Thus, typically, the relationship between probe spots on the microarray and a subject biomarker is a two to one correspondence, a three to one correspondence, or some other form of correspondence. However, it can be the case that there is a unique one-to-one correspondence between probes on a microarray and biomarkers.

A “phenotypic change” is a detectable change in a parameter associated with a given state of the subject. For instance, a phenotypic change can include an increase or decrease of a biomarker in a bodily fluid, where the change is associated with SIRS, sepsis, the onset of sepsis or with a particular stage in the progression of sepsis. A phenotypic change can further include a change in a detectable aspect of a given state of the subject that is not a change in a measurable aspect of a biomarker. For example, a change in phenotype can include a detectable change in body temperature, respiration rate, pulse, blood pressure, or other physiological parameter. Such changes can be determined via clinical observation and measurement using conventional techniques that are well-known to the skilled artisan.

As used herein, the term “complementary,” in the context of a nucleic acid sequence (e.g., a nucleotide sequence encoding a gene described herein), refers to the chemical affinity between specific nitrogenous bases as a result of their hydrogen bonding properties. For example, guanine (G) forms a hydrogen bond with only cytosine (C), while adenine forms a hydrogen bond only with thymine (T) in the case of DNA, and uracil (U) in the case of RNA. These reactions are described as base pairing, and the paired bases (G with C, or A with T/U) are said to be complementary. Thus, two nucleic acid sequences may be complementary if their nitrogenous bases are able to form hydrogen bonds. Such sequences are referred to as “complements” of each other. Such complement sequences can be naturally occurring, or, they can be chemically synthesized by any method known to those skilled in the art, as for example, in the case of antisense nucleic acid molecules which are complementary to the sense strand of a DNA molecule or an RNA molecule (e.g., an mRNA transcript). See, e.g., Lewin, 2002, Genes VII. Oxford University Press Inc., New York, NY, which is hereby incorporated by reference.

As used herein, “conventional techniques” in the context of diagnosing or predicting sepsis or SIRS are those techniques that classify a subject based on phenotypic changes without obtaining a biomarker profile according to the present invention.

A “decision rule” is a method used to evaluate biomarker profiles. Such decision rules can take on one or more forms that are known in the art, as exemplified in Hastie et al., 2001, The Elements of Statistical Learning, Springer-Verlag, New York. which is hereby incorporated by reference in its entirety. A decision rule may be used to act on a data set of features to, inter alia, predict the onset of sepsis, to determine the progression of sepsis, or to diagnose sepsis. Exemplary decision rules that can be used in some embodiments of the present invention are described in further detail in Section 5.5, below.

“Predicting the development of sepsis” is the determination as to whether a subject will develop sepsis. Any such prediction is limited by the accuracy of the means used to make this determination. The present invention provides a method, e.g., by utilizing a decision rule(s), for making this determination with an accuracy that is 60% or greater. As used herein, the terms “predicting the development of sepsis” and “predicting sepsis” are interchangeable. In some embodiments, the act of predicting the development of sepsis (predicting sepsis) is accomplished by evaluating one or more biomarker profiles from a subject using a decision rule that is indicative of the development of sepsis and, as a result of this evaluation, receiving a result from the decision rule that indicates that the subject will become septic. Such an evaluation of one or more biomarker profiles from a test subject using a decision rule uses some or all the features in the one or more biomarker profiles to obtain such a result.

The terms “obtain” and “obtaining,” as used herein, mean “to come into possession of,” or “coming into possession of,” respectively. This can be done, for example, by retrieving data from a data store in a computer system. This can also be done, for example, by direct measurement.

As used herein, the term “specifically,” and analogous terms, in the context of an antibody, refers to peptides, polypeptides, and antibodies or fragments thereof that specifically bind to an antigen or a fragment and do not specifically bind to other antigens or other fragments. A peptide or polypeptide that specifically binds to an antigen may bind to other peptides or polypeptides with lower affinity, as determined by standard experimental techniques, for example, by any immunoassay well-known to those skilled in the art. Such immunoassays include, but are not limited to, radioimmunoassays (RIAs) and enzyme-linked immunosorbent assays (ELISAs). Antibodies or fragments that specifically bind to an antigen may be cross-reactive with related antigens. Preferably, antibodies or fragments thereof that specifically bind to an antigen do not cross-react with other antigens. See, e.g., Paul, ed., 2003, Fundamental Immunology, 5th ed., Raven Press, New York at pages 69-105, which is incorporated by reference herein, for a discussion regarding antigen-antibody interactions, specificity and cross-reactivity, and methods for determining all of the above.

As used herein, a “subject” is an animal, preferably a mammal, more preferably a non-human primate, and most preferably a human. The terms “subject” “individual” and “patient” are used interchangeably herein.

As used herein, a “test subject,” typically, is any subject that is not in a training population used to construct a decision rule. A test subject can optionally be suspected of either having sepsis at risk of developing sepsis.

As used herein, a “tissue type,” is a type of tissue. A tissue is an association of cells of a multicellular organism, with a common embryoloical origin or pathway and similar structure and function. Often, cells of a tissue are contiguous at cell membranes but occasionally the tissue may be fluid (e.g., blood). Cells of a tissue may be all of one type (a simple tissue, e.g., squamous epithelium, plant parentchyma) or of more than one type (a mixed tissue, e.g., connective tissue).

As used herein, a “training population” is a set of samples from a population of subjects used to construct a decision rule, using a data analysis algorithm, for evaluation of the biomarker profiles of subjects at risk for developing sepsis. In a preferred embodiment, a training population includes samples from subjects that are converters and subjects that are nonconverters.

As used herein, a “data analysis algorithm” is an algorithm used to construct a decision rule using biomarker profiles of subjects in a training population. Representative data analysis algorithms are described in Section 5.5. A “decision rule” is the final product of a data analysis algorithm, and is characterized by one or more value sets, where each of these value sets is indicative of an aspect of SIRS, the onset of sepsis, sepsis, or a prediction that a subject will acquire sepsis. In one specific example, a value set represents a prediction that a subject will develop sepsis. In another example, a value set represents a prediction that a subject will not develop sepsis.

As used herein, a “validation population” is a set of samples from a population of subjects used to determine the accuracy of a decision rule. In a preferred embodiment, a validation population includes samples from subjects that are converters and subjects that are nonconverters. In a preferred embodiment, a validation population does not include subjects that are part of the training population used to train the decision rule for which an accuracy measurement is sought.

As used herein, a “value set” is a combination of values, or ranges of values for features in a biomarker profile. The nature of this value set and the values therein is dependent upon the type of features present in the biomarker profile and the data analysis algorithm used to construct the decision rule that dictates the value set. To illustrate, reconsider exemplary biomarker profile 2: Exemplary biomarker profile 2.

                     Feature
                     Abundance in sample
Biomarker            in relative units
transcript of gene A 300
transcript of gene B 400

In this example, the biomarker profile of each member of a training population is obtained. Each such biomarker profile includes a measured feature, here abundance, for the transcript of gene A, and a measured feature, here abundance, for the transcript of gene B. These feature values, here abundance values, are used by a data analysis algorithm to construct a decision rule. In this example, the data analysis algorithm is a decision tree, described in Section 5.5.1 and the final product of this data analysis algorithm, the decision rule, is a decision tree. An exemplary decision tree is illustrated in Figure. 1. The decision rule defines value sets. One such value set is predictive of the onset of sepsis. A subject whose biomarker feature values satisfy this value set is likely to become septic. An exemplary value set of this class is exemplary value set 1: Exemplary value set 1.

                     Value set component
                     (Abundance in sample
Biomarker            in relative units)
transcript of gene A <400
transcript of gene B <600

Another such value set is predictive of a septic-free state. A subject whose biomarker feature values satisfy this value set is not likely to become septic. An exemplary value set of this class is exemplary value set 2: Exemplary value set 2.

                     Value set component
                     (Abundance in sample
Biomarker            in relative units)
transcript of gene A >400
transcript of gene B >600

In the case where the data analysis algorithm is a neural network analysis and the final product of this neural network analysis is an appropriately weighted neural network, one value set is those ranges of biomarker profile feature values that will cause the weighted neural network to indicate that onset of sepsis is likely. Another value set is those ranges of biomarker profile feature values that will cause the weighted neural network to indicate that onset of sepsis is not likely.

As used herein, the term “probe spot” in the context of a microarray refers to a single stranded DNA molecule (e.g., a single stranded cDNA molecule or synthetic DNA oligomer), referred to herein as a “probe,” that is used to determine the abundance of a particular nucleic acid in a sample. For example, a probe spot can be used to determine the level of mRNA in a biological sample (e.g., a collection of cells) from a test subject. In a specific embodiment, a typical microarray comprises multiple probe spots that are placed onto a glass slide (or other substrate) in known locations on a grid. The nucleic acid for each probe spot is a single stranded contiguous portion of the sequence of a gene or gene of interest (e.g., a 10-mer, 11-mer, 12-mer, 13-mer, 14-mer, 15-mer, 16-mer, 17-mer, 18-mer, 19-mer, 20-mer, 21-mer, 22-mer, 23-mer, 24-mer, 25-mer or larger) and is a probe for the mRNA encoded by the particular gene or gene of interest. Each probe spot is characterized by a single nucleic acid sequence, and is hybridized under conditions that cause it to hybridize only to its complementary DNA strand or mRNA molecule. As such, there can be many probe spots on a substrate, and each can represent a unique gene or sequence of interest. In addition, two or more probe spots can represent the same gene sequence. In some embodiments, a labeled nucleic sample is hybridized to a probe spot, and the amount of labeled nucleic acid specifically hybridized to a probe spot can be quantified to determine the levels of that specific nucleic acid (e.g., mRNA transcript of a particular gene) in a particular biological sample. Probes, probe spots, and microarrays, generally, are described in Draghici, 2003, Data Analysis Tools for DNA Microarrays, Chapman & Hall/CRC, Chapter, 2, which is hereby incorporated by reference in its entirety.

As used herein, the term “annotation data” refers to any type of data that describes a property of a biomarker. Annotation data includes, but is not limited to, biological pathway membership, enzymatic class (e.g., phosphodiesterase, kinase, metalloproteinase, etc.), protein domain information, enzymatic substrate information, enzymatic reaction information, protein interaction data, disease association, cellular localization, tissue type localization, and cell type localization.

As used herein, the term “T₋₁₂” refers to the last time blood was obtained from a subject before the subject is clinically diagnosed with sepsis. Since, in the present invention, blood is collected from subjects each 24 hour period, T₋₁₂ references the average time period prior to the onset of sepsis for a pool of patients, with some patients turning septic prior to the 12 hour mark and some patients turning septic after the 12 hour mark. However, across a pool of subjects, the average time period for this last blood sample is the 12 hour mark, hence the name “T₋₁₂”

5.2 Methods for Screening Subjects

The present invention allows for accurate, rapid prediction and/or diagnosis of sepsis through detection of two or more features of a biomarker profile of a test individual suspected of or at risk for developing sepsis in each of one or more biological samples from a test subject. In one embodiment, only a single biological sample taken at a single point in time from the test subject is needed to construct a biomarker profile that is used to make this prediction or diagnosis of sepsis. In another embodiment, multiple biological samples taken at different points in time from the test subject are used to construct a biomarker profile that is used to make this prediction or diagnosis of sepsis.

In specific embodiments of the invention, subjects at risk for developing sepsis or SIRS are screened using the methods of the present invention. In accordance with these embodiments, the methods of the present invention can be employed to screen, for example, subjects admitted to an ICU and/or those who have experienced some sort of trauma (such as, e.g., surgery, vehicular accident, gunshot wound, etc.).

In specific embodiments, a biological sample such as, for example, blood, is taken upon admission. In some embodiments, a biological sample is blood, plasma, serum, saliva, sputum, urine, cerebral spinal fluid, cells, a cellular extract, a tissue specimen, a tissue biopsy, or a stool specimen. In some embodiments a biological sample is whole blood and this whole blood is used to obtain measurements for a biomarker profile. In some embodiments a biological sample is some component of whole blood. For example, in some embodiments some portion of the mixture of proteins, nucleic acid, and/or other molecules (e.g., metabolites) within a cellular fraction or within a liquid (e.g., plasma or serum fraction) of the blood is resolved as a biomarker profile. This can be accomplished by measuring features of the biomarkers in the biomarker profile. In some embodiments, the biological sample is whole blood but the biomarker profile is resolved from biomarkers in a specific cell type that is isolated from the whole blood. In some embodiments, the biological sample is whole blood but the biomarker profile is resolved from biomarkers expressed or otherwise found in monocytes that are isolated from the whole blood. In some embodiments, the biological sample is whole blood but the biomarker profile is resolved from biomarkers expressed or otherwise found in red blood cells that are isolated from the whole blood. In some embodiments, the biological sample is whole blood but the biomarker profile is resolved from biomarkers expressed or otherwise found in platelets that are isolated from the whole blood. In some embodiments, the biological sample is whole blood but the biomarker profile is resolved from biomarkers expressed or otherwise found in neutriphils that are isolated from the whole blood. In some embodiments, the biological sample is whole blood but the biomarker profile is resolved from biomarkers expressed or otherwise found in eosinophils that are isolated from the whole blood. In some embodiments, the biological sample is whole blood but the biomarker profile is resolved from biomarkers expressed or otherwise found in basophils that are isolated from the whole blood. In some embodiments, the biological sample is whole blood but the biomarker profile is resolved from biomarkers expressed or otherwise found in lymphocytes that are isolated from the whole blood. In some embodiments, the biological sample is whole blood but the biomarker profile is resolved from biomarkers expressed or otherwise found in monocytes that are isolated from the whole blood. In some embodiments, the biological sample is whole blood but the biomarker profile is resolved from one, two, three, four, five, six, or seven cell types from the group of cells types consisting of red blood cells, platelets, neutrophils, eosinophils, basophils, lymphocytes, and monocytes.

A biomarker profile comprises a plurality of one or more types of biomarkers (e.g., an mRNA molecule, a cDNA molecule, a protein and/or a carbohydrate, etc.), or an indication thereof, together with features, such as a measurable aspect (e.g., abundance) of the biomarkers. A biomarker profile can comprise at least two such biomarkers or indications thereof, where the biomarkers can be in the same or different classes, such as, for example, a nucleic acid and a carbohydrate. In some embodiments, a biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150, 155, 160, 165, 170, 175, 180, 185, 190, 195 or 200 or more biomarkers or indications thereof. In one embodiment, a biomarker profile comprises hundreds, or even thousands, of biomarkers or indications thereof. In some embodiments, a biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, or more biomarkers or indications thereof. In one example, in some embodiments, a biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, or more biomarkers selected from Table I of Section 5.11, or indications thereof. In another example, in some embodiments, a biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40 or more biomarkers selected from Table J of Section 5.11, or indications thereof. In another example, in some embodiments, a biomarker profile comprises any 2, 3, 4, 5, 6, 7, 8, 9, or all ten biomarkers in Table K of Section 5.11. or indications thereof.

In typical embodiments, each biomarker in the biomarker profile is represented by a feature. In other words, there is a correspondence between biomarkers and features. In some embodiments, the correspondence between biomarkers and features is 1:1, meaning that for each biomarker there is a feature. In some embodiments, there is more than one feature for each biomarker. In some embodiments the number of features corresponding to one biomarker in the biomarker profile is different than then number of features corresponding to another biomarker in the biomarker profile. As such, in some embodiments, a biomarker profile can include at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150, 155, 160, 165, 170, 175, 180, 185, 190, 195 or 200 or more features, provided that there are at least 2, 3, 4, 5, 6, or 7 or more biomarkers in the biomarker profile. In some embodiments, a biomarker profile can include at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, or more features. Regardless of embodiment, these features can be determined through the use of any reproducible measurement technique or combination of measurement techniques. Such techniques include those that are well known in the art including any technique described herein or, for example, any technique disclosed in Section 5.4, infra. Typically, such techniques are used to measure feature values using a biological sample taken from a subject at a single point in time or multiple samples taken at multiple points in time. In one embodiment, an exemplary technique to obtain a biomarker profile from a sample taken from a subject is a cDNA microarray (see, e.g., Section 5.4.1.2 and Section 6, infra). In another embodiment, an exemplary technique to obtain a biomarker profile from a sample taken from a subject is a protein-based assay or other form of protein-based technique such as described in the BD Cytometric Bead Array (CBA) Human Inflammation Kit Instruction Manual (BD Biosciences) or the bead assay described in U.S. Pat. No. 5,981,180, each of which is incorporated herein by reference in their entirety, and in particular for their teachings of various methods of assay protein concentrations in biological samples. In still another embodiment, the biomarker profile is mixed, meaning that it comprises some biomarkers that are nucleic acids, or indications thereof, and some biomarkers that are proteins, or indications thereof. In such embodiments, both protein based and nucleic acid based techniques are used to obtain a biomarker profile from one or more samples taken from a subject. In other words, the feature values for the features associated with the biomarkers in the biomarker profile that are nucleic acids are obtained by nucleic acid based measurement techniques (e.g., a nucleic acid microarray) and the feature values for the features associated with the biomarkers in the biomarker profile that are proteins are obtained by protein based measurement techniques. In some embodiments biomarker profiles can be obtained using a kit, such as a kit described in Section 5.3 below.

In specific embodiments, a subject is screened using the methods and compositions of the invention as frequently as necessary (e.g., during their stay in the ICU) to diagnose or predict sepsis or SIRS in a subject. In a preferred embodiment, the subject is screened soon after they arrive in the ICU. In some embodiments, the subject is screened daily after they arrive in the ICU. In some embodiments, the subject is screened every 1 to 4 hours, 1 to 8 hours, 8 to 12 hours, 12 to 16 hours, or 16 to 24 hours after they arrive in the ICU.

5.3 Kits

The invention also provides kits that are useful in diagnosing or predicting the development of sepsis or diagnosing SIRS in a subject. In some embodiments, the kits of the present invention comprise at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150, 155, 160, 165, 170, 175, 180, 185, 190, 195 or 200 or more biomarkers and/or reagents to detect the presence or abundance of such biomarkers. In other embodiments, the kits of the present invention comprise at least 2, but as many as several hundred or more biomarkers. In some embodiments, the kits of the present invention comprise at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50 or more biomarkers selected from Table I of Section 5.11. In some embodiments, the kits of the present invention comprise at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40 or more biomarkers selected from Table J of Section 5.11. In some embodiments, the kits of the present invention comprise at least 2, 3, 4, 5, 6, 7, 8, 9, or all 10 of the biomarkers in Table K of Section 5.11. In accordance with the definition of biomarkers given in Section 5.1, in some instances, a biomarker is in fact a discriminating molecule of, for example, a gene, mRNA, or protein rather than the gene, mRNA, or protein itself. Thus, a biomarker could be a molecule that indicates the presence or abundance of a particular gene or protein, or fragment thereof, identified in any one of Tables 1, J, or K of Section 5.11 rather than the actual gene or protein itself. Such discriminating molecules are sometimes referred to in the art as “reagents.” In some embodiments, the kits of the present invention comprise at least 2, but as many as several hundred or more biomarkers.

The biomarkers of the kits of the present invention can be used to generate biomarker profiles according to the present invention. Examples of classes of compounds of the kit include, but are not limited to, proteins and fragments thereof, peptides, proteoglycans, glycoproteins, lipoproteins, carbohydrates, lipids, nucleic acids (e.g., DNA, such as cDNA or amplified DNA, or RNA, such as mRNA), organic or inorganic chemicals, natural or synthetic polymers, small molecules (e.g., metabolites), or discriminating molecules or discriminating fragments of any of the foregoing. In a specific embodiment, a biomarker is of a particular size, (e.g., at least 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150, 155, 160, 165, 170, 175, 180, 185, 190, 195, 200, 1000, 2000, 3000, 5000, 10 k, 20 k, 100 k Daltons or greater). The biomarker(s) may be part of an array, or the biomarker(s) may be packaged separately and/or individually. The kit may also comprise at least one internal standard to be used in generating the biomarker profiles of the present invention. Likewise, the internal standard or standards can be any of the classes of compounds described above.

In one embodiment, the invention provides kits comprising probes and/or primers that may or may not be immobilized at an addressable position on a substrate, such as found, for example, in a microarray. In a particular embodiment, the invention provides such a microarray.

In a specific embodiment, the invention provides a kit for predicting the development of sepsis in a test subject that comprises a plurality of antibodies that specifically bind the protein-based biomarkers listed in any one of Tables 30, 31, 32, 33, 34, 36, 1, J, or K. In such embodiments, the antibodies themselves are biomarkers within the scope of the present invention. In accordance with this embodiment, the kit may comprise a set of antibodies or functional fragments or derivatives thereof (e.g., Fab, F(ab′)₂, Fv, or scFv fragments) that specifically bind at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150, 155, 160, 165, 170, 175, 180, 185, 190, 195 or 200 or more of the protein-based biomarkers set forth in any one of Tables 30, 31, 32, 33, 34, 36, 1, J, or K. In accordance with this embodiment, the kit may include antibodies, fragments or derivatives thereof (e.g., Fab, F(ab′)₂, Fv, or scFv fragments) that are specific for the biomarkers of the present invention. In one embodiment, the antibodies may be detectably labeled.

In a specific embodiment, the invention provides a kit for predicting the development of sepsis in a test subject comprises a plurality of antibodies that specifically bind a plurality of the protein-based biomarkers listed in Table I of Section 5.11. In accordance with this embodiment, the kit may comprise a set of antibodies or functional fragments or derivatives thereof (e.g., Fab, F(ab′)₂, Fv, or scFv fragments) that specifically bind at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50 or more of the biomarkers set forth in Table I. In accordance with this embodiment, the kit may include antibodies, fragments or derivatives thereof (e.g., Fab, F(ab′)₂, Fv, or scFv fragments) that are specific for the biomarkers of the present invention. In one embodiment, the antibodies may be detectably labeled.

In other embodiments of the invention, a kit may comprise a specific biomarker binding component, such as an aptamer. If the biomarkers comprise a nucleic acid, the kit may provide an oligonucleotide probe that is capable of forming a duplex with the biomarker or with a complementary strand of a biomarker. The oligonucleotide probe may be detectably labeled. In such embodiments, the probes are themselves biomarkers that fall within the scope of the present invention.

The kits of the present invention may also include additional compositions, such as buffers, that can be used in constructing the biomarker profile. Prevention of the action of microorganisms can be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include isotonic agents such as sugars, sodium chloride, and the like.

Some kits of the present invention comprise a microarray. In one embodiment this microarray comprises a plurality of probe spots, wherein at least twenty percent of the probe spots in the plurality of probe spots correspond to biomarkers in any one of Tables 30, 31, 32, 33, 34, 36, 1, J, or K. In some embodiments, at least twenty-five percent, at least thirty percent, at least thirty-five percent, at least forty percent, or at least sixty percent, or at least eighty percent of the probe spots in the plurality of probe spots correspond to biomarkers in any one of Tables 30, 31, 32, 33, 34, 36, I, J, or K. Such probe spots are biomarkers within the scope of the present invention. In some embodiments, the microarray consists of between about three and about one hundred probe spots on a substrate. In some embodiments, the microarray consists of between about three and about one hundred probe spots on a substrate. As used in this context, the term “about” means within five percent of the stated value, within ten percent of the stated value, or within twenty-five percent of the stated value. In some embodiments, such microarrays contain one or more probe spots for inter-microarray calibration or for calibration with other microarrays such as reference microarrays using techniques that are known to those of skill in the art. In some embodiments such microarrays are nucleic acid microarrays. In some embodiments, such microarrays are protein microarrays.

Some kits of the invention may further comprise a computer program product for use in conjunction with a computer system, wherein the computer program product comprises a computer readable storage medium and a computer program mechanism embedded therein. In such kits, the computer program mechanism comprises instructions for evaluating whether a plurality of features in a biomarker profile of a test subject at risk for developing sepsis satisfies a first value set. Satisfying the first value set predicts that the test subject is likely to develop sepsis. In one embodiment, the plurality of features corresponds to biomarkers listed in any one of Tables 30, 31, 32, 33, 34, 36, 1. J, or K. In some kits, the computer program product further comprises instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a second value set. Satisfying the second value set predicts that the test subject is not likely to develop sepsis.

Some kits of the present invention comprise a computer having a central processing unit and a memory coupled to the central processing unit. The memory stores instructions for evaluating whether a plurality of features in a biomarker profile of a test subject at risk for developing sepsis satisfies a first value set. Satisfying the first value set predicts that the test subject is likely to develop sepsis. In one embodiment, the plurality of features corresponds to biomarkers listed in any one of Tables 30, 31, 32, 33, 34, 36, I, J, or K.

FIG. 35 details an exemplary system that supports the functionality described above. The system is preferably a computer system 10 having:

• • a central processing unit 22;
  • a main non-volatile storage unit 14, for example, a hard disk drive, for storing software and data, the storage unit 14 controlled by storage controller 12;
  • a system memory 36, preferably high speed random-access memory (RAM), for storing system control programs, data, and application programs, comprising programs and data loaded from non-volatile storage unit 14: system memory 36 may also include read-only memory (ROM);
  • a user interface 32, comprising one or more input devices (e.g., keyboard 28) and a display 26 or other output device;
  • a network interface card 20 for connecting to any wired or wireless communication network 34 (e.g., a wide area network such as the Internet);
  • an internal bus 30 for interconnecting the aforementioned elements of the system; and
  • a power source 24 to power the aforementioned elements.

Operation of computer 10 is controlled primarily by operating system 40, which is executed by central processing unit 22. Operating system 40 can be stored in system memory 36. In addition to operating system 40, in a typical implementation, system memory 36 includes:

• • file system 42 for controlling access to the various files and data structures used by the present invention;
  • a training data set 44 for use in construction one or more decision rules in accordance with the present invention;
  • a data analysis algorithm module 54 for processing training data and constructing decision rules;
  • one or more decision rules 56;
  • a biomarker profile evaluation module 60 for determining whether a plurality of features in a biomarker profile of a test subject satisfies a first value set or a second value set;
  • a test subject biomarker profile 62 comprising biomarkers 64 and, for each such biomarkers, features 66; and
  • a database 68 of select biomarkers of the present invention (e.g., Table 30 and/or Table I and/or Table J and/or Table K, and/or Table L and/or Table M and/or Table N and/or Table O etc.) and/or one or features for each of these select biomarkers.

Training data set 46 comprises data for a plurality of subjects 46. For each subject 46 there is a subject identifier 48 and a plurality of biomarkers 50. For each biomarker 50, there is at least one feature 52. Although not shown in FIG. 35, for each feature 52, there is a feature value. For each decision rule 56 constructed using data analysis algorithms, there is at least one decision rule value set 58.

As illustrated in FIG. 35, computer 10 comprises software program modules and data structures. The data structures stored in computer 10 include training data set 44, decision rules 56, test subject biomarker profile 62, and biomarker database 68. Each of these data structures can comprise any form of data storage system including, but not limited to, a flat ASCII or binary file, an Excel spreadsheet, a relational database (SQL), or an on-line analytical processing (OLAP) database (MDX and/or variants thereof). In some specific embodiments, such data structures are each in the form of one or more databases that include hierarchical structure (e.g., a star schema). In some embodiments, such data structures are each in the form of databases that do not have explicit hierarchy (e.g., dimension tables that are not hierarchically arranged).

In some embodiments, each of the data structures stored or accessible to system 10 are single data structures. In other embodiments, such data structures in fact comprise a plurality of data structures (e.g., databases, files, archives) that may or may not all be hosted by the same computer 10. For example, in some embodiments, training data set 44 comprises a plurality of Excel spreadsheets that are stored either on computer 10 and/or on computers that are addressable by computer 10 across wide area network 34. In another example, training data set 44 comprises a database that is either stored on computer 10 or is distributed across one or more computers that are addressable by computer 10 across wide area network 34.

It will be appreciated that many of the modules and data structures illustrated in FIG. 35 can be located on one or more remote computers. For example, some embodiments of the present application are web service-type implementations. In such embodiments, biomarker profile evaluation module 60 and/or other modules can reside on a client computer that is in communication with computer 10 via network 34. In some embodiments, for example, biomarker profile evaluation module 60 can be an interactive web page.

In some embodiments, training data set 44, decision rules 56, and/or biomarker database 68 illustrated in FIG. 35 are on a single computer (computer 10) and in other embodiments one or more of such data structures and modules are hosted by one or more remote computers (not shown). Any arrangement of the data structures and software modules illustrated in FIG. 35 on one or more computers is within the scope of the present invention so long as these data structures and software modules are addressable with respect to each other across network 34 or by other electronic means. Thus, the present invention fully encompasses a broad array of computer systems.

Still another kit of the present invention comprises computers and computer readable media for evaluating whether a test subject is likely to develop sepsis or SIRS. For instance, one embodiment of the present invention provides a computer program product for use in conjunction with a computer system. The computer program product comprises a computer readable storage medium and a computer program mechanism embedded therein. The computer program mechanism comprises instructions for evaluating whether a plurality of features in a biomarker profile of a test subject at risk for developing sepsis satisfies a first value set. Satisfaction of the first value set predicts that the test subject is likely to develop sepsis. The plurality of features are measurable aspects of a plurality of biomarkers, the plurality of biomarkers comprising at least three biomarkers listed in Table I. In certain embodiments, the plurality of biomarkers comprises at least six biomarkers listed in Table I, wherein the plurality of biomarkers comprises both IL-6 and IL-8. In some embodiments, the computer program product further comprises instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a second value set. Satisfaction of the second value set predicts that the test subject is not likely to develop sepsis. In some embodiments, the biomarker profile has between 3 and 50 biomarkers listed in Table I, between 3 and 40 biomarkers listed in Table I, at least four biomarkers listed in Table I, or at least eight biomarkers listed in Table 1.

Another kit of the present invention comprises a central processing unit and a memory coupled to the central processing unit. The memory stores instructions for evaluating whether a plurality of features in a biomarker profile of a test subject at risk for developing sepsis satisfies a first value set. Satisfaction of the first value set predicts that the test subject is likely to develop sepsis. The plurality of features are measurable aspects of a plurality of biomarkers. This plurality of biomarkers comprises at least three biomarkers from Table I. In some embodiments, the plurality of biomarkers comprises at least six biomarkers listed in Table I when the plurality of biomarkers comprises both IL-6 and IL-8. In some embodiments, the memory further stores instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a second value set, wherein satisfying the second value set predicts that the test subject is not likely to develop sepsis. In some embodiments, the biomarker profile consists of between 3 and 50 biomarkers listed in Table I, between 3 and 40 biomarkers listed in Table I, at least four biomarkers listed in Table I., or at least eight biomarkers listed in Table I.

Another kit in accordance with the present invention comprises a computer system for determining whether a subject is likely to develop sepsis. The computer system comprises a central processing unit and a memory, coupled to the central processing unit. The memory stores instructions for obtaining a biomarker profile of a test subject. The biomarker profile comprises a plurality of features. Each feature in the plurality of features is a measurable aspect of a corresponding biomarker in a plurality of biomarkers. The plurality of biomarkers comprises at least three biomarkers listed in Table I. The memory further comprises instructions for transmitting the biomarker profile to a remote computer. The remote computer includes instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a first value set. Satisfaction of the first value set predicts that the test subject is likely to develop sepsis. The memory further comprises instructions for receiving a determination, from the remote computer, as to whether the plurality of features in the biomarker profile of the test subject satisfies the first value set. The memory also comprises instructions for reporting whether the plurality of features in the biomarker profile of the test subject satisfies the first value set. In some embodiments, the plurality of biomarkers comprises at least six biomarkers listed in Table I when the plurality of biomarkers comprises both IL-6 and IL-8. In some embodiments, the remote computer further comprises instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a second value set. Satisfaction of the second value set predicts that the test subject is not likely to develop sepsis. In such embodiments, the memory further comprises instructions for receiving a determination, from the remote computer, as to whether the plurality of features in the biomarker profile of the test subject satisfies the second set as well as instructions for reporting whether the plurality of features in the biomarker profile of the test subject satisfies the second value set. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least six biomarkers listed in Table I.

Still another aspect of the present invention comprises a digital signal embodied on a carrier wave comprising a respective value for each of a plurality of features in a biomarker profile. The plurality of features are measurable aspects of a plurality of biomarkers. The plurality of biomarkers comprises at least three biomarkers listed in Table 1. In some embodiments, the plurality of biomarkers comprises at least six biomarkers listed in Table I when the plurality of biomarkers comprises both IL-6 and TL-8. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least eight biomarkers listed in Table I.

Still another aspect of the present invention provides a digital signal embodied on a carrier wave comprising a determination as to whether a plurality of features in a biomarker profile of a test subject satisfies a value set. The plurality of features are measurable aspects of a plurality of biomarkers. This plurality of biomarkers comprises at least three biomarkers listed in Table I. Satisfying the value set predicts that the test subject is likely to develop sepsis. In some embodiments, the plurality of biomarkers comprises at least six biomarkers listed in Table 1 when the plurality of biomarkers comprises both 1L-6 and IL-8. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least eight biomarkers listed in Table I.

Still another embodiment provides a digital signal embodied on a carrier wave comprising a determination as to whether a plurality of features in a biomarker profile of a test subject satisfies a value set. The plurality of features are measurable aspects of a plurality of biomarkers. The plurality of biomarkers comprise at least three biomarkers listed in Table I. Satisfaction of the value set predicts that the test subject is not likely to develop sepsis. In some embodiments, the plurality of biomarkers comprises at least six biomarkers listed in Table I when the plurality of biomarkers comprises both IL-6 and IL-8. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least eight biomarkers listed in Table I.

Still another embodiment of the present invention provides a graphical user interface for determining whether a subject is likely to develop sepsis. The graphical user interface comprises a display field for a displaying a result encoded in a digital signal embodied on a carrier wave received from a remote computer. The plurality of features are measurable aspects of a plurality of biomarkers. The plurality of biomarkers comprise at least three biomarkers listed in Table I. The result has a first value when a plurality of features in a biomarker profile of a test subject satisfies a first value set. The result has a second value when a plurality of features in a biomarker profile of a test subject satisfies a second value set. In some embodiments, the plurality of biomarkers comprises at least six biomarkers listed in Table I when the plurality of biomarkers comprises IL-6 and IL-8. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least eight biomarkers listed in Table I.

Yet another kit of the present invention provides a computer system for determining whether a subject is likely to develop sepsis. The computer system comprises a central processing unit and a memory, coupled to the central processing unit. The memory stores instructions for obtaining a biomarker profile of a test subject. The biomarker profile comprises a plurality of features. The plurality of features are measurable aspects of a plurality of biomarkers. The plurality of biomarkers comprise at least three biomarkers listed in Table I. The memory further stores instructions for evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a first value set. Satisfying the first value set predicts that the test subject is likely to develop sepsis. The memory also stores instructions for reporting whether the plurality of features in the biomarker profile of the test subject satisfies the first value set. In some embodiments, the plurality of biomarkers comprises at least six biomarkers listed in Table I when the plurality of biomarkers comprises both IL-6 and IL-8. In some embodiments, the plurality of biomarkers comprises at least four biomarkers listed in Table I. In some embodiments, the plurality of biomarkers comprises at least eight biomarkers listed in Table I.

5.4 Generation of Biomarker Profiles

According to one embodiment, the methods of the present invention comprise generating a biomarker profile from a biological sample taken from a subject. The biological sample may be, for example, whole blood, plasma, serum, red blood cells, platelets, neutrophils, eosinophils, basophils, lymphocytes, monocytes, saliva, sputum, urine, cerebral spinal fluid, cells, a cellular extract, a tissue sample, a tissue biopsy, a stool sample or any sample that may be obtained from a subject using techniques well known to those of skill in the art. In a specific embodiment, a biomarker profile is determined using samples collected from a subject at one or more separate time points. In another specific embodiment, a biomarker profile is generated using samples obtained from a subject at separate time points. In one example, these samples are obtained from the subject either once or, alternatively, on a daily basis, or more frequently, e.g., every 4, 6, 8 or 12 hours. In a specific embodiment, a biomarker profile is determined using samples collected from a single tissue type. In another specific embodiment, a biomarker profile is determined using samples collected from at least two different tissue types.

5.4.1 Methods of Detecting Nucleic Add Biomarkers

In specific embodiments of the invention, biomarkers in a biomarker profile are nucleic acids. Such biomarkers and corresponding features of the biomarker profile may be generated, for example, by detecting the expression product (e.g., a polynucleotide or polypeptide) of one or more genes described herein (e.g., a gene listed in Table 30. Table I, Table J, or Table K.). In a specific embodiment, the biomarkers and corresponding features in a biomarker profile are obtained by detecting and/or analyzing one or more nucleic acids expressed from a gene disclosed herein (e.g., a gene listed in Table 30, Table I, Table J, or Table K) using any method well known to those skilled in the art including, but by no means limited to, hybridization, microarray analysis, RT-PCR, nuclease protection assays and Northern blot analysis.

In certain embodiments, nucleic acids detected and/or analyzed by the methods and compositions of the invention include RNA molecules such as, for example, expressed RNA molecules which include messenger RNA (mRNA) molecules, mRNA spliced variants as well as regulatory RNA, cRNA molecules (e.g., RNA molecules prepared from cDNA molecules that are transcribed in vitro) and discriminating fragments thereof. Nucleic acids detected and/or analyzed by the methods and compositions of the present invention can also include, for example, DNA molecules such as genomic DNA molecules, cDNA molecules, and discriminating fragments thereof (e.g., oligonucleotides, ESTs, STSs, etc.).

The nucleic acid molecules detected and/or analyzed by the methods and compositions of the invention may be naturally occurring nucleic acid molecules such as genomic or extragenomic DNA molecules isolated from a sample, or RNA molecules, such as mRNA molecules, present in, isolated from or derived from a biological sample. The sample of nucleic acids detected and/or analyzed by the methods and compositions of the invention comprise, e.g., molecules of DNA, RNA, or copolymers of DNA and RNA. Generally, these nucleic acids correspond to particular genes or alleles of genes, or to particular gene transcripts (e.g., to particular mRNA sequences expressed in specific cell types or to particular cDNA sequences derived from such mRNA sequences). The nucleic acids detected and/or analyzed by the methods and compositions of the invention may correspond to different exons of the same gene, e.g., so that different splice variants of that gene may be detected and/or analyzed.

In specific embodiments, the nucleic acids are prepared in vitro from nucleic acids present in, or isolated or partially isolated from biological a sample. For example, in one embodiment, RNA is extracted from a sample (e.g., total cellular RNA, poly(A)+messenger RNA, fraction thereof) and messenger RNA is purified from the total extracted RNA. Methods for preparing total and poly(A)+RNA are well known in the art, and are described generally, e.g., in Sambrook et al., 2001, Molecular Cloning: A Laboratory Manual. 3^rd ed. Cold Spring Harbor Laboratory Press (Cold Spring Harbor, New York), which is incorporated by reference herein in its entirety. In one embodiment, RNA is extracted from a sample using guanidinium thiocyanate lysis followed by CsCl centrifugation and an oligo dT purification (Chirgwin et al., 1979, Bichemistrv 18:5294-5299). In another embodiment, RNA is extracted from a sample using guanidinium thiocyanate lysis followed by purification on RNeasy columns (Qiagen, Valencia, California). cDNA is then synthesized from the purified mRNA using, e.g., oligo-dT or random primers. In specific embodiments, the target nucleic acids are cRNA prepared from purified messenger RNA extracted from a sample. As used herein, cRNA is defined here as RNA complementary to the source RNA. The extracted RNAs are amplified using a process in which doubled-stranded cDNAs are synthesized from the RNAs using a primer linked to an RNA polymerase promoter in a direction capable of directing transcription of anti-sense RNA. Anti-sense RNAs or cRNAs are then transcribed from the second strand of the double-stranded cDNAs using an RNA polymerase (see, e.g., U.S. Pat. Nos. 5,891,636, 5,716,785; 5,545,522 and 6,132,997, which are hereby incorporated by reference). Both oligo-dT primers (U.S. Pat. Nos. 5,545,522 and 6,132,997, hereby incorporated by reference herein) or random primers that contain an RNA polymerase promoter or complement thereof can be used. In some embodiments the target nucleic acids are short and/or fragmented nucleic acid molecules which are representative of the original nucleic acid population of the sample.

In one embodiment, nucleic acids of the invention can be detectably labeled. For example, cDNA can be labeled directly, e.g., with nucleotide analogs, or indirectly, e.g., by making a second, labeled cDNA strand using the first strand as a template. Alternatively, the double-stranded cDNA can be transcribed into cRNA and labeled.

In some embodiments the detectable label is a fluorescent label, e.g., by incorporation of nucleotide analogs. Other labels suitable for use in the present invention include, but are not limited to, biotin, imminobiotin, antigens, cofactors, dinitrophenol, lipoic acid, olefinic compounds, detectable polypeptides, electron rich molecules, enzymes capable of generating a detectable signal by action upon a substrate, and radioactive isotopes. Suitable radioactive isotopes include ³²P, ³⁵S, ²⁴C, ¹⁵N and ¹²⁵I. Fluorescent molecules suitable for the present invention include, but are not limited to, fluorescein and its derivatives, rhodamine and its derivatives, Texas red, 5′carboxy-fluorescein (“FMA”), 6-carboxy-4′,5′-dichloro-2′,7′-dimethoxyfluorescein, succinimidyl ester (“JOE”), 6-carboxytetramethylrhodamine (“TAMRA”), 6 carboxy-X-rhodamine (“ROX”), HEX, TET, IRD40, and IRD41. Fluorescent molecules that are suitable for the invention further include, but are not limited to: cyamine dyes. including by not limited to Cy3, Cy3.5 and Cy5; BODIPY dyes including but not limited to BODIPY-FL, BODIPY-TR, BODIPY-TMR, BODIPY-630/650, BODIPY-650/670; and ALEXA dyes, including but not limited to ALEXA-488, ALEXA-532, ALEXA-546, ALEXA-568, and ALEXA-594; as well as other fluorescent dyes which will be known to those who are skilled in the art. Electron-rich indicator molecules suitable for the present invention include, but are not limited to, ferritin, hemocyanin, and colloidal gold. Alternatively, in some embodiments the target nucleic acids may be labeled by specifically complexing a first group to the nucleic acid. A second group, covalently linked to an indicator molecules and which has an affinity for the first group, can be used to indirectly detect the target nucleic acid. In such an embodiment, compounds suitable for use as a first group include, but are not limited to, biotin and iminobiotin. Compounds suitable for use as a second group include, but are not limited to, avidin and streptavidin.

5.4.1.1 Nucleic Add Arrays

In certain embodiments of the invention, nucleic acid arrays are employed to generate features of biomarkers in a biomarker profile by detecting the expression of any one or more of the genes described herein (e.g., a gene listed in Table 30. Table I, Table J or Table K). In one embodiment of the invention, a microarray, such as a cDNA microarray, is used to determine feature values of biomarkers in a biomarker profile. The diagnostic use of cDNA arrays is well known in the art. (See, e.g., Zou et. al., 2002, Oncogene 21:4855-4862; as well as Draghici, 2003, Data Analysis Tools for DNA Microarrays, Chapman & Hall/CRC, each of which is hereby incorporated by reference herein in its entirety). Exemplary methods for cDNA microarray analysis are described below, and in the examples in Section 6, infra.

In certain embodiments, the feature values for biomarkers in a biomarker profile are obtained by hybridizing to the array detectably labeled nucleic acids representing or corresponding to the nucleic acid sequences in mRNA transcripts present in a biological sample (e.g., fluorescently labeled cDNA synthesized from the sample) to a microarray comprising one or more probe spots.

Nucleic acid arrays, for example, microarrays, can be made in a number of ways, of which several are described herein below. Preferably, the arrays are reproducible, allowing multiple copies of a given array to be produced and results from said microarrays compared with each other. Preferably, the arrays are made from materials that are stable under binding (e.g., nucleic acid hybridization) conditions. Those skilled in the art will know of suitable supports, substrates or carriers for hybridizing test probes to probe spots on an array, or will be able to ascertain the same by use of routine experimentation.

Arrays, for example, microarrays, used can include one or more test probes. In some embodiments each such test probe comprises a nucleic acid sequence that is complementary to a subsequence of RNA or DNA to be detected. Each probe typically has a different nucleic acid sequence, and the position of each probe on the solid surface of the array is usually known or can be determined. Arrays useful in accordance with the invention can include, for example, oligonucleotide microarrays, cDNA based arrays, SNP arrays, spliced variant arrays and any other array able to provide a qualitative, quantitative or semi-quantitative measurement of expression of a gene described herein (e.g., a gene listed in Table 30, Table I, Table J or Table K). Some types of microarrays are addressable arrays. More specifically, some microarrays are positionally addressable arrays. In some embodiments, each probe of the array is located at a known, predetermined position on the solid support so that the identity (e.g., the sequence) of each probe can be determined from its position on the array (e.g., on the support or surface). In some embodiments, the arrays are ordered arrays. Microarrays are generally described in Draghici, 2003, Data Analysis Tools for DNA Microarrays, Chapman & Hall/CRC, which is hereby incorporated herein by reference in its entirety.

In some embodiments of the present invention, an expressed transcript (e.g., a transcript of a gene described herein) is represented in the nucleic acid arrays. In such embodiments, a set of binding sites can include probes with different nucleic acids that are complementary to different sequence segments of the expressed transcript. Exemplary nucleic acids that fall within this class can be of length of 15 to 200 bases, 20 to 100 bases, 25 to 50 bases, 40 to 60 bases or some other range of bases. Each probe sequence can also comprise one or more linker sequences in addition to the sequence that is complementary to its target sequence. As used herein, a linker sequence is a sequence between the sequence that is complementary to its target sequence and the surface of support. For example, the nucleic acid arrays of the invention can comprise one probe specific to each target gene or exon. However, if desired, the nucleic acid arrays can contain at least 2, 5, 10, 100, or 1000 or more probes specific to some expressed transcript (e.g., a transcript of a gene described herein, e.g., in Table 30, Table I, Table J, or Table K). For example, the array may contain probes tiled across the sequence of the longest mRNA isoform of a gene.

It will be appreciated that when cDNA complementary to the RNA of a cell, for example, a cell in a biological sample, is made and hybridized to a microarray under suitable hybridization conditions, the level of hybridization to the site in the array corresponding to a gene described herein (e.g., a gene listed in Table 30, Table I, Table J, or Table K) will reflect the prevalence in the cell of mRNA or mRNAs transcribed from that gene. Alternatively, in instances where multiple isoforms or alternate splice variants produced by particular genes are to be distinguished, detectably labeled (e.g., with a fluorophore) cDNA complementary to the total cellular mRNA can be hybridized to a microarray, and the site on the array corresponding to an exon of the gene that is not transcribed or is removed during RNA splicing in the cell will have little or no signal (e.g., fluorescent signal), and a site corresponding to an exon of a gene for which the encoded mRNA expressing the exon is prevalent will have a relatively strong signal. The relative abundance of different mRNAs produced from the same gene by alternative splicing is then determined by the signal strength pattern across the whole set of exons monitored for the gene.

In one embodiment, hybridization levels at different hybridization times are measured separately on different, identical microarrays. For each such measurement, at hybridization time when hybridization level is measured, the microarray is washed briefly, preferably in room temperature in an aqueous solution of high to moderate salt concentration (e.g., 0.5 to 3 M salt concentration) under conditions which retain all bound or hybridized nucleic acids while removing all unbound nucleic acids. The detectable label on the remaining, hybridized nucleic acid molecules on each probe is then measured by a method which is appropriate to the particular labeling method used. The resulting hybridization levels are then combined to form a hybridization curve. In another embodiment, hybridization levels are measured in real time using a single microarray. In this embodiment, the microarray is allowed to hybridize to the sample without interruption and the microarray is interrogated at each hybridization time in a non-invasive manner. In still another embodiment, one can use one array, hybridize for a short time, wash and measure the hybridization level, put back to the same sample, hybridize for another period of time, wash and measure again to get the hybridization time curve.

In some embodiments, nucleic acid hybridization and wash conditions are chosen so that the nucleic acid biomarkers to be analyzed specifically bind or specifically hybridize to the complementary nucleic acid sequences of the array, typically to a specific array site, where its complementary DNA is located.

Arrays containing double-stranded probe DNA situated thereon can be subjected to denaturing conditions to render the DNA single-stranded prior to contacting with the target nucleic acid molecules. Arrays containing single-stranded probe DNA (e.g., synthetic oligodeoxyribonucleic acids) may need to be denatured prior to contacting with the target nucleic acid molecules, e.g., to remove hairpins or dimers which form due to self complementary sequences.

Optimal hybridization conditions will depend on the length (e.g., oligomer versus polynucleotide greater than 200 bases) and type (e.g., RNA, or DNA) of probe and target nucleic acids. General parameters for specific (i.e., stringent) hybridization conditions for nucleic acids are described in Sambrook et al., (supra), and in Ausubel et al., 1988, Current Protocols in Molecular Biology, Greene Publishing and Wiley-Interscience, New York. When the cDNA microarrays of Shena et al. are used, typical hybridization conditions are hybridization in 5×SSC plus 0.2% SDS at 65° C. for four hours, followed by washes at 25° C. in low stringency wash buffer (1×SSC plus 0.2% SDS), followed by 10 minutes at 25° C. in higher stringency wash buffer (0.1×SSC plus 0.2% SDS) (Shena et al., 1996, Proc. Natl. Acad. Sci. U.S.A. 93:10614). Useful hybridization conditions are also provided in, e.g., Tijessen, 1993, Hybridization With Nucleic Acid Probes, Elsevier Science Publishers B.V.; Kricka.1992, Nonisotopic DNA Probe Techniques, Academic Press, San Diego, CA; and Zou et. al., 2002, Oncogene 21:4855-4862; and Draghici, Data Analysis Toolsfor DNA Microanalysis, 2003, CRC Press LLC, Boca Raton, Florida, pp. 342-343, which are hereby incorporated by reference herein in their entirety.

In a specific embodiment, a microarray can be used to sort out RT-PCR products that have been generated by the methods described, for example, below in Section 5.4.1.2.

5.4.1.2 RT-PCR

In certain embodiments, to determine the feature values of biomarkers in a biomarker profile of the invention, the level of expression of one or more of the genes described herein (e.g., a gene listed in Table 30, Table I. Table J. or Table K) is measured by amplifying RNA from a sample using reverse transcription (RT) in combination with the polymerase chain reaction (PCR). In accordance with this embodiment, the reverse transcription may be quantitative or semi-quantitative. The RT-PCR methods taught herein may be used in conjunction with the microarray methods described above, for example, in Section 5.4.1.1. For example, a bulk PCR reaction may be performed, the PCR products may be resolved and used as probe spots on a microarray. See also Section 6.10, infra.

Total RNA, or mRNA from a sample is used as a template and a primer specific to the transcribed portion of the gene(s) is used to initiate reverse transcription. Methods of reverse transcribing RNA into cDNA are well known and described in Sambrook et al., 2001, supra. Primer design can be accomplished based on known nucleotide sequences that have been published or available from any publicly available sequence database such as GenBank. For example, primers may be designed for any of the genes described herein (see, e.g., in Table 30, Table I, Table J, or Table K). Further, primer design may be accomplished by utilizing commercially available software (e.g., Primer Designer 1.0, Scientific Software etc.). The product of the reverse transcription is subsequently used as a template for PCR.

PCR provides a method for rapidly amplifying a particular nucleic acid sequence by using multiple cycles of DNA replication catalyzed by a thermostable, DNA-dependent DNA polymerase to amplify the target sequence of interest. PCR requires the presence of a nucleic acid to be amplified, two single-stranded oligonucleotide primers flanking the sequence to be amplified, a DNA polymerase, deoxyribonucleoside triphosphates, a buffer and salts. The method of PCR is well known in the art. PCR, is performed, for example, as described in Mullis and Faloona, 1987, Methods Enzymol. 155:335, which is hereby incorporated herein by reference in its entirety.

PCR can be performed using template DNA or cDNA (at least 1 fg; more usefully, 1-1000 ng) and at least 25 pmol of oligonucleotide primers. A typical reaction mixture includes: 2 μl of DNA, 25 pmol of oligonucleotide primer, 2.5 μl of 10 M PCR buffer I (Perkin-Elmer, Foster City, CA), 0.4 μl of 1.25 M dNTP, 0.15 μl (or 2.5 units) of Taq DNA polymerase (Perkin Elmer, Foster City, CA) and deionized water to a total volume of 25 μl. Mineral oil is overlaid and the PCR is performed using a programmable thermal cycler.

The length and temperature of each step of a PCR cycle, as well as the number of cycles, are adjusted according to the stringency requirements in effect. Annealing temperature and timing are determined both by the efficiency with which a primer is expected to anneal to a template and the degree of mismatch that is to be tolerated. The ability to optimize the stringency of primer annealing conditions is well within the knowledge of one of moderate skill in the art. An annealing temperature of between 30° C. and 72° C. is used. Initial denaturation of the template molecules normally occurs at between 92° C. and 99° C. for 4 minutes, followed by 20-40 cycles consisting of denaturation (94-99° C. for 15 seconds to 1 minute), annealing (temperature determined as discussed above; 1-2 minutes), and extension (72° C. for 1 minute). The final extension step is generally carried out for 4 minutes at 72° C., and may be followed by an indefinite (0-24 hour) step at 4° C.

Quantitative RT-PCR (“QRT-PCR”), which is quantitative in nature, can also be performed to provide a quantitative measure of gene expression levels. In QRT-PCR reverse transcription and PCR can be performed in two steps, or reverse transcription combined with PCR can be performed concurrently. One of these techniques, for which there are commercially available kits such as Taqman (Perkin Elmer, Foster City, California) or as provided by Applied Biosystems (Foster City, California) is performed with a transcript-specific antisense probe. This probe is specific for the PCR product (e.g. a nucleic acid fragment derived from a gene) and is prepared with a quencher and fluorescent reporter probe complexed to the 5′ end of the oligonucleotide. Different fluorescent markers are attached to different reporters, allowing for measurement of two products in one reaction. When Taq DNA polymerase is activated, it cleaves off the fluorescent reporters of the probe bound to the template by virtue of its 5′-to-3′ exonuclease activity. In the absence of the quenchers, the reporters now fluoresce. The color change in the reporters is proportional to the amount of each specific product and is measured by a fluorometer; therefore, the amount of each color is measured and the PCR product is quantified. The PCR reactions are performed in 96-well plates so that samples derived from many individuals are processed and measured simultaneously. The Taqman system has the additional advantage of not requiring gel electrophoresis and allows for quantification when used with a standard curve.

A second technique useful for detecting PCR products quantitatively is to use an intercolating dye such as the commercially available QuantiTect SYBR Green PCR (Qiagen, Valencia California). RT-PCR is performed using SYBR green as a fluorescent label which is incorporated into the PCR product during the PCR stage and produces a flourescense proportional to the amount of PCR product.

Both Taqman and QuantiTect SYBR systems can be used subsequent to reverse transcription of RNA. Reverse transcription can either be performed in the same reaction mixture as the PCR step (one-step protocol) or reverse transcription can be performed first prior to amplification utilizing PCR (two-step protocol).

Additionally, other systems to quantitatively measure mRNA expression products are known including Molecular Beacons* which uses a probe having a fluorescent molecule and a quencher molecule, the probe capable of forming a hairpin structure such that when in the hairpin form, the fluorescence molecule is quenched, and when hybridized the fluorescence increases giving a quantitative measurement of gene expression.

Additional techniques to quantitatively measure RNA expression include, but are not limited to, polymerase chain reaction, ligase chain reaction, Qbeta replicase (see, e.g., International Application No. PCT/US87/00880, which is hereby incorporated by reference), isothermal amplification method (see, e.g., Walker et al., 1992, PNAS 89:382-396, which is hereby incorporated herein by reference), strand displacement amplification (SDA), repair chain reaction, Asymmetric Quantitative PCR (see, e.g., U.S. Publication No. US 2003/30134307A1, herein incorporated by reference) and the multiplex microsphere bead assay described in Fuja et al., 2004, Journal of Biotechnology 108:193-205, herein incorporated by reference.

The level of expression of one or more of the genes described herein (e.g., the genes listed in Table 30, Table I, Table J, or Table K) can, for example, be measured by amplifying RNA from a sample using amplification (NASBA). See, e.g., Kwoh et al., 1989, PNAS USA 86:1173; International Publication No. WO 88/10315; and U.S. Pat. No. 6,329,179, each of which is hereby incorporated by reference. In NASBA, the nucleic acids may be prepared for amplification using conventional methods, e.g., phenol/chloroform extraction, heat denaturation, treatment with lysis buffer and minispin columns for isolation of DNA and RNA or guanidinium chloride extraction of RNA. These amplification techniques involve annealing a primer that has target specific sequences. Following polymerization, DNA/RNA hybrids are digested with RNase H while double stranded DNA molecules are heat denatured again. In either case the single stranded DNA is made fully double stranded by addition of second target specific primer, followed by polymerization. The double-stranded DNA molecules are then multiply transcribed by a polymerase such as T7 or SP6. In an isothermal cyclic reaction, the RNA's are reverse transcribed into double stranded DNA, and transcribed once with a polymerase such as T7 or SP6. The resulting products, whether truncated or complete, indicate target specific sequences.

Several techniques may be used to separate amplification products. For example, amplification products may be separated by agarose, agarose-acrylamide or polyacrylamide gel electrophoresis using conventional methods. See Sambrook et al., 2001. Several techniques for detecting PCR products quantitatively without electrophoresis may also be used according to the invention (see, e.g., PCR Protocols. A Guide to Methods and Applications, Innis et al., 1990, Academic Press, Inc. N.Y., which is hereby incorporated by reference). For example, chromatographic techniques may be employed to effect separation. There are many kinds of chromatography which may be used in the present invention: adsorption. partition, ion-exchange and molecular sieve, HPLC, and many specialized techniques for using them including column, paper, thin-layer and gas chromatography (Freifelder, Physical Biochemistry Applications to Biochemistry and Molecular Biology, 2nd ed., Wm. Freeman and Co., New York, N.Y., 1982, which is hereby incorporated by reference).

Another example of a separation methodology is to covalently label the oligonucleotide primers used in a PCR reaction with various types of small molecule ligands. In one such separation, a different ligand is present on each oligonucleotide. A molecule, perhaps an antibody or avidin if the ligand is biotin, that specifically binds to one of the ligands is used to coat the surface of a plate such as a 96 well ELISA plate. Upon application of the PCR reactions to the surface of such a prepared plate, the PCR products are bound with specificity to the surface. After washing the plate to remove unbound reagents, a solution containing a second molecule that binds to the first ligand is added. This second molecule is linked to some kind of reporter system. The second molecule only binds to the plate if a PCR product has been produced whereby both oligonucleotide primers are incorporated into the final PCR products. The amount of the PCR product is then detected and quantified in a commercial plate reader much as ELISA reactions are detected and quantified. An ELISA-like system such as the one described here has been developed by Raggio Italgene (under the C-Track tradename.

Amplification products should be visualized in order to confirm amplification of the nucleic acid sequences of interest, i.e., nucleic acid sequences of one or more of the genes described herein (e.g., a gene listed in Table 30, Table I, Table J, or Table K). One typical visualization method involves staining of a gel with ethidium bromide and visualization under UV light. Alternatively, if the amplification products are integrally labeled with radio- or fluorometrically-labeled nucleotides, the amplification products may then be exposed to x-ray film or visualized under the appropriate stimulating spectra, following separation.

In one embodiment, visualization is achieved indirectly. Following separation of amplification products, a labeled, nucleic acid probe is brought into contact with the amplified nucleic acid sequence of interest, i.e., nucleic acid sequences of one or more of the genes described herein (e.g., a gene listed in Table 30, Table I, Table J, or Table K). The probe preferably is conjugated to a chromophore but may be radiolabeled. In another embodiment, the probe is conjugated to a binding partner, such as an antibody or biotin, where the other member of the binding pair carries a detectable moiety.

In another embodiment, detection is by Southern blotting and hybridization with a labeled probe. The techniques involved in Southern blotting are well known to those of skill in the art and may be found in many standard books on molecular protocols. See Sambrook et al., 2001. Briefly, amplification products are separated by gel electrophoresis. The gel is then contacted with a membrane, such as nitrocellulose, permitting transfer of the nucleic acid and non-covalent binding. Subsequently, the membrane is incubated with a chromophore-conjugated probe that is capable of hybridizing with a target amplification product. Detection is by exposure of the membrane to x-ray film or ion-emitting detection devices. One example of the foregoing is described in U.S. Pat. No. 5,279,721, incorporated by reference herein, which discloses an apparatus and method for the automated electrophoresis and transfer of nucleic acids. The apparatus permits electrophoresis and blotting without external manipulation of the gel and is ideally suited to carrying out methods according to the present invention.

5.4.1.3 Nuclease Protection Assays

In particular embodiments, feature values for biomarkers in a biomarker profile can be obtained by performing nuclease protection assays (including both ribonuclease protection assays and S1 nuclease assays) to detect and quantify specific mRNAs (e.g., mRNAs of a gene described in Table 30, Table I, Table J, or Table K). Such assays are described in, for example. Sambrook et al., 2001, supra. In nuclease protection assays, an antisense probe (labeled with, e.g., radiolabeled or nonisotopic) hybridizes in solution to an RNA sample. Following hybridization, single-stranded, unhybridized probe and RNA are degraded by nucleases. An acrylamide gel is used to separate the remaining protected fragments. Typically, solution hybridization is more efficient than membrane-based hybridization, and it can accommodate up to 100 μg of sample RNA, compared with the 20-30 μg maximum of blot hybridizations.

The ribonuclease protection assay, which is the most common type of nuclease protection assay, requires the use of RNA probes. Oligonucleotides and other single-stranded DNA probes can only be used in assays containing SI nuclease. The single-stranded, antisense probe must typically be completely homologous to target RNA to prevent cleavage of the probe:target hybrid by nuclease.

5.4.1.4 Northern Blot Assays

Any hybridization technique known to those of skill in the art can be used to generate feature values for biomarkers in a biomarker profile. In other particular embodiments, feature values for biomarkers in a biomarker profile can be obtained by Northern blot analysis (to detect and quantify specific RNA molecules (e.g., RNAs of a gene described in Table 30, Table I, Table J, or Table K). A standard Northern blot assay can be used to ascertain an RNA transcript size, identify alternatively spliced RNA transcripts, and the relative amounts of one or more genes described herein (in particular, mRNA) in a sample, in accordance with conventional Northern hybridization techniques known to those persons of ordinary skill in the art. In Northern blots, RNA samples are first separated by size via electrophoresis in an agarose gel under denaturing conditions. The RNA is then transferred to a membrane, crosslinked and hybridized with a labeled probe. Nonisotopic or high specific activity radiolabeled probes can be used including random-primed, nick-translated, or PCR-generated DNA probes, in vitro transcribed RNA probes, and oligonucleotides. Additionally, sequences with only partial homology (e.g., cDNA from a different species or genomic DNA fragments that might contain an exon) may be used as probes. The labeled probe, e.g., a radiolabelled cDNA, either containing the full-length, single stranded DNA or a fragment of that DNA sequence may be at least 20, at least 30, at least 50, or at least 100 consecutive nucleotides in length. The probe can be labeled by any of the many different methods known to those skilled in this art. The labels most commonly employed for these studies are radioactive elements, enzymes, chemicals that fluoresce when exposed to ultraviolet light, and others. A number of fluorescent materials are known and can be utilized as labels. These include, but are not limited to, fluorescein, rhodamine, auramine, Texas Red, AMCA blue and Lucifer Yellow. The radioactive label can be detected by any of the currently available counting procedures. Non-limiting examples of isotopes include ³H, ¹⁴C, ³²P, ³⁵S, ³⁶Cl, ⁵¹Cr, ⁵⁷Co, ⁵⁸Co, ⁵⁹Fe, ⁹⁰Y, ¹²⁵I, ¹³¹I, and “Re. Enzyme labels are likewise useful, and can be detected by any of the presently utilized colorimetric, spectrophotometric, fluorospectrophotometric, amperometric or gasometric techniques. The enzyme is conjugated to the selected particle by reaction with bridging molecules such as carbodiimides, diisocyanates, glutaraldehyde and the like. Any enzymes known to one of skill in the art can be utilized. Examples of such enzymes include, but are not limited to, peroxidase, beta-D-galactosidase, urease, glucose oxidase plus peroxidase and alkaline phosphatase. U.S. Pat. Nos. 3,654,090, 3,850,752, and 4,016,043 are referred to by way of example for their disclosure of alternate labeling material and methods.

5.4.2 Methods of Detecting Proteins

In specific embodiments of the invention, feature values of biomarkers in a biomarker profile can be obtained by detecting proteins, for example, by detecting the expression product (e.g., a nucleic acid or protein) of one or more genes described herein (e.g., a gene listed in Table 30, Table I, Table J, or Table K), or post-translationally modified, or otherwise modified, or processed forms of such proteins. In a specific embodiment, a biomarker profile is generated by detecting and/or analyzing one or more proteins and/or discriminating fragments thereof expressed from a gene disclosed herein (e.g., a gene listed in Table 30, Table I, Table J, or Table K) using any method known to those skilled in the art for detecting proteins including, but not limited to protein microarray analysis, immunohistochemistry and mass spectrometry.

Standard techniques may be utilized for determining the amount of the protein or proteins of interest (e.g., proteins expressed from genes listed in Table 30, Table I, Table J, or Table K) present in a sample. For example, standard techniques can be employed using, e.g., immunoassays such as, for example Western blot, immunoprecipitation followed by sodium dodecyl sulfate polyacrylamide gel electrophoresis, (SDS-PAGE), immunocytochemistry, and the like to determine the amount of protein or proteins of interest present in a sample. One exemplary agent for detecting a protein of interest is an antibody capable of specifically binding to a protein of interest, preferably an antibody detectably labeled, either directly or indirectly.

For such detection methods, if desired a protein from the sample to be analyzed can easily be isolated using techniques which are well known to those of skill in the art. Protein isolation methods can, for example, be such as those described in Harlow and Lane, 1988, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory Press (Cold Spring Harbor, New York), which is incorporated by reference herein in its entirety.

In certain embodiments, methods of detection of the protein or proteins of interest involve their detection via interaction with a protein-specific antibody. For example, antibodies directed to a protein of interest (e.g., a protein expressed from a gene described herein, e.g., a protein listed in Table 30, Table I, Table J, or Table K). Antibodies can be generated utilizing standard techniques well known to those of skill in the art. In specific embodiments, antibodies can be polyclonal, or more preferably, monoclonal. An intact antibody, or an antibody fragment (e.g., scFv, Fab or F(ab′)₂) can, for example, be used.

For example, antibodies, or fragments of antibodies, specific for a protein of interest can be used to quantitatively or qualitatively detect the presence of a protein. This can be accomplished, for example, by immunofluorescence techniques. Antibodies (or fragments thereof) can, additionally, be employed histologically, as in immunofluorescence or immunoelectron microscopy, for in situ detection of a protein of interest. In situ detection can be accomplished by removing a biological sample (e.g., a biopsy specimen) from a patient, and applying thereto a labeled antibody that is directed to a protein of interest (e.g., a protein expressed from a gene in Table 30, Table I, Table J, or Table K). The antibody (or fragment) is preferably applied by overlaying the antibody (or fragment) onto a biological sample. Through the use of such a procedure, it is possible to determine not only the presence of the protein of interest, but also its distribution, in a particular sample. A wide variety of well-known histological methods (such as staining procedures) can be utilized to achieve such in situ detection.

Immunoassays for a protein of interest typically comprise incubating a biological sample of a detectably labeled antibody capable of identifying a protein of interest, and detecting the bound antibody by any of a number of techniques well-known in the art. As discussed in more detail, below, the term “labeled” can refer to direct labeling of the antibody via, e.g., coupling (i.e., physically linking) a detectable substance to the antibody, and can also refer to indirect labeling of the antibody by reactivity with another reagent that is directly labeled. Examples of indirect labeling include detection of a primary antibody using a fluorescently labeled secondary antibody.

The biological sample can be brought in contact with and immobilized onto a solid phase support or carrier such as nitrocellulose, or other solid support which is capable of immobilizing cells, cell particles or soluble proteins. The support can then be washed with suitable buffers followed by treatment with the detectably labeled fingerprint gene-specific antibody. The solid phase support can then be washed with the buffer a second time to remove unbound antibody. The amount of bound label on solid support can then be detected by conventional methods.

By “solid phase support or carrier” is intended any support capable of binding an antigen or an antibody. Well-known supports or carriers include glass, polystyrene, polypropylene, polyethylene, dextran, nylon, amylases, natural and modified celluloses, polyacrylamides and magnetite. The nature of the carrier can be either soluble to some extent or insoluble for the purposes of the present invention. The support material can have virtually any possible structural configuration so long as the coupled molecule is capable of binding to an antigen or antibody. Thus, the support configuration can be spherical, as in a bead, or cylindrical, as in the inside surface of a test tube, or the external surface of a rod. Alternatively, the surface can be flat such as a sheet, test strip, etc. Preferred supports include polystyrene beads. Those skilled in the art will know many other suitable carriers for binding antibody or antigen, or will be able to ascertain the same by use of routine experimentation.

One of the ways in which an antibody specific for a protein of interest can be detectably labeled is by linking the same to an enzyme and use in an enzyme immunoassay (EIA) (Voller, 1978, “The Enzyme Linked Immunosorbent Assay (ELISA)”, Diagnostic Horizons 2:1-7, Microbiological Associates Quarterly Publication, Walkersville, MD; Voller et al., 1978, J. Clin. Pathol. 31:507-520; Butler, J. E., 1981, Meth. Enzymol. 73:482-523; Maggio (ed.), 1980, Enzyme Immunoassay, CRC Press, Boca Raton, FL; Ishikawa et al., (eds.), 1981, Enzyme Immunoassay, Kgaku Shoin, Tokyo, each of which is hereby incorporated by reference in its entirety). The enzyme which is bound to the antibody will react with an appropriate substrate, preferably a chromogenic substrate, in such a manner as to produce a chemical moiety which can be detected, for example, by spectrophotometric, fluorimetric or by visual means. Enzymes which can be used to detectably label the antibody include, but are not limited to, malate dehydrogenase, staphylococcal nuclease, delta-5-steroid isomerase, yeast alcohol dehydrogenase, alpha-glycerophosphate, dehydrogenase, triose phosphate isomerase, horseradish peroxidase, alkaline phosphatase, asparaginase, glucose oxidase, beta-galactosidase, ribonuclease, urease, catalase, glucose-6-phosphate dehydrogenase, glucoamylase and acetylcholinesterase. The detection can be accomplished by colorimetric methods which employ a chromogenic substrate for the enzyme. Detection can also be accomplished by visual comparison of the extent of enzymatic reaction of a substrate in comparison with similarly prepared standards.

Detection can also be accomplished using any of a variety of other immunoassays. For example, by radioactively labeling the antibodies or antibody fragments, it is possible to detect a protein of interest through the use of a radioimmunoassay (RIA) (see, for example, Weintraub, 1986, Principles of Radioimmunoassays, Seventh Training Course on Radioligand Assay Techniques, The Endocrine Society, which is hereby incorporated by reference herein). The radioactive isotope (e.g., ¹²⁵I, ¹³¹I, ³⁵S or ³H) can be detected by such means as the use of a gamma counter or a scintillation counter or by autoradiography.

It is also possible to label the antibody with a fluorescent compound. When the fluorescently labeled antibody is exposed to light of the proper wavelength, its presence can then be detected due to fluorescence. Among the most commonly used fluorescent labeling compounds are fluorescein isothiocyanate, rhodamine, phycoerythrin, phycocyanin, allophycocyanin, o-phthaldehyde and fluorescamine.

The antibody can also be detectably labeled using fluorescence emitting metals such as ¹⁵²Eu, or others of the lanthanide series. These metals can be attached to the antibody using such metal chelating groups as diethylenetriaminepentacetic acid (DTPA) or ethylenediaminetetraacetic acid (EDTA).

The antibody also can be detectably labeled by coupling it to a chemiluminescent compound. The presence of the chemiluminescent-tagged antibody is then determined by detecting the presence of luminescence that arises during the course of a chemical reaction. Examples of particularly useful chemiluminescent labeling compounds are luminol, isoluminol, theromatic acridinium ester, imidazole, acridinium salt and oxalate ester.

Likewise, a bioluminescent compound can be used to label the antibody of the present invention. Bioluminescence is a type of chemiluminescence found in biological systems in, which a catalytic protein increases the efficiency of the chemiluminescent reaction. The presence of a bioluminescent protein is determined by detecting the presence of luminescence. Important bioluminescent compounds for purposes of labeling are luciferin, luciferase and aequorin.

In another embodiment, specific binding molecules other than antibodies, such as aptamers, may be used to bind the biomarkers. In yet another embodiment, the biomarker profile may comprise a measurable aspect of an infectious agent (e.g., lipopolysaccharides or viral proteins) or a component thereof.

In some embodiments, a protein chip assay (e.g., The ProteinChip® Biomarker System, Ciphergen, Fremont, California) is used to measure feature values for the biomarkers in the biomarker profile. See also, for example, Lin, 2004, Modern Pathology, 1-9; Li, 2004, Journal of Urology 171, 1782-1787: Wadsworth, 2004, Clinical Cancer Research, 10, 1625-1632; Prieto, 2003, Journal of Liquid Chromatography & Related Technologies 26, 2315-2328; Coombes, 2003. Clinical Chemistry 49, 1615-1623; Mian, 2003, Proteomics 3, 1725-1737; Lehre et al., 2003, BJU International 92, 223-225; and Diamond, 2003, Journal of the American Society for Mass Spectrometry 14, 760-765, each of which is hereby incorporated by reference in its entirety.

In some embodiments, a bead assay is used to measure feature values for the biomarkers in the biomarker profile. One such bead assay is the Becton Dickinson Cytometric Bead Array (CBA). CBA employs a series of particles with discrete fluorescence intensities to simultaneously detect multiple soluble analytes. CBA is combined with flow cytometry to create a multiplexed assay. The Becton Dickinson CBA system, as embodied for example in the Becton Dickinson Human Inflammation Kit, uses the sensitivity of amplified fluorescence detection by flow cytometry to measure soluble analytes in a particle-based immunoassay. Each bead in a CBA provides a capture surface for a specific protein and is analogous to an individually coated well in an ELISA plate. The BD CBA capture bead mixture is in suspension to allow for the detection of multiple analytes in a small volume sample.

In some embodiments the multiplex analysis method described in U.S. Pat. No. 5,981,180 (“the '180 patent”), herein incorporated by reference in its entirety, and in particular for its teachings of the general methodology, bead technology, system hardware and antibody detection, is used to measure feature values for the biomarkers in a biomarker profile. For this analysis, a matrix of microparticles is synthesized, where the matrix consists of different sets of microparticles. Each set of microparticles can have thousands of molecules of a distinct antibody capture reagent immobilized on the microparticle surface and can be color-coded by incorporation of varying amounts of two fluorescent dyes. The ratio of the two fluorescent dyes provides a distinct emission spectrum for each set of microparticles, allowing the identification of a microparticle a set following the pooling of the various sets of microparticles. U.S. Pat. Nos. 6,268,222 and 6,599,331 also are incorporated herein by reference in their entirety, and in particular for their teachings of various methods of labeling microparticles for multiplex analysis.

5.4.3 Use of other methods of detection

In some embodiments, a separation method may be used determine feature values for biomarkers in a biomarker profile, such that only a subset of biomarkers within the sample is analyzed. For example, the biomarkers that are analyzed in a sample may be mRNA species from a cellular extract which has been fractionated to obtain only the nucleic acid biomarkers within the sample, or the biomarkers may be from a fraction of the total complement of proteins within the sample, which have been fractionated by chromatographic techniques.

Feature values for biomarkers in a biomarker profile can also, for example, be generated by the use of one or more of the following methods described below. For example, methods may include nuclear magnetic resonance (NMR) spectroscopy, a mass spectrometry method, such as electrospray ionization mass spectrometry (ESI-MS). ESI-MS/MS, ESI-MS/(MS)ⁿ (n is an integer greater than zero), matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS), surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF-MS), desorption/ionization on silicon (DIOS), secondary ion mass spectrometry (SIMS), quadrupole time-of-flight (Q-TOF), atmospheric pressure chemical ionization mass spectrometry (APCI-MS), APCI-MS/MS, APCI-(MS)ⁿ, atmospheric pressure photoionization mass spectrometry (APPI-MS), APPI-MS/MS, and APPI-(MS)ⁿ. Other mass spectrometry methods may include, inter alia, quadrupole, Fourier transform mass spectrometry (FTMS) and ion trap. Other suitable methods may include chemical extraction partitioning, column chromatography, ion exchange chromatography, hydrophobic (reverse phase) liquid chromatography, isoelectric focusing, one-dimensional polyacrylamide gel electrophoresis (PAGE), two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) or other chromatography, such as thin-layer, gas or liquid chromatography, or any combination thereof. In one embodiment, the biological sample may be fractionated prior to application of the separation method.

In one embodiment, laser desorption/ionization time-of-flight mass spectrometry is used to create determine feature values in a biomarker profile where the biomarkers are proteins or protein fragments that have been ionized and vaporized off an immobilizing support by incident laser radiation and the feature values are the presence or absence of peaks representing these fragments in the mass spectra profile. A variety of laser desorption/ionization techniques are known in the art (see, e.g., Guttman et al., 2001, Anal. Chem. 73:1252-62 and Wei et al., 1999, Nature 399:243-246, each of which is hereby incorporated by herein be reference in its entirety).

Laser desorption/ionization time-of-flight mass spectrometry allows the generation of large amounts of information in a relatively short period of time. A biological sample is applied to one of several varieties of a support that binds all of the biomarkers, or a subset thereof, in the sample. Cell lysates or samples are directly applied to these surfaces in volumes as small as 0.5 μL, with or without prior purification or fractionation. The lysates or sample can be concentrated or diluted prior to application onto the support surface. Laser desorption/ionization is then used to generate mass spectra of the sample, or samples, in as little as three hours.

5.5 Data Analysis Algorithms

Biomarkers whose corresponding feature values are capable of discriminating between converters and nonconverters are identified in the present invention. The identity of these biomarkers and their corresponding features (e.g., expression levels) can be used to develop a decision rule, or plurality of decision rules, that discriminate between converters and nonconverters. Section 6 below illustrates how data analysis algorithms can be used to construct a number of such decision rules. Each of the data analysis algorithms described in Section 6 use features (e.g., expression values) of a subset of the biomarkers identified in the present invention across a training population that includes converters and nonconverters. Typically, a SIRS subject is considered a nonconverter when the subject does not develop sepsis in a defined time period (e.g., observation period). This defined time period can be, for example, twelve hours, twenty four hours, forty-eight hours, a day, a week, a month, or longer. Specific data analysis algorithms for building a decision rule, or plurality of decision rules, that discriminate between subjects that develop sepsis and subjects that do not develop sepsis during a defined period will be described in the subsections below. Once a decision rule has been built using these exemplary data analysis algorithms or other techniques known in the art, the decision rule can be used to classify a test subject into one of the two or more phenotypic classes (e.g., a converter or a nonconverter). This is accomplished by applying the decision rule to a biomarker profile obtained from the test subject. Such decision rules, therefore, have enormous value as diagnostic indicators.

The present invention provides, in one aspect, for the evaluation of a biomarker profile from a test subject to biomarker profiles obtained from a training population. In some embodiments, each biomarker profile obtained from subjects in the training population, as well as the test subject, comprises a feature for each of a plurality of different biomarkers. In some embodiments, this comparison is accomplished by (i) developing a decision rule using the biomarker profiles from the training population and (ii) applying the decision rule to the biomarker profile from the test subject. As such, the decision rules applied in some embodiments of the present invention are used to determine whether a test subject having SIRS will or will not likely acquire sepsis.

In some embodiments of the present invention, when the results of the application of a decision rule indicate that the subject will likely acquire sepsis, the subject is diagnosed as a “sepsis” subject. If the results of an application of a decision rule indicate that the subject will not acquire sepsis, the subject is diagnosed as a “SIRS” subject. Thus, in some embodiments, the result in the above-described binary decision situation has four possible outcomes:

• • (i) truly septic, where the decision rule indicates that the subject will acquire sepsis and the subject does in fact acquire sepsis during the definite time period (true positive, TP);
  • (ii) falsely septic, where the decision rule indicates that the subject will acquire sepsis and the subject, in fact, does not acquire sepsis during the definite time period (false positive, FP);
  • (iii) truly SIRS, where the decision rule indicates that the subject will not acquire sepsis and the subject, in fact, does not acquire sepsis during the definite time period (true negative, TN); or
  • (iv) falsely SIRS. where the decision rule indicates that the subject will not acquire sepsis and the subject, in fact, does acquire sepsis during the definite time period (false negative, FN).

It will be appreciated that other definitions for TP, FP, TN, FN can be made. For example, TP could have been defined as instances where the decision rule indicates that the subject will not acquire sepsis and the subject, in fact, does not acquire sepsis during the definite time period. While all such alternative definitions are within the scope of the present invention, for ease of understanding the present invention, the definitions for TP, FP, TN, and FN given by definitions (i) through (iv) above will be used herein, unless otherwise stated.

As will be appreciated by those of skill in the art, a number of quantitative criteria can be used to communicate the performance of the comparisons made between a test biomarker profile and reference biomarker profiles (e.g., the application of a decision rule to the biomarker profile from a test subject). These include positive predicted value (PPV), negative predicted value (NPV), specificity, sensitivity, accuracy, and certainty. In addition, other constructs such a receiver operator curves (ROC) can be used to evaluate decision rule performance. As used herein:

$PPV=\frac{TP}{TP+FP}$ $NPV=\frac{TN}{TN+FN}$ $\mathrm{specificity}=\frac{TN}{TN+FP}$ $\mathrm{sensitivity}=\frac{TP}{TP+FN}$ $\mathrm{accuracy}=\mathrm{certainty}=\frac{TP+TN}{N}$

Here, N is the number of samples compared (e.g., the number of test samples for which a determination of sepsis or SIRS is sought). For example, consider the case in which there are ten subjects for which SIRS/sepsis classification is sought. Biomarker profiles are constructed for each of the ten test subjects. Then, each of the biomarker profiles is evaluated by applying a decision rule, where the decision rule was developed based upon biomarker profiles obtained from a training population. In this example, N, from the above equations, is equal to 10. Typically, N is a number of samples, where each sample was collected from a different member of a population. This population can, in fact, be of two different types. In one type, the population comprises subjects whose samples and phenotypic data (e.g., feature values of biomarkers and an indication of whether or not the subject acquired sepsis) was used to construct or refine a decision rule. Such a population is referred to herein as a training population. In the other type, the population comprises subjects that were not used to construct the decision rule. Such a population is referred to herein as a validation population. Unless otherwise stated, the population represented by N is either exclusively a training population or exclusively a validation population, as opposed to a mixture of the two population types. It will be appreciated that scores such as accuracy will be higher (closer to unity) when they are based on a training population as opposed to a validation population. Nevertheless, unless otherwise explicitly stated herein, all criteria used to assess the performance of a decision rule (or other forms of evaluation of a biomarker profile from a test subject) including certainty (accuracy) refer to criteria that were measured by applying the decision rule corresponding to the criteria to either a training population or a validation population. Furthermore, the definitions for PPV, NPV, specificity, sensitivity, and accuracy defined above can also be found in Draghici, Data Analysis Tools for DNA Microanalysis, 2003, CRC Press LLC, Boca Raton, Florida, pp. 342-343, which is hereby incorporated herein by reference.

In some embodiments the training population comprises nonconverters and converters. In some embodiments, biomarker profiles are constructed from this population using biological samples collected from the training population at some time period prior to the onset of sepsis by the converters of the population. As such, for the converters of the training population, a biological sample can be collected two week before, one week before, four days before, three days before, one day before, or any other time period before the converters became septic. In practice, such collections are obtained by collecting a biological sample at regular time intervals after admittance into the hospital with a SIRS diagnosis. For example, in one approach, subjects who have been diagnosed with SIRS in a hospital are used as a training population. Once admitted to the hospital with SIRS, the biological samples are collected from the subjects at selected times (e.g., hourly, every eight hours, every twelve hours, daily, etc.). A portion of the subjects acquire sepsis and a portion of the subjects do not acquire sepsis. For the subjects that acquire sepsis, the biological sample taken from the subjects just prior to the onset of sepsis are termed the T₋₁₂ biological samples. All other biological samples from the subjects are retroactively indexed relative to these biological samples. For instance, when a biological sample has been taken from a subject on a daily basis, the biological sample taken the day before the T₋₁₂ sample is referred to as the T₋₃₆ biological sample. Time points for biological samples for a nonconverter in the training population are identified by “time-matching” the nonconverter subject with a converter subject. To illustrate, consider the case in which a subject in the training population became clinically-defined as septic on his sixth day of enrollment. For the sake of illustration, for this subject. T₋₃₆ is day four of the study, and the T₋₃₆ biological sample is the biological sample that was obtained on day four of the study. Likewise, T₋₃₆ for the matched nonconverter subject is deemed to be day four of the study on this paired nonconverter subject.

In some embodiments, N is more than one, more than five, more than ten, more than twenty, between ten and 100, more than 100, or less than 1000 subjects. A decision rule (or other forms of comparison) can have at least about 99% certainty, or even more, in some embodiments, against a training population or a validation population. In other embodiments, the certainty is at least about 97%, at least about 95%, at least about 90%, at least about 85%, at least about 80%, at least about 75%, at least about 70%, at least about 65%, or at least about 60% against a training population or a validation population (and therefore against a single subject that is not part of a training population such as a clinical patient). The useful degree of certainty may vary, depending on the particular method of the present invention. As used herein, “certainty” means “accuracy.” In one embodiment, the sensitivity and/or specificity is at is at least about 97%, at least about 95%, at least about 90%, at least about 85%, at least about 80%, at least about 75%. or at least about 70% against a training population or a validation population. In some embodiments, such decision rules are used to predict the development of sepsis with the stated accuracy. In some embodiments, such decision rules are used to diagnoses sepsis with the stated accuracy. In some embodiments, such decision rules are used to determine a stage of sepsis with the stated accuracy.

The number of features that may be used by a decision rule to classify a test subject with adequate certainty is two or more. In some embodiments, it is three or more, four or more, ten or more, or between 10 and 200. Depending on the degree of certainty sought, however, the number of features used in a decision rule can be more or less, but in all cases is at least two. In one embodiment, the number of features that may be used by a decision rule to classify a test subject is optimized to allow a classification of a test subject with high certainty.

In some of the examples in Section 6 below, microarray data abundance data was collected for a plurality of biomarkers in each subject. That is, for each biomarker in a biomarker profile, a feature, microarray abundance data for the biomarker, was measured. Decision rules are developed from such biomarker profiles from a training population using data analysis algorithms in order to predict sample phenotypes based on observed gene expression patterns. While new and microarray specific classification tools are constantly being developed, the existing body of pattern recognition and prediction algorithms provide effective data analysis algorithms for constructing decision rules. See, for example, National Research Council; Panel on Discriminant Analysis Classification and Clustering, Discriminant Analysis and Clustering, Washington, D.C.: National Academy Press, which is hereby incorporated by reference. Furthermore, the techniques described in Dudoit et al., 2002. “Comparison of discrimination methods for the classification of tumors using gene expression data.” JASA 97; 77-87, hereby incorporated by reference herein in its entirety, can be used to develop such decision rules.

Relevant data analysis algorithms for developing a decision rule include, but are not limited to, discriminant analysis including linear, logistic, and more flexible discrimination techniques (see, e.g., Gnanadesikan, 1977, Methodsfor Statistical Data Analysis of Multivariate Observations, New York: Wiley 1977, which is hereby incorporated by reference herein in its entirety); tree-based algorithms such as classification and regression trees (CART) and variants (see, e.g., Breiman, 1984, Classification and Regression Trees, Belmont, California: Wadsworth International Group, which is hereby incorporated by reference herein in its entirety, as well as Section 5.1.3, below); generalized additive models (see, e.g., Tibshirani, 1990, Generalized Additive Models, London: Chapman and Hall, which is hereby incorporated by reference herein in its entirety); and neural networks (see, e.g., Neal, 1996. Bayesian Learning for Neural Networks, New York: Springer-Verlag; and Insua, 1998, Feedforward neural networks for nonparametric regression In: Practical Nonparametric and Semiparametric Bayesian Statistics, pp. 181-194, New York: Springer, which is hereby incorporated by reference herein in its entirety. as well as Section 5.5.6, below).

In one embodiment, comparison of a test subject's biomarker profile to a biomarker profiles obtained from a training population is performed, and comprises applying a decision rule. The decision rule is constructed using a data analysis algorithm, such as a computer pattern recognition algorithm. Other suitable data analysis algorithms for constructing decision rules include, but are not limited to, logistic regression (see Section 5.5.10, below) or a nonparametric algorithm that detects differences in the distribution of feature values (e.g., a Wilcoxon Signed Rank Test (unadjusted and adjusted)). The decision rule can be based upon two, three, four, five, 10, 20 or more features, corresponding to measured observables from one, two, three, four, five, 10, 20 or more biomarkers. In one embodiment, the decision rule is based on hundreds of features or more. Decision rules may also be built using a classification tree algorithm. For example, each biomarker profile from a training population can comprise at least three features, where the features are predictors in a classification tree algorithm (see Section 5.5.1, below). The decision rule predicts membership within a population (or class) with an accuracy of at least about at least about 70%, of at least about 75%, of at least about 80%, of at least about 85%, of at least about 90%, of at least about 95%, of at least about 97%, of at least about 98%, of at least about 99%, or about 100%.

Suitable data analysis algorithms are known in the art, some of which are reviewed in Hastie et al., supra. In a specific embodiment, a data analysis algorithm of the invention comprises Classification and Regression Tree (CART; Section 5.5.1, below), Multiple Additive Regression Tree (MART; Section 5.5.4. below), Prediction Analysis for Microarrays (PAM; Section 5.5.2, below) or Random Forest analysis (Section 5.5.1, below). Such algorithms classify complex spectra from biological materials, such as a blood sample, to distinguish subjects as normal or as possessing biomarker expression levels characteristic of a particular disease state. In other embodiments, a data analysis algorithm of the invention comprises ANOVA and nonparametric equivalents, linear discriminant analysis (Section 5.5.10, below), logistic regression analysis (Section 5.5.10, below), nearest neighbor classifier analysis (Section 5.5.9, below), neural networks (Section 5.5.6, below), principal component analysis (Section 5.5.8, below), quadratic discriminant analysis (Section 5.5.11. below), regression classifiers (Section 5.5.5, below) and support vector machines (Section 5.5.12, below). While such algorithms may be used to construct a decision rule and/or increase the speed and efficiency of the application of the decision rule and to avoid investigator bias, one of ordinary skill in the art will realize that computer-based algorithms are not required to carry out the methods of the present invention. Decision rules can be used to evaluate biomarker profiles, regardless of the method that was used to generate the biomarker profile. For example, suitable decision rules that can be used to evaluate biomarker profiles generated using gas chromatography, as discussed in Harper, “Pyrolysis and GC in Polymer Analysis,” Dekker, New York (1985). Further, Wagner et al., 2002, Anal. Chem. 74:1824-1835 disclose a decision rule that improves the ability to classify subjects based on spectra obtained by static time-of-flight secondary ion mass spectrometry (TOF-SIMS). Additionally, Bright et al., 2002, J. Microbiol. Methods 48:127-38, hereby incorporated by reference herein in its entirety, disclose a method of distinguishing between bacterial strains with high certainty (79-89% correct classification rates) by analysis of MALDI-TOF-MS spectra. Dalluge, 2000, Fresenius J. Anal. Chem. 366:701-711. hereby incorporated by reference herein in its entirety, discusses the use of MALDI-TOF-MS and liquid chromatography-electrospray ionization mass spectrometry (LCESI-MS) to classify profiles of biomarkers in complex biological samples.

5.5.1 Decision Trees

One type of decision rule that can be constructed using the feature values of the biomarkers identified in the present invention is a decision tree. Here, the “data analysis algorithm” is any technique that can build the decision tree, whereas the final “decision tree” is the decision rule. A decision tree is constructed using a training population and specific data analysis algorithms. Decision trees are described generally by Duda, 2001, Pattern Classification, John Wiley & Sons, Inc., New York. pp. 395-396, which is hereby incorporated by reference. Tree-based methods partition the feature space into a set of rectangles, and then fit a model (like a constant) in each one.

The training population data includes the features (e.g., expression values, or some other observable) for the biomarkers of the present invention across a training set population. One specific algorithm that can be used to construct a decision tree is a classification and regression tree (CART). Other specific decision tree algorithms include, but are not limited to, ID3, C4.5, MART, and Random Forests. CART, ID3, and C4.5 are described in Duda, 2001, Pattern Classification, John Wiley & Sons, Inc., New York. pp. 396-408 and pp. 411-412, which is hereby incorporated by reference. CART, MART, and C4.5 are described in Hastie et al., 2001, The Elements of Statistical Leaming, Springer-Verlag, New York, Chapter 9, which is hereby incorporated by reference in its entirety. Random Forests are described in Breiman, 1999, “Random Forests-Random Features,” Technical Report 567, Statistics Department. U.C.Berkeley, September 1999, which is hereby incorporated by reference in its entirety.

In some embodiments of the present invention, decision trees are used to classify subjects using features for combinations of biomarkers of the present invention. Decision tree algorithms belong to the class of supervised learning algorithms. The aim of a decision tree is to induce a classifier (a tree) from real-world example data. This tree can be used to classify unseen examples that have not been used to derive the decision tree. As such, a decision tree is derived from training data. Exemplary training data contains data for a plurality of subjects (the training population). For each respective subject there is a plurality of features the class of the respective subject (e.g., sepsis/SIRS). In one embodiment of the present invention, the training data is expression data for a combination of biomarkers across the training population.

The following algorithm describes an exemplary decision tree derivation:

Tree(Examples,Class,Features)
Create a root node
If all Examples have the same Class value, give the root this label
Else if Features is empty label the root according to the
most common value
Else begin
Calculate the information gain for each Feature
Select the Feature A with highest information gain
and make this the root Feature
For each possible value, v, of this Feature
Add a new branch below the root, corresponding to A = v
Let Examples(v) be those examples with A = v
If Examples(v) is empty, make the new branch a leaf
node labeled with the most common value among Examples
Else let the new branch be the tree created by
Tree(Examples(v),Class,Features - {A})
end

A more detailed description of the calculation of information gain is shown in the following. If the possible classes vi of the examples have probabilities P(vi) then the information content I of the actual answer is given by:

$I\left(P\left(v_1\right),\dots ,P\left(v_n\right)\right)=\sum _{i=1}^n-P\left(v_1\right){\log }_{2}P\left(v_i\right)$

The I-value shows how much information we need in order to be able to describe the outcome of a classification for the specific dataset used. Supposing that the dataset contains p positive (e.g. will develop sepsis) and n negative (e.g. will not develop sepsis) examples (e.g. subjects), the information contained in a correct answer is:

$I\left(\frac{p}{p+n},\frac{n}{p+n}\right)=-\frac{p}{p+n}{\log }_2\frac{p}{p+n}-\frac{n}{p+n}{\log }_2\frac{n}{p+n}$

where log₂ is the logarithm using base two. By testing single features the amount of information needed to make a correct classification can be reduced. The remainder for a specific feature A (e.g. representing a specific biomarker) shows how much the information that is needed can be reduced.

$\mathrm{Remainder}\left(A\right)=\sum _{i=1}^v\frac{p_i+n_i}{p+n}I\left(\frac{p_i}{p_i+n_i},\frac{n_i}{p_i+n_i}\right)$

“v” is the number of unique attribute values for feature A in a certain dataset, “i” is a certain attribute value, “pi” is the number of examples for feature A where the classification is positive (e.g. will develop sepsis), “n_i” is the number of examples for feature A where the classification is negative (e.g. will not develop sepsis).

The information gain of a specific feature A is calculated as the difference between the information content for the classes and the remainder of feature A:

$\mathrm{Gain}\left(A\right)=I\left(\frac{p}{p+n},\frac{n}{p+n}\right)-\mathrm{Remainder}\left(A\right)$

The information gain is used to evaluate how important the different features are for the classification (how well they split up the examples), and the feature with the highest information.

In general there are a number of different decision tree algorithms, many of which are described in Duda, Pattern Classification, Second Edition, 2001, John Wiley & Sons, Inc. Decision tree algorithms often require consideration of feature processing, impurity measure, stopping criterion, and pruning. Specific decision tree algorithms include, but are not limited to classification and regression trees (CART), multivariate decision trees, ID3, and C4.5.

In one approach, when a decision tree is used, the gene expression data for a select combination of genes described in the present invention across a training population is standardized to have mean zero and unit variance. The members of the training population are randomly divided into a training set and a test set. For example, in one embodiment, two thirds of the members of the training population are placed in the training set and one third of the members of the training population are placed in the test set. The expression values for a select combination of biomarkers described in the present invention is used to construct the decision tree. Then, the ability for the decision tree to correctly classify members in the test set is determined. In some embodiments, this computation is performed several times for a given combination of biomarkers. In each computational iteration, the members of the training population are randomly assigned to the training set and the test set. Then, the quality of the combination of biomarkers is taken as the average of each such iteration of the decision tree computation.

In addition to univariate decision trees in which each split is based on a feature value for a corresponding biomarker, among the set of biomarkers of the present invention, or the relative feature values of two such biomarkers, multivariate decision trees can be implemented as a decision rule. In such multivariate decision trees, some or all of the decisions actually comprise a linear combination of feature values for a plurality of biomarkers of the present invention. Such a linear combination can be trained using known techniques such as gradient descent on a classification or by the use of a sum-squared-error criterion. To illustrate such a decision tree, consider the expression:

0.04 x_i+0.16 x₂<500

Here, x₁ and x₂ refer to two different features for two different biomarkers from among the biomarkers of the present invention. To poll the decision rule, the values of features x_i and x₂ are obtained from the measurements obtained from the unclassified subject. These values are then inserted into the equation. If a value of less than 500 is computed, then a first branch in the decision tree is taken. Otherwise, a second branch in the decision tree is taken. Multivariate decision trees are described in Duda, 2001, Pattern Classification, John Wiley & Sons, Inc., New York, pp. 408-409, which is hereby incorporated by reference.

Another approach that can be used in the present invention is multivariate adaptive regression splines (MARS). MARS is an adaptive procedure for regression, and is well suited for the high-dimensional problems addressed by the present invention. MARS can be viewed as a generalization of stepwise linear regression or a modification of the CART method to improve the performance of CART in the regression setting. MARS is described in Hastie et al., 2001, The Elements of Statistical Learning, Springer-Verlag, New York, pp. 283-295, which is hereby incorporated by reference in its entirety.

5.5.2 Predictive Analysis of Microarrays (PAM)

One approach to developing a decision rule using feature values of biomarkers of the present invention is the nearest centroid classifier. Such a technique computes, for each class (sepsis and SIRS), a centroid given by the average feature levels of the biomarkers in the class, and then assigns new samples to the class whose centroid is nearest. This approach is similar to k-means clustering except clusters are replaced by known classes. This algorithm can be sensitive to noise when a large number of biomarkers are used. One enhancement to the technique uses shrinkage: for each biomarker, differences between class centroids are set to zero if they are deemed likely to be due to chance. This approach is implemented in the Prediction Analysis of Microarray, or PAM. See, for example, Tibshirani et al., 2002, Proceedings of the National Academy of Science USA 99; 6567-6572, which is hereby incorporated by reference in its entirety. Shrinkage is controlled by a threshold below which differences are considered noise. Biomarkers that show no difference above the noise level are removed. A threshold can be chosen by cross-validation. As the threshold is decreased, more biomarkers are included and estimated classification errors decrease, until they reach a bottom and start climbing again as a result of noise biomarkers—a phenomenon known as overfitting.

5.5.3 Bagging, Boosting, and the Random Subspace Method

Bagging, boosting, the random subspace method, and additive trees are data analysis algorithms known as combining techniques that can be used to improve weak decision rules. These techniques are designed for, and usually applied to, decision trees, such as the decision trees described in Section 5.5.1, above. In addition, such techniques can also be useful in decision rules developed using other types of data analysis algorithms such as linear discriminant analysis.

In bagging, one samples the training set, generating random independent bootstrap replicates, constructs the decision rule on each of these, and aggregates them by a simple majority vote in the final decision rule. See, for example, Breiman, 1996, Machine Learning 24, 123-140; and Efron & Tibshirani, An Introduction to Boostrap, Chapman & Hall, New York, 1993, which is hereby incorporated by reference in its entirety.

In boosting, decision rules are constructed on weighted versions of the training set, which are dependent on previous classification results. Initially, all features under consideration have equal weights, and the first decision rule is constructed on this data set. Then, weights are changed according to the performance of the decision rule. Erroneously classified features get larger weights, and the next decision rule is boosted on the reweighted training set. In this way, a sequence of training sets and decision rules is obtained, which is then combined by simple majority voting or by weighted majority voting in the final decision rule. See, for example, Freund & Schapire. “Experiments with a new boosting algorithm,” Proceedings 13th International Conference on Machine Learning, 1996, 148-156, which is hereby incorporated by reference in its entirety.

To illustrate boosting, consider the case where there are two phenotypes exhibited by the population under study, phenotype I (e.g., acquiring sepsis during a defined time periond), and phenotype 2 (e.g., SIRS only, meaning that the subject does acquire sepsis within a defined time period). Given a vector of predictor biomarkers (e.g., a vector of features that represent such biomarkers) from the training set data, a decision rule G(X) produces a prediction taking one of the type values in the two value set:{phenotype 1, phenotype 21. The error rate on the training sample is

$\stackrel{\_}{\mathrm{err}}=\frac{1}{N}\sum _{i=1}^{N}I\left(y_i\ne G\left(x_i\right)\right)$

where N is the number of subjects in the training set (the sum total of the subjects that have either phenotype 1 or phenotype 2). For example, if there are 49 organisms that acquire sepsis and 72 organisms that remain in the SIRS state, N is 121. A weak decision rule is one whose error rate is only slightly better than random guessing. In the boosting algorithm, the weak decision rule is repeatedly applied to modified versions of the data, thereby producing a sequence of weak decision rules G_m(x), m, =1, 2, . . . , M. The predictions from all of the decision rules in this sequence are then combined through a weighted majority vote to produce the final decision rule:

$G\left(x\right)=\mathrm{sign}\left(\sum _{m=1}^M{\alpha }_m{G}_m\left(x\right)\right)$

Here α₁, α₂, . . . , α_M are computed by the boosting algorithm and their purpose is to weigh the contribution of each respective decision rule Gm(x). Their effect is to give higher influence to the more accurate decision rules in the sequence.

The data modifications at each boosting step consist of applying weights w₁, w₂, . . . , w to each of the training observations (x_i, y_i), i=1, 2, . . . , N. Initially all the weights are set to w_i=1/N, so that the first step simply trains the decision rule on the data in the usual manner. For each successive iteration m=2, 3, . . . , M the observation weights are individually modified and the decision rule is reapplied to the weighted observations. At step m, those observations that were misclassified by the decision rule G-l(x) induced at the previous step have their weights increased, whereas the weights are decreased for those that were classified correctly. Thus as iterations proceed, observations that are difficult to correctly classify receive ever-increasing influence. Each successive decision rule is thereby forced to concentrate on those training observations that are missed by previous ones in the sequence.

The exemplary boosting algorithm is summarized as follows:

1. Initialize the observation weights wi = 1/N, i = 1, 2, . . . , N.
2. For m = 1 to M:
   (a) Fit a decision rule Gm(x) to the training set using weights wi.
   (b) Compute
   errm=∑i=1N⁢wi⁢I⁡(yi≠Gm(xi))∑i=1N⁢wi
   (c) Compute αm = log((1 − errm)/errm).
   (d) Set wi ← wi · exp[αm · I(yi ≠ Gm(xi))], i = 1, 2, . . . , N.
3. Output                      ⁢                                                                    G                        ⁡                        (                        x                        )                                                              =                                          sign                      ⁢                                              ⌊                                                                                                            ∑                                                                                                                    m                              =                              1                                                        M                                                    ⁢                                                      α                            m                                                    ⁢                                                                                    G                              m                                                        (                            x                            )                                                                          ⌋

In one embodiment in accordance with this algorithm, each object is, in fact, a factor. Furthermore, in the algorithm, the current decision rule G_m(x) is induced on the weighted observations at line 2a. The resulting weighted error rate is computed at line 2b. Line 2c calculates the weight am given to G_m(x) in producing the final classifier G(x) (line 3). The individual weights of each of the observations are updated for the next iteration at line 2d. Observations misclassified by G_m(x) have their weights scaled by a factor exp(am), increasing their relative influence for inducing the next classifier G.+1(x) in the sequence. In some embodiments, modifications of the Freund and Schapire, 1997, Journal of Computer and System Sciences 55, pp. 119-139, boosting methods are used. See, for example, Hasti et al., The Elements of Statistical Learning, 2001, Springer, New York, Chapter 10, which is hereby incorporated by reference in its entirety. For example, in some embodiments, feature preselection is performed using a technique such as the nonparametric scoring methods of Park et al., 2002, Pac. Symp. Biocomput. 6, 52-63, which is hereby incorporated by reference in its entirety. Feature preselection is a form of dimensionality reduction in which the genes that discriminate between classifications the best are selected for use in the classifier. Then, the LogitBoost procedure introduced by Friedman et al., 2000, Ann Stat 28, 337-407 is used rather than the boosting procedure of Freund and Schapire. In some embodiments, the boosting and other classification methods of Ben-Dor et al., 2000, Journal of Computational Biology 7, 559-583, hereby incorporated by reference in its entirety, are used in the present invention. In some embodiments, the boosting and other classification methods of Freund and Schapire, 1997, Journal of Computer and System Sciences 55, 119-139, hereby incorporated by reference in its entirety, are used.

In the random subspace method, decision rules are constructed in random subspaces of the data feature space. These decision rules are usually combined by simple majority voting in the final decision rule. See, for example, Ho, “The Random subspace method for constructing decision forests,” IEEE Trans Pattern Analysis and Machine Intelligence, 1998; 20(8): 832-844, which is hereby incorporated by reference in its entirety.

5.5.4 Multiple Additive Regression Trees

Multiple additive regression trees (MART) represents another way to construct a decision rule that can be used in the present invention. A generic algorithm for MART is:

1. Initialize f( )(x) = arg min γ Σi=1N L(yi, γ).
2. For m = 1 to M:
   (a) For I = 1, 2, . . . , N compute
r                      im                                        =                                          -                                                                        [                                                                                    ∂                                                              L                                ⁡                                (                                                                                                      y                                    i                                                                    ,                                                                      f                                    ⁡                                    (                                                                          x                                      i                                                                        )                                                                                                  )                                                                                                                    ∂                                                              f                                ⁡                                (                                                                  x                                  i                                                                )                                                                                                              ]                                                                          f                          =                                                      f                                                          m                              -                              1
   (b) Fit a regression tree to the targets rim giving terminal regions
Rjm, j =  1,2, . . . , Jm.
   (c) For j = 1, 2, . . . , Jm compute
   γjm=argminγ∑xt∈RjmL⁡(yi,fm-1(xi)+γ).
   (d) Update fm(x) = fm − 1(x) + Σj=1Jm γjmI(x ∈ Rjm)
3. Output {circumflex over (f)}(x) = fM(x).

Specific algorithms are obtained by inserting different loss criteria L(y,f(x)). The first line of the algorithm initializes to the optimal constant model, which is just a single terminal node tree. The components of the negative gradient computed in line 2(a) are referred to as generalized pseudo residuals, r. Gradients for commonly used loss functions are summarized in Table 10.2, of Hastie et al., 2001, The Elements of Statistical Learning, Springer-Verlag, New York, p. 321, which is hereby incorporated by reference. The algorithm for classification is similar and is described in Hastie et al., Chapter 10, which is hereby incorporated by reference in its entirety. Tuning parameters associated with the MART procedure are the number of iterations M and the sizes of each of the constituent trees J_m, m=1, 2, . . . , M.

5.5.5 Decision Rules Derived by Regression

In some embodiments, a decision rule used to classify subjects is built using regression. In such embodiments, the decision rule can be characterized as a regression classifier, preferably a logistic regression classifier. Such a regression classifier includes a coefficient for each of the biomarkers (e.g., a feature for each such biomarker) used to construct the classifier. In such embodiments, the coefficients for the regression classifier are computed using, for example, a maximum likelihood approach. In such a computation, the features for the biomarkers (e.g., RT-PCR, microarray data) is used. In particular embodiments, molecular marker data from only two trait subgroups is used (e.g., trait subgroup a: will acquire sepsis in a defined time period and trait subgroup b: will not acquire sepsis in a defined time period) and the dependent variable is absence or presence of a particular trait in the subjects for which biomarker data is available.

In another specific embodiment, the training population comprises a plurality of trait subgroups (e.g., three or more trait subgroups, four or more specific trait subgroups, etc.). These multiple trait subgroups can correspond to discrete stages in the phenotypic progression from healthy, to SIRS, to sepsis, to more advanced stages of sepsis in a training population. In this specific embodiment, a generalization of the logistic regression model that handles multicategory responses can be used to develop a decision that discriminates between the various trait subgroups found in the training population. For example, measured data for selected molecular markers can be applied to any of the multi-category logit models described in Agresti, An Introduction to Categorical Data Analysis, 1996, John Wiley & Sons, Inc., New York. Chapter 8, hereby incorporated by reference in its entirety, in order to develop a classifier capable of discriminating between any of a plurality of trait subgroups represented in a training population.

5.5.6 Neural Networks

In some embodiments, the feature data measured for select biomarkers of the present invention (e.g., RT-PCR data, mass spectrometry data, microarray data) can be used to train a neural network. A neural network is a two-stage regression or classification decision rule. A neural network has a layered structure that includes a layer of input units (and the bias) connected by a layer of weights to a layer of output units. For regression, the layer of output units typically includes just one output unit. However, neural networks can handle multiple quantitative responses in a seamless fashion.

In multilayer neural networks, there are input units (input layer), hidden units (hidden layer), and output units (output layer). There is, furthermore, a single bias unit that is connected to each unit other than the input units. Neural networks are described in Duda et al., 2001, Pattern Classification, Second Edition, John Wiley & Sons, Inc., New York; and Hastie et al., 2001, The Elements of Statistical Learning, Springer-Verlag, New York, each of which is hereby incorporated by reference in its entirety. Neural networks are also described in Draghici, 2003. Data Analysis Tools for DNA Microarrays, Chapman & Hall/CRC; and Mount, 2001, Bioinformatics: sequence and genome analysis, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, each of which is hereby incorporated by reference in its entirety. What is disclosed below is some exemplary forms of neural networks.

The basic approach to the use of neural networks is to start with an untrained network, present a training pattern to the input layer, and to pass signals through the net and determine the output at the output layer. These outputs are then compared to the target values; any difference corresponds to an error. This error or criterion function is some scalar function of the weights and is minimized when the network outputs match the desired outputs. Thus, the weights are adjusted to reduce this measure of error. For regression, this error can be sum-of-squared errors. For classification, this error can be either squared error or cross-entropy (deviation). See, e.g., Hastie et al., 2001, The Elements of Statistical Learning, Springer-Verlag, New York, which is hereby incorporated by reference in its entirety.

Three commonly used training protocols are stochastic, batch, and on-line. In stochastic training, patterns are chosen randomly from the training set and the network weights are updated for each pattern presentation. Multilayer nonlinear networks trained by gradient descent methods such as stochastic back-propagation perform a maximum-likelihood estimation of the weight values in the classifier defined by the network topology. In batch training, all patterns are presented to the network before learning takes place. Typically, in batch training, several passes are made through the training data. In online training, each pattern is presented once and only once to the net.

In some embodiments, consideration is given to starting values for weights. If the weights are near zero, then the operative part of the sigmoid commonly used in the hidden layer of a neural network (see, e.g., Hastie et al., 2001, The Elements of Statistical Learning, Springer-Verlag, New York, hereby incorporated by reference) is roughly linear, and hence the neural network collapses into an approximately linear classifier. In some embodiments, starting values for weights are chosen to be random values near zero. Hence the classifier starts out nearly linear, and becomes nonlinear as the weights increase. Individual units localize to directions and introduce nonlinearities where needed. Use of exact zero weights leads to zero derivatives and perfect symmetry, and the algorithm never moves. Alternatively, starting with large weights often leads to poor solutions.

Since the scaling of inputs determines the effective scaling of weights in the bottom layer, it can have a large effect on the quality of the final solution. Thus, in some embodiments, at the outset all expression values are standardized to have mean zero and a standard deviation of one. This ensures all inputs are treated equally in the regularization process, and allows one to choose a meaningful range for the random starting weights. With standardization inputs, it is typical to take random uniform weights over the range [−0.7, +0.7].

A recurrent problem in the use of three-layer networks is the optimal number of hidden units to use in the network. The number of inputs and outputs of a three-layer network are determined by the problem to be solved. In the present invention, the number of inputs for a given neural network will equal the number of biomarkers selected from the training population. The number of output for the neural network will typically be just one. However, in some embodiments more than one output is used so that more than just two states can be defined by the network. For example, a multi-output neural network can be used to discriminate between, healthy phenotypes, various stages of SIRS, and/or various stages of sepsis. If too many hidden units are used in a neural network, the network will have too many degrees of freedom and is trained too long, there is a danger that the network will overfit the data. If there are too few hidden units, the training set cannot be learned. Generally speaking, however, it is better to have too many hidden units than too few. With too few hidden units, the classifier might not have enough flexibility to capture the nonlinearities in the date; with too many hidden units, the extra weight can be shrunk towards zero if appropriate regularization or pruning, as described below, is used. In typical embodiments, the number of hidden units is somewhere in the range of 5 to 100, with the number increasing with the number of inputs and number of training cases.

One general approach to determining the number of hidden units to use is to apply a regularization approach. In the regularization approach, a new criterion function is constructed that depends not only on the classical training error, but also on classifier complexity. Specifically, the new criterion function penalizes highly complex classifiers: searching for the minimum in this criterion is to balance error on the training set with error on the training set plus a regularization term, which expresses constraints or desirable properties of solutions:

J=J _pat +λj _reg.

The parameter;. is adjusted to impose the regularization more or less strongly. In other words, larger values for A will tend to shrink weights towards zero: typically cross-validation with a validation set is used to estimate A. This validation set can be obtained by setting aside a random subset of the training population. Other forms of penalty have been proposed, for example the weight elimination penalty (see, e.g., Hastie et al., 2001, The Elements of Statistical Learning, Springer-Verlag, New York, hereby incorporated by reference).

Another approach to determine the number of hidden units to use is to eliminate—prune—weights that are least needed. In one approach, the weights with the smallest magnitude are eliminated (set to zero). Such magnitude-based pruning can work, but is nonoptimal; sometimes weights with small magnitudes are important for learning and training data. In some embodiments, rather than using a magnitude-based pruning approach, Wald statistics are computed. The fundamental idea in Wald Statistics is that they can be used to estimate the importance of a hidden unit (weight) in a classifier. Then, hidden units having the least importance are eliminated (by setting their input and output weights to zero). Two algorithms in this regard are the Optimal Brain Damage (OBD) and the Optimal Brain Surgeon (OBS) algorithms that use second-order approximation to predict how the training error depends upon a weight, and eliminate the weight that leads to the smallest increase in training error.

Optimal Brain Damage and Optimal Brain Surgeon share the same basic approach of training a network to local minimum error at weight w, and then pruning a weight that leads to the smallest increase in the training error. The predicted functional increase in the error for a change in full weight vector δw is:

$\delta J={\left(\frac{\partial J}{\partial w}\right)}^t·\delta w+\frac{1}{2}\delta w^t·\frac{{\partial }^{2}J}{\partial w^2}·\delta w+O\left({\delta w}^3\right)$ $\mathrm{where}$ $\frac{{\partial }^{2}J}{\partial w^2}$

is the Hessian matrix. The first term vanishes at a local minimum in error; third and higher order terms are ignored. The general solution for minimizing this function given the constraint of deleting one weight is:

$\delta w=-\frac{w_q}{{\left[H^{-1}\right]}_{qq}}{H}^{-1}·u_q$ $\mathrm{and}$ $L_q=\frac{1}{2}-\frac{w_q^2}{{\left[H^{-1}\right]}_{\mathrm{qq}}}$

Here, u_q is the unit vector along the qth direction in weight space and L_q is approximation to the saliency of the weight q—the increase in training error if weight q is pruned and the other weights updated δw. These equations require the inverse of H. One method to calculate this inverse matrix is to start with a small value, H₀⁻¹=α⁻¹I, where α is a small parameter—effectively a weight constant. Next the matrix is updated with each pattern according to

$\begin{array}{cc}{H}_{m+1}^{-1}=H_m^{-1}-\frac{H_m^{-1}{X}_{m+1}{X}_{m+1}^T{H}_m^{-1}}{\frac{n}{a_m}+X_{m+1}^r{H}_m^{-1}{X}_{m+1}}& \mathrm{Eqn}.1\end{array}$

where the subscripts correspond to the pattern being presented and am decreases with m. After the full training set has been presented, the inverse Hessian matrix is given by H⁻¹=H_n⁻¹. In algorithmic form, the Optimal Brain Surgeon method is:

begin initialize nH, w, θ
train a reasonably large network to minimum error
do compute H−1 by Eqn. 1
q*←argminqwq2/(2⁢⌊H-1⌋qq)⁢(saliency⁢Lq)
w←w-wq*[H-1]q*⁢q*⁢H-1⁢eq*⁢(saliency⁢Lq)
until J(w) > θ
return w
end

The Optimal Brain Damage method is computationally simpler because the calculation of the inverse Hessian matrix in line 3 is particularly simple for a diagonal matrix. The above algorithm terminates when the error is greater than a criterion initialized to be 0. Another approach is to change line 6 to terminate when the change in J(w) due to elimination of a weight is greater than some criterion value. In some embodiments, the back-propagation neural network See, for example Abdi. 1994, “A neural network primer,” J. Biol System. 2, 247-283, hereby incorporated by reference in its entirety.

5.5.7 Clustering

In some embodiments, features for select biomarkers of the present invention are used to cluster a training set. For example, consider the case in which ten features (corresponding to ten biomarkers) described in the present invention is used. Each member m of the training population will have feature values (e.g. expression values) for each of the ten biomarkers. Such values from a member m in the training population define the vector:

X1m

X2m

X3m

X4m

X5m

X6m

X7m

X8m

X9m

X10m

where X_im is the expression level of the i^th biomarker in organism m. If there are m organisms in the training set, selection of i biomarkers will define m vectors. Note that the methods of the present invention do not require that each the expression value of every single biomarker used in the vectors be represented in every single vector m. In other words, data from a subject in which one of the P* biomarkers is not found can still be used for clustering. In such instances, the missing expression value is assigned either a “zero” or some other normalized value. In some embodiments, prior to clustering, the feature values are normalized to have a mean value of zero and unit variance.

Those members of the training population that exhibit similar expression patterns across the training group will tend to cluster together. A particular combination of genes of the present invention is considered to be a good classifier in this aspect of the invention when the vectors cluster into the trait groups found in the training population. For instance, if the training population includes class a: subjects that do not develop sepsis, and class b: subjects that develop sepsis, an ideal clustering classifier will cluster the population into two groups, with one cluster group uniquely representing class a and the other cluster group uniquely representing class b.

Clustering is described on pages 211-256 of Duda and Hart, Pattern Classification and Scene Analysis, 1973, John Wiley & Sons, Inc., New York, (hereinafter “Duda 1973”) which is hereby incorporated by reference in its entirety. As described in Section 6.7 of Duda 1973, the clustering problem is described as one of finding natural groupings in a dataset. To identify natural groupings, two issues are addressed. First, a way to measure similarity (or dissimilarity) between two samples is determined. This metric (similarity measure) is used to ensure that the samples in one cluster are more like one another than they are to samples in other clusters. Second, a mechanism for partitioning the data into clusters using the similarity measure is determined.

Similarity measures are discussed in Section 6.7 of Duda 1973, where it is stated that one way to begin a clustering investigation is to define a distance function and to compute the matrix of distances between all pairs of samples in a dataset. If distance is a good measure of similarity, then the distance between samples in the same cluster will be significantly less than the distance between samples in different clusters. However, as stated on page 215 of Duda 1973, clustering does not require the use of a distance metric. For example, a nonmetric similarity function s(x, x′) can be used to compare two vectors x and x′. Conventionally, s(x, x′) is a symmetric function whose value is large when x and x′ are somehow “similar”. An example of a nonmetric similarity function s(x, x′) is provided on page 216 of Duda 1973.

Once a method for measuring “similarity” or “dissimilarity” between points in a dataset has been selected, clustering requires a criterion function that measures the clustering quality of any partition of the data. Partitions of the data set that extremize the criterion function are used to cluster the data. See page 217 of Duda 1973. Criterion functions are discussed in Section 6.8 of Duda 1973.

More recently, Duda et al., Pattern Classification, 2^nd edition, John Wiley & Sons, Inc. New York, has been published. Pages 537-563 describe clustering in detail. More information on clustering techniques can be found in Kaufman and Rousseeuw, 1990, Finding Groups in Data: An Introduction to Cluster Analysis, Wiley, New York, NY; Everitt, 1993, Cluster analysis (3d ed.), Wiley, New York, NY; and Backer, 1995, Computer-Assisted Reasoning in Cluster Analysis, Prentice Hall, Upper Saddle River, New Jersey. Particular exemplary clustering techniques that can be used in the present invention include, but are not limited to, hierarchical clustering (agglomerative clustering using nearest-neighbor algorithm, farthest-neighbor algorithm, the average linkage algorithm, the centroid algorithm, or the sum-of-squares algorithm), k-means clustering, fuzzy k-means clustering algorithm, and Jarvis-Patrick clustering.

5.5.8 Principle Component Analysis

Principal component analysis (PCA) has been proposed to analyze gene expression data. More generally, PCA can be used to analyze feature value data of biomarkers of the present invention in order to construct a decision rule that discriminates converters from nonconverters. Principal component analysis is a classical technique to reduce the dimensionality of a data set by transforming the data to a new set of variable (principal components) that summarize the features of the data. See, for example, Jolliffe, 1986, Principal Component Analysis, Springer, New York, which is hereby incorporated by reference. Principal component analysis is also described in Draghici, 2003, Data Analysis Toolsfor DNA Microarravs, Chapman & Hall/CRC, which is hereby incorporated by reference. What follows is non-limiting examples of principal components analysis.

Principal components (PCs) are uncorrelated and are ordered such that the k^thPC has the kth largest variance among PCs. The k^th PC can be interpreted as the direction that maximizes the variation of the projections of the data points such that it is orthogonal to the first k−1 PCs. The first few PCs capture most of the variation in the data set. In contrast, the last few PCs are often assumed to capture only the residual ‘noise’ in the data.

PCA can also be used to create a classifier in accordance with the present invention. In such an approach, vectors for the select biomarkers of the present invention can be constructed in the same manner described for clustering above. In fact, the set of vectors, where each vector represents the feature values (e.g., abundance values) for the select genes from a particular member of the training population. can be viewed as a matrix. In some embodiments, this matrix is represented in a Free-Wilson method of qualitative binary description of monomers (Kubinyi, 1990, 3D QSAR in drug design theory methods and applications, Pergamon Press, Oxford, pp 589-638), and distributed in a maximally compressed space using PCA so that the first principal component (PC) captures the largest amount of variance information possible, the second principal component (PC) captures the second largest amount of all variance information, and so forth until all variance information in the matrix has been considered.

Then, each of the vectors (where each vector represents a member of the training population) is plotted. Many different types of plots are possible. In some embodiments, a one-dimensional plot is made. In this one-dimensional plot, the value for the first principal component from each of the members of the training population is plotted. In this form of plot, the expectation is that members of a first subgroup (e.g. those subjects that do not develop sepsis in a determined time period) will cluster in one range of first principal component values and members of a second subgroup (e.g., those subjects that develop sepsis in a determined time period) will cluster in a second range of first principal component values.

In one ideal example, the training population comprises two subgroups: “sepsis” and “SIRS.” The first principal component is computed using the molecular marker expression values for the select biomarkers of the present invention across the entire training population data set. Then, each member of the training set is plotted as a function of the value for the first principal component. In this ideal example, those members of the training population in which the first principal component is positive are the “responders” and those members of the training population in which the first principal component is negative are “subjects with sepsis.”

In some embodiments, the members of the training population are plotted against more than one principal component. For example, in some embodiments, the members of the training population are plotted on a two-dimensional plot in which the first dimension is the first principal component and the second dimension is the second principal component. In such a two-dimensional plot, the expectation is that members of each subgroup represented in the training population will cluster into discrete groups. For example, a first cluster of members in the two-dimensional plot will represent subjects that develop sepsis in a given time period and a second cluster of members in the two-dimensional plot will represent subjects that do not develop sepsis in a given time period.

5.5.9 Nearest Neighbor Analysis

Nearest neighbor classifiers are memory-based and require no classifier to be fit. Given a query point x₀, the k training points x_(r), r, . . . , k closest in distance to x₀ are identified and then the point x₀ is classified using the k nearest neighbors. Ties can be broken at random. In some embodiments, Euclidean distance in feature space is used to determine distance as:

d _(i) =∥x _(i) −x _o∥.

Typically, when the nearest neighbor algorithm is used, the expression data used to compute the linear discriminant is standardized to have mean zero and variance 1. In the present invention, the members of the training population are randomly divided into a training set and a test set. For example, in one embodiment, two thirds of the members of the training population are placed in the training set and one third of the members of the training population are placed in the test set. A select combination of biomarkers of the present invention represents the feature space into which members of the test set are plotted. Next, the ability of the training set to correctly characterize the members of the test set is computed. In some embodiments, nearest neighbor computation is performed several times for a given combination of biomarkers of the present invention. In each iteration of the computation, the members of the training population are randomly assigned to the training set and the test set. Then, the quality of the combination of biomarkers is taken as the average of each such iteration of the nearest neighbor computation.

The nearest neighbor rule can be refined to deal with issues of unequal class priors, differential misclassification costs, and feature selection. Many of these refinements involve some form of weighted voting for the neighbors. For more information on nearest neighbor analysis, see Duda, Pattern Classification, Second Edition, 2001, John Wiley & Sons, Inc; and Hastie, 2001, The Elements of Statistical Learning, Springer, New York, each of which is hereby incorporated by reference in its entirety.

5.5.10 Linear Discriminant Analysis

Linear discriminant analysis (LDA) attempts to classify a subject into one of two categories based on certain object properties. In other words, LDA tests whether object attributes measured in an experiment predict categorization of the objects. LDA typically requires continuous independent variables and a dichotomous categorical dependent variable. In the present invention, the feature values for the select combinations of biomarkers of the present invention across a subset of the training population serve as the requisite continuous independent variables. The trait subgroup classification of each of the members of the training population serves as the dichotomous categorical dependent variable.

LDA seeks the linear combination of variables that maximizes the ratio of between-group variance and within-group variance by using the grouping information. Implicitly, the linear weights used by LDA depend on how the feature values of a molecular marker across the training set separates in the two groups (e.g., a group a that develops sepsis during a defined time period and a group b that does not develop sepsis during a defined time period) and how these feature values correlate with the feature values of other biomarkers. In some embodiments, LDA is applied to the data matrix of the N members in the training sample by K biomarkers in a combination of biomarkers described in the present invention. Then, the linear discriminant of each member of the training population is plotted. Ideally, those members of the training population representing a first subgroup (e.g. those subjects that develop sepsis in a defined time period) will cluster into one range of linear discriminant values (e.g., negative) and those member of the training population representing a second subgroup (e.g. those subjects that will not develop sepsis in a defined time period) will cluster into a second range of linear discriminant values (e.g., positive). The LDA is considered more successful when the separation between the clusters of discriminant values is larger. For more information on linear discriminant analysis, see Duda, Pattern Classification, Second Edition, 2001, John Wiley & Sons, Inc; and Hastie, 2001, The Elements of Statistical Learning, Springer, New York; and Venables & Ripley, 1997, Modern Applied Statistics with s-plus, Springer, New York, each of which is hereby incorporated by reference in its entirety.

5.5.11 Quadratic Discriminant Analysis

Quadratic discriminant analysis (QDA) takes the same input parameters and returns the same results as LDA. QDA uses quadratic equations, rather than linear equations, to produce results. LDA and QDA are interchangeable, and which to use is a matter of preference and/or availability of software to support the analysis. Logistic regression takes the same input parameters and returns the same results as LDA and QDA.

5.5.12 Support Vector Machines

In some embodiments of the present invention, support vector machines (SVMs) are used to classify subjects using feature values of the genes described in the present invention. SVMs are a relatively new type of learning algorithm. See, for example, Cristianini and Shawe-Taylor, 2000, An Introduction to Support Vector Machines, Cambridge University Press, Cambridge; Boser et al., 1992, “A training algorithm for optimal margin classifiers,” in Proceedings of the 5^th Annual ACM Workshop on Computational Learning Theory, ACM Press, Pittsburgh, PA, pp. 142-152; Vapnik, 1998, Statistical Learning Theory, Wiley, New York; Mount, 2001, Bioinformatics: sequence and genome analysis, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, Duda, Pattern Classification, Second Edition, 2001, John Wiley & Sons, Inc.; and Hastie, 2001, The Elements of Statistical Learning, Springer, New York; and Furey et al., 2000, Bioinformatics 16, 906-914, each of which is hereby incorporated by reference in its entirety. When used for classification, SVMs separate a given set of binary labeled data training data with a hyper-plane that is maximally distance from them. For cases in which no linear separation is possible, SVMs can work in combination with the technique of ‘kernels’, which automatically realizes a non-linear mapping to a feature space. The hyper-plane found by the SVM in feature space corresponds to a non-linear decision boundary in the input space.

In one approach, when a SVM is used, the feature data is standardized to have mean zero and unit variance and the members of a training population are randomly divided into a training set and a test set. For example, in one embodiment, two thirds of the members of the training population are placed in the training set and one third of the members of the training population are placed in the test set. The expression values for a combination of genes described in the present invention is used to train the SVM. Then the ability for the trained SVM to correctly classify members in the test set is determined. In some embodiments, this computation is performed several times for a given combination of molecular markers. In each iteration of the computation, the members of the training population are randomly assigned to the training set and the test set. Then, the quality of the combination of biomarkers is taken as the average of each such iteration of the SVM computation.

5.5.13 Evolutionary Methods

Inspired by the process of biological evolution, evolutionary methods of decision rule design employ a stochastic search for an decision rule. In broad overview, such methods create several decision rules—a population—from a combination of biomarkers described in the present invention. Each decision rule varies somewhat from the other. Next, the decision rules are scored on feature data across the training population. In keeping with the analogy with biological evolution, the resulting (scalar) score is sometimes called the fitness. The decision rules are ranked according to their score and the best decision rules are retained (some portion of the total population of decision rules). Again, in keeping with biological terminology, this is called survival of the fittest. The decision rules are stochastically altered in the next generation—the children or offspring. Some offspring decision rules will have higher scores than their parent in the previous generation, some will have lower scores. The overall process is then repeated for the subsequent generation: the decision rules are scored and the best ones are retained, randomly altered to give yet another generation, and so on. In part, because of the ranking, each generation has, on average, a slightly higher score than the previous one. The process is halted when the single best decision rule in a generation has a score that exceeds a desired criterion value. More information on evolutionary methods is found in, for example, Duda, Pattern Classification, Second Edition, 2001, John Wiley & Sons, Inc.

5.5.14 Other Data Analysis Algorithms

The data analysis algorithms described above are merely examples of the types of methods that can be used to construct a decision rule for discriminating converters from nonconverters. Moreover, combinations of the techniques described above can be used. Some combinations, such as the use of the combination of decision trees and boosting, have been described. However, many other combinations are possible. In addition, in other techniques in the art such as Projection Pursuit and Weighted Voting can be used to construct decision rules.

5.6 Biomarkers

In specific embodiments, the present invention provides biomarkers that are useful in diagnosing or predicting sepsis and/or its stages of progression in a subject. While the methods of the present invention may use an unbiased approach to identifying predictive biomarkers, it will be clear to the artisan that specific groups of biomarkers associated with physiological responses or with various signaling pathways may be the subject of particular attention. This is particularly the case where biomarkers from a biological sample are contacted with an array that can be used to measure the amount of various biomarkers through direct and specific interaction with the biomarkers (e.g., an antibody array or a nucleic acid array). In this case, the choice of the components of the array may be based on a suggestion that a particular pathway is relevant to the determination of the status of sepsis or SIRS in a subject. The indication that a particular biomarker has a feature that is predictive or diagnostic of sepsis or SIRS may give rise to an expectation that other biomarkers that are physiologically regulated in a concerted fashion likewise may provide a predictive or diagnostic feature. The artisan will appreciate, however, that such an expectation may not be realized because of the complexity of biological systems. For example, if the amount of a specific mRNA biomarker were a predictive feature, a concerted change in mRNA expression of another biomarker might not be measurable, if the expression of the other biomarker was regulated at a post-translational level. Further, the mRNA expression level of a biomarker may be affected by multiple converging pathways that may or may not be involved in a physiological response to sepsis.

Biomarkers can be obtained from any biological sample, which can be, by way of example and not of limitation, whole blood, plasma, saliva, serum, red blood cells, platelets, neutrophils, eosinophils, basophils, lymphocytes, monocytes, urine, cerebral spinal fluid, sputum, stool, cells and cellular extracts, or other biological fluid sample, tissue sample or tissue biopsy from a host or subject. The precise biological sample that is taken from the subject may vary, but the sampling preferably is minimally invasive and is easily performed by conventional techniques.

Measurement of a phenotypic change may be carried out by any conventional technique. Measurement of body temperature, respiration rate, pulse, blood pressure, or other physiological parameters can be achieved via clinical observation and measurement. Measurements of biomarker molecules may include, for example, measurements that indicate the presence, concentration, expression level, or any other value associated with a biomarker molecule. The form of detection of biomarker molecules typically depends on the method used to form a profile of these biomarkers from a biological sample. See Section 5.4, above, and Tables 30. i, J. K, L, and M below.

In a particular embodiment, the biomarker profile comprises at least two different biomarkers listed in column four or five of Table 30. The biomarker profile further comprises a respective corresponding feature for the at least two biomarkers. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example amplified nucleic acid, or proteins. Generally, the at least two biomarkers are derived from at least two different genes. In the case where a biomarker in the at least two different biomarkers is listed in column four of Table 30, the biomarker can be, for example, a transcript made by the listed gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein listed in column five of Table 30, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In accordance with this embodiment, the biomarker profiles of the present invention can be obtained using any standard assay known to those skilled in the art, or in an assay described herein, to detect a biomarker. Such assays are capable, for example, of detecting the products of expression (e.g., nucleic acids and/or proteins) of a particular gene or allele of a gene of interest (e.g., a gene disclosed in Table 30). In one embodiment, such an assay utilizes a nucleic acid microarray.

In a particular embodiment, the biomarker profile comprises at least two different biomarkers that each contain one of the probesets listed in column 2 of Table 30, biomarkers that contain the complement of one of the probesets of Table 30, or biomarkers that contain an amino acid sequence encoded by a gene that either contains one of the probesets of Table 30 or the complement of one of the probesets of Table 30. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example amplified nucleic acid, or proteins. The biomarker profile further comprises a respective corresponding feature for the at least two biomarkers. Generally, the at least two biomarkers are derived from at least two different genes. In the case where a biomarker is based upon a gene that includes the sequence of a probeset listed in Table 30, the biomarker can be, for example, a transcript made by the gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein encoded by a gene that includes a probeset sequence described in Table 30, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein.

In some embodiments the biomarker profile has between 2 and 626 biomarkers listed in Table 30. In some embodiments, the biomarker profile has between 3 and 50 biomarkers listed in Table 30. In some embodiments, the biomarker profile has between 4 and 25 biomarkers listed in Table 30. In some embodiments, the biomarker profile has at least 3 biomarkers listed in Table 30. In some embodiments, the biomarker profile has at least 4 biomarkers listed in Table 30. In some embodiments, the biomarker profile has at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, or 100 biomarkers listed in Table 30. In some embodiments, each such biomarker is a nucleic acid. In some embodiments, each such biomarker is a protein.

In some embodiments, some of the biomarkers in the biomarker profile are nucleic acids and some of the biomarkers in the biomarker profile are proteins. In some embodiments the biomarker profile has between 2 and 130 biomarkers listed in Table 31. In some embodiments, the biomarker profile has between 3 and 50 biomarkers listed in Table 31. In some embodiments, the biomarker profile has between 4 and 25 biomarkers listed in Table 31. In some embodiments, the biomarker profile has at least 3 biomarkers listed in Table 31. In some embodiments, the biomarker profile has at least 4 biomarkers listed in Table 30. In some embodiments, the biomarker profile has at least 6, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, or 100 biomarkers listed in Table 31.

In some embodiments the biomarker profile has between 2 and 10 biomarkers listed in Table 33. In some embodiments, the biomarker profile has between 3 and 10 biomarkers listed in Table 32. In some embodiments, the biomarker profile has between 4 and 10 biomarkers listed in Table 32. In some embodiments, the biomarker profile has at least 3 biomarkers listed in Table 32. In some embodiments, the biomarker profile has at least 4 biomarkers listed in Table 32. In some embodiments, the biomarker profile has at least 6, 7, 8, 9, or 10 biomarkers listed in Table 32. In some embodiments, each such biomarker is a nucleic acid. In some embodiments, each such biomarker is a protein. In some embodiments, some of the biomarkers in the biomarker profile are nucleic acids and some of the biomarkers in the biomarker profile are proteins.

In some embodiments the biomarker profile has between 2 and 10 biomarkers listed in Table 33. In some embodiments, the biomarker profile has between 3 and 10 biomarkers listed in Table 33. In some embodiments, the biomarker profile has between 4 and 10 biomarkers listed in Table 33. In some embodiments, the biomarker profile has at least 3 biomarkers listed in Table 33. In some embodiments, the biomarker profile has at least 4 biomarkers listed in Table 33. In some embodiments, the biomarker profile has at least 6, 7, 8, 9, or 10 biomarkers listed in Table 33. In some embodiments, each such biomarker is a nucleic acid. In some embodiments, each such biomarker is a protein. In some embodiments, some of the biomarkers in the biomarker profile are nucleic acids and some of the biomarkers in the biomarker profile are proteins.

In some embodiments the biomarker profile has between 2 and 130 biomarkers listed in Table 34. In some embodiments, the biomarker profile has between 3 and 40 biomarkers listed in Table 34. In some embodiments, the biomarker profile has between 4 and 25 biomarkers listed in Table 34. In some embodiments, the biomarker profile has at least 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, or 40 biomarkers listed in Table 34. In some embodiments, each such biomarker is a nucleic acid. In some embodiments, each such biomarker is a protein. In some embodiments, some of the biomarkers in the biomarker profile are nucleic acids and some of the biomarkers in the biomarker profile are proteins.

In some embodiments the biomarker profile has between 2 and 7 biomarkers listed in Table 36. In some embodiments, the biomarker profile has between 3 and 6 biomarkers listed in Table 36. In some embodiments, the biomarker profile has between 4 and 7 biomarkers listed in Table 36. In some embodiments, the biomarker profile has at least 3 biomarkers listed in Table 36. In some embodiments, the biomarker profile has at least 4 biomarkers listed in Table 36. In some embodiments, the biomarker profile has at least 6, 7, 8, 9, or 10 biomarkers listed in Table 36. In some embodiments, each such biomarker is a nucleic acid. In some embodiments, each such biomarker is a protein. In some embodiments, some of the biomarkers in the biomarker profile are nucleic acids and some of the biomarkers in the biomarker profile are proteins.

In some embodiments the biomarker profile has between 2 and 53 biomarkers listed in Table I. In some embodiments, the biomarker profile has between 3 and 50 biomarkers listed in Table I. In some embodiments, the biomarker profile has between 4 and 25 biomarkers listed in Table I. In some embodiments, the biomarker profile has at least 3 biomarkers listed in Table I. In some embodiments, the biomarker profile has at least 4 biomarkers listed in Table I. In some embodiments, the biomarker profile has at least 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 15, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, or 53 biomarkers listed in Table I. In some embodiments, each of the biomarkers in the biomarker profile is a nucleic acid in Table I. In some embodiments, each of the biomarkers in the biomarker profile is a protein in Table I. In some embodiments, some of the biomarkers in a biomarker profile are proteins in Table I and some of the biomarkers in the same biomarker profile are nucleic acids in Table I.

In some embodiments the biomarker profile has between 2 and 44 biomarkers listed in Table J. In some embodiments, the biomarker profile has between 3 and 44 biomarkers listed in Table J. In some embodiments, the biomarker profile has between 4 and 25 biomarkers listed in Table J. In some embodiments, the biomarker profile has at least 3 biomarkers listed in Table J. In some embodiments, the biomarker profile has at least 4 biomarkers listed in Table J. In some embodiments, the biomarker profile has at least 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 15, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, or 43 biomarkers listed in Table J. In some embodiments, each of the biomarkers in the biomarker profile is a nucleic acid in Table J. In some embodiments, each of the biomarkers in the biomarker profile is a protein in Table J. In some embodiments, some of the biomarkers in a biomarker profile are proteins in Table J and some of the biomarkers in the same biomarker profile are nucleic acids in Table J.

In some embodiments the biomarker profile has between 2 and 10 biomarkers listed in Table K. In some embodiments, the biomarker profile has between 3 and 10 biomarkers listed in Table K. In some embodiments, the biomarker profile has between 4 and 10 biomarkers listed in Table K. In some embodiments, the biomarker profile has at least 3 biomarkers listed in Table K. In some embodiments, the biomarker profile has at least 4 biomarkers listed in Table K. In some embodiments, the biomarker profile has at least 5, 6, 7, 8, or 9 biomarkers listed in Table K. In some embodiments, each of the biomarkers in the biomarker profile is a nucleic acid in Table K. In some embodiments, each of the biomarkers in the biomarker profile is a protein in Table K. In some embodiments, some of the biomarkers in a biomarker profile are proteins in Table K and some of the biomarkers in the same biomarker profile are nucleic acids in Table K.

5.6.1 Isolation of Useful Biomarkers

The biomarkers of the present invention may, for example, be used to raise antibodies that bind the biomarker if it is a protein (using methods described in Section 5.4.2, supra, or any method well known to those of skill in the art), or they may be used to develop a specific oligonucleotide probe, if it is a nucleic acid, for example, using a method described in Section 5.4.1, supra, or any method well known to those of skill in the art. The skilled artisan will readily appreciate that useful features can be further characterized to determine the molecular structure of the biomarker. Methods for characterizing biomarkers in this fashion are well-known in the art and include X-ray crystallography, high-resolution mass spectrometry, infrared spectrometry, ultraviolet spectrometry and nuclear magnetic resonance. Methods for determining the nucleotide sequence of nucleic acid biomarkers, the amino acid sequence of polypeptide biomarkers, and the composition and sequence of carbohydrate biomarkers also are well-known in the art.

5.7 Application of the Present Invention to Sirs Subjects

In one embodiment, the presently described methods are used to screen SIRS subjects who are at risk for developing sepsis. A biological sample is taken from a SIRS-positive subject and used to construct a biomarker profile. The biomarker profile is then evaluated to determine whether the feature values of the biomarker profile satisfy a first value set associated with a particular decision rule. This evaluation classifies the subject as a converter or a nonconverter. A treatment regimen may then be initiated to forestall or prevent the progression of sepsis when the subject is classified as a converter.

5.8 Application of the Present Invention to Stages of Sepsis

In one embodiment, the presently described methods are used to screen subjects who are particularly at risk for developing a certain stage of sepsis. A biological sample is taken from a subject and used to construct a biomarker profile. The biomarker profile is then evaluated to determine whether the feature values of the biomarker profile satisfy a first value set associated with a particular decision rule. This evaluation classifies the subject as having or not having a particular stage of sepsis. A treatment regimen may then be initiated to treat the specific stage of sepsis. In some embodiments, the stage of sepsis is for example, onset of sepsis, severe sepsis, septic shock, or multiple organ dysfunction.

5.9 Exemplary Embodiments

In some embodiments of the present invention, a biomarker profile is obtained using a biological sample from a test subject, particularly a subject at risk of developing sepsis, having sepsis, or suspected of having sepsis. The biomarker profile in such embodiments is evaluated. This evaluation can be made, for example, by applying a decision rule to the test subject. The decision rule can, for example, be or have been constructed based upon the biomarker profiles obtained from subjects in the training population. The training population, in one embodiment, includes (a) subjects that had SIRS and were then diagnosed as septic during an observation time period as well as (b) subjects that had SIRS and were not diagnosed as septic during an observation time period. If the biomarker profile from the test subject contains appropriately characteristic features, then the test subject is diagnosed as having a more likely chance of becoming septic, as being afflicted with sepsis or as being at the particular stage in the progression of sepsis. Various populations of subjects including those who are suffering from SIRS (e.g., SIRS-positive subjects) or those who are suffering from an infection but who are not suffering from SIRS (e.g., SIRS-negative subjects) can serve as training populations. Accordingly, the present invention allows the clinician to distinguish, inter alia, between those subjects who do not have SIRS, those who have SIRS but are not likely to develop sepsis within a given time frame, those who have SIRS and who are at risk of eventually becoming septic, and those who are suffering from a particular stage in the progression of sepsis. For more details on suitable training populations and suitable data collected from such populations, see Section 5.5, above.

5.10 Use of Annotation Data to Identify Discriminating Biomarkers

In some embodiments, data analysis algorithms identify a large set of biomarkers whose features discriminate between converters and nonconverters. For example, in some embodiments, application of a data analysis algorithm to a training population results in the selection of more than 500 biomarkers, more than 1000 biomarkers, or more than 10,000 biomarkers. In some embodiments, further reduction in the number of biomarkers that are deemed to be discriminating is desired. Accordingly, in some embodiments, filtering rules that are complementary to data analysis algorithms (e.g., the data analysis algorithms of Section 5.5) are used to further reduce the list of discriminating biomarkers identified by the data analysis algorithms. Specifically, the list of biomarkers identified by application of one or more data analysis algorithms to the biomarker profile data measured in a training population is further refined by application of annotation data based filtering rules to the list. In such embodiments, those biomarkers in the set of biomarkers identified by the one or more data analysis algorithms that satisfy the one or more applied annotation data based filtering rules remain in the set of discriminating biomarkers. In some instances, those biomarkers in the set of biomarkers identified by the one or more data analysis algorithms that do not satisfy the one or more applied annotation data based filtering rules are removed from the set. In other instances, those biomarkers in the set of biomarkers identified by the one or more data analysis algorithms that do not satisfy the one or more applied annotation data based filtering rules stay in the set and those that satisfy the one or more applied annotation data based filtering rules are removed from the set. In this way, annotation data can be used to reduce the number of biomarkers in the set of discriminating biomarkers identified by the data analysis algorithms.

Annotation data based filtering rules are rules based upon annotation data. Annotation data refers to any type of data that describes a property of a biomarker. An example of annotation data is the identification of biological pathways to which a given biomarker belongs. Another example of annotation data is enzymatic class (e.g., phosphodiesterases, kinases, metalloproteinases, etc.). Still other examples of annotation data include, but are not limited to, protein domain information, enzymatic substrate information, enzymatic reaction information, and protein interaction data. Yet another example of annotation data is disease association, in other words, which disease process a given biomarker has been linked to or otherwise affects. Another form of annotation data is any type of data that associates biomarker expression, other forms of biomarker abundance, and/or biomarker activity, with cellular localization, tissue type localization, and/or cell type localization.

As the name implies, annotation data is used to construct an annotation data based filtering rule. An example of an annotation data based filtering rule is:

Annotation rule 1:

• • remove all transcription factors from the training set.Application of this filtering rule to a set of biomarkers will remove all transcription factors from the set.

Another type of annotation data based filtering rule is: Annotation rule 2: keep all biomarkers that are enriched for annotation X in a biomarker list.

Application of this filtering rule will only keep those biomarkers in a given list that are enriched (overrepresented) for annotation X in the list. To more fully appreciate this filtering rule, consider an exemplary biomarker set that has been identified by application of a data analysis algorithm (Section 5.5) to biomarker profiles measured using training population data measured in accordance with a technique disclosed in Section 5.4. This exemplary biomarker set has 500 biomarkers. Assume, for in this illustrative example, that the full set of biomarkers in a human consists of 25,000 biomarkers. Here, the 25,000 biomarkers is a population and the 500 biomarker set is the sample. As used here, the term “population” consists of all possible observable biomarkers. The term “sample” is the data that is actually considered. Now, for this example, let X=kinases. Suppose there are 800 known human kinases and further suppose that the set of 500 biomarkers was randomly selected with respect to kinases. Under these circumstances, the list of 500 biomarkers identified by the data analysis algorithms should select about (500/25,000)*800=16 kinases. Since there are, in fact, 50 kinases in the sample, a conclusion can be reached that kinases are indeed enriched in the sample relative to the population.

More formally, in this example, a determination can be made as to whether kinases are enriched in the set of biomarkers identified by the data analysis algorithm (the sample) relative to the population by analysis of the two-way contingency table that describes the observed sample and population:

		Kinase
	Group	Yes	No	Total
	Population	800	24,200	25,000
	Sample	50	450	500

Following Agresti, 1996, An Introduction to Categorical Data Analysis, John Wiley & Sons, New York, which is hereby incorporated by reference in its entirety, this two-way contingency table can be analyzed by treating each row as an independent bionomial variable. In such instances, the true difference in proportions, termed π₁-π₂, compares the probabilities in the two rows. This difference falls between −1 and +1. It equals zero when π₁=π₂; that is, when the selection of kinases in the sample from the population is independent of the kinase annotation. Of the N_i=25,000 biomarkers in the population, 800 are kinases, a proportion of p₁=800/25,000=0.032. Of the N₂=500 biomarkers in the sample identified using a data analysis algorithm, 50 are kinases, a proportion p₂ of 50/500=0.10. The sample difference of proportions is 0.032-0.10=−0.068. In accordance with Agresti, when the counts in the two rows are independent binomial samples, the estimated standard error of p₁-p₂ is:

$\stackrel{}{\sigma }\left(p_1-p_2\right)=\sqrt{\frac{p_1\left(1-p_1\right)}{N_1}+\frac{p_2\left(1-p_2\right)}{N_2}}$

where N₁ and N₂ are the samples sizes for the population and the sample selected by data analysis algorithm, respectively. The standard error decreases, and hence the estimate of n₁-π₂ improves, as the sample sizes increase. A large-sample (100(1−α))% confidence interval for π₁-π₂ is

(p₁+p₂)±z_a/2=:z_0.025=1.96

Thus, for this example, the estimated error is

$\sqrt{\frac{0.032\left(1-0.032\right)}{25,000}+\frac{0.10\left(1-0.1\right)}{500}=}0.013$

and a 95% confidence interval for the true difference π₁-π₂ is −0.068±1.96(0.013), or −0.068±0.025. Since the 95% confidence interval contains only negative values, the conclusion can be reached that kinases are enriched in the sample (the biomarker set produced by the data analysis algorithm) relative to the population of 25,000 biomarkers.

The two-way contingency table in the example above can be analysed using methods known in the art other than the one disclosed above. For example, the chi-square test for independence and/or Fisher's exact test can be used to test the null hypothesis that the row and column classification variables of the two-way contingency table are independent.

The term “X” in annotation rule 2 can be any form of annotation data. In one embodiment, “X” is any biological pathway. As such the annotation data based filtering rule has the following form.

Annotation rule 3:Select all biomarkers that are in any biological pathway that is enriched in the biomarker list.To determine whether a particular biological pathway is enriched, the number of biomarkers in a particular biological pathway in the sample is compared with the number of biomarkers that are in the particular biological pathway in the population using, for example, the two-way contingency table analysis described above, or other techniques known in the art. If the biological pathway is enriched in the sample, then all biomarkers in the sample that are also in the biological pathway are retained for further analysis, in accordance with the annotation data based filtering rule.

An example of enrichment, in which it was shown that the proportion of kinases in the sample was greater than the proportion of kinases in the population across its entire 95% confidence interval has been given. In one embodiment, biomarkers having a given annotation are considered enriched in the sample relative to the population when the proportion of biomarkers having the annotation in the sample is greater than the proportion of biomarkers having the annotation in the population across its entire 95% degree confidence interval as determined by two-way contingency table analysis. In another embodiment, biomarkers having a given annotation are considered enriched in the sample relative to the population if a p value as determined by the Fisher exact test, Chi-square test, or relative algorithms is 0.05 or less, 0.005 or less or 0.0005 or less.

Another form of annotation data based filtering rule has the following form:

Annotation rule 4:Select all biomarkers that are in biological pathway X.

In an embodiment, a set of biomarkers is determined using a data analysis algorithm. Exemplary data analysis algorithms are disclosed in Section 5.5. In addition, Section 6 describes certain tests that can also serve as data analysis algorithms. These tests include, but are not limited to a Wilcoxon test and the like with a statistically significant p value (e.g., 0.05 or less, 0.04, or less, etc.), and/or a requirement that a biomarker exhibit a mean differential abundance between biological samples obtained from converters and biological samples obtained from nonconverters in a training population. Upon application of the data analysis algorithm, a set of biomarkers that discriminates between converters and nonconverters is determined. Next, an annotation rule, for example annotation rule 4, is applied to the set of discriminating biomarkers in order to further reduce the set of biomarkers. Those of skill in the art will appreciate that the order in which these rules are applied is generally not important. For example, annotation rule 4 can be applied first and then certain data analysis algorithms can be applied, or vice versa. In some embodiments, biomarkers ultimately deemed as discriminating between converters and nonconverters satisfy each of the following criteria: (i) a p value of 0.05 or less (p<0.05) as determined from a Wilcoxon adjusted test using static (single time point) data; (ii) a mean-fold change of 1.2 or greater between converters and nonconverters across the training set using static (single time point data), and (iii) present in a specific biological pathway. See also. Section 6.7, infra, for a detailed example. In this example, there is no requirement that members of the pathway are enriched in the set of biomarkers identified by the data analysis algorithms. Furthermore, it is noted that criteria (i) and (ii) are forms of data analysis algorithms and criterion (iii) is a annotation data based filtering rule.

In another embodiment, once a list of discriminating biomarkers is identified, the biomarkers can then be used to determine the identity of the particular biological pathways from which the discriminating biomarkers are implicated. In certain embodiments, annotation data-based filtering rules are applied to the list of discriminating biomarkers identified by the methods of the present invention (e.g., the methods described in Sections 5.4, 5.5 and 6). Such annotation data-based filtering rules identify the particular biological pathway or pathways that are enriched in the discriminating list of biomarkers identified by the data analysis algorithms. In an exemplary embodiment of the invention, DAVID 2.0 software, available at appsl.niaid.nih.gov/david/, is used to identify and apply such annotation data-based filtering rules to the set of biomarkers identified by the data analysis algorithms in order to identify pathways that are enriched in the set. In some embodiments, those biomarkers that are in an enriched biological pathway are selected for use as discriminating biomarkers in the kits of the present invention.

In some embodiments of the present invention, biomarkers that are in biological pathways that are enriched in the biomarker set determined by application of a data analysis algorithm to a training population that includes converters and nonconverters can be used as filtering step to reduce the number of biomarkers in the set. In one such approach, biological samples from subjects in a training population are obtained using, e.g., any of one or more of the methods described in Section 5.4, supra, and in Section 6, infra. In accordance with this embodiment, a nucleic acid array, such as a cDNA microarray, may be employed to generate features of biomarkers in a biomarker profile by detecting the expression of any one or more of the genes known to be or suspected to be involved in the selected biological pathways. Data derived from the cDNA microarray analysis may then be analyzed using any one or more of the analysis algorithms described in Section 5.5, supra, to identify biomarkers whose features discriminate between converters and nonconverters. Biomarkers whose corresponding feature values are capable of discriminating, for example, between converters (i.e., SIRS patients who subsequently develop sepsis) and non-converters (i.e., SIRS patients who do not subsequently develop sepsis) can thus be identified and classified as discriminating biomarkers. Biomarkers that are in enriched biological pathways can be selected from this set by applying Annotation rule 3, from above. Representative biological pathways that could be found include, for example, genes involved in the Th1/Th2 cell differentiation pathway). In one embodiments, biomarkers ultimately deemed as discriminating between converters and nonconverters satisfy each of the following criteria: (i) a p value of 0.05 or less (p<0.05) as determined from a Wilcoxon adjusted test; (ii) a mean-fold change of 1.2 or greater between converters and nonconverters across the training set, and (iii) present in a biological pathway that is enriched in the set of biomarkers derived by application of criteria (i) and (ii).

In some embodiments of the present invention, annotation data based filtering rules are used to identify biological pathways that are enriched in a given biomarker set. This biomarker set can be, for example, a set of biomarkers that is identified by application of a data analysis algorithm to training data comprising converters and nonconverters. Then, biomarkers in these enriched biological pathways are analyzed using any of the data analysis algorithms disclosed herein in order to identify biomarkers that discriminate between converters and nonconverters. In some instances, some of the biomarkers analyzed in the enriched biological pathways were not among the biomarkers in the original given biomarker set. In some instances, some of the biomarkers in the enriched biological pathways are among the biomarkers in the original given biomarker set. In some embodiments, a secondary assay is used to collect feature data for biomarkers that are in enriched pathways and it is this data that is used to determine whether the biomarkers in the enriched biological pathways discriminate between converters and nonconverters.

In some embodiments, biomarkers in biological pathways of interest are identified. In one example, genes involved in the Th1/Th2 cell differentiation pathway are identified. Then, these biomarkers are evaluated using the data analysis algorithms disclosed herein to determine whether they discriminate between converters and nonconverters.

5.11 Representative Embodiment in Accordance with the Present Invention

Sections 6.11 through 6.13 identify a number of biomarkers that are of interest in one embodiment in accordance with the present invention. Specifically, one embodiment of the present invention comprises the 10 biomarkers identified in Table 48 of Section 6.11.1, the 34 biomarkers listed in Table 59 of Section 6.11.2, and the 10 biomarkers listed in Table 93 of Section 6.13.1, below. Table 48 and Table 93 each identify MMP9 as a discriminating biomarker. Thus, the total number of biomarkers in Table I is one less than the sum of the biomarkers identified in Tables 48, Table 59, and Table 93, (34+10+10-1) or 53. These biomarkers are reproduced in Table I, below. Section 5.11.1 provides details on each of the individual biomarkers. Section 5.11.2, below, provides more details on select combinations of the biomarkers listed in Tables I, J, and K. Each of the biomarkers listed in Table I were selected based on the experimental results summarized in Sections 6.11 through 6.13. In some experiments, the identified biomarkers were proteins or fragments thereof. Such protein biomarkers, which discriminate between sepsis and SIRS, are listed in Table I with a “P” designation in column 5. In some experiments, the identified biomarkers were nucleic acids or fragment thereof. Such nucleic acid biomarkers, which discriminate between sepsis and SIRS, are listed in Table I with an “N” designation in column 5. As indicated above, one biomarker MMP9, was identified both as a protein and as a nucleic acid biomarker. Table J below lists the biomarkers in accordance with one embodiment of the present invention in which the biomarkers were discovered using nucleic acid based assays described in Section 6. such as RT-PCR. Table K below lists the biomarkers in accordance with one embodiment of the present invention in which the biomarkers were discovered using protein based assays, described in Section 6, such as bead assays. One embodiment of the invention comprises at least 3, 4, 5, 6, 7, 8, 9, or 10 biomarkers from any one of Tables 48, 59, or 93.

Unless indicated in specific embodiments below, the biomarkers of Tables I, J and K are not limited by their physical form in the experiments summarized in Sections 6.11 through 6.13. For example, although the discriminatory nature of a biomarker may have been discovered by the abundance of the biomarker, in nucleic acid form, in a nucleic acid assay such as RT-PCR and accordingly listed in Table I on this basis with an “N” designation in column 5 of Table I, the physical manifestation of the biomarker in the methods, kits, and biomarker profiles of the present invention is not limited to nucleic acids. Rather, any physical manifestation of the biomarker as defined for the term “biomarker” in Section 5.1 is encompassed in the present invention. Column 6 of Table I indicates, based on the data summarized in Section 6 below, whether the biomarker is up-regulated or down-regulated in the subjects that will convert to sepsis (the converters) relative to the subjects that will not convert (the SIRS subjects). Thus, if a biomarker has the designation UP, in column 6, that means that the biomarker, in the form indicated in column 5, was, on average, more abundant in subjects that will convert to sepsis (sepsis subjects) relative to subjects that will not convert to sepsis (SIRS subjects). Furthermore, if a biomarker has the designation DOWN, in column 6, that means that the biomarker, in the form indicated in column 5, was, on average, less abundant in subjects that will convert to sepsis (sepsis subjects), relative to subjects that will not convert to sepsis (SIRS subjects).

TABLE I
Biomarkers in accordance with an embodiment of the present invention.
		Gene	Protein
Gene		Accession	Accession		Regulation
Symbol	Gene Name	Number	Number	Source	in SEPSIS
1	2	3	4	5	6
AFP	ALPHA-FETOPROTEIN	NM_001134	CAA79592	P	UP
ANKRD22	ANKYRIN REPEAT	NM_144590	NP_653191	N	UP
	DOMAIN 22
ANXA3	ANNEXIN A3	NM_005139	NP_005130	N	UP
APOC3	APOLIPOPROTEIN CIII	NM_000040	CAA25648	P	DOWN
ARG2	ARGINASE TYPE II	NM_001172	CAG38787	N	UP
B2M	BETA-2	NM_004048	AAA51811	P	UP
	MICROGLOBULIN
BCL2A1	BCL2-RELATED	NM_004049	NP_004040	N	UP
	PROTEIN A1
CCL5	CHEMOKINE (C-C	NM_002985	NP_002976	N	DOWN
	MOTIF) LIGAND 5
CD86	CD86 ANTIGEN (CD28	NM_006889	NP_008820	N	DOWN
	ANTIGEN LIGAND 2,	NM_175862	NP_787058
	B7-2 ANTIGEN)
CEACAM1	CARCINOEMBRYONIC	NM_001712	NP_001703	N	UP
	ANTIGEN-RELATED
	CELL ADHESION
	MOLECULE 1
CRP	C REACTIVE PROTEIN	NM_000567	CAA39671	P	UP
CRTAP	CARTILAGE-	NM_006371	NP_006362	N	DOWN
	ASSOCIATED
	PROTEIN
CSF1R	COLONY	NM_005211	NP_005202	N	DOWN
	STIMULATING
	FACTOR 1 RECEPTOR,
	FORMERLY
	MCDONOUGH FELINE
	SARCOMA VIRAL (V-
	FMS) ONCOGENE
	HOMOLOG
FAD104	FIBRONECTIN TYPE	NM_022763	NP_073600	N	UP
	III DOMAIN
	CONTAINING 3B
	(FNDC3B)
FCGR1A	FC FRAGMENT OF	NM_000566	NP_000557	N	UP
	IGG, HIGH AFFINITY
	IA
GADD45A	GROWTH ARREST	NM_001924	NP_001915	N	UP
	AND DNA-DAMAGE-
	INDUCIBLE, ALPHA
GADD45B	GROWTH ARREST-	NM_015675	NP_056490	N	UP
	AND DNA DAMAGE-
	INDUCIBLE GENE
	GADD45
HLA-DRA	MAJOR	NM_002123	NP_002114	N	DOWN
	HISTOCOMPATIBILITY
	COMPLEX, CLASS
	II, DR ALPHA
IFNGR1	INTERFERON GAMMA	NM_000416	NP_000407	N	UP
	RECEPTOR 1
IL1RN	INTERLEUKIN = 1	NM_000577,	AAN87150	N	UP
	RECEPTOR	NM_173841,
	ANTAGONIST GENE	NM_173842,
		NM_173843
IL-6	INTERLEUKIN 6	NM_000600	NP_000591	P	UP
IL-8	INTERLEUKIN 8	M28130	AAA59158	P	UP
IL-10	INTERLEUKIN 10	NM_000572	CAH73907	P	UP
IL10RA	INTERLEUKIN 10	NM_001558	NP_001549	N	DOWN
	RECEPTOR, ALPHA
IL18R1	INTERLEUKIN 18	NM_003855	NP_003846	N	UP
	RECEPTOR 1
INSL3	INSULIN-LIKE 3	NM_005543	NP_005534	N	UP
	(LEYDIG CELL)
IRAK2	INTERLEUKIN-1	NM_001570	NP_001561	N	UP
	RECEPTOR-
	ASSOCIATED KINASE
	2
IRAK4	INTERLEUKIN-1	NM_016123	NP_057207	N	UP
	RECEPTOR-
	ASSOCIATED KINASE
	4
ITGAM	INTEGRIN, ALPHA M	NM_000632	NP_000623	N	UP
	(COMPLEMENT
	COMPONENT
	RECEPTOR 3, ALPHA;
	ALSO KNOWN AS
	CD11B (P170),
	MACROPHAGE
	ANTIGEN ALPHA
	POLYPEPTIDE)
JAK2	JANUS KINASE 2 (A	NM_004972	NP_004963	N	UP
	PROTEIN TYROSINE
	KINASE)
LDLR	LOW DENSITY	NM_000527	NP_000518	N	UP
	LIPOPROTEIN
	RECEPTOR
LY96	LYMPHOCYTE	NM_015364	NP_056179	N	UP
	ANTIGEN 96
MAP2K6	MITOGEN-	NM_002758	NP_002749	N	UP
	ACTIVATED PROTEIN	NM_031988	NP_114365
	KINASE KINASE 6
MAPK14	MAPK14 MITOGEN-	NM_001315	NP_001306	N	UP
	ACTIVATED PROTEIN	NM_139012	NP_620581
	KINASE 14	NM_139013	NP_620582
		NM_139014	NP_620583
MCP1	MONOCYTE	AF493698,	AAQ75526	P	UP
	CHEMOATTRACTANT	AF493697
	PROTEIN 1
MKNK1	MAP KINASE	NM_003684	NP_003675	N	UP
	INTERACTING	NM_198973	NP_945324
	SERINE/THREONINE
	KINASE 1
MMP9	MATRIX	NM_004994	NP_004985	N/P	UP (both
	METALLOPROTEINASE				protein and
	9 (GELATINASE B,				nucleic
	92KDA GELATINASE,				acid)
	92KDA TYPE IV
	COLLAGENASE)
NCR1	NATURAL	NM_004829	NP_004820	N	UP
	CYTOTOXICITY
	TRIGGERING
	RECEPTOR 1
OSM	ONCOSTATIN M	NM_020530	NP_065391	N	UP
PFKFB3	6-PHOSPHOFRUCTO-	NM_004566	NP_004557	N	UP
	2-KINASE/FRUCTOSE-
	2,6-BISPHOSPHATASE
	3
PRV1	NEUTROPHIL-	NM_020406	NP_065139	N	UP
	SPECIFIC ANTIGEN 1
	(POLYCYTHEMIA
	RUBRA VERA 1)
PSTPIP2	PROLINE/SERINE/	NM_024430	NP_077748	N	UP
	THREONINE
	PHOSPHATASE-
	INTERACTING
	PROTEIN 1 (PROLINE-
	SERINE-THREONINE
	PHOSPHATASE
	INTERACTING
	PROTEIN 2)
SOCS3	SUPPRESSOR OF	NM_003955	NP_003946	N	UP
	CYTOKINE
	SIGNALING 3
SOD2	SUPEROXIDE	NM_000636	NP_000627	N	UP
	DISMUTASE 2,
	MITOCHONDRIAL
TDRD9	TUDOR DOMAIN	NM_153046	NP_694591	N	UP
	CONTAINING 9
TGFBI	TRANSFORMING	NM_000358	NP_000349	N	DOWN
	GROWTH FACTOR,
	BETA-1
	(TRANSFORMING
	GROWTH FACTOR,
	BETA-INDUCED,
	68KDA)
TIFA	TRAF-INTERACTING	NM_052864	NP_443096	N	UP
	PROTEIN WITH A
	FORKHEAD-
	ASSOCIATED
	DOMAIN
TIMP1	TISSUE INHIBITOR OF	NM_003254	AAA75558	P	UP
	METALLOPROTEINASE
	1
TLR4	TOLL-LIKE	AH009665	AAF05316	N	UP
	RECEPTOR 4
TNFRSF6	TUMOR NECROSIS	NM_152877	NP_000034	N	UP
	FACTOR RECEPTOR
	SUPERFAMILY,
	MEMBER 6
TNFSF10	TUMOR NECROSIS	NM_003810	NP_003801	N	UP
	FACTOR (LIGAND)
	SUPERFAMILY,
	MEMBER 10
TNFSF13B	TUMOR NECROSIS	NM_006573	NP_006564	N	UP
	FACTOR (LIGAND)
	SUPERFAMILY,
	MEMBER 13B
VNN1	VANIN 1	NM_004666	NP_004657	N	UP

Each of the sequences, genes, proteins, and probesets identified in Table I is hereby incorporated by reference.

TABLE J
Biomarkers identified based on the ability of the nucleic acid
form of the biomarker to discriminate between SIRS and sepsis
		Gene	Protein
Gene		Accession	Accession
Symbol	Gene Name	Number	Number
1	2	3	4
FCGR1A	FC FRAGMENT OF	NM_000566	NP_000557
	IGG, HIGH AFFINITY
	IA
MMP9	MATRIX	NM_004994	NP_004985
	METALLOPROTEINASE
	9
IL18R1	INTERLEUKIN 18	NM_003855	NP_003846
	RECEPTOR 1
ARG2	ARGINASE TYPE II	NM_001172	CAG38787
IL1RN	INTERLEUKIN-1	NM_000577,	AAN87150
	RECEPTOR	NM_173841,
	ANTAGONIST GENE	NM_173842,
		NM_173843
TNFSF13B	TUMOR NECROSIS	NM_006573	NP_006564
	FACTOR
	SUPERFAMILY,
	MEMBER 13B
ITGAM	INTEGRIN, ALPHA M	NM_000632	NP_000623
TGFB1	TRANSFORMING	NM_000358	NP_000349
	GROWTH FACTOR,
	BETA-1
CD86	CD86 ANTIGEN	NM_006889	NP_008820
		NM_175682	NP_787058
TLR4	TOLL-LIKE	AH009665	AAF05316
	RECEPTOR 4
	BCL2-RELATED	NM_004049	NP_004040
	PROTEIN A1
CCL5	CHEMOKINE (C-C	NM_002985	NP_002976
	MOTIF) LIGAND 5
CSF1R	COLONY	NM_005211	NP_005202
	STIMULATING
	FACTOR 1 RECEPTOR,
	FORMERLY
	MCDONOUGH FELINE
	SARCOMA VIRAL (V-
	FMS) ONCOGENE
	HOMOLOG
GADD45A	GROWTH ARREST	NM_001924	NP_001915
	AND DNA-DAMAGE-
	INDUCIBLE, ALPHA
GADD45B	GROWTH ARREST-	NM_015675	NP_056490
	AND DNA DAMAGE-
	INDUCIBLE GENE
	GADD45
IFNGR1	INTERFERON	NM_000416	NP_000407
	GAMMA RECEPTOR 1
IL10RA	INTERLEUKIN 10	NM_001558	NP_001549
	RECEPTOR, ALPHA
IRAK2	INTERLEUKIN-1	NM_001570	NP_001561
	RECEPTOR-
	ASSOCIATED KINASE
	2
IRAK4	INTERLEUKIN-1	NM_016123	NP_057207
	RECEPTOR-
	ASSOCIATED KINASE
	4
JAK2	JANUS KINASE 2 (A	NM_004972	NP_004963
	PROTEIN TYROSINE
	KINASE)
LY96	LYMPHOCYTE	NM_015364	NP_056179
	ANTIGEN 96
MAP2K6	MITOGEN-	NM_002758	NP_002749
	ACTIVATED PROTEIN	NM_031988	NP_114365
	KINASE 6
MAPK14	MAPK14 MITOGEN-	NM_001315	NP_001306
	ACTIVATED PROTEIN	NM_139012	NP_620581
	KINASE 14	NM_139013	NP_620582
		NM_139014	NP_620583
MKNK1	MAP KINASE	NM_003684	NP_003675
	INTERACTING	NM_198973	NP_945324
	SERINE/THREONINE
	KINASE 1
OSM	ONCOSTATIN M	NM_020530	NP_065391
SOCS3	SUPPRESSOR OF	NM_003955	NP_003946
	CYTOKINE
	SIGNALING 3
TDRD9	TUDOR DOMAIN	NM_153046	NP_694591
	CONTAINING 9
TNFRSF6	TUMOR NECROSIS	NM_152877	NP_000034
	FACTOR RECEPTOR
	SUPERFAMILY,
	MEMBER 6
TNFSF10	TUMOR NECROSIS	NM_003810	NP_003801
	FACTOR (LIGAND)
	SUPERFAMILY,
	MEMBER 10
ANKRD22	ANKYRIN REPEAT	NM_144590	NP_653191
	DOMAIN 22
ANXA3	ANNEXIN A3	NM_005139	NP_005130
CEACAM1	CARCINOEMBRYONIC	NM_001712	NP_001703
	ANTIGEN-RELATED
	CELL ADHESION
	MOLECULE 1
LDLR	LOW DENSITY	NM_000527	NP_000518
	LIPOPROTEIN
	RECEPTOR
PFKFB3	6-PHOSPHOFRUCTO-	NM_004566	NP_004557
	2-KINASE/FRUCTOSE-
	2,6-BISPHOSPHATASE
	3
PRV1	NEUTROPHIL-	NM_020406	NP_065139
	SPECIFIC ANTIGEN 1
	(POLYCYTHEMIA
	RUBRA VERA 1)
PSTPIP2	PROLINE/SERINE/	NM_024430	NP_077748
	THREONINE
	PHOSPHATASE-
	INTERACTING
	PROTEIN 1 (PROLINE-
	SERINE-THREONINE
	PHOSPHATASE
	INTERACTING
	PROTEIN 2)
TIFA	TRAF-INTERACTING	NM_052864	NP_443096
	PROTEIN WITH A
	FORKHEAD-
	ASSOCIATED
	DOMAIN
VNN1	VANIN 1	NM_004666	NP004657
NCR1	NATURAL	NM_004829	NP_004820
	CYTOTOXICITY
	TRIGGERING
	RECEPTOR 1
FAD104	FIBRONECTIN TYPE	NM_022763	NP_073600
	III DOMAIN
	CONTAINING 3B
	(FNDC3B)
INSL3	INSULIN-LIKE 3	NM_005543	NP_005534
	(LEYDIG CELL)
CRTAP	CARTILAGE-	NM_006371	NP_006362
	ASSOCIATED
	PROTEIN
HLA-DRA	MAJOR	NM_002123	NP_002114
	HISTOCOMPATIBILITY
	COMPLEX, CLASS
	II, DR ALPHA
SOD2	SUPEROXIDE	NM_000636	NP_000627
	DISMUTASE 2,
	MITOCHONDRIAL

TABLE K
Biomarkers identified based on the ability of the protein form
of the biomarker to discriminate between SIRS and sepsis
		Gene	Protein
Gene		Accession	Accession
Symbol	Gene Name	Number	Number
1	2	3	4
IL-6	INTERLEUKIN 6	NM_000600	NP_000591
IL-8	INTERLEUKIN 8	M28130	AAA59158
CRP	C Reactive protein	CAA39671	NM_000567
IL-10	INTERLEUKIN 10	NM_000572	CAH73907
APOC3	APOLIPOPROTEIN CIII	NM_000040	CAA25648
MMP9	MATRIX	NM_004994	NP_004985
	METALLOPROTEINASE 9
	(GELATINASE B, 92KDA
	GELATINASE, 92KDA TYPE
	IV COLLAGENASE)
TIMP1	TISSUE INHIBITOR OF	NM_003254	AAA75558
	METALLOPROTEINASE 1
MCP1	MONOCYTE	AF493698,	AAQ75526
	CHEMOATTRACTANT	AF493697
	PROTEIN 1
AFP	ALPHA-FETOPROTEIN	NM_001134	CAA79592
B2M	BETA-2 MICROGLOBULIN	NM_004048	AAA51811

5.11.1 Biomarker Descriptions

The references for the biomarkers in this section merely provide exemplary sequences for the biomarkers set forth in the present application.

The nucleotide sequence of AFP (identified by accession no. NM_001134) is disclosed in, e.g., Beattie et al., 1982, “Structure and evolution of human alpha-fetoprotein deduced from partial sequence of cloned cDNA” Gene 20 (3): 415-422, Harper, M. E. et al., 1983, “Linkage of the evolutionarily-related serum albumin and alpha-fetoprotein genes within q11-22 of human chromosome 4,” Am. J. Hum. Genet. 35 (4):565-572, Morinaga, T. et al., 1983, “Primary structures of human alpha-fetoprotein and its mRNA,” Proc. Natl. Acad. Sci. U.S.A. 80 (15):4604-4608, and the amino acid sequence of AFP (identified by accession no. CAA79592) is disclosed in, e.g., McVey, 1993, Direct Submission, Clinical Research Centre, Haemostasis Research Group, Watford Road, Harrow, UK, HA1 3UJ, McVey et al., 1993, “A G-->A substitution in an HNF I binding site in the human alpha-fetoprotein gene is associated with hereditary persistence of alpha-fetoprotein (HPAFP),” Hum. Mol. Genet. 2 (4): 379-384, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of ANKRD22 (identified by accession no. NM_144590) is disclosed in, e.g., Strausberg, 2002, “Homo sapiens ankyrin repeat domain 22, mRNA (cDNA clone MGC:22805 IMAGE:3682099),” unpublished, and the amino acid sequence of ANKRD22 (identified by accession no. NP_653191) is disclosed in, e.g., Strausberg, 2002, “Homo sapiens ankyrin repeat domain 22, mRNA (cDNA clone MGC:22805 IMAGE:3682099),” unpublished, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of ANXA3 (identified by accession no. NM_005139) is disclosed in, e.g., Pepinsky, R. B. et al., 1988,” Five distinct calcium and phospholipid binding proteins share homology with lipocortin I,” J. Biol. Chem. 263 (22): 10799-10811, Tait. J. F. et al., 1988, “Placental anticoagulant proteins: isolation and comparative characterization four members of the lipocortin family,” Biochemistry 27 (17):6268-6276, Ross, T. S. et al., 1990, “Identity of inositol 1,2-cyclic phosphate 2-phosphohydrolase with lipocortin III,” Science 248 (4955):605-607, and the amino acid sequence of ANXA3 (identified by accession no. NP_005130) is disclosed in, e.g., Pepinsky, R. B et al., 1988,” Five distinct calcium and phospholipid binding proteins share homology with lipocortin I,” J. Biol. Chem. 263 (22): 10799-10811, Tait, J. F. et al., 1988, “Placental anticoagulant proteins: isolation and comparative characterization four members of the lipocortin family,” Biochemistry 27 (17):6268-6276, Ross, T. S. et al., 1990, “Identity of inositol 1,2-cyclic phosphate 2-phosphohydrolase with lipocortin IlI,” Science 248 (4955):605-607, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of Apolipoprotein CIII (APOC3) (identified by accession no. NM_000040) is disclosed in, e.g., Ruiz-Narvaez. et al., 2005 “APOC3/A5 haplotypes, lipid levels, and risk of myocardial infarction in the Central Valley of Costa Rica,” J. Lipid Res. 46 (12), 2605-2613; Garenc et al., 2005, “Effect of the APOC3 Sst I SNP on fasting triglyceride levels in men heterozygous for the LPL P207L deficiency,” Eur. J. Hum. Genet. 13, 1159-1165; Baum. et al., 2005, “Effect of hepatic lipase −514C->T polymorphism and its interactions with apolipoprotein C3-482C->T and apolipoprotein E exon 4 polymorphisms on the risk of nephropathy in chinese type 2 diabetic patients.” Diabetes Care 28, 1704-1709, and the amino acid sequence of APOC3 (identified by accession no. CAA25648) is disclosed in, e.g., Protter et al., 1984, “Isolation and sequence analysis of the human apolipoprotein CIII gene and the intergenic region between the apo A1 and apo CHI,” DNA 3, 449-456, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of ARG2 (identified by accession no. NM_001172) is disclosed in, e.g., Gotoh et al.,1996 “Molecular cloning of cDNA for nonhepatic mitochondrial arginase(arginase II) and comparison of its induction with nitric oxide synthase in a murine macrophage-like cell line,” FEBS Lett. 395 (2-3):119-122, Vockley et al., 1996, “Cloning and characterization of the human type II arginase gene,” Genomics 38 (2):118-123, Gotoh et al., 1997, “Chromosomal localization of the human arginase II gene and tissue distribution of its mRNA,” Biochem. Biophys. Res. Commun. 233 (2):487-491, and the amino acid sequence of ARG2 (identified by accession no. CAG38787) is disclosed in, e.g., Halleck et al., 2004, Direct Submission, RZPD Deutsches Ressourcenzentrum fuer Genomforschung GmbH, Im Neuenheimer Feld 580, D-69120 Heidelberg, Germany, Halleck et al., unpublished, “Cloning of human full open reading frames in Gateway™ system entry vector (pDONR201).” each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of B2M (identified by accession no. NM_004048) is disclosed in, e.g., Krangel, M. S. et al., 1979, “Assembly and maturation of HLA-A and HLA-B antigens in vivo,” Cell 18 (4):979-991, Suggs, S. V. et al., 1981, “Use of synthetic oligonucleotides as hybridization probes: isolation of cloned cDNA sequences for human beta 2-microglobulin,” Proc. Natl. Acad. Sci. U.S.A. 78 (11):6613-6617, Rosa, F. et al., 1983. “The beta2-microglobulin mRNA in human Daudi cells has a mutated initiation codon but is still inducible by interferon,” EMBO J. 2 (2):239-243, and the amino acid sequence of B2M (identified by accession no. AAA51811) is disclosed in, e.g., Gussow, D. et al., 1987, “The human beta 2-microglobulin gene. Primary structure and definition of the transcriptional unit,” J. Immunol. 139 (9): 3132-3138, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of BCL2A1 (identified by accession no. NM_004049) is disclosed in, e.g., Lin, E. Y. et al., 1993, “Characterization of A1. a novel hemopoietic-specific early-response gene with sequence similarity to bcl-2,” J. Immunol. 151 (4):1979-1988, Savitsky, K. et al., “The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different species,” Hum. Mol. Genet. 4 (11):2025-2032, Choi, S. S. et al., 1995, “A novel Bcl-2 related gene, Bfl-1, is overexpressed in stomach cancer and preferentially expressed in bone marrow,” Oncogene 11 (9):1693-1698, and the amino acid sequence of BCL2A1 (identified by accession no. NP_004040) is disclosed in, e.g., Lin, E. Y. et al., 1993, “Characterization of A1, a novel hemopoietic-specific early-response gene with sequence similarity to bcl-2,” J. Immunol. 151 (4):1979-1988, Savitsky, K. et al., “The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different species,” Hum. Mol. Genet. 4 (11):2025-2032, Choi, S. S. et al., 1995, “A novel Bcl-2 related gene, Bfl-1, is overexpressed in stomach cancer and preferentially expressed in bone marrow,” Oncogene 11 (9):1693-1698, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of CCL5 (identified by accession no. NM_002985) is disclosed in, e.g., Schall, T. J. et al., 1988, “A human T cell-specific molecule is a member of a new gene family,” J. Immunol. 141 (3):1018-1025, Donlon, T. A. et al., 1990, “Localization of a human T-cell-specific gene, RANTES (D17S136E), to chromosome 17q1 1.2-q12,” Genomics 6 (3):548-553, Kameyoshi, Y. et al., 1992, “Cytokine RANTES released by thrombin-stimulated platelets is a potent attractant for human eosinophils,” J. Exp. Med. 176 (2):587-592, and the amino acid sequence of CCL5 (identified by accession no. NP_002976) is disclosed in, e.g., Schall, T. J. et al., 1988, “A human T cell-specific molecule is a member of a new gene family,” J. Immunol. 141 (3):1018-1025, Donlon, T. A. et al., 1990, “Localization of a human T-cell-specific gene, RANTES (D17S136E), to chromosome 17911.2-q12,” Genomics 6 (3):548-553, Kameyoshi, Y. et al., 1992. “Cytokine RANTES released by thrombin-stimulated platelets is a potent attractant for human eosinophils,” J. Exp. Med. 176 (2):587-592, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of CD86 (identified by accession nos. NM_006889, NM_l75862) is disclosed in, e.g., Azuma, M. et al., 1993, “B70 antigen is a second ligand for CTLA-4 and CD28,” Nature 366 (6450):76-79, Freeman, G. J. et al., 1993, “Cloning of B7-2: a CTLA-4 counter-receptor that costimulates human T cell proliferation,” Science 262 (5135):909-911. Chen, C. et al., 1994, “Molecular cloning and expression of early T cell costimulatory molecule-1 and its characterization as B7-2 molecule,” J. Immunol. 152 (10):4929-4936, and the amino acid sequence of CD86 (identified by accession nos. NP_008820, NP_787058) is disclosed in, e.g., Azuma, M. et al., 1993. “B70 antigen is a second ligand for CTLA-4 and CD28,” Nature 366 (6450):76-79, Azuma, M. et al., 1993, “B70 antigen is a second ligand for CTLA-4 and CD28,” Nature 366 (6450):76-79, Freeman, G. J. et al., 1993, “Cloning of B7-2: a CTLA-4 counter-receptor that costimulates human T cell proliferation,” Science 262 (5135):909-911, Chen, C. et al., 1994, “Molecular cloning and expression of early T cell costimulatory molecule-1 and its characterization as B7-2 molecule,” J. Immunol. 152 (10):4929-4936, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of CEACAM1 (identified by accession no. NM_001712) is disclosed in, e.g., Svenberg, T. et al., 1979, “Immunofluorescence studies on the occurrence and localization of the CEA-related biliary glycoprotein I (BGP I) in normal human gastrointestinal tissues,” Clin. Exp. Immunol. 36 (3):436-441, Hinoda, Y. et al., 1988, “Molecular cloning of a cDNA coding biliary glycoprotein I: primary structure of a glycoprotein immunologically crossreactive with carcinoembryonic antigen,” Proc. Natl. Acad. Sci. U.S.A. 85 (18):6959-6963, Barnett, T. R. et al., 1989, “Carcinoembryonic antigens: alternative splicing accounts for the multiple mRNAs that code for novel members of the carcinoembryonic antigen family,” J. Cell Biol. 108 (2):267-276, and the amino acid sequence of CEACAM1 (identified by accession no. NP_001703) is disclosed in, e.g., Svenberg, T. et al., 1979, “Immunofluorescence studies on the occurrence and localization of the CEA-related biliary glycoprotein I (BGP I) in normal human gastrointestinal tissues,” Clin. Exp. Immunol. 36 (3):436-441. Hinoda, Y. et al., 1988, “Molecular cloning of a cDNA coding biliary glycoprotein I: primary structure of a glycoprotein immunologically crossreactive with carcinoembryonic antigen,” Proc. Natl. Acad. Sci. U.S.A. 85 (18):6959-6963, Barnett, T. R. et al., 1989, “Carcinoembryonic antigens: alternative splicing accounts for the multiple mRNAs that code for novel members of the carcinoembryonic antigen family,” J. Cell Biol. 108 (2):267-276, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of C Reactive Protein (CRP) (identified by accession no. NM_000567) is disclosed in, e.g., Song et al., 2006, “C-reactive protein contributes to the hypercoagulable state in coronary artery disease,” J. Thromb. Haemost. 4 (1), 98-106; Wakugawa et al., 2006, “C-reactive protein and risk of first-ever ischemic and hemorrhagic stroke in a general Japanese population: the Hisayama Study,” Stroke 37, 27-32; Tong et al., 2005, “Association of testosterone, insulin-like growth factor-T. and C-reactive protein with metabolic syndrome in Chinese middle-aged men with a family history of type 2 diabetes,” J. Clin. Endocrinol. Metab. 90, 6418-6423, and the amino acid sequence of CRP (identified by accession no. CAA39671 is described in a direct submissiong by Tenchini et al., 1990, Tenchini M. L., Dipartimento di Biologia e Genetica per le Scienze mediche, via Viotti 3, 20133 Milano, Italy, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of CRTAP (identified by accession no. NM_006371) is disclosed in, e.g., Castagnola, P. et al., 1997, “Cartilage associated protein (CASP) is a novel developmentally regulated chick embryo protein,” J. Cell. Sci. 110 (PT 12):1351-1359; Tonachini, L. et al., 1999, “cDNA cloning, characterization and chromosome mapping of the gene encoding human cartilage associated protein (CRTAP),” Cytogenet. Cell Genet. 87:(3-4); Morello, R. et al., 1999, “cDNA cloning, characterization and chromosome mapping of Crtap encoding the mouse cartilage associated protein,” Matrix Biol. 18 (3):319-324, and the amino acid sequence of CRTAP (identified by accession no. NP_006362) is disclosed in, e.g., Castagnola, P. et al., 1997, “Cartilage associated protein (CASP) is a novel developmentally regulated chick embryo protein,” J. Cell. Sci. 110 (PT 12):1351-1359, Tonachini, L. et al., 1999, “cDNA cloning, characterization and chromosome mapping of the gene encoding human cartilage associated protein (CRTAP),” Cytogenet. Cell Genet. 87:(3-4), Morello, R. et al., 1999, “cDNA cloning, characterization and chromosome mapping of Crtap encoding the mouse cartilage associated protein,” Matrix Biol. 18 (3):319-324, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of CSFIR (identified by accession no. NM_005211) is disclosed in, e.g., Verbeek, J. S. et al., 1985, “Human c-fms proto-oncogene: comparative analysis with an abnormal allele,” Mol. Cell. Biol. 5 (2):422-426; Xu, D. Q. et al., 1985, “Restriction fragment length polymorphism of the human c-fms gene,” Proc. Natl. Acad. Sci. U.S.A. 82 (9):2862-2865; Sherr, C. J. et al., 1985, “The c-fms proto-oncogene product is related to the receptor for the mononuclear phagocyte growth factor, CSF-1,” Cell 41 (3):665-676, and the amino acid sequence of CSFIR (identified by accession no. NP_005202) is disclosed in, e.g., Verbeek, J. S. et al., 1985, “Human c-fins proto-oncogene: comparative analysis with an abnormal allele,” Mol. Cell. Biol. 5 (2):422-426, Xu, D. Q. et al., 1985, “Restriction fragment length polymorphism of the human c-fms gene,” Proc. Natl. Acad. Sci. U.S.A. 82 (9):2862-2865, Sherr, C. J. et al., 1985, “The c-fms proto-oncogene product is related to the receptor for the mononuclear phagocyte growth factor, CSF-1,” Cell 41 (3):665-676, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of FAD104 (identified by accession no. NM_022763) is disclosed in, e.g., Clark, H. F. et al., 2003, “The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins:a bioinformatics assessment,” Genome Res. 13 (10):2265-2270, Tominaga, K. et al., 2004, “The novel gene fad104, containing a fibronectin type III domain, has a significant role in adipogenesis,” FEBS Lett. 577 (1-2):49-54, and the amino acid sequence of FAD104 (identified by accession no. NP_073600) is disclosed in, e.g., Clark, H. F. et al., 2003, “The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins:a bioinformatics assessment,” Genome Res. 13 (10):2265-2270, Tominaga, K. et al., 2004, “The novel gene fad104, containing a fibronectin type III domain, has a significant role in adipogenesis,” FEBS Lett. 577 (1-2):49-54, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of FCGR1A (identified by accession no. NM_000566) is disclosed in, e.g., Eizuru, Y. et al., 1988, “Induction of Fc (IgG) receptor(s) by simian cytomegaloviruses in human embryonic lung fibroblasts,” Intervirology 29 (6):339-345, Allen, J. M. et al., 1988, “Nucleotide sequence of three cDNAs for the human high affinity Fc receptor (FcRI),” Nucleic Acids Res. 16 (24):11824, van de Winkel, J. G. et al., 1991, “Gene organization of the human high affinity receptor for IgG, Fc gamma RI (CD64). Characterization and evidence for a second gene,” J. Biol. Chem. 266 (20):13449-1345, and the amino acid sequence of FCGR1A (identified by accession no. NP_000557) is disclosed in, e.g., Eizuru, Y. et al., 1988, “Induction of Fe (IgG) receptor(s) by simian cytomegaloviruses in human embryonic lung fibroblasts,” Intervirology 29 (6):339-345. Allen, J. M. et al., 1988, “Nucleotide sequence of three cDNAs for the human high affinity Fc receptor (FcRI),” Nucleic Acids Res. 16 (24):11824, van de Winkel, J. G. et al., 1991, “Gene organization of the human high affinity receptor for IgG, Fc gamma RI (CD64). Characterization and evidence for a second gene,” J. Biol. Chem. 266 (20):13449-1345, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of GADD45A (identified by accession no. NM_001924) is disclosed in, e.g., Papathanasiou, M. A. et al., 1991, “Induction by ionizing radiation of the gadd45 gene in cultured human cells: lack of mediation by protein kinase C,” Mol. Cell. Biol. I1 (2):1009-1016, Hollander, M. C. et al., 1993, “Analysis of the mammalian gadd45 gene and its response to DNA damage,” J. Biol. Chem. 268 (32):24385-24393, Smith, M. L. et al., 1994. “Interaction of the p53-regulated protein Gadd45 with proliferating cell nuclear antigen,” Science 266 (5189):1376-1380, and the amino acid sequence of GADD45A (identified by accession no. NP_001915) is disclosed in, e.g., Papathanasiou, M. A. et al., 1991, “Induction by ionizing radiation of the gadd45 gene in cultured human cells: lack of mediation by protein kinase C,” Mol. Cell. Biol. 11 (2):1009-1016, Hollander, M. C. et al., 1993, “Analysis of the mammalian gadd45 gene and its response to DNA damage,” J. Biol. Chem. 268 (32):24385-24393, Smith, M. L. et al., 1994, “Interaction of the p53-regulated protein Gadd45 with proliferating cell nuclear antigen,” Science 266 (5189):1376-1380, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of GADD45B (identified by accession no. NM_015675) is disclosed in, e.g., Abdollahi, A. et al., 1991, “Sequence and expression of a cDNA encoding MyD118: a novel myeloid differentiation primary response gene induced by multiple cytokines,” Oncogene 6 (1): 165-167, Vairapandi, M. et al., 1996, “The differentiation primary response gene MyD118, related to GADD45, encodes for a nuclear protein which interacts with PCNA and p21WAF1/CIP1,” Oncogene 12 (12):2579-2594, Koonin, E. V., 1997, “Cell cycle and apoptosis: possible roles of Gadd45 and MyD118 proteins inferred from their homology to ribosomal proteins,” J. Mol. Med. 75 (4):236-238, and the amino acid sequence of GADD45B (identified by accession no. NP_056490) is disclosed in, e.g., Abdollahi, A. et al., 1991, “Sequence and expression of a cDNA encoding MyD118: a novel myeloid differentiation primary response gene induced by multiple cytokines,” Oncogene 6 (1):165-167, Vairapandi, M. et al., 1996. “The differentiation primary response gene MyD118, related to GADD45, encodes for a nuclear protein which interacts with PCNA and p21WAF1/CIP1,” Oncogene 12 (12):2579-2594, Koonin, E. V., 1997. “Cell cycle and apoptosis: possible roles of Gadd45 and MyD118 proteins inferred from their homology to ribosomal proteins,” J. Mol. Med. 75 (4):236-238, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of HLA-DRA (identified by accession no. NM_002123) is disclosed in, e.g., Larhammar, D. et al., 1981, Evolutionary relationship between HLA-DR antigen beta-chains, HLA-A, B, C antigen subunits and immunoglobulin chains,” Scand. J. Immunol. 14 (6):617-622, Wiman, K. et al., 1982, “Isolation and identification of a cDNA clone corresponding to an HLA-DR antigen beta chain,” Proc. Natl. Acad. Sci. U.S.A. 79 (6):1703-1707. Larhammar, D. et al., 1982, “Complete amino acid sequence of an HLA-DR antigen-like beta chain as predicted from the nucleotide sequence: similarities with immunoglobulins and HLA-A, -B, and -C antigens,” Proc. Natl. Acad. Sci. U.S.A. 79 (12):3687-3691, and the amino acid sequence of HLA-DRA (identified by accession no. NP_002114) is disclosed in, e.g., Larhammar, D. et al., 1981, Evolutionary relationship between HLA-DR antigen beta-chains, HLA-A, B, C antigen subunits and immunoglobulin chains,” Scand. J. Immunol. 14 (6):617-622, Wiman, K. et al., 1982. “Isolation and identification of a cDNA clone corresponding to an HLA-DR antigen beta chain,” Proc. Natl. Acad. Sci. U.S.A. 79 (6):1703-1707, Larhammar, D. et al., 1982, “Complete amino acid sequence of an HLA-DR antigen-like beta chain as predicted from the nucleotide sequence: similarities with immunoglobulins and HLA-A, -B, and -C antigens,” Proc. NatI. Acad. Sci. U.S.A. 79 (12):3687-3691. each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of IFNGR1 (identified by accession no. NM_000416) is disclosed in, e.g., Novick, D. et al., 1987, “The human interferon-gamma receptor. Purification, characterization, and preparation of antibodies, each of which is incorporated by reference herein in its entirety,” J. Biol. Chem. 262 (18): 8483-8487, Aguet, M. et al., 1988, “Molecular cloning and expression of the human interferon-gamma receptor,” Cell 55 (2): 273-280, Le Coniat, M. et al., 1989, “Human interferon gamma receptor 1 (TFNGR 1) gene maps to chromosome region 6q23-6q24,” Hum. Genet. 84 (1):92-94, and the amino acid sequence of IFNGR1 (identified by accession no. NP_000407) is disclosed in, e.g., Novick, D. et al., 1987, “The human interferon-gamma receptor. Purification, characterization, and preparation of antibodies,” J. Biol. Chem. 262 (18):8483-8487, Aguet, M. et al., 1988, “Molecular cloning and expression of the human interferon-gamma receptor,” Cell 55 (2): 273-280, Le Coniat, M. et al., 1989, “Human interferon gamma receptor 1 (IFNGR1) gene maps to chromosome region 6q23-6q24,” Hum. Genet. 84 (1):92-94, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of IL1RN (identified by accession nos. NM_000577, NM_173841, NM_173842, NM_173843) is disclosed in, e.g., Eisenberg, S. P. et al., 1990, “Primary structure and functional expression from complementary DNA of a human interleukin-1 receptor antagonist,” Nature 343 (6256):341-346, Carter, D. B. et al., 1990, “Purification, cloning, expression and biological characterization of an interleukin-1 receptor antagonist protein,” Nature 344 (6267):633-638, Seckinger, P. et al., 1990, “Natural and recombinant human IL-1 receptor antagonists block the effects of IL-1 on bone resorption and prostaglandin production,” J. Immunol. 145 (12):4181-4184, and the amino acid sequence of ILIRN (identified by accession no. AAN87150) is disclosed in, e.g., Rieder, M. J. et al., 2002, Direct Submission, Genome Sciences, University of Washington, 1705 NE Pacific, Seattle, WA 98195, USA, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of TL-6 (identified by accession no. NM_000600) is disclosed in, e.g., Haegeman, G. et al., 1986, “Structural analysis of the sequence coding for an inducible 26-kDa protein in human fibroblasts,” Eur. J. Biochem. 159 (3):625-632, Zilberstein, A. et al., 1986, “Structure and expression of cDNA and genes for human interferon-beta-2, a distinct species inducible by growth-stimulatory cytokines,” EMBO J. 5 (10):2529-2537, Hirano, T. et al., 1986, “Complementary DNA for a novel human interleukin (BSF-2) that induces B lymphocytes to produce immunoglobulin,” Nature 324 (6092):73-76, and the amino acid sequence of IL-6 (identified by accession no. NP_000591) is disclosed in, e.g., Haegeman, G. et al., 1986, “Structural analysis of the sequence coding for an inducible 26-kDa protein in human fibroblasts,” Eur. J. Biochem. 159 (3):625-632, Zilberstein, A. et al., 1986, “Structure and expression of cDNA and genes for human interferon-beta-2, a distinct species inducible by growth-stimulatory cytokines,” EMBO J. 5 (10):2529-2537, Hirano, T. et al., 1986, “Complementary DNA for a novel human interleukin (BSF-2) that induces B lymphocytes to produce immunoglobulin,” Nature 324 (6092):73-76, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of TL-8 (identified by accession no. M28130) and the amino acid sequence of IL-8 (identified by accession no.AAA59158) are each disclosed in, e.g., Mukaida et al., 1989, “Genomic structure of the human monocyte-derived neutrophil chemotactic factor IL-8,” J. Immunol. 143, 1366-1371 which is incorporated by reference herein in its entirety.

The nucleotide sequence of IL-10 (identified by accession no. NM_000572) is disclosed in, e.g., Ghosh, S. et al., 1975, “Anaerobic acidogenesis of wastewater sludge,” Breast Cancer Res. Treat. 47 (1):30-45, Hsu, D. H. et al., 1990. “Expression of interleukin-10 activity by Epstein-Barr virus protein BCRF1,” Science 250 (4982):830-832, Vieira, P. et al., 1991, “Isolation and expression of human cytokine synthesis inhibitory factor cDNA clones: homology to Epstein-Barr virus open reading frame BCRF1,” Proc. Natl. Acad. Sci. U.S.A. 88 (4):1172-1176, and the amino acid sequence of IL-10 (identified by accession no. CAH73907) is disclosed in, e.g., Tracey, A., 2005, Direct Submission, Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, CB10 1SA, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of ILIORA (identified by accession no. NM_001558) is disclosed in, e.g., Tan, J. C. et al., 1993, “Characterization of interleukin-10 receptors on human and mouse cells,” J. Biol. Chem. 268 (28):21053-21059, Ho, A. S. et al., 1993, “A receptor for interleukin 10 is related to interferon receptors,” Proc. Natl. Acad. Sci. U.S.A. 90 (23):11267-11271. Liu, Y. et al., 1994, “Expression cloning and characterization of a human IL-10 receptor,” J. Immunol. 152 (4):1821-1829, and the amino acid sequence of IL10RA (identified by accession no. NP_001549) is disclosed in, e.g., Tan, J. C. et al., 1993, “Characterization of interleukin-10 receptors on human and mouse cells,” J. Biol. Chem. 268 (28):21053-21059, Ho, A. S. et al., 1993, “A receptor for interleukin 10 is related to interferon receptors,” Proc. Natl. Acad. Sci. U.S.A. 90 (23):11267-11271, Liu, Y. et al., 1994, “Expression cloning and characterization of a human IL-10 receptor,” J. Immunol. 152 (4):1821-1829, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of IL18R1 (identified by accession no. NM_003855) is disclosed in, e.g., Parnet, P. et al., 1996, “IL-1Rrp is a novel receptor-like molecule similar to the type I interleukin-1 receptor and its homologues T/ST2 and IL-IR AcP,” J. Biol. Chem. 271 (8):3967-3970, Lovenberg, T. W. et al., 1996, “Cloning of a cDNA encoding a novel interleukin-1 receptor related protein (IL 1R-rp2),” J. Neuroimmunol. 70 (2):113-122, Torigoe, K. et al., 1997, “Purification and characterization of the human interleukin-18 receptor,” J. Biol. Chem. 272 (41):25737-25742, and the amino acid sequence of IL18R1 (identified by accession no. NP_003846) is disclosed in, e.g., Parnet, P. et al., 1996, “IL-1Rrp is a novel receptor-like molecule similar to the type I interleukin-1 receptor and its homologues T1/ST2 and IL-IR AcP,” J. Biol. Chem. 271 (8):3967-3970, Lovenberg, T. W. et al., 1996, “Cloning of a cDNA encoding a novel interleukin-1 receptor related protein (IL 1R-rp2),” J. Neuroimmunol. 70 (2):113-122, Torigoe, K. et al., 1997, “Purification and characterization of the human interleukin-18 receptor,” J. Biol. Chem. 272 (41):25737-25742, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of INSL3 (identified by accession no. NM_005543) is disclosed in, e.g., Adham, I. M. et al., 1993, “Cloning of a cDNA for a novel insulin-like peptide of the testicular Leydig cells,” J. Biol. Chem. 268 (35):26668-26672, Burkhardt, E. et al., 1994, “Structural organization of the porcine and human genes coding for a Leydig cell-specific insulin-like peptide (LEY T-L) and chromosomal localization of the human gene (INSL3),” Genomics 20 (1):13-19, Burkhardt, E. et al., 1994, “A human cDNA coding for the Leydig insulin-like peptide (Ley I-L),” Hum. Genet. 94 (1):91-94, and the amino acid sequence of TNSL3 (identified by accession no. NP_005534) is disclosed in, e.g., Adham, I. M. et al., 1993, “Cloning of a cDNA for a novel insulin-like peptide of the testicular Leydig cells,” J. Biol. Chem. 268 (35):26668-26672, Burkhardt, E. et al., 1994, “Structural organization of the porcine and human genes coding for a Leydig cell-specific insulin-like peptide (LEY I-L) and chromosomal localization of the human gene (TNSL3),” Genomics 20 (1):13-19, Burkhardt, E. et al., 1994, “A human cDNA coding for the Leydig insulin-like peptide (Ley 1-L),” Hum. Genet. 94 (1):91-94, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of IRAK2 (identified by accession no. NM_001570) is disclosed in, e.g., Muzio, M. et al., 1997, “IRAK (Pelle) family member IRAK-2 and MyD88 as proximal mediators of IL-1 signaling,” Science 278 (5343):1612-1615, Auron, P. E., 1998, “The interleukin I receptor: ligand interactions and signal transduction,” Cytokine Growth Factor Rev. 9 (3-4):221-237, Maschera, B. et al., 1999, “Overexpression of an enzymically inactive interleukin-1-receptor-associated kinase activates nuclear factor-kappaB,” Biochem. J. 339 (PT 2):227-231, and the amino acid sequence of IRAK2 (identified by accession no. NP_001561) is disclosed in, e.g., Muzio, M. et al., 1997, “IRAK (Pelle) family member TRAK-2 and MyD88 as proximal mediators of IL-1 signaling,” Science 278 (5343):1612-1615, Auron, P. E., 1998, “The interleukin 1 receptor: ligand interactions and signal transduction,” Cytokine Growth Factor Rev. 9 (3-4):221-237, Maschera, B. et al., 1999, “Overexpression of an enzymically inactive interleukin-1-receptor-associated kinase activates nuclear factor-kappaB,” Biochem. J. 339 (PT 2):227-231, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of IRAK4 (identified by accession no. NM_016123) is disclosed in, e.g., Siu, G. et al., 1986, “Analysis of a human V beta gene subfamily,” J. Exp. Med. 164 (5):1600-1614, Scanlan, M. J. et al., 1999, “Antigens recognized by autologous antibody in patients with renal-cell carcinoma,” Int. J. Cancer 83 (4):456-464, Li, S. et al., 2002. “IRAK-4: a novel member of the IRAK family with the properties of an IRAK-kinase,” Proc. Natl. Acad. Sci. U.S.A. 99 (8):5567-5572, and the amino acid sequence of IRAK4 (identified by accession no. NP_057207) is disclosed in, e.g., Siu, G. et al., 1986, “Analysis of a human V beta gene subfamily,” J. Exp. Med. 164 (5):1600-1614, Scanlan, M. J. et al., 1999, “Antigens recognized by autologous antibody in patients with renal-cell carcinoma,” Int. J. Cancer 83 (4):456-464, Li, S. et al., 2002, “IRAK-4: a novel member of the IRAK family with the properties of an IRAK-kinase,” Proc. Natl. Acad. Sci. U.S.A. 99 (8):5567-5572, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of ITGAM (identified by accession no. NM_000632) is disclosed in, e.g., Micklem, K. J. et al., 1985, “Isolation of complement-fragment-iC3b-binding proteins by affinity chromatography. The identification of p150,95 as an iC3b-binding protein,” Biochem. J. 231 (1):233-236, Pierce, M. W. et al., 1986, “N-terminal sequence of human leukocyte glycoprotein Mol:conservation across species and homology to platelet IIb/IIIa,” Biochim. Biophys. Acta 874 (3):368-371, Arnaout, M. A. et al., 1988. “Molecular cloning of the alpha subunit of human and guinea pig leukocyte adhesion glycoprotein Mol: chromosomal localization and homology to the alpha subunits of integrins,” Proc. Natl. Acad. Sci. U.S.A. 85 (8):2776-2780, and the amino acid sequence of ITGAM (identified by accession no. NP_000623) is disclosed in, e.g., Micklem, K. J. et al., 1985, “Isolation of complement-fragment-iC3b-binding proteins by affinity chromatography. The identification of p150,95 as an iC3b-binding protein,” Biochem. J. 231 (1):233-236, Pierce, M. W. et al., 1986, “N-terminal sequence of human leukocyte glycoprotein Mol:conservation across species and homology to platelet IIb/Ia,” Biochim. Biophys. Acta 874 (3):368-371, Arnaout, M. A. et al., 1988, “Molecular cloning of the alpha subunit of human and guinea pig leukocyte adhesion glycoprotein Mo1: chromosomal localization and homology to the alpha subunits of integrins,” Proc. Natl. Acad. Sci. U.S.A. 85 (8):2776-2780, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of JAK2 (identified by accession no. NM_004972) is disclosed in, e.g., Wilks, A. F. et al., 1991, “Two novel protein-tyrosine kinases, each with a second phosphotransferase-related catalytic domain, define a new class of protein kinase,” Mol. Cell. Biol. 11 (4):2057-2065, Pritchard, M. A. et al., 1992, “Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24,” Mamm. Genome 3 (1):36-38, Witthuhn, B. A. et al., 1993, “JAK2 associates with the erythropoietin receptor and is tyrosine phosphorylated and activated following stimulation with erythropoietin,” Cell 74 (2):227-236, and the amino acid sequence of JAK2 (identified by accession no. NP_004963) is disclosed in, e.g., Wilks, A. F. et al., 1991, “Two novel protein-tyrosine kinases, each with a second phosphotransferase-related catalytic domain, define a new class of protein kinase,” Mol. Cell. Biol. 11 (4):2057-2065, Pritchard, M. A. et al., 1992, “Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24,” Mamm. Genome 3 (1):36-38, Witthuhn, B. A. et al., 1993. “JAK2 associates with the erythropoietin receptor and is tyrosine phosphorylated and activated following stimulation with erythropoietin,” Cell 74 (2):227-236, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of LDLR (identified by accession no. NM_000527) is disclosed in, e.g., Brown, M. S. et al., 1979, “Receptor-mediated endocytosis: insights from the lipoprotein receptor system,” Proc. Natl. Acad. Sci. U.S.A. 76 (7):3330-3337, Goldstein, J. L. et al., 1982, “Receptor-mediated endocytosis and the cellular uptake of low density lipoprotein.” Ciba Found. Symp. 92, 77-95, Tolleshaug H. et al., 1983, “The LDL receptor locus in familial hypercholesterolemia: multiple mutations disrupt transport and processing of a membrane receptor,” Cell 32 (3):941-951, and the amino acid sequence of LDLR (identified by accession no. NP_000518) is disclosed in, e.g., Brown, M. S. et al., 1979, “Receptor-mediated endocytosis: insights from the lipoprotein receptor system,” Proc. Natl. Acad. Sci. U.S.A. 76 (7):3330-3337, Goldstein, J. L. et al., 1982, “Receptor-mediated endocytosis and the cellular uptake of low density lipoprotein,” Ciba Found. Symp. 92, 77-95. Tolleshaug. H. et al., 1983, “The LDL receptor locus in familial hypercholesterolemia: multiple mutations disrupt transport and processing of a membrane receptor,” Cell 32 (3):941-951, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of LY96 (identified by accession no. NM_015364) is disclosed in, e.g., Shimazu, R. et al., 1999, “MD-2, a molecule that confers lipopolysaccharide responsiveness on Toll-like receptor 4,” J. Exp. Med. 189 (11):1777-1782, Kato, K. et al., 2000, “ESOP-1, a secreted protein expressed in the hematopoietic, nervous, and reproductive systems of embryonic and adult mice,” Blood 96 (1):362-364, Dziarski, R. et al., 2001, “MD-2 enables Toll-like receptor 2 (TLR2)-mediated responses to lipopolysaccharide and enhances TLR2-mediated responses to Gram-positive and Gram-negative bacteria and their cell wall components,” J. Immunol. 166 (3):1938-1944, and the amino acid sequence of LY96 (identified by accession no. NP_056179) is disclosed in, e.g., Shimazu, R. et al., 1999, “MD-2, a molecule that confers lipopolysaccharide responsiveness on Toll-like receptor 4,” J. Exp. Med. 189 (11):1777-1782, Kato, K. et al., 2000, “ESOP-1, a secreted protein expressed in the hematopoietic, nervous, and reproductive systems of embryonic and adult mice,” Blood 96 (1):362-364, Dziarski, R. et al., 2001, “MD-2 enables Toll-like receptor 2 (TLR2)-mediated responses to lipopolysaccharide and enhances TLR2-mediated responses to Gram-positive and Gram-negative bacteria and their cell wall components,” J. Immunol. 166 (3):1938-1944, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of MAP2K6 (identified by accession nos. NM_002758, NM_031988) is disclosed in, e.g., Han, J. et al., 1996, “Characterization of the structure and function of a novel MAP kinase kinase (MKK6), J. Biol. Chem. 271 (6):2886-2891, Raingeaud, J. et al., 1996, “MKK3- and MKK6-regulated gene expression is mediated by the p38 mitogen-activated protein kinase signal transduction pathway,” Mol. Cell. Biol. 16 (3), 1247-1255, Stein, B. et al., 1996, “Cloning and characterization of MEK6, a novel member of the mitogen-activated protein kinase kinase cascade.” J. Biol. Chem. 271 (19): 11427-11433, and the amino acid sequence of MAP2K6 (identified by accession nos. NP_002749, NP_114365) is disclosed in, e.g., Han, J. et al., 1996, “Characterization of the structure and function of a novel MAP kinase kinase (MKK6), J. Biol. Chem. 271 (6):2886-2891, Raingeaud, J. et al., 1996, “MKK3- and MKK6-regulated gene expression is mediated by the p38 mitogen-activated protein kinase signal transduction pathway,” Mol. Cell. Biol. 16 (3), 1247-1255, Stein, B. et al., 1996, “Cloning and characterization of MEK6, a novel member of the mitogen-activated protein kinase kinase cascade,” J. Biol. Chem. 271 (19): 11427-11433, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of MAPK14 (identified by accession nos. NM_001315, NM_139012, NM_139013, NM_139014) is disclosed in, e.g., Zhukov-Verezhnikov, N. N. et al., 1976, “Study of the heterogenetic antigens in vaccinal preparations of V. cholerae,” Biochem. Biophys. Res. Commun. 82 (8):961-962, Schultz, S. J. et al., 1993, Identification of 21 novel human protein kinases, including 3 members of a family related to the cell cycle regulator nimA of Aspergillus nidulans,” Cell Growth Differ. 4 (10):821-830, Lee, J. C. et al., 1994, “A protein kinase involved in the regulation of inflammatory cytokine biosynthesis,” Nature 372 (6508):739-746, and the amino acid sequence of MAPK14 (identified by accession nos. NP_001306, NP_620581, NP_620582, NP_620583) is disclosed in, e.g., Zhukov-Verezhnikov, N. N. et al., 1976, “Study of the heterogenetic antigens in vaccinal preparations of V. cholerae,” Biochem. Biophys. Res. Commun. 82 (8):961-962. Schultz, S. J. et al., 1993, Identification of 21 novel human protein kinases, including 3 members of a family related to the cell cycle regulator nimA of Aspergillus nidulans,” Cell Growth Differ. 4 (10):821-830, Lee, J. C. et al., 1994, “A protein kinase involved in the regulation of inflammatory cytokine biosynthesis,” Nature 372 (6508):739-746, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of Monocyte Chemoattractant Protein 1 (MCP1) (identified by accession nos. AF493698 and AF493697) is disclosed in, e.g., Shanmugasundaram et al., 2002, Virology II, National Institute of Immunology, Aruna Asag Ali Marg, J.N.U. Campus, New Delhi 110 067, India, and the amino acid sequence of MCP1 (identified by accession no. AAQ75526) is disclosed in, e.g., Nyquist et al., 2003, direct submission, Medicine, Inova Fairfax, 3300 Gallows Road, Falls Church, Virginia 22402-3300, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of MKNKI (identified by accession nos. NM_003684, NM 198973) is disclosed in, e.g., Fukunaga et al., 1997, “MNK1, a new MAP kinase-activated protein kinase, isolated by a novel expression screening method for identifying protein kinase substrates, EMBO J. 16: 1921-1933; Pyronnet et al., 1999. “Human eukaryotic translation initiation factor 4G (eIF4G) recruits mnk1 to phosphorylate eIF4E,” EMBO J. 18: 270-279; Cuesta et al., 2000, “Chaperone hsp27 inhibits translation during heat shock by binding eIF4G and facilitating dissociation of cap-initiation complexes,” Genes Dev. 14: 1460-1470, and the amino acid sequence of MKNK1 (identified by accession nos. NP_003675, NP_945324) is disclosed in, e.g., Fukunaga et al., 1997, “MNK1, a new MAP kinase-activated protein kinase, isolated by a novel expression screening method for identifying protein kinase substrates.” EMBO J. 16:1921-1933, Pyronnet et al., 1999, “Human eukaryotic translation initiation factor 4G (eIF4G) recruits mnkl to phosphorylate eIF4E,” EMBO J. 18: 270-279, Cuesta et al., 2000, “Chaperone hsp27 inhibits translation during heat shock by binding eIF4G and facilitating dissociation of cap-initiation complexes,” Genes Dev. 14: 1460-1470, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of MMP9 (identified by accession no. NM_004994) is disclosed in, e.g., Wilhelm et al., 1989, “SV40-transformed human lung fibroblasts secrete a 92-kDa type IV collagenase which is identical to that secreted by normal human macrophages” J. Biol. Chem. 264: 17213-17221, Huhtala et al., 1990, “Completion of the primary structure of the human type IV collagenase preproenzyme and assignment of the gene (CLG4) to the q21 region of chromosome 16,” Genomics 6: 554-559, Collier et al., 1991, “On the structure and chromosome location of the 72- and 92-kDa human type IV collagenase genes,” Genomics 9: 429-434, and the amino acid sequence of MMP9 (identified by accession no. NP_004985) is disclosed in, e.g., Wilhelm et al., 1989, “SV40-transformed human lung fibroblasts secrete a 92-kDa type IV collagenase which is identical to that secreted by normal human macrophages,” J. Biol. Chem. 264: 17213-17221, Huhtala et al., 1990. “Completion of the primary structure of the human type IV collagenase preproenzyme and assignment of the gene (CLG4) to the q21 region of chromosome 16,” Genomics 6: 554-559, Collier et al., 1991, “On the structure and chromosome location of the 72- and 92-kDa human type IV collagenase genes,” Genomics 9: 429-434, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of NCR1 (identified by accession no. NM_004829) is disclosed in, e.g., Sivori et al., 1997, “p46, a novel natural killer cell-specific surface molecule that mediates cell activation.” J. Exp. Med. 186:1129-1136, Vitale.M. et al., NKp44, 1998, “NKp44, a novel triggering surface molecule specifically expressed by activated natural killer cells, is involved in non-major histocompatibility complex-restricted tumor cell lysis,” J. Exp. Med. 187: 2065-2072, Pessino et al., 1998, “Molecular cloning of NKp46: a novel member of the immunoglobulin superfamily involved in triggering of natural cytotoxicity,” J. Exp. Med. 188: 953-960, and the amino acid sequence of NCRI (identified by accession no. NP_004820) is disclosed in, e.g., Sivori et al., 1997, “p46, a novel natural killer cell-specific surface molecule that mediates cell activation,” J. Exp. Med. 186:1129-1136, Vitale et al., NKp44, 1998, “NKp44, a novel triggering surface molecule specifically expressed by activated natural killer cells, is involved in non-major histocompatibility complex-restricted tumor cell lysis,” J. Exp. Med. 187: 2065-2072, Pessino et al., 1998, “Molecular cloning of NKp46: a novel member of the immunoglobulin superfamily involved in triggering of natural cytotoxicity,” J. Exp. Med. 188: 953-96, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of OSM (identified by accession no. NM_020530) is disclosed in, e.g., Zarling et al., 1986, “Oncostatin M: a growth regulator produced by differentiated histiocytic lymphoma cells,” Proc. Natl. Acad. Sci. U.S.A. 83 (24):9739-9743, Malik et al., 1989, “Molecular cloning, sequence analysis, and functional expression of a novel growth regulator, oncostatin M,” Mol. Cell. Biol. 9 (7):2847-2853, Linsley, P. S. et al., 1990, “Cleavage of a hydrophilic C-terminal domain increases growth-inhibitory activity of oncostatin M,” Mol. Cell. Biol. 10 (5):1882-1890, and the amino acid sequence of OSM (identified by accession no. NP_065391) is disclosed in, e.g., Zarling, J. M. et al., 1986, “Oncostatin M: a growth regulator produced by differentiated histiocytic lymphoma cells,” Proc. Natl. Acad. Sci. U.S.A. 83 (24):9739-9743, Malik, N. et al., 1989, “Molecular cloning, sequence analysis, and functional expression of a novel growth regulator, oncostatin M,” Mol. Cell. Biol. 9 (7):2847-2853, Linsley, P. S. et al., 1990, “Cleavage of a hydrophilic C-terminal domain increases growth-inhibitory activity of oncostatin M.” Mol. Cell. Biol. 10 (5):1882-1890, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of PFKFB3 (identified by accession no. NM_004566) is disclosed in, e.g., Sakai, A. et al., 1996, “Cloning of cDNA encoding for a novel isozyme of fructose 6-phosphate, 2-kinase/fructose 2,6-bisphosphatase from human placenta,” J. Biochem. 19 (3):506-511, Hamilton, J. A. et al., 1997, “Identification of PRG1, a novel progestin-responsive gene with sequence homology to 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase,”

Mol. Endocrinol. 11 (4):490-502, Nicholl, J. et al., “The third human isoform of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFKFB3) map position 10p14-p15, Chromosome Res. 5 (2):150, and the amino acid sequence of PFKFB3 (identified by accession no. NP_004557) is disclosed in, e.g., Sakai, A. et al., 1996, “Cloning of cDNA encoding for a novel isozyme of fructose 6-phosphate, 2-kinase/fructose 2,6-bisphosphatase from human placenta,” J. Biochem. 119 (3):506-511, Hamilton, J. A. et al., 1997, “Identification of PRG1, a novel progestin-responsive gene with sequence homology to 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase,” Mol. Endocrinol. 11 (4):490-502, Nicholl, J. et al., “The third human isoform of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFKFB3) map position 10p14-p15, Chromosome Res. 5 (2):150, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of PRV I (identified by accession no. NM_020406) is disclosed in, e.g., Lalezari, P. et al., 1971, “NB1, a new neutrophil-specific antigen involved in the pathogenesis of neonatal neutropenia,” J. Clin. Invest. 50 (5):1108-1115, Goldschmeding, R. et al., 1992, “Further characterization of the NB 1 antigen as a variably expressed 56-62 kD GPI-linked glycoprotein of plasma membranes and specific granules of neutrophils,” Br. J. Haematol. 81 (3):336-345, Stroncek, D. F. et al., “Neutrophil-specific antigen NB1 inhibits neutrophil-endothelial cell interactions,” J. Lab. Clin. Med. 123 (2):247-255, and the amino acid sequence of PRV1 (identified by accession no. NP_065139) is disclosed in, e.g., Lalezari, P. et al., 1971, “NB1, a new neutrophil-specific antigen involved in the pathogenesis of neonatal neutropenia,” J. Clin. Invest. 50 (5):1108-1115, Goldschmeding, R. et al., 1992, “Further characterization of the NB 1 antigen as a variably expressed 56-62 kD GPI-linked glycoprotein of plasma membranes and specific granules of neutrophils,” Br. J. Haematol. 81 (3):336-345, Stroncek, D. F. et al., “Neutrophil-specific antigen NBI inhibits neutrophil-endothelial cell interactions,” J. Lab. Clin. Med. 123 (2):247-255, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of PSTPTP2 (identified by accession no. NM_024430) is disclosed in, e.g., Hillier, L. D. et al., 1996, “Generation and analysis of 280,000 human expressed sequence tags,” Genome Res. 6 (9):807-828, Wu, Y. et al., 1998, “PSTPIP 2, a second tyrosine phosphorylated, cytoskeletal-associated protein that binds a PEST-type protein-tyrosine phosphatase,” J. Biol. Chem. 273 (46):30487-30496, Yeung, Y. G. et al., 1998, “A novel macrophage actin-associated protein (MAYP) is tyrosine-phosphorylated following colony stimulating factor-1 stimulation,” J. Biol. Chem. 273 (46): 30638-30642, and the amino acid sequence of PSTPIP2 (identified by accession no. NP_077748) is disclosed in, e.g., Hillier, L. D. et al., 1996, “Generation and analysis of 280,000 human expressed sequence tags,” Genome Res. 6 (9):807-828, Wu, Y. et al., 1998, “PSTPIP 2, a second tyrosine phosphorylated, cytoskeletal-associated protein that binds a PEST-type protein-tyrosine phosphatase,” J. Biol. Chem. 273 (46):30487-30496, Yeung, Y. G. et al., 1998, “A novel macrophage actin-associated protein (MAYP) is tyrosine-phosphorylated following colony stimulating factor-1 stimulation,” J. Biol. Chem. 273 (46): 30638-30642, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of SOCS3 (identified by accession no. NM_003955) is disclosed in, e.g., Minamoto, S. et al., 1997, “Cloning and functional analysis of new members of STAT induced STAT inhibitor (SSI) family: SSI-2 and SSI-3,” Biochem. Biophys. Res. Commun. 237 (1):79-83, Masuhara, M. et al., 1997, “Cloning and characterization of novel CIS family genes,” Biochem. Biophys. Res. Commun. 239 (2):439-446, Zhang, J. G. et al., 1999, “The conserved SOCS box motif in suppressors of cytokine signaling binds to elongins B and C and may couple bound proteins to proteasomal degradation,” Proc. Natl. Acad. Sci. U.S.A. 96 (5):2071-2076, and the amino acid sequence of SOCS3 (identified by accession no. NP_003946) is disclosed in, e.g., Minamoto, S. et al., 1997, “Cloning and functional analysis of new members of STAT induced STAT inhibitor (SSI) family: SSI-2 and SSI-3,” Biochem. Biophys. Res. Commun. 237 (1):79-83, Masuhara, M. et al., 1997, “Cloning and characterization of novel CIS family genes,” Biochem. Biophys. Res. Commun. 239 (2):439-446, Zhang, J. G. et al., 1999, “The conserved SOCS box motif in suppressors of cytokine signaling binds to elongins B and C and may couple bound proteins to proteasomal degradation,” Proc. Natl. Acad. Sci. U.S.A. 96 (5):2071-2076, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of SOD2 (identified by accession no. NM_000636) is disclosed in, e.g., Smith, M. et al., 1978. “Regional localization of HLA, MES, and SODM on chromosome 6,” Cytogenet. Cell Genet. 22 (1-6):428-433, Beck, Y. et al., 1987, “Human Mn superoxide dismutase cDNA sequence,” Nucleic Acids Res. 15 (21):9076, Ho, Y. S. et al., 1988, “Isolation and characterization of complementary DNAs encoding human manganese-containing superoxide dismutase,” FEBS Lett. 229 (2):256-260, and the amino acid sequence of SOD2 (identified by accession no. NP_000627) is disclosed in, e.g., Smith, M. et al., 1978, “Regional localization of HLA, MES, and SODM on chromosome 6,” Cytogenet. Cell Genet. 22 (1-6):428-433, Beck, Y. et al., 1987, “Human Mn superoxide dismutase cDNA sequence,” Nucleic Acids Res. 15 (21):9076, Ho, Y. S. et al., 1988, “Isolation and characterization of complementary DNAs encoding human manganese-containing superoxide dismutase,” FEBS Lett. 229 (2):256-260, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of TDRD9 (identified by accession no. NM_153046) is disclosed in, e.g., Isogai et al., 2003, “Homo sapiens cDNA FU43990 fis, clone TEST14019566, weakly similar to Dosage compensation regulator,” unpublished, and the amino acid sequence of TDRD9 (identified by accession no. NP_694591) is disclosed in, e.g., Isogai et al., 2003, “Homo sapiens cDNA FLJ43990 fis, clone TEST14019566, weakly similar to Dosage compensation regulator,” unpublished, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of TGFBI (identified by accession no. NM_000358) is disclosed in, e.g., Skonier et al., 1992, “cDNA cloning and sequence analysis of beta ig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor-beta,” DNA Cell Biol. 11 (7):511-522. Stone et al., 1994, “Three autosomal dominant corneal dystrophies map to chromosome 5q,” Nat. Genet. 6 (1):47-51, Skonier et al., 1994, “beta ig-h3: a transforming growth factor-beta-responsive gene encoding a secreted protein that inhibits cell attachment in vitro and suppresses the growth of CHO cells in nude mice,” DNA Cell Biol. 13 (6):571-584, and the amino acid sequence of TGFBI (identified by accession no. NP_000349) is disclosed in, e.g., Skonier et al., 1992, “cDNA cloning and sequence analysis of beta ig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor-beta,” DNA Cell Biol. I1 (7):511-522; Stone et al., 1994, “Three autosomal dominant corneal dystrophies map to chromosome 5q,” Nat. Genet. 6 (1):47-51; Skonier et al., 1994, “beta ig-h3: a transforming growth factor-beta-responsive gene encoding a secreted protein that inhibits cell attachment in vitro and suppresses the growth of CHO cells in nude mice,” DNA Cell Biol. 13: 571-584, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of TIFA (identified by accession no. NM_052864) is disclosed in, e.g., Kananori, M. et aL., 2002, “T2BP, a novel TRAF2 binding protein, can activate NF-kappaB and AP-1 without TNF stimulation,” Biochem. Biophys. Res. Commun. 290 (3):1108-1113, Takatsuna, H. et aL., 2003, “Identification of TIFA as an adapter protein that links tumor necrosis factor receptor-associated factor 6 (TRAF6) to interleukin-1 (IL-1) receptor-associated kinase-1 (IRAK-1) in IL-1 receptor signaling,” J. Biol. Chem. 278 (14):12144-12150, Matsuda et al., 2003, “Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways,” Oncogene 22 (21):3307-3318, and the amino acid sequence of TIFA (identified by accession no. NP_443096) is disclosed in, e.g., Kananori et al., 2002, “T2BP, a novel TRAF2 binding protein, can activate NF-kappaB and AP-I without TNF stimulation,” Biochem. Biophys. Res. Commun. 290:1108-1113, Takatsuna et al., 2003, “Identification of TIFA as an adapter protein that links tumor necrosis factor receptor-associated factor 6 (TRAF6) to interleukin-1 (IL-I) receptor-associated kinase-I (IRAK-1) in IL-1 receptor signaling,” J. Biol. Chem. 278 (14):12144-12150, Matsuda et al., 2003, “Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways,” Oncogene 22 (21):3307-3318, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of Tissue Inhibitor of Metalloproteinase 1 (TIMP1) (identified by accession no. NM_003254) is disclosed in, e.g., Domeij et al., 2005, “ell expression of MMP-1 and TIMP-1 in co-cultures of human gingival fibroblasts and monocytes: the involvement of ICAM-1,” Biochem. Biophys. Res. Commun. 338, 1825-1833; Zureik et al., “Serum tissue inhibitors of metalloproteinases 1 (TIMP-1) and carotid atherosclerosis and aortic arterial stiffness”, J. Hypertens. 23, 2263-2268; Crombez, 2005, “High level production of secreted proteins: example of the human tissue inhibitor of metalloproteinases 1”, Biochem. Biophys. Res. Commun. 337, 908-915 and the amino acid sequence of TIMPI (identified by accession no. AAA75558) is disclosed in, e.g., Hardcastle et al., 1997, “Genomic organization of the human TIMP-1 gene. Investigation of a causative role in the pathogenesis of X-linked retinitis pigmentosa,” Invest. Ophthalmol. Vis. Sci. 38, 1893-1896, which is incorporated by reference herein in its entirety.

The nucleotide sequence of TLR4 (identified by accession no. AH009665) is disclosed in, e.g., Arbour, N.C. et al., 1999, Direct Submission, Medicine, University of Iowa, 2182 Med Labs, Iowa City, IA 52242, USA, Arbour, N.C. et aL., A Genetic Basis for a Blunted Response to Endotoxin in Humans, Arbour, N.C. et al., unpublished, “A Genetic Basis for a Blunted Response to Endotoxin in Humans”, and the amino acid sequence of TLR4 (identified by accession no. AAF05316) is disclosed in, e.g., Beutler, 1999, Direct Submission, Department of Internal Medicine, University of Texas Southwestern Medical Center and the Howard Hughes Medical Institute, 5323 Harry Hines Boulevard, Dallas, TX 75235-9050, USA, Smirnova, I. et al., 2000, “Phylogenetic variation and polymorphism at the toll-like receptor 4 locus (TLR4),” Genome Biol. 1, res. 002.1-002.10, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of TNFRSF6 (identified by accession no. NM_152877) is disclosed in, e.g., Oehm, A. et al., 1992, “Purification and molecular cloning of the APO-1 cell surface antigen, a member of the tumor necrosis factor/nerve growth factor receptor superfamily. Sequence identity with the Fas antigen,” J. Biol. Chem. 267 (15):10709-10715, Inazawa, J. et al., 1992, “Assignment of the human Fas antigen gene (Fas) to 10q24.1,” Genomics 14 (3):821-822, Cheng, J. et al., 1994, “Protection from Fas-mediated apoptosis by a soluble form of the Fas molecule,” Science 263 (5154):1759-1762, and the amino acid sequence of TNFRSF6 (identified by accession no. NP_000034) is disclosed in, e.g., Oehm, A. et al., 1992, “Purification and molecular cloning of the APO-l cell surface antigen, a member of the tumor necrosis factor/nerve growth factor receptor superfamily. Sequence identity with the Fas antigen,” J. Biol. Chem. 267 (15):10709-10715, Inazawa, J. et al., 1992, “Assignment of the human Fas antigen gene (Fas) to 10q24.1,” Genomics 14 (3):821-822, Cheng, J. et al., 1994, “Protection from Fas-mediated apoptosis by a soluble form of the Fas molecule,” Science 263 (5154):1759-1762, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of TNFSF10 (identified by accession no. NM_003810) is disclosed in, e.g., Wiley, S. R. et al., 1995, “Identification and characterization of a new member of the TNF family that induces apoptosis,” Immunity 3 (6):673-682, Pitti, R. M. et al., 1996, “Induction of apoptosis by Apo-2 ligand, a new member of the tumor necrosis factor cytokine family,” J. Biol. Chem. 271 (22):12687-12690, Pan, G. et al., 1997, “The receptor for the cytotoxic ligand TRAIL,” Science 276 (5309):111-113, and the amino acid sequence of TNFSF10 (identified by accession no. NP_003801) is disclosed in, e.g., Wiley, S. R. el al., 1995, “Identification and characterization of a new member of the TNF family that induces apoptosis,” Immunity 3 (6):673-682, Pitti, R. M. et al., 1996, “Induction of apoptosis by Apo-2 ligand, a new member of the tumor necrosis factor cytokine family,” J. Biol. Chem. 271 (22):12687-12690, Pan, G. et al., 1997, “The receptor for the cytotoxic ligand TRAIL,” Science 276 (5309):111-113, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of TNFSF13B (identified by accession no. NM_006573) is disclosed in, e.g., Shu, H. B. et al., 1999, “TALL-1 is a novel member of the TNF family that is down-regulated by mitogens,” J. Leukoc. Biol. 65 (5): 680-683, Mukhopadhyay, A. et al., 1999, “Identification and characterization of a novel cytokine, THANK, a TNF homologue that activates apoptosis, nuclear factor-kappaB, and c-Jun NH2-terminal kinase,” J. Biol. Chem. 274 (23):15978-15981, Schneider, P. et al., 1999, “BAFF. a novel ligand of the tumor necrosis factor family, stimulates B cell growth,” J. Exp. Med. 189 (11):1747-1756, and the amino acid sequence of TNFSF13B (identified by accession no. NP_006564) is disclosed in, e.g., Shu, H. B. et al., 1999, “TALL-1 is a novel member of the TNF family that is down-regulated by mitogens,” J. Leukoc. Biol. 65 (5): 680-683, Mukhopadhyay, A. et al., 1999, “Identification and characterization of a novel cytokine, THANK, a TNF homologue that activates apoptosis, nuclear factor-kappaB, and c-Jun NH2-terminal kinase,” J. Biol. Chem. 274 (23):15978-15981, Schneider, P. et al., 1999, “BAFF, a novel ligand of the tumor necrosis factor family, stimulates B cell growth,” J. Exp. Med. 189 (11):1747-1756, each of which is incorporated by reference herein in its entirety.

The nucleotide sequence of VNN1 (identified by accession no. NM_004666) is disclosed in, e.g., Aurrand-Lions, M. et al., 1996, “Vanin-1, a novel GPI-linked perivascular molecule involved in thymus homing,” Immunity 5 (5):391-405, Galland, F. et al., 1998, “Two human genes related to murine vanin-1 are located on the long arm of human chromosome 6,” Genomics 53 (2):203-213, Maras, B. et al., 1999, “Is pantetheinase the actual identity of mouse and human vanin-1 proteins?,” FEBS Lett. 461 (3):149-152, and the amino acid sequence of VNN1 (identified by accession no. NP_004657) is disclosed in, e.g., Aurrand-Lions, M. et al., 1996, “Vanin-1, a novel GPI-linked perivascular molecule involved in thymus homing,” Immunity 5 (5):391-405, Galland, F. et al., 1998, “Two human genes related to murine vanin-1 are located on the long arm of human chromosome 6,” Genomics 53 (2):203-213, Maras, B. et al., 1999, “is pantetheinase the actual identity of mouse and human vanin-1 proteins?,” FEBS Lett. 461 (3):149-152, each of which is incorporated by reference herein in its entirety.

5.11.2 Exemplary Combinations of Biomarkers in Accordance with Embodiments of the Invention

In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, 50, or more biomarkers selected from Table I regardless of whether each such biomarker has an “N” designation or a “P” designation in Table I. In some nonlimiting exemplary embodiments, between 2 and 53, between 3 and 40, between 4 and 30, or between 5 and 20 such biomarkers are used.

Nucleic acid based kits and methods. In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, or more biomarkers selected from Table J. Typically, in these embodiments, each biomarker is a nucleic acid (e.g., DNA, such as cDNA or amplified DNA, or RNA, such as mRNA), or a discriminating molecule or discriminating fragment of a nucleic acid. In some nonlimiting exemplary embodiments, between 2 and 44, between 3 and 35, between 4 and 25, or between 5 and 20 such biomarkers are used.

Protein or peptide based kits and methods. In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 of the biomarkers selected from Table K. Typically, such biomarkers are peptide-based (e.g., a peptide, a full length protein, etc.), or a discriminating molecule or discriminating fragment of the foregoing. In some embodiments, the biomarkers in the kit are specific antibodies to two or more of the biomarkers listed in Table K. In some nonlimiting exemplary embodiments, between 2 and 10, between 3 and 10, between 4 and 10, or between 5 and 10 such biomarkers are used.

Homogenous kits and methods. In some embodiments, each of the biomarkers in the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use at least two or more biomarkers selected from Table I where each biomarker used in such methods or kits is in the same physical form. In one example in accordance with such embodiments, each biomarker in a method or kit in accordance Section 5.2 and Section 5.3, respectively, is a biomarker selected from Table I and is a nucleic acid or a discriminating molecule of a nucleic acid in the method or kit. In another example in accordance with such embodiments, each biomarker in a method or kit in accordance Section 5.2 and Section 5.3, respectively, is a biomarker selected from Table I and is peptide-based (e.g., a peptide, a full length protein. etc.) or a discriminating molecule of the forgoing. In these embodiments, biomarkers are selected without regard as to whether they are designated “P” or “N” in Table I. Thus, a kit in accordance with these embodiments can include a biomarker in nucleic acid form, even when the biomarker is designated “P” on Table I. Correspondingly, a kit in accordance with this embodiment can include a biomarker in peptidic form, even when the biomarker is designated “N” on Table I.

Heterogeneous kits and methods. In some embodiments, each of the biomarkers in the methods and kits respectively described or referenced in Section 5.2 and Section 5.3 use at least two or more biomarkers selected from Table I where each such biomarker is in the same physical form that the biomarker was in when identified in Sections 6.11 through 6.13 below. In other words, if the biomarker has an “N” designation in Table I, a nucleic acid form of the biomarker is used in the methods and kits respectively described or referenced in Section 5.2 and 5.3 in accordance with this embodiment of the invention. If the biomarker has a “P” designation in Table I, a peptidic form of the biomarker is used in the methods and kits respectively described or referenced in Section 5.2 and 5.3 in accordance with this embodiment of the invention. Further, there is at least one biomarker used in such methods or kits that has an “N” designation in Table I and at least one biomarker that has a “P” designation. In such embodiments, biomarkers having an N designation in Table I are nucleic acids and biomarkers having a P designation in Table I are peptide-based or protein-based.

A non-limiting exemplary kit in accordance with such mixed embodiments use two biomarkers from among the biomarkers listed in Table J, in nucleic acid form, and three biomarkers from among the biomarkers listed in Table K, in peptidic-based form. In some embodiments, the non-limiting methods and kits respectively described or referenced in Sections 5.2 and 5.3 use at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, or more biomarkers from Table J, in nucleic acid form, and 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 biomarkers from Table K in peptide-based or protein-based form.

Additional kits and methods. In some embodiments, each of the biomarkers in the methods and kits respectively described or referenced in Section 5.2 and Section 5.3 use at least one biomarkers selected from Table I and at least one different biomarker from Table 31. In some embodiments, each of the biomarkers in the methods and kits respectively described or referenced in Section 5.2 and Section 5.3 use at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 biomarkers selected from Table I and at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 different biomarkers from Table 31.

In some embodiments, each of the biomarkers in the methods and kits respectively described or referenced in Section 5.2 and Section 5.3 use at least one biomarker in, nucleic acid form, selected from Table J and at least one different biomarker from Table 31. In some embodiments, each of the biomarkers in the methods and kits respectively described or referenced in Section 5.2 and Section 5.3 use at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 biomarkers selected from Table I, each in nucleic acid form, and at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 different biomarkers from Table 31.

In some embodiments, each of the biomarkers in the methods and kits respectively described or referenced in Section 5.2 and Section 5.3 use at least one biomarker in, protein form, selected from Table K and at least one different biomarker from Table 31. In some embodiments, each of the biomarkers in the methods and kits respectively described or referenced in Section 5.2 and Section 5.3 use at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 biomarkers selected from Table I, each in protein form, and at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 different biomarkers from Table 31.

In some embodiments, each of the biomarkers in the methods and kits respectively described or referenced in Section 5.2 and Section 5.3 use at least one biomarker from among the biomarkers listed in Table J, in nucleic acid form, and at least one biomarkers from among the biomarkers listed in Table K, in protein form. In some embodiments, the non-limiting methods and kits respectively described or referenced in Sections 5.2 and 5.3 use at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, or more biomarkers from Table J, in nucleic acid form, and 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 biomarkers from Table K in protein form.

In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the IL-6, IL-8, MMP9, B2M, HLA-DRA, and MCP1 biomarkers are not used in such methods or kits. For example, in embodiments where certain monocytes are isolated from whole blood and tested, such biomarkers are not utilized, especially when such biomarkers are nucleic acids. In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the IL-6, IL-8, IL-10, and CRP protein biomarkers are not used in such methods or kits. In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the IL-6, IL-8, IL-10, and CRP nucleic acid biomarkers are not used in such methods or kits. In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the IL-6 and MAPK biomarkers are not used in such methods or kits. In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the TL-6, IL-8, and IL-10 biomarkers are not used in such methods or kits. In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the CD86, IL-6, IL-8. IL-10, and CRP biomarkers are not used in such methods or kits. In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the IL-6 and IL-10 biomarkers are not used in such methods or kits. In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the IL-6 and CRP biomarkers are not used in such methods or kits. In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the CRP biomarker is not used in such methods or kits. In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the IL-8 biomarker is not used in such methods or kits. In some embodiments, any of the above-described combinations of biomarkers are used in methods or kits in accordance Section 5.2 and Section 5.3 with the exception that the B2M biomarker is not used in such methods or kits.

5.11.3 Exemplary Subcombinations of Biomarkers in Accordance with Embodiments of the Invention

In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use any one biomarker set listed in Table L. The biomarker sets listed in Table L were identified in the computational experiments described in Section 6.14.1, below, in which 4600 random subcombinations of the biomarkers listed in Table J were tested. Table L, below, lists some of the biomarker sets that provided high accuracy scores against the validation population described in Section 6.14.1. Each row of Table L lists a single biomarker set that can be used in the methods and kits respectively referenced in Sections 5.2 and 5.3. In other words, each row of Table L describes a biomarker set that can be used to discriminate between sepsis and SIRS subjects (e.g., to determine whether a subject is likely to acquire sepsis). In some embodiments, nucleic acid forms of the biomarkers listed in a biomarker set in Table L are used in the methods and kits respectively referenced in Sections 5.2 and 5.3. In some embodiments, protein forms of the biomarkers listed in a biomarker set in Table L are used in the methods and kits respectively referenced in Sections 5.2 and 5.3. In some hybrid embodiments, some of the biomarkers in a biomarker set listed in Table L are in protein form and some of the biomarkers in the same biomarker set from Table L are in nucleic acid form in the methods and kits respectively referenced in Sections 5.2 and 5.3.

In some embodiments, a given biomarker set listed in Table L is used with the addition of one, two, three, four, five, six, seven, eight, or nine or more additional biomarkers listed in Table I that are not within the given set of biomarkers from Table L. In some embodiments, a given biomarker set listed in Table L is used with the addition of one, two, three, four, five, six, seven, eight, or nine or more additional biomarkers from any one of Tables I, 30, 31, 32, 33, 34, or 36 that are not within the given biomarker set from Table L. In Table L, accuracy, specificity, and sensitivity are described with reference to T₋₁₂ time point data described in Section 6.14.1, below.

TABLE L
Exemplary sets of biomarkers used in the methods or kits referenced in Sections 5.2 and 5.3
BIOMARKER SET	ACCURACY	SPECIFICITY	SENSISTIVITY
INSL3, BCL2A1, CD86	0.82	0.82	0.83
MAP2K6, INSL3, CD86	0.82	0.75	0.87
ARG2, MAP2K6, SOCS3	0.82	0.75	0.87
NCR1, GADD45A, OSM	0.81	0.77	0.85
GADD45B, TNFSF13B, PFKFB3	0.80	0.74	0.87
TLR4, FCGR1A, CSF1R	0.80	0.82	0.78
SOCS3, FCGR1A, PSTPIP2	0.80	0.79	0.81
TGFBI, MAP2K6, PSTPIP2	0.80	0.76	0.83
IFNGR1, JAK2, TNFRSF6, OSM	0.83	0.80	0.87
IRAK2, GADD45A, CD86, JAK2	0.83	0.86	0.81
GADD45A, PRV1, OSM, FCGR1A	0.83	0.80	0.86
IRAK4, CCL5, INSL3, CD86	0.83	0.76	0.90
VNN1, BCL2A1, GADD45B, FAD104	0.82	0.83	0.81
OSM, CD86, PRV1, BCL2A1	0.82	0.78	0.85
VNN1, SOCS3, CSF1R, FCGR1A	0.82	0.78	0.85
VNN1, CCL5, ANKRD22, OSM	0.82	0.77	0.86
LDLR, SOCS3, CD86, IL10alpha	0.81	0.78	0.85
TLR4, SOCS3, IRAK2, CSF1R	0.81	0.76	0.85
IL1RN, SOCS3, ARG2, LDLR	0.81	0.76	0.84
IL18R1, MAP2K6, TGFBI, OSM	0.80	0.86	0.75
FCGR1A, HLA-DRA, IL18R1, PSTPIP2	0.80	0.79	0.82
OSM, IL1RN, SOD2, SOCS3	0.80	0.78	0.82
NCR1, JAK2, TNFSF13B, FCGR1A	0.80	0.76	0.86
TIFA, VNN1, ANXA3, ITGAM	0.80	0.73	0.88
PFKFB3, IRAK2, CSF1R, CD86, PSTPIP2	0.88	0.83	0.91
PSTPIP2, FAD104, TIFA, CD86, LY96	0.84	0.85	0.84
IL1RN, IL10alpha, IFNGR1, OSM, MKNK1	0.83	0.78	0.89
IL18R1, CCL5, JAK2, SOCS3, SOD2	0.83	0.81	0.84
JAK2, MKNK1, TNFSF13B, PRV1, TNFSF10	0.83	0.81	0.84
MAP2K6, ARG2, OSM, ANKRD22,	0.83	0.8	0.85
Gene_MMP9
SOCS3, IL1RN, ARG2, FCGR1A, CCL5	0.83	0.78	0.87
CCL5, INSL3, SOD2, TLR4, ARG2	0.83	0.78	0.87
FCGR1A, ARG2, CD86, MAPK14, TNFRSF6	0.82	0.83	0.82
INSL3, TLR4, SOCS3, CSF1R, FCGR1A	0.82	0.79	0.85
CEACAM1, TNFRSF6, MAPK14, IL10alpha,	0.82	0.79	0.84
CSF1R
ANKRD22, CD86, CRTAP, OSM, PFKFB3	0.82	0.79	0.84
OSM, IL18R1, LDLR, GADD45B, MKNK1	0.82	0.76	0.86
CRTAP, SOCS3, PSTPIP2, TIFA, FAD104	0.81	0.82	0.81
PSTPIP2, ARG2, IL10alpha, TLR4, CSF1R	0.81	0.81	0.82
TIFA, PFKFB3, CSF1R, LDLR, Gene_MMP9	0.81	0.79	0.83
NCR1, PSTPIP2, GADD45A, LY96, MAPK14	0.81	0.77	0.86
ARG2, BCL2A1, NCR1, PSTPIP2, IL10alpha	0.81	0.82	0.8
PFKFB3, OSM, CSF1R, CD86, TIFA	0.81	0.81	0.81
IL10alpha, CD86, SOCS3, GADD45A, TGFBI	0.81	0.78	0.84
PSTPIP2, PFKFB3, INSL3, PRV1, IL1RN	0.81	0.78	0.85
ITGAM, PRV1, IL18R1, INSL3, JAK2	0.81	0.77	0.85
PSTPIP2, OSM, IL18R1, TNFSF13B, ITGAM	0.81	0.72	0.9
CD86, TIFA, CSF1R, FCGR1A, CRTAP	0.81	0.84	0.78
LY96, TGFBI, SOCS3, ANKRD22, MAPK14	0.81	0.83	0.79
IL1RN, SOD2, VNN1, OSM, TNFSF10	0.81	0.79	0.82
CRTAP, NCR1, OSM, PRV1, ANXA3	0.81	0.76	0.85
TDRD9, LY96, CEACAM1, OSM, NCR1	0.81	0.72	0.88
TGFBI, INSL3, GADD45A, LDLR, PSTPIP2	0.8	0.75	0.85
PFKFB3, IRAK2, CSF1R, CD86, PSTPIP2	0.88	0.83	0.91
MAP2K6, ARG2, CD86, PRV1, FAD104,	0.85	0.86	0.84
MAPK14
ARG2, LY96, INSL3, MAP2K6, TNFSF10,	0.85	0.86	0.84
NCR1
SOCS3, GADD45B, CSF1R, ARG2, PSTPIP2,	0.85	0.83	0.86
OSM
GADD45B, PFKFB3, PSTPIP2, FCGR1A,	0.85	0.81	0.88
HLA-DRA, ARG2
TIFA, IL18R1, MAPK14, CD86, ARG2,	0.84	0.8	0.88
TNFSF13B
FCGR1A, ARG2, GADD45B, IL10alpha,	0.84	0.81	0.86
NCR1, LDLR
TGFBI, INSL3, IRAK4, GADD45B, SOCS3,	0.84	0.8	0.87
CSF1R
SOCS3, CSF1R, CEACAM1, ARG2,	0.83	0.82	0.85
IL10alpha, IFNGR1
TLR4, PFKFB3, ARG2, PRV1, LDLR,	0.83	0.81	0.85
TNFSF13B
PSTPIP2, OSM, TLR4, INSL3, IRAK4,	0.83	0.8	0.85
IL18R1
GADD45A, CCL5, FCGR1A, PSTPIP2,	0.82	0.83	0.82
MAP2K6, IL1RN
OSM, FAD104, JAK2, CRTAP, TDRD9,	0.82	0.79	0.85
TNFSF13B
FAD104, SOCS3, TNFSF13B, GADD45B,	0.82	0.84	0.81
CRTAP, TGFBI
IL18R1, TNFRSF6, INSL3, CD86, ANXA3,	0.82	0.79	0.84
PSTPIP2
HLA-DRA, INSL3, ARG2, CD86, CCL5,	0.82	0.79	0.84
SOCS3
TNFRSF6, IL18R1, CD86, PFKFB3,	0.81	0.82	0.81
IL10alpha, FAD104
FAD104, TGFBI, TDRD9, CD86, SOD2,	0.81	0.79	0.83
ARG2
CD86, ARG2, GADD45A, TLR4, BCL2A1,	0.81	0.79	0.83
GADD45B
SOD2, CEACAM1, OSM, GADD45A,	0.81	0.74	0.88
PSTPIP2, IL10alpha
FCGR1A, CSF1R, NCR1, ANXA3, SOCS3,	0.81	0.81	0.8
Gene_MMP9
TNFSF10, IL1RN, OSM, CSF1R, PSTPIP2,	0.81	0.78	0.83
JAK2
CD86, VNN1, LDLR, IL1RN, MAP2K6,	0.81	0.76	0.84
TDRD9
ARG2, OSM, CSF1R, ITGAM, CRTAP,	0.81	0.76	0.85
SOCS3
ANXA3, CSF1R, CEACAM1, Gene_MMP9,	0.8	0.8	0.81
CD86, OSM
LY96, VNN1, SOD2, TGFBI, ARG2, CSF1R	0.8	0.78	0.83
GADD45A, PSTPIP2, BCL2A1, ANKRD22,	0.8	0.77	0.83
HLA-DRA, ANXA3
TGFBI, FCGR1A, ARG2, CD86, PFKFB3,	0.86	0.86	0.85
BCL2A1, TNFRSF6
SOCS3, ITGAM, TDRD9, INSL3, PRV1,	0.84	0.81	0.87
TGFBI, ARG2
MKNK1, GADD45B, IRAK2, TIFA, OSM,	0.83	0.81	0.85
VNN1, PSTPIP2
SOCS3, PSTPIP2, TDRD9, IL10alpha, ARG2,	0.83	0.82	0.84
CD86, CCL5
CSF1R, PSTPIP2, MAPK14, INSL3, IL18R1,	0.83	0.78	0.87
JAK2, OSM
MKNK1, PSTPIP2, ARG2, LY96, ANKRD22,	0.82	0.85	0.8
SOCS3, IRAK4
PSTPIP2, FAD104, TNFSF13B, ITGAM,	0.82	0.83	0.82
BCL2A1, FCGR1A, ANXA3
SOCS3, IRAK2, IFNGR1, CD86, OSM,	0.82	0.81	0.83
PSTPIP2, GADD45A
INSL3, NCR1, PSTPIP2, PFKFB3,	0.82	0.8	0.84
ANKRD22, HLA-DRA, MKNK1
FCGR1A, HLA-DRA, CSF1R, SOCS3,	0.82	0.76	0.88
IRAK4, TIFA, ARG2
FAD104, TGFBI, MAP2K6, IRAK4, LY96,	0.82	0.81	0.83
CD86, ANKRD22
LDLR, INSL3, GADD45B, ARG2, PFKFB3,	0.82	0.78	0.86
HLA-DRA, ITGAM
FCGR1A, TIFA, CD86, PFKFB3, TDRD9,	0.82	0.79	0.85
GADD45A, LDLR
SOCS3, CSF1R, SOD2, CD86, MAP2K6,	0.82	0.76	0.86
GADD45B, PSTPIP2
MKNK1, CD86, FAD104, PRV1, SOCS3,	0.82	0.76	0.87
IL10alpha, MAP2K6
TIFA, JAK2, LDLR, IRAK2, VNN1, CD86,	0.81	0.81	0.81
ARG2
ANKRD22, MAPK14, INSL3, BCL2A1,	0.81	0.79	0.83
CRTAP, IRAK2, FCGR1A
FAD104, INSL3, CD86, TNFRSF6,	0.81	0.79	0.83
GADD45A, IFNGR1, JAK2
CSF1R, INSL3, VNN1, TIFA, IFNGR1,	0.81	0.79	0.83
LDLR, ARG2
PFKFB3, BCL2A1, ANXA3, IL10alpha,	0.81	0.79	0.84
FAD104, VNN1, INSL3
CSF1R, CEACAM1, MAP2K6, GADD45B,	0.81	0.82	0.8
TNFSF10, TNFSF13B, TIFA
FCGR1A, ARG2, IRAK2, GADD45A, CD86,	0.81	0.82	0.79
Gene_MMP9, BCL2A1
CRTAP, CEACAM1, FAD104, MKNK1,	0.81	0.76	0.84
INSL3, ITGAM, SOD2
OSM, TDRD9, BCL2A1, IRAK2, GADD45A,	0.8	0.77	0.84
CD86, LDLR
PFKFB3, CCL5, CSF1R, LDLR, TLR4, LY96,	0.8	0.77	0.84
FAD104
IRAK4, GADD45B, CEACAM1, FAD104,	0.8	0.75	0.85
CSF1R, IRAK2, MAPK14
IFNGR1, FAD104, MAP2K6, TNFRSF6,	0.8	0.74	0.86
FCGR1A, IRAK2, ARG2
TGFBI, IRAK2, CRTAP, BCL2A1, ITGAM,	0.8	0.81	0.79
ANXA3, FCGR1A
SOD2, PFKFB3, GADD45B, IRAK2, PRV1,	0.8	0.77	0.82
SOCS3, FCGR1A
TNFRSF6, TLR4, IRAK2, ITGAM, JAK2,	0.8	0.77	0.83
OSM, NCR1
IL10alpha, ANKRD22, Gene_MMP9, IL1RN,	0.8	0.76	0.84
LY96, FAD104, PSTPIP2
IRAK4, INSL3, CSF1R, ITGAM, VNN1,	0.8	0.74	0.86
HLA-DRA, IL18R1
IRAK2, TGFBI, MAP2K6, IL18R1, IFNGR1,	0.8	0.73	0.87
CRTAP, PSTPIP2
TDRD9, ITGAM, OSM, NCR1, CD86,	0.8	0.73	0.87
MAP2K6, CCL5
ANXA3, FCGR1A, TNFSF10, VNN1,	0.85	0.86	0.84
TNFSF13B, ARG2, 12, CD86
INSL3, PFKFB3, MAPK14, FCGR1A,	0.85	0.84	0.85
TDRD9, CSF1R, 12, IRAK4
VNN1, CSF1R, ANKRD22, OSM,	0.85	0.78	0.9
GADD45A, LY96, 12, MAP2K6
ITGAM, OSM, LY96, TDRD9, ANKRD22,	0.84	0.84	0.83
TLR4, 12, MKNK1
ARG2, ANXA3, MAP2K6, CCL5, CD86,	0.84	0.84	0.83
OSM, 12, LDLR
OSM, IL1RN, FCGR1A, GADD45A, ARG2,	0.84	0.82	0.86
IL10alpha, 12, ITGAM
TIFA, ANKRD22, TNFSF13B, CRTAP,	0.84	0.81	0.86
MAP2K6, IRAK4, 12, ARG2
IRAK2, TLR4, IL10alpha, TGFBI, PRV1,	0.83	0.8	0.86
FAD104, 12, MAP2K6
IL18R1, FAD104, TNFSF13B, MAP2K6,	0.83	0.81	0.85
OSM, SOD2, 12, TNFRSF6
OSM, LDLR, VNN1, LY96, ARG2, MAPK14,	0.83	0.8	0.85
12, IRAK2
PRV1, ITGAM, SOD2, Gene_MMP9, OSM,	0.83	0.79	0.86
JAK2, 12, ARG2
ANXA3, TNFSF10, CEACAM1, FCGR1A,	0.83	0.78	0.86
HLA-DRA, IL10alpha, 12, SOCS3
ITGAM, CD86, CEACAM1, TDRD9,	0.83	0.77	0.88
GADD45A, PFKFB3, 12, SOCS3
SOCS3, PRV1, ARG2, CEACAM1, LDLR,	0.82	0.83	0.82
GADD45A, 12, IL10alpha
INSL3, CSF1R, IL1RN, PSTPIP2, MKNK1,	0.82	0.8	0.84
SOCS3, 12, JAK2
TDRD9, LY96, ITGAM, NCR1, PSTPIP2,	0.82	0.75	0.9
IL10alpha, 12, OSM
PFKFB3, MAP2K6, ARG2, TGFBI, LDLR,	0.82	0.84	0.8
FAD104, 12, MAPK14
ARG2, IL18R1, NCR1, CD86, FCGR1A,	0.82	0.79	0.84
TGFBI, 12, IL1RN
HLA-DRA, CEACAM1, IFNGR1, MKNK1,	0.82	0.76	0.87
LDLR, GADD45B, 12, CSF1R
IL10alpha, IL1RN, OSM, PSTPIP2, INSL3,	0.82	0.81	0.82
TIFA, 12, TLR4
MKNK1, CSF1R, VNN1, OSM, ARG2,	0.81	0.81	0.82
GADD45B, 12, SOCS3
IL18R1, GADD45B, TNFRSF6, TNFSF10,	0.81	0.79	0.84
TIFA, JAK2, 12, GADD45A
LDLR, IL10alpha, PRV1, LY96, ANXA3,	0.81	0.76	0.86
TNFRSF6, 12, CCL5
IL18R1, CD86, PFKFB3, ANKRD22, CSF1R,	0.81	0.8	0.82
SOCS3, 12, TIFA
CCL5, TDRD9, PSTPIP2, ARG2, INSL3,	0.81	0.77	0.85
OSM, 12, CSF1R
CEACAM1, IL10alpha, IL18R1, PSTPIP2,	0.81	0.77	0.85
TGFBI, TIFA, 12, VNN1
GADD45B, Gene_MMP9, TLR4, PFKFB3,	0.81	0.76	0.85
VNN1, JAK2, 12, IL18R1
FAD104, MAPK14, IFNGR1, IL18R1,	0.81	0.76	0.86
TNFSF10, CD86, 12, HLA-DRA
PSTPIP2, SOCS3, OSM, CSF1R, PFKFB3,	0.81	0.75	0.86
NCR1, 12, PRV1
TGFBI, SOCS3, ITGAM, TNFSF13B,	0.81	0.8	0.81
IL18R1, PSTPIP2, 12, ANKRD22
CEACAM1, SOCS3, PFKFB3, TNFRSF6,	0.81	0.79	0.82
PSTPIP2, OSM, 12, BCL2A1
TNFRSF6, ITGAM, BCL2A1, INSL3, CD86,	0.81	0.77	0.84
TIFA, 12, PFKFB3
PFKFB3, PSTPIP2, MAP2K6, IRAK4, OSM,	0.81	0.76	0.85
CCL5, 12, TNFSF10
MKNK1, TIFA, IL1RN, ARG2, SOCS3,	0.81	0.76	0.85
IL10alpha, 12, IFNGR1
FAD104, TNFSF13B, OSM, BCL2A1,	0.8	0.8	0.8
TDRD9, LY96, 12, SOD2
CD86, SOCS3, PSTPIP2, CCL5, OSM, TLR4,	0.8	0.77	0.83
12, MAPK14
TGFBI, LDLR, CRTAP, CSF1R, NCR1,	0.8	0.82	0.78
LY96, 12, PSTPIP2
JAK2, TIFA, TNFSF10, IL18R1, CCL5,	0.8	0.82	0.78
INSL3, 12, VNN1
TIFA, IL1RN, MAP2K6, HLA-DRA, OSM,	0.8	0.8	0.8
FAD104, 12, INSL3
JAK2, IRAK2, PRV1, TNFSF13B, OSM,	0.8	0.8	0.8
HLA-DRA, 12, IFNGR1
ANXA3, CSF1R, TLR4, SOCS3, IRAK4,	0.8	0.8	0.8
PRV1, 12, INSL3
TGFBI, IRAK4, PFKFB3, SOD2, ANXA3,	0.8	0.8	0.8
ITGAM, 12, TDRD9
TIFA, FCGR1A, TNFRSF6, LY96, IL10alpha,	0.8	0.78	0.81
SOCS3, 12, OSM
PRV1, TLR4, CSF1R, IL18R1, PSTPIP2,	0.8	0.78	0.82
TDRD9, 12, HLA-DRA
LY96, TNFSF13B, OSM, TGFBI, TIFA,	0.8	0.77	0.82
FAD104, 12, NCR1
ITGAM, ARG2, IL10alpha, SOD2, LY96,	0.8	0.76	0.83
OSM, 12, FCGR1A
ANKRD22, HLA-DRA, PRV1, NCR1,	0.8	0.76	0.84
CSF1R, PSTPIP2, 12, LY96
Gene_MMP9, PSTPIP2, GADD45B, SOD2,	0.8	0.74	0.86
ANKRD22, TNFSF13B, 12, ITGAM
ANXA3, FCGR1A, TNFSF10, VNN1,	0.85	0.86	0.84
TNFSF13B, ARG2, 12, CD86
CSF1R, PFKFB3, BCL2A1, SOCS3, NCR1,	0.86	0.87	0.85
TNFSF10, FCGR1A, ARG2, CD86
PSTPIP2, ITGAM, IRAK2, OSM, NCR1,	0.84	0.81	0.87
CEACAM1, PFKFB3, TLR4, ANXA3
INSL3, ARG2, LDLR, HLA-DRA, NCR1,	0.84	0.78	0.9
TIFA, LY96, ITGAM, SOCS3
CD86, CSF1R, SOD2, OSM, SOCS3,	0.83	0.79	0.87
BCL2A1, GADD45B, ARG2, HLA-DRA
ARG2, CD86, MAP2K6, HLA-DRA,	0.83	0.82	0.84
IL10alpha, IRAK2, GADD45B, MKNK1,
IL18R1
IFNGR1, BCL2A1, ARG2, TNFSF13B,	0.83	0.8	0.86
GADD45A, FCGR1A, TNFRSF6, CD86,
MAP2K6
OSM, TNFSF10, CSF1R, CCL5, IRAK2,	0.83	0.82	0.83
INSL3, ARG2, TNFSF13B, TNFRSF6
LY96, TNFSF10, GADD45B, CRTAP, ARG2,	0.82	0.87	0.77
ANXA3, CSF1R, CCL5, OSM
NCR1, LY96, FAD104, ANKRD22, BCL2A1,	0.82	0.79	0.84
PSTPIP2, ARG2, PRV1, IL18R1
SOD2, IRAK2, JAK2, CCL5, IL10alpha,	0.82	0.77	0.86
ARG2, BCL2A1, SOCS3, CSF1R
TNFRSF6, TGFBI, FCGR1A, IRAK4,	0.82	0.81	0.83
GADD45A, LDLR, IFNGR1, CSF1R, TIFA
GADD45B, ITGAM, PRV1, SOD2,	0.81	0.79	0.83
TNFSF13B, HLA-DRA, FAD104, TNFRSF6,
TLR4
IRAK2, SOCS3, GADD45B, MAP2K6, PRV1,	0.81	0.83	0.8
PFKFB3, CD86, IFNGR1, ANKRD22
HLA-DRA, GADD45A, FCGR1A,	0.81	0.81	0.81
ANKRD22, ARG2, NCR1, BCL2A1, IRAK2,
SOCS3
IRAK4, SOCS3, MKNK1, JAK2, OSM,	0.81	0.79	0.83
ANXA3, VNN1, ITGAM, TNFRSF6
SOD2, JAK2, FAD104, CD86, ARG2, CCL5,	0.81	0.79	0.83
MAP2K6, IFNGR1, PFKFB3
IL18R1, CSF1R, IRAK2, HLA-DRA,	0.81	0.78	0.83
PFKFB3, CRTAP, CD86, TIFA, TNFSF10
MAP2K6, FAD104, TGFBI, IRAK4, CRTAP,	0.81	0.77	0.84
LDLR, IRAK2, FCGR1A, ARG2
CEACAM1, SOD2, GADD45A, VNN1,	0.81	0.73	0.88
IRAK4, OSM, TDRD9, GADD45B, PSTPIP2
PSTPIP2, ANKRD22, TNFSF10, INSL3,	0.81	0.84	0.78
HLA-DRA, NCR1, TNFSF13B, CSF1R,
Gene_MMP9
JAK2, MAP2K6, CSF1R, IRAK2, TNFSF10,	0.81	0.81	0.8
LDLR, OSM, BCL2A1, ARG2
Gene_MMP9, MAP2K6, IL18R1, VNN1,	0.81	0.8	0.81
INSL3, ANKRD22, CCL5, PFKFB3,
MAPK14
IL18R1, ARG2, FCGR1A, CRTAP,	0.81	0.8	0.82
GADD45B, FAD104, IRAK4, MAPK14,
TDRD9
SOD2, PRV1, MKNK1, FCGR1A, CD86,	0.81	0.78	0.83
GADD45A, IL18R1, TNFSF13B, HLA-DRA
ANXA3, TNFRSF6, MAP2K6, OSM,	0.81	0.78	0.83
ANKRD22, IL18R1, MAPK14, GADD45A,
GADD45B
OSM, IRAK2, ANXA3, TNFSF13B, IL18R1,	0.81	0.78	0.83
ANKRD22, MAP2K6, IL10alpha, FAD104
ITGAM, SOD2, CSF1R, TGFBI, IFNGR1,	0.81	0.73	0.87
TDRD9, JAK2, ARG2, GADD45A
INSL3, ITGAM, OSM, TIFA, IRAK2,	0.8	0.84	0.77
MKNK1, SOCS3, TNFSF10, ANKRD22
GADD45A, PFKFB3, SOD2, IRAK2,	0.8	0.79	0.82
MAPK14, INSL3, IRAK4, ITGAM, ARG2
NCR1, INSL3, ARG2, IFNGR1, LDLR, OSM,	0.8	0.78	0.83
PRV1, GADD45B, CD86
IRAK2, FAD104, TLR4, CSF1R, PRV1, OSM,	0.8	0.77	0.83
MKNK1, BCL2A1, CD86
NCR1, SOCS3, HLA-DRA, PFKFB3,	0.8	0.74	0.86
FAD104, IRAK4, VNN1, CCL5, MAP2K6
CRTAP, TLR4, PFKFB3, CSF1R, TIFA,	0.8	0.82	0.78
PSTPIP2, PRV1, IFNGR1, CCL5
LY96, SOD2, IL18R1, TNFRSF6, TLR4,	0.8	0.81	0.79
MAP2K6, FAD104, Gene_MMP9, NCR1
ITGAM, SOD2, SOCS3, LDLR, MAP2K6,	0.8	0.8	0.8
FAD104, NCR1, CSF1R, CD86
CRTAP, ARG2, SOD2, TDRD9, TNFRSF6,	0.8	0.8	0.8
TIFA, OSM, Gene_MMP9, HLA-DRA
OSM, LY96, CEACAM1, IRAK4, INSL3,	0.8	0.78	0.82
PSTPIP2, PRV1, IRAK2, JAK2
CD86, IL1RN, IFNGR1, ANXA3, CSF1R,	0.8	0.78	0.82
ITGAM, NCR1, TDRD9, MAP2K6
TNFSF13B, JAK2, IRAK4, TDRD9, HLA-	0.8	0.78	0.82
DRA, SOCS3, PSTPIP2, FAD104, SOD2
Gene_MMP9, SOD2, JAK2, CD86, HLA-	0.8	0.74	0.85
DRA, IRAK2, CEACAM1, MAPK14, ANXA3
GADD45B, ITGAM, TLR4, NCR1, CD86,	0.8	0.71	0.88
TNFSF13B, HLA-DRA, FCGR1A, OSM
OSM, GADD45B, CSF1R, CCL5, ANXA3,	0.85	0.85	0.84
CEACAM1, CD86, TNFSF10, ARG2, LY96,
TDRD9
NCR1, HLA-DRA, BCL2A1, ARG2, SOCS3,	0.84	0.84	0.84
IL18R1, PSTPIP2, VNN1, CD86, GADD45A,
CCL5
PFKFB3, SOCS3, TNFRSF6, GADD45A,	0.84	0.8	0.87
OSM, TDRD9, IL18R1, NCR1, CSF1R,
ANXA3, PSTPIP2
ARG2, IFNGR1, MAPK14, Gene_MMP9,	0.84	0.8	0.88
IRAK4, CEACAM1, ITGAM, ANKRD22,
GADD45B, VNN1, OSM
BCL2A1, LY96, GADD45B, IL10alpha,	0.84	0.82	0.86
CRTAP, OSM, IFNGR1, IL1RN, TIFA,
IRAK4, GADD45A
TGFBI, SOCS3, MAP2K6, ANXA3, TLR4,	0.83	0.77	0.89
IL1RN, VNN1, HLA-DRA, TIFA, JAK2,
TDRD9
TNFSF13B, GADD45A, ANXA3, IL18R1,	0.83	0.83	0.83
FCGR1A, JAK2, CD86, SOCS3, INSL3,
CRTAP, NCR1
LY96, INSL3, TNFSF10, MAP2K6, OSM,	0.83	0.78	0.88
ITGAM, JAK2, CD86, FCGR1A, IL10alpha,
CCL5
ARG2, OSM, TLR4, NCR1, CCL5, BCL2A1,	0.83	0.76	0.88
IL1RN, GADD45A, MAPK14, SOCS3,
TDRD9
INSL3, IL18R1, IFNGR1, ARG2, IL10alpha,	0.83	0.82	0.83
LY96, CRTAP, LDLR, JAK2, CSF1R, VNN1
ANXA3, IFNGR1, GADD45A, TNFRSF6,	0.83	0.79	0.86
CCL5, JAK2, FAD104, IL1RN, ARG2,
IL10alpha, INSL3
CRTAP, TNFRSF6, LDLR, VNN1, HLA-	0.82	0.86	0.79
DRA, SOCS3, TGFBI, TNFSF10, IFNGR1,
ARG2, FCGR1A
GADD45A, VNN1, MKNK1, CCL5,	0.82	0.83	0.82
IL10alpha, PSTPIP2, IRAK2, TNFRSF6,
CEACAM1, FAD104, TGFBI
HLA-DRA, BCL2A1, PSTPIP2, PFKFB3,	0.82	0.82	0.83
JAK2, TNFSF10, ARG2, CEACAM1, IL18R1,
MAPK14, CSF1R
GADD45B, TNFSF10, TNFSF13B, OSM,	0.82	0.82	0.83
VNN1, PRV1, MKNK1, Gene_MMP9,
ANXA3, TGFBI, HLA-DRA
GADD45A, IFNGR1, IRAK4, TGFBI, NCR1,	0.82	0.75	0.88
FAD104, INSL3, IL10alpha, OSM, TIFA,
CSF1R
Gene_MMP9, IRAK2, JAK2, TGFBI,	0.82	0.83	0.81
BCL2A1, PSTPIP2, GADD45A, ARG2, OSM,
CEACAM1, IFNGR1
MAP2K6, FCGR1A, TNFSF13B, SOD2,	0.82	0.79	0.85
NCR1, ANXA3, TLR4, CD86, ITGAM,
IRAK2, INSL3
FAD104, ARG2, NCR1, ANKRD22, OSM,	0.82	0.78	0.85
CSF1R, BCL2A1, CRTAP, LY96, SOD2,
TNFRSF6
LY96, TDRD9, CD86, GADD45A, ARG2,	0.82	0.82	0.81
VNN1, IL10alpha, SOD2, CRTAP, TIFA,
FCGR1A
BCL2A1, VNN1, LDLR, TLR4, OSM,	0.82	0.82	0.81
IRAK4, IRAK2, CRTAP, IFNGR1, TGFBI,
CD86
CCL5, IFNGR1, TIFA, SOCS3, INSL3, TLR4,	0.82	0.81	0.82
IRAK4, ANXA3, TGFBI, TDRD9, CSF1R
VNN1, SOD2, CCL5, BCL2A1, HLA-DRA,	0.82	0.79	0.85
ANKRD22, CD86, TDRD9, TLR4, FCGR1A,
TNFSF10
CEACAM1, OSM, IRAK4, MAP2K6,	0.82	0.77	0.85
PSTPIP2, GADD45A, IRAK2, PRV1, IL1RN,
TNFSF10, PFKFB3
TNFSF10, IL1RN, IFNGR1, TIFA, FCGR1A,	0.81	0.82	0.81
PSTPIP2, OSM, ANXA3, TGFBI, INSL3,
CRTAP
LDLR, VNN1, GADD45B, IL18R1,	0.81	0.8	0.83
GADD45A, Gene_MMP9, FAD104, IL1RN,
IRAK4, JAK2, TGFBI
FCGR1A, OSM, GADD45A, IL18R1,	0.81	0.79	0.83
GADD45B, TLR4, MAP2K6, CRTAP, TIFA,
CCL5, BCL2A1
CSF1R, ITGAM, HLA-DRA, MAP2K6,	0.81	0.78	0.85
JAK2, FCGR1A, OSM, LDLR, SOCS3,
TNFRSF6, IL18R1
IL10alpha, IRAK2, OSM, TIFA, TNFSF10,	0.81	0.75	0.87
FAD104, GADD45B, ITGAM, CD86, VNN1,
SOD2
ARG2, GADD45A, LDLR, TNFRSF6,	0.81	0.84	0.78
CEACAM1, ANKRD22, MAPK14, IRAK4,
SOD2, INSL3, PSTPIP2
TGFBI, TNFRSF6, IRAK4, IRAK2, OSM,	0.81	0.82	0.79
TNFSF13B, TIFA, FAD104, ANKRD22,
MAPK14, CD86
VNN1, INSL3, TNFSF10, TGFBI, JAK2,	0.81	0.82	0.8
CRTAP, IRAK2, TNFRSF6, TNFSF13B,
LY96, OSM
GADD45B, OSM, SOD2, FCGR1A, VNN1,	0.81	0.77	0.85
CEACAM1, TIFA, PSTPIP2, IL1RN, TDRD9,
LY96
PFKFB3, LDLR, IL10alpha, IRAK4, ANXA3,	0.81	0.77	0.85
NCR1, IL18R1, VNN1, TDRD9, TNFSF13B,
CSF1R
CD86, TNFRSF6, PFKFB3, MKNK1, OSM,	0.81	0.76	0.85
JAK2, FAD104, IL10alpha, BCL2A1, SOCS3,
IRAK4
OSM, GADD45A, TNFSF10, IFNGR1,	0.81	0.75	0.87
CRTAP, JAK2, ANKRD22, HLA-DRA,
TNFSF13B, SOCS3, FCGR1A
CCL5, CD86, HLA-DRA, SOCS3, TGFBI,	0.84	0.85	0.82
PSTPIP2, ANXA3, GADD45A, CSF1R,
IRAK4, FAD104, MAPK14
IRAK2, CD86, IL1RN, TLR4, ANKRD22,	0.84	0.82	0.85
ANXA3, IL10alpha, GADD45B, BCL2A1,
CSF1R, INSL3, FCGR1A
CD86, TNFRSF6, TIFA, GADD45B,	0.84	0.8	0.87
CEACAM1, TNFSF13B, OSM, IL18R1,
CCL5, ITGAM, TGFBI, FAD104
NCR1, CCL5, BCL2A1, IL18R1, ARG2,	0.83	0.82	0.85
MKNK1, FCGR1A, CD86, GADD45B,
INSL3, IRAK4, ANXA3
TNFSF13B, IFNGR1, Gene_MMP9, SOD2,	0.83	0.8	0.86
LDLR, NCR1, CD86, INSL3, SOCS3, VNN1,
PSTPIP2, CEACAM1
SOD2, INSL3, TDRD9, OSM, TNFSF13B,	0.83	0.82	0.84
BCL2A1, JAK2, CSF1R, ANXA3, TNFSF10,
GADD45A, CRTAP
IL10alpha, MKNK1, GADD45A, TGFBI,	0.83	0.79	0.86
MAPK14, IRAK4, TDRD9, IL1RN,
TNFRSF6, FCGR1A, ITGAM, CD86
TNFRSF6, IL10alpha, PSTPIP2, HLA-DRA,	0.83	0.78	0.87
CRTAP, ARG2, MKNK1, NCR1, OSM,
INSL3, VNN1, FAD104
ANXA3, PRV1, LDLR, TNFSF13B, PFKFB3,	0.82	0.8	0.84
TNFRSF6, VNN1, ARG2, ANKRD22, INSL3,
NCR1, OSM
FCGR1A, HLA-DRA, IFNGR1, CD86, LY96,	0.82	0.76	0.89
ANXA3, MAP2K6, TDRD9, IL18R1, PRV1,
SOCS3, TIFA
GADD45B, OSM, ITGAM, CSF1R, CD86,	0.82	0.84	0.8
CEACAM1, IFNGR1, SOCS3, MAP2K6,
IL1RN, FAD104, CCL5
TGFBI, PRV1, JAK2, FCGR1A, ANKRD22,	0.82	0.83	0.81
TNFSF10, VNN1, SOCS3, PSTPIP2, IRAK2,
INSL3, FAD104
FCGR1A, GADD45A, SOD2, OSM, ARG2,	0.82	0.8	0.83
PFKFB3, ANKRD22, IL10alpha, CCL5,
SOCS3, CD86, ITGAM
LDLR, MAP2K6, INSL3, TDRD9, NCR1,	0.82	0.84	0.79
IL1RN, HLA-DRA, ARG2, MKNK1,
MAPK14, OSM, PFKFB3
IL1RN, PFKFB3, TIFA, OSM, IRAK2,	0.82	0.83	0.81
TGFBI, INSL3, TNFSF13B, TNFRSF6,
MAP2K6, PSTPIP2, CEACAM1
LY96, TNFSF13B, HLA-DRA, IRAK2,	0.82	0.82	0.82
FCGR1A, ANXA3, CEACAM1, FAD104,
TDRD9, IL1RN, ARG2, LDLR
IL1RN, ARG2, IRAK2, IRAK4, SOCS3,	0.82	0.81	0.82
IL10alpha, CCL5, Gene_MMP9, MAPK14,
FAD104, LY96, TGFBI
BCL2A1, LY96, ITGAM, OSM, TNFSF10,	0.81	0.81	0.82
INSL3, CD86, IRAK2, MAP2K6, IFNGR1,
PRV1, TNFRSF6
BCL2A1, ANXA3, LY96, TNFSF10, NCR1,	0.83	0.83	0.83
OSM, MAPK14, MKNK1, IFNGR1,
GADD45A, INSL3, ANKRD22, TNFSF13B
LY96, GADD45B, MAPK14, OSM, MKNK1,	0.83	0.82	0.84
BCL2A1, ARG2, IL1RN, INSL3, PFKFB3,
LDLR, CRTAP, TIFA
OSM, CD86, GADD45B, IRAK4, MAPK14,	0.83	0.82	0.84
SOCS3, VNN1, ARG2, TNFSF13B, TDRD9,
PRV1, IL1RN, IL18R1
OSM, NCR1, HLA-DRA, TNFSF10, PSTPIP2,	0.83	0.82	0.84
IL1RN, SOCS3, INSL3, TNFRSF6, MAPK14,
Gene_MMP9, CEACAM1, IL18R1
CCL5, ARG2, IL10alpha, MAPK14, CSF1R,	0.83	0.8	0.85
GADD45B, LDLR, SOD2, Gene_MMP9,
IFNGR1, IL18R1, CEACAM1, CD86
TDRD9, SOCS3, Gene_MMP9, IL18R1,	0.83	0.85	0.81
CRTAP, ANXA3, PRV1, ARG2, CD86,
ITGAM, OSM, NCR1, VNN1
SOD2, JAK2, PSTPIP2, MAPK14, MAP2K6,	0.83	0.83	0.83
FCGR1A, CCL5, ITGAM, CD86, GADD45B,
IL1RN, HLA-DRA, VNN1
IRAK4, JAK2, SOD2, Gene_MMP9, PSTPIP2,	0.83	0.81	0.84
PFKFB3, HLA-DRA, TNFRSF6, FAD104,
ARG2, IFNGR1, IRAK2, MAP2K6
PSTPIP2, MAPK14, CCL5, Gene_MMP9,	0.83	0.79	0.86
TNFRSF6, IL10alpha, LY96, IL1RN, ARG2,
SOCS3, TLR4, OSM, HLA-DRA
CRTAP, CEACAM1, ARG2, JAK2,	0.83	0.79	0.87
TNFSF10, VNN1, PSTPIP2, IRAK2,
TNFRSF6, ITGAM, SOCS3, OSM, IL18R1
VNN1, PSTPIP2, GADD45B, ITGAM,	0.83	0.77	0.88
IL1RN, FAD104, NCR1, TIFA, OSM,
TDRD9, SOD2, ARG2, TGFBI
TGFBI, IL1RN, INSL3, PSTPIP2, NCR1,	0.82	0.84	0.81
FAD104, HLA-DRA, CD86, IRAK4,
IL10alpha, ARG2, CSF1R, MAP2K6
FAD104, IRAK2, TIFA, TGFBI, IL18R1,	0.82	0.82	0.83
MAPK14, SOCS3, PSTPIP2, CD86, PRV1,
NCR1, FCGR1A, ANXA3
GADD45A, HLA-DRA, INSL3, ANKRD22,	0.82	0.79	0.85
ANXA3, CD86, IRAK4, GADD45B, PFKFB3,
ITGAM, VNN1, NCR1, JAK2
MKNK1, CCL5, PSTPIP2, ANXA3, VNN1,	0.82	0.86	0.78
LY96, IRAK2, IFNGR1, CRTAP, PFKFB3,
IL18R1, LDLR, FAD104
TNFSF10, OSM, FCGR1A, IRAK4, TLR4,	0.82	0.81	0.83
SOCS3, IL18R1, CRTAP, GADD45B, IL1RN,
IL10alpha, PRV1, JAK2
FAD104, ITGAM, ARG2, PSTPIP2, TLR4,	0.82	0.79	0.84
NCR1, IL1RN, MAP2K6, FCGR1A, PFKFB3,
LDLR, IFNGR1, BCL2A1
LDLR, ARG2, NCR1, MKNK1, GADD45B,	0.82	0.79	0.84
GADD45A, CEACAM1, PSTPIP2,
Gene_MMP9, CCL5, BCL2A1, TIFA, TDRD9
IRAK2, Gene_MMP9, INSL3, ARG2, OSM,	0.81	0.81	0.82
ITGAM, PSTPIP2, TNFSF13B, FCGR1A,
BCL2A1, CRTAP, PRV1, MAP2K6
CEACAM1, PSTPIP2, TLR4, IFNGR1,	0.85	0.89	0.83
GADD45B, CSF1R, CD86, VNN1, IL18R1,
ANKRD22, MAPK14, OSM, CCL5, IRAK4
LY96, ANKRD22, Gene_MMP9, ARG2,	0.85	0.84	0.86
GADD45A, MKNK1, CD86, PSTPIP2, OSM,
FAD104, FCGR1A, IL18R1, TIFA, ITGAM
ARG2, ANKRD22, VNN1, TLR4, OSM,	0.84	0.82	0.86
TIFA, TGFBI, TDRD9, ANXA3, CCL5,
TNFRSF6, GADD45B, FAD104, CD86
IFNGR1, TLR4, CRTAP, ANKRD22,	0.84	0.79	0.87
Gene_MMP9, JAK2, INSL3, ITGAM, IRAK4,
HLA-DRA, BCL2A1, OSM, TNFSF10, NCR1
TNFSF10, VNN1, TDRD9, CSF1R, OSM,	0.83	0.83	0.83
IFNGR1, TLR4, PSTPIP2, TIFA, ARG2,
FCGR1A, CD86, MAPK14, MAP2K6
LDLR, IL18R1, BCL2A1, IL1RN, ARG2,	0.83	0.83	0.84
IRAK2, JAK2, GADD45A, ANKRD22,
MAP2K6, OSM, CD86, IRAK4, SOD2
IL1RN, IRAK4, VNN1, CRTAP, TNFSF10,	0.83	0.8	0.86
IFNGR1, FAD104, ARG2, OSM, NCR1,
JAK2, ANXA3, CEACAM1, TDRD9
CD86, FCGR1A, MKNK1, TNFRSF6,	0.83	0.78	0.88
GADD45B, LY96, NCR1, PSTPIP2, HLA-
DRA, VNN1, ANXA3, IRAK4, ARG2, TGFBI
IRAK2, ANKRD22, JAK2, CD86, INSL3,	0.83	0.77	0.88
TNFSF10, OSM, PSTPIP2, IL10alpha, CCL5,
TDRD9, GADD45B, Gene_MMP9, LY96
LY96, FCGR1A, CCL5, IL18R1, VNN1,	0.83	0.83	0.83
TNFSF10, MAP2K6, PRV1, IRAK4, IL1RN,
TLR4, PSTPIP2, PFKFB3, TGFBI
SOD2, IL1RN, JAK2, PRV1, IRAK2, CD86,	0.83	0.83	0.83
TGFBI, CCL5, MAPK14, TLR4, INSL3,
PFKFB3, GADD45B, LY96
TDRD9, FCGR1A, NCR1, IFNGR1, ARG2,	0.83	0.81	0.85
SOD2, TNFRSF6, CD86, PFKFB3, LDLR,
JAK2, CCL5, ANKRD22, FAD104
MAPK14, INSL3, MAP2K6, CCL5, CSF1R,	0.83	0.82	0.83
CD86, GADD45A, SOCS3, GADD45B,
ANXA3, TGFBI, TNFRSF6, IFNGR1,
CRTAP
GADD45B, MAPK14, GADD45A, IL1RN,	0.83	0.81	0.84
CEACAM1, CRTAP, MKNK1, IL18R1,
NCR1, FCGR1A, TIFA, MAP2K6, CD86,
TLR4
ARG2, ANKRD22, OSM, LDLR, CCL5,	0.82	0.83	0.82
IL1RN, FCGR1A, PFKFB3, CSF1R, ANXA3,
HLA-DRA, INSL3, NCR1, TIFA
TNFSF10, ANXA3, OSM, JAK2, VNN1,	0.82	0.81	0.83
ANKRD22, INSL3, IFNGR1, CD86,
MAPK14, GADD45B, TNFRSF6, MAP2K6,
LY96
TGFBI, IL18R1, IFNGR1, TDRD9, ANXA3,	0.82	0.8	0.84
TNFSF10, ANKRD22, CD86, TNFRSF6,
BCL2A1, FAD104, Gene_MMP9, TNFSF13B,
CRTAP
OSM, ANXA3, SOCS3, INSL3, ITGAM,	0.82	0.87	0.79
SOD2, NCR1, TNFSF10, BCL2A1, PSTPIP2,
TLR4, IRAK2, Gene_MMP9, IL18R1
SOD2, IRAK4, TNFRSF6, PRV1, FCGR1A,	0.82	0.84	0.8
LDLR, MAP2K6, TIFA, CEACAM1, IL18R1,
SOCS3, OSM, IL10alpha, MKNK1
TLR4, MKNK1, SOD2, SOCS3, FAD104,	0.85	0.83	0.86
HLA-DRA, PSTPIP2, ANKRD22, TIFA,
TNFRSF6, JAK2, TNFSF10, ARG2, CSF1R,
TLR4
CCL5, MAP2K6, SOCS3, IFNGR1, TGFBI,	0.84	0.85	0.83
ANXA3, OSM, GADD45A, TNFSF10,
Gene_MMP9, TNFRSF6, TIFA, ARG2,
INSL3, SOCS3
ANXA3, IL18R1, VNN1, NCR1, TIFA,	0.84	0.84	0.83
INSL3, TGFBI, MAPK14, CEACAM1,
CRTAP, CSF1R, TDRD9, IL10alpha, CCL5,
MAPK14
TLR4, MKNK1, SOD2, SOCS3, FAD104,	0.85	0.83	0.86
HLA-DRA, PSTPIP2, ANKRD22, TIFA,
TNFRSF6, JAK2, TNFSF10, ARG2, CSF1R,
IRAK4
CCL5, MAP2K6, SOCS3, IFNGR1, TGFBI,	0.84	0.85	0.83
ANXA3, OSM, GADD45A, TNFSF10,
Gene_MMP9, TNFRSF6, TIFA, ARG2,
INSL3, TLR4
ANXA3, IL18R1, VNN1, NCR1, TIFA,	0.84	0.84	0.83
INSL3, TGFBI, MAPK14, CEACAM1,
CRTAP, CSF1R, TDRD9, IL10alpha, CCL5,
SOCS3
IL18R1, MAP2K6, INSL3, IRAK4, CCL5,	0.84	0.79	0.88
PFKFB3, CSF1R, LDLR, ITGAM,
GADD45A, ARG2, PSTPIP2, TLR4, CD86,
MAPK14
SOD2, IFNGR1, CEACAM1, OSM, FAD104,	0.83	0.84	0.83
HLA-DRA, CRTAP, IL10alpha, TGFBI,
GADD45A, ITGAM, IL18R1, CCL5, TLR4,
FCGR1A
SOCS3, OSM, TIFA, TNFRSF6, INSL3,	0.83	0.83	0.84
LDLR, IL18R1, PFKFB3, TGFBI, IL10alpha,
GADD45B, ARG2, TNFSF10, VNN1,
ANXA3
PRV1, PFKFB3, CEACAM1, FCGR1A, TIFA,	0.83	0.82	0.85
MKNK1, ARG2, GADD45B, IL18R1, CD86,
ITGAM, VNN1, IFNGR1, OSM, JAK2
NCR1, INSL3, HLA-DRA, TNFSF10,	0.83	0.82	0.84
TNFRSF6, FCGR1A, OSM, GADD45B,
MKNK1, TNFSF13B, CSF1R, LY96,
MAPK14, PRV1, CCL5
FCGR1A, CD86, CEACAM1, ANXA3,	0.83	0.79	0.87
FAD104, CRTAP, JAK2, MKNK1, MAPK14,
IFNGR1, GADD45A, PFKFB3, ANKRD22,
IL18R1, LY96
IRAK2, IL10alpha, INSL3, FAD104, TIFA,	0.83	0.78	0.87
SOD2, IFNGR1, IL1RN, HLA-DRA, LY96,
IL18R1, CCL5, CD86, TDRD9, TNFSF10
LY96, BCL2A1, Gene_MMP9, OSM, ARG2,	0.83	0.8	0.85
MAP2K6, INSL3, ITGAM, MAPK14, TIFA,
IRAK2, PSTPIP2, FCGR1A, CEACAM1,
IFNGR1
IL18R1, BCL2A1, PFKFB3, Gene_MMP9,	0.83	0.76	0.88
IL1RN, IL10alpha, SOCS3, PSTPIP2, CRTAP,
OSM, CD86, FCGR1A, FAD104, JAK2,
SOD2
MKNK1, CRTAP, PRV1, IL1RN, GADD45A,	0.82	0.82	0.82
TNFRSF6, FAD104, HLA-DRA, CEACAM1,
PSTPIP2, OSM, JAK2, IL18R1, LDLR,
IRAK4
FCGR1A, BCL2A1, IFNGR1, CRTAP, VNN1,	0.82	0.8	0.84
TIFA, CCL5, NCR1, OSM, HLA-DRA,
IRAK4, INSL3, MAP2K6, TNFSF13B, ARG2
FAD104, BCL2A1, PRV1, MKNK1, CRTAP,	0.82	0.77	0.87
IRAK4, PFKFB3, SOD2, CD86, ARG2,
FCGR1A, ANKRD22, INSL3, IFNGR1,
LDLR
SOCS3, CD86, FCGR1A, MAP2K6, TGFBI,	0.82	0.84	0.8
IRAK2, PSTPIP2, CCL5, IL1RN, GADD45B,
TDRD9, OSM, IL10alpha, PFKFB3, FAD104
TIFA, SOD2, LDLR, FCGR1A, BCL2A1,	0.86	0.84	0.87
TNFSF13B, ARG2, PSTPIP2, MAPK14,
LY96, Gene_MMP9, IFNGR1, GADD45B,
ANXA3, PRV1, CD86
HLA-DRA, IRAK2, FCGR1A, ANXA3,	0.84	0.83	0.84
ITGAM, LY96, TDRD9, SOCS3, IL1RN,
PFKFB3, GADD45B, TNFSF13B, TLR4,
ARG2, CSF1R, FAD104
OSM, CRTAP, CEACAM1, NCR1, IRAK4,	0.83	0.81	0.86
TLR4, FAD104, MKNK1, TDRD9, PSTPIP2,
IL1RN, CSF1R, MAP2K6, ITGAM, ARG2,
IFNGR1
TIFA, IL10alpha, VNN1, OSM, MAP2K6,	0.83	0.77	0.9
GADD45B, PSTPIP2, TDRD9, TNFRSF6,
INSL3, IL1RN, FAD104, TNFSF10, TGFBI,
IL18R1, TLR4
GADD45A, CSF1R, INSL3, BCL2A1,	0.83	0.82	0.84
TDRD9, LDLR, HLA-DRA, MAP2K6,
PSTPIP2, CCL5, ANXA3, PRV1, TNFRSF6,
TLR4, CD86, JAK2
TDRD9, PFKFB3, MAPK14, IL1RN,	0.83	0.85	0.8
IFNGR1, FCGR1A, MAP2K6, TNFRSF6,
ARG2, VNN1, CRTAP, LDLR, CEACAM1,
FAD104, NCR1, TNFSF10
ARG2, IL10alpha, TLR4, PRV1, INSL3,	0.83	0.82	0.83
OSM, CD86, TGFBI, SOCS3, GADD45B,
TIFA, LDLR, IRAK2, GADD45A, SOD2,
TNFSF13B
TNFSF10, PRV1, SOCS3, FAD104,	0.83	0.8	0.85
TNFRSF6, ARG2, Gene_MMP9, FCGR1A,
TGFBI, NCR1, CRTAP, MAP2K6, ANXA3,
CSF1R, HLA-DRA, JAK2
TNFRSF6, BCL2A1, VNN1, ANXA3, SOCS3,	0.83	0.8	0.85
GADD45A, CRTAP, CCL5, FAD104,
ANKRD22, MKNK1, FCGR1A, SOD2,
IRAK2, MAPK14, Gene_MMP9
FAD104, OSM, LDLR, TNFSF10, GADD45B,	0.82	0.78	0.87
HLA-DRA, TNFRSF6, GADD45A, CD86,
TDRD9, ITGAM, ANXA3, IFNGR1,
MAPK14, CSF1R, TGFBI
CSF1R, PRV1, ANXA3, SOD2, PSTPIP2,	0.82	0.77	0.87
CEACAM1, IFNGR1, IRAK4, LY96,
MAPK14, IL10alpha, MKNK1, TNFRSF6,
OSM, TGFBI, INSL3
PSTPIP2, ARG2, MAP2K6, INSL3, SOCS3,	0.82	0.76	0.89
JAK2, FAD104, ANKRD22, HLA-DRA,
ITGAM, GADD45B, LY96, IRAK2, PFKFB3,
TNFRSF6, IFNGR1
CRTAP, MKNK1, BCL2A1, PRV1, CD86,	0.82	0.88	0.77
TNFRSF6, PSTPIP2, MAPK14, TNFSF13B,
ARG2, PFKFB3, CEACAM1, FAD104,
Gene_MMP9, OSM, SOD2
MKNK1, SOCS3, CRTAP, FCGR1A, CD86,	0.82	0.82	0.82
IL10alpha, GADD45A, IL18R1, IRAK2,
CCL5, JAK2, ANKRD22, TIFA, TGFBI,
CSF1R, BCL2A1
GADD45B, CEACAM1, ANKRD22, IRAK4,	0.82	0.81	0.82
LDLR, CRTAP, MKNK1, OSM, MAPK14,
MAP2K6, INSL3, GADD45A, PFKFB3,
TNFSF10, CSF1R, TIFA
CSF1R, INSL3, TNFRSF6, BCL2A1, CD86,	0.82	0.79	0.85
CEACAM1, IL10alpha, IL18R1, TLR4,
ITGAM, TNFSF10, OSM, ARG2, SOD2,
FCGR1A, PSTPIP2
NCR1, LDLR, MKNK1, INSL3, BCL2A1,	0.82	0.78	0.85
JAK2, FCGR1A, IL1RN, TNFRSF6, PRV1,
GADD45B, ARG2, MAP2K6, OSM, VNN1,
TDRD9
TLR4, CD86, MAPK14, TNFSF13B, INSL3,	0.82	0.85	0.79
CRTAP, NCR1, ARG2, GADD45A, CSF1R,
TNFRSF6, MAP2K6, JAK2, MKNK1,
ANKRD22, OSM
CSF1R, CCL5, ARG2, BCL2A1, FCGR1A,	0.82	0.85	0.79
MKNK1, TDRD9, IFNGR1, PFKFB3,
ITGAM, JAK2, OSM, GADD45B, FAD104,
NCR1, HLA-DRA
IFNGR1, FCGR1A, TLR4, OSM, PSTPIP2,	0.86	0.82	0.9
IL18R1, NCR1, SOCS3, PFKFB3, INSL3,
LDLR, TNFRSF6, SOD2, GADD45B,
IL10alpha, CCL5, IL1RN
CEACAM1, IL18R1, SOCS3, CRTAP, LDLR,	0.86	0.84	0.88
HLA-DRA, LY96, IL1RN, IL10alpha,
BCL2A1, GADD45A, TIFA, FAD104,
ANKRD22, OSM, CCL5, IFNGR1
FAD104, GADD45B, HLA-DRA, VNN1,	0.85	0.79	0.91
IL10alpha, CD86, JAK2, INSL3, TDRD9,
TLR4, IRAK4, SOD2, LDLR, CCL5,
MKNK1, ARG2, IL18R1
IL18R1, PRV1, IL1RN, TNFSF10, FAD104,	0.85	0.81	0.89
ITGAM, FCGR1A, INSL3, MAP2K6, LDLR,
TNFSF13B, IRAK2, OSM, PFKFB3, TGFBI,
IL10alpha, LY96
IRAK2, HLA-DRA, IFNGR1, MAP2K6,	0.85	0.81	0.89
TLR4, ITGAM, SOCS3, CD86, ARG2, VNN1,
IL18R1, ANXA3, FCGR1A, IL1RN,
Gene_MMP9, TGFBI, IL10alpha
MAP2K6, IL18R1, IL1RN, CSF1R,	0.84	0.81	0.87
TNFRSF6, FCGR1A, NCR1, TDRD9,
TNFSF10, SOCS3, CCL5, IFNGR1, TIFA,
CRTAP, GADD45B, IL10alpha, TGFBI
CD86, CCL5, IRAK4, GADD45A, ANXA3,	0.84	0.8	0.88
OSM, JAK2, INSL3, SOCS3, BCL2A1,
FAD104, MAPK14, TIFA, TLR4, NCR1,
PRV1, TDRD9
BCL2A1, IL18R1, TLR4, OSM, CD86,	0.84	0.8	0.89
FAD104, PRV1, JAK2, MAPK14, TNFRSF6,
CEACAM1, IL1RN, IL10alpha, SOD2,
Gene_MMP9, CSF1R, PFKFB3
LY96, TIFA, IL10alpha, ANXA3, LDLR,	0.84	0.81	0.87
JAK2, IFNGR1, IRAK2, MAP2K6, TGFBI,
MAPK14, TDRD9, FCGR1A, ITGAM,
TNFSF10, GADD45B, SOCS3
TNFSF13B, FAD104, SOD2, SOCS3,	0.84	0.85	0.83
CEACAM1, TDRD9, ARG2, CD86, IRAK2,
PFKFB3, FCGR1A, NCR1, MAPK14,
CRTAP, LDLR, GADD45A, TNFRSF6
IRAK2, MKNK1, PSTPIP2, ANXA3, HLA-	0.84	0.83	0.84
DRA, TNFSF10, IFNGR1, PFKFB3, OSM,
PRV1, IL1RN, IL10alpha, FAD104, CD86,
TIFA, BCL2A1, TNFSF13B
VNN1, IFNGR1, LY96, SOD2, IL18R1,	0.84	0.82	0.86
SOCS3, FCGR1A, ARG2, CSF1R,
Gene_MMP9, IRAK4, MAP2K6, TIFA,
FAD104, HLA-DRA, GADD45B, IL1RN
CD86, Gene_MMP9, IL18R1, TNFSF13B,	0.83	0.82	0.84
FCGR1A, TNFRSF6, INSL3, IL1RN,
PFKFB3, PSTPIP2, NCR1, GADD45B,
VNN1, CRTAP, IRAK4, MAP2K6, OSM
TNFSF13B, FAD104, PRV1, TIFA, SOD2,	0.83	0.79	0.88
TDRD9, TLR4, TNFRSF6, MKNK1, OSM,
MAP2K6, CCL5, ARG2, LDLR, HLA-DRA,
PSTPIP2, IL18R1
IRAK4, MAP2K6, JAK2, LY96, ITGAM,	0.83	0.82	0.84
CCL5, CSF1R, ARG2, FCGR1A, FAD104,
CD86, TNFSF10, IL18R1, CRTAP,
GADD45A, TLR4, Gene_MMP9
IRAK2, OSM, MAP2K6, TNFSF13B,	0.83	0.8	0.86
ANKRD22, HLA-DRA, SOD2, TNFSF10,
VNN1, ARG2, IRAK4, LY96, IFNGR1, JAK2,
BCL2A1, FCGR1A, CSF1R
IL10alpha, FCGR1A, TGFBI, ANKRD22,	0.83	0.78	0.87
IRAK4, CD86, TNFSF13B, TNFRSF6,
IL18R1, JAK2, IL1RN, PSTPIP2, OSM,
MAP2K6, GADD45A, Gene_MMP9,
MAPK14
PRV1, IRAK4, MKNK1, JAK2, OSM,	0.82	0.83	0.82
MAP2K6, BCL2A1, GADD45B,
Gene_MMP9, IL10alpha, FAD104, ARG2,
PSTPIP2, SOD2, TNFRSF6, TNFSF10,
IL1RN
IL1RN, OSM, FAD104, CRTAP, IRAK4,	0.82	0.82	0.83
IL10alpha, LDLR, INSL3, TNFSF10, CCL5,
IL18R1, ANXA3, PRV1, ARG2,
Gene_MMP9, CEACAM1, SOCS3
TNFRSF6, MAP2K6, FCGR1A, MAPK14,	0.82	0.81	0.83
ARG2, INSL3, TNFSF10, NCR1, PRV1,
CEACAM1, ANXA3, IL18R1, TIFA,
IFNGR1, IRAK4, CCL5, VNN1
IRAK2, ANKRD22, MAPK14, TIFA,	0.85	0.83	0.87
GADD45B, OSM, IL10alpha, SOD2, CCL5,
GADD45A, CD86, IRAK4, SOCS3, TDRD9,
MAP2K6, FAD104, PRV1, ANXA3
TLR4, LDLR, OSM, MAP2K6, GADD45A,	0.85	0.84	0.86
TIFA, NCR1, IL18R1, IFNGR1, INSL3,
ANXA3, IL10alpha, IL1RN, CSF1R,
GADD45B, PFKFB3, TGFBI, CRTAP
HLA-DRA, GADD45A, ANXA3, ARG2,	0.84	0.85	0.83
FAD104, PFKFB3, ITGAM, JAK2, MAPK14,
OSM, CD86, LDLR, TIFA, CCL5, NCR1,
IRAK2, SOD2, PRV1
GADD45A, INSL3, IRAK2, TNFSF10,	0.83	0.82	0.85
TGFBI, IRAK4, NCR1, HLA-DRA,
CEACAM1, GADD45B, MAPK14, CD86,
IL18R1, CRTAP, ANKRD22, PSTPIP2, LY96,
PFKFB3
MAP2K6, IL1RN, TIFA, TLR4, OSM, TGFBI,	0.83	0.85	0.81
ANXA3, NCR1, IL18R1, ANKRD22,
GADD45A, TNFSF10, PRV1, IRAK2,
TDRD9, JAK2, Gene_MMP9, CSF1R
CD86, GADD45A, GADD45B, TNFSF13B,	0.83	0.83	0.83
CRTAP, TNFRSF6, NCR1, IL10alpha,
CSF1R, OSM, MKNK1, CEACAM1, TLR4,
IFNGR1, IRAK2, SOCS3, TGFBI,
Gene_MMP9
BCL2A1, ANKRD22, OSM, CD86, ITGAM,	0.83	0.82	0.84
ANXA3, FCGR1A, CCL5, TIFA, IRAK4,
HLA-DRA, NCR1, CRTAP, TLR4,
CEACAM1, FAD104, ARG2, MAP2K6
GADD45A, IFNGR1, MAP2K6, CRTAP,	0.83	0.82	0.84
MAPK14, TNFSF10, LDLR, TIFA, OSM,
SOCS3, CD86, ARG2, PSTPIP2, IL1RN,
LY96, GADD45B, ANKRD22, TGFBI
INSL3, TLR4, BCL2A1, ANKRD22, FAD104,	0.83	0.81	0.85
MAP2K6, GADD45B, ARG2, NCR1,
MKNK1, ITGAM, CSF1R, IL1RN, HLA-
DRA, LDLR, CRTAP, PRV1, LY96
CRTAP, HLA-DRA, ARG2, PSTPIP2,	0.83	0.81	0.86
MKNK1, INSL3, TIFA, CEACAM1, JAK2,
Gene_MMP9, TLR4, IRAK4, CD86, FAD104,
CCL5, TNFSF10, LDLR, IFNGR1
IL18R1, TNFRSF6, PFKFB3, FAD104,	0.83	0.8	0.86
GADD45A, OSM, JAK2, VNN1, MKNK1,
BCL2A1, SOCS3, NCR1, TLR4, FCGR1A,
CSF1R, ITGAM, IRAK4, CRTAP
FAD104, TNFRSF6, OSM, TIFA, PSTPIP2,	0.83	0.78	0.87
ANXA3, TLR4, CD86, IRAK4, TNFSF13B,
IL1RN, IFNGR1, ITGAM, BCL2A1,
CEACAM1, MKNK1, TGFBI, ARG2
TNFSF10, BCL2A1, TGFBI, LY96, PRV1,	0.83	0.85	0.81
MKNK1, SOD2, ARG2, SOCS3, CD86,
IL10alpha, TNFSF13B, ITGAM, OSM,
MAPK14, PSTPIP2, ANXA3, CCL5
SOCS3, OSM, CCL5, JAK2, MAP2K6,	0.83	0.85	0.81
IL18R1, NCR1, CEACAM1, IRAK2, ARG2,
LY96, PRV1, ITGAM, TNFSF13B, TNFSF10,
TGFBI, IL10alpha, LDLR
ARG2, IRAK2, Gene_MMP9, GADD45B,	0.83	0.83	0.82
MKNK1, PFKFB3, MAPK14, IRAK4, CSF1R,
FCGR1A, GADD45A, TDRD9, TIFA, CD86,
IL18R1, BCL2A1, CRTAP, TNFRSF6
FAD104, IL1RN, TGFBI, TLR4, BCL2A1,	0.83	0.82	0.83
IFNGR1, IRAK4, PRV1, ANKRD22, CRTAP,
TNFRSF6, CSF1R, ARG2, OSM, GADD45A,
VNN1, INSL3, CEACAM1
CSF1R, SOCS3, FAD104, TLR4, INSL3,	0.83	0.81	0.84
ANXA3, NCR1, CRTAP, IFNGR1, TIFA,
OSM, MAPK14, TDRD9, IL1RN, ANKRD22,
TNFRSF6, IRAK2, BCL2A1
MAP2K6, IFNGR1, CD86, FCGR1A, IRAK2,	0.83	0.81	0.84
MKNK1, CRTAP, FAD104, IL10alpha,
VNN1, ANXA3, NCR1, IL18R1, CEACAM1,
CCL5, ARG2, MAPK14, SOCS3
IL1RN, IRAK4, JAK2, CD86, BCL2A1,	0.83	0.79	0.86
TGFBI, Gene_MMP9, NCR1, IFNGR1,
VNN1, SOCS3, CCL5, TNFSF13B, TDRD9,
MAPK14, PRV1, OSM, TLR4
MAP2K6, CSF1R, HLA-DRA, ANKRD22,	0.82	0.8	0.85
MKNK1, SOCS3, TNFSF10, LDLR, FAD104,
CEACAM1, TNFSF13B, TDRD9, IRAK4,
VNN1, IL18R1, OSM, PSTPIP2, Gene_MMP9
CCL5, SOD2, JAK2, IRAK4, IRAK2,	0.84	0.79	0.89
Gene_MMP9, IFNGR1, TLR4, GADD45A,
TNFSF10, CSF1R, IL18R1, PRV1,
TNFSF13B, HLA-DRA, LDLR, CD86,
SOCS3, FAD104
MAP2K6, TNFSF13B, SOD2, GADD45B,	0.84	0.84	0.84
HLA-DRA, CSF1R, CCL5, TIFA, NCR1,
IFNGR1, OSM, CD86, SOCS3, ARG2,
IL10alpha, BCL2A1, TDRD9, LDLR,
GADD45A
IFNGR1, OSM, MAPK14, CEACAM1,	0.84	0.83	0.85
PFKFB3, TLR4, CSF1R, JAK2, IL18R1,
TGFBI, CD86, IL10alpha, INSL3, BCL2A1,
FCGR1A, GADD45B, LDLR, PSTPIP2,
FAD104
ARG2, PRV1, IRAK4, TNFRSF6, MAP2K6,	0.84	0.8	0.86
SOCS3, IL18R1, HLA-DRA, IFNGR1,
ANXA3, TNFSF10, JAK2, FCGR1A,
GADD45A, INSL3, IL1RN, TNFSF13B,
ITGAM, CSF1R
LDLR, INSL3, JAK2, TNFRSF6, PRV1,	0.83	0.82	0.84
IFNGR1, OSM, ITGAM, FCGR1A, IL10alpha,
NCR1, TDRD9, MAP2K6, TNFSF13B, TIFA,
HLA-DRA, ANKRD22, GADD45B, IL1RN
MAPK14, SOD2, CSF1R, ITGAM, MAP2K6,	0.83	0.82	0.84
TLR4, ANXA3, BCL2A1, CRTAP, IL10alpha,
IRAK4, CCL5, SOCS3, TNFSF13B, ARG2,
FCGR1A, CEACAM1, OSM, IL1RN
LY96, IL10alpha, GADD45A, GADD45B,	0.83	0.78	0.87
IL1RN, IL18R1, PSTPIP2, ARG2, IRAK2,
CEACAM1, MKNK1, PFKFB3, TNFSF10,
ANKRD22, ANXA3, SOD2, MAP2K6,
IRAK4, SOCS3
IL18R1, MAP2K6, ARG2, CD86, TNFSF13B,	0.82	0.82	0.83
MAPK14, TNFSF10, CRTAP, GADD45A,
NCR1, GADD45B, JAK2, MKNK1,
TNFRSF6, VNN1, FAD104, LY96,
CEACAM1, PRV1
HLA-DRA, CD86, SOCS3, TIFA, TNFSF13B,	0.82	0.79	0.85
FCGR1A, JAK2, PFKFB3, MAP2K6, OSM,
TGFBI, ANKRD22, CEACAM1, IRAK4,
ARG2, IL18R1, SOD2, MKNK1, GADD45B
TDRD9, IRAK2, PFKFB3, CSF1R, TGFBI,	0.82	0.79	0.85
SOCS3, IL10alpha, IFNGR1, TNFRSF6,
VNN1, FCGR1A, PRV1, TNFSF13B,
MAPK14, BCL2A1, CD86, SOD2, INSL3,
ARG2
LDLR, ITGAM, IL18R1, ANXA3,	0.82	0.79	0.86
GADD45A, VNN1, TDRD9, LY96, BCL2A1,
CD86, IRAK2, FAD104, Gene_MMP9, TLR4,
TIFA, OSM, ARG2, CRTAP, PSTPIP2
CCL5, TGFBI, BCL2A1, VNN1, TDRD9,	0.82	0.8	0.84
SOCS3, CRTAP, CD86, TNFRSF6, LDLR,
CSF1R, PRV1, IL18R1, INSL3, GADD45B,
TNFSF13B, PFKFB3, JAK2, SOD2
SOD2, ARG2, HLA-DRA, LY96,	0.82	0.8	0.84
Gene_MMP9, VNN1, CD86, IL10alpha,
CSF1R, PSTPIP2, JAK2, TNFSF13B, IRAK2,
CCL5, ANKRD22, TLR4, IL1RN, OSM,
GADD45B
SOCS3, TGFBI, FCGR1A, TDRD9,	0.82	0.78	0.86
GADD45A, TIFA, IFNGR1, VNN1, ITGAM,
MAPK14, OSM, ANXA3, TNFSF13B,
IL1RN, HLA-DRA, ARG2, MAP2K6, TLR4,
PSTPIP2
CD86, INSL3, MAPK14, TIFA, MAP2K6,	0.82	0.76	0.87
Gene_MMP9, CRTAP, CSF1R, MKNK1,
IL10alpha, FAD104, PRV1, BCL2A1, NCR1,
LDLR, IRAK4, HLA-DRA, IFNGR1, TDRD9
NCR1, LDLR, IRAK2, TNFRSF6, CD86,	0.82	0.74	0.89
SOD2, TNFSF13B, VNN1, GADD45A,
Gene_MMP9, PFKFB3, ANKRD22, PSTPIP2,
PRV1, FCGR1A, IL18R1, TIFA, INSL3,
CRTAP
IL1RN, TLR4, PSTPIP2, IL18R1, GADD45A,	0.82	0.82	0.82
IL10alpha, BCL2A1, MKNK1, IRAK2, HLA-
DRA, ANKRD22, NCR1, CEACAM1,
IRAK4, OSM, TIFA, SOD2, TGFBI,
Gene_MMP9
GADD45A, LY96, ITGAM, CCL5, TNFSF10,	0.82	0.78	0.85
TNFSF13B, HLA-DRA, CSF1R, TIFA,
SOCS3, MKNK1, ARG2, IFNGR1, IL1RN,
BCL2A1, OSM, PFKFB3, PSTPIP2, IRAK2
Gene_MMP9, GADD45A, PSTPIP2, INSL3,	0.82	0.78	0.85
IRAK4, HLA-DRA, CCL5, TGFBI, OSM,
LY96, TDRD9, NCR1, PFKFB3, IFNGR1,
IRAK2, VNN1, CRTAP, TIFA, CD86
LDLR, ARG2, MAP2K6, MAPK14, IL18R1,	0.85	0.81	0.9
CCL5, PSTPIP2, ANKRD22, OSM, TDRD9,
HLA-DRA, SOCS3, ANXA3, TNFRSF6,
TIFA, CD86, FAD104, MKNK1, BCL2A1,
IRAK2
FCGR1A, FAD104, Gene_MMP9, LDLR,	0.85	0.8	0.88
ANKRD22, VNN1, SOCS3, TNFSF13B,
TLR4, TDRD9, CEACAM1, PSTPIP2,
MAPK14, ARG2, IRAK4, OSM, PRV1,
TNFRSF6, IL10alpha, PFKFB3
TNFSF10, IRAK2, TDRD9, TGFBI, PFKFB3,	0.84	0.8	0.88
CD86, OSM, IFNGR1, FAD104, ANXA3,
CCL5, IRAK4, PSTPIP2, GADD45A, SOCS3,
CSF1R, NCR1, CRTAP, IL1RN, BCL2A1
IFNGR1, TIFA, ARG2, IRAK2, CCL5, LDLR,	0.84	0.83	0.85
OSM, SOCS3, SOD2, IL1RN, PSTPIP2,
BCL2A1, FAD104, IL18R1, IL10alpha, CD86,
FCGR1A, ITGAM, JAK2, Gene_MMP9
PSTPIP2, SOCS3, OSM, FCGR1A, IL1RN,	0.84	0.82	0.85
IRAK4, ITGAM, ARG2, TGFBI,
Gene_MMP9, CSF1R, TLR4, GADD45A,
GADD45B, PRV1, IFNGR1, IL18R1, VNN1,
FAD104, PFKFB3
TNFRSF6, TIFA, PFKFB3, PRV1, OSM,	0.84	0.8	0.87
JAK2, TGFBI, IL10alpha, CEACAM1, INSL3,
IRAK2, LY96, ARG2, CD86, FAD104,
MAP2K6, TLR4, SOCS3, IL18R1, ITGAM
FCGR1A, HLA-DRA, ARG2, CRTAP,	0.84	0.83	0.84
CEACAM1, TNFSF13B, OSM, ANXA3,
IL1RN, Gene_MMP9, TNFRSF6, FAD104,
JAK2, IFNGR1, MKNK1, LDLR, IL10alpha,
TGFBI, SOD2, CCL5
GADD45A, MAPK14, ARG2, TDRD9, NCR1,	0.84	0.83	0.85
IL18R1, SOD2, ITGAM, FCGR1A, SOCS3,
HLA-DRA, IRAK4, TNFRSF6, PRV1, CD86,
TGFBI, TNFSF13B, TIFA, VNN1, FAD104
HLA-DRA, ARG2, IL1RN, SOCS3, PSTPIP2,	0.84	0.79	0.88
CCL5, IFNGR1, CD86, TLR4, TGFBI, LY96,
TNFRSF6, OSM, MAP2K6, VNN1, ITGAM,
TNFSF10, NCR1, IRAK4, MAPK14
BCL2A1, ITGAM, ANKRD22, ARG2,	0.84	0.79	0.87
FAD104, OSM, GADD45A, CCL5, TGFBI,
CD86, PSTPIP2, PFKFB3, IFNGR1, IL18R1,
CEACAM1, Gene_MMP9, IRAK2, IL1RN,
NCR1, LY96
JAK2, VNN1, CSF1R, TLR4, OSM, SOCS3,	0.84	0.79	0.88
ANXA3, LY96, MKNK1, TDRD9, ITGAM,
Gene_MMP9, TGFBI, CEACAM1, CD86,
MAP2K6, CCL5, TNFSF10, IL1RN, IL18R1
FAD104, PSTPIP2, CEACAM1, MAP2K6,	0.83	0.84	0.83
TIFA, ANKRD22, INSL3, TLR4, CRTAP,
LY96, SOCS3, MAPK14, JAK2, ARG2,
MKNK1, IL18R1, CSF1R, CD86, PRV1, OSM
CEACAM1, SOCS3, FCGR1A, ARG2,	0.83	0.8	0.87
INSL3, FAD104, IRAK4, GADD45A,
ITGAM, PRV1, TNFSF13B, NCR1,
Gene_MMP9, IL18R1, SOD2, MAPK14,
TIFA, IRAK2, ANKRD22, IL1RN
GADD45B, SOD2, CRTAP, OSM,	0.83	0.78	0.88
TNFSF13B, CCL5, CD86, INSL3, HLA-DRA,
TNFRSF6, TGFBI, GADD45A, FCGR1A,
FAD104, JAK2, IL1RN, PFKFB3, MAP2K6,
CEACAM1, TDRD9
FCGR1A, GADD45A, ANKRD22, IL1RN,	0.83	0.78	0.88
PFKFB3, CCL5, TIFA, IL10alpha, CRTAP,
MKNK1, PSTPIP2, PRV1, CSF1R, ANXA3,
NCR1, JAK2, VNN1, IRAK4, CD86,
MAP2K6
TLR4, GADD45A, JAK2, OSM, CD86,	0.83	0.78	0.88
SOCS3, CEACAM1, IL18R1, MAP2K6,
PRV1, FAD104, BCL2A1, VNN1, INSL3,
PSTPIP2, ANKRD22, TNFSF10, IFNGR1,
CRTAP, HLA-DRA
FAD104, IL18R1, TIFA, TNFRSF6,	0.83	0.77	0.88
Gene_MMP9, ARG2, OSM, TNFSF13B,
FCGR1A, CD86, CEACAM1, LY96, NCR1,
TNFSF10, PFKFB3, PRV1, GADD45A,
SOCS3, HLA-DRA, IRAK2
TDRD9, MKNK1, PFKFB3, IRAK2, INSL3,	0.83	0.82	0.84
ITGAM, MAPK14, JAK2, HLA-DRA,
CSF1R, CRTAP, NCR1, SOD2, TIFA, IRAK4,
CD86, OSM, BCL2A1, LY96, ANKRD22
ANKRD22, CRTAP, NCR1, OSM, INSL3,	0.83	0.82	0.84
CD86, CCL5, JAK2, CSF1R, GADD45B,
ANXA3, SOCS3, PSTPIP2, FCGR1A, HLA-
DRA, IRAK2, IL1RN, IL18R1, PFKFB3,
Gene_MMP9
IL1RN, LY96, ARG2, PRV1, GADD45A,	0.85	0.84	0.85
TNFSF10, FCGR1A, IL10alpha, LDLR,
PFKFB3, CRTAP, SOD2, CEACAM1,
IL18R1, CCL5, PSTPIP2, TLR4, VNN1,
HLA-DRA, JAK2, ANKRD22
CD86, LDLR, CRTAP, OSM, TGFBI,	0.84	0.88	0.82
FCGR1A, NCR1, MAPK14, GADD45A,
ARG2, TLR4, GADD45B, INSL3, TNFSF10,
ANXA3, MKNK1, PSTPIP2, CSF1R, SOD2,
MAP2K6, BCL2A1
IRAK4, GADD45A, MAP2K6, ANKRD22,	0.84	0.82	0.85
Gene_MMP9, TDRD9, PSTPIP2, VNN1,
IL18R1, ARG2, IL1RN, PFKFB3, FCGR1A,
TNFRSF6, JAK2, NCR1, TLR4, FAD104,
SOCS3, IFNGR1, SOD2
SOCS3, ITGAM, Gene_MMP9, MKNK1,	0.84	0.82	0.86
ARG2, CRTAP, BCL2A1, PRV1, NCR1,
HLA-DRA, MAP2K6, FCGR1A, CD86,
FAD104, CCL5, TGFBI, TDRD9, OSM,
GADD45B, IRAK4, LY96
INSL3, BCL2A1, PSTPIP2, OSM, MAP2K6,	0.83	0.84	0.83
CCL5, MKNK1, FAD104, ITGAM, MAPK14,
IL1RN, VNN1, IRAK2, FCGR1A, CD86,
PFKFB3, TDRD9, HLA-DRA, ARG2, TLR4,
CEACAM1
TIFA, MKNK1, TNFSF13B, CSF1R, HLA-	0.83	0.82	0.84
DRA, IL18R1, MAPK14, INSL3, PFKFB3,
ANKRD22, LDLR, ARG2, CCL5, LY96,
PSTPIP2, GADD45A, CEACAM1, JAK2,
TGFBI, VNN1, IL1RN
CRTAP, FAD104, TIFA, BCL2A1, IRAK2,	0.83	0.81	0.85
PSTPIP2, PFKFB3, MKNK1, ANKRD22,
IL18R1, GADD45B, TDRD9, TLR4, INSL3,
CEACAM1, MAP2K6, ARG2, CD86, NCR1,
TNFSF13B, PRV1
JAK2, SOCS3, IFNGR1, IL1RN, OSM,	0.83	0.81	0.85
BCL2A1, SOD2, ITGAM, FAD104, IL18R1,
PSTPIP2, ARG2, PRV1, TNFSF13B,
FCGR1A, IRAK2, IL10alpha, PFKFB3,
MAPK14, INSL3, TGFBI
GADD45A, CCL5, LDLR, ARG2, IRAK2,	0.83	0.86	0.8
SOCS3, SOD2, PRV1, MAP2K6, INSL3,
TNFSF10, IL18R1, IL1RN, MAPK14,
FAD104, IFNGR1, HLA-DRA, PSTPIP2,
ITGAM, CSF1R, IL10alpha
CD86, TGFBI, ITGAM, IL10alpha, JAK2,	0.83	0.79	0.86
TIFA, FAD104, CRTAP, IL1RN, BCL2A1,
CCL5, GADD45B, HLA-DRA, SOD2, OSM,
NCR1, VNN1, IL18R1, ANXA3,
Gene_MMP9, PSTPIP2
IL10alpha, TNFSF13B, GADD45B, MAP2K6,	0.83	0.76	0.89
CCL5, IRAK2, MKNK1, LDLR, VNN1,
GADD45A, ARG2, OSM, IFNGR1, IL18R1,
ANKRD22, JAK2, TLR4, TGFBI, TNFRSF6,
FAD104, PFKFB3
MAPK14, SOD2, PRV1, GADD45B,	0.83	0.83	0.82
MKNK1, IL18R1, INSL3, NCR1, LY96,
IRAK2, CSF1R, TNFRSF6, HLA-DRA,
VNN1, IRAK4, FAD104, CEACAM1,
IFNGR1, FCGR1A, TIFA, CD86
IL1RN, PFKFB3, IL18R1, PRV1, CRTAP,	0.83	0.81	0.84
ITGAM, TNFRSF6, IL10alpha, SOCS3,
VNN1, BCL2A1, MAPK14, GADD45A,
IRAK2, CCL5, ARG2, TLR4, CD86,
ANKRD22, TNFSF10, TGFBI
HLA-DRA, PRV1, GADD45A, IL1RN,	0.83	0.81	0.84
IL18R1, TNFRSF6, LDLR, IRAK4, BCL2A1,
TIFA, PSTPIP2, SOCS3, IL10alpha, FAD104,
MKNK1, TNFSF13B, JAK2, TDRD9,
TNFSF10, FCGR1A, CD86
INSL3, GADD45A, TGFBI, JAK2, IRAK2,	0.82	0.82	0.82
OSM, TIFA, TNFSF13B, HLA-DRA,
FCGR1A, BCL2A1, PRV1, CEACAM1,
SOCS3, MAPK14, IRAK4, ANXA3,
TNFRSF6, FAD104, IFNGR1, Gene_MMP9
BCL2A1, ANKRD22, IL10alpha, HLA-DRA,	0.82	0.8	0.84
VNN1, GADD45B, TNFRSF6, CSF1R,
IRAK4, ITGAM, IL1RN, IRAK2, LY96,
MAPK14, JAK2, Gene_MMP9, TLR4, ARG2,
CCL5, SOCS3, MAP2K6
TDRD9, VNN1, GADD45A, ANKRD22,	0.82	0.79	0.85
PFKFB3, TNFSF13B, SOCS3, IL18R1,
IL1RN, ARG2, CSF1R, HLA-DRA, PRV1,
CEACAM1, CD86, IFNGR1, CCL5,
MAP2K6, TGFBI, IL10alpha, Gene_MMP9
CRTAP, IL1RN, TIFA, IRAK4, ANXA3,	0.82	0.78	0.86
SOCS3, CD86, CSF1R, FCGR1A, FAD104,
ANKRD22, TNFSF13B, PSTPIP2, TDRD9,
ARG2, TGFBI, Gene_MMP9, CCL5,
IL10alpha, GADD45B, TNFRSF6
ANXA3, TNFRSF6, TDRD9, IRAK2,	0.82	0.78	0.87
MAP2K6, INSL3, FCGR1A, GADD45A,
NCR1, ARG2, VNN1, PRV1, MAPK14,
IRAK4, SOCS3, ITGAM, HLA-DRA, CD86,
CEACAM1, LY96, GADD45B
VNN1, CCL5, IFNGR1, LY96, IL10alpha,	0.87	0.84	0.89
ITGAM, FCGR1A, FAD104, NCR1,
TNFRSF6, TNFSF13B, SOCS3, TIFA,
TNFSF10, PSTPIP2, ARG2, IL18R1, CSF1R,
OSM, PFKFB3, LDLR, IRAK2
IL18R1, GADD45A, BCL2A1, HLA-DRA,	0.84	0.79	0.88
PSTPIP2, ANKRD22, CRTAP, FAD104,
CD86, TNFRSF6, Gene_MMP9, IRAK2,
SOD2, IL10alpha, IFNGR1, FCGR1A, TIFA,
OSM, CCL5, GADD45B, TGFBI, TLR4
TNFSF13B, LDLR, GADD45B, MAPK14,	0.84	0.79	0.89
PFKFB3, CRTAP, MAP2K6, NCR1, CCL5,
ARG2, SOD2, BCL2A1, MKNK1, TIFA,
ANKRD22, Gene_MMP9, TGFBI, IL1RN,
HLA-DRA, IL18R1, VNN1, CSF1R
TNFRSF6, PSTPIP2, CD86, VNN1, CCL5,	0.83	0.85	0.82
MAPK14, TLR4, BCL2A1, ANKRD22,
ARG2, ITGAM, IL10alpha, IRAK4, SOCS3,
LY96, CRTAP, JAK2, IL1RN, FCGR1A,
MAP2K6, TNFSF10, GADD45A
TDRD9, CRTAP, ANKRD22, TNFSF13B,	0.83	0.82	0.85
ANXA3, CCL5, FCGR1A, TNFSF10,
TNFRSF6, PRV1, IRAK2, CEACAM1,
SOCS3, CSF1R, FAD104, PSTPIP2, VNN1,
ARG2, IL1RN, HLA-DRA, BCL2A1, INSL3
TNFSF10, TLR4, MAP2K6, PFKFB3,	0.83	0.79	0.86
FCGR1A, INSL3, MAPK14, PSTPIP2,
IFNGR1, CD86, PRV1, IL10alpha, OSM,
FAD104, ITGAM, ANXA3, TIFA,
CEACAM1, IL18R1, TNFRSF6, NCR1,
GADD45A
GADD45B, HLA-DRA, NCR1, TGFBI, OSM,	0.83	0.8	0.86
MKNK1, TLR4, ARG2, CCL5, LDLR,
IFNGR1, SOCS3, INSL3, TIFA, TNFSF10,
CD86, IL10alpha, GADD45A, CSF1R,
TDRD9, BCL2A1, ANXA3
TLR4, ANXA3, IL10alpha, NCR1, JAK2,	0.83	0.76	0.88
TNFSF13B, GADD45A, OSM, SOCS3,
CEACAM1, BCL2A1, MKNK1, ARG2,
CRTAP, TNFRSF6, Gene_MMP9, PSTPIP2,
SOD2, CD86, IL1RN, FCGR1A, CSF1R
LY96, TIFA, TLR4, PSTPIP2, Gene_MMP9,	0.83	0.82	0.83
PRV1, HLA-DRA, CEACAM1, FCGR1A,
ARG2, IRAK4, IL1RN, OSM, IFNGR1,
TNFSF13B, CSF1R, TDRD9, GADD45B,
ANXA3, SOCS3, GADD45A, LDLR
INSL3, PSTPIP2, MKNK1, FCGR1A,	0.83	0.82	0.83
PFKFB3, OSM, TGFBI, MAPK14, IRAK2,
GADD45A, ANKRD22, CCL5, HLA-DRA,
IL10alpha, SOCS3, CD86, IFNGR1, ARG2,
Gene_MMP9, GADD45B, VNN1, IL1RN
IL1RN, IFNGR1, CCL5, GADD45B, VNN1,	0.83	0.78	0.87
CSF1R, TNFSF10, LDLR, TNFRSF6, INSL3,
CD86, OSM, FCGR1A, BCL2A1, CRTAP,
TLR4, NCR1, PSTPIP2, SOCS3, MAP2K6,
TNFSF13B, Gene_MMP9
ARG2, GADD45B, TNFSF10, IRAK2,	0.82	0.83	0.82
MAPK14, IL1RN, MKNK1, CRTAP,
TNFSF13B, PRV1, SOD2, VNN1, IL18R1,
HLA-DRA, MAP2K6, INSL3, CEACAM1,
IL10alpha, LY96, SOCS3, FCGR1A,
ANKRD22
IFNGR1, LDLR, ITGAM, VNN1, IL18R1,	0.82	0.83	0.82
TGFBI, SOCS3, ANKRD22, HLA-DRA,
TIFA, OSM, TLR4, IRAK4, INSL3, SOD2,
TNFSF13B, LY96, IRAK2, BCL2A1,
MAPK14, CCL5, MKNK1
Gene_MMP9, BCL2A1, TDRD9, OSM,	0.82	0.81	0.83
MAPK14, IRAK2, CRTAP, MAP2K6, TGFBI,
IL18R1, TNFSF10, ANXA3, IFNGR1,
GADD45A, TIFA, PSTPIP2, SOCS3, ITGAM,
ARG2, HLA-DRA, FAD104, IRAK4
IRAK2, IL1RN, ITGAM, LY96, IFNGR1,	0.82	0.81	0.84
TGFBI, TIFA, PFKFB3, Gene_MMP9,
FAD104, TNFSF13B, VNN1, LDLR, INSL3,
HLA-DRA, NCR1, TDRD9, TNFRSF6,
ANXA3, CSF1R, SOCS3, IL18R1
TNFRSF6, INSL3, LDLR, CD86, TGFBI,	0.82	0.8	0.84
NCR1, Gene_MMP9, CRTAP, HLA-DRA,
BCL2A1, MKNK1, IL18R1, TLR4,
CEACAM1, PRV1, CCL5, OSM, TDRD9,
PFKFB3, IFNGR1, IRAK2, PSTPIP2
PFKFB3, ITGAM, ANKRD22, MAPK14,	0.82	0.8	0.85
TGFBI, PSTPIP2, BCL2A1, IFNGR1,
MKNK1, NCR1, ARG2, HLA-DRA, INSL3,
CRTAP, FCGR1A, LDLR, CCL5, JAK2,
IRAK4, TLR4, LY96, IL10alpha
TIFA, IFNGR1, HLA-DRA, Gene_MMP9,	0.82	0.8	0.84
PRV1, FAD104, IL10alpha, GADD45B,
IRAK4, IL1RN, TDRD9, IL18R1, BCL2A1,
CD86, GADD45A, CCL5, ANXA3, OSM,
SOCS3, PFKFB3, LDLR, CSF1R
FAD104, NCR1, BCL2A1, IRAK2, TLR4,	0.82	0.8	0.84
IL18R1, SOD2, MAPK14, GADD45B, CD86,
FCGR1A, CSF1R, OSM, MAP2K6, PFKFB3,
LY96, TIFA, MKNK1, PSTPIP2, CRTAP,
TGFBI, GADD45A
GADD45A, CSF1R, IL18R1, TGFBI,	0.85	0.81	0.89
TNFSF13B, ANXA3, OSM, SOCS3, LY96,
TDRD9, ITGAM, FCGR1A, IFNGR1,
FAD104, HLA-DRA, PSTPIP2, MKNK1,
CRTAP, GADD45B, Gene_MMP9, LDLR,
TLR4, VNN1
MAP2K6, TGFBI, HLA-DRA, IL10alpha,	0.85	0.82	0.87
VNN1, GADD45B, CEACAM1, PRV1, OSM,
IRAK4, IRAK2, ITGAM, CSF1R, TDRD9,
NCR1, TNFSF13B, CRTAP, BCL2A1, TIFA,
IFNGR1, GADD45A, IL18R1, SOD2
GADD45B, MAPK14, TDRD9, CCL5, OSM,	0.84	0.83	0.85
TNFSF13B, ANXA3, TIFA, ANKRD22,
TNFRSF6, TNFSF10, PSTPIP2, TLR4, VNN1,
FCGR1A, IL18R1, NCR1, GADD45A, LY96,
INSL3, ITGAM, BCL2A1, IRAK2
HLA-DRA, PFKFB3, IRAK4, MKNK1,	0.84	0.8	0.88
TGFBI, CRTAP, ANXA3, CEACAM1, CCL5,
JAK2, TNFSF10, IL1RN, CSF1R, IFNGR1,
ARG2, LY96, Gene_MMP9, PRV1, CD86,
IRAK2, ITGAM, IL10alpha, OSM
FAD104, LY96, NCR1, TLR4, TNFSF13B,	0.84	0.8	0.89
MAPK14, MAP2K6, HLA-DRA, FCGR1A,
CD86, ANKRD22, LDLR, IL1RN, IFNGR1,
TDRD9, TGFBI, GADD45A, PRV1, PFKFB3,
ITGAM, JAK2, PSTPIP2, CRTAP
BCL2A1, FCGR1A, CRTAP, Gene_MMP9,	0.84	0.82	0.85
TDRD9, CEACAM1, SOCS3, SOD2, LDLR,
GADD45B, LY96, CSF1R, ARG2, TNFRSF6,
PSTPIP2, PFKFB3, IL1RN, IL10alpha, VNN1,
GADD45A, INSL3, JAK2, IFNGR1
Gene_MMP9, LDLR, CEACAM1, MAPK14,	0.84	0.82	0.86
TLR4, ANXA3, IRAK4, FCGR1A,
GADD45B, GADD45A, TGFBI, BCL2A1,
CSF1R, PRV1, TNFRSF6, IFNGR1, TDRD9,
LY96, MAP2K6, OSM, CRTAP, CD86,
FAD104
FCGR1A, ANXA3, MAPK14, TNFRSF6,	0.83	0.82	0.84
PSTPIP2, INSL3, ANKRD22, CD86, CRTAP,
FAD104, GADD45B, IL18R1, TLR4, IRAK2,
ITGAM, JAK2, GADD45A, BCL2A1,
IFNGR1, CSF1R, TIFA, NCR1, IRAK4
CRTAP, OSM, TNFRSF6, IRAK2, VNN1,	0.83	0.8	0.85
IRAK4, ANXA3, SOD2, ANKRD22, ITGAM,
TLR4, MKNK1, IL18R1, CEACAM1, TGFBI,
PRV1, Gene_MMP9, TNFSF13B, BCL2A1,
HLA-DRA, INSL3, NCR1, CSF1R
FAD104, CEACAM1, CCL5, PSTPIP2,	0.83	0.79	0.87
TNFSF10, VNN1, CRTAP, IRAK2, FCGR1A,
TNFSF13B, CD86, IL10alpha, ARG2,
BCL2A1, IFNGR1, PRV1, IL18R1, TNFRSF6,
TIFA, TLR4, JAK2, MAPK14, MAP2K6
ARG2, MAPK14, IRAK4, LDLR, IL10alpha,	0.83	0.84	0.81
Gene_MMP9, NCR1, OSM, CEACAM1,
SOD2, CSF1R, CCL5, GADD45A, ITGAM,
BCL2A1, HLA-DRA, PFKFB3, TNFSF13B,
TNFSF10, IRAK2, VNN1, JAK2, PRV1
FAD104, IFNGR1, INSL3, PFKFB3,	0.83	0.83	0.83
MAP2K6, LDLR, CD86, ARG2, PRV1,
IL1RN, OSM, ITGAM, VNN1, MKNK1,
ANXA3, JAK2, GADD45B, CSF1R,
TNFSF13B, PSTPIP2, FCGR1A, CRTAP,
TGFBI
VNN1, SOCS3, ANKRD22, FAD104, IL18R1,	0.83	0.77	0.89
OSM, ITGAM, CCL5, TGFBI, MAPK14,
MKNK1, HLA-DRA, LDLR, PSTPIP2,
ARG2, CSF1R, IL10alpha, MAP2K6, LY96,
FCGR1A, TNFSF10, JAK2, TLR4
CEACAM1, MAP2K6, IL18R1, TIFA, HLA-	0.82	0.82	0.83
DRA, FAD104, TGFBI, LDLR, ANKRD22,
IL1RN, SOCS3, TNFSF13B, NCR1, CD86,
BCL2A1, IL10alpha, TLR4, CRTAP,
MKNK1, ITGAM, JAK2, OSM, ARG2
VNN1, FCGR1A, SOD2, CRTAP, TGFBI,	0.82	0.81	0.84
LDLR, FAD104, NCR1, TNFRSF6, ARG2,
GADD45A, OSM, ANXA3, ITGAM,
BCL2A1, CSF1R, IFNGR1, TIFA,
CEACAM1, CCL5, SOCS3, ANKRD22,
Gene_MMP9
CCL5, IL1RN, TIFA, PRV1, TNFSF13B,	0.82	0.81	0.84
INSL3, IRAK2, MKNK1, MAPK14,
FCGR1A, SOCS3, JAK2, FAD104, IFNGR1,
CRTAP, IL18R1, GADD45B, SOD2,
TNFSF10, HLA-DRA, TNFRSF6, ANKRD22,
LDLR
PRV1, BCL2A1, SOD2, VNN1, FAD104,	0.82	0.74	0.9
TIFA, IL10alpha, SOCS3, ITGAM, IL18R1,
CEACAM1, MAP2K6, TNFSF13B, JAK2,
IRAK4, TNFRSF6, OSM, CRTAP, PSTPIP2,
TLR4, CSF1R, IL1RN, FCGR1A
TNFRSF6, TNFSF10, CD86, IL10alpha,	0.82	0.81	0.83
ARG2, TLR4, JAK2, MAP2K6, GADD45B,
LDLR, TIFA, IRAK2, BCL2A1, SOD2, LY96,
PFKFB3, HLA-DRA, CSF1R, FAD104,
CRTAP, FCGR1A, ANXA3, SOCS3
TNFSF13B, IRAK4, CD86, LDLR, OSM,	0.82	0.8	0.83
CCL5, ANXA3, IL1RN, GADD45B, SOCS3,
TGFBI, BCL2A1, FAD104, IRAK2,
IL10alpha, NCR1, MAP2K6, INSL3, TIFA,
CEACAM1, MKNK1, MAPK14, JAK2
LY96, ANXA3, TIFA, CSF1R, GADD45B,	0.85	0.8	0.89
PFKFB3, IL1RN, IL18R1, LDLR, TNFRSF6,
OSM, INSL3, CRTAP, MAP2K6, IRAK2,
ARG2, IL10alpha, NCR1, FAD104, IRAK4,
MKNK1, VNN1, IFNGR1, SOD2
NCR1, IL1RN, PRV1, IL18R1, HLA-DRA,	0.84	0.82	0.86
BCL2A1, GADD45A, FAD104, TLR4, OSM,
FCGR1A, TNFSF10, CRTAP, INSL3,
GADD45B, LY96, IRAK2, CD86, VNN1,
CCL5, JAK2, IL10alpha, MKNK1, IRAK4
GADD45A, MKNK1, ANXA3, TLR4,	0.84	0.83	0.85
MAP2K6, TIFA, FCGR1A, IRAK2, TDRD9,
VNN1, CSF1R, GADD45B, LDLR, IL1RN,
ANKRD22, JAK2, HLA-DRA, IL10alpha,
PSTPIP2, Gene_MMP9, CRTAP, IL18R1,
MAPK14, ARG2
FAD104, IL18R1, IRAK2, TIFA, IL10alpha,	0.83	0.83	0.84
ITGAM, SOCS3, TDRD9, PSTPIP2, ARG2,
INSL3, IL1RN, TLR4, IFNGR1, VNN1,
MAPK14, TNFRSF6, SOD2, ANKRD22,
NCR1, ANXA3, FCGR1A, CD86, OSM
TLR4, TGFBI, CEACAM1, OSM, CRTAP,	0.83	0.83	0.83
IL1RN, TNFRSF6, PRV1, SOD2, MKNK1,
VNN1, CSF1R, IL18R1, ANKRD22,
MAPK14, ANXA3, TNFSF10, TDRD9,
BCL2A1, IRAK4, FCGR1A, CCL5,
TNFSF13B, GADD45B
ARG2, JAK2, CSF1R, NCR1, LY96, HLA-	0.83	0.82	0.84
DRA, ANXA3, PSTPIP2, IRAK4, BCL2A1,
IL1RN, IFNGR1, FCGR1A, VNN1, TNFSF10,
MAPK14, TGFBI, GADD45B, INSL3,
IRAK2, OSM, CD86, CRTAP, TNFSF13B
HLA-DRA, INSL3, PRV1, MAP2K6, TIFA,	0.83	0.81	0.84
NCR1, CSF1R, TDRD9, IL18R1, MKNK1,
TNFRSF6, TNFSF10, LDLR, IRAK4,
FAD104, ITGAM, PSTPIP2, MAPK14,
TNFSF13B, GADD45B, CEACAM1, IL1RN,
ANXA3, PFKFB3
INSL3, TDRD9, GADD45A, BCL2A1,	0.83	0.78	0.87
PFKFB3, TNFRSF6, MAP2K6, GADD45B,
TGFBI, IRAK2, CEACAM1, ITGAM,
IL10alpha, ANXA3, JAK2, IL1RN, CRTAP,
PRV1, SOCS3, TIFA, CCL5, LY96,
TNFSF10, OSM
VNN1, LDLR, FAD104, HLA-DRA, ARG2,	0.82	0.85	0.8
IFNGR1, IRAK4, TNFRSF6, TIFA, MAP2K6,
NCR1, OSM, PRV1, CSF1R, INSL3,
TNFSF13B, JAK2, MAPK14, BCL2A1,
IRAK2, TLR4, PSTPIP2, TDRD9, ANXA3
ANXA3, TNFSF10, TGFBI, MKNK1,	0.82	0.83	0.82
PSTPIP2, GADD45A, CRTAP, LDLR, INSL3,
MAPK14, IFNGR1, BCL2A1, TNFSF13B,
GADD45B, Gene_MMP9, IRAK2,
CEACAM1, PRV1, SOD2, FAD104, JAK2,
NCR1, ARG2, IL1RN
TDRD9, LY96, PFKFB3, IRAK2, FAD104,	0.82	0.8	0.85
NCR1, Gene_MMP9, MAPK14, CCL5,
LDLR, PSTPIP2, OSM, VNN1, IRAK4,
BCL2A1, TIFA, GADD45A, TGFBI,
ANKRD22, FCGR1A, IFNGR1, ARG2, CD86,
IL18R1
CD86, TNFSF13B, PSTPIP2, IL10alpha,	0.82	0.8	0.84
HLA-DRA, MAP2K6, FCGR1A,
Gene_MMP9, JAK2, SOCS3, CSF1R,
TDRD9, ARG2, NCR1, OSM, FAD104,
BCL2A1, TNFRSF6, INSL3, VNN1, ITGAM,
PRV1, TLR4, CEACAM1
IL18R1, ARG2, VNN1, TNFRSF6, TIFA,	0.82	0.78	0.86
MKNK1, IL10alpha, CD86, NCR1, OSM,
ANKRD22, TDRD9, PSTPIP2, ITGAM,
IFNGR1, MAP2K6, BCL2A1, IRAK2, TLR4,
LY96, SOCS3, GADD45B, IRAK4, PRV1
TNFSF10, ITGAM, MAP2K6, TIFA, CSF1R,	0.82	0.78	0.86
TDRD9, FAD104, TLR4, GADD45B, HLA-
DRA, IRAK2, IRAK4, OSM, FCGR1A,
CCL5, SOD2, VNN1, MKNK1, ARG2,
Gene_MMP9, TGFBI, TNFSF13B, MAPK14,
PFKFB3
TNFSF10, CEACAM1, IFNGR1, TIFA,	0.82	0.75	0.88
MKNK1, ANXA3, IL1RN, IL10alpha,
IL18R1, HLA-DRA, SOCS3, Gene_MMP9,
MAPK14, TGFBI, JAK2, IRAK2, TLR4,
CSF1R, BCL2A1, PSTPIP2, MAP2K6, CD86,
ITGAM, SOD2
SOD2, PFKFB3, MAP2K6, HLA-DRA,	0.82	0.85	0.79
ANKRD22, IL18R1, Gene_MMP9, LDLR,
ARG2, GADD45A, JAK2, MKNK1, PRV1,
FCGR1A, ITGAM, OSM, NCR1, VNN1,
LY96, IFNGR1, TIFA, PSTPIP2, IL1RN,
TLR4
CSF1R, FCGR1A, IL18R1, ANKRD22,	0.82	0.81	0.83
MKNK1, NCR1, IRAK2, TDRD9, GADD45A,
CRTAP, GADD45B, JAK2, PRV1, SOCS3,
CD86, MAPK14, MAP2K6, IFNGR1, LY96,
FAD104, OSM, SOD2, TLR4, IL10alpha
ARG2, TGFBI, TIFA, IL18R1, TNFRSF6,	0.82	0.8	0.83
CSF1R, CCL5, SOCS3, LY96, MKNK1,
BCL2A1, SOD2, FCGR1A, PSTPIP2,
GADD45B, IFNGR1, NCR1, TNFSF10,
LDLR, PRV1, IL1RN, TDRD9, ANKRD22,
TLR4
IL1RN, IL10alpha, IFNGR1, TDRD9,	0.82	0.8	0.84
PFKFB3, GADD45B, TNFSF10, PSTPIP2,
SOCS3, TIFA, MAPK14, CSF1R, TNFSF13B,
CRTAP, TNFRSF6, ARG2, IL18R1, LY96,
TGFBI, CD86, TLR4, GADD45A, OSM,
Gene_MMP9
SOD2, IRAK4, SOCS3, VNN1, IL1RN,	0.86	0.88	0.85
ITGAM, TNFSF10, GADD45A, CCL5,
CEACAM1, ANKRD22, NCR1, IL18R1,
OSM, ARG2, INSL3, MAPK14, MAP2K6,
TGFBI, TNFSF13B, PFKFB3, MKNK1,
LY96, FCGR1A, CSF1R
LDLR, VNN1, GADD45A, SOCS3, TLR4,	0.85	0.85	0.85
SOD2, BCL2A1, IL18R1, IRAK2, HLA-DRA,
TIFA, CEACAM1, OSM, INSL3, TNFSF13B,
TNFRSF6, Gene_MMP9, CRTAP, ARG2,
LY96, GADD45B, CSF1R, FCGR1A, IL1RN,
PFKFB3
ARG2, PRV1, TNFSF10, FAD104, SOD2,	0.85	0.84	0.86
ANXA3, IL18R1, JAK2, LDLR, OSM,
IFNGR1, PSTPIP2, TNFRSF6, IRAK4,
IL1RN, VNN1, FCGR1A, ITGAM, IL10alpha,
IRAK2, INSL3, CD86, TDRD9, TIFA,
MKNK1
GADD45B, IRAK2, MAPK14, Gene_MMP9,	0.85	0.81	0.89
CD86, CEACAM1, SOD2, SOCS3, ARG2,
ANXA3, LDLR, JAK2, VNN1, IFNGR1,
FAD104, NCR1, PRV1, OSM, TDRD9,
MKNK1, ITGAM, INSL3, IL1RN,
ANKRD22, CCL5
IL10alpha, IRAK2, HLA-DRA, Gene_MMP9,	0.84	0.85	0.84
TGFBI, LDLR, TIFA, GADD45A, ARG2,
CSF1R, MAP2K6, CEACAM1, PRV1, OSM,
CD86, TNFRSF6, LY96, FAD104, PSTPIP2,
ANXA3, IFNGR1, NCR1, CCL5, GADD45B,
PFKFB3
GADD45A, SOCS3, SOD2, TGFBI, HLA-	0.84	0.84	0.85
DRA, VNN1, CD86, CCL5, BCL2A1,
CRTAP, MAP2K6, PRV1, IL18R1, CSF1R,
OSM, IRAK2, PSTPIP2, TLR4, FCGR1A,
ANKRD22, CEACAM1, JAK2, INSL3,
TDRD9, TNFSF10
FCGR1A, TLR4, ANKRD22, CEACAM1,	0.84	0.78	0.9
IRAK4, LY96, TDRD9, ARG2, CRTAP,
ANXA3, LDLR, MAPK14, CD86,
Gene_MMP9, INSL3, GADD45B, TNFSF10,
VNN1, IRAK2, PSTPIP2, TIFA, TNFRSF6,
TGFBI, IL18R1, IL1RN
SOCS3, VNN1, FCGR1A, SOD2, OSM,	0.84	0.83	0.84
TNFSF10, LY96, Gene_MMP9, GADD45B,
CRTAP, PRV1, HLA-DRA, GADD45A,
TLR4, ARG2, IRAK2, FAD104, INSL3,
PSTPIP2, TIFA, TGFBI, IL18R1, MAP2K6,
LDLR, ANXA3
MAP2K6, LDLR, TIFA, TNFSF13B, IL18R1,	0.84	0.83	0.84
ITGAM, SOCS3, OSM, ANXA3, GADD45A,
Gene_MMP9, CD86, IL1RN, IFNGR1, PRV1,
FCGR1A, MAPK14, CCL5, VNN1, ARG2,
PSTPIP2, IRAK2, NCR1, TDRD9, TNFRSF6
TIFA, ANKRD22, TNFSF13B, SOCS3,	0.84	0.82	0.86
NCR1, IRAK4, JAK2, GADD45A, CCL5,
LDLR, MAPK14, IL18R1, SOD2, TGFBI,
CSF1R, IFNGR1, MAP2K6, TNFSF10,
IRAK2, LY96, IL1RN, TNFRSF6, VNN1,
INSL3, PFKFB3
MAP2K6, FAD104, CCL5, IL18R1, NCR1,	0.84	0.81	0.86
VNN1, IL10alpha, ANKRD22, IFNGR1,
MAPK14, CD86, MKNK1, TLR4, LY96,
TIFA, PSTPIP2, TNFRSF6, LDLR, CSF1R,
ARG2, TGFBI, JAK2, PFKFB3, OSM,
TDRD9
JAK2, OSM, IRAK4, VNN1, SOCS3,	0.83	0.84	0.83
GADD45B, IL1RN, FCGR1A, TNFRSF6,
Gene_MMP9, ANKRD22, ARG2, IL10alpha,
CCL5, IL18R1, ANXA3, LY96, PSTPIP2,
TIFA, TNFSF10, FAD104, MAP2K6,
MKNK1, PFKFB3, CRTAP
TIFA, IRAK2, ANKRD22, CCL5, IL10alpha,	0.83	0.85	0.82
INSL3, CEACAM1, TLR4, FCGR1A, NCR1,
CD86, BCL2A1, GADD45A, ITGAM,
MAP2K6, CRTAP, VNN1, TDRD9, SOCS3,
ANXA3, TNFSF10, LY96, MKNK1, JAK2,
ARG2
PSTPIP2, CEACAM1, FAD104, TIFA,	0.83	0.82	0.84
ANKRD22, OSM, TNFSF13B, IRAK4,
INSL3, GADD45A, IL10alpha, CSF1R, HLA-
DRA, SOCS3, GADD45B, CCL5,
Gene_MMP9, LY96, TLR4, IFNGR1, TGFBI,
BCL2A1, MAP2K6, CD86, PFKFB3
IL1RN, JAK2, PFKFB3, OSM, CD86, IL18R1,	0.83	0.82	0.84
SOD2, GADD45B, ITGAM, TNFRSF6,
MAP2K6, LDLR, TLR4, TIFA, INSL3,
SOCS3, IFNGR1, ANKRD22, GADD45A,
IRAK4, CRTAP, CSF1R, TNFSF13B, PRV1,
PSTPIP2
IFNGR1, VNN1, ANKRD22, FCGR1A, JAK2,	0.83	0.78	0.87
MAP2K6, SOD2, TNFSF13B, IRAK4,
CEACAM1, LY96, MAPK14, INSL3, NCR1,
Gene_MMP9, CCL5, HLA-DRA, LDLR,
TNFRSF6, PFKFB3, ANXA3, SOCS3, ARG2,
ITGAM, CSF1R
LDLR, GADD45A, IFNGR1, ARG2,	0.83	0.83	0.82
MAPK14, HLA-DRA, CRTAP, OSM,
TDRD9, CSF1R, FCGR1A, Gene_MMP9,
NCR1, PRV1, IRAK4, TGFBI, TLR4, LY96,
IL1RN, FAD104, SOD2, CCL5, TNFRSF6,
MAP2K6, TNFSF13B
IL18R1, IL1RN, IRAK4, CEACAM1,	0.83	0.83	0.83
ITGAM, LY96, ANKRD22, ARG2, TDRD9,
LDLR, NCR1, IL10alpha, ANXA3, CD86,
MAPK14, TNFRSF6, SOD2, MKNK1,
GADD45B, CRTAP, PFKFB3, CSF1R,
INSL3, PSTPIP2, CCL5
PSTPIP2, NCR1, MKNK1, SOCS3, IL1RN,	0.83	0.81	0.84
IFNGR1, IL18R1, CSF1R, ITGAM, LDLR,
TIFA, CRTAP, OSM, TLR4, CEACAM1,
Gene_MMP9, INSL3, MAP2K6, CCL5,
FAD104, HLA-DRA, PRV1, VNN1, PFKFB3,
JAK2

In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use any one of the biomarker sets listed in Table M. The biomarker sets listed in Table M were identified in the computational experiments described in Section 6.14.2, below, in which 1600 random subcombinations of the biomarkers listed in Table K were tested. Table M lists some of the biomarker sets that provided high accuracy scores against the validation population described in Section 6.14.2. Each row of Table M lists a single biomarker set that can be used in the methods and kits respectively referenced in Sections 5.2 and 5.3. In other words, each row of Table M describes a biomarker set that can be used to discriminate between sepsis and SIRS subjects (e.g., to determine whether a subject is likely to acquire SEPSIS). In some embodiments, nucleic acid forms of the biomarkers listed in Table M are used in the methods and kits respectively referenced in Sections 5.2 and 5.3. In some embodiments, protein forms of the biomarkers listed in Table M are used. In some hybrid embodiments, some of the biomarkers in a biomarker set from Table M are in protein form and some of the biomarkers in the same biomarker set from Table M are in nucleic acid form in the methods and kits respectively referenced in Sections 5.2 and 5.3.

In some embodiments, a given biomarker set listed in Table M is used with the addition of one, two, three, four, five, six, seven, eight, or nine or more additional biomarkers from Table I that are not within the given set of biomarkers from Table M. In some embodiments, a given set of biomarkers from Table M is used with the addition of one, two, three, four, five, six, seven, eight, or nine or more additional biomarkers from any one of Table 1, 30, 31, 32, 33, 34, or 36 that are not within the given biomarker set from Table M. In Table M, accuracy, specificity, and sensitivity are described with reference to T₋₁₂ time point data described in Section 6.14.2, below.

TABLE M
Exemplary sets of biomarkers used in the methods or kits referenced in
Sections 5.2 and 5.3
BIOMARKER SET	ACCURACY	SPECIFICITY	SENSISTIVIY
ALPHAFETOPROTEIN, IL6, IL8	0.78	0.76	0.8
CREACTIVEPROTEIN, TIMP1, IL6	0.78	0.75	0.8
PROTEIN_MMP9, IL8, IL6	0.77	0.8	0.74
IL8, IL6, IL10	0.77	0.72	0.81
CREACTIVEPROTEIN, IL6,	0.77	0.77	0.76
PROTEIN_MMP9
APOLIPOPROTEINCIII, IL8, IL6	0.76	0.74	0.78
IL6, IL8, CREACTIVEPROTEIN	0.76	0.74	0.79
ALPHAFETOPROTEIN, MCP1, IL10, IL6	0.8	0.8	0.8
ALPHAFETOPROTEIN, IL10, IL6,	0.79	0.7	0.86
PROTEIN_MMP9
ALPHAFETOPROTEIN,	0.78	0.74	0.81
PROTEIN_MMP9, IL6,
APOLIPOPROTEINCIII
APOLIPOPROTEINCIII, IL6,	0.78	0.73	0.81
BETA2MICROGLOBULIN, TIMP1
IL6, BETA2MICROGLOBULIN, IL10,	0.77	0.73	0.81
APOLIPOPROTEINCIII
IL6, PROTEIN_MMP9, IL10, MCP1	0.77	0.81	0.73
APOLIPOPROTEINCIII,	0.77	0.78	0.75
ALPHAFETOPROTEIN,
PROTEIN_MMP9, IL6
IL10, TIMP1, IL6, ALPHAFETOPROTEIN	0.77	0.71	0.83
TIMP1, IL6, CREACTIVEPROTEIN,	0.76	0.8	0.73
BETA2MICROGLOBULIN
PROTEIN_MMP9, CREACTIVEPROTEIN,	0.8	0.78	0.81
MCP1, IL10, IL6
APOLIPOPROTEINCIII,	0.79	0.81	0.78
CREACTIVEPROTEIN, IL10,
ALPHAFETOPROTEIN, IL6
CREACTIVEPROTEIN,	0.79	0.77	0.81
ALPHAFETOPROTEIN, IL6,
PROTEIN_MMP9, IL8
IL6, TIMP1, MCP1,	0.78	0.75	0.82
APOLIPOPROTEINCIII,
CREACTIVEPROTEIN
CREACTIVEPROTEIN,	0.78	0.79	0.76
APOLIPOPROTEINCIII, TIMP1, IL8,
PROTEIN_MMP9
CREACTIVEPROTEIN, IL10, MCP1, IL6,	0.77	0.78	0.77
TIMP1
IL10, IL8, APOLIPOPROTEINCIII, IL6,	0.77	0.73	0.8
TIMP1
IL10, CREACTIVEPROTEIN, MCP1, IL6,	0.77	0.72	0.82
APOLIPOPROTEINCIII
IL6, ALPHAFETOPROTEIN, IL8,	0.77	0.75	0.78
CREACTIVEPROTEIN, TIMP1
TIMP1, MCP1, PROTEIN_MMP9, IL6,	0.8	0.81	0.79
APOLIPOPROTEINCIII,
CREACTIVEPROTEIN
TIMP1, IL6, IL10, CREACTIVEPROTEIN,	0.79	0.77	0.8
APOLIPOPROTEINCIII, PROTEIN_MMP9
MCP1, PROTEIN_MMP9,	0.79	0.75	0.82
APOLIPOPROTEINCIII, IL6, TIMP1, IL10
IL10, CREACTIVEPROTEIN, IL6,	0.78	0.78	0.79
ALPHAFETOPROTEIN, TIMP1,
PROTEIN_MMP9
PROTEIN_MMP9, CREACTIVEPROTEIN,	0.78	0.77	0.79
ALPHAFETOPROTEIN, IL10, IL6, MCP1
IL6, MCP1, IL10, TIMP1,	0.78	0.76	0.79
APOLIPOPROTEINCIII, IL8
TIMP1, IL6, IL10,	0.77	0.72	0.83
BETA2MICROGLOBULIN,
PROTEIN_MMP9, APOLIPOPROTEINCIII
IL10, MCP1, ALPHAFETOPROTEIN,	0.77	0.76	0.78
APOLIPOPROTEINCIII, IL6,
PROTEIN_MMP9
BETA2MICROGLOBULIN, IL6, TIMP1,	0.77	0.74	0.79
ALPHAFETOPROTEIN,
CREACTIVEPROTEIN, PROTEIN_MMP9
MCP1, IL10, IL8, IL6, TIMP1,	0.79	0.77	0.81
PROTEIN_MMP9, CREACTIVEPROTEIN
PROTEIN_MMP9,	0.79	0.77	0.8
BETA2MICROGLOBULIN,
APOLIPOPROTEINCIII, IL8, IL6,
ALPHAFETOPROTEIN,
CREACTIVEPROTEIN
IL8, MCP1, CREACTIVEPROTEIN,	0.79	0.71	0.85
APOLIPOPROTEINCIII,
ALPHAFETOPROTEIN,
PROTEIN_MMP9, IL6
TIMP1, IL6, CREACTIVEPROTEIN,	0.78	0.76	0.8
APOLIPOPROTEINCIII,
PROTEIN_MMP9, IL8,
ALPHAFETOPROTEIN
IL10, IL6, BETA2MICROGLOBULIN,	0.78	0.7	0.85
CREACTIVEPROTEIN,
APOLIPOPROTEINCIII, MCP1, IL8
APOLIPOPROTEINCIII,	0.78	0.8	0.76
PROTEIN_MMP9, MCP1, IL6,
ALPHAFETOPROTEIN, IL10, TIMP1
IL10, CREACTIVEPROTEIN,	0.78	0.74	0.82
ALPHAFETOPROTEIN,
BETA2MICROGLOBULIN, IL8,
PROTEIN_MMP9, APOLIPOPROTEINCIII
TIMP1, IL10, CREACTIVEPROTEIN,	0.78	0.81	0.74
APOLIPOPROTEINCIII, IL6, IL8, MCP1
IL8, TIMP1, CREACTIVEPROTEIN, IL6,	0.78	0.8	0.76
IL10, BETA2MICROGLOBULIN,
APOLIPOPROTEINCIII
APOLIPOPROTEINCIII,	0.78	0.78	0.77
CREACTIVEPROTEIN, IL8, IL10,
PROTEIN_MMP9, IL6,
BETA2MICROGLOBULIN
TIMP1, MCP1, IL10,	0.8	0.74	0.86
BETA2MICROGLOBULIN,
PROTEIN_MMP9, IL6,
ALPHAFETOPROTEIN,
APOLIPOPROTEINCIII
TIMP1, PROTEIN_MMP9, IL6,	0.79	0.77	0.82
ALPHAFETOPROTEIN, IL10,
APOLIPOPROTEINCIII, MCP1, IL8
IL10, IL6, MCP1, CREACTIVEPROTEIN,	0.79	0.79	0.79
APOLIPOPROTEINCIII,
PROTEIN_MMP9,
BETA2MICROGLOBULIN,
ALPHAFETOPROTEIN
TIMP1, MCP1, IL10,	0.79	0.76	0.81
CREACTIVEPROTEIN,
ALPHAFETOPROTEIN, IL6,
PROTEIN_MMP9, IL8
APOLIPOPROTEINCIII,	0.79	0.73	0.83
ALPHAFETOPROTEIN, TIMP1,
BETA2MICROGLOBULIN, MCP1, IL10,
IL6, IL8
CREACTIVEPROTEIN, TIMP1,	0.78	0.78	0.79
APOLIPOPROTEINCIII, MCP1, IL6,
ALPHAFETOPROTEIN,
BETA2MICROGLOBULIN,
PROTEIN_MMP9
BETA2MICROGLOBULIN, IL10, IL8,	0.78	0.73	0.83
APOLIPOPROTEINCIII,
PROTEIN_MMP9, IL6, TIMP1,
CREACTIVEPROTEIN
APOLIPOPROTEINCIII, IL8,	0.78	0.78	0.77
ALPHAFETOPROTEIN, IL6,
PROTEIN_MMP9, IL10, TIMP1, MCP1
APOLIPOPROTEINCIII, IL6, IL8,	0.78	0.71	0.83
PROTEIN_MMP9, TIMP1,
BETA2MICROGLOBULIN, IL10,
CREACTIVEPROTEIN
APOLIPOPROTEINCIII, MCP1, IL10,	0.77	0.76	0.78
PROTEIN_MMP9, TIMP1,
ALPHAFETOPROTEIN,
CREACTIVEPROTEIN, IL6
PROTEIN_MMP9, CREACTIVEPROTEIN,	0.79	0.78	0.81
IL6, TIMP1, BETA2MICROGLOBULIN,
IL10, APOLIPOPROTEINCIII, MCP1,
ALPHAFETOPROTEIN
APOLIPOPROTEINCIII,	0.79	0.77	0.81
PROTEIN_MMP9,
ALPHAFETOPROTEIN,
CREACTIVEPROTEIN, IL6, IL10, IL8,
TIMP1, BETA2MICROGLOBULIN
ALPHAFETOPROTEIN, TIMP1,	0.79	0.79	0.79
PROTEIN_MMP9, MCP1, IL6,
APOLIPOPROTEINCIII,
BETA2MICROGLOBULIN, IL10,
CREACTIVEPROTEIN
APOLIPOPROTEINCIII,	0.79	0.78	0.79
PROTEIN_MMP9, MCP1,
BETA2MICROGLOBULIN, IL8, IL6, IL10,
CREACTIVEPROTEIN, TIMP1
TIMP1, APOLIPOPROTEINCIII, IL6,	0.79	0.72	0.84
CREACTIVEPROTEIN, MCP1,
PROTEIN_MMP9, IL8,
BETA2MICROGLOBULIN,
ALPHAFETOPROTEIN
BETA2MICROGLOBULIN, IL8,	0.78	0.77	0.79
CREACTIVEPROTEIN, TIMP1, IL6,
ALPHAFETOPROTEIN,
APOLIPOPROTEINCIII,
PROTEIN_MMP9, IL10
IL6, IL8, TIMP1, PROTEIN_MMP9, IL10,	0.78	0.73	0.83
BETA2MICROGLOBULIN,
APOLIPOPROTEINCIII,
CREACTIVEPROTEIN,
ALPHAFETOPROTEIN
PROTEIN_MMP9, IL10, MCP1,	0.78	0.8	0.75
CREACTIVEPROTEIN,
ALPHAFETOPROTEIN, IL6, TIMP1,
APOLIPOPROTEINCIII,
BETA2MICROGLOBULIN
IL10, IL8, ALPHAFETOPROTEIN, IL6,	0.78	0.79	0.76
TIMP1, PROTEIN_MMP9, MCP1,
BETA2MICROGLOBULIN,
CREACTIVEPROTEIN
ALPHAFETOPROTEIN, MCP1, IL6,	0.78	0.78	0.78
BETA2MICROGLOBULIN,
PROTEIN_MMP9, CREACTIVEPROTEIN,
TIMP1, APOLIPOPROTEINCIII, IL10
TIMP1, IL6, CREACTIVEPROTEIN,	0.79	0.78	0.81
ALPHAFETOPROTEIN, IL10,
BETA2MICROGLOBULIN, MCP1,
APOLIPOPROTEINCIII, IL8,
PROTEIN_MMP9
IL8, CREACTIVEPROTEIN, TIMP1, IL10,	0.79	0.78	0.8
MCP1, IL6, ALPHAFETOPROTEIN,
PROTEIN_MMP9,
APOLIPOPROTEINCIII,
BETA2MICROGLOBULIN
MCP1, TIMP1, APOLIPOPROTEINCIII,	0.78	0.8	0.77
ALPHAFETOPROTEIN,
PROTEIN_MMP9, IL10,
CREACTIVEPROTEIN,
BETA2MICROGLOBULIN, IL8, IL6
BETA2MICROGLOBULIN, MCP1, IL6,	0.78	0.78	0.79
CREACTIVEPROTEIN, IL10, IL8,
ALPHAFETOPROTEIN,
APOLIPOPROTEINCIII, TIMP1,
PROTEIN_MMP9
CREACTIVEPROTEIN, TIMP1, IL10, IL6,	0.78	0.76	0.8
ALPHAFETOPROTEIN,
APOLIPOPROTEINCIII, IL8,
BETA2MICROGLOBULIN, MCP1,
PROTEIN_MMP9
MCP1, TIMP1, IL6,	0.78	0.78	0.78
ALPHAFETOPROTEIN,
PROTEIN_MMP9,
BETA2MICROGLOBULIN,
APOLIPOPROTEINCIII,
CREACTIVEPROTEIN, IL8, IL10
ALPHAFETOPROTEIN,	0.78	0.8	0.75
APOLIPOPROTEINCIII,
PROTEIN_MMP9,
BETA2MICROGLOBULIN, IL10, TIMP1,
MCP1, IL6, IL8, CREACTIVEPROTEIN
TIMP1, IL10, BETA2MICROGLOBULIN,	0.78	0.76	0.8
IL8, APOLIPOPROTEINCIII, IL6, MCP1,
CREACTIVEPROTEIN,
ALPHAFETOPROTEIN, PROTEIN_MMP9
BETA2MICROGLOBULIN,	0.77	0.74	0.8
ALPHAFETOPROTEIN, MCP1, IL10,
APOLIPOPROTEINCIII, TIMP1,
CREACTIVEPROTEIN, IL8,
PROTEIN_MMP9, IL6
IL8, MCP1, BETA2MICROGLOBULIN,	0.77	0.79	0.75
PROTEIN_MMP9, IL10, TIMP1, IL6,
CREACTIVEPROTEIN,
ALPHAFETOPROTEIN,
APOLIPOPROTEINCIII

In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use any one of the subsets of biomarkers listed in Table N. The subsets of biomarkers listed in Table N were identified in the computational experiments described in Section 6.14.5, below, in which 4600 random subcombinations of the biomarkers listed in Table I were tested. Table N lists some of the biomarker sets that provided high accuracy scores against the validation population described in Section 6.14.5. Each row of Table N lists a single set of biomarkers that can be used in the methods and kits respectively referenced in Sections 5.2 and 5.3. In other words, each row of Table N describes a set of biomarkers that can be used to discriminate between sepsis and SIRS subjects. In some embodiments, nucleic acid forms of the biomarkers listed in Table N are used in the methods and kits respectively referenced in Sections 5.2 and 5.3. In some embodiments, protein forms of the biomarkers listed in Table N are used. In some embodiments, some of the biomarkers in a biomarker set from Table N are in protein form and some of the biomarkers in the same biomarker set from Table N are in nucleic acid form in the methods and kits respectively referenced in Sections 5.2 and 5.3.

In some embodiments, a given set of biomarkers from Table N is used with the addition of one, two, three, four, five, six, seven, eight, or nine or more additional biomarkers from any one of Table 30, 31, 32, 33, 34, or 36 that are not within the given set of biomarkers from Table N. In Table N, accuracy, specificity, and sensitivity are described with reference to T₋₁₂ time point data described in Section 6.14.5, below.

TABLE N
Exemplary sets of biomarkers used in the methods or kits referenced in
Sections 5.2 and 5.3
BIOMARKER SET	ACCURACY	SPECIFICITY	SENSISTIVIY
TLR4, ARG2, OSM	0.85	0.83	0.88
IRAK4, OSM, TNFSF10	0.83	0.79	0.87
PSTPIP2, SOCS3, TIMP1	0.82	0.81	0.83
FCGR1A, IL6, MAP2K6	0.81	0.84	0.79
SOCS3, TNFSF10, NCR1	0.81	0.73	0.87
IL8, IL18R1, Beta2Microglobulin	0.81	0.79	0.82
OSM, NCR1, IL8	0.81	0.77	0.83
PFKFB3, MKNK1, FCGR1A	0.8	0.79	0.81
TIMP1, IL18R1, ARG2	0.8	0.78	0.83
FCGR1A, MAP2K6, IRAK4	0.8	0.75	0.86
Gene_MMP9, IL8, GADD45B	0.8	0.75	0.84
INSL3, ANKRD22, MAP2K6, LDLR	0.87	0.83	0.9
PSTPIP2, ARG2, CRTAP, GADD45A	0.83	0.81	0.85
CEACAM1, GADD45B, GADD45A, OSM	0.83	0.75	0.91
OSM, CSF1R, IL10, ANKRD22	0.83	0.88	0.78
TIMP1, ARG2, GADD45B, VNN1	0.83	0.83	0.82
HLA-DRA, PSTPIP2, INSL3, MKNK1	0.83	0.79	0.86
CD86, TGFBI, ANKRD22, SOCS3	0.82	0.82	0.83
GADD45A, PSTPIP2, GADD45B, IL18R1	0.82	0.76	0.86
ANKRD22, MAP2K6, Protein_MMP9,	0.81	0.8	0.82
FAD104
IFNGR1, FAD104, CSF1R, IL8	0.81	0.78	0.84
OSM, TDRD9, ARG2, HLA-DRA	0.81	0.77	0.85
ANKRD22, CReactiveProtein, OSM, IL10	0.81	0.76	0.85
TDRD9, TNFSF13B, CReactiveProtein,	0.81	0.76	0.85
MAP2K6
TNFSF10, Gene_MMP9, IL8, FCGR1A	0.8	0.79	0.81
IL10, NCR1, IL6, INSL3	0.8	0.79	0.81
CD86, FCGR1A, BCL2A1, LY96	0.8	0.79	0.81
IL8, VNN1, IL6, GADD45B	0.8	0.79	0.82
HLA-DRA, TNFSF10, OSM, MKNK1	0.8	0.76	0.84
PFKFB3, INSL3, IL10alpha, FCGR1A	0.8	0.76	0.84
TNFSF10, IRAK4, OSM, ARG2, MAPK14	0.85	0.84	0.86
CD86, CEACAM1, IL18R1, GADD45B,	0.83	0.85	0.81
CCL5
MCP1, CSF1R, GADD45B, Protein_MMP9,	0.83	0.83	0.82
Beta2Microglobulin
IL8, CD86, IRAK2, IL1RN, TIFA	0.82	0.84	0.81
IRAK4, OSM, INSL3, CEACAM1,	0.82	0.82	0.82
TNFSF13B
CReactiveProtein, SOCS3, HLA-DRA,	0.82	0.76	0.88
GADD45B, OSM
CD86, NCR1, PRV1, IL1RN, GADD45B	0.82	0.77	0.86
TNFRSF6, ITGAM, PSTPIP2, ARG2,	0.82	0.77	0.87
BCL2A1
IRAK4, LDLR, OSM, PSTPIP2, GADD45A	0.81	0.81	0.82
Gene_MMP9, SOD2, PFKFB3, ARG2,	0.81	0.78	0.84
CD86
CReactiveProtein, IL18R1, NCR1, CD86,	0.81	0.78	0.84
GADD45A
IL8, IL18R1, LDLR, SOD2, PSTPIP2	0.81	0.77	0.84
Gene_MMP9, CSF1R, TGFBI, MAP2K6,	0.81	0.8	0.81
ANKRD22
CReactiveProtein, LDLR, IRAK2, OSM,	0.81	0.8	0.82
PSTPIP2
ITGAM, SOCS3, IL8, ARG2, JAK2	0.81	0.79	0.83
TNFSF10, LY96, IL10alpha, IL10, OSM	0.8	0.83	0.78
GADD45B, IL6, INSL3, ANKRD22, IL8	0.8	0.81	0.8
CSF1R, IL6, IL1RN, TLR4, JAK2	0.8	0.79	0.81
TDRD9, OSM, ITGAM, ANKRD22,	0.8	0.73	0.87
Gene_MMP9
IL8, TNFRSF6, CReactiveProtein, IRAK4,	0.8	0.79	0.81
PRV1
OSM, IL1RN, JAK2, GADD45B, CSF1R	0.8	0.78	0.82
CD86, Beta2Microglobulin, PFKFB3,	0.8	0.78	0.82
TNFSF13B, TNFRSF6
MAPK14, TGFBI, GADD45A, ANKRD22,	0.8	0.75	0.85
CReactiveProtein
MKNK1, CD86, OSM, TIFA, HLA-DRA,	0.85	0.79	0.89
SOCS3
CD86, CEACAM1, LDLR, NCR1,	0.83	0.81	0.84
AlphaFetoprotein, IRAK2
INSL3, PRV1, LY96, Protein_MMP9, IL8,	0.82	0.82	0.82
OSM
FAD104, ARG2, FCGR1A, SOCS3, HLA-	0.82	0.8	0.84
DRA, ANXA3
CCL5, TIMP1, ARG2, IL6, IFNGR1, SOD2	0.82	0.77	0.87
CRTAP, OSM, GADD45B, TNFSF10,	0.82	0.75	0.88
MKNK1, TGFBI
LDLR, OSM, IL6, JAK2, INSL3, FCGR1A	0.82	0.82	0.81
Beta2Microglobulin, FAD104, TGFBI,	0.82	0.82	0.82
NCR1, ARG2, GADD45B
CSF1R, VNN1, MAP2K6, LY96, OSM,	0.82	0.81	0.82
Beta2Microglobulin
ApolipoproteinCIII, HLA-DRA, GADD45A,	0.82	0.8	0.83
ITGAM, TNFRSF6, MAP2K6
PRV1, TGFBI, VNN1, GADD45B, IL1RN,	0.81	0.8	0.82
CSF1R
IRAK4, TIMP1, ANKRD22, GADD45B,	0.81	0.78	0.83
OSM, TLR4
SOD2, MKNK1, MCP1, OSM, TIFA,	0.81	0.77	0.84
SOCS3
FAD104, TGFBI, ANXA3, IL18R1, PRV1,	0.81	0.77	0.85
IL10alpha
FCGR1A, IL8, Beta2Microglobulin,	0.81	0.83	0.79
GADD45B, ANKRD22, TNFSF10
TIFA, Beta2Microglobulin, IL18R1,	0.81	0.8	0.81
CRTAP, IL6, TGFBI
CD86, IL10, MCP1, TIMP1, OSM, ANXA3	0.81	0.79	0.82
INSL3, FAD104, TGFBI, CEACAM1,	0.81	0.77	0.85
CSF1R, PFKFB3
PRV1, IL8, TNFSF10, FCGR1A, IFNGR1,	0.81	0.77	0.84
CReactiveProtein
ANKRD22, BCL2A1, CRTAP, NCR1,	0.81	0.72	0.88
SOCS3, IL18R1
INSL3, IRAK2, CD86, JAK2, IL10,	0.8	0.84	0.77
FAD104
MCP1, PSTPIP2, AlphaFetoprotein,	0.8	0.81	0.8
CReactiveProtein, IL6, ApolipoproteinCIII
CSF1R, OSM, IFNGR1, TDRD9,	0.8	0.8	0.8
Gene_MMP9, FCGR1A
TIMP1, IFNGR1, TNFSF10, GADD45A,	0.8	0.8	0.81
BCL2A1, SOD2
FCGR1A, MKNK1, CRTAP, LDLR,	0.8	0.79	0.81
Gene_MMP9, Beta2Microglobulin
ITGAM, AlphaFetoprotein, FCGR1A,	0.8	0.78	0.82
MCP1, MKNK1, GADD45A
MCP1, FCGR1A, OSM, PFKFB3, FAD104,	0.8	0.77	0.82
TDRD9
TNFSF10, Gene_MMP9, FCGR1A,	0.86	0.85	0.86
AlphaFetoprotein, INSL3, CSF1R, IL8
OSM, Beta2Microglobulin, ANKRD22,	0.84	0.85	0.83
CSF1R, GADD45B, TNFRSF6,
ApolipoproteinCIII
BCL2A1, TDRD9, OSM, PRV1, IRAK2,	0.84	0.83	0.85
TLR4, MAPK14
LDLR, OSM, ApolipoproteinCIII, IL6,	0.83	0.83	0.83
TIMP1, ARG2, TNFRSF6
IL1RN, TNFSF13B, AlphaFetoprotein,	0.83	0.8	0.85
MCP1, ANKRD22, ARG2, OSM
NCR1, ARG2, PSTPIP2, GADD45A, LY96,	0.83	0.81	0.84
OSM, BCL2A1
FCGR1A, TNFSF13B, INSL3, TIFA,	0.83	0.79	0.87
ApolipoproteinCIII, ITGAM, CD86
LY96, CReactiveProtein, FCGR1A,	0.82	0.85	0.8
Beta2Microglobulin, IL8, OSM, VNN1
PSTPIP2, ARG2, IRAK2, TNFSF13B,	0.82	0.85	0.8
GADD45A, IL8, CRTAP
MCP1, SOCS3, HLA-DRA,	0.82	0.84	0.81
ApolipoproteinCIII, IL10alpha, GADD45A,
MAP2K6
IL18R1, MAPK14, Gene_MMP9, TIFA,	0.82	0.75	0.89
FCGR1A, SOCS3, MKNK1
Beta2Microglobulin, CRTAP, ARG2,	0.82	0.82	0.82
ANKRD22, TNFRSF6, IRAK4, OSM
PFKFB3, IRAK2, IRAK4, OSM, JAK2,	0.82	0.82	0.82
Beta2Microglobulin, CEACAM1
TIFA, CRTAP, PFKFB3, JAK2, IL6,	0.82	0.82	0.82
TGFBI, CD86
GADD45B, Gene_MMP9, TNFSF13B,	0.82	0.76	0.88
IRAK2, VNN1, TIFA, SOCS3
INSL3, IL6, CD86, IL10alpha,	0.82	0.86	0.78
CReactiveProtein, TGFBI, ITGAM
GADD45B, MCP1, INSL3,	0.82	0.81	0.82
CReactiveProtein, ARG2, CCL5, SOCS3
TNFSF10, IL8, ApolipoproteinCIII, TGFBI,	0.82	0.8	0.83
CSF1R, OSM, SOD2
PRV1, PSTPIP2, ARG2, TIMP1,	0.82	0.79	0.84
Protein_MMP9, IL6, SOD2
CD86, LY96, MAP2K6, IL6, IL10, IRAK2,	0.81	0.78	0.84
TNFSF10
BCL2A1, MCP1, ARG2, SOCS3, NCR1,	0.81	0.8	0.81
IL10, LY96
SOCS3, ApolipoproteinCIII, NCR1,	0.81	0.8	0.82
CEACAM1, ANKRD22, FCGR1A, IL6
INSL3, TNFSF10, SOD2, FCGR1A,	0.81	0.77	0.85
PSTPIP2, IL10, IL8
FCGR1A, OSM, Protein_MMP9,	0.81	0.76	0.84
GADD45A, PSTPIP2, ARG2, Gene_MMP9
TIMP1, SOCS3, LY96, CSF1R,	0.81	0.84	0.77
CReactiveProtein, CCL5, TNFSF13B
ANKRD22, CEACAM1, TLR4,	0.81	0.82	0.8
ApolipoproteinCIII, SOCS3, ITGAM, IL10
INSL3, IRAK2, FCGR1A, MAP2K6,	0.81	0.81	0.8
CRTAP, ITGAM, CSF1R
VNN1, SOCS3, Beta2Microglobulin,	0.81	0.81	0.81
MAP2K6, IL6, ANKRD22, IL10
TNFSF10, TGFBI, CReactiveProtein,	0.81	0.8	0.82
Beta2Microglobulin, TNFRSF6, ARG2,
PRV1
IL18R1, IL6, CRTAP, IRAK4, GADD45A,	0.8	0.81	0.79
Protein_MMP9, TNFSF13B
AlphaFetoprotein, ARG2, NCR1, PSTPIP2,	0.8	0.8	0.81
ApolipoproteinCIII, CD86, GADD45B
ANKRD22, TIFA, JAK2, IL10, IL6, CCL5,	0.8	0.79	0.82
CSF1R
PRV1, TNFSF13B, TLR4, OSM, ARG2,	0.8	0.78	0.82
AlphaFetoprotein, HLA-DRA
CSF1R, TLR4, SOD2, FCGR1A, CRTAP,	0.8	0.78	0.83
TNFSF13B, GADD45A
JAK2, IRAK2, ITGAM, IL6, MKNK1,	0.8	0.77	0.83
Gene_MMP9, FCGR1A
GADD45B, PRV1, CSF1R, NCR1, CD86,	0.8	0.76	0.83
MKNK1, JAK2
Beta2Microglobulin, TNFSF10, IL18R1,	0.8	0.75	0.85
GADD45B, Protein_MMP9, FAD104,
PSTPIP2
MAPK14, TIFA, ITGAM, MKNK1, CSF1R,	0.8	0.73	0.86
IRAK4, Protein_MMP9
TIFA, TNFSF13B, LY96, GADD45B, IL6,	0.8	0.8	0.8
INSL3, OSM
IL6, GADD45B, CEACAM1, IRAK4,	0.8	0.8	0.8
TGFBI, INSL3, TNFSF13B
GADD45B, ARG2, IL18R1, ANKRD22,	0.8	0.8	0.8
AlphaFetoprotein, IL10, PSTPIP2
TNFSF13B, IFNGR1, OSM, FAD104,	0.8	0.8	0.8
CSF1R, PSTPIP2, TIFA
TDRD9, ITGAM, TNFSF10, ANXA3,	0.8	0.8	0.8
ApolipoproteinCIII, MCP1, INSL3
SOCS3, Protein_MMP9, SOD2, LY96,	0.8	0.78	0.82
ARG2, IRAK2, OSM
CEACAM1, IL10, TNFRSF6, IL18R1,	0.8	0.78	0.82
ARG2, FCGR1A, CReactiveProtein
CCL5, FCGR1A, CReactiveProtein,	0.8	0.74	0.86
ApolipoproteinCIII, IL18R1,
Protein_MMP9, ITGAM
NCR1, SOD2, IRAK2, IL8, OSM, HLA-	0.86	0.89	0.84
DRA, ARG2, GADD45A
PFKFB3, PSTPIP2, GADD45B, INSL3,	0.85	0.86	0.84
FAD104, TNFRSF6, ARG2, IL10alpha
CSF1R, CEACAM1, GADD45B, OSM,	0.84	0.86	0.82
LDLR, MCP1, ARG2, AlphaFetoprotein
TIFA, NCR1, BCL2A1, OSM, CCL5, TLR4,	0.82	0.82	0.82
CD86, CEACAM1
FAD104, LDLR, INSL3, IRAK4, LY96,	0.82	0.81	0.83
TLR4, GADD45B, TIMP1
FAD104, JAK2, TNFSF13B, ARG2,	0.82	0.79	0.85
CReactiveProtein, IL10alpha, TLR4, PRV1
CRTAP, LY96, TDRD9, Gene_MMP9,	0.82	0.79	0.85
HLA-DRA, SOCS3, IL8, Protein_MMP9
CRTAP, GADD45B, TIFA,	0.81	0.83	0.8
ApolipoproteinCIII, LY96, IL8, GADD45A,
MKNK1
IL8, CSF1R, ARG2, TGFBI, PRV1,	0.81	0.82	0.81
TNFRSF6, CEACAM1, JAK2
ARG2, Beta2Microglobulin, GADD45A,	0.81	0.79	0.83
IL6, INSL3, IL8, JAK2, TIMP1
SOD2, IL10, IL8, ARG2, PSTPIP2, INSL3,	0.81	0.77	0.86
CSF1R, ANXA3
CD86, IL6, BCL2A1, CCL5, GADD45B,	0.81	0.86	0.76
IRAK4, LDLR, ARG2
ANXA3, MAP2K6, VNN1, GADD45A,	0.81	0.81	0.81
CSF1R, FAD104, IL6, IRAK2
IL8, GADD45A, TDRD9,	0.81	0.8	0.82
Beta2Microglobulin, ANKRD22,
GADD45B, PRV1, CSF1R
IRAK4, PRV1, GADD45A, IL8,	0.81	0.79	0.82
TNFSF13B, CD86, FCGR1A, TIMP1
IRAK4, MAPK14, GADD45B, HLA-DRA,	0.81	0.77	0.84
JAK2, PRV1, SOD2, IL6
IL18R1, IL6, GADD45B, MAPK14, IL10,	0.81	0.76	0.86
JAK2, IL8, ANKRD22
TLR4, IRAK2, TNFRSF6, TGFBI, IL8,	0.81	0.88	0.74
ARG2, GADD45B, GADD45A
ANXA3, IFNGR1, SOCS3, VNN1, TIFA,	0.81	0.8	0.81
CReactiveProtein, IRAK4, AlphaFetoprotein
ANKRD22, CCL5, TGFBI, CEACAM1,	0.81	0.8	0.82
CD86, Gene_MMP9, IFNGR1, GADD45B
NCR1, ARG2, TIMP1, Beta2Microglobulin,	0.81	0.77	0.84
ANXA3, TIFA, BCL2A1, MAP2K6
OSM, TIMP1, IL1RN, IL8, BCL2A1,	0.81	0.76	0.84
IFNGR1, CSF1R, CD86
IL10, NCR1, IRAK2, IL18R1, ARG2,	0.81	0.76	0.84
PSTPIP2, Gene_MMP9, LY96
IL18R1, TNFSF10, SOCS3,	0.81	0.74	0.88
ApolipoproteinCIII, HLA-DRA, GADD45A,
Beta2Microglobulin, ARG2
IL10alpha, IL10, MKNK1, LY96, OSM,	0.8	0.8	0.81
JAK2, IFNGR1, CEACAM1
HLA-DRA, TIMP1, OSM, CD86, NCR1,	0.8	0.78	0.82
IL1RN, TNFSF10, FAD104
CSF1R, TNFSF13B, ANKRD22, IFNGR1,	0.8	0.77	0.82
Protein_MMP9, PFKFB3, NCR1, TGFBI
ANXA3, IL10alpha, PSTPIP2, CSF1R,	0.8	0.77	0.83
IL1RN, FAD104, CD86, CReactiveProtein
CSF1R, ANKRD22, TGFBI, IRAK4,	0.8	0.77	0.83
Protein_MMP9, TIMP1, HLA-DRA,
PFKFB3
TNFSF13B, JAK2, ARG2, CCL5, IL18R1,	0.8	0.76	0.85
GADD45B, CD86, GADD45A
GADD45B, BCL2A1, IL1RN, FCGR1A,	0.8	0.76	0.84
MAPK14, SOCS3, ITGAM, PRV1
IL6, JAK2, CReactiveProtein, MCP1,	0.8	0.85	0.76
TIMP1, BCL2A1, GADD45B, LY96
AlphaFetoprotein, ApolipoproteinCIII,	0.8	0.84	0.77
CEACAM1, CRTAP, IL18R1, NCR1,
TIMP1, TGFBI
ANXA3, FAD104, MKNK1,	0.8	0.82	0.78
CReactiveProtein, AlphaFetoprotein, CSF1R,
IRAK4, IL6
TIMP1, VNN1, TIFA, CCL5, TDRD9,	0.8	0.82	0.78
FCGR1A, ApolipoproteinCIII, IL1RN
TNFSF10, TLR4, JAK2, OSM,	0.8	0.8	0.81
Beta2Microglobulin, ITGAM, IL1RN, HLA-
DRA
ApolipoproteinCIII, MAPK14, IRAK2,	0.8	0.79	0.81
TNFSF13B, GADD45B, SOCS3,
CEACAM1, TNFSF10
IL1RN, ANKRD22, FCGR1A, GADD45A,	0.8	0.79	0.81
TGFBI, CSF1R, MCP1, MAPK14
SOCS3, HLA-DRA, IRAK2,	0.8	0.79	0.81
Protein_MMP9, MAP2K6, INSL3,
CReactiveProtein, Gene_MMP9
INSL3, BCL2A1, ARG2, GADD45B,	0.8	0.78	0.82
MAPK14, ITGAM, IRAK2, LDLR
GADD45B, Beta2Microglobulin,	0.8	0.77	0.82
Protein_MMP9, IFNGR1, IRAK2, PSTPIP2,
IL8, FCGR1A
CSF1R, HLA-DRA, IRAK4, FAD104,	0.84	0.88	0.82
CRTAP, MCP1, GADD45B, CCL5, IL6
HLA-DRA, Gene_MMP9, FAD104, IRAK2,	0.84	0.85	0.83
TNFRSF6, LY96, CReactiveProtein,
FCGR1A, CD86
GADD45A, GADD45B, OSM, ARG2,	0.84	0.81	0.86
FAD104, MAPK14, IRAK2, ITGAM,
MKNK1
IL6, IL18R1, IL1RN, HLA-DRA, CD86,	0.83	0.88	0.8
IRAK2, NCR1, TNFSF10, CCL5
CD86, IRAK2, ARG2, PFKFB3, MAPK14,	0.83	0.85	0.82
PRV1, VNN1, HLA-DRA, FAD104
TDRD9, FCGR1A, ARG2,	0.83	0.8	0.86
AlphaFetoprotein, JAK2,
ApolipoproteinCIII, TIMP1, MAP2K6,
CCL5
PFKFB3, CReactiveProtein, TDRD9, OSM,	0.83	0.85	0.81
IFNGR1, CCL5, TIMP1, ARG2, ITGAM
NCR1, CSF1R, MAP2K6, INSL3, IFNGR1,	0.83	0.85	0.81
FAD104, IL6, ARG2, IL18R1
PSTPIP2, OSM, LDLR, Protein_MMP9,	0.83	0.82	0.84
LY96, TNFSF13B, ANXA3, IL1RN,
Beta2Microglobulin
FAD104, NCR1, VNN1, IRAK2,	0.83	0.81	0.84
ApolipoproteinCIII, IL10alpha, LDLR,
FCGR1A, IRAK4
IL10alpha, HLA-DRA, TGFBI, FCGR1A,	0.82	0.84	0.81
CSF1R, IRAK2, GADD45A, PFKFB3,
SOCS3
IL8, IRAK4, CSF1R, IL18R1,	0.82	0.83	0.81
AlphaFetoprotein, IL1RN, BCL2A1,
TNFSF13B, INSL3
SOCS3, MAP2K6, PSTPIP2, OSM,	0.82	0.82	0.82
MAPK14, MKNK1, ApolipoproteinCIII,
IL18R1, TLR4
TIMP1, IL8, PFKFB3, CD86, SOCS3,	0.82	0.81	0.83
JAK2, IRAK2, IL10alpha, Protein_MMP9
TIMP1, INSL3, TNFRSF6, PFKFB3, CD86,	0.82	0.8	0.85
JAK2, IL8, CRTAP, Protein_MMP9
IRAK4, MAPK14, ApolipoproteinCIII, IL6,	0.82	0.88	0.76
MAP2K6, MCP1, TIFA, ARG2, CD86
TLR4, IL10alpha, IL8, GADD45A, IRAK2,	0.82	0.82	0.81
MAP2K6, MCP1, HLA-DRA, MAPK14
LY96, MCP1, CD86, VNN1, OSM, ARG2,	0.81	0.83	0.8
TDRD9, CCL5, INSL3
CCL5, CRTAP, ApolipoproteinCIII,	0.81	0.81	0.81
Gene_MMP9, IFNGR1, TNFSF13B,
ANKRD22, GADD45A, OSM
MCP1, IL6, FCGR1A, PSTPIP2, VNN1,	0.81	0.79	0.83
TNFSF10, TIMP1, Protein_MMP9,
CReactiveProtein
PFKFB3, IL6, NCR1, MAP2K6, FAD104,	0.81	0.79	0.84
CD86, TLR4, TDRD9, OSM
ApolipoproteinCIII, CReactiveProtein,	0.81	0.77	0.86
TGFBI, MKNK1, PRV1, FAD104, HLA-
DRA, ARG2, TIMP1
IL10alpha, IL10, ANXA3, IL6, CSF1R,	0.81	0.82	0.8
TGFBI, PSTPIP2, IL8, INSL3
IL6, IRAK2, CReactiveProtein, CCL5,	0.81	0.8	0.82
ANKRD22, MCP1, GADD45A, PFKFB3,
IL10alpha
TIFA, IL1RN, IL6, ITGAM,	0.81	0.79	0.82
CReactiveProtein, CCL5, TGFBI, IL10,
NCR1
CEACAM1, IFNGR1, TNFSF10, INSL3,	0.81	0.78	0.84
BCL2A1, Beta2Microglobulin, IL10, ARG2,
SOCS3
SOCS3, LDLR, SOD2, FAD104, MAP2K6,	0.81	0.75	0.86
PSTPIP2, GADD45B, IRAK4, GADD45A
MKNK1, IL8, TNFSF13B, FAD104,	0.81	0.83	0.78
ITGAM, GADD45B, NCR1, IL18R1,
ApolipoproteinCIII
IL8, Gene_MMP9, TNFSF10, MKNK1,	0.81	0.82	0.79
MCP1, IL6, CCL5, ApolipoproteinCIII,
SOD2
NCR1, PFKFB3, ApolipoproteinCIII,	0.81	0.78	0.83
INSL3, OSM, VNN1, AlphaFetoprotein,
TNFSF10, CRTAP
FCGR1A, CReactiveProtein, PRV1, NCR1,	0.81	0.75	0.86
ARG2, INSL3, IL10, TGFBI, MAPK14
IL8, IRAK2, PFKFB3, CEACAM1, TIFA,	0.8	0.8	0.81
Protein_MMP9, IRAK4, CRTAP, TDRD9
ARG2, INSL3, CSF1R, TNFSF13B,	0.8	0.79	0.82
Beta2Microglobulin, PRV1, FCGR1A,
GADD45B, CRTAP
GADD45A, IL8, TIMP1, CReactiveProtein,	0.8	0.77	0.84
MAP2K6, TGFBI, CRTAP, TNFRSF6,
BCL2A1
HLA-DRA, ApolipoproteinCIII, INSL3,	0.8	0.77	0.84
FAD104, TIMP1, IRAK4, FCGR1A, IL6,
GADD45A
ARG2, JAK2, IL1RN, VNN1, IRAK4,	0.8	0.84	0.77
CSF1R, ANKRD22, BCL2A1, TDRD9
CReactiveProtein, PFKFB3, CD86, IL1RN,	0.8	0.8	0.8
TLR4, Beta2Microglobulin, IRAK2,
TNFSF10, TNFRSF6
GADD45B, MAP2K6, JAK2, MAPK14,	0.8	0.79	0.81
TIMP1, IRAK4, CReactiveProtein, TLR4,
TGFBI
JAK2, TLR4, CCL5, IL6, CReactiveProtein,	0.8	0.73	0.87
IFNGR1, ApolipoproteinCIII, GADD45B,
NCR1
CSF1R, TNFRSF6, INSL3, MKNK1, IL8,	0.86	0.85	0.86
MAP2K6, FAD104, NCR1, IL1RN, MCP1
IL8, PRV1, SOCS3, IRAK2, ARG2,	0.85	0.86	0.83
IL10alpha, NCR1, CCL5, CReactiveProtein,
MKNK1
TNFSF13B, TLR4, ARG2, IL6, SOCS3,	0.84	0.8	0.88
Beta2Microglobulin, FAD104, MCP1, HLA-
DRA, PSTPIP2
IL6, MCP1, Beta2Microglobulin, IL1RN,	0.84	0.82	0.86
TDRD9, IFNGR1, ApolipoproteinCIII,
FCGR1A, OSM, IL8
FCGR1A, IL6, LY96, LDLR, IL18R1,	0.84	0.81	0.87
CSF1R, CCL5, NCR1, TNFRSF6, IRAK4
IL6, TGFBI, IL18R1, ANXA3, IL1RN,	0.83	0.84	0.82
GADD45B, ANKRD22, LDLR, TLR4,
CEACAM1
MAPK14, IL6, CSF1R, IL1RN, ITGAM,	0.83	0.86	0.79
Beta2Microglobulin, MAP2K6, IL10,
PSTPIP2, FAD104
CReactiveProtein, FCGR1A, CCL5,	0.83	0.86	0.8
ApolipoproteinCIII, OSM, IRAK2,
GADD45A, CRTAP, PFKFB3, ITGAM
TNFSF10, AlphaFetoprotein, CCL5, IL8,	0.82	0.79	0.85
IRAK4, OSM, IL10alpha, ARG2,
CReactiveProtein, TIFA
TDRD9, TNFSF10, GADD45B,	0.82	0.85	0.78
CReactiveProtein, IL8, ARG2, ANXA3,
TGFBI, IL1RN, CCL5
IL10alpha, ANXA3, TNFSF10, IL1RN,	0.82	0.85	0.78
TGFBI, FAD104, INSL3, MAP2K6,
MAPK14, ApolipoproteinCIII
TIMP1, Beta2Microglobulin, ITGAM,	0.82	0.82	0.81
LDLR, MCP1, IL8, FCGR1A, TIFA,
IL10alpha, MAP2K6
TNFRSF6, TGFBI, JAK2, SOD2, ANXA3,	0.82	0.82	0.81
VNN1, CCL5, INSL3, CSF1R, IL10
TDRD9, IL10alpha, MAPK14, NCR1,	0.82	0.8	0.83
LY96, GADD45B, IRAK2,
CReactiveProtein, INSL3, ITGAM
LDLR, JAK2, IFNGR1, IRAK2, SOCS3,	0.82	0.79	0.84
ITGAM, Protein_MMP9, INSL3,
ApolipoproteinCIII, CEACAM1
CSF1R, Beta2Microglobulin, IRAK4,	0.82	0.78	0.85
MKNK1, PRV1, TNFRSF6, PSTPIP2,
IL18R1, HLA-DRA, CCL5
BCL2A1, TLR4, IL8, TIMP1, SOD2,	0.82	0.77	0.86
CReactiveProtein, CRTAP,
ApolipoproteinCIII, GADD45B, FAD104
ARG2, OSM, TNFSF13B, CReactiveProtein,	0.81	0.86	0.77
AlphaFetoprotein, IL6, CRTAP,
Beta2Microglobulin, MCP1, TDRD9
FAD104, TNFSF13B, IL1RN, GADD45B,	0.81	0.82	0.8
IFNGR1, IL18R1, TNFRSF6, MCP1, PRV1,
IL8
IL8, ITGAM, CSF1R, TNFRSF6, INSL3,	0.81	0.82	0.81
IL10alpha, IFNGR1, IL10, IL1RN, SOD2
MCP1, IFNGR1, TNFRSF6, MAPK14,	0.81	0.78	0.84
FAD104, IL18R1, IRAK4, INSL3,
IL10alpha, Beta2Microglobulin
NCR1, PRV1, Protein_MMP9, TIMP1,	0.81	0.74	0.88
ANKRD22, INSL3, CD86, CCL5, MKNK1,
Gene_MMP9
NCR1, INSL3, CEACAM1, FAD104,	0.81	0.86	0.76
IL10alpha, TIFA, TNFSF13B, IL6, CCL5,
CReactiveProtein
CRTAP, IL1RN, IL18R1, FAD104, NCR1,	0.81	0.8	0.82
HLA-DRA, TGFBI, LY96, IL6, IRAK4
OSM, NCR1, IL8, GADD45B,	0.81	0.8	0.82
Protein_MMP9, TNFRSF6, TNFSF13B,
Beta2Microglobulin, IL1RN, IRAK2
CD86, IL10alpha, CSF1R, IRAK2,	0.81	0.79	0.83
ANKRD22, OSM, AlphaFetoprotein,
Gene_MMP9, IL10, IRAK4
ARG2, IRAK4, GADD45A, VNN1, IL18R1,	0.81	0.79	0.83
JAK2, ANXA3, CSF1R, HLA-DRA,
PFKFB3
LY96, TDRD9, NCR1, TNFRSF6, CSF1R,	0.81	0.76	0.86
PRV1, IL18R1, ARG2, Beta2Microglobulin,
IL10alpha
INSL3, TDRD9, CRTAP, TNFRSF6,	0.81	0.75	0.88
IRAK4, SOD2, LDLR, ANKRD22, OSM,
CSF1R
FAD104, PFKFB3, IL18R1, IL10, MAPK14,	0.81	0.83	0.79
ARG2, CD86, IL1RN, CCL5, GADD45A
TNFSF10, CSF1R, TNFSF13B, MKNK1,	0.81	0.81	0.8
ITGAM, PFKFB3, AlphaFetoprotein,
SOCS3, TNFRSF6, FAD104
CSF1R, PFKFB3, ApolipoproteinCIII,	0.81	0.81	0.81
TLR4, ARG2, PRV1, ANKRD22, ITGAM,
TIFA, TNFRSF6
TGFBI, IL10, TDRD9, PFKFB3, INSL3,	0.81	0.8	0.81
CSF1R, PSTPIP2, MKNK1, NCR1, HLA-
DRA
ANKRD22, TIMP1, CRTAP, HLA-DRA,	0.81	0.78	0.83
ApolipoproteinCIII, CD86, TNFRSF6,
Gene_MMP9, VNN1, IL10
ARG2, NCR1, IRAK4, FCGR1A, FAD104,	0.81	0.77	0.84
TNFRSF6, PFKFB3, MAP2K6, TGFBI,
MKNK1
TLR4, ANKRD22, IL10alpha, VNN1,	0.81	0.76	0.84
Protein_MMP9, TNFRSF6, ARG2,
TNFSF10, OSM, FCGR1A
FAD104, PRV1, Protein_MMP9, IL10alpha,	0.81	0.75	0.86
ARG2, TNFSF13B, FCGR1A, CEACAM1,
CCL5, IL1RN
TNFRSF6, IL6, TGFBI, PSTPIP2, ANXA3,	0.8	0.83	0.78
ANKRD22, ApolipoproteinCIII, OSM,
SOCS3, MAPK14
IL8, OSM, IRAK4, TDRD9, LDLR,	0.8	0.81	0.8
TNFSF13B, IL10, IFNGR1, ARG2, SOD2
PSTPIP2, BCL2A1, CD86, ANXA3,	0.8	0.84	0.77
IL10alpha, SOD2, OSM, INSL3,
TNFSF13B, GADD45B
IL6, ANXA3, SOCS3, MAP2K6, TGFBI,	0.8	0.83	0.77
ANKRD22, CRTAP, BCL2A1, CCL5, TLR4
HLA-DRA, CSF1R, TGFBI, MAP2K6,	0.8	0.82	0.78
BCL2A1, CD86, TLR4, IL1RN, IL6,
ApolipoproteinCIII
ApolipoproteinCIII, CCL5, SOCS3, TIMP1,	0.8	0.81	0.79
Gene_MMP9, AlphaFetoprotein, ITGAM,
INSL3, CEACAM1, LDLR
IL8, TNFRSF6, IL6, IL1RN, PSTPIP2,	0.8	0.79	0.81
ApolipoproteinCIII, CD86, JAK2, TLR4,
Protein_MMP9
IL10alpha, JAK2, MCP1, CEACAM1,	0.8	0.78	0.82
ApolipoproteinCIII, BCL2A1, PRV1,
Protein_MMP9, MAP2K6, IFNGR1
FCGR1A, LY96, JAK2, GADD45B, LDLR,	0.8	0.77	0.82
IL6, VNN1, MCP1, Gene_MMP9, SOD2
CSF1R, TNFRSF6, INSL3, MKNK1, IL8,	0.86	0.85	0.86
MAP2K6, FAD104, NCR1, IL1RN, MCP1
IL8, PRV1, SOCS3, IRAK2, ARG2,	0.85	0.86	0.83
IL10alpha, NCR1, CCL5, CReactiveProtein,
MKNK1
LDLR, CD86, NCR1, IRAK4, IL18R1,	0.85	0.84	0.87
Protein_MMP9, PRV1, GADD45B, ARG2,
LY96, AlphaFetoprotein
MAP2K6, CD86, INSL3,	0.85	0.81	0.88
ApolipoproteinCIII, IL8, OSM, TNFSF13B,
IL1RN, BCL2A1, FAD104, GADD45A
NCR1, GADD45B, TNFSF10, IL10alpha,	0.84	0.87	0.82
FAD104, LY96, IL6, IL10, ARG2,
CReactiveProtein, TGFBI
CD86, CEACAM1, INSL3, PFKFB3,	0.83	0.86	0.81
IL10alpha, FAD104, SOD2, Gene_MMP9,
SOCS3, ApolipoproteinCIII, FCGR1A
SOCS3, ARG2, ApolipoproteinCIII, IRAK4,	0.83	0.84	0.82
PFKFB3, IFNGR1, NCR1, IL8,
CReactiveProtein, VNN1, TDRD9
ARG2, OSM, CReactiveProtein, SOD2,	0.83	0.85	0.81
CEACAM1, FCGR1A, TIMP1, IL10,
IL18R1, ANKRD22, IRAK2
TGFBI, SOD2, IL10, CD86, CEACAM1,	0.83	0.83	0.83
TDRD9, IRAK4, ANXA3, LDLR, OSM,
ARG2
CReactiveProtein, IL10alpha, TIMP1, LY96,	0.83	0.83	0.83
IL8, SOD2, MAP2K6, MAPK14, TLR4,
PSTPIP2, INSL3
ARG2, PSTPIP2, SOD2, INSL3, FAD104,	0.83	0.8	0.86
JAK2, TIFA, PFKFB3, IRAK2, IL6,
ANXA3
PSTPIP2, CEACAM1, GADD45A,	0.83	0.84	0.82
ApolipoproteinCIII, ITGAM, PRV1, TLR4,
IL10alpha, ARG2, SOCS3, NCR1
OSM, SOCS3, CSF1R, IRAK2, VNN1, IL6,	0.83	0.82	0.83
SOD2, LDLR, BCL2A1, ANKRD22, CD86
CRTAP, LDLR, TGFBI, INSL3, TIFA,	0.83	0.82	0.83
FAD104, AlphaFetoprotein, IL8, JAK2,
IRAK4, BCL2A1
CD86, ITGAM, PSTPIP2, IL18R1, IL6,	0.83	0.77	0.87
IFNGR1, GADD45B, IL10,
Beta2Microglobulin, FCGR1A, FAD104
PRV1, Beta2Microglobulin, IL1RN, NCR1,	0.82	0.84	0.81
CSF1R, IFNGR1, TIMP1, SOCS3, LDLR,
TIFA, ARG2
IL10alpha, GADD45A, LDLR, SOCS3,	0.82	0.83	0.81
MAP2K6, LY96, CSF1R, Protein_MMP9,
MCP1, TDRD9, IL8
CSF1R, TDRD9, TIMP1, SOD2, FCGR1A,	0.82	0.83	0.82
IFNGR1, INSL3, CD86, TNFRSF6, HLA-
DRA, MAP2K6
IL8, IL18R1, BCL2A1, MKNK1,	0.82	0.82	0.83
CReactiveProtein, CCL5, IL6, SOCS3,
FCGR1A, PSTPIP2, ApolipoproteinCIII
ANXA3, IL6, CD86, SOD2, CEACAM1,	0.82	0.8	0.85
FCGR1A, ANKRD22, NCR1, PSTPIP2, IL8,
MAPK14
Protein_MMP9, TNFRSF6, ITGAM,	0.82	0.79	0.85
CSF1R, INSL3, TIFA, BCL2A1, IL1RN,
TGFBI, FCGR1A, ApolipoproteinCIII
ANKRD22, IL10alpha, SOCS3, IRAK4,	0.82	0.76	0.88
OSM, INSL3, TGFBI, MCP1, IL8,
TNFSF13B, PRV1
ANKRD22, LDLR, VNN1, TIMP1, IRAK2,	0.82	0.85	0.8
IL10alpha, GADD45B, ARG2, MAPK14,
CSF1R, TNFRSF6
TIFA, ARG2, TNFSF10, INSL3, CD86, IL8,	0.82	0.82	0.82
IRAK2, OSM, CSF1R, HLA-DRA, ITGAM
ANKRD22, TIFA, PSTPIP2, CCL5,	0.82	0.79	0.84
Gene_MMP9, Beta2Microglobulin, NCR1,
FCGR1A, INSL3, SOCS3, IL10alpha
ApolipoproteinCIII, AlphaFetoprotein,	0.82	0.82	0.81
NCR1, CCL5, GADD45A, IL18R1, JAK2,
TDRD9, OSM, TLR4, Gene_MMP9
CReactiveProtein, IL18R1, TGFBI,	0.82	0.8	0.83
TNFSF10, MAP2K6, LDLR, FAD104,
ARG2, HLA-DRA, GADD45B, ANXA3
IL18R1, IRAK4, LY96, INSL3, TNFRSF6,	0.82	0.8	0.83
CReactiveProtein, CD86, GADD45B,
CRTAP, IL8, MAPK14
IL8, FCGR1A, CSF1R, VNN1, IL10alpha,	0.81	0.85	0.78
PSTPIP2, IL6, IL1RN, TLR4, GADD45B,
LY96
HLA-DRA, IL6, FAD104, GADD45A,	0.81	0.79	0.84
INSL3, ITGAM, CSF1R, IFNGR1,
Protein_MMP9, SOCS3, NCR1
IL10, LDLR, AlphaFetoprotein, IL1RN,	0.81	0.79	0.84
INSL3, ApolipoproteinCIII, PSTPIP2,
CCL5, SOD2, TGFBI, VNN1
Protein_MMP9, IL10, TGFBI, INSL3,	0.81	0.84	0.78
IRAK2, TNFRSF6, IL8, PSTPIP2, OSM,
AlphaFetoprotein, NCR1
IL8, TLR4, MCP1, ApolipoproteinCIII,	0.81	0.83	0.79
Beta2Microglobulin, IL6, IL10, VNN1,
CD86, PSTPIP2, ITGAM
FAD104, GADD45A, SOCS3, PSTPIP2,	0.81	0.81	0.81
IL6, TGFBI, TIMP1, HLA-DRA, TNFSF10,
IL10alpha, MKNK1
PRV1, IL8, FCGR1A, GADD45A, IRAK2,	0.81	0.81	0.81
VNN1, CD86, IL18R1, Protein_MMP9,
MAP2K6, ITGAM
CRTAP, JAK2, IRAK2, CEACAM1, PRV1,	0.81	0.79	0.82
CCL5, SOD2, BCL2A1, SOCS3, IL1RN,
ApolipoproteinCIII
MCP1, CCL5, HLA-DRA, IRAK4, OSM,	0.81	0.76	0.85
LDLR, PFKFB3, CReactiveProtein,
MKNK1, GADD45A, LY96
ARG2, INSL3, IL6, ITGAM, TGFBI, LDLR,	0.81	0.82	0.79
IL10, CD86, IL8, TNFSF13B, IL10alpha
Protein_MMP9, CD86, GADD45B, LY96,	0.81	0.82	0.8
SOD2, FCGR1A, IL8, AlphaFetoprotein,
CSF1R, FAD104, CRTAP
TNFSF13B, ApolipoproteinCIII, LDLR,	0.81	0.77	0.84
TDRD9, CEACAM1, AlphaFetoprotein,
IRAK4, INSL3, GADD45A, CRTAP,
IFNGR1
MKNK1, PSTPIP2, Beta2Microglobulin,	0.8	0.82	0.79
ANKRD22, TIFA, IL10alpha, TGFBI,
AlphaFetoprotein, NCR1, PRV1, SOCS3
TIFA, MKNK1, IL6, ANXA3, FAD104,	0.8	0.82	0.79
PSTPIP2, TNFSF13B, LDLR, INSL3,
SOD2, JAK2
TNFSF13B, IFNGR1, IL18R1, CD86,	0.8	0.81	0.8
Beta2Microglobulin, TGFBI, CSF1R,
CReactiveProtein, CRTAP, MCP1, JAK2
TNFSF13B, Beta2Microglobulin, CSF1R,	0.8	0.79	0.82
JAK2, CRTAP, IL1RN, IL10, SOCS3,
ANKRD22, PFKFB3, LDLR
TNFRSF6, OSM, PRV1, INSL3, TLR4,	0.8	0.77	0.83
MKNK1, IRAK4, HLA-DRA, VNN1,
IL10alpha, FCGR1A
IL8, ApolipoproteinCIII, GADD45B,	0.8	0.77	0.83
SOCS3, ARG2, TNFSF13B, IL1RN, CCL5,
ANXA3, CReactiveProtein, TIFA
TNFSF13B, SOCS3, Protein_MMP9, SOD2,	0.8	0.76	0.86
TNFRSF6, NCR1, FAD104, IL6, OSM,
CCL5, TDRD9
CD86, INSL3, ANXA3, GADD45B, VNN1,	0.8	0.84	0.77
IFNGR1, IL6, PFKFB3, PSTPIP2,
Beta2Microglobulin, IRAK2
IL6, Gene_MMP9, FAD104, TIFA, TGFBI,	0.8	0.82	0.78
Beta2Microglobulin, IL10alpha, ANXA3,
IL18R1, NCR1, INSL3
CEACAM1, JAK2, MCP1, OSM, IL18R1,	0.8	0.82	0.78
MKNK1, ANKRD22, TLR4, CSF1R,
PSTPIP2, IL1RN
CSF1R, AlphaFetoprotein, HLA-DRA,	0.8	0.8	0.8
TDRD9, ITGAM, SOCS3, FCGR1A,
IRAK2, TIFA, TNFSF10, Protein_MMP9
CSF1R, IL10alpha, TNFRSF6, TNFSF13B,	0.8	0.79	0.81
LDLR, INSL3, AlphaFetoprotein, IL10,
TIFA, VNN1, HLA-DRA
IL18R1, MCP1, ANKRD22, TGFBI, ARG2,	0.8	0.77	0.83
ANXA3, GADD45A, IL1RN, TNFRSF6,
PSTPIP2, IRAK2
IL10alpha, IFNGR1, MAPK14, FCGR1A,	0.8	0.76	0.83
Gene_MMP9, GADD45A, VNN1,
ANKRD22, TNFSF13B, CCL5, IRAK2
IL8, CReactiveProtein, CSF1R, TLR4,	0.85	0.85	0.85
TNFRSF6, Gene_MMP9, TDRD9, OSM,
PFKFB3, IFNGR1, ApolipoproteinCIII,
PSTPIP2
JAK2, OSM, GADD45B, MCP1, IL1RN,	0.85	0.81	0.88
ANKRD22, IL18R1, Gene_MMP9, ITGAM,
NCR1, ApolipoproteinCIII, PFKFB3
TNFSF10, MKNK1, PFKFB3, ANXA3,	0.84	0.84	0.84
CRTAP, CD86, MAPK14, IL8, OSM,
GADD45B, HLA-DRA, INSL3
IL1RN, AlphaFetoprotein, ARG2, MAP2K6,	0.83	0.86	0.82
CEACAM1, GADD45B, CRTAP, ANXA3,
INSL3, ApolipoproteinCIII, NCR1, FAD104
IL6, LDLR, TDRD9, TNFRSF6, NCR1,	0.83	0.84	0.83
ITGAM, AlphaFetoprotein, FCGR1A,
ARG2, TNFSF10, OSM, BCL2A1
IL10, SOD2, GADD45A, TNFSF13B,	0.83	0.86	0.81
IRAK4, LY96, HLA-DRA, PSTPIP2, IL6,
IFNGR1, ARG2, LDLR
CCL5, CSF1R, LDLR, GADD45A, INSL3,	0.83	0.8	0.86
JAK2, AlphaFetoprotein, OSM,
Beta2Microglobulin, PRV1, HLA-DRA,
MKNK1
ANKRD22, TNFSF13B, TIMP1, VNN1,	0.83	0.83	0.83
IRAK4, FCGR1A, CEACAM1, IRAK2,
ARG2, ANXA3, CD86, IL1RN
JAK2, AlphaFetoprotein, IL1RN, SOCS3,	0.82	0.83	0.82
ANKRD22, IL10alpha, IL8, TGFBI, CD86,
IL10, CSF1R, CReactiveProtein
VNN1, GADD45B, MAP2K6, TNFSF13B,	0.82	0.79	0.85
IRAK2, TLR4, CReactiveProtein, PSTPIP2,
MCP1, CSF1R, IL8, TDRD9
SOD2, IL10, CReactiveProtein,	0.82	0.77	0.86
ApolipoproteinCIII, Beta2Microglobulin,
IFNGR1, OSM, TNFSF13B, VNN1,
GADD45B, CD86, PFKFB3
LDLR, CRTAP, PSTPIP2, GADD45B, IL8,	0.82	0.82	0.82
TNFRSF6, MAP2K6, IL10, ARG2, LY96,
MAPK14, IL18R1
IFNGR1, NCR1, ApolipoproteinCIII,	0.82	0.82	0.82
ANXA3, CSF1R, CCL5, FCGR1A, TIFA,
TLR4, INSL3, IL8, ARG2
LY96, Beta2Microglobulin, CCL5, LDLR,	0.82	0.78	0.86
IRAK4, TIMP1, MKNK1,
ApolipoproteinCIII, IL8, SOCS3,
ANKRD22, PRV1
Protein_MMP9, MAPK14, IL1RN, SOCS3,	0.82	0.77	0.87
MKNK1, ApolipoproteinCIII, IL10, OSM,
MAP2K6, TNFSF13B, NCR1, IL18R1
TNFSF13B, FAD104, OSM, TNFRSF6,	0.82	0.81	0.83
TDRD9, TIFA, IL10alpha, INSL3,
Protein_MMP9, HLA-DRA,
Beta2Microglobulin, ApolipoproteinCIII
TLR4, Protein_MMP9, VNN1, IFNGR1,	0.82	0.78	0.85
ITGAM, MCP1, LY96, IRAK2, OSM,
TDRD9, IL8, ApolipoproteinCIII
MAP2K6, OSM, GADD45B, IL1RN,	0.81	0.81	0.81
MAPK14, ARG2, LY96, VNN1, TNFRSF6,
TGFBI, CD86, Beta2Microglobulin
MKNK1, ARG2, CEACAM1, GADD45A,	0.81	0.81	0.81
AlphaFetoprotein, GADD45B, HLA-DRA,
CReactiveProtein, SOD2, TLR4, LDLR,
TNFRSF6
Protein_MMP9, TGFBI, PRV1,	0.81	0.81	0.82
Beta2Microglobulin, TNFSF13B, TLR4,
INSL3, Gene_MMP9, ARG2,
ApolipoproteinCIII, MKNK1, IL10alpha
TLR4, TGFBI, FCGR1A, NCR1, LY96,	0.81	0.81	0.82
IL10, CCL5, IRAK2, INSL3, TDRD9, OSM,
BCL2A1
Gene_MMP9, FCGR1A, PSTPIP2, TIFA,	0.81	0.81	0.82
CSF1R, SOD2, ITGAM, PFKFB3, JAK2,
IL8, LY96, OSM
CRTAP, MKNK1, TDRD9, LY96, TLR4,	0.81	0.8	0.83
TNFSF10, SOD2, JAK2,
Beta2Microglobulin, CD86, PSTPIP2,
MAP2K6
TGFBI, TDRD9, ARG2, OSM, TNFSF13B,	0.81	0.78	0.85
CEACAM1, CCL5, CReactiveProtein,
TLR4, IL10alpha, LY96, SOCS3
IRAK2, LDLR, ARG2, SOD2, IL10alpha,	0.81	0.78	0.84
ANKRD22, FCGR1A, Beta2Microglobulin,
FAD104, ITGAM, PRV1, OSM
FAD104, IL10alpha, INSL3, IL18R1,	0.81	0.83	0.79
IL1RN, MKNK1, MAP2K6, Gene_MMP9,
IRAK2, PSTPIP2, CEACAM1, IL6
VNN1, ApolipoproteinCIII, IL10, JAK2,	0.81	0.82	0.8
Protein_MMP9, INSL3, Beta2Microglobulin,
OSM, IRAK4, MAP2K6, IL1RN,
AlphaFetoprotein
BCL2A1, GADD45A, JAK2, FCGR1A,	0.81	0.81	0.81
FAD104, Gene_MMP9, CRTAP, TDRD9,
MAP2K6, CSF1R, PRV1, Protein_MMP9
INSL3, TIFA, LY96, FAD104, PSTPIP2,	0.81	0.8	0.82
PFKFB3, Beta2Microglobulin, TIMP1,
IL18R1, GADD45A, IL6, AlphaFetoprotein
TDRD9, PFKFB3, CSF1R, ITGAM, MCP1,	0.81	0.79	0.83
ARG2, TNFSF13B, PSTPIP2, MAP2K6,
ANXA3, OSM, TGFBI
TNFSF10, TNFRSF6, Beta2Microglobulin,	0.81	0.77	0.84
PRV1, SOCS3, IL8, VNN1, TDRD9,
CReactiveProtein, GADD45B, TNFSF13B,
CD86
MAP2K6, IFNGR1, LY96,	0.81	0.76	0.85
Beta2Microglobulin, GADD45B,
ANKRD22, SOCS3, ANXA3, INSL3,
Protein_MMP9, CD86, HLA-DRA
SOD2, TIMP1, ApolipoproteinCIII,	0.81	0.76	0.85
Protein_MMP9, FAD104, ANXA3, TLR4,
CCL5, ITGAM, IRAK4, SOCS3, HLA-DRA
ITGAM, INSL3, FCGR1A, ARG2, IRAK2,	0.85	0.82	0.88
FAD104, IRAK4, MAPK14, LY96, TIMP1,
PRV1, TLR4, CD86
PRV1, MKNK1, IL8, FAD104, VNN1,	0.85	0.84	0.86
SOCS3, ARG2, MAP2K6, IL1RN, SOD2,
IL18R1, NCR1, BCL2A1
NCR1, CEACAM1, IRAK4, ARG2,	0.85	0.79	0.89
TNFSF13B, PFKFB3, OSM, TNFRSF6,
SOCS3, HLA-DRA, TNFSF10, JAK2,
SOD2
MCP1, Protein_MMP9, IL10alpha, FAD104,	0.84	0.81	0.87
FCGR1A, ITGAM, TGFBI,
ApolipoproteinCIII, ARG2, PRV1, CRTAP,
TIFA, LDLR
ARG2, ANKRD22, GADD45B, IRAK2,	0.84	0.83	0.85
OSM, MKNK1, ANXA3, IL18R1,
TNFRSF6, MAP2K6, AlphaFetoprotein,
MCP1, ApolipoproteinCIII
HLA-DRA, NCR1, CEACAM1,	0.83	0.82	0.85
Beta2Microglobulin, VNN1,
AlphaFetoprotein, MCP1, IL6, FCGR1A,
OSM, CSF1R, IRAK2, CRTAP
CReactiveProtein, SOD2, GADD45A,	0.83	0.86	0.81
ARG2, IRAK4, FCGR1A, IL18R1, TLR4,
JAK2, BCL2A1, IL10alpha, TGFBI,
AlphaFetoprotein
ApolipoproteinCIII, HLA-DRA, TNFSF10,	0.83	0.83	0.83
TLR4, IL10, GADD45B, BCL2A1, IL6,
CCL5, INSL3, MAP2K6, LDLR, IFNGR1
TIFA, JAK2, HLA-DRA, SOCS3, ARG2,	0.83	0.79	0.87
OSM, AlphaFetoprotein, MAPK14, IRAK2,
IFNGR1, FCGR1A, MAP2K6, PRV1
Beta2Microglobulin, IRAK2, MKNK1,	0.83	0.83	0.83
ANKRD22, CD86, OSM, CSF1R, TNFSF10,
IFNGR1, TLR4, MCP1, FAD104, TGFBI
VNN1, FCGR1A, ANKRD22, CRTAP,	0.83	0.82	0.84
ANXA3, IL8, PFKFB3, NCR1, TLR4,
AlphaFetoprotein, TIFA, IRAK4, CD86
Gene_MMP9, INSL3, FCGR1A, LDLR,	0.83	0.81	0.84
OSM, PFKFB3, ANKRD22, IL1RN, IL8,
IFNGR1, TDRD9, BCL2A1, TNFSF13B
PFKFB3, AlphaFetoprotein, IRAK4, NCR1,	0.82	0.81	0.84
TNFSF10, TDRD9, JAK2, FAD104,
IL10alpha, PRV1, CReactiveProtein, TGFBI,
Protein_MMP9
Gene_MMP9, MAP2K6, MAPK14,	0.82	0.76	0.88
CReactiveProtein, PFKFB3, CCL5, CSF1R,
INSL3, MKNK1, ARG2, FAD104, SOD2,
Protein_MMP9
IL8, TNFSF13B, ARG2, TIFA, CRTAP,	0.82	0.85	0.79
OSM, IL18R1, MCP1, IRAK4, LY96,
AlphaFetoprotein, TDRD9,
CReactiveProtein
PSTPIP2, CEACAM1, GADD45B,	0.82	0.83	0.81
MAPK14, ARG2, FCGR1A, ITGAM,
TGFBI, IL10alpha, OSM, PRV1, IL8, TLR4
OSM, CReactiveProtein, CD86, LY96,	0.82	0.82	0.82
IL10alpha, FAD104, TDRD9, IL6,
ApolipoproteinCIII, LDLR, CSF1R, IL18R1,
MCP1
JAK2, IL8, ARG2, OSM, BCL2A1, TIFA,	0.82	0.83	0.8
IL6, Gene_MMP9, PRV1, TLR4, IL1RN,
LY96, IRAK2
IL6, INSL3, BCL2A1, TLR4, HLA-DRA,	0.82	0.81	0.82
IL10alpha, MKNK1, TDRD9, GADD45A,
OSM, SOCS3, CCL5, MAPK14
LDLR, FCGR1A, SOD2, LY96, MKNK1,	0.82	0.77	0.86
PRV1, MAP2K6, NCR1, Protein_MMP9,
SOCS3, AlphaFetoprotein, IFNGR1, INSL3
TNFRSF6, ARG2, INSL3, ANXA3, IL10,	0.82	0.77	0.87
TIFA, ITGAM, VNN1, SOD2, TIMP1,
CSF1R, Protein_MMP9, SOCS3
IL10alpha, TNFRSF6, ARG2, TIMP1, IL8,	0.81	0.85	0.78
CSF1R, MAP2K6, IRAK4, PFKFB3,
FCGR1A, AlphaFetoprotein, OSM, HLA-
DRA
Protein_MMP9, CD86, IFNGR1, TIMP1,	0.81	0.81	0.81
IL1RN, FCGR1A, ARG2, TIFA, IL8,
CRTAP, CSF1R, IL6, ITGAM
CEACAM1, ANKRD22, CCL5, TLR4,	0.81	0.81	0.82
IRAK4, Beta2Microglobulin, MAP2K6,
PRV1, TGFBI, FAD104, SOD2, JAK2,
MCP1
CD86, VNN1, PSTPIP2, PFKFB3,	0.81	0.86	0.77
CReactiveProtein, IL6, TLR4, CCL5,
FCGR1A, TDRD9, TNFRSF6, CSF1R,
CRTAP
LDLR, OSM, MCP1, CD86, IL1RN,	0.81	0.83	0.78
Protein_MMP9, MAP2K6, FCGR1A, IL8,
CEACAM1, PFKFB3, IRAK4, LY96
CReactiveProtein, TNFSF13B,	0.81	0.79	0.82
ApolipoproteinCIII, IRAK2, VNN1,
FCGR1A, PFKFB3, HLA-DRA, ANKRD22,
SOD2, CD86, TGFBI, Beta2Microglobulin
LY96, TNFSF10, PRV1, PSTPIP2, SOCS3,	0.81	0.79	0.83
TIMP1, IFNGR1, ARG2, CEACAM1,
CCL5, TNFSF13B, LDLR,
ApolipoproteinCIII
PRV1, JAK2, FCGR1A, VNN1, SOCS3,	0.81	0.79	0.83
TIFA, CRTAP, INSL3, IFNGR1, TDRD9,
CEACAM1, Protein_MMP9, IL8
GADD45A, SOCS3, OSM, CD86, ITGAM,	0.81	0.77	0.84
ApolipoproteinCIII, FAD104, INSL3,
PSTPIP2, IL18R1, AlphaFetoprotein,
TDRD9, MAP2K6
PSTPIP2, VNN1, IL1RN, CSF1R, CD86,	0.81	0.77	0.85
TLR4, IRAK4, IFNGR1, CRTAP, TNFSF10,
SOD2, TIFA, TDRD9
TNFRSF6, IFNGR1, TNFSF13B, MAP2K6,	0.85	0.88	0.83
MKNK1, ANXA3, TGFBI, OSM, ARG2,
Beta2Microglobulin, CReactiveProtein,
LY96, ApolipoproteinCIII, TIFA
CSF1R, TLR4, IL6, TNFSF13B,	0.84	0.85	0.83
Beta2Microglobulin, IRAK4, FCGR1A,
CCL5, ITGAM, VNN1, TIFA, CRTAP,
PFKFB3, TDRD9
CReactiveProtein, IL6, MAP2K6, OSM,	0.84	0.82	0.85
ARG2, ANKRD22, JAK2, HLA-DRA,
ApolipoproteinCIII, MAPK14, TLR4,
TNFSF13B, IFNGR1, IL10alpha
VNN1, GADD45B, IRAK2, TGFBI, NCR1,	0.84	0.77	0.89
IL6, CEACAM1, CRTAP, Gene_MMP9,
TNFRSF6, CD86, TDRD9,
CReactiveProtein, IL10
CRTAP, IL18R1, Beta2Microglobulin,	0.83	0.81	0.85
ANXA3, TDRD9, MKNK1, Protein_MMP9,
IL6, TNFSF10, OSM, MCP1, PFKFB3,
ApolipoproteinCIII, VNN1
PSTPIP2, IL8, IL18R1, CEACAM1, HLA-	0.83	0.79	0.86
DRA, OSM, NCR1, MCP1, FCGR1A,
TNFRSF6, TLR4, IRAK2, Protein_MMP9,
CReactiveProtein
PRV1, IRAK4, FAD104, TGFBI,	0.83	0.83	0.82
Protein_MMP9, INSL3, AlphaFetoprotein,
CD86, VNN1, CSF1R, Beta2Microglobulin,
GADD45B, BCL2A1, IL10
CD86, MAP2K6, PSTPIP2, TNFSF10,	0.83	0.81	0.84
OSM, GADD45B, TLR4, HLA-DRA, LY96,
TNFSF13B, ARG2, SOD2, PRV1,
Beta2Microglobulin
TIFA, CSF1R, IL10alpha, IFNGR1,	0.83	0.77	0.87
CEACAM1, CRTAP, ANKRD22, FCGR1A,
MAP2K6, FAD104, PSTPIP2, MAPK14,
ARG2, IRAK2
CReactiveProtein, TDRD9, IL8, ITGAM,	0.82	0.86	0.78
IL10alpha, TNFRSF6, SOD2, MCP1,
SOCS3, MKNK1, FAD104, MAP2K6,
IFNGR1, AlphaFetoprotein
TLR4, ANKRD22, IL10alpha,	0.82	0.86	0.78
CReactiveProtein, ApolipoproteinCIII,
BCL2A1, FCGR1A, SOD2, OSM, IFNGR1,
TGFBI, TIFA, VNN1, CEACAM1
FCGR1A, IRAK4, MAP2K6, ANXA3,	0.82	0.86	0.79
MAPK14, INSL3, AlphaFetoprotein, IL8,
MKNK1, ARG2, VNN1, TIMP1, CSF1R,
GADD45A
ANKRD22, HLA-DRA, IFNGR1,	0.82	0.81	0.84
GADD45A, TNFSF13B, FAD104, LDLR,
IL10alpha, IL6, MAPK14,
ApolipoproteinCIII, PRV1,
CReactiveProtein, TIMP1
IL10, PSTPIP2, INSL3, LY96, NCR1,	0.82	0.76	0.87
MAPK14, VNN1, MCP1, PRV1,
ApolipoproteinCIII, TIMP1, Protein_MMP9,
TDRD9, PFKFB3
TNFRSF6, TGFBI, LY96, TDRD9, CRTAP,	0.82	0.85	0.79
AlphaFetoprotein, TNFSF10, CCL5, JAK2,
IL6, IRAK2, HLA-DRA, OSM,
ApolipoproteinCIII
TIFA, Gene_MMP9, IL18R1, TDRD9,	0.82	0.84	0.8
SOCS3, TIMP1, IL6, CCL5, ARG2, CSF1R,
OSM, IL10alpha, IL8, TNFSF13B
PSTPIP2, PRV1, MAPK14, OSM, CRTAP,	0.82	0.82	0.82
IFNGR1, IL6, FAD104, IL18R1, JAK2,
GADD45B, LY96, BCL2A1, TLR4
GADD45A, IL6, TGFBI, BCL2A1, CRTAP,	0.82	0.8	0.84
CCL5, TIFA, TLR4, CD86, PRV1, FAD104,
TDRD9, TNFSF10, SOCS3
Beta2Microglobulin, JAK2, TDRD9,	0.82	0.79	0.85
PSTPIP2, HLA-DRA, IL1RN, TGFBI,
INSL3, ARG2, LDLR, AlphaFetoprotein,
IRAK2, SOD2, MAPK14
CD86, FAD104, AlphaFetoprotein,	0.82	0.77	0.86
Gene_MMP9, MCP1, HLA-DRA, INSL3,
PSTPIP2, IL1RN, ITGAM, TIMP1,
Protein_MMP9, IL6, IRAK4
ANKRD22, MAPK14, GADD45A, TDRD9,	0.82	0.88	0.75
IL10alpha, Protein_MMP9, ARG2, CD86,
TIMP1, IRAK2, TIFA, VNN1, OSM,
ITGAM
SOCS3, IL1RN, CEACAM1, FCGR1A,	0.82	0.85	0.79
LDLR, CCL5, CReactiveProtein,
AlphaFetoprotein, ARG2, IL6, CD86,
MCP1, INSL3, IL18R1
ANKRD22, FAD104, ApolipoproteinCIII,	0.82	0.84	0.79
IRAK2, TNFSF13B, TGFBI, TLR4,
CRTAP, MCP1, LDLR, JAK2, SOD2,
PSTPIP2, Protein_MMP9
BCL2A1, IL1RN, FCGR1A, GADD45A,	0.82	0.84	0.79
JAK2, NCR1, TDRD9, TIFA, TNFSF10,
Protein_MMP9, CRTAP, CSF1R, IL6,
INSL3
SOD2, ITGAM, ApolipoproteinCIII,	0.82	0.8	0.83
ANXA3, FAD104, IL6, ARG2, CD86,
TGFBI, SOCS3, OSM, TDRD9, IL18R1,
LY96
VNN1, IRAK2, ApolipoproteinCIII, IL10,	0.82	0.79	0.84
TDRD9, FCGR1A, IL8, TIMP1, MCP1,
JAK2, TIFA, TGFBI, OSM, MAPK14
ApolipoproteinCIII, IL10, TDRD9, ARG2,	0.82	0.78	0.85
IRAK4, ANXA3, TNFRSF6,
CReactiveProtein, INSL3, JAK2, IL1RN,
IL6, NCR1, Gene_MMP9
CD86, CSF1R, TNFSF13B, FCGR1A,	0.81	0.83	0.79
MCP1, GADD45A, LDLR, IRAK2, CCL5,
Beta2Microglobulin, SOCS3, MAP2K6,
LY96, INSL3
MCP1, NCR1, TGFBI, TDRD9, MAP2K6,	0.81	0.83	0.8
ApolipoproteinCIII, INSL3, LY96, IFNGR1,
JAK2, Protein_MMP9, GADD45B, IRAK4,
CCL5
Beta2Microglobulin, FCGR1A, TNFSF13B,	0.81	0.82	0.8
OSM, IRAK4, IRAK2, IL8, MAPK14,
PSTPIP2, TIFA, TIMP1, ApolipoproteinCIII,
MAP2K6, TLR4
TNFSF13B, LY96, OSM, MAP2K6, IRAK2,	0.81	0.82	0.81
CRTAP, JAK2, PFKFB3, BCL2A1,
CReactiveProtein, INSL3, GADD45A,
TIFA, IL10alpha
OSM, JAK2, GADD45A, CEACAM1,	0.81	0.82	0.81
ARG2, NCR1, TLR4, PRV1, PFKFB3, IL8,
Beta2Microglobulin, GADD45B, HLA-
DRA, INSL3
LY96, TIFA, CSF1R, IL10, SOCS3, ARG2,	0.81	0.79	0.83
IRAK4, CD86, IL10alpha, Protein_MMP9,
TNFSF10, ITGAM, Gene_MMP9, LDLR
AlphaFetoprotein, ApolipoproteinCIII,	0.81	0.78	0.84
SOD2, PSTPIP2, CSF1R,
Beta2Microglobulin, NCR1, GADD45B,
FCGR1A, CReactiveProtein, CEACAM1,
CD86, Protein_MMP9, HLA-DRA
MAPK14, ARG2, TNFSF10, TNFSF13B,	0.81	0.74	0.88
FAD104, ANKRD22, GADD45A, ANXA3,
CReactiveProtein, NCR1, IFNGR1, OSM,
Protein_MMP9, IL18R1
VNN1, NCR1, IL10alpha, ARG2, IL6,	0.81	0.84	0.79
LY96, CReactiveProtein, JAK2, TGFBI,
SOCS3, CRTAP, ITGAM, IRAK4, PRV1
TNFSF13B, CReactiveProtein, INSL3,	0.81	0.78	0.84
CEACAM1, Beta2Microglobulin, CD86,
IL6, JAK2, ApolipoproteinCIII, IL18R1,
ANXA3, PSTPIP2, SOD2, IL1RN
IRAK2, FCGR1A, Gene_MMP9, BCL2A1,	0.81	0.78	0.84
TGFBI, PSTPIP2, CEACAM1, GADD45A,
CCL5, TNFSF13B, ARG2, IL8, TIFA,
IL18R1

In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use any one of the subsets of biomarkers listed in Table O. The subsets of biomarkers listed in Table O were identified in the computational experiments described in Section 6.14.5, below, in which 4600 random subcombinations of the biomarkers listed in Table I were tested. Table O lists some of the biomarker sets that provided high accuracy scores against the validation population described in Section 6.14.5. Each row of Table O lists a single set of biomarkers that can be used in the methods and kits respectively referenced in Sections 5.2 and 5.3. In other words, each row of Table O describes a set of biomarkers that can be used to discriminate between sepsis and SIRS subjects. In some embodiments, nucleic acid forms of the biomarkers listed in Table O are used in the methods and kits respectively referenced in Sections 5.2 and 5.3. In some embodiments, protein forms of the biomarkers listed in Table O are used. In some embodiments, some of the biomarkers in a biomarker set from Table O are in protein form and some of the biomarkers in the same biomarker set from Table O are in nucleic acid form in the methods and kits respectively referenced in Sections 5.2 and 5.3.

In some embodiments, a given set of biomarkers from Table O is used with the addition of one, two, three, four, five, six, seven, eight, or nine or more additional biomarkers from any one of Table 30, 31, 32, 33, 34, or 36 that are not within the given set of biomarkers from Table O. In Table O, accuracy, specificity, and sensitivity are described with reference to T₋₃₆ time point data described in Section 6.14.6, below.

TABLE O
Exemplary sets of biomarkers used in the methods or kits referenced in
Sections 5.2 and 5.3
BIOMARKER SET	ACCURACY	SPECIFICITY	SENSISTIVITY
SOCS3, ApolipoproteinCIII, NCR1	0.81	0.75	0.85
IL8, PRV1, CEACAM1	0.8	0.79	0.8
PSTPIP2, TLR4, GADD45B	0.8	0.72	0.87
ARG2, PRV1, MKNK1	0.79	0.71	0.85
CD86, SOCS3, TLR4	0.79	0.74	0.82
PRV1, GADD45B, TNFSF13B, ITGAM	0.83	0.73	0.91
PRV1, ApolipoproteinCIII, FCGR1A,	0.81	0.78	0.84
LDLR
TNFRSF6, MAP2K6, PRV1, ANKRD22	0.81	0.77	0.85
PRV1, ARG2, CD86, CEACAM1	0.81	0.8	0.82
GADD45B, CReactiveProtein, PRV1, CD86	0.81	0.73	0.88
GADD45B, TNFSF13B, FAD104, PFKFB3	0.81	0.73	0.86
PRV1, FAD104, IL18R1, MCP1	0.8	0.69	0.88
PRV1, IRAK2, PSTPIP2, ANXA3	0.8	0.68	0.87
FCGR1A, JAK2, MKNK1, PRV1	0.8	0.65	0.91
IL10, TNFSF13B, GADD45B, CEACAM1	0.79	0.73	0.85
Beta2Microglobulin, GADD45B, ARG2,	0.81	0.73	0.88
TNFSF13B, OSM
CD86, BCL2A1, PSTPIP2, PRV1, JAK2	0.8	0.71	0.89
GADD45A, GADD45B, CSF1R, MAP2K6,	0.8	0.69	0.88
PSTPIP2
AlphaFetoprotein, CReactiveProtein,	0.8	0.76	0.82
GADD45B, MAPK14, ANXA3
PRV1, FCGR1A, NCR1, CReactiveProtein,	0.8	0.74	0.84
TNFRSF6
MAPK14, CSF1R, OSM, IL1RN, TLR4	0.8	0.74	0.84
IRAK4, MAPK14, GADD45B, TNFSF13B,	0.8	0.71	0.86
CSF1R
ITGAM, ANXA3, Beta2Microglobulin,	0.79	0.76	0.82
PRV1, IRAK2
NCR1, MCP1, PRV1, CD86, FCGR1A	0.79	0.72	0.86
CRTAP, Beta2Microglobulin, TDRD9,	0.79	0.65	0.91
GADD45A, PRV1
PRV1, PFKFB3, FCGR1A, TIFA,	0.79	0.73	0.84
ANKRD22
PRV1, ApolipoproteinCIII, FCGR1A,	0.79	0.72	0.85
Protein_MMP9, TIMP1
FCGR1A, IRAK2, TNFSF13B, OSM,	0.84	0.79	0.89
CRTAP, PFKFB3
ANXA3, CEACAM1, PRV1, OSM, MCP1,	0.81	0.77	0.84
CCL5
IRAK4, TNFSF10, MCP1, PRV1, MKNK1,	0.81	0.75	0.84
SOCS3
TGFBI, CEACAM1, CD86, MAPK14,	0.8	0.76	0.83
LDLR, PRV1
MCP1, GADD45B, CEACAM1, TIMP1,	0.8	0.76	0.83
MAP2K6, IFNGR1
LY96, PRV1, MCP1, IRAK2, CD86,	0.8	0.76	0.83
TNFSF10
BCL2A1, PRV1, LDLR, TNFSF10,	0.8	0.73	0.85
IL18R1, SOCS3
SOCS3, ApolipoproteinCIII, FCGR1A,	0.79	0.7	0.87
TNFSF13B, IFNGR1, Beta2Microglobulin
ARG2, PSTPIP2, TNFRSF6, GADD45B,	0.79	0.82	0.77
MAPK14, TIMP1
NCR1, IL8, FCGR1A, IL1RN,	0.79	0.73	0.84
ApolipoproteinCIII, IFNGR1
LDLR, MAP2K6, PRV1, TIMP1, HLA-	0.79	0.72	0.85
DRA, CCL5
TIFA, GADD45B, HLA-DRA, CEACAM1,	0.79	0.74	0.83
OSM, ARG2
TIMP1, GADD45A, MKNK1, SOCS3,	0.79	0.73	0.83
LDLR, TNFSF10
SOD2, LY96, PRV1, FAD104, BCL2A1,	0.79	0.72	0.83
GADD45A
CEACAM1, BCL2A1, IRAK4, LDLR,	0.79	0.69	0.85
TIFA, IL10alpha
TNFSF10, TIFA, GADD45B, ANXA3,	0.78	0.65	0.88
BCL2A1, TNFRSF6
Beta2Microglobulin, TIMP1, GADD45A,	0.78	0.79	0.77
CRTAP, FAD104, GADD45B
ApolipoproteinCIII, IL18R1, CSF1R,	0.78	0.72	0.83
LDLR, FCGR1A, MCP1
MKNK1, GADD45B, IL1RN, NCR1, IL10,	0.78	0.71	0.83
LDLR
CD86, IL10, IFNGR1, SOCS3, TDRD9,	0.78	0.7	0.85
MCP1
PRV1, SOD2, INSL3, TIFA, IRAK2, MCP1	0.78	0.7	0.84
AlphaFetoprotein, Protein_MMP9,	0.83	0.79	0.87
ANKRD22, HLA-DRA, MAP2K6,
GADD45B, CEACAM1
TNFSF13B, OSM, PRV1, CSF1R, IFNGR1,	0.83	0.79	0.85
TNFRSF6, FCGR1A
FCGR1A, CCL5, TNFSF13B,	0.81	0.83	0.8
Gene_MMP9, IL6, MAP2K6, OSM
GADD45B, IL1RN, Beta2Microglobulin,	0.81	0.68	0.91
VNN1, PRV1, CD86, IL10
IL8, TIFA, IL18R1, SOD2, CSF1R,	0.8	0.81	0.8
FAD104, PRV1
MAP2K6, SOD2, IL18R1, LDLR, ANXA3,	0.8	0.78	0.82
CD86, GADD45B
ANKRD22, PRV1, TIMP1, NCR1,	0.8	0.75	0.84
GADD45A, FCGR1A, TNFSF13B
IL10alpha, CRTAP, IL10, TIMP1, TIFA,	0.8	0.73	0.87
PRV1, ARG2
TNFRSF6, TLR4, LY96, CSF1R,	0.8	0.7	0.88
GADD45B, CCL5, INSL3
TDRD9, ANXA3, TNFSF10, TNFRSF6,	0.8	0.68	0.9
PRV1, CCL5, IFNGR1
CD86, GADD45B, CReactiveProtein,	0.8	0.82	0.78
LDLR, CCL5, FAD104, IL8
IRAK4, TGFBI, PRV1, CEACAM1,	0.8	0.75	0.83
IFNGR1, PSTPIP2, TLR4
OSM, Gene_MMP9, TLR4, TDRD9, CCL5,	0.8	0.72	0.84
CRTAP, HLA-DRA
CRTAP, CEACAM1, FAD104, GADD45A,	0.79	0.72	0.84
PRV1, MAP2K6, TNFSF10
TNFRSF6, MKNK1, SOD2, TGFBI, MCP1,	0.79	0.72	0.86
GADD45B, ANKRD22
TIMP1, BCL2A1, TNFSF10, PRV1, HLA-	0.79	0.7	0.86
DRA, CRTAP, PFKFB3
INSL3, ANXA3, Beta2Microglobulin,	0.79	0.7	0.86
GADD45B, TNFRSF6, ANKRD22, LDLR
TIFA, GADD45B, HLA-DRA, CD86, IL10,	0.79	0.72	0.83
IL10alpha, MCP1
FCGR1A, CReactiveProtein, BCL2A1,	0.79	0.71	0.83
GADD45B, PRV1, PFKFB3, MAP2K6
IL8, INSL3, ANKRD22, TNFSF10, HLA-	0.79	0.7	0.85
DRA, PFKFB3, CSF1R
IL10alpha, MCP1, SOD2, TNFSF13B,	0.78	0.75	0.81
CRTAP, MAP2K6, PRV1
FAD104, SOD2, LY96, IL8, IRAK4, PRV1,	0.78	0.73	0.83
Protein_MMP9
MAPK14, OSM, PRV1, CRTAP,	0.78	0.7	0.85
IL10alpha, MKNK1, IFNGR1
OSM, AlphaFetoprotein, IFNGR1, SOD2,	0.78	0.73	0.82
GADD45A, CEACAM1, MKNK1
IL18R1, TDRD9, INSL3, JAK2,	0.78	0.7	0.85
Protein_MMP9, TNFRSF6, NCR1
IFNGR1, CEACAM1, JAK2, SOD2, HLA-	0.83	0.82	0.84
DRA, MAPK14, PRV1, VNN1
NCR1, IRAK2, MAP2K6,	0.83	0.83	0.82
CReactiveProtein, FCGR1A, ARG2, CD86,
SOCS3
GADD45B, ARG2, GADD45A, IL10alpha,	0.81	0.75	0.84
TDRD9, PFKFB3, CReactiveProtein, OSM
PRV1, ITGAM, IL1RN, MAPK14,	0.81	0.74	0.85
TNFSF10, SOD2, ARG2, PFKFB3
TNFRSF6, Beta2Microglobulin, PSTPIP2,	0.81	0.73	0.87
IL8, SOCS3, GADD45B, CRTAP, IFNGR1
CReactiveProtein, LY96, MAP2K6,	0.8	0.78	0.82
IL18R1, INSL3, OSM, CSF1R, IL6
ITGAM, PRV1, MAP2K6, IL8, OSM,	0.8	0.74	0.86
SOD2, IRAK4, CCL5
CReactiveProtein, OSM, PSTPIP2,	0.8	0.73	0.85
TNFSF10, ANKRD22, TDRD9, INSL3,
CD86
ANKRD22, CD86, PRV1, ANXA3, IL10,	0.79	0.81	0.78
TNFSF13B, TIFA, AlphaFetoprotein
ApolipoproteinCIII, MKNK1, FCGR1A,	0.79	0.75	0.82
PSTPIP2, VNN1, TNFRSF6,
AlphaFetoprotein, OSM
PRV1, CCL5, PFKFB3, TNFSF13B,	0.79	0.74	0.83
TIMP1, LDLR, ANKRD22, MAP2K6
ARG2, VNN1, ANKRD22, IFNGR1,	0.79	0.74	0.85
IL1RN, CD86, FAD104, GADD45B
IL10, PFKFB3, NCR1, TNFSF13B, MCP1,	0.79	0.7	0.86
MAPK14, PRV1, TIMP1
ApolipoproteinCIII, INSL3, IL10alpha,	0.79	0.74	0.83
FCGR1A, IL1RN, IL6, TNFRSF6, IL8
IL10, FAD104, CCL5, SOCS3, CD86,	0.79	0.79	0.78
HLA-DRA, LDLR, GADD45A
PFKFB3, CReactiveProtein, MAPK14,	0.79	0.74	0.81
TNFSF10, BCL2A1, ITGAM, IL10alpha,
TDRD9
Beta2Microglobulin, TNFSF13B,	0.78	0.73	0.82
ANKRD22, MCP1, TDRD9, IRAK4,
TIMP1, OSM
PSTPIP2, MAP2K6, AlphaFetoprotein,	0.78	0.69	0.84
TDRD9, PFKFB3, IL8, ANXA3, PRV1
TIFA, AlphaFetoprotein, PRV1, IL18R1,	0.78	0.68	0.87
Gene_MMP9, VNN1, TDRD9, TNFRSF6
IRAK2, FAD104, PRV1, GADD45A, TIFA,	0.78	0.72	0.83
MCP1, TIMP1, SOD2
IL6, CSF1R, MAP2K6, ANXA3, MCP1,	0.78	0.72	0.82
PRV1, ITGAM, AlphaFetoprotein
CCL5, IL10alpha, GADD45B, LDLR,	0.78	0.69	0.84
PSTPIP2, CD86, HLA-DRA, TLR4
LDLR, CRTAP, NCR1, TNFRSF6,	0.78	0.69	0.84
ApolipoproteinCIII, MAPK14, FCGR1A,
IRAK2
TGFBI, ANXA3, IL18R1, MAP2K6,	0.78	0.67	0.87
FCGR1A, IL10, OSM, PRV1
NCR1, JAK2, ANKRD22, IL1RN, ANXA3,	0.82	0.78	0.86
LDLR, CD86, IFNGR1, OSM
CSF1R, TDRD9, FAD104, TNFSF10,	0.82	0.79	0.84
OSM, LDLR, MAPK14, TIFA, BCL2A1
TNFSF10, IFNGR1, TNFRSF6, GADD45B,	0.82	0.75	0.87
CCL5, TNFSF13B, ANXA3, JAK2, PRV1
TNFSF13B, CD86, TIFA, SOCS3,	0.81	0.68	0.91
GADD45B, ARG2, TNFSF10, IRAK4,
IL10
FCGR1A, PSTPIP2, CEACAM1, IL1RN,	0.81	0.79	0.83
FAD104, IL6, INSL3, CSF1R, PRV1
IL1RN, SOD2, TGFBI, ApolipoproteinCIII,	0.8	0.83	0.78
JAK2, CEACAM1, IRAK2, IFNGR1, OSM
TDRD9, CD86, Protein_MMP9, TNFRSF6,	0.8	0.78	0.82
SOCS3, MCP1, AlphaFetoprotein, TIFA,
INSL3
BCL2A1, TGFBI, TLR4, IL8, LDLR,	0.8	0.77	0.83
ANKRD22, TNFSF13B, IL10, GADD45B
TNFSF13B, AlphaFetoprotein, TDRD9,	0.8	0.73	0.86
MAPK14, SOCS3, ANXA3, IL1RN,
CRTAP, TNFRSF6
IL6, TNFRSF6, MCP1, JAK2, GADD45A,	0.8	0.75	0.84
TIFA, ARG2, FCGR1A, ANKRD22
PSTPIP2, ANXA3, MCP1, FAD104, PRV1,	0.8	0.73	0.86
ANKRD22, NCR1, HLA-DRA, FCGR1A
IL8, PRV1, TDRD9, Beta2Microglobulin,	0.8	0.73	0.86
IL10alpha, VNN1, INSL3, TIFA, CSF1R
GADD45B, TNFRSF6, OSM, IRAK4,	0.8	0.71	0.88
AlphaFetoprotein, IL1RN, TNFSF13B,
MCP1, FAD104
ANKRD22, OSM, INSL3, IFNGR1,	0.8	0.69	0.89
MKNK1, GADD45B, TDRD9, MAP2K6,
IRAK4
NCR1, JAK2, ANKRD22, IL1RN, ANXA3,	0.82	0.78	0.86
LDLR, CD86, IFNGR1, OSM
ApolipoproteinCIII, ANXA3, IL18R1,	0.84	0.73	0.93
PRV1, CD86, LDLR, TDRD9,
CReactiveProtein, MAP2K6, CSF1R,
CRTAP
CCL5, Protein_MMP9, NCR1, PRV1,	0.82	0.74	0.88
TNFRSF6, TGFBI, HLA-DRA, FCGR1A,
IFNGR1, CSF1R, MCP1
GADD45B, CSF1R, IL1RN, PSTPIP2,	0.81	0.81	0.81
PRV1, ApolipoproteinCIII, ARG2, SOCS3,
FAD104, ITGAM, TIMP1
JAK2, MKNK1, CRTAP, GADD45B,	0.81	0.79	0.83
OSM, INSL3, TIMP1, TIFA, TNFRSF6,
AlphaFetoprotein, CD86
ApolipoproteinCIII, CD86, FCGR1A,	0.81	0.73	0.88
ARG2, GADD45B, IL8, CRTAP, IFNGR1,
TIMP1, ANXA3, HLA-DRA
MCP1, IL8, TNFSF13B, AlphaFetoprotein,	0.81	0.78	0.83
LDLR, Protein_MMP9, JAK2, FAD104,
IRAK2, TNFRSF6, GADD45B
TLR4, NCR1, CCL5, IL6,	0.81	0.76	0.85
CReactiveProtein, IRAK4,
AlphaFetoprotein, FCGR1A,
ApolipoproteinCIII, GADD45B, PRV1
ANKRD22, OSM, VNN1, LDLR,	0.8	0.81	0.8
ApolipoproteinCIII, IL1RN, SOCS3,
MAPK14, GADD45B, JAK2, ITGAM
NCR1, ARG2, GADD45B, GADD45A,	0.8	0.76	0.84
CD86, TNFSF10, CCL5, PSTPIP2,
Beta2Microglobulin, CRTAP, LDLR
SOCS3, JAK2, IL1RN, IFNGR1, CRTAP,	0.8	0.76	0.84
TIMP1, Protein_MMP9, VNN1, TNFRSF6,
CD86, ANKRD22
OSM, PSTPIP2, IL1RN, AlphaFetoprotein,	0.8	0.86	0.75
PRV1, IL6, LY96, IL18R1, CSF1R,
TNFSF13B, LDLR
IL10alpha, CReactiveProtein, TIFA, NCR1,	0.8	0.75	0.84
CRTAP, TGFBI, PFKFB3, LDLR, IRAK4,
GADD45B, TDRD9
ApolipoproteinCIII, ANXA3, IL18R1,	0.84	0.73	0.93
PRV1, CD86, LDLR, TDRD9,
CReactiveProtein, MAP2K6, CSF1R,
CRTAP

In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use at least two different biomarkers that each contain a probeset listed in any one of FIGS. 6, 14, 17, or 26. In a particular embodiment, a biomarker profile comprises at least two different biomarkers that each contain one of the probesets listed in any one of FIGS. 6, 14, 17, or 26, biomarkers that each contain the complement of one of the probesets of any one of FIGS. 6, 14, 17, or 26, or biomarkers that each contain an amino acid sequence encoded by a gene that either contains one of the probesets of any one of FIGS. 6, 14, 17, or 26, or the complement of one of the probesets of any one of FIGS. 6, 14, 17, or 26. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example, amplified nucleic acid, or proteins. The biomarker profile further comprises a respective corresponding feature for the at least two biomarkers. Generally, the at least two biomarkers are derived from at least two different genes. In the case where a biomarker is based upon a gene that includes the sequence of a probeset listed in any one of FIGS. 6, 14, 17, or 26, the biomarker can be, for example, a transcript made by the gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein encoded by a gene that includes a probeset sequence described in any one of FIGS. 6, 14, 17, or 26, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In some embodiments, the biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9. or 10 different biomarkers that each contains a probeset listed in any one of FIGS. 6, 14, 17, or 26.

In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use at least two different biomarkers listed in any one of FIGS. 39, 43, 52, 53, or 56. In a particular embodiment, the biomarker profile comprises at least two different biomarkers listed in any one of FIGS. 39, 43, 52, 53, or 56. The biomarker profile further comprises a respective corresponding feature for the at least two biomarkers. Generally, the at least two biomarkers are derived from at least two different genes. In the case where a biomarker in the at least two different biomarkers is listed in any one of FIGS. 39, 43, 52, 53, or 56, the biomarker can be, for example, a transcript made by the listed gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein encoded by a gene listed in any one of FIGS. 39, 43, 52, 53, or 56, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In accordance with this embodiment, the biomarker profiles of the present invention can be obtained using any standard assay known to those skilled in the art, or in an assay described herein, to detect a biomarker. Such assays are capable, for example, of detecting the products of expression (e.g., nucleic acids and/or proteins) of a particular gene or allele of a gene of interest (e.g., a gene disclosed in Table 30). In one embodiment, such an assay utilizes a nucleic acid microarray. In some embodiments, the biomarker profile comprises at least two different biomarkers from any one of FIGS. 39, 43, 52, 53, or 56. In some embodiments, the biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 different biomarkers from any one of FIGS. 39, 43, 52, 53, or 56.

In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use specific biomarkers containing probes from any one of the probeset collections listed in Table P. In a particular embodiment, a biomarker profile comprises at least two different biomarkers that each contain one of the probesets listed in any one of the probeset collections of Table P, biomarkers that each contain the complement of one of the probesets from any one of the probeset collections of Table P, or biomarkers that each contain an amino acid sequence encoded by a gene that either contains one of the probesets from any one of the probeset collections of Table P, or the complement of one of the probesets of any one of the probeset collections of Table P. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example, amplified nucleic acid, or proteins. The biomarker profile further comprises a respective corresponding feature for the at least two biomarkers. Generally, the at least two biomarkers are derived from at least two different genes. In the case where a biomarker is based upon a gene that includes the sequence of a probeset listed in any one of the probeset collections of Table P, the biomarker can be, for example, a transcript made by the gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein encoded by a gene that includes a probeset sequence from any one of the probeset collections listed in Table P, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In some embodiments, the biomarker profile comprises at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 different biomarkers that each contains a probeset from any one of probeset collections listed in Table P.

TABLE P
Exemplary probesets
PROBESET
COLLECTION IDENTITY OF PROBE IN PROBESET COLLECTION
1          X206513_at, X214681_at, X235359_at, X221850_x_at, X213524_s_at,
           X225656_a, X200881_s_at, X229743_at, X215178_x_at, X215178_x_at,
           X216841_s_at, X216841_at, X244158_at, X238858_at, X205287_s_at,
           X233651_s_at, X229572_at, X214765_s_at.
2          X206513_at, X213524_s_at, X200881_s_at, X218992_at, X238858_at,
           X221123_x_at, X228402_at, X230585_at, X209304_x_at, X214681_at.
3          X204102_s_at, X236013_at, X213668_s_at, X1556639_at, X218220_at,
           X207860_at, X232422_at, X218578_at, X205875_s_at, X226043_at,
           X225879_at, X224618_at, X216316_x_at, X243159_x_at,
           X202200_s_at, X201936_s_at, X242492_at, X216609_at, X214328_s_at,
           X228648_at, X223797_at, X225622_at, X205988_at, X201978_s_at,
           X200874_s_at, X210105_s_at, X203913_s_at, X204225_at, X227587_at,
           X220865_s_at, X206682_at, X222664_at, X212264_s_at, X219669_at,
           X221971_x_at, X1554464_a_at, X242590_at, X227925_at,
           X221926_s_at, X202101_s_at, X211078_s_at, X44563_at, X206513_at,
           X215178_x_at, X235359_at, X225656_at, X244158_at, X214765_s_at,
           X229743_at, X214681.

In some embodiments, the methods or kits respectively described or referenced in Section 5.2 and Section 5.3 use at least two different biomarkers listed in any one of the biomarker sets in Table Q. In a particular embodiment, the biomarker profile comprises at least two different biomarkers listed in any one of the biomarker sets in Table Q. The biomarker profile further comprises a respective corresponding feature for the at least two biomarkers listed in any of the biomarker sets in Table Q. Generally, the at least two biomarkers are derived from at least two different genes. In the case where a biomarker in the at least two different biomarkers is listed in any one of biomarker sets of Table Q. the biomarker can be, for example, a transcript made by the listed gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein encoded by a gene listed in any one of the biomarker sets in Table Q, or a discriminating fragment of the protein, or an indication of any of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In accordance with this embodiment, the biomarker profiles of the present invention can be obtained using any standard assay known to those skilled in the art, or in an assay described herein, to detect a biomarker. Such assays are capable, for example, of detecting the products of expression (e.g., nucleic acids and/or proteins) of a particular gene or allele of a gene of interest (e.g., a gene disclosed in any on of the biomarker sets of Table Q). In one embodiment, such an assay utilizes a nucleic acid microarray. In some embodiments, a biomarker profile comprising at least 2 or 3 different biomarkers from any one of the biomarker sets of Table Q is used.

TABLE Q
Exemplary biomarker sets
BIOMARKER
SET NUMBER IDENTITY OF BIOMARKERS
1          IL18R1, ARG2, FCGR1A
2          ITGAM, TGFB1, TLR4, TNFSF, FCGR1A, IL18R1,
           ARG2
3          ARG2, TGFB1, MMP9, TLR4, ITGAM, IL18R1,
           TNFSF, IL1RN, FCGR1A
4          OSM, GADD45B, ARG2, IL18R1, TDRD9, PFKFB3,
           MAPK14, PRV1, MAP2K6, TNFRSF6, FCGR1A,
           INSL3, LY96, PSTPIP2, ANKRD22, TNFSF10,
           HLA-DRA, FNDC3B, TIFA, GADD45A, VNN1,
           ITGAM, BCL2A1, TLR4, TNFSF13B, SOCS3,
           IL1RN, CEACAM1, SOD2
5          ARG2, GADD45B, OSM, LY96, INSL3, ANKRD22,
           MAP2K6, PSTPIP2, TGFB1, GADD45B, TDRD9,
           MAP2K6, OSM, TNFSF10, ANKRD22

6. EXAMPLES

The following examples are representative of the embodiments encompassed by the present invention and in no way limit the subject embraced by the present invention. In the following examples, data was collected at twenty-four hour time intervals from each subject in a population of subjects. The population included two subject types. The first subject type was those that initially had SIRS and developed sepsis at a terminal time point in the analysis. The second subject type was those that initially had SIRS and did not develop sepsis at the terminal time point in the analysis. For subjects that initially had SIRS and developed sepsis, a T₋₁₂ time point was defined as the time frame immediate prior to the onset of clinically-diagnosed sepsis. In practice, the T₋₁₂ time point for each respective sepsis subject was the day the last blood sample was collected from the respective subject prior to being diagnosed with sepsis.

For each time point, two types of analyses were performed, a static and a baseline analysis. In the static analysis, only data from a single time point was considered. In particular, univariate and/or multivariate techniques were used to identify biomarkers whose abundance on corresponding microarray probesets on the U133 plus 2.0 (Affymetrix, Santa Clara, California) discriminate between those subjects that develop sepsis from those subjects that do not develop sepsis during the study. To illustrate, consider the case in which there are two subjects in the population, subject A, who develops sepsis shortly after time period T₋₁₂, and subject B, who does not develop sepsis in any of the observed time points. In the static analysis, microarray biomarker abundance data from the two subjects that was collected at a particular single time point is evaluated in order to identify those biomarkers that have different abundance levels in the two subjects, as determined by a U133 plus 2.0 microarray experiment. In fact, in the present examples, a whole population of subjects of type A and type B are evaluated and parametric and/or nonparametric statistical techniques are used to identify those biomarkers whose abundance levels discriminate between subjects that develop sepsis at some point during the observation period and subjects that do not develop sepsis during the observation period. Here, an observation period refers to a time period that was a matter of hours, days, or weeks.

In addition to static analyses, baseline analyses were performed in the examples below. In a baseline analysis, rather than identifying biomarkers whose corresponding features (e.g. abundance value) at a single time point discriminate between sepsis subjects (subjects that develop sepsis at some point during the observation time period) and subjects that do not develop sepsis during the observed time frame, biomarkers whose change in abundance value across two or more time points discriminates between the two populations types were identified. For example, again consider subject A, who develops sepsis shortly after time period T₁₂, and subject B, who does not develop sepsis in any of the observed time points. In the basesline analysis, what were needed are biomarker abundance values for each subject from two different time points (e.g., time point 1 and time point 2). For each respective biomarker considered, the difference in the abundance of the biomarker at the two different time points was computed. These differential abundances from each of the subjects is then used to determine which corresponding biomarkers, expressed as a differential between two different time points, discriminate between subjects that develop sepsis during the observation period and subjects that do not develop sepsis during the observation time period.

6.1 Data Collection

SIRS positive subjects admitted to an ICU were recruited for the study. Subjects were eighteen years of age or older and gave informed consent to comply with the study protocol. Subjects were excluded from the study if they were (i) pregnant, (ii) taking antibiotics to treat a suspected infection, (iii) were taking systemic corticosteroids (total dosage greater than 100 mg hydrocortisone or equivalent in the past 48 hours prior to study entry), (iv) had a spinal cord injury or other illness requiring high-dose corticosteroid therapy, (v) pharmacologically immunosuppressed (e.g., azathioprine, methotrexate, cyclosporin, tacrolimus, cyclophosphamide, etanercept, anakinra, infliximab, leuflonamide, mycophenolic acid, OKT3, pentoxyphylin, etc.), (vi) were an organ transplant recipient, (vii) had active or metastatic cancer, (viii) had received chemotherapy or radiation therapy within 8 weeks prior to enrollment, and/or (ix) had taken investigational use drugs within thirty days prior to enrollment.

In the study SIRS criteria were evaluated daily. APACHE II and SOFA scoring was performed following ICU admission. APACHE II is a system for rating the severity of medical illness. APACHE stands for “Acute Physiology And Chronic Health Evaluation,” and is most frequently used to predict in-hospital death for patients in an intensive care unit. See, for example, Gupta et al., 2004, Indian Journal of Medical Research 119, 273-282, which is hereby incorporated herein by reference in its entirety. SOFA is a test to measure the severity of sepsis. See, for example, Vincent et al., 1996, Intensive Care Med. 22, 707-710, which is hereby incorporated herein by reference in its entirety. Patients were monitored daily for up to two weeks for clinical suspicion of sepsis including, but not limited to, any of the following signs and symptoms:

• • pneumonia: temperature >38.3° C. or <36° C. +white blood cell count (WBC)>12,000/mm³ or <4,000/mm³+new-onset of purulent sputum+new or progressive infiltrate on chest radiograph (3 out of 4 findings);
  • wound infection: temperature >38.3° C. or <36° C.+pain+erythema+purulent discharge (3 out of 4 findings);
  • urinary tract infection: temperature >38.3° C. or WBC>12,000/mm³ or <4,000/mm³+bacteruria and pyuria (>10 WBC/hpf or positive leukocyte esterase) (all findings);
  • line sepsis: temperature >38.3° C. or <36° C.+erythema/pain/purulence at catheter exit site (3 out of 4 findings, including fever);
  • intra-abdominal abscess: temperature >38.3° C. or <36° C.+WBC >12,000/mm³ or <4,000/mm³+radiographic evidence of fluid collection (2 out of 3 criteria);
  • CNS Infection: temperature >38.3° C. or <36° C.+WBC>12,000/mm³ or <4,000/mm³+CSF pleocytosis via LP or Ventricular drainage.

Blood was drawn daily for a minimum of four consecutive days beginning within 24 hours following study entry. Patients were followed and blood samples were drawn daily for a maximum of fourteen consecutive days unless clinical suspicion of infection occurred. The maximum volume of blood drawn from any one subject did not exceed 210 mL over the course of a 14 day study maximum. Blood draws for the study were discontinued if the loss of blood posed risk to the patient as defined by physician's judgment. Each patient had two Paxgene (RNA) tubes drawn on each day. One tube was used for the microarray analysis described in Section 6.2. The other tube was used for the RT-PCR analysis described in Section 6.10.

6.2 Microarray Analysis

RNA was extracted from each blood sample described in Section 6.1, labeled, reversed transcribed to generate cDNA which was labeled, and the labeled cDNA was hybridized to Affymetrix (Santa Clara, California) U133 plus 2.0 human genome chips containing 54,675 probesets. To enhance detection sensitivity of the microarray, globin mRNA molecules were removed from the total RNA extracted from the blood samples using the methods described in. for example, U.S. Patent Publication 20050221310, filed Aug. 9, 2004, and Ser. No. 10/948,635, filed Sep. 24, 2004, both entitled “Methods of Enhancing Gene Expression Analysis,” each of which is incorporated by reference herein in its entirety. The U133 plus 2.0 has 62 probesets designed for special functions, such as measuring supplementally added transcripts. This leaves 54,613 probesets designed specifically for the detection of human genes. The Affymetrix human genome U133 (HG-U133) set, consisting of two microarrays, contains almost 45,000 probesets representing more than 39,000 transcripts derived from approximately 33,000 human genes. This set design uses sequences selected from GenBank, dbEST, and RefSeq. As used herein, the abundance value measured for each of the biomarkers that bind to these probesets is referred to as a feature. The examples below discuss abundance values of biomarkers that bind to particular probesets in the U133 plus 2.0 human genome chip.

6.3 Static T₋₃₆ Data Analysis

In one experiment, a T₋₃₆ static analysis was performed. In the T₋₃₆ static analysis, biomarkers features are determined using a specific blood sample, designated the T₋₃₆ blood sample, from each subject in a training population. The identity of this specific blood sample from each respective subject in the training population is dependent upon whether the subject was a SIRS subject (did not develop sepsis during the observation period) or was a sepsis subject (did develop sepsis during the observation period). In the case of a sepsis subject, the T₋₃₆ sample is defined as the second to last blood sample taken from the subject before the subject acquired sepsis. Identification of T₋₃₆ samples in the SIRS subjects in the training population was more discretionary than for the sepsis counterpart subjects because there was no significant event in which the SIRS subjects became septic. Because of this, the identity of the T₋₃% samples for the sepsis subjects in the training population was used to identify the T₋₃₆ samples in the SIRS subjects in the training population. Specifically, T₋₃₆ time points (blood samples) for SIRS subjects in the training population were identified by “time-matching” a septic subject and a SIRS subject. For example, consider the case in which a subject that entered the study became clinically-defined as septic on their sixth day of enrollment. For this subject, T₋₃₆ is day four of the study, and the T₋₃₆ blood sample is the blood sample that was obtained on day four of the study. Likewise, T₋₃₆ for the SIRS subject that was matched to this sepsis subject is deemed to be day four of the study on this paired SIRS subject.

Although SIRS subjects did not progress on to develop sepsis, they did have changes in their expressed genes (and proteins, etc.) over time. Thus, a one-to-one time matching of sepsis subjects to SIRS subjects for the purpose of obtaining a relevant set of T₋₃₆ blood samples from the SIRS subjects was sought in the manner described above. Just as subjects who progressed to become septic did so at varying rates, this time matching was done to mimic feature variability in SIRS subjects. While time matching between arbitrary pairs of SIRS and sepsis subjects was done to identify T₋₃₆ blood samples for as many of the SIRS subjects in the training population as possible, in some instances, T₋₃₆ samples from SIRS subjects had to be selected from time points based on sample availability.

For the T₋₃₆ static analysis there were 54,613 biomarkers measured on 84 samples for a total of 84 corresponding microarray experiments from 84 different subjects. Each sample was collected from a different subject in the population of 84 subject. Of the 54,613 probesets measured in each microarray experiment, 30,464 were transformed by log transformations. The log transformation is described in Draghici, 2003, Data Analysis Toolsfor DNA Microarrays, Chapman & Hall/CRC, Boca Raton, pp. 309-311, which is hereby incorporated by reference in its entirety. Further, of the 54,613 probesets in each microarray experiment, 2317 were transformed by a square root transformation. The square root transformation is described in Ramdas, 2001, Genome Biology 2, 47.1-47.7, which is hereby incorporated by reference in its entirety. The remaining 21,832 probesets in each microarray experiment were not transformed.

The 84 member population was initially split into a training set (n=64) and a validation set (n=20). The training set was used to estimate the appropriate classification algorithm parameters while the trained algorithm was applied to the validation set to independently assess performance. Of the 64 training samples, 35 were Sepsis, meaning that the subjects developed sepsis at some point during the observation time period, and 29 were SIRS, meaning that they did not develop sepsis during the observation time period. Table I provides distributions of the race, gender and age for these samples.

TABLE 1
Distributions of the race, gender, and age for the training data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	10	13	1
	Female	0	10	1
SIRS	Male	5	17	0
	Female	0	7	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	42	41	80
SIRS	18	43	40	90

For the 20 validation samples, 9 were Sepsis and 11 were SIRS. Table 2 provides distributions of the race, gender and age for these samples.

TABLE 2
Distributions of the race, gender, and age for the validation data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	1	7	0
	Female	0	3	0
SIRS	Male	0	6	0
	Female	0	3	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	41.8	43	81
SIRS	19	47.7	51	77

Each sample in the training data was randomly assigned to one of ten groups used for cross-validation. The number of training samples in these groups ranged from 6 to 7. The samples were assigned in way that attempted to balance the number of sepsis and SIRS samples across folds. As described in more detail below, several different methods were used to judge whether select biomarkers, which bind to particular probesets in the microarray, discriminate between the Sepsis and SIRS groups.

Wilcoxon and Q-value tests. The first method used to identify discriminating biomarkers was a Wilcoxon test (unadjusted). The Wilcoxon test is a distribution-free test is resistant to extreme values. The Wilcoxon test is described in Agresti, 1996, An Introduction to Categorical Data Analysis, John Wiley & Sons, Inc, New York, Chapter 2, which is hereby incorporated by reference in its entirety. The Wilcoxon test produces a p value. The abundance value for a given biomarker from all samples in the training data is subjected to the Wilcoxon test. The Wilcoxon test considers both group classification (sepsis versus SIRS) and abundance value in order to compute a p value for the given biomarker. The p value provides an indication of how well the abundance value for the given biomarker across the samples collected in the training set discriminates between the sepsis and SIRS state. When the p value is less than a specific confidence level, such as 0.05, an inference is made that the biomarker discriminates between Sepsis and SIRS. There were 9520 significant biomarkers using this method (see Table 3).

The second method used to identify discriminating biomarkers was the Wilcoxon Test (adjusted). Due to the large number of biomarkers, 54613, and the relatively small number of samples, 84, there was a high risk of finding falsely significant biomarkers. An adjusted p-value was used to counter this risk. In particular, the method of Benjamini and Hochberg, 1995. J. R. Statist. Soc. B 57, pp 289-300, which is hereby incorporated by reference in its entirety, was used to control the false discovery rate. Here, the false discovery rate is defined as the number of biomarkers truly significant divided by the number of biomarkers declared significant. For example, if the adjusted p-value is less than 0.05, there is a 5% chance that the biomarker is a false discovery. Results using this test are reported in Table 3. There were 1618 significant biomarkers using this method (see Table 3). As used, herein, a biomarker is considered significant if the feature values corresponding to the biomarker have a p-value of less than 0.05 as determined by the Wilcoxon test (adjusted).

The third method used to identify discriminating biomarkers was the use of Q values. Q-values are described in Storey, 2002, J. R. Statist. Soc. B 64, Part 3, pp. 479-498, which is hereby incorporated by reference in its entirety. The biomarkers are ordered by their q-values and if a biomarker has a q-value of X, then this biomarker and all others more significant have a combined false discovery rate of X. However, the false discovery rate for any one biomarker may be much larger. There were 2431 significant markers using this method (see Table 3).

TABLE 3
Cumulative number of significant calls for the three methods.
Note that all 84 samples (training and validation)
were used to compare converters and nonconverters.
Missing biomarker values were not included in the analyses.
	≤1e−04	≤0.001	≤0.01	≤0.025	≤0.05	≤0.1	≤1
p-value	0	1362	4210	6637	9520	13945	54613
(unadjusted)
p-value	0	0	0	584	1618	3315	54613
(adjusted)
q-value	0	0	0	1055	2431	4785	54613

CART. In addition to analyzing the microarray data using Wilcoxon test and Q-value tests in order to identify biomarkers that discriminate between the sepsis and SIRS subpopulations in the training set, classification and regression tree (CART) analysis was used. CART is described in Section 5.5.1, above. Specifically, the data summarized above was used to predict the disease state by iteratively partitioning the data based on the best single-variable (feature of biomarker across training set) split of the data. In other words, at each stage of the tree building process, the biomarker whose abundance value across the training population best discriminates between the sepsis and SIRS population was invoked as a decision branch. Cross-validation was carried out, with the optimal number of splits estimated independently in each of the 10 iterations. The final tree is depicted in FIG. 1. In FIG. 1, decision 102 makes a decision based on the abundance of the biomarker that binds to X204319_s_at. If the biomarker that binds to X204319_s_at has an abundance that is greater than 2.331 units in a biological sample from a subject to be diagnosed (test biological sample), then control passes to decision 104. If, on the other hand, the biomarker that binds to probeset X204319_s_at has abundance that is less than 2.331 units in the test biological sample, decision control passes to decision 106. Decisions are made in this manner until a terminal leaf of the decision tree is reached, at which point diagnoses of sepsis or SIRS is made. The decision tree in FIG. 1 makes use of the biomarkers that bind to the following five probesets: X204319_s_at, X1562290_at, X1552501_a_at, X1552283_s_at, and X117_at.

FIG. 2 shows the distribution of the biomarkers that bind to the five probesets used in the decision tree between the sepsis and SIRS groups in the training data set. In FIG. 2, the top of each box denotes the 75^th percentile of the data across the training set and the bottom of each box denotes the 25^th percentile, and the median value for each biomarker across the training set is drawn as a line within each box. The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 4. From this confusion matrix. the overall accuracy was estimated to be 70.3% with a 95% confidence interval of 57.6% to 81.1%. The estimated sensitivity was 60% and the estimated specificity was 82.8%.

TABLE 4
Confusion matrix for training samples using
the cross-validated CART algorithm of FIG. 1.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	21	5
SIRS	14	24

For the 20 validation samples held back from training data set, the overall accuracy was estimated to be 70% with a 95% confidence interval of 45.7% to 88.1%, sensitivity 88.9% and specificity 54.5%. Table 5 shows the confusion matrix for the validation samples.

TABLE 5
Confusion matrix for validation samples using
the cross-validated CART algorithm of FIG. 1.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	8	5
SIRS	1	6

Random Forests. Another decision rule that can be developed using biomarkers of the present invention is a Random Forests decision tree. Random Forests is a tree based method that uses bootstrapping instead of cross-validation. For each iteration, a random sample (with replacement) is drawn and the largest tree possible is grown. Each tree receives a vote in the final class prediction. To fit a random forest, the number of trees (e.g. bootstrap iterations) is specified. No more than 500 were used in this example, but at least 50 are needed for a burn-in period. The number of trees was chosen based on the accuracy of the training data. For this data, 500 trees were used to train the algorithm (see FIG. 3). In FIG. 3, curve 302 is a smoothed estimate of overall accuracy as a function of tree number. Curve 304 is a smoothed curve of tree sensitivity as a function of tree number. Curve 306 is a smoothed curve of tree specificity as a function of tree number. Using this algorithm, 901 biomarkers had non-zero importance and were used in the model. The random forest algorithm gauges biomarker importance by the average reduction in the training accuracy. The biomarkers were ranked by this method and are shown in FIG. 4. In FIG. 4, the biomarkers are labeled by the name of the U133 plus 2.0 probeset to which they bind. The figure only reflects the 50 most important biomarkers found by using Random Forest analysis. However, 901 biomarkers were actually found to have discriminating significance. The random forest method uses a number of different decision trees. A biomarker is considered to have discriminating significance if it served as a decision branch of a decision tree from a significant random forest analysis. As used herein, a significant random forest analysis is one where the lower 95% confidence interval on accuracy by cross validation on a training data set is greater than 50% and the point estimate for accuracy on a validation set is greater than 65%.

The predicted confusion matrix for the training dataset using the decision tree developed using the Random Forest method is given in Table 6. From this confusion matrix, the overall accuracy was estimated to be 68.8% (confidence intervals cannot be computed when using the bootstrap accuracy estimate). The estimated sensitivity was 74.3% and the estimated specificity was 62.1%.

TABLE 6
Confusion matrix for training samples against
the decision tree developed using the Random
Forest method.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	18	9
SIRS	11	26

For the 20 validation samples held back from training, the overall accuracy was estimated to be 65% with a 95% confidence interval of 40.8% to 84.6%. sensitivity 66.7% and specificity 63.6%. Table 7 shows the confusion matrix for the validation samples.

TABLE 7
Confusion matrix for the 20 validation samples
against the decision tree developed using the
Random Forest method.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	6	4
SIRS	3	7

PAM. Yet another decision rule developed using the biomarkers of the present invention is predictive analysis of microarrays (PAM), which is described in Section 5.5.2, above. In this method, a shrinkage parameter that determines the number of biomarkers used to classify samples is specified. This parameter was chosen via cross-validation. There were no biomarkers with missing values. Based on cross-validation, the optimal threshold value was 2.07, corresponding to 258 biomarkers. FIG. 5 shows the accuracy across different thresholds. In FIG. 5, curve 502 is the overall accuracy (with 95% confidence interval bars). Curve 504 shows decision rule sensitivity as a function of threshold value. Curve 506 shows decision rule specificity as a function of threshold value. Using the threshold of 2.07, the overall accuracy for the training samples was estimated to be 73.4% with 95% a confidence interval of 61.4% to 82.8%. The estimated sensitivity was 79.3% and the estimated specificity was 68.6%.

TABLE 8
Confusion matrix for training samples using
cross-validated PAM algorithm
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	23	11
SIRS	6	24

For the twenty validation samples held back from training, the overall accuracy was estimated to be 70% with a 95% confidence interval of 45.7% to 88.1%, sensitivity 66.7% and specificity 72.7%. Table 9 shows the confusion matrix for the validation samples.

TABLE 9
Confusion matrix for training samples using
cross-validated PAM algorithm
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	6	3
SIRS	3	8

FIG. 6 shows the selected biomarkers, ranked by their relative discriminatory power, and their relative importance in the model. FIG. 6 only shows the fifty most important biomarkers found using the PAM analysis. However, 258 important biomarkers were found. The biomarkers in FIG. 6 are labeled based upon the U133 plus 2.0 probeset to which they bind.

FIG. 7 provides a summary of the CART, PAM, and random forests classification algorithm (decision rule) performance and associated 95% confidence intervals. Fifty distinct biomarkers were selected from across all the algorithms illustrated in FIG. 7. FIG. 8 illustrates the number of times that common biomarkers were selected across the techniques of Wilcoxon (adjusted), CART, PAM, and RF. FIG. 9 illustrates an overall ranking of biomarkers for the T₋₃₆ data set. For the selected biomarkers, the x-axis depicts the percentage of times that it was selected. Within the percentage of times that biomarkers were selected, the biomarkers are ranked. The biomarkers in FIG. 7 are labeled based upon the probeset (oligonucleotide identity) to which they bind.

6.4 Static T₋₁₂ Data Analysis

In another experiment, a T₋₁₂ static analysis was performed. In the T₋₁₂ static analysis, biomarkers features were measured using a specific blood sample, designated the T₋₁₂ blood sample, obtained from each subject in the training population. The identity of this specific blood sample from a given subject in the training population was dependent upon whether the subject was a SIRS subject (did not develop sepsis during the observation period) or a sepsis subject (did develop sepsis during the observation period). In the case of a sepsis subject, the T₋₁₂ sample was defined as the last blood sample taken from the subject before the subject acquired sepsis. Identification of T₋₁₂ samples in the SIRS subjects in the training population was more discretionary than for the sepsis counterpart subjects because there was no significant event in which the SIRS subjects became septic. Because of this, the identity of the T₋₁₂ samples for the sepsis subjects in the training population was used to identify the T₋₁₂ samples in the SIRS subjects in the training population. Specifically, T-?time points (blood samples) for SIRS subjects in the training population were identified by “time-matching” a septic subject and a SIRS subject. For example, consider the case in which a subject that entered the study became clinically-defined as septic on their sixth day of enrollment. For this subject, T₋₁ was day five of the study (1-24 hours prior to sepsis), and the T₋₂ blood sample was the blood sample that was obtained on day five of the study. Likewise, T₋₁₂ for the SIRS subject that was matched to this sepsis subject was deemed to be day five of study on this paired SIRS subject. While time matching between arbitrary pairs of SIRS and sepsis subjects was done to identify T₋₁₂ blood samples for as many of the SIRS subjects in the training population as possible, in some instances, T₋₁₂ samples from SIRS subjects had to be selected from the time points based on sample availability.

For the T₋₁ static analysis, there were 54,613 biomarkers measured on 90 samples for a total of 90 corresponding microarray experiments from 90 different subjects. Each sample was collected from a different member the population. Of the 54,613 probesets in each microarray experiment, 31,047 were transformed by log transformations. Further, of the 54,613 probesets in each microarray experiment, 2518 were transformed by a square root transformation. The remaining 21,048 probesets in each microarray experiment were not transformed.

The 90 member population was initially split into a training set (n=69) and a validation set (n=21). The training set was used to estimate the appropriate classification algorithm parameters while the trained algorithm was applied to the validation set to independently assess performance. Of the 69 training samples, 34 were labeled Sepsis, meaning that the subjects developed sepsis at some point during the observation time period, and 35 were SIRS, meaning that they did not develop sepsis during the observation time period. Table 10 provides distributions of the race, gender and age for these samples.

TABLE 10
Distributions of the race, gender, and age for the training data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	9	13	1
	Female	0	10	1
SIRS	Male	5	20	0
	Female	0	10	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	42.1	39	80
SIRS	18	44.1	40	90

For the 21 validation samples, 11 were labeled Sepsis and 10 were labeled SIRS. Table 11 provides distributions of the race, gender and age for these samples.

TABLE 11
Distributions of the race, gender, and age for the validation data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	0	7	0
	Female	0	3	0
SIRS	Male	2	6	0
	Female	0	3	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	43.3	40	81
SIRS	19	53	52	85

Each sample in the training data was randomly assigned to one of ten groups used for cross-validation. The number of training samples in these groups ranged from 6 to 8. The samples were assigned in way that attempted to balance the number of sepsis and SIRS samples across folds. As described in more detail below, several different methods were used to judge whether select biomarkers discriminate between the Sepsis and SIRS groups.

Wilcoxon and Q-value tests. The first method used to identify discriminating biomarkers was a Wilcoxon test (unadjusted). The abundance value for a given biomarker across the samples in the training data was subjected to the Wilcoxon test. The Wilcoxon test considers both group classification (sepsis versus SIRS) and abundance value in order to compute a p value for the given biomarker. The p value provides an indication of how well the abundance value for the given biomarker across the samples collected in the training set discriminates between the sepsis and SIRS state. The lower the p value, the better the discrimination. When the p value is less than a specific confidence level, such as 0.05, an inference is made that the biomarker discriminates between the sepsis and SIRS phenotype. There were 19,791 significant biomarkers using this method (see Table 12).

The second method used to identify discriminating biomarkers was the Wilcoxon Test (adjusted). Due to the large number of biomarkers, 54613, and the relatively small number of samples, 90, there was a high risk of finding falsely significant biomarkers. An adjusted p-value was used to counter this risk. In particular, the method of Benjamini and Hochberg, 1995, J. R. Statist. Soc. B 57, pp 289-300, which is hereby incorporated by reference in its entirety, was used to control the false discovery rate. Here, the false discovery rate is defined as the number of biomarkers truly significant divided by the number of biomarkers declared significant. For example, if the adjusted p-value is less than 0.05, there is a 5% chance that the biomarker is a false discovery. Results using this test are reported in Table 12. There were 11851 significant biomarkers using this method (see Table 12). As used, herein, a biomarker is considered significant if it has a p-value of less than 0.05 as determined by the Wilcoxon test (adjusted).

The third method used to identify discriminating biomarkers was the use of Q values. In such an approach, the biomarkers are ordered by their q-values and if a respective biomarker has a q-value of X, then respective biomarker and all others more significant have a combined false discovery rate of X. However, the false discovery rate for any one biomarker may be much larger. There were 11851 significant biomarkers using this method (see Table 12).

TABLE 12
Cumulative number of significant calls for the three methods.
Note that all 90 samples (training and validation)
were used to compare Sepsis and SIRS groups. Missing
biomarker feature values were not included in the analyses.
	≤1e−04	≤0.001	≤0.01	≤0.025	≤0.05	≤0.1	≤1
p-value	0	5417	11537	15769	19791	24809	54613
(unadjusted)
p-value	0	0	5043	8374	11851	16973	54613
(adjusted)
q-value	0	0	7734	12478	17820	24890	54613

CART. In addition to analyzing the microarray data using Wilcoxon test and Q-value tests in order to identify biomarkers that discriminate between the sepsis and SIRS subpopulations in the training set, classification and regression tree (CART) analysis was used. CART is described in Section 5.5.1, above. Specifically, the data summarized above was used to predict the disease state by iteratively partitioning the data based on the best single-variable split of the data. In other words, at each stage of the tree building process, the biomarker whose expression values across the training population best discriminate between the sepsis and SIRS population was invoked as a decision branch. Cross-validation was carried out, with the optimal number of splits estimated independently in each of the 10 iterations. The final tree is depicted in FIG. 10. In FIG. 10, decision 1002 makes a decision based on the abundance of the biomarker that binds to probeset X214681_at. If biomarker X214681_at has an abundance that is greater than 7.862 units in a biological sample from a subject to be diagnosed (test biological sample), than control passes to decision 1004. If, on the other hand, if the biomarker that binds to probeset (U133 plus 2.0 oligonucleotide) X214681_at has an abundance that is less than 7.862 units in the test biological sample, decision control passes to decision 1006. Decisions are made in this manner until a terminal leaf of the decision tree is reached, at which point diagnoses of sepsis or SIRS is made. The decision tree in FIG. 10 makes use of the biomarkers that bind to the following four probesets: X214681_at, X1560432_at, X230281_at, and X1007_s_at.

FIG. 11 shows the distribution of the four biomarkers used in the decision tree between the sepsis and SIRS groups in the training data set. In FIG. 11, the top of each box denotes the 75^th percentile of the data across the training set and the bottom of each box denotes the 25^th percentile, and the median value for each biomarker across the training set is drawn as a line within each box. The biomarkers are labeled in FIG. 11 based on the identity of the U133 plus 2.0 probes to which they bind). The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 13. From this confusion matrix, the overall accuracy was estimated to be 65.2% with a 95% confidence interval of 52.8% to 76.3%. The estimated sensitivity was 61.8% and the estimated specificity was 68.6%.

TABLE 13
Confusion matrix for training samples using
the cross-validated CART algorithm of FIG. 10
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	21	11
	SIRS	13	24

For the 21 validation samples held back from training data set, the overall accuracy was estimated to be 71.4% with a 95% confidence interval of 47.8% to 88.7%, sensitivity 90.9% and specificity 50%. Table 14 shows the confusion matrix for the validation samples.

TABLE 14
Confusion matrix for validation samples using
the cross-validated CART algorithm of FIG. 10
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	10	5
	SIRS	1	5

Random Forests. Another decision rule that can be developed using biomarkers of the present invention is a Random Forests decision tree. Random Forests is a tree based method that uses bootstrapping instead of cross-validation. For each iteration, a random sample (with replacement) is drawn and the largest tree possible is grown. Each tree receives a vote in the final class prediction. To fit a random forest, the number of trees (e.g. bootstrap iterations) is specified. No more than 500 were used in this example, but at least 50 are needed for a burn-in period. The number of trees was chosen based on the accuracy of the training data. For this data, 439 trees were used to train the algorithm (see FIG. 12). In FIG. 12, curve 1202 is a smoothed estimate of overall accuracy as a function of tree number. Curve 1204 is a smoothed curve of tree sensitivity as a function of tree number. Curve 1206 is a smoothed curve of tree specificity as a function of tree number. Using this algorithm, 845 biomarkers had non-zero importance and were used in the model. The random forest algorithm gauges biomarker importance by the average reduction in the training accuracy. The biomarkers were ranked by this method and are shown in FIG. 13. The figure only reflects the 50 most important biomarkers found by using Random Forest analysis. However, 845 biomarkers were actually found to have discriminating significance. The random forest method uses a number of different decision trees. A biomarker is considered to have discriminating significance if it served as a decision branch of a decision tree from a significant random forest analysis. As used herein, a significant random forest analysis is one where the lower 95% confidence interval on accuracy by cross validation on a training data set is greater than 50% and the point estimate for accuracy on a validation set is greater than 65%.

The predicted confusion matrix for the training dataset using the decision tree developed using the Random Forest method is given in Table 15. From this confusion matrix, the overall accuracy was estimated to be 75.4% (confidence intervals cannot be computed when using the bootstrap accuracy estimate). The estimated sensitivity was 73.5% and the estimated specificity was 77.1%.

TABLE 15
Confusion matrix for training samples against the decision
tree developed using the Random Forest method.
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	27	9
	SIRS	8	25

For the 21 validation samples held back from training, the overall accuracy was estimated to be 95.2% with a 95% confidence interval of 76.2% to 99.9%, sensitivity 100% and specificity 90%. Table 16 shows the confusion matrix for the validation samples.

TABLE 16
Confusion matrix for the 20 validation samples against the
decision tree developed using the Random Forest method.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	11	1
SIRS	0	9

MART. Multiple Additive Regression Trees (MART), also known as “gradient boosting machines,” was used to simultaneously assess the importance of biomarkers and classify the subject samples. Several fitting parameters are specified in this approach including (i) number of trees, (ii) step size (commonly referred to as “shrinkage”), and (iii) degree of interaction (related to the number of splits for each tree). More information on MART is described in Section 5.5.4 above. The degree of interaction was set to 1 to enforce an additive model (e.g. each tree has one split and only uses one biomarker).

Estimating interactions may require more data to function well. The step size was set to 0.05 so that the model complexity was dictated by the number of trees. The optimal number of trees was estimated by leaving out a random subset of cases at each fitting iteration, then assessing quality of prediction on that subset. After fitting more trees than were warranted, the point at which prediction performance stopped improving was estimated as the optimal point.

The estimated model used 28 trees and 17 biomarkers across all trees. The MART algorithm also provides a calculation of biomarker importance (summing to 100%), which are given in FIG. 14. Biomarkers with zero importance were excluded. In FIG. 14, biomarkers are labeled by the U133 plus 2.0 oligonucleotide to which they bind. FIG. 15 shows the distribution of the selected biomarkers between the Sepsis and SIRS groups. In FIG. 15, biomarkers are labeled by the U133 plus 2.0 oligonucleotide to which they bind.

Cross-validation was carried out, with the optimal number of trees estimated independently in each of the 10 iterations. The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 17. From this confusion matrix, the overall accuracy was estimated to be 76.8% with a 95% confidence interval of 65.1% to 86.1%. The estimated sensitivity was 76.5% and the estimated specificity was 77.1%.

TABLE 17
Confusion matrix for the training samples using the
cross-validated MART algorithm.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	26	8
SIRS	8	27

For the 21 validation samples held back from training, the overall accuracy was estimated to be 85.7% with a 95% confidence interval of 63.7% to 97%, sensitivity 80% and specificity 90.9%. Table 18 shows the confusion matrix for the validation samples.

TABLE 18
Confusion matrix for the validation samples
using the MART algorithm.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	8	1
SIRS	2	10

PAM. Yet another decision rule developed using biomarkers of the present invention is predictive analysis of microarrays (PAM), which is described in Section 5.5.2, above. In this method, a shrinkage parameter that determines the number of biomarkers used to classify samples is specified. This parameter was chosen via cross-validation. There were no biomarkers with missing values. Based on cross-validation, the optimal threshold value was 2.1, corresponding to 820 biomarkers. FIG. 16 shows the accuracy across different thresholds. In FIG. 16, curve 1602 is the overall accuracy (with 95% confidence interval bars). Curve 1604 shows decision rule sensitivity as a function of threshold value. Curve 1606 shows decision rule specificity as a function of threshold value. Using the threshold of 2.1. the overall accuracy for the training samples was estimated to be 80.9% with a 95% confidence interval of 73.4% to 86.7%. The estimated sensitivity was 85.7% and the estimated specificity was 76.5%. Table 19 shows the confusion matrix for the training data where the predicted classifications were made from the cross-validated models.

TABLE 19
Confusion matrix for training samples using cross-validated
PAM algorithm
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	30	8
SIRS	5	26

For the 21 validation samples held back from training, the overall accuracy was estimated to be 95.2% with a 95% confidence interval of 76.2% to 99.9%, sensitivity 100% and specificity 90%. Table 20 shows the confusion matrix for the validation samples.

TABLE 20
Confusion matrix for validation samples using cross-validated
PAM algorithm
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	11	1
SIRS	0	9

FIG. 17 shows the selected biomarkers, ranked by their relative discriminatory power, and their relative importance in the model. FIG. 17 only shows the fifty most important biomarkers found using the PAM analysis. However, 820 important biomarkers were found. In FIG. 17, biomarkers are labeled by the U133 plus 2.0 oligonucleotide to which they bind.

FIG. 18 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals. Fifty distinct biomarkers were selected from across all the algorithms illustrated in FIG. 18. The identity of these fifty selected features is shown in FIG. 20. FIG. 19 illustrates the number of times that common biomarkers were selected across the techniques of CART, MART, PAM, RF, and Wilcoxon (adjusted). FIG. 20 illustrates an overall ranking of biomarkers for the T₋₁₂ data set. For the selected biomarkers, the x-axis depicts the percentage of times that it was selected. Within the percentage of times that biomarkers were selected, the biomarkers are ranked. In FIG. 20, biomarkers are labeled by the U1 33 plus 2.0 oligonucleotide to which they bind.

6.5 Baseline T₋₂ Data Analysis

In another example, a baseline T₋₁₂ analysis was performed. Feature values for biomarkers in this example were computed as the differential between two time points. The two time points for each respective subject in a training population were (i) the T₋₂ time point and (ii) the first measurement, T_first, taken of the respective subject. It will be appreciated that T_first could differ across the training population. For example, in some subjects, T_first was two days before T₋₁₂, in some subjects T_first was three days before T₁₂.and so forth. To illustrate the computation of a feature value in accordance with the T₁₂ baseline analysis, consider the case in which biomarker A was evaluated. To compute a feature value for biomarker A for the purposes of the baseline T₋₁₂ analysis, the abundance of biomarker A in the T₋₁₂ blood sample for a respective subject in the training population [A]_T−12. was obtained. Further, the abundance of biomarker A from the first blood sample taken for the respective subject, [A]_first, was obtained. The feature value for A for this respective subject was then computed as ΔA=[A]_T−12-[A]_first. This calculation was repeated for each subject in the training population and for each biomarker under consideration.

For the baseline T₋₁₂ analysis, there were 54,613 probesets measured on 89 samples for a total of 89 corresponding microarray experiments from 89 different subjects. Each sample was collected from a different member of the population. Of the 54,613 probesets in each microarray experiment, 31,047 were transformed by log transformations. Further, of the 54,613 probesets in each microarray experiment, 2518 were transformed by a square root transformation. The remaining 21,048 probesets in each microarray experiment were not transformed.

The 89 member population was initially split into a training set (n=68) and a validation set (n=21). The training set was used to estimate the appropriate classification algorithm parameters while the trained algorithm was applied to the validation set to independently assess performance. Of the 68 training samples, 33 were Sepsis, meaning that the subjects developed sepsis at some point during the observation time period, and 35 were SIRS, meaning that they did not develop sepsis during the observation time period. Table 21 provides distributions of the race, gender and age for these samples.

TABLE 21
Distributions of the race, gender, and age for the training data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	9	12	1
	Female	0	10	1
SIRS	Male	5	20	0
	Female	0	10	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	42.7	39	80
SIRS	18	44.1	40	90

For the 21 validation samples, 11 were Sepsis and 10 were SIRS. Table 22 provides distributions of the race, gender and age for these samples.

TABLE 22
Distributions of the race, gender, and age for the validation data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	0	7	0
	Female	0	3	0
SIRS	Male	2	6	0
	Female	0	3	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	43.3	40	81
SIRS	19	53	52	85

Each sample in the training data was randomly assigned to one of ten groups used for cross-validation. The number of training samples in these groups ranged from 6 to 8. The samples were assigned in way that attempted to balance the number of sepsis and SIRS samples across folds. As described in more detail below, several different methods were used to judge whether select biomarkers discriminate between the Sepsis and SIRS groups.

Wilcoxon and Q-value tests. The first method used to identify discriminating biomarkers was a Wilcoxon test (unadjusted). The abundance value for a given biomarker from all samples in the training data was subjected to the Wilcoxon test. The Wilcoxon test considers both group classification (sepsis versus SIRS) and abundance value in order to compute a p value for the given biomarker. The p value provides an indication of how well the abundance value for the given biomarker across the samples collected in the training set discriminates between the sepsis and SIRS state. The lower the p value, the better the discrimination. When the p value is less than a specific confidence level, such as 0.05, an inference is made that the biomarker discriminates between the sepsis and SIRS phenotype. There were 6427 significant biomarkers using this method (see Table 23).

The second method used to identify discriminating biomarkers was the Wilcoxon Test (adjusted). Due to the large number of biomarkers, 54613, and the relatively small number of samples, 89, there was a high risk of finding falsely significant biomarkers. An adjusted p-value was used to counter this risk. In particular, the method of Benjamini and Hochberg, 1995, J. R. Statist. Soc. B 57, pp 289-300, which is hereby incorporated by reference in its entirety, was used to control the false discovery rate. Here, the false discovery rate is defined as the number of biomarkers truly significant divided by the number of biomarkers declared significant. For example, if the adjusted p-value is less than 0.05, there is a 5% chance that the biomarker is a false discovery. Results using this test are reported in Table 12. There were 482 significant biomarkers using this method (see Table 23). As used, herein, a biomarker is considered significant if it has a p-value of less than 0.05 as determined by the Wilcoxon test (adjusted).

The third method used to identify discriminating biomarkers was the use of Q values. The biomarkers are ordered by their q-values and if a biomarker has a q-value of X, then this biomarker and all others more biomarkers have a combined false discovery rate of X. However, the false discovery rate for any one biomarker may be much larger. There were 482 significant biomarkers using this method (see Table 23).

TABLE 23
Cumulative number of significant calls for the three methods.
Note that all 89 samples (training and validation)
were used to compare Sepsis and SIRS groups. Missing
biomarker values were not included in the analyses.
	≤1e−04	≤0.001	≤0.01	≤0.025	≤0.05	≤0.1	≤1
p-value	0	808	2486	4230	6427	10051	54613
(un-adjusted)
p-value	0	0	0	0	482	1035	54613
(adjusted)
q-value	0	0	0	0	606	1283	54613

CART. In addition to analyzing the microarray data using Wilcoxon test and Q-value tests in order to identify biomarkers that discriminate between the sepsis and SIRS subpopulations in the training set, classification and regression tree (CART) analysis was used. CART is described in Section 5.5.1, above. Specifically, the data summarized above was used to predict the disease state by iteratively partitioning the data based on the best single-variable (biomarker) split of the data. In other words, at each stage of the tree building process, the biomarker whose abundance value across the training population best discriminates between the sepsis and SIRS population was invoked as a decision branch. Cross-validation was carried out, with the optimal number of splits estimated independently in each of the 10 iterations. The final tree is depicted in FIG. 21. In FIG. 21, decision 2102 makes a decision based on the abundance of the biomarker that bind to U133 plus 2.0 probe X210119_at. If this biomarker that binds to X210119_at has an abundance that is less than −0.03669 units in a biological sample from a subject to be diagnosed (test biological sample), then control passes to decision 2104. If, on the other hand, the biomarker that binds to probeset X210119_at has an abundance that is greater than −0.03669 units in the test biological sample, decision control passes to decision 2106. Decisions are made in this manner until a terminal leaf of the decision tree is reached, at which point diagnoses of sepsis or SIRS is made. The decision tree in FIG. 21 makes use of the biomarkers that bind to the following five U133 plus 2.0 oligonucleotides: X210119_at, X1552554_a_at, X1554390_s_at, X1552301_a_at, and X1555868_at.

FIG. 22 shows the distribution of the five biomarkers used in the decision tree between the sepsis and SIRS groups in the training data set. In FIG. 22, the top of each box denotes the 75^th percentile of the data across the training set and the bottom of each box denotes the 25^th percentile, and the median value for each biomarker across the training set is drawn as a line within each box. In FIG. 22, biomarkers are labeled by the U133 plus 2.0 oligonucleotides to which they bind. The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 24. From this confusion matrix, the overall accuracy was estimated to be 80.9% with a 95% confidence interval of 69.5% to 89.4%. The estimated sensitivity was 93.9% and the estimated specificity was 68.6%.

TABLE 24
Confusion matrix for training samples using the cross-validated
CART algorithm of FIG. 21.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	31	11
SIRS	2	24

For the 21 validation samples held back from training data set, the overall accuracy was estimated to be 71.4% with a 95% confidence interval of 47.8% to 88.7%, sensitivity 72.7% and specificity 70%. Table 25 shows the confusion matrix for the validation samples.

TABLE 25
Confusion matrix for validation samples using the
cross-validated CART algorithm of FIG. 21.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	10	5
SIRS	1	5

Random Forests. Another decision rule that can be developed using biomarkers is a Random Forests decision tree. To fit a random forest, the number of trees (e.g. bootstrap iterations) is specified. No more than 500 were used in this example, but at least 50 are needed for a burn-in period. The number of trees was chosen based on the accuracy of the training data. For this data, 482 trees were used to train the algorithm (see FIG. 23). In FIG. 23, curve 2302 is a smoothed estimate of overall accuracy as a function of tree number. Curve 2304 is a smoothed curve of tree sensitivity as a function of tree number. Curve 2306 is a smoothed curve of tree specificity as a function of tree number. Using this algorithm, 482 biomarkers had non-zero importance and were used in the model. The random forest algorithm gauges biomarker importance by the average reduction in the training accuracy. The biomarkers were ranked by this method and are shown in FIG. 24. The figure only reflects the 50 most important biomarkers found by using Random Forest analysis. However, 893 biomarkers were actually found to have discriminating significance. The random forest method uses a number of different decision trees. A biomarker is considered to have discriminating significance if it served as a decision branch of a decision tree from a significant random forest analysis. As used herein, a significant random forest analysis is one where the lower 95% confidence interval on accuracy by cross validation on a training data set is greater than 50% and the point estimate for accuracy on a validation set is greater than 65%.

The predicted confusion matrix for the training dataset using the decision tree developed using the Random Forest method is given in Table 26. From this confusion matrix, the overall accuracy was estimated to be 61.8% (confidence intervals cannot be computed when using the bootstrap accuracy estimate). The estimated sensitivity was 57.6% and the estimated specificity was 65.7%.

TABLE 26
Confusion matrix for training samples against the decision
tree developed using the Random Forest method.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	23	14
SIRS	12	19

For the 21 validation samples held back from training, the overall accuracy was estimated to be 72.6% with a 95% confidence interval of 52.8% to 91.8%, sensitivity 63.9% and specificity 90%. Table 27 shows the confusion matrix for the validation samples.

TABLE 27
Confusion matrix for the 20 validation samples against
the decision tree developed using the Random Forest method.
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	7	1
SIRS	4	9

PAM. Yet another decision rule developed using biomarkers is predictive analysis of microarrays (PAM), which is described in Section 5.5.2, above. In this method, a shrinkage parameter that determines the number of biomarkers used to classify samples is specified. This parameter was chosen via cross-validation. There were no biomarkers with missing values. Based on cross-validation, the optimal threshold value was 1.62, corresponding to 269 biomarkers. FIG. 25 shows the accuracy across different thresholds. In FIG. 25, curve 2502 is the overall accuracy (with 95% confidence interval bars). Curve 2504 shows decision rule sensitivity as a function of threshold value. Curve 2506 shows decision rule specificity as a function of threshold value. Using the threshold of 1.62, the overall accuracy for the training samples was estimated to be 67.7% with a 95% confidence interval of 55.9% to 77.6%. The estimated sensitivity was 68.6% and the estimated specificity was 66.7%. Table 28 shows the confusion matrix for the training data where the predicted classifications were made from the cross-validated models.

TABLE 28
Confusion matrix for training samples using cross-validated
PAM algorithm
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	24	11
SIRS	11	22

For the 21 validation samples held back from training, the overall accuracy was estimated to be 81% with a 95% confidence interval of 58.1% to 94.6%, sensitivity 72.7% and specificity 100%. Table 26 shows the confusion matrix for the validation samples.

TABLE 29
Confusion matrix for validation samples using cross-validated
PAM algorithm
	True Diagnosis
Predicted	Sepsis	SIRS
Sepsis	8	1
SIRS	3	9

FIG. 26 shows the selected biomarkers, ranked by their relative discriminatory power, and their relative importance in the model. FIG. 26 only shows the fifty most important biomarkers found using the PAM analysis. However, 269 biomarker were found. In FIG. 26, biomarkers are labeled by the U1 33 plus 2.0 oligonucleotides to which they bind.

FIG. 27 provides a summary of the CART, PAM and random forests classification algorithm (decision rule) performance and associated 95% confidence intervals. Fifty distinct biomarkers were selected from across all the algorithms illustrated in FIG. 27. FIG. 28 illustrates the number of times that common biomarkers were selected across the techniques of CART, PAM, RF, and Wilcoxon (adjusted). In FIG. 28, biomarkers are labeled by the U1 33 plus 2.0 oligonucleotide to which they bind. FIG. 29 illustrates an overall ranking of biomarkers for the To base data set. In FIG. 29, biomarkers are labeled by the U133 plus 2.0 oligonucleotide to which they bind. For the selected biomarkers, the x-axis depicts the percentage of times that it was selected. Within the percentage of times that biomarkers were selected, the biomarkers are ranked.

6.6 Select Biomarkers

Sections 6.3 through 6.5 describe experiments in which blood samples from SIRS positive subjects have been tested using Affymetrix U133 plus 2.0 human genome chips containing 54,613 probesets. This section describes the criteria applied to the data described in Sections 6.3 through 6.5 in order to identify a list of biomarkers that discriminate between subjects likely to develop sepsis in a defined time period (sepsis subjects) and subjects not likely to develop sepsis in a defined time period (SIRS subjects). FIG. 30 illustrates the filters applied to identify this list of biomarkers.

A first criterion that was imposed was a requirement that a biomarker discriminate between SIRS and sepsis with a p value of 0.05 or less, as determined by the Wilcoxon test after correction for multiple comparisons, at any time point measured or the biomarker was used in a multivariate analysis with significant classification performance where significant classification performance is defined by having a lower 95^th percentile for accuracy on a training data set that is greater than 50% and a point estimate for accuracy on the validation set greater than 65% at any time point measured. At T₋₃₆ (Section 6.3), 1,618 biomarkers met this criterion. At T₋₁ (Section 6.4), 12,728 biomarkers met this criterion. Some biomarkers met this criterion at both T₋₁₂ and T₋₃ time points. In total, there were 14,346 biomarkers (including duplicates from T₁₂ and T₋₃₆ time points) that discriminated between the sepsis and SIRS states. Thus, the first filter criterion reduced the number of eligible biomarkers from 54,613 to 14,346.

The second criterion that was imposed was a requirement that each respective biomarker under consideration exhibit at least a 1.2× fold change between the median value for the respective biomarker among the subjects that acquired sepsis during a defined time period (sepsis subjects) and the median value for the respective biomarker among subjects that do not acquire sepsis during the defined time period (SIRS subjects) at the T₋₃₆ time or the T₋₁₂ time point period. Furthermore, to satisfy the second criterion, the biomarker must have been used in at least one multivariate analysis with significant classification performance where significant classification performance is defined by having a lower 95^th percentile for accuracy on a training data set that is greater than 50% and a point estimate for accuracy on the validation set that is greater then 65% at any time point measured. As noted in FIG. 30, application of the third filter criterion reduced the number of eligible biomarkers from 14,346 to 626.

In column one of Table 30, each biomarker is listed by a gene name, such as, for example. a Human Gene Nomenclature Database (HUGO) symbol set forth by the Gene Nomenclature Committee, Department of Biology, University College London. As is known in the art, some human genome genes are represented by more than one probeset in the U133 plus 2.0 array. Furthermore, some of the oligonucleotides in the U133 plus 2.0 array represent expressed sequence tags (ESTs) that do not correspond to a known gene (see column two of Table 30). Where known, the names of the different human genes are listed in column three of Table 30.

In the case where a biomarker is based upon a gene that includes the sequence of a probeset listed in Table 30 or a complement thereof, the biomarker can be, for example, a transcript made by the gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein encoded by a gene that includes a probeset sequence described in Table 30 or a discriminating fragment of the protein, or an indication of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In one embodiment, a biomarker profile of the present invention comprises a plurality of biomarkers that contain at least five, at least ten at least fifteen, at least twenty, at least thirty, between 2 and 5, between 3 and 7, or less than 15 of the sequences of the probesets of Table 30, or complements thereof, or genes including one of at least five of the sequences or complements thereof, or a discriminating fragment thereof, or an amino acid sequence encoded by any of the foregoing nucleic acid sequences, or any discriminating fragment of such an amino acid sequence. Such biomarkers can be mRNA transcripts, cDNA or some other form of amplified nucleic acid or proteins. In some embodiments a biomarker is any gene that includes the sequence in an Affymetrix probeset given in Table 30, or any gene that includes a complement of the sequence in an Affymetrix probeset given in Table 30, or any mRNA, cDNA or other form of amplified nucleic acid of the foregoing, for any discriminating fragment of the foregoing, or any amino acid sequence coded by the foregoing, or any discriminating fragment of such a protein.

TABLE 30
Exemplary biomarkers that discriminate between responders and nonresponders
			Gene	Protein
	Affymetrix		Accession	Accession
Gene Symbol	Probeset name	Gene Name	Number	Number
Column	Column	Column	Column	Column
1	2	3	4	5
FLJ20445	218582_at	HYPOTHETICAL PROTEIN	NM_017824
		FLJ20445
3′HEXO	231852_at	HISTONE MRNA 3′ END	NM_153332	NP_699163
		EXORIBONUCLEASE
3′HEXO	226416_at	HISTONE MRNA 3′ END	NM_153332	NP_699163
		EXORIBONUCLEASE
ABCA2	212772_s_at	ATP-BINDING CASSETTE,	NM_001606	NP_001597
		SUB-FAMILY A (ABC1),	NM_212533	NP_997698
		MEMBER 2
ABHD2	228490_at	ABHYDROLASE DOMAIN	NM_007011	NP_008942
		CONTAINING 2	NM_152924	NP_690888
ACN9	218981_at	ACN9 HOMOLOG	NM_020186	NP_064571
		(S.CEREVISIAE)
ACSL1	201963_at	ACYL-COA SYNTHETASE	NM_001995	NP_001986
		LONG-CHAIN FAMILY
		MEMBER 1
ACSL3	201660_at	ACYL-COA SYNTHETASE	NM_004457NM_203372	NP_004448
		LONG-CHAIN FAMILY		NP_976251
		MEMBER 3
ACSL4	202422_s_at	ACYL-COA SYNTHETASE	NM_004458	NP_004449
		LONG-CHAIN FAMILY	NM_022977	NP_075266
		MEMBER 4
ACTR3	213101_s_at	ARP3 ACTIN-RELATED	NM_005721	NP_005712
		PROTEIN 3 HOMOLOG
		(YEAST)
ADM	202912_at	ADRENOMEDULLIN	NM_001124	NP_001115
ADORA2A	205013_s_at	ADENOSINE A2	NM_000675	NP_000666
		RECEPTOR
AIM2	206513_at	ABSENT IN MELANOMA 2	NM_004833	NP_004824
ALOX5AP	204174_at	ARACHIDONATE 5-	NM_001629	NP_001620
		LIPOXYGENASE-
		ACTIVATING PROTEIN
AMPD2	212360_at	ADENOSINE	NM_004037	NP_004028
		MONOPHOSPHATE	NM_139156	NP_631895
		DEAMINASE 2 (ISOFORM L)	NM_203404	NP_981949
ANKRD22	238439_at	ANKYRIN REPEAT	NM_144590	NP_653191
		DOMAIN 22
ANKRD22	239196_at	ANKYRIN REPEAT	NM_144590	NP_653191
		DOMAIN 22
ANXA3	209369_at	ANNEXIN A3	NM_005139	NP_005130
APG3L	220237_at	APG3 AUTOPHAGY 3-LIKE	NM_022488	NP_071933
		(S.CEREVISIAE)
ARHGAP8	47069_at	RHO GTPASE	NM_015366	NP_056181
		ACTIVATING PROTEIN 8	NM_017701	NP_060171
			NM_181333	NP_851850
			NM_181334	NP_851851
			NM_181335	NP_851852
ARID5B	212614_at	AT RICH INTERACTIVE	XM_084482	XP_084482
		DOMAIN 5B (MRF1-LIKE)
ASAHL	214765_s_at	N-ACYLSPHINGOSINE	NM_014435	NP_055250
		AMIDOHYDROLASE-LIKE
		PROTEIN
ASAHL	232072_at	N-ACYLSPHINGOSINE	NM_014435	NP_055250
		AMIDOHYDROLASE-LIKE
		PROTEIN
ASAHL	227135_at	N-ACYLSPHINGOSINE	NM_014435	NP_055250
		AMIDOHYDROLASE-LIKE
		PROTEIN
ASPH	242037_at	ASPARTATE BETA-	NM_004318	NP_004309
		HYDROXYLASE	NM_020164	NP_064549
			NM_032466	NP_115855
			NM_032467	NP_115856
			NM_032468	NP_115857
ATP11B	1554557_at	ATPASE, CLASS VI, TYPE	XM_087254	XP_087254
		11B
ATP11B	1564064_a_at	ATPASE, CLASS VI, TYPE	XM_087254	XP_087254
		11B
ATP11B	1554556_a_at	ATPASE, CLASS VI, TYPE	XM_087254	XP_087254
		11B
ATP11B	212536_at	ATPASE, CLASS VI, TYPE	XM_087254	XP_087254
		11B
ATP11B	1564063_a_at	ATPASE, CLASS VI, TYPE	XM_087254	XP_087254
		11B
ATP6V1C1	202872_at	ATPASE, H+	NM_001007254	NP_001007255
		TRANSPORTING,	NM_001695	NP_001686
		LYSOSOMAL, 42-KD, V1
		SUBUNIT C, ISOFORM 1
ATP6V1C1	202874_s_at	ATPASE, H+	NM_001007254	NP_001007255
		TRANSPORTING,	NM_001695	NP_001686
		LYSOSOMAL, 42-KD, V1
		SUBUNIT C, ISOFORM 1
ATP6V1C1	226463_at	ATPASE, H+	NM_001007254	NP_001007255
		TRANSPORTING,	NM_001695	NP_001686
		LYSOSOMAL, 42-KD, V1
		SUBUNIT C, ISOFORM 1
ATP9A	212062_at	ATPASE, CLASS II, TYPE 9A	XM_030577	XP_030577
B4GALT5	221485_at	BETA-1,4-	NM_004776	NP_004767
		GALACTOSYLTRANSFERASE
BASP1	202391_at	BRAIN-ABUNDANT	NM_006317	NP_006308
		SIGNAL PROTEIN
BAT5	224756_s_at	HLA-B ASSOCIATED	NM_021160	NP_066983
		TRANSCRIPT 5
BATF	205965_at	BASIC LEUCINE ZIPPER	NM_006399	NP_006390
		TRANSCRIPTION FACTOR,
		ATF-LIKE
BAZ1A	217986_s_at	BROMODOMAIN	NM_013448	NP_038476
		ADJACENT TO ZINC	NM_182648	NP_872589
		FINGER DOMAIN, 1A
BAZ1A	217985_s_at	BROMODOMAIN	NM_013448	NP_038476
		ADJACENT TO ZINC	NM_182648	NP_872589
		FINGER DOMAIN, 1A
BCL2A1	205681_at	BCL2-RELATED PROTEIN A1	NM_004049	NP_004040
BCL3	204908_s_at	B-CELL CLL/LYMPHOMA 3	NM_005178	NP_005169
BCL3	204907_s_at	B-CELL CLL/LYMPHOMA 3	NM_005178	NP_005169
BCL6	203140_at	B-CELL LYMPHOMA 6	NM_001706	NP_001697
			NM_138931	NP_620309
BCL6	215990_s_at	B-CELL LYMPHOMA 6	NM_001706	NP_001697
			NM_138931	NP_620309
BIK	205780_at	BCL2-INTERACTING	NM_001197	NP_001188
		KILLER (APOPTOSIS-
		INDUCING)
BMX	206464_at	BONE MARROW KINASE,	NM_001721	NP_001712
		X-LINKED	NM_203281	NP_975010
C13orf12	217769_s_at	CHROMOSOME 13 OPEN	NM_015932	NP_057016
		READING FRAME 12
C14orf101	225675_at	CHROMOSOME 14 OPEN	NM_017799	NP_060269
		READING FRAME 101
C14orf101	219757_s_at	CHROMOSOME 14 OPEN	NM_017799	NP_060269
		READING FRAME 101
C14orf147	213508_at	CHROMOSOME 14 OPEN	NM_138288	NP_612145
		READING FRAME 147
C16orf30	219315_s_at	CHROMOSOME 16 OPEN	NM_024600	NP_078876
		READING FRAME 30
C16orf7	205781_at	CHROMOSOME 16 OPEN-	NM_004913	NP_004904
		READING FRAME 7
C1GALT1	219439_at	CORE 1 SYNTHASE,	NM_020156	NP_064541
		GLYCOPROTEIN-N-
		ACETYLGALACTOSAMINE
		3-BETA-
		GALACTOSYLTRANSFERASE
C1GALT1C1	219283_at	C1GALT1-SPECIFIC	NM_001011551	NP_001011551
		CHAPERONE 1	NM_152692	NP_689905
C1GALT1C1	238989_at	C1GALT1-SPECIFIC	NM_001011551	NP_001011551
		CHAPERONE 1	NM_152692	NP_689905
C1orf8	200620_at	CHROMOSOME 1 OPEN	NM_004872	NP_004863
		READING FRAME 8
C1RL	218983_at	COMPLEMENT	NM_016546	NP_057630
		COMPONENT 1, R
		SUBCOMPONENT-LIKE
C20orf24	217835_x_at	CHROMOSOME 20 OPEN	NM_018840	NP_061328
		READING FRAME 24	NM_199483	NP_955777
			NM_199484	NP_955778
			NM_199485	NP_955779
C20orf24	223880_x_at	CHROMOSOME 20 OPEN	NM_018840	NP_061328
		READING FRAME 24	NM_199483	NP_955777
			NM_199484	NP_955778
			NM_199485	NP_955779
C20orf32	1554786_at	CHROMOSOME 20 OPEN-	NM_020356	NP_065089
		READING FRAME 32
C21orf91	220941_s_at	CHROMOSOME 21 OPEN	NM_017447	NP_059143
		READING FRAME 91
C2orf25	217883_at	CHROMOSOME 2 OPEN	NM_015702	NP_056517
		READING FRAME 25
C2orf33	223354_x_at	CHROMOSOME 2 OPEN	NM_020194	NP_064579
		READING FRAME 33
C6orf83	225850_at	CHROMOSOME 6 OPEN	NM_145169	NP_660152
		READING FRAME 83
C9orf19	225604_s_at	CHROMOSOME 9 OPEN	NM_022343	NP_071738
		READING FRAME 19
C9orf46	218992_at	CHROMOSOME 9 OPEN	NM_018465	NP_060935
		READING FRAME 46
C9orf84	1553920_at	CHROMOSOME 9 OPEN	NM_173521	NP_775792
		READING FRAME 84
CA4	206208_at	CARBONIC ANHYDRASE IV	NM_000717	NP_000708
CA4	206209_s_at	CARBONIC ANHYDRASE IV	NM_000717	NP_000708
CAB39	217873_at	CALCIUM BINDING	NM_016289	NP_057373
		PROTEIN 39
CACNA1E	236013_at	CALCIUM CHANNEL,	NM_000721	NP_000712
		VOLTAGE-DEPENDENT,
		ALPHA 1E SUBUNIT
CACNA2D3	219714_s_at	CALCIUM CHANNEL,	NM_018398	NP_060868
		VOLTAGE-DEPENDENT,
		ALPHA 2/DELTA 3
		SUBUNIT
CAPZA2	1569450_at	CAPPING PROTEIN (ACTIN	NM_006136	NP_006127
		FILAMENT) MUSCLE Z-
		LINE, ALPHA 2
CARD12	1552553_a_at	CASPASE RECRUITMENT	NM_021209	NP_067032
		DOMAIN FAMILY,
		MEMBER 12
CASP4	209310_s_at	CASPASE 4, APOPTOSIS-	NM_001225	NP_001216
		RELATED CYSTEINE	NM_033306	NP_150649
		PROTEASE	NM_033307	NP_150650
CCL5	1555759_a_at	CHEMOKINE (C-C MOTIF)	NM_002985	NP_002976
		LIGAND 5
CCPG1	221511_x_at	CELL CYCLE	NM_004748	NP_004739
		PROGRESSION 1	NM_020739	NP_065790
CD4	203547_at	CD4 ANTIGEN (P55)	NM_000616	NP_000607
CD48	237759_at	CD48 ANTIGEN (B-CELL	NM_001778	NP_001769
		MEMBRANE PROTEIN)
CD58	211744_s_at	CD58 ANTIGEN,	NM_001779	NP_001770
		(LYMPHOCYTE
		FUNCTION-ASSOCIATED
		ANTIGEN 3)
CD58	205173_x_at	CD58 ANTIGEN,	NM_001779	NP_001770
		(LYMPHOCYTE
		FUNCTION-ASSOCIATED
		ANTIGEN 3)
CD58	216942_s_at	CD58 ANTIGEN,	NM_001779	NP_001770
		(LYMPHOCYTE
		FUNCTION-ASSOCIATED
		ANTIGEN 3)
CD59	228748_at	CD59 ANTIGEN P18-20	NM_000611	NP_000602
		(ANTIGEN IDENTIFIED BY	NM_203329	NP_976074
		MONOCLONAL	NM_203330	NP_976075
		ANTIBODIES 16.3A5, EJ16,	NM_203331	NP_976076
		EJ30, EL32 AND G344)
CD59	200985_s_at	CD59 ANTIGEN P18-20	NM_000611	NP_000602
		(ANTIGEN IDENTIFIED BY	NM_203329	NP_976074
		MONOCLONAL	NM_203330	NP_976075
		ANTIBODIES 16.3A5, EJ16,	NM_203331	NP_976076
		EJ30, EL32 AND G344)
CD59	200984_s_at	CD59 ANTIGEN P18-20	NM_000611	NP_000602
		(ANTIGEN IDENTIFIED BY	NM_203329	NP_976074
		MONOCLONAL	NM_203330	NP_976075
		ANTIBODIES 16.3A5, EJ16,	NM_203331	NP_976076
		EJ30, EL32 AND G344)
CD59	212463_at	CD59 ANTIGEN P18-20	NM_000611	NP_000602
		(ANTIGEN IDENTIFIED BY	NM_203329	NP_976074
		MONOCLONAL	NM_203330	NP_976075
		ANTIBODIES 16.3A5, EJ16,	NM_203331	NP_976076
		EJ30, EL32 AND G344)
CD74	209619_at	CD74 ANTIGEN	NM_004355	NP_004346
		(INVARIANT
		POLYPEPTIDE OF MAJOR
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II
		ANTIGEN-ASSOCIATED)
CD74	1567628_at	CD74 ANTIGEN	NM_004355	NP_004346
		(INVARIANT
		POLYPEPTIDE OF MAJOR
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II
		ANTIGEN-ASSOCIATED)
CD86	210895_s_at	CD86 ANTIGEN (CD28	NM_006889	NP_008820
		ANTIGEN LIGAND 2, B7-2	NM_175862	NP_787058
		ANTIGEN)
CDKN3	209714_s_at	CYCLIN-DEPENDENT	NM_005192	NP_005183
		KINASE INHIBITOR 3
		(CDK2-ASSOCIATED
		DUAL SPECIFICITY
		PHOSPHATASE)
CEACAM1	209498_at	CARCINOEMBRYONIC	NM_001712	NP_001703
		ANTIGEN-RELATED CELL
		ADHESION MOLECULE 1
CEACAM1	206576_s_at	CARCINOEMBRYONIC	NM_001712	NP_001703
		ANTIGEN-RELATED CELL
		ADHESION MOLECULE 1
CEACAM1	211889_x_at	CARCINOEMBRYONIC	NM_001712	NP_001703
		ANTIGEN-RELATED CELL
		ADHESION MOLECULE 1
CEACAM1	211883_x_at	CARCINOEMBRYONIC	NM_001712	NP_001703
		ANTIGEN-RELATED CELL
		ADHESION MOLECULE 1
CEACAM3	208052_x_at	CARCINOEMBRYONIC	NM_001815	NP_001806
		ANTIGEN-RELATED CELL
		ADHESION MOLECULE 3
CECR1	219505_at	CAT EYE SYNDROME	NM_017424	NP_059120
		CHROMOSOME REGION,	NM_177405	NP_803124
		CANDIDATE 1
CHCHD7	222701_s_at	COILED-COIL-HELIX	NM_001011667	NP_001011667
		DOMAIN-CONTAINING	NM_001011668	NP_001011668
		PROTEIN 7	NM_001011669	NP_001011669
			NM_001011670	NP_001011670
			NM_001011671	NP_001011671
			NM_024300	NP_077276
CHSY1	203044_at	CARBOHYDRATE	NM_014918	NP_055733
		SYNTHASE 1
CIR	209571_at	CBF1 INTERACTING	NM_004882	NP_004873
		COREPRESSOR	NM_199075	NP_951057
CKLF	223451_s_at	CHEMOKINE-LIKE	NM_016326	NP_057410
		FACTOR	NM_016951	NP_058647
			NM_181640	NP_857591
			NM_181641	NP_857592
CKLF	219161_s_at	CHEMOKINE-LIKE	NM_016326	NP_057410
		FACTOR	NM_016951	NP_058647
			NM_181640	NP_857591
			NM_181641	NP_857592
CKLF	221058_s_at	CHEMOKINE-LIKE	NM_016326	NP_057410
		FACTOR	NM_016951	NP_058647
			NM_181640	NP_857591
			NM_181641	NP_857592
CKLFSF1	235286_at	CHEMOKINE-LIKE	NM_052999	NP_443725
		FACTOR SUPER FAMILY 1	NM_181268	NP_851785
			NM_181269	NP_851786
			NM_181270	NP_851787
			NM_181271	NP_851788
			NM_181272	NP_851789
			NM_181283	NP_851800
			NM_181285	NP_851802
			NM_181286	NP_851803
			NM_181287	NP_851804
			NM_181288	NP_851805
			NM_181289	NP_851806
			NM_181290	NP_851807
			NM_181292	NP_851809
			NM_181293	NP_851810
			NM_181294	NP_851811
			NM_181295	NP_851812
			NM_181296	NP_851813
			NM_181297	NP_851814
			NM_181298	NP_851815
			NM_181299	NP_851816
			NM_181300	NP_851817
			NM_181301	NP_851818
CLEC10A	206682_at	C-TYPE LECTIN DOMAIN	NM_006344	NP_006335
		FAMILY 10, MEMBER A	NM_182906	NP_878910
CLEC4D	1552772_at	C-TYPE LECTIN DOMAIN	NM_080387	NP_525126
		FAMILY 4, MEMBER D
CLEC4E	219859_at	C-TYPE LECTIN DOMAIN	NM_014358	NP_055173
		FAMILY 4, MEMBER E
CLEC5A	219890_at	C-TYPE LECTIN DOMAIN	NM_013252	NP_037384
		FAMILY 5, MEMBER A
COL4A3BP	223465_at	COLLAGEN, TYPE IV,	NM_005713	NP_005704
		ALPHA 3 (GOODPASTURE	NM_031361	NP_112729
		ANTIGEN) BINDING
		PROTEIN
COP1	1552701_a_at	CARD ONLY PROTEIN	NM_052889	NP_443121
COX15	235204_at	COX15 HOMOLOG,	NM_004376	NP_004367
		CYTOCHROME C	NM_078470	NP_510870
		OXIDASE ASSEMBLY
		PROTEIN (YEAST)
CPD	201941_at	CARBOXYPEPTIDASE D	NM_001304	NP_001295
CPD	201940_at	CARBOXYPEPTIDASE D	NM_001304	NP_001295
CPEB4	242384_at	CYTOPLASMIC	NM_030627	NP_085130
		POLYADENYLATION
		ELEMENT BINDING
		PROTEIN 4
CPEB4	224829_at	CYTOPLASMIC	NM_030627	NP_085130
		POLYADENYLATION
		ELEMENT BINDING
		PROTEIN 4
CPVL	208146_s_at	CARBOXYPEPTIDASE,	NM_019029	NP_061902
		VITELLOGENIC-LIKE	NM_031311	NP_112601
CR1	206244_at	COMPLEMENT	NM_000573	NP_000564
		COMPONENT (3B/4B)	NM_000651	NP_000642
		RECEPTOR 1, INCLUDING
		KNOPS BLOOD GROUP SYSTEM
CRTAP	1554464_a_at	CARTILAGE-ASSOCIATED	NM_006371	NP_006362
		PROTEIN
CRTAP	1555889_a_at	CARTILAGE-ASSOCIATED	NM_006371	NP_006362
		PROTEIN
CSF1R	203104_at	COLONY STIMULATING	NM_005211	NP_005202
		FACTOR 1 RECEPTOR,
		FORMERLY MCDONOUGH
		FELINE SARCOMA VIRAL
		(V-FMS) ONCOGENE
		HOMOLOG
CTGLF1	221850_x_at	CENTAURIN, GAMMA-	NM_133446	NP_597703
		LIKE FAMILY, MEMBER 1
CYP4F2	210452_x_at	CYTOCHROME P450,	NM_001082	NP_001073
		FAMILY 4, SUBFAMILY F,
		POLYPEPTIDE 2
DCP2	235258_at	DCP2 DECAPPING	NM_152624	NP_689837
		ENZYME HOMOLOG
		(S.CEREVISIAE)
DDAH2	202262_x_at	DIMETHYLARGININE	NM_013974	NP_039268
		DIMETHYLAMINOHYDROLASE 2
DDAH2	215537_x_at	DIMETHYLARGININE	NM_013974	NP_039268
		DIMETHYLAMINOHYDROLASE 2
DDAH2	214909_s_at	DIMETHYLARGININE	NM_013974	NP_039268
		DIMETHYLAMINOHYDROLASE 2
DDX26	222239_s_at	DEAD/H (Asp-Glu-Ala-Asp/His)	NM_012141	NP_036273
		BOX POLYPEPTIDE 26
DHRS9	223952_x_at	MEMBRANE PROTEIN,	NM_005771	NP_005762
		PALMITOYLATED 3; MPP3	NM_199204	NP_954674
DHRS9	224009_x_at	MEMBRANE PROTEIN,	NM_005771	NP_005762
		PALMITOYLATED 3; MPP3	NM_199204	NP_954674
DHRS9	219799_s_at	MEMBRANE PROTEIN,	NM_005771	NP_005762
		PALMITOYLATED 3; MPP3	NM_199204	NP_954674
DKFZP564B1023	228385_at	KINESIN FAMILY	XM_375825	XP_375825
		MEMBER 14 (KIF14)
DKFZP566M1046	223637_s_at	HYPOTHETICAL PROTEIN	NM_032127	NP_115503
		DKFZP566M1046
DKFZp667F0711	1559756_at	HYPOTHETICAL PROTEIN	XM_374767	XP_374767
		DKFZp667F0711
DLGAP1	239421_at	DISCS, LARGE	NM_001003809	NP_001003809
		(DROSOPHILA)	NM_004746	NP_004737
		HOMOLOG-ASSOCIATED
		PROTEIN 1
DNAJA1	200881_s_at	DNAJ (HSP40) HOMOLOG,	NM_001539	NP_001530
		SUBFAMILY A, MEMBER 1
DR1	216652_s_at	DOWN-REGULATOR OF	NM_001938	NP_001929
		TRANSCRIPTION 1, TBP-
		BINDING (NEGATIVE
		COFACTOR 2)
E2F3	203693_s_at	E2F TRANSCRIPTION	NM_001949	NP_001940
		FACTOR 3
EFHC1	225656_at	EF-HAND DOMAIN (C-	NM_018100	NP_060570
		TERMINAL) CONTAINING 1
EGFL5	212831_at	EGF-LIKE-DOMAIN,	XM_376905	XP_376905
		MULTIPLE 5
EIF4E	201435_s_at	EUKARYOTIC	NM_001968	NP_001959
		TRANSLATION
		INITIATION FACTOR 4E
EIF4E3	225941_at	EUKARYOTIC	NM_173359	NP_775495
		TRANSLATION
		INITIATION FACTOR 4E
		MEMBER 3
EIF4E3	225940_at	EUKARYOTIC	NM_173359	NP_775495
		TRANSLATION
		INITIATION FACTOR 4E
		MEMBER 3
EIF4E3	238461_at	EUKARYOTIC	NM_173359	NP_775495
		TRANSLATION
		INITIATION FACTOR 4E
		MEMBER 3
EIF4G3	201935_s_at	EUKARYOTIC	NM_003760	NP_003751
		TRANSLATION
		INITIATION FACTOR 4-
		GAMMA, 3
EIF4G3	201936_s_at	EUKARYOTIC	NM_003760	NP_003751
		TRANSLATION
		INITIATION FACTOR 4-
		GAMMA, 3
EIF4G3	243149_at	EUKARYOTIC	NM_003760	NP_003751
		TRANSLATION
		INITIATION FACTOR 4-
		GAMMA, 3
EMILIN2	242288_s_at	ELASTIN MICROFIBRIL	NM_032048	NP_114437
		INTERFACER 2
ETS2	201328_at	V-ETS	NM_005239	NP_005230
		ERYTHROBLASTOSIS
		VIRUS E26 ONCOGENE
		HOMOLOG 2 (AVIAN)
EXOSC4	91684_g_at	EXOSOME COMPONENT 4	NM_019037	NP_061910
EXOSC4	218695_at	EXOSOME COMPONENT 4	NM_019037	NP_061910
EXOSC4	58696_at	EXOSOME COMPONENT 4	NM_019037	NP_061910
FAD104	244022_at	FIBRONECTIN TYPE III	NM_022763	NP_073600
		DOMAIN CONTAINING 3B
		(FNDC3B)
FAM53C	218023_s_at	FAMILY WITH SEQUENCE	NM_016605	NP_057689
		SIMILARITY 53, MEMBER C
FAS	204781_s_at	FAS (TNF RECEPTOR	NM_000043	NP_000034
		SUPERFAMILY, MEMBER 6)	NM_152871	NP_690610
			NM_152872	NP_690611
			NM_152873	NP_690612
			NM_152874	NP_690613
			NM_152875	NP_690614
			NM_152876	NP_690615
			NM_152877	NP_690616
FAS	204780_s_at	FAS (TNF RECEPTOR	NM_000043	NP_000034
		SUPERFAMILY, MEMBER 6)	NM_152871	NP_690610
			NM_152872	NP_690611
			NM_152873	NP_690612
			NM_152874	NP_690613
			NM_152875	NP_690614
			NM_152876	NP_690615
			NM_152877	NP_690616
FBXL13	1553798_a_at	F-BOX AND LEUCINE-	NM_145032	NP_659469
		RICH REPEAT PROTEIN 13
FBXO9	1559094_at	F-BOX PROTEIN 9	NM_012347	NP_036479
			NM_033480	NP_258441
			NM_033481	NP_258442
FBXO9	1559096_x_at	F-BOX PROTEIN 9	NM_012347	NP_036479
			NM_033480	NP_258441
			NM_033481	NP_258442
FCAR	211307_s_at	FC FRAGMENT OF IGA,	NM_002000	NP_001991
		RECEPTOR FOR	NM_133269	NP_579803
			NM_133271	NP_579805
			NM_133272	NP_579806
			NM_133273	NP_579807
			NM_133274	NP_579808
			NM_133277	NP_579811
			NM_133278	NP_579812
			NM_133279	NP_579813
			NM_133280	NP_579814
FCAR	211306_s_at	FC FRAGMENT OF IGA,	NM_002000	NP_001991
		RECEPTOR FOR	NM_133269	NP_579803
			NM_133271	NP_579805
			NM_133272	NP_579806
			NM_133273	NP_579807
			NM_133274	NP_579808
			NM_133277	NP_579811
			NM_133278	NP_579812
			NM_133279	NP_579813
			NM_133280	NP_579814
FCAR	207674_at	FC FRAGMENT OF IGA,	NM_002000	NP_001991
		RECEPTOR FOR	NM_133269	NP_579803
			NM_133271	NP_579805
			NM_133272	NP_579806
			NM_133273	NP_579807
			NM_133274	NP_579808
			NM_133277	NP_579811
			NM_133278	NP_579812
			NM_133279	NP_579813
			NM_133280	NP_579814
FCAR	211305_x_at	FC FRAGMENT OF IGA,	NM_002000	NP_001991
		RECEPTOR FOR	NM_133269	NP_579803
			NM_133271	NP_579805
			NM_133272	NP_579806
			NM_133273	NP_579807
			NM_133274	NP_579808
			NM_133277	NP_579811
			NM_133278	NP_579812
			NM_133279	NP_579813
			NM_133280	NP_579814
FCGR1A	216950_s_at	FC FRAGMENT OF IGG,	NM_000566	NP_000557
		HIGH AFFINITY IA
FCGR1A	216951_at	FC FRAGMENT OF IGG,	NM_000566	NP_000557
		HIGH AFFINITY IA
FCGR1A	214511_x_at
LOC440607
FEM1C	213341_at	FEM-1 HOMOLOG C	NM_020177	NP_064562
		(C.ELEGANS)
FLJ10213	219906_at	HYPOTHETICAL PROTEIN	NM_018029	NP_060499
		FLJ10213
FLJ10521	1570511_at	HYPOTHETICAL PROTEIN	NM_001011722	NP_001011722
		FLJ10521	NM_018125	NP_060595
FLJ11011	222657_s_at	HYPOTHETICAL PROTEIN	NM_001001481	NP_001001481
		FLJ11011	NM_001001482	NP_001001482
			NM_018299	NP_060769
FLJ11259	218627_at	HYPOTHETICAL PROTEIN	NM_018370	NP_060840
		FLJ11259
FLJ11795	220112_at	HYPOTHETICAL PROTEIN	NM_024669	NP_078945
		FLJ11795
FLJ12770	226059_at	HYPOTHETICAL PROTEIN	NM_032174	NP_115550
		FLJ12770
FLJ13154	218060_s_at	HYPOTHETICAL PROTEIN	NM_024598	NP_078874
		FLJ13154
FLJ13448	219397_at	HYPOTHETICAL PROTEIN	NM_025147	NP_079423
		FLJ13448
FLJ14001	238983_at	HYPOTHETICAL PROTEIN	NM_024677	NP_078953
		FLJ14001
FLJ20273	218035_s_at	RNA-BINDING PROTEIN	NM_019027	NP_061900
FLJ20273	222496_s_at	RNA-BINDING PROTEIN	NM_019027	NP_061900
FLJ20481	227889_at	HYPOTHETICAL PROTEIN	NM_017839	NP_060309
		FLJ20481
FLJ20481	222833_at	HYPOTHETICAL PROTEIN	NM_017839	NP_060309
		FLJ20481
FLJ20701	219093_at	HYPOTHETICAL PROTEIN	NM_017933	NP_060403
		FLJ20701
FLJ22833	219334_s_at	HYPOTHETICAL PROTEIN	NM_022837	NP_073748
		FLJ22833
FLJ22833	233085_s_at	HYPOTHETICAL PROTEIN	NM_022837	NP_073748
		FLJ22833
FLJ22833	222872_x_at	HYPOTHETICAL PROTEIN	NM_022837	NP_073748
		FLJ22833
FLJ23231	218810_at	MCP-1 TREATMENT-	NM_025079	NP_079355
		INDUCED PROTEIN
		(MCPIP)
FLJ25416	228281_at	HYPOTHETICAL PROTEIN	NM_145018	NP_659455
		FLJ25416
FLJ31033	228152_s_at	HYPOTHETICAL PROTEIN	XM_037817	XP_037817
		FLJ31033	XM_376353	XP_376353
FLJ36031	226756_at	HYPOTHETICAL PROTEIN	NM_175884	NP_787080
		FLJ36031
FLJ37858	227354_at	FLJ37858 PROTEIN	NM_001007549	NP_001007550
FLOT1	210142_x_at	FLOTILLIN 1	NM_005803	NP_005794
FNDC3B	225032_at	FIBRONECTIN TYPE III	NM_022763	NP_073600
		DOMAIN CONTAINING 3B
FNDC3B	222692_s_at	FIBRONECTIN TYPE III	NM_022763	NP_073600
		DOMAIN CONTAINING 3B
FNDC3B	222693_at	FIBRONECTIN TYPE III	NM_022763	NP_073600
		DOMAIN CONTAINING 3B
FNDC3B	229865_at	FIBRONECTIN TYPE III	NM_022763	NP_073600
		DOMAIN CONTAINING 3B
FNDC3B	218618_s_at	FIBRONECTIN TYPE III	NM_022763	NP_073600
		DOMAIN CONTAINING 3B
FTS	218373_at	FUSED TOES HOMOLOG	NM_001012398	NP_001012398
		(MOUSE)	NM_022476	NP_071921
FYB	227266_s_at	FYN BINDING PROTEIN	NM_001465	NP_001456
		(FYB-120/130)	NM_199335	NP_955367
FYB	211795_s_at	FYN BINDING PROTEIN	NM_001465	NP_001456
		(FYB-120/130)	NM_199335	NP_955367
G0S2	213524_s_at	PUTATIVE LYMPHOCYTE	NM_015714	NP_056529
		G0/G1 SWITCH GENE
GAB2	238405_at	GRB2-ASSOCIATED	NM_012296	NP_036428
		BINDING PROTEIN 2	NM_080491	NP_536739
GADD45A	203725_at	GROWTH ARREST AND	NM_001924	NP_001915
		DNA-DAMAGE-
		INDUCIBLE, ALPHA
GADD45B	209304_x_at	GROWTH ARREST- AND	NM_015675	NP_056490
		DNA DAMAGE-
		INDUCIBLE GENE
		GADD45
GADD45B	207574_s_at	GROWTH ARREST- AND	NM_015675	NP_056490
		DNA DAMAGE-
		INDUCIBLE GENE
		GADD45
GALNT3	203397_s_at	UDP-N-ACETYL-ALPHA-D-	NM_004482	NP_004473
		GALACTOSAMINE:POLYPEPTIDE
		N-
		ACETYLGALACTOSAMINYL
		TRANSFERASE 3
		(GALNAC-T3)
GBA	210589_s_at	GLUCOSIDASE, BETA;	NM_000157	NP_000148
		ACID (INCLUDES	NM_001005741	NP_001005741
		GLUCOSYLCERAMIDASE)	NM_001005742	NP_001005742
			NM_001005749	NP_001005749
			NM_001005750	NP_001005750
GBA	209093_s_at	GLUCOSIDASE, BETA;	NM_000157	NP_000148
		ACID (INCLUDES	NM_001005741	NP_001005741
		GLUCOSYLCERAMIDASE)	NM_001005742	NP_001005742
			NM_001005749	NP_001005749
			NM_001005750	NP_001005750
GBP2	242907_at	GUANYLATE BINDING	NM_004120	NP_004111
		PROTEIN 2, INTERFERON-
		INDUCIBLE
GCA	203765_at	GRANCALCIN, EF-HAND	NM_012198	NP_036330
		CALCIUM BINDING
		PROTEIN
GCLM	203925_at	GLUTAMATE-CYSTEINE	NM_002061	NP_002052
		LIGASE, MODIFIER
		SUBUNIT
GK	214681_at	GLYCEROL KINASE	NM_000167	NP_000158
			NM_203391	NP_976325
GK	207387_s_at	GLYCEROL KINASE	NM_000167	NP_000158
			NM_203391	NP_976325
GK	217167_x_at	GLYCEROL KINASE	NM_000167	NP_000158
			NM_203391	NP_976325
GK	216316_x_at	GLYCEROL KINASE	NM_000167	NP_000158
			NM_203391	NP_976325
GK	215977_x_at	GLYCEROL KINASE	NM_000167	NP_000158
			NM_203391	NP_976325
GNAI3	201180_s_at	GUANINE NUCLEOTIDE	NM_006496	NP_006487
		BINDING PROTEIN (G
		PROTEIN), ALPHA
		INHIBITING ACTIVITY
		POLYPEPTIDE 3
GNG5	207157_s_at	GUANINE NUCLEOTIDE	NM_005274	NP_005265
		BINDING PROTEIN (G
		PROTEIN), GAMMA 5
GNS	212335_at	GLUCOSAMINE (N-	NM_002076	NP_002067
		ACETYL)-6-SULFATASE
		(SANFILIPPO DISEASE IIID)
GPR160	223423_at	G PROTEIN-COUPLED	NM_014373	NP_055188
		RECEPTOR 160
GPR43	221345_at	G PROTEIN-COUPLED	NM_005306	NP_005297
		RECEPTOR 43
GPR84	223767_at	G PROTEIN-COUPLED	NM_020370	NP_065103
		RECEPTOR 84
GPR97	220404_at	G PROTEIN-COUPLED	NM_170776	NP_740746
		RECEPTOR 97
GTDC1	219770_at	GLYCOSYLTRANSFERASE-	NM_001006636	NP_001006637
		LIKE DOMAIN	NM_024659	NP_078935
		CONTAINING 1
GTF2B	208066_s_at	GENERAL	NM_001514	NP_001505
		TRANSCRIPTION FACTOR
		IIB
GYG	201554_x_at	GLYCOGENIN	NM_004130	NP_004121
GYG	211275_s_at	GLYCOGENIN	NM_004130	NP_004121
HAGH	205012_s_at	HYDROXYACYLGLUTATHIONE	NM_005326	NP_005317
		HYDROLASE
HDAC4	204225_at	HISTONE DEACETYLASE 4	NM_006037	NP_006028
HGF	209960_at	HEPATOCYTE GROWTH	NM_000601	NP_000592
		FACTOR (HEPAPOIETIN A;	NM_001010931	NP_001010931
		SCATTER FACTOR)	NM_001010932	NP_001010932
			NM_001010933	NP_001010933
			NM_001010934	NP_001010934
HIP1	226364_at	HUNTINGTIN	NM_005338	NP_005329
		INTERACTING PROTEIN 1
HIP1	205425_at	HUNTINGTIN	NM_005338	NP_005329
		INTERACTING PROTEIN 1
HIP1	205426_s_at	HUNTINGTIN	NM_005338	NP_005329
		INTERACTING PROTEIN 1
HIST1H2BD	209911_x_at	HISTONE 1, H2BD	NM_021063	NP_066407
			NM_138720	NP_619790
HIST2H2AA	214290_s_at	HISTONE 2, H2AA	NM_003516	NP_003507
HLA-DMA	217478_s_at	HLA-D	NM_006120	NP_006111
		HISTOCOMPATIBILITY
		TYPE
HLA-DMB	203932_at	MAJOR	NM_002118	NP_002109
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DM
		BETA
HLA-DPA1	211990_at	MAJOR	NM_033554	NP_291032
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DP
		ALPHA 1
HLA-DPA1	211991_s_at	MAJOR	NM_033554	NP_291032
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DP
		ALPHA 1
HLA-DPB1	201137_s_at	MAJOR	NM_002121	NP_002112
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DP
		BETA 1
HLA-DQB1	209823_x_at	MAJOR	NM_002123	NP_002114
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DQ
		BETA 1
HLA-DQB1	211656_x_at	MAJOR	NM_002123	NP_002114
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DQ
		BETA 1
HLA-DRA	208894_at	MAJOR	NM_002123	NP_002114
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DR
		ALPHA
HLA-DRA	210982_s_at	MAJOR	NM_002123	NP_002114
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DR
		ALPHA
HLA-DRB1	208306_x_at	MAJOR	NM_002124	NP_002115
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DR
		BETA 1
HLA-DRB1	204670_x_at	MAJOR	NM_002124	NP_002115
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DR
		BETA 1
HLA-DRB1	209312_x_at	MAJOR	NM_002124	NP_002115
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DR
		BETA 1
HLA-DRB1	215193_x_at	MAJOR	NM_002124	NP_002115
		HISTOCOMPATIBILITY
		COMPLEX, CLASS II, DR
		BETA 1
HNRPLL	241692_at	HETEROGENEOUS	NM_138394	NP_612403
		NUCLEAR
		RIBONUCLEOPROTEIN L-
		LIKE
HPGD	203913_s_at	HYDROXYPROSTAGLANDIN	NM_000860	NP_000851
		DEHYDROGENASE 15-
		(NAD)
HRPT2	218578_at	HYPERPARATHYROIDISM	NM_024529	NP_078805
		2 (WITH JAW TUMOR)
HSPC163	228306_at	HSPC163 PROTEIN	NM_014184	NP_054903
HSPC163	218728_s_at	HSPC163 PROTEIN	NM_014184	NP_054903
HSPC163	228437_at	HSPC163 PROTEIN	NM_014184	NP_054903
HSPC163	223993_s_at	HSPC163 PROTEIN	NM_014184	NP_054903
HSPC163	243051_at	HSPC163 PROTEIN	NM_014184	NP_054903
HSPCA	214328_s_at	HEAT SHOCK 90 KDA	NM_005348	NP_005339
		PROTEIN 1, ALPHA
HTATIP2	209448_at	HIV-1 TAT INTERACTIVE	NM_006410	NP_006401
		PROTEIN 2, 30 KDA
HTATIP2	210253_at	HIV-1 TAT INTERACTIVE	NM_006410	NP_006401
		PROTEIN 2, 30 KDA
IDI1	204615_x_at	ISOPENTENYL-	NM_004508	NP_004499
		DIPHOSPHATE DELTA
		ISOMERASE
IDI1	208881_x_at	ISOPENTENYL-	NM_004508	NP_004499
		DIPHOSPHATE DELTA
		ISOMERASE
IFNAR1	225669_at	INTERFERON (ALPHA,	NM_000629	NP_000620
		BETA AND OMEGA)
		RECEPTOR 1
IFNAR1	225661_at	INTERFERON (ALPHA,	NM_000629	NP_000620
		BETA AND OMEGA)
		RECEPTOR 1
IFNAR2	204786_s_at	INTERFERON (ALPHA,	NM_000874	NP_000865
		BETA AND OMEGA)	NM_207584	NP_997467
		RECEPTOR 2	NM_207585	NP_997468
IFNGR1	202727_s_at	INTERFERON GAMMA	NM_000416	NP_000407
		RECEPTOR 1
IGSF2	207167_at	IMMUNOGLOBULIN	NM_004258	NP_004249
		SUPERFAMILY, MEMBER 2
IL10RA	204912_at	INTERLEUKIN 10	NM_001558	NP_001549
		RECEPTOR, ALPHA
IL18R1	206618_at	INTERLEUKIN 18	NM_003855	NP_003846
		RECEPTOR 1
IL1R1	202948_at	INTERLEUKIN 1	NM_000877	NP_000868
		RECEPTOR, TYPE I
IL1R2	211372_s_at	INTERLEUKIN 1	NM_004633	NP_004624
		RECEPTOR, TYPE II	NM_173343	NP_775465
IL1R2	205403_at	INTERLEUKIN 1	NM_004633	NP_004624
		RECEPTOR, TYPE II	NM_173343	NP_775465
IL1RAP	205227_at	INTERLEUKIN 1	NM_002182	NP_002173
		RECEPTOR ACCESSORY	NM_134470	NP_608273
		PROTEIN
INSL3	214572_s_at	INSULIN-LIKE 3 (LEYDIG	NM_005543	NP_005534
		CELL)
IRAK2	231779_at	INTERLEUKIN-1	NM_001570	NP_001561
		RECEPTOR-ASSOCIATED
		KINASE 2
IRAK3	220034_at	INTERLEUKIN-1	NM_007199	NP_009130
		RECEPTOR-ASSOCIATED
		KINASE 3
IRAK4	219618_at	INTERLEUKIN-1	NM_016123	NP_057207
		RECEPTOR-ASSOCIATED
		KINASE 4
ITGAM	205786_s_at	INTEGRIN, ALPHA M	NM_000632	NP_000623
		(COMPLEMENT
		COMPONENT RECEPTOR
		3, ALPHA; ALSO KNOWN
		AS CD11B (P170),
		MACROPHAGE ANTIGEN
		ALPHA POLYPEPTIDE)
ITGB3	216261_at	INTEGRIN, BETA 3	NM_000212	NP_000203
		(PLATELET
		GLYCOPROTEIN IIIA,
		ANTIGEN CD61)
IVNS1ABP	201362_at	INFLUENZA VIRUS NS1A	NM_006469	NP_006460
		BINDING PROTEIN	NM_016389	NP_057473
JAK2	205842_s_at	JANUS KINASE 2 (A	NM_004972	NP_004963
		PROTEIN TYROSINE
		KINASE)
JAK2	205841_at	JANUS KINASE 2 (A	NM_004972	NP_004963
		PROTEIN TYROSINE
		KINASE)
JAK3	211108_s_at	JANUS KINASE 3 (A	NM_000215	NP_000206
		PROTEIN TYROSINE
		KINASE, LEUKOCYTE)
JAK3	227677_at	JANUS KINASE 3 (A	NM_000215	NP_000206
		PROTEIN TYROSINE
		KINASE, LEUKOCYTE)
JUNB	201473_at	JUN B PROTO-ONCOGENE	NM_002229	NP_002220
KCNE1	236407_at	POTASSIUM VOLTAGE-	NM_000219	NP_000210
		GATED CHANNEL, ISK-
		RELATED FAMILY,
		MEMBER 1
KCNJ15	238428_at	POTASSIUM INWARDLY-	NM_002243	NP_002234
		RECTIFYING CHANNEL,	NM_170736	NP_733932
		SUBFAMILY J, MEMBER 15	NM_170737	NP_733933
KCNJ15	210119_at	POTASSIUM INWARDLY-	NM_002243	NP_002234
		RECTIFYING CHANNEL,	NM_170736	NP_733932
		SUBFAMILY J, MEMBER 15	NM_170737	NP_733933
KIAA0040	203144_s_at	KIAA0040	NM_014656	NP_055471
KIAA0103	203584_at	KIAA0103	NM_014673	NP_055488
KIAA0182	212057_at	KIAA0182 PROTEIN	NM_014615	NP_055430
KIAA0261	212264_s_at	KIAA0261	NM_015045	NP_055860
KIAA0635	206003_at	CENTROSOMAL PROTEIN 4	NM_025009	NP_079285
KIAA0746	212314_at	KIAA0746 PROTEIN	NM_015187	NP_056002
KIAA1160	223831_x_at	KIAA1160 PROTEIN	NM_020701	NP_065752
KIAA1533	244808_at	KIAA1533	NM_020895	NP_065946
KIAA1533	224807_at	KIAA1533	NM_020895	NP_065946
KIAA1600	226155_at	KIAA1600	NM_020940	NP_065991
KIAA1632	227638_at	KIAA1632	NM_020964	NP_066015
KIAA1991	242808_at	HYPOTHETICAL PROTEIN	XM_495886	XP_495886
		KIAA1991
KIF1B	225878_at	KINESIN FAMILY	NM_015074	NP_055889
		MEMBER 1B	NM_183416	NP_904325
KIF1B	209234_at	KINESIN FAMILY	NM_015074	NP_055889
		MEMBER 1B	NM_183416	NP_904325
KIF1B	241216_at	KINESIN FAMILY	NM_015074	NP_055889
		MEMBER 1B	NM_183416	NP_904325
KLF11	218486_at	KRUPPEL-LIKE FACTOR 11	NM_003597	NP_003588
KLF7	204334_at	KRUPPEL-LIKE FACTOR 7	NM_003709	NP_003700
		(UBIQUITOUS)
KLHL2	219157_at	KELCH-LIKE 2, MAYVEN	NM_007246	NP_009177
		(DROSOPHILA)
KLHL6	1560396_at	KELCH-LIKE 6	NM_130446	NP_569713
		(DROSOPHILA)
KPNA4	225267_at	KARYOPHERIN ALPHA 4	NM_002268	NP_002259
		(IMPORTIN ALPHA 3)
KPNA4	209653_at	KARYOPHERIN ALPHA 4	NM_002268	NP_002259
		(IMPORTIN ALPHA 3)
KREMEN1	227250_at	KRINGLE CONTAINING	NM_032045	NP_114434
		TRANSMEMBRANE	NM_153379	NP_700358
		PROTEIN 1
KREMEN1	235370_at	KRINGLE CONTAINING	NM_032045	NP_114434
		TRANSMEMBRANE	NM_153379	NP_700358
		PROTEIN 1
KREMEN1	224534_at	KRINGLE CONTAINING	NM_032045	NP_114434
		TRANSMEMBRANE	NM_153379	NP_700358
		PROTEIN 1
LDLR	202068_s_at	LOW DENSITY	NM_000527	NP_000518
		LIPOPROTEIN RECEPTOR
LFNG	228762_at	LUNATIC FRINGE	NM_002304	NP_002295
		HOMOLOG (DROSOPHILA)
LGALS8	208934_s_at	LECTIN, GALACTOSIDE-	NM_006499	NP_006490
		BINDING, SOLUBLE, 8	NM_201543	NP_963837
		(GALECTIN 8)	NM_201544	NP_963838
			NM_201545	NP_963839
LIMK2	1561654_at	LIM DOMAIN KINASE 2	NM_005569	NP_005560
			NM_016733	NP_057952
LIMK2	202193_at	LIM DOMAIN KINASE 2	NM_005569	NP_005560
			NM_016733	NP_057952
LIMK2	210582_s_at	LIM DOMAIN KINASE 2	NM_005569	NP_005560
			NM_016733	NP_057952
LIMK2	217475_s_at	LIM DOMAIN KINASE 2	NM_005569	NP_005560
			NM_016733	NP_057952
LIN7A	240027_at	LIN-7 HOMOLOG A	NM_004664	NP_004655
		(C.ELEGANS)
LIN7A	206440_at	LIN-7 HOMOLOG A	NM_004664	NP_004655
		(C.ELEGANS)
LIR9	1555634_a_at	LEUKOCYTE	NM_021250	NP_067073
		IMMUNOGLOBULIN-LIKE	NM_181879	NP_870994
		RECEPTOR, SUBFAMILY B	NM_181985	NP_871714
		(WITH TM AND ITIM	NM_181986	NP_871715
		DOMAINS), MEMBER 7
		(LILRB7)
LMNB1	203276_at	LAMIN B1	NM_005573	NP_005564
LMTK2	226375_at	LEMUR TYROSINE	NM_014916	NP_055731
		KINASE 2
LOC145758	226513_at	HYPOTHETICAL PROTEIN
		LOC145758
LOC153561	232889_at	HYPOTHETICAL PROTEIN	NM_207331	NP_997214
		LOC153561
LOC199675	235568_at	HYPOTHETICAL PROTEIN	NM_174918	NP_777578
		LOC199675
LOC220929	229743_at	HYPOTHETICAL PROTEIN	NM_182755	NP_877432
		LOC220929
LOC285771	237870_at	HYPOTHETICAL PROTEIN
		LOC285771
LOC286044	222662_at	HYPOTHETICAL PROTEIN
		LOC286044
LOC338758	238893_at	HYPOTHETICAL PROTEIN
		LOC338758
LOC401152	224602_at	HCV F-TRANSACTIVATED	NM_001001701	NP_001001701
		PROTEIN 1
LOC440731	237563_s_at	LOC440731	XM_498838	XP_498838
LOC440823	227168_at
LOC57149	203897_at	HYPOTHETICAL PROTEIN	NM_020424	NP_065157
		A-211C6.1
LOC88523	214748_at	CG016	NM_033111	NP_149102
LRG1	228648_at	LEUCINE-RICH ALPHA-2-	NM_052972	NP_443204
		GLYCOPROTEIN 1
LRPAP1	201186_at	LOW DENSITY	NM_002337	NP_002328
		LIPOPROTEIN RECEPTOR-
		RELATED PROTEIN
		ASSOCIATED PROTEIN 1
LRRC17	1560527_at	LEUCINE RICH REPEAT	NM_005824	NP_005815
		CONTAINING 17
LTB4R	236172_at	LEUKOTRIENE B4	NM_181657	NP_858043
		RECEPTOR
LTBP2	204682_at	LATENT TRANSFORMING	NM_000428	NP_000419
		GROWTH FACTOR BETA
		BINDING PROTEIN 2
LY86	205859_at	LYMPHOCYTE ANTIGEN 86	NM_004271	NP_004262
LY96	206584_at	LYMPHOCYTE ANTIGEN 96	NM_015364	NP_056179
MAP2K1IP1	217971_at	MITOGEN-ACTIVATED	NM_021970	NP_068805
		PROTEIN KINASE KINASE
		1 INTERACTING PROTEIN 1
MAP2K6	205698_s_at	MITOGEN-ACTIVATED	NM_002758	NP_002749
		PROTEIN KINASE KINASE 6	NM_031988	NP_114365
MAPK14	210449_x_at	MAPK14 MITOGEN-	NM_001315	NP_001306
		ACTIVATED PROTEIN	NM_139012	NP_620581
		KINASE 14	NM_139013	NP_620582
			NM_139014	NP_620583
MAPK14	211561_x_at	MAPK14 MITOGEN-	NM_001315	NP_001306
		ACTIVATED PROTEIN	NM_139012	NP_620581
		KINASE 14	NM_139013	NP_620582
			NM_139014	NP_620583
MAPK14	211087_x_at	MAPK14 MITOGEN-	NM_001315	NP_001306
		ACTIVATED PROTEIN	NM_139012	NP_620581
		KINASE 14	NM_139013	NP_620582
			NM_139014	NP_620583
MAPK14	202530_at	MAPK14 MITOGEN-	NM_001315	NP_001306
		ACTIVATED PROTEIN	NM_139012	NP_620581
		KINASE 14	NM_139013	NP_620582
			NM_139014	NP_620583
MARCKSL1	200644_at	MARCKS-LIKE 1	NM_023009	NP_075385
MCTP2	220603_s_at	MULTIPLE C2-DOMAINS	NM_018349	NP_060819
		WITH TWO
		TRANSMEMBRANE
		REGIONS 2
MCTP2	229005_at	MULTIPLE C2-DOMAINS	NM_018349	NP_060819
		WITH TWO
		TRANSMEMBRANE
		REGIONS 2
MCTP2	239893_at	MULTIPLE C2-DOMAINS	NM_018349	NP_060819
		WITH TWO
		TRANSMEMBRANE
		REGIONS 2
MEF2A	214684_at	MADS BOX	NM_005587	NP_005578
		TRANSCRIPTION
		ENHANCER FACTOR 2,
		POLYPEPTIDE A
		(MYOCYTE ENHANCER
		FACTOR 2A)
MEF2C	236395_at	MADS BOX	NM_002397	NP_002388
		TRANSCRIPTION
		ENHANCER FACTOR 2,
		POLYPEPTIDE C
		(MYOCYTE ENHANCER
		FACTOR 2C)
MGC11324	224480_s_at	HYPOTHETICAL PROTEIN	NM_032717	NP_116106
		MGC11324
MGC15619	226879_at	HYPOTHETICAL PROTEIN	NM_032369	NP_115745
		MGC15619
MGC15887	226448_at	HYPOTHETICAL GENE	NM_198552	NP_940954
		SUPPORTED BY BC009447
MGC17301	227055_at	HYPOTHETICAL PROTEIN	NM_152637	NP_689850
		MGC17301
MGC23280	226121_at	HYPOTHETICAL PROTEIN	NM_144683	NP_653284
		MGC23280
MKNK1	209467_s_at	MAP KINASE	NM_003684	NP_003675
		INTERACTING	NM_198973	NP_945324
		SERINE/THREONINE
		KINASE 1
MLKL	238025_at	MIXED LINEAGE KINASE	NM_152649	NP_689862
		DOMAIN-LIKE
MLLT2	201924_at	MYELOID/LYMPHOID OR	NM_005935	NP_005926
		MIXED-LINEAGE
		LEUKEMIA (TRITHORAX
		HOMOLOG,
		DROSOPHILA);
		TRANSLOCATED TO, 2
MMP9	203936_s_at	MATRIX	NM_004994	NP_004985
		METALLOPROTEINASE 9
		(GELATINASE B, 92 KDA
		GELATINASE, 92 KDA
		TYPE IV COLLAGENASE)
MOBK1B	201298_s_at	MOB1, MPS ONE BINDER	NM_018221	NP_060691
		KINASE ACTIVATOR-LIKE
		1B (YEAST)
MOBKL2C	227066_at	MOB1, MPS ONE BINDER	NM_145279	NP_660322
		KINASE ACTIVATOR-LIKE	NM_201403	NP_958805
		2C (YEAST)
MPEG1	226818_at	MACROPHAGE	XM_166227	XP_166227
		EXPRESSED GENE 1
MPEG1	226841_at	MACROPHAGE	XM_166227	XP_166227
		EXPRESSED GENE 1
MSL3L1	207551_s_at	MALE-SPECIFIC LETHAL	NM_006800	NP_006791
		3-LIKE 1 (DROSOPHILA)	NM_078628	NP_523352
			NM_078629	NP_523353
			NM_078630	NP_523354
MSL3L1	214009_at	MALE-SPECIFIC LETHAL	NM_006800	NP_006791
		3-LIKE 1 (DROSOPHILA)	NM_078628	NP_523352
			NM_078629	NP_523353
			NM_078630	NP_523354
MSRB2	218773_s_at	METHIONINE SULFOXIDE	NM_012228	NP_036360
		REDUCTASE B2
MTF1	227150_at	METAL-REGULATORY	NM_005955	NP_005946
		TRANSCRIPTION FACTOR 1
MTMR6	214429_at	MYOTUBULARIN	NM_004685	NP_004676
		RELATED PROTEIN 6
MYO10	201976_s_at	MYOSIN X	NM_012334	NP_036466
NALP1	210113_s_at	NACHT, LEUCINE RICH	NM_014922	NP_055737
		REPEAT AND PYD (PYRIN	NM_033004	NP_127497
		DOMAIN) CONTAINING 1	NM_033006	NP_127499
			NM_033007	NP_127500
NALP1	211824_x_at	NACHT, LEUCINE RICH	NM_014922	NP_055737
		REPEAT AND PYD (PYRIN	NM_033004	NP_127497
		DOMAIN) CONTAINING 1	NM_033006	NP_127499
			NM_033007	NP_127500
NARF	219862_s_at	NUCLEAR PRELAMIN A	NM_012336	NP_036468
		RECOGNITION FACTOR	NM_031968	NP_114174
NBS1	202906_s_at	NIJMEGEN BREAKAGE	NM_002485	NP_002476
		SYNDROME 1 (NIBRIN)
NBS1	217299_s_at	NIJMEGEN BREAKAGE	NM_002485	NP_002476
		SYNDROME 1 (NIBRIN)
NCR1	207860_at	NATURAL	NM_004829	NP_004820
		CYTOTOXICITY
		TRIGGERING RECEPTOR 1
NDST2	203916_at	N-DEACETYLASE/N-	NM_003635	NP_003626
		SULFOTRANSFERASE
		(HEPARAN
		GLUCOSAMINYL) 2
NDUFA1	202298_at	NADH DEHYDROGENASE	NM_004541	NP_004532
		(UBIQUINONE) 1 ALPHA
		SUBCOMPLEX, 1, 7.5 KDA
NDUFB3	203371_s_at	NADH DEHYDROGENASE	NM_002491	NP_002482
		(UBIQUINONE) 1 BETA
		SUBCOMPLEX, 3, 12 KDA
NFKBIZ	223218_s_at	NUCLEAR FACTOR OF	NM_001005474	NP_001005474
		KAPPA LIGHT	NM_031419	NP_113607
		POLYPEPTIDE GENE
		ENHANCER IN B-CELLS
		INHIBITOR, ZETA
NMI	203964_at	N-MYC (AND STAT)	NM_004688	NP_004679
		INTERACTOR
NT5C2	209155_s_at	5′-NUCLEOTIDASE,	NM_012229	NP_036361
		CYTOSOLIC II
NTNG2	233072_at	NETRIN G2	NM_032536	NP_115925
NUPL1	204435_at	NUCLEOPORIN LIKE 1	NM_001008564	NP_001008564
			NM_001008565	NP_001008565
			NM_014089	NP_054808
OACT2	226726_at	O-ACYLTRANSFERASE	NM_138799	NP_620154
		(MEMBRANE BOUND)
		DOMAIN CONTAINING 2
OAT	201599_at	ORNITHINE	NM_000274	NP_000265
		AMINOTRANSFERASE
		(GYRATE ATROPHY)
OMG	207093_s_at	OLIGODENDROCYTE	NM_002544	NP_002535
		MYELIN GLYCOPROTEIN
OPLAH	222025_s_at	5-OXOPROLINASE (ATP-	NM_017570	NP_060040
		HYDROLYSING)
ORF1-FL49	224707_at	PUTATIVE NUCLEAR	NM_032412	NP_115788
		PROTEIN ORF1-FL49
OSM	230170_at	ONCOSTATIN M	NM_020530	NP_065391
OSTalpha	229230_at	ORGANIC SOLUTE	NM_152672	NP_689885
		TRANSPORTER ALPHA
OTUD1	226140_s_at	OTU DOMAIN	XM_166659	XP_166659
		CONTAINING 1
P2RX1	210401_at	PURINERGIC RECEPTOR	NM_002558	NP_002549
		P2X, LIGAND-GATED ION
		CHANNEL, 1
PAG	225622_at	PHOSPHOPROTEIN	NM_018440	NP_060910
		ASSOCIATED WITH
		GLYCOSPHINGOLIPID-
		ENRICHED
		MICRODOMAINS
PAM	202336_s_at	PEPTIDYLGLYCINE	NM_000919	NP_000910
		ALPHA-AMIDATING	NM_138766	NP_620121
		MONOOXYGENASE	NM_138821	NP_620176
			NM_138822	NP_620177
PAPSS1	209043_at	3′-PHOSPHOADENOSINE	NM_005443	NP_005434
		5′-PHOSPHOSULFATE
		SYNTHASE 1
PBEF1	217738_at	PRE-B-CELL COLONY	NM_005746	NP_005737
		ENHANCING FACTOR 1	NM_182790	NP_877591
PBEF1	217739_s_at	PRE-B-CELL COLONY	NM_005746	NP_005737
		ENHANCING FACTOR 1	NM_182790	NP_877591
PBEF1	1555167_s_at	PRE-B-CELL COLONY	NM_005746	NP_005737
		ENHANCING FACTOR 1	NM_182790	NP_877591
PBEF1	243296_at	PRE-B-CELL COLONY	NM_005746	NP_005737
		ENHANCING FACTOR 1	NM_182790	NP_877591
PCGF5	227935_s_at	POLYCOMB GROUP RING	NM_032373	NP_115749
		FINGER 5
PCMT1	208857_s_at	PROTEIN-L-	NM_005389	NP_005380
		ISOASPARTATE (D-
		ASPARTATE) O-
		METHYLTRANSFERASE
PCMT1	210156_s_at	PROTEIN-L-	NM_005389	NP_005380
		ISOASPARTATE (D-
		ASPARTATE) O-
		METHYLTRANSFERASE
PCMT1	205202_at	PROTEIN-L-	NM_005389	NP_005380
		ISOASPARTATE (D-
		ASPARTATE) O-
		METHYLTRANSFERASE
PDCD1LG1	227458_at	CD274 ANTIGEN (CD274)	NM_014143	NP_054862
PDCD1LG1	223834_at	CD274 ANTIGEN (CD274)	NM_014143	NP_054862
PDE5A	239556_at	PHOSPHODIESTERASE 5A,	NM_001083	NP_001074
		CGMP-SPECIFIC	NM_033430	NP_236914
			NM_033437	NP_246273
			NM_033431	NP_237223
PDK1	226452_at	PYRUVATE	NM_002610	NP_002601
		DEHYDROGENASE
		KINASE, ISOENZYME 1
PEA15	200788_s_at	PHOSPHOPROTEIN	NM_003768	NP_003759
		ENRICHED IN
		ASTROCYTES 15
PFKFB2	209992_at	6-PHOSPHOFRUCTO-2-	NM_006212	NP_006203
		KINASE/FRUCTOSE-2,6-
		BIPHOSPHATASE 2
PFKFB2	226733_at	6-PHOSPHOFRUCTO-2-	NM_006212	NP_006203
		KINASE/FRUCTOSE-2,6-
		BIPHOSPHATASE 2
PFKFB3	202464_s_at	6-PHOSPHOFRUCTO-2-	NM_004566	NP_004557
		KINASE/FRUCTOSE-2,6-
		BISPHOSPHATASE 3
PFTK1	204604_at	PFTAIRE PROTEIN	NM_012395	NP_036527
		KINASE 1
PGLYRP1	207384_at	PEPTIDOGLYCAN	NM_005091	NP_005082
		RECOGNITION PROTEIN 1
PGM2	225366_at	PHOSPHOGLUCOMUTASE 2	NM_018290	NP_060760
PGS1	219394_at	PHOSPHATIDYLGLYCERO-	NM_024419	NP_077733
		PHOSPHATE SYNTHASE
PHTF1	210191_s_at	PUTATIVE	NM_006608	NP_006599
		HOMEODOMAIN
		TRANSCRIPTION FACTOR 1
PHTF1	215285_s_at	PUTATIVE	NM_006608	NP_006599
		HOMEODOMAIN
		TRANSCRIPTION FACTOR 1
PHTF1	205702_at	PUTATIVE	NM_006608	NP_006599
		HOMEODOMAIN
		TRANSCRIPTION FACTOR 1
PIK3AP1	226459_at	PHOSPHOINOSITIDE-3-	NM_152309	NP_689522
		KINASE ADAPTOR
		PROTEIN 1
PIK3CB	212688_at	PHOSPHOINOSITIDE-3-	NM_006219	NP_006210
		KINASE, CATALYTIC,
		BETA POLYPEPTIDE
PIM3	224739_at	PIM-3 ONCOGENE	NM_001001852	NP_001001852
PIP5K1A	235646_at	PHOSPHATIDYLINOSITOL-	NM_003557	NP_003548
		4-PHOSPHATE 5-KINASE,
		TYPE I, ALPHA
PLSCR1	244315_at	PHOSPHOLIPID	NM_021105	NP_066928
		SCRAMBLASE 1
PLSCR1	241916_at	PHOSPHOLIPID	NM_021105	NP_066928
		SCRAMBLASE 1
POR	208928_at	P450 (CYTOCHROME)	NM_000941	NP_000932
		OXIDOREDUCTASE
PPP1R12A	201602_s_at	PROTEIN PHOSPHATASE	NM_002480	NP_002471
		1, REGULATORY
		(INHIBITOR) SUBUNIT 12A
PPP4R2	225519_at	PROTEIN PHOSPHATASE	NM_174907	NP_777567
		4, REGULATORY SUBUNIT 2
PPP4R2	226317_at	PROTEIN PHOSPHATASE	NM_174907	NP_777567
		4, REGULATORY SUBUNIT 2
PRO0149	225183_at	PRO0149 PROTEIN	NM_014117	NP_054836
PRV1	219669_at	NEUTROPHIL-SPECIFIC	NM_020406	NP_065139
		ANTIGEN 1
		(POLYCYTHEMIA RUBRA
		VERA 1)
PSTPIP2	219938_s_at	PROLINE/SERINE/THREONINE	NM_024430	NP_077748
		PHOSPHATASE-
		INTERACTING PROTEIN 1
		(PROLINE-SERINE-
		THREONINE
		PHOSPHATASE
		INTERACTING PROTEIN 2)
PTDSR	212723_at	CHROMOSOME 17	NM_015167	NP_055982
		GENOMIC CONTIG,
		ALTERNATE ASSEMBLY
		(PHOSPHATIDYLSERINE
		RECEPTOR)
PTDSR	212722_s_at	CHROMOSOME 17	NM_015167	NP_055982
		GENOMIC CONTIG,
		ALTERNATE ASSEMBLY
		(PHOSPHATIDYLSERINE
		RECEPTOR)
PTGFR	207177_at	CHROMOSOME 17	NM_015167	NP_055982
		GENOMIC CONTIG,
		ALTERNATE ASSEMBLY
		(PHOSPHATIDYLSERINE
		RECEPTOR)
PTPN1	202716_at	PROTEIN TYROSINE	NM_002827	NP_002818
		PHOSPHATASE, NON-
		RECEPTOR TYPE 1
PTX1	226422_at	PTX1 PROTEIN	NM_016570	NP_057654
QSCN6	201482_at	QUIESCIN Q6	NM_001004128	NP_001004128
			NM_002826	NP_002817
RAB10	222981_s_at	RAB10, MEMBER RAS	NM_016131	NP_057215
		ONCOGENE FAMILY
RAB20	219622_at	RAB20, MEMBER RAS	NM_017817	NP_060287
		ONCOGENE FAMILY
RAB24	225251_at	RAB24, MEMBER RAS	NM_130781	NP_570137
		ONCOGENE FAMILY
RAB27A	209514_s_at	RAB27A, MEMBER RAS	NM_004580	NP_004571
		ONCOGENE FAMILY	NM_183234	NP_899057
			NM_183235	NP_899058
			NM_183236	NP_899059
RAB27A	210951_x_at	RAB27A, MEMBER RAS	NM_004580	NP_004571
		ONCOGENE FAMILY	NM_183234	NP_899057
			NM_183235	NP_899058
			NM_183236	NP_899059
RAB43	225632_s_at	RAB43, MEMBER RAS	NM_198490	NP_940892
		ONCOGENE FAMILY
RAB8B	219210_s_at	RAB8B, MEMBER RAS	NM_016530	NP_057614
		ONCOGENE FAMILY
RABGEF1	218310_at	RAB GUANINE	NM_014504	NP_055319
		NUCLEOTIDE EXCHANGE
		FACTOR (RAB GUANINE
		NUCLEOTIDE EXCHANGE
		FACTOR (GEF) 1)
RAD23B	201222_s_at	RAD23 HOMOLOG B	NM_002874	NP_002865
		(S.CEREVISIAE)
RALB	202101_s_at	V-RAL SIMIAN LEUKEMIA	NM_002881	NP_002872
		VIRAL ONCOGENE
		HOMOLOG B (RAS
		RELATED; GTP BINDING
		PROTEIN)
RAPGEFL1	218657_at	RAP GUANINE	NM_014504	NP_055319
		NUCLEOTIDE EXCHANGE
		FACTOR (GEF)-LIKE 1
RARA	228037_at	RETINOIC ACID	NM_000964	NP_000955
		RECEPTOR, ALPHA
RASSF4	226436_at	RAS ASSOCIATION	NM_032023	NP_114412
		(RALGDS/AF-6) DOMAIN	NM_178145	NP_835281
		FAMILY 4
RB1CC1	202033_s_at	RB1-INDUCIBLE COILED-	NM_014781	NP_055596
		COIL 1
RBMS1	225265_at	RNA BINDING MOTIF,	NM_002897	NP_002888
		SINGLE STRANDED	NM_016836	NP_058520
		INTERACTING PROTEIN 1	NM_016839	NP_058523
RBMS1	238317_x_at	RNA BINDING MOTIF,	NM_002897	NP_002888
		SINGLE STRANDED	NM_016836	NP_058520
		INTERACTING PROTEIN 1	NM_016839	NP_058523
RFWD2	234950_s_at	RING FINGER AND WD	NM_001001740	NP_001001740
		REPEAT DOMAIN 2	NM_022457	NP_071902
Rgr	235816_s_at	RAL-GDS RELATED	NM_153615	NP_705843
		PROTEIN RGR
RGS10	204319_s_at	REGULATOR OF G-	NM_001005339	NP_001005339
		PROTEIN SIGNALLING 10	NM_002925	NP_002916
RHOT1	222148_s_at	RAS HOMOLOG GENE	NM_018307	NP_060777
		FAMILY, MEMBER T1
RIT1	209882_at	RAS-LIKE WITHOUT CAAX 1	NM_006912	NP_008843
RNASE6	213566_at	RIBONUCLEASE, RNASE A	NM_005615	NP_005606
		FAMILY, K6
RNASEL	229285_at	RIBONUCLEASE L (2′,5′-	NM_021133	NP_066956
		OLIGOISOADENYLATE
		SYNTHETASE-
		DEPENDENT)
RNF13	201779_s_at	RING FINGER PROTEIN 13	NM_007282	NP_009213
			NM_183381	NP_899237
			NM_183382	NP_899238
			NM_183383	NP_899239
			NM_183384	NP_899240
RNF13	201780_s_at	RING FINGER PROTEIN 13	NM_007282	NP_009213
			NM_183381	NP_899237
			NM_183382	NP_899238
			NM_183383	NP_899239
			NM_183384	NP_899240
ROD1	224618_at	ROD1 REGULATOR OF	NM_005156	NP_005147
		DIFFERENTIATION 1
		(S.POMBE)
ROD1	214697_s_at	ROD1 REGULATOR OF	NM_005156	NP_005147
		DIFFERENTIATION 1
		(S.POMBE)
RRM2	209773_s_at	RIBONUCLEOTIDE	NM_001034	NP_001025
		REDUCTASE M2
		POLYPEPTIDE
RSBN1	213694_at	ROUND SPERMATID	NM_018364	NP_060834
		BASIC PROTEIN 1
RTN1	203485_at	RETICULON 1	NM_021136	NP_066959
			NM_206852	NP_996734
			NM_206857	NP_996739
RTN4	214629_x_at	RETICULON 4	NM_007008	NP_008939
			NM_020532	NP_065393
			NM_153828	NP_722550
			NM_207520	NP_997403
			NM_207521	NP_997404
RY1	212438_at	PUTATIVE NUCLEIC ACID	NM_006857	NP_006848
		BINDING PROTEIN RY-1
S100A12	205863_at	S100 CALCIUM BINDING	NM_005621	NP_005612
		PROTEIN A12
		(CALGRANULIN C)
SAMSN1	1555638_a_at	SAM DOMAIN, SH3	NM_022136	NP_071419
		DOMAIN, AND NUCLEAR
		LOCALIZATION SIGNALS, 1
SAMSN1	220330_s_at	SAM DOMAIN, SH3	NM_022136	NP_071419
		DOMAIN, AND NUCLEAR
		LOCALIZATION SIGNALS, 1
SAP30L	219129_s_at	SIN3A ASSOCIATED	NM_024632	NP_078908
		PROTEIN P30-LIKE
SART2	218854_at	SQUAMOUS CELL	NM_013352	NP_037484
		CARCINOMA ANTIGEN
		RECOGNIZED BY T CELLS 2
SBNO1	218737_at	SNO, STRAWBERRY	NM_018183	NP_060653
		NOTCH HOMOLOG 1
		(DROSOPHILA)
SDF2	203090_at	STROMAL CELL-DERIVED	NM_006923	NP_008854
		FACTOR 2
SDHC	238056_at	SUCCINATE	NM_003001	NP_002992
		DEHYDROGENASE
		COMPLEX, SUBUNIT C,
		INTEGRAL MEMBRANE
		PROTEIN, 15 KDA
SEC15L1	226259_at	SEC15-LIKE 1 (S.CEREVISIAE)	NM_019053	NP_061926
			NM_001013848	NP_001013870
SEC15L1	233924_s_at	SEC15-LIKE 1 (S.CEREVISIAE)	NM_019053	NP_061926
			NM_001013848	NP_001013870
SEC24A	212902_at	SEC24 RELATED GENE	XM_094581	XP_094581
		FAMILY, MEMBER A
		(S.CEREVISIAE)
SEL1L	202064_s_at	SEL-1 SUPPRESSOR OF	NM_005065	NP_005056
		LIN-12-LIKE (C.ELEGANS)
SERPINB1	228726_at	SERINE (OR CYSTEINE)	NM_030666	NP_109591
		PROTEINASE INHIBITOR,
		CLADE B (OVALBUMIN),
		MEMBER 1
SERPINB1	212268_at	SERINE (OR CYSTEINE)	NM_030666	NP_109591
		PROTEINASE INHIBITOR,
		CLADE B (OVALBUMIN),
		MEMBER 1
SF3B14	223416_at	SPLICING FACTOR 3B, 14 KDA	NM_016047	NP_057131
		SUBUNIT
SH3GLB1	209091_s_at	SH3-DOMAIN GRB2-LIKE	NM_016009	NP_057093
		ENDOPHILIN B1
SH3GLB1	210101_x_at	SH3-DOMAIN GRB2-LIKE	NM_016009	NP_057093
		ENDOPHILIN B1
SIPA1L2	225056_at	SIGNAL-INDUCED	NM_020808	NP_065859
		PROLIFERATION-
		ASSOCIATED GENE 1
		(SIGNAL-INDUCED
		PROLIFERATION-
		ASSOCIATED 1 LIKE 2)
SLA	203761_at	SRC-LIKE-ADAPTOR	NM_006748	NP_006739
SLA	244492_at	SRC-LIKE-ADAPTOR	NM_006748	NP_006739
SLC22A4	205896_at	SOLUTE CARRIER	NM_003059	NP_003050
		FAMILY 22 (ORGANIC
		CATION TRANSPORTER),
		MEMBER 4
SLC25A28	221432_s_at	SOLUTE CARRIER	NM_031212	NP_112489
		FAMILY 25, MEMBER 28
SLC26A8	237340_at	SOLUTE CARRIER	NM_052961	NP_443193
		FAMILY 26, MEMBER 8	NM_138718	NP_619732
SLC2A3	202497_x_at	SOLUTE CARRIER	NM_006931	NP_008862
		FAMILY 2 (FACILITATED
		GLUCOSE
		TRANSPORTER), MEMBER 3
SLC2A3	202498_s_at	SOLUTE CARRIER	NM_006931	NP_008862
		FAMILY 2 (FACILITATED
		GLUCOSE
		TRANSPORTER), MEMBER 3
SLC2A3	216236_s_at	SOLUTE CARRIER	NM_006931	NP_008862
		FAMILY 2 (FACILITATED
		GLUCOSE
		TRANSPORTER), MEMBER 3
SLC2A3	202499_s_at	SOLUTE CARRIER	NM_006931	NP_008862
		FAMILY 2 (FACILITATED
		GLUCOSE
		TRANSPORTER), MEMBER 3
SLC2A3	222088_s_at	SOLUTE CARRIER	NM_006931	NP_008862
		FAMILY 2 (FACILITATED
		GLUCOSE
		TRANSPORTER), MEMBER 3
SLC2A3	236571_at	SOLUTE CARRIER	NM_006931	NP_008862
		FAMILY 2 (FACILITATED
		GLUCOSE
		TRANSPORTER), MEMBER 3
SLC37A3	223304_at	SOLUTE CARRIER	NM_032295	NP_115671
		FAMILY 37 (GLYCEROL-3-	NM_207113	NP_996996
		PHOSPHATE
		TRANSPORTER), MEMBER 3
SLC38A2	220924_s_at	SOLUTE CARRIER	NM_018976	NP_061849
		FAMILY 38, MEMBER 2
SMPDL3A	213624_at	SPHINGOMYELIN	NM_006714	NP_006705
		PHOSPHODIESTERASE,
		ACID-LIKE 3A
SOCS3	227697_at	SUPPRESSOR OF	NM_003955	NP_003946
		CYTOKINE SIGNALING 3
SOCS3	206359_at	SUPPRESSOR OF	NM_003955	NP_003946
		CYTOKINE SIGNALING 3
SOD2	216841_s_at	SUPEROXIDE DISMUTASE	NM_000636	NP_000627
		2, MITOCHONDRIAL
SP100	202863_at	NUCLEAR ANTIGEN SP100	NM_003113	NP_003104
SPPL2A	226353_at	SIGNAL PEPTIDE	NM_032802	NP_116191
		PEPTIDASE-LIKE 2A
SQRDL	217995_at	SULFIDE QUINONE	NM_021199	NP_067022
		REDUCTASE-LIKE (YEAST)
SRPK1	202200_s_at	PROTEIN KINASE,	NM_003137	NP_003128
		SERINE/ARGININE-
		SPECIFIC, 1 (SFRS
		PROTEIN KINASE 1)
ST3GAL4	203759_at	ST3 BETA-GALACTOSIDE	NM_006278	NP_006269
		ALPHA-2,3-
		SIALYLTRANSFERASE 4
ST6GALNAC4	223285_s_at	ST6 (ALPHA-N-ACETYL-	NM_014403	NP_055218
		NEURAMINYL-2,3-BETA-	NM_175039	NP_778204
		GALACTOSYL-1,3)-N-	NM_175040	NP_778205
		ACETYLGALACTOSAMINIDE
		ALPHA-2,6-
		SIALYLTRANSFERASE 4
STAT5B	1555086_at	SIGNAL TRANSDUCER	NM_012448	NP_036580
		AND ACTIVATOR OF
		TRANSCRIPTION 5B
STK17B	205214_at	SERINE/THREONINE	NM_004226	NP_004217
		KINASE 17B (APOPTOSIS-
		INDUCING)
STK3	204068_at	SERINE/THREONINE	NM_006281	NP_006272
		PROTEIN KINASE 3
		(SERINE/THREONINE
		KINASE 3 (STE20
		HOMOLOG, YEAST))
STOM	201060_x_at	STOMATIN	NM_004099	NP_004090
			NM_198194	NP_937837
STX3A	209238_at	SYNTAXIN 3A	NM_004177	NP_004168
SULF2	233555_s_at	SULFATASE 2	NM_018837	NP_061325
			NM_198596	NP_940998
SULF2	224724_at	SULFATASE 2	NM_018837	NP_061325
			NM_198596	NP_940998
SULT1A1	203615_x_at	SULFOTRANSFERASE	NM_001055	NP_001046
		FAMILY, CYTOSOLIC, 1A,	NM_177529	NP_803565
		PHENOL-PREFERRING,	NM_177530	NP_803566
		MEMBER 1	NM_177534	NP_803878
			NM_177536	NP_803880
SULT1B1	207601_at	SULFOTRANSFERASE	NM_014465	NP_055280
		FAMILY, CYTOSOLIC, 1B,
		MEMBER 1
TBC1D15	218268_at	TBC1 DOMAIN FAMILY,	NM_022771	NP_073608
		MEMBER 15
TBC1D8	204526_s_at	TBC1 DOMAIN FAMILY,	NM_007063	NP_008994
		MEMBER 8 (WITH GRAM
		DOMAIN)
TCTEL1	201999_s_at	T-COMPLEX-	NM_006519	NP_006510
		ASSOCIATED-TESTIS-
		EXPRESSED 1 (T-
		COMPLEX-ASSOCIATED-
		TESTIS-EXPRESSED 1-LIKE 1
TCTEL1	242109_at	T-COMPLEX-	NM_006519	NP_006510
		ASSOCIATED-TESTIS-
		EXPRESSED 1 (T-
		COMPLEX-ASSOCIATED-
		TESTIS-EXPRESSED 1-LIKE 1
TDRD9	228285_at	TUDOR DOMAIN	NM_153046	NP_694591
		CONTAINING 9
TGFBI	201506_at	TRANSFORMING	NM_000358	NP_000349
		GROWTH FACTOR, BETA-
		1 (TRANSFORMING
		GROWTH FACTOR, BETA-
		INDUCED, 68 KDA)
TIAM2	222942_s_at	T-CELL LYMPHOMA	NM_001010927	NP_001010927
		INVASION AND	NM_012454	NP_036586
		METASTASIS 2
TIFA	238858_at	TRAF-INTERACTING	NM_052864	NP_443096
		PROTEIN WITH A
		FORKHEAD-ASSOCIATED
		DOMAIN
TIFA	226117_at	TRAF-INTERACTING	NM_052864	NP_443096
		PROTEIN WITH A
		FORKHEAD-ASSOCIATED
		DOMAIN
TIFA	235971_at	TRAF-INTERACTING	NM_052864	NP_443096
		PROTEIN WITH A
		FORKHEAD-ASSOCIATED
		DOMAIN
TLR5	210166_at	TOLL-LIKE RECEPTOR 5	NM_003268	NP_003259
TMEM2	218113_at	TRANSMEMBRANE	NM_013390	NP_037522
		PROTEIN 2
TMEM33	235907_at	TRANSMEMBRANE	NM_018126	NP_060596
		PROTEIN 33
TMOD3	223078_s_at	TROPOMODULIN 3	NM_014547	NP_055362
		(UBIQUITOUS)
TncRNA	214657_s_at	TROPHOBLAST-DERIVED
		NONCODING RNA
TNFAIP6	206026_s_at	TUMOR NECROSIS	NM_007115	NP_009046
		FACTOR, ALPHA-
		INDUCED PROTEIN 6
TNFAIP6	206025_s_at	TUMOR NECROSIS	NM_007115	NP_009046
		FACTOR, ALPHA-
		INDUCED PROTEIN 6
TNFAIP9	225987_at	TUMOR NECROSIS	NM_024636	NP_078912
		FACTOR, ALPHA-
		INDUCED PROTEIN 9
TNFSF10	202687_s_at	TUMOR NECROSIS	NM_003810	NP_003801
		FACTOR (LIGAND)
		SUPERFAMILY, MEMBER 10
TNFSF13B	223501_at	TUMOR NECROSIS	NM_006573	NP_006564
		FACTOR (LIGAND)
		SUPERFAMILY, MEMBER 13B
TOP1	208901_s_at	TOPOISOMERASE (DNA) I	NM_003286	NP_003277
TOSO	221602_s_at	FAS APOPTOTIC	NM_005449	NP_005440
		INHIBITORY MOLECULE
		(FAIM3)
TPARL	218095_s_at	TPA REGULATED LOCUS	NM_018475	NP_060945
TPCN1	242108_at	TWO PORE SEGMENT	NM_017901	NP_060371
		CHANNEL 1
TPRT	220865_s_at	TRANS-	NM_014317	NP_055132
		PRENYLTRANSFERASE
TRA@	234013_at	T CELL RECEPTOR ALPHA
		LOCUS
TRA@	211902_x_at	T CELL RECEPTOR ALPHA
		LOCUS
TRBC1	211796_s_at	T CELL RECEPTOR BETA
		CONSTANT 1
TRIB1	202241_at	TRIBBLES HOMOLOG 1	NM_025195	NP_079471
		(DROSOPHILA)
TRPM6	224412_s_at	TRANSIENT RECEPTOR	NM_017662	NP_060132
		POTENTIAL CATION
		CHANNEL, SUBFAMILY
		M, MEMBER 6
TTN	240793_at	TITIN	NM_003319	NP_003310
			NM_133378	NP_596869
			NM_133379	NP_596870
			NM_133432	NP_597676
			NM_133437	NP_597681
TTYH2	223741_s_at	TWEETY, DROSOPHILA,	NM_032646	NP_116035
		HOMOLOG OF, 2	NM_052869	NP_443101
TXN	208864_s_at	THIOREDOXIN	NM_003329	NP_003320
UBE2H	222421_at	UBIQUITIN-	NM_003344	NP_003335
		CONJUGATING ENZYME	NM_182697	NP_874356
		E2H (UBC8 HOMOLOG,
		YEAST)
UBE2J1	217826_s_at	UBIQUITIN-	NM_016021	NP_057105
		CONJUGATING ENZYME
		E2, J1 (UBC6 HOMOLOG,
		YEAST)
UBQLN2	215884_s_at	UBIQUILIN 2	NM_013444	NP_038472
UNC84B	229548_at	UNC-84 HOMOLOG B	NM_015374	NP_056189
		(C.ELEGANS)
USP38	223289_s_at	UBIQUITIN SPECIFIC	NM_032557	NP_115946
		PROTEASE 38
USP9X	201099_at	UBIQUITIN SPECIFIC	NM_004652	NP_004643
		PROTEASE 9, X-LINKED	NM_021906	NP_068706
		(FAT FACETS-LIKE,
		DROSOPHILA)
VAV3	218807_at	VAV 3 ONCOGENE	NM_006113	NP_006104
WBP4	203598_s_at	WW DOMAIN BINDING	NM_007187	NP_009118
		PROTEIN 4 (FORMIN
		BINDING PROTEIN 21)
WDFY3	212606_at	WD REPEAT AND FYVE	NM_014991	NP_055806
		DOMAIN CONTAINING 3	NM_178583	NP_848698
			NM_178585	NP_848700
WDFY3	212602_at	WD REPEAT AND FYVE	NM_014991	NP_055806
		DOMAIN CONTAINING 3	NM_178583	NP_848698
			NM_178585	NP_848700
WDFY3	212598_at	WD REPEAT AND FYVE	NM_014991	NP_055806
		DOMAIN CONTAINING 3	NM_178583	NP_848698
			NM_178585	NP_848700
WSB1	227501_at	WD REPEAT AND SOCS	NM_015626	NP_056441
		BOX-CONTAINING 1	NM_134264	NP_599026
			NM_134265	NP_599027
WSB1	210561_s_at	WD REPEAT AND SOCS	NM_015626	NP_056441
		BOX-CONTAINING 1	NM_134264	NP_599026
			NM_134265	NP_599027
WSB1	201296_s_at	WD REPEAT AND SOCS	NM_015626	NP_056441
		BOX-CONTAINING 1	NM_134264	NP_599026
			NM_134265	NP_599027
XRN1	1555785_a_at	5′-3′ EXORIBONUCLEASE 1	NM_019001	NP_061874
XRN1	233632_s_at	5′-3′ EXORIBONUCLEASE 1	NM_019001	NP_061874
ZC3HAV1	225634_at	ZINC FINGER CCCH TYPE,	NM_020119	NP_064504
		ANTIVIRAL 1	NM_024625	NP_078901
ZCSL2	225195_at	ZINC FINGER, CSL	NM_206831	NP_996662
		DOMAIN CONTAINING 2
ZDHHC19	231122_x_at	ZINC FINGER, DHHC	NM_144637	NP_653238
		DOMAIN CONTAINING 19
ZDHHC19	1553952_at	ZINC FINGER, DHHC	NM_144637	NP_653238
		DOMAIN CONTAINING 19
ZFP276	213778_x_at	ZINC FINGER PROTEIN 276	NM_152287	NP_689500
		HOMOLOG (MOUSE)
ZFP36L2	201367_s_at	ZINC FINGER PROTEIN 36,	NM_006887	NP_008818
		C3H TYPE-LIKE 2; ZFP36L2
ZFP36L2	201369_s_at	ZINC FINGER PROTEIN 36,	NM_006887	NP_008818
		C3H TYPE-LIKE 2; ZFP36L2
ZNF167	206314_at	ZINC FINGER PROTEIN 167	NM_018651	NP_061121
			NM_025169	NP_079445
	230585_at	EST
	200880_at	EST
	230267_at	EST
	215966_x_at	EST
	237071_at	EST
	230683_at	EST
	241388_at	EST
	204166_at	EST
	241652_x_at	EST
	229968_at	EST
	223596_at	EST
	240310_at	EST
	216609_at	EST
	224604_at	EST
	223797_at	EST
	238973_s_at	EST
	230632_at	EST
	230575_at	EST
	1559777_at	EST
	244313_at	EST
	242582_at	EST
	233264_at	EST
	219253_at	EST
	235427_at	EST
	1555311_at	EST
	229934_at	EST
	231035_s_at	EST
	230999_at	EST
	224261_at	EST
	239780_at	EST
	239669_at	EST
	213002_at	EST
	227925_at	EST
	235456_at	EST
	233312_at	EST
	239167_at	EST
	1569263_at	EST
	216198_at	EST
	232876_at	EST
	237387_at	EST
	216621_at	EST
	235352_at	EST
	1564933_at	EST
	222376_at	EST
	205922_at	EST
	1557626_at	EST
	228758_at	EST
	1557733_a_at	EST
	236898_at	EST

Each of the sequences, genes, proteins, and probesets identified in Table 30 is hereby incorporated by reference.

6.7 Exemplary Biomarker Combinations

In one embodiment of the present invention, an additional criterion was applied to the set of biomarkers identified in Section 6.6. Specifically, the additional criterion that was imposed was a requirement that each respective biomarker under consideration exhibit at least a 1.2× fold change between the median value for the respective biomarker among the subjects that acquired sepsis during a defined time period (sepsis subjects) and the median value for the respective biomarker among subjects that do not acquire sepsis during the defined time period (SIRS subjects) at the T₋₁₂ static time and at the T₋₃ static time periods. Furthermore, to satisfy the third criterion, the biomarker must have been used in at least one multivariate analysis with significant classification performance where significant classification performance is defined by having a lower 95^th percentile for accuracy on a training data set that is grater than 50% and a point estimate for accuracy on the validation set that is greater than 65% at any time point measured. As noted in FIG. 30, application of this third filter criterion reduced the number of eligible biomarkers from 626 to 130. These biomarkers are listed column two of Table 31. In column two of Table 31, the biomarkers are indicated by the U133 plus 2.0 probeset to which they bind. However, in some embodiments, each such biomarker is, in fact, an mRNA, cDNA, or other such nucleic acid molecule corresponding to the identified U133 plus 2.0 oligonucleotide probe listed in column two of Table 31.

In column one of Table 31, each biomarker is listed by a gene name, such as, for example, a Human Gene Nomenclature Database (HUGO) symbol set forth by the Gene Nomenclature Committee, Department of Biology, University College London. As is known in the art, some human genome genes are represented by more than one probeset in the U133 plus 2.0 array. Furthermore, some of the oligonucleotides in the U133 plus 2.0 array represent expression sequence tags (ESTs) that do not correspond to a known gene. As a result, the 130 biomarkers listed in Table 31, in fact, represent 95 different known genes (see FIG. 30). Where known, the names of the 95 different human genes are listed in column three of Table 31.

In column four of Table 31, the median fold change between the mean value of the biomarker measured from T₋₁₂ samples of those subjects in the training population that develop sepsis (sepsis subjects) versus the mean value of the biomarker measured from T., samples of those subjects in the training population that do not develop sepsis (SIRS subjects) is given. In column five of Table 31, the direction of the fold change, where “+” indicates that the mean value in the sepsis subjects is greater than in the SIRS subjects, is given.

In column six of Table 31, the median fold change between the mean value of the biomarker measured from T₋₃₆ samples of those subjects in the training population that develop sepsis (sepsis subjects) versus the mean value of the biomarker measured from T₋₃₆ samples of those subjects in the training population that do not develop sepsis (SIRS subjects) is given. In column seven of Table 31, the direction of the fold change, where “+” indicates that the mean value in the sepsis subjects is greater than in the SIRS subjects, is given.

In a particular embodiment, the biomarker profile comprises at least two different biomarkers that each contain one of the probesets of Table 32, biomarkers that contain the complement of one of the probesets of Table 32, or biomarkers that contain an amino acid sequence encoded by a gene that contains one of the probesets of Table 32. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example amplified nucleic acid, or proteins. The biomarker profile further comprises a respective corresponding feature for the at least two biomarkers. Generally, the at least two biomarkers are derived from at least two different genes. In the case where a biomarker is based upon a gene that includes the sequence of a probeset listed in Table 32 or a complement thereof, the biomarker can be, for example, a transcript made by the gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still, the biomarker can be, for example, a protein encoded by a gene that includes a probeset sequence described in Table 32 or a discriminating fragment of the protein, or an indication of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein. In one embodiment, a biomarker profile of the present invention comprises a plurality of biomarkers that contain at least five, at least ten at least fifteen, at least twenty, at least thirty, between 2 and 5, between 3 and 7, or less than 15 of the sequences of the probesets of Table 32, or complements thereof, or genes including one of at least five of the sequences or complements thereof, or a discriminating fragment thereof, or an amino acid sequence encoded by any of the foregoing nucleic acid sequences, or any discriminating fragment of such an amino acid sequence. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example amplified nucleic acid, or proteins. In some embodiments a biomarker is any gene that includes the sequence in an Affymetrix probeset given in Table 31, or any gene that includes a complement of the sequence in an Affymetrix probeset given in Table 32, or any mRNA, cDNA or other form of amplified nucleic acid of the foregoing, for any discriminating fragment of the foregoing, or any amino acid sequence coded by the foregoing, or any discriminating fragment of such a protein.

TABLE 31
Exemplary biomarkers that discriminate between converters and non-converters
			T−12 Values	T−36 Values
Gene	Affymetrix	Gene	Median		Median
Symbol	Probeset name	Name	FC	Direction	FC	Direction
Column	Column	Column	Column	Column	Column	Column
1	2	3	3	4	5	6
	1555785_a_at	EST	1.34	Up	1.31	up
	227150_at	EST	1.45	Up	1.34	up
	238973_s_at	EST	1.33	Up	1.25	up
	239893_at	EST	1.89	Up	1.46	up
	237563_s_at	EST	1.84	Up	1.60	up
	244313_at	EST	1.87	Up	1.80	up
	237071_at	EST	1.73	up	1.37	up
	229934_at	EST	1.67	up	1.41	up
	1555311_at	EST	1.31	up	1.21	up
	233264_at	EST	1.52	up	1.36	up
	239780_at	EST	1.93	up	1.42	up
	238405_at	EST	3.02	up	2.23	up
3′HEXO	226416_at	HISTONE	1.70	up	1.41	up
		MRNA 3′ END
		EXORIBO-
		NUCLEASE
3′HEXO	231852_at		1.45	up	1.22	up
ADORA2A	205013_s_at	ADENOSINE	1.32	up	1.33	up
		A2 RECEPTOR
ANXA3	209369_at	ANNEXIN A3	2.82	up	2.23	up
ASAHL	214765_s_at	N-	1.28	down	1.29	down
		ACYLSPHIN-
		GOSINE
		AMIDO-
		HYDROLASE-
		LIKE
		PROTEIN
ASAHL	232072_at		1.23	down	1.31	down
ASAHL	227135_at		1.24	down	1.26	down
ATP11B	1554557_at	ATPASE,	1.70	up	1.49	up
		CLASS VI,
		TYPE 11B
ATP6V1C1	202872_at	ATPASE, H+	1.85	up	1.49	up
		TRANSPORTING,
		LYSOSOMAL,
		42-KD, V1
		SUBUNIT C,
		ISOFORM 1
B4GALT5	221485_at	BETA-1,4-	1.67	up	1.43	up
		GALACTOSYL-
		TRANSFERASE
BASP1	202391_at	BRAIN-	1.42	up	1.23	up
		ABUNDANT
		SIGNAL
		PROTEIN
BAZ1A	217986_s_at	BROMODOMA	1.89	up	1.57	up
		IN ADJACENT
		TO ZINC
		FINGER
		DOMAIN, 1A
BCL6	203140_at	B-CELL	1.46	up	1.33	up
		LYMPHOMA 6
BMX	206464_at	BONE	1.87	up	1.52	up
		MARROW
		KINASE, X-
		LINKED
C16orf7	205781_at	CHROMOSOME	1.96	up	1.49	up
		16 OPEN-
		READING
		FRAME 7
C20orf32	1554786_at	CHROMOSOME	1.27	down	1.24	down
		20 OPEN-
		READING
		FRAME 32
C3F	203547_at	COMPLEMENT	1.28	down	1.26	down
		COMPONENT 3
C8FW	202241_at	C8FW GENE;	1.57	up	1.34	up
		PHOSPHO-
		PROTEIN.
CEACAM1	209498_at	CARCINO-	2.78	up	2.20	up
		EMBRYONIC
		ANTIGEN-
		RELATED
		CELL
		ADHESION
		MOLECULE 1
CEACAM1	211883_x_at		1.87	up	1.61	up
CECR1	219505_at	CAT EYE	1.25	down	1.26	down
		SYNDROME
		CHROMOSOME
		REGION,
		CANDIDATE 1
CHCHD7	222701_s_at	COILED-COIL-	1.58	up	1.26	up
		HELIX
		DOMAIN-
		CONTAINING
		PROTEIN 7
CHSY1	203044_at	CARBO-	1.78	up	1.24	up
		HYDRATE
		SYNTHASE 1
CKLF	223451_s_at	CHEMOKINE-	1.59	up	1.40	up
		LIKE FACTOR
CKLF	219161_s_at		1.38	up	1.31	up
CL25022	217883_at		1.36	up	1.31	up
CPD	201940_at	CARBOXY-	1.61	up	1.38	up
		PEPTIDASE D
CPD	201941_at		1.61	up	1.35	up
CRTAP	1554464_a_at	CARTILAGE-	1.23	down	1.21	down
		ASSOCIATED
		PROTEIN
DHRS9	219799_s_at	MEMBRANE	1.94	up	1.52	up
		PROTEIN,
		PALM-
		ITOYLATED
		3; MPP3
EIF4G3	201936_s_at	EUKARYOTIC	1.58	up	1.28	up
		TRANSLATION
		INITIATION
		FACTOR 4-
		GAMMA, 3
FAD104	218618_s_at	FIBRONECTIN	1.61	up	1.38	up
		TYPE III
		DOMAIN
		CONTAINING
		3B (FNDC3B
FAD104	225032_at		1.63	up	1.41	up
FAD104	222692_s_at		1.74	up	1.59	up
FAD104	222693_at		1.88	up	1.92	up
FCGR1A	214511_x_at	FC	2.37	up	1.71	up
		FRAGMENT
		OF IGG, HIGH
		AFFINITY IA
FCGR1A	216950_s_at		2.56	up	1.60	up
FLJ11175	229005_at		1.77	up	1.50	up
FLJ11175	220603_s_at		2.12	up	1.77	up
FLJ11259	218627_at		1.54	up	1.25	up
FLJ11795	220112_at		1.80	up	1.62	up
FLJ22833	219334_s_at		1.49	up	1.28	up
G0S2	213524_s_at		1.69	up	1.30	up
GADD45B	207574_s_at	GROWTH	1.55	up	1.37	up
		ARREST-
		AND DNA
		DAMAGE-
		INDUCIBLE
		GENE GADD45
GADD45B	209304_x_at		1.42	up	1.25	up
GK	214681_at	GLYCEROL	1.76	up	1.39	up
		KINASE
GPR160	223423_at	G PROTEIN-	1.83	up	1.54	up
		COUPLED
		RECEPTOR 160
HLA-DMA	217478_s_at	HLA-D	1.32	down	1.27	down
		HISTOCOMPAT-
		IBILITY
		TYPE
HLA-DMB	203932_at		1.29	down	1.27	down
HLA-	211991_s_at		1.34	down	1.27	down
DPA1
HLA-	209823_x_at		1.31	down	1.20	down
DQB1
HLA-DRA	210982_s_at		1.25	down	1.24	down
HLA-DRA	208894_at		1.29	down	1.23	down
HLA-	215193_x_at		1.30	down	1.30	down
DRB1
HLA-	209312_x_at		1.27	down	1.30	down
DRB1
HLA-	204670_x_at		1.25	down	1.27	down
DRB4
HLA-	208306_x_at		1.27	down	1.27	down
DRB4
HPGD	203913_s_at	15-	2.01	up	1.57	up
		HYDROXY-
		PROSTA-
		GLANDIN
		DEHYDRO-
		GENASE
HRPT2	218578_at	HYPERPARA-	1.43	up	1.27	up
		THYROIDISM 2
HSPC163	228437_at	HSPC163	1.64	up	1.46	up
		PROTEIN
HSPC163	218728_s_at		2.00	up	1.52	up
IDI1	204615_x_at	ISOPENTENYL-	1.51	up	1.31	up
		DIPHOSPHATE
		DELTA-
		ISOMERASE
IL18R1	206618_at	INTERLEUKIN	3.18	up	2.37	up
		18 RECEPTOR 1
KCNE1	236407_at	POTASSIUM	1.68	up	1.45	up
		CHANNEL,
		VOLTAGE-
		GATED, ISK-
		RELATED
		SUBFAMILY
KIF1B	225878_at	KINESIN	2.04	up	1.62	up
		FAMILY
		MEMBER 1B;
KREMEN1	227250_at	KRINGLE	2.11	up	1.32	up
		CONTAINING
		TRANS-
		MEMBRANE
		PROTEIN 1
LDLR	202068_s_at	LOW DENSITY	1.55	up	1.52	up
		LIPOPROTEIN
		RECEPTOR
LIMK2	202193_at	LIM DOMAIN	2.05	up	1.51	up
		KINASE 2
LOC199675	235568_at		2.91	up	2.03	up
LOC284829	225669_at		1.48	up	1.30	up
LOC285771	237870_at		1.40	up	1.34	up
LRG1	228648_at	LEUCINE-	2.08	up	1.62	up
		RICH ALPHA-
		2-
		GLYCO-
		PROTEIN 1
MGC22805	239196_at	NOVEL GENE	2.30	up	1.86	up
		(MGC22805),
MGC22805	238439_at		3.38	up	2.24	up
MPEG1	226841_at	MACROPHAGE	1.23	down	1.21	down
		EXPRESSED
		GENE 1
OAT	201599_at	ORNITHINE	1.53	up	1.44	up
		AMINOTRANS-
		FERASE
		DEFICIENCY
ORF1-FL49	224707_at		1.75	up	1.65	up
PDCD1LG1	227458_at	PROGRAMMED	2.22	up	1.86	up
		CELL
		DEATH 1
		LIGAND 1
PFKFB2	226733_at	6-PHOSPHO-	1.70	up	1.28	up
		FRUCTO-
		2-KINASE
PFKFB2	209992_at		1.65	up	1.43	up
PFKFB3	202464_s_at	6-	3.02	up	1.95	up
		PHOSPHO-
		FRUCTO-2-
		KINASE/
		FRUCTOSE-2,6-
		BISPHOSPHA-
		TASE 3
PGS1	219394_at	PHOSPHA-	2.32	up	1.70	up
		TIDYLGLYCERO-
		PHOSPHATE
		SYNTHASE
PHTF1	205702_at	PUTATIVE	1.37	up	1.20	up
		HOMEODOMAIN
		TRANSCRIPTION
		FACTOR 1
PIK3AP1	226459_at	PHOSPHO-	1.64	up	1.39	up
		INOSITIDE 3-
		KINASE
		ADAPTOR
		PROTEIN 1
PLSCR1	241916_at	PHOSPHOLIPID	2.01	up	1.57	up
		SCRAMBLASE 1
PRO2852	223797_at		1.62	up	1.42	up
PRV1	219669_at	NEUTROPHIL-	7.08	up	4.72	up
		SPECIFIC
		ANTIGEN 1
PSTPIP2	219938_s_at	PROLINE/	2.54	up	1.82	up
		SERINE/
		THREONINE
		PHOSPHATASE-
		INTERACTING
		PROTEIN 1
PTDSR	212723_at	CHROMOSOME	1.45	up	1.34	up
		17 GENOMIC
		CONTIG,
		ALTERNATE
		ASSEMBLY
RABGEF1	218310_at	RAB GUANINE	2.03	up	1.59	up
		NUCLEOTIDE
		EXCHANGE
		FACTOR
RARA	228037_at	RETINOIC	1.54	up	1.20	up
		ACID
		RECEPTOR,
		ALPHA
RNASEL	229285_at	RIBONUCLEASE	1.68	up	1.36	up
		L
SAMSN1	1555638_a_at	SAM DOMAIN,	2.22	up	1.42	up
		SH3 DOMAIN,
		AND
		NUCLEAR
		LOCALIZATION
		SIGNALS 1
SAMSN1	220330_s_at		2.29	up	2.10	up
SEC15L1	226259_at	SEC15-LIKE 1	1.64	up	1.43	up
		(S.
		CEREVISIAE)
		(SEC15L1),
		MRNA
SIPA1L2	225056_at	SIGNAL-	2.02	up	1.52	up
		INDUCED
		PROLIFERATION-
		ASSOCIATED
		GENE 1
SLC26A8	237340_at		2.01	up	1.48	up
SLC2A3	202499_s_at	SOLUTE	1.87	up	1.71	up
		CARRIER
		FAMILY 2
		(FACILITATED
		GLUCOSE
		TRANSPORTER),
		MEMBER 3
SOCS3	227697_at	SUPPRESSOR	2.84	up	2.15	up
		OF CYTOKINE
		SIGNALING 3
SOD2	216841_s_at	SUPEROXIDE	1.56	up	1.55	up
		DISMUTASE 2
SPPL2A	226353_at	SIGNAL	1.48	up	1.51	up
		PEPTIDE
		PEPTIDASE-
		LIKE 2A
SRPK1	202200_s_at	PROTEIN	1.80	up	1.46	up
		KINASE,
		SERINE/
		ARGININE-
		SPECIFIC, 1
STK3	204068_at	SERINE/	1.74	up	1.33	up
		THREONINE
		PROTEIN
		KINASE 3
SULF2	224724_at	SULFATASE 2	1.36	down	1.35	down
		(SULF2),
		TRANSCRIPT
		VARIANT 2
SULF2	233555_s_at		1.37	down	1.30	down
T2BP	226117_at	TRAF-2	2.90	up	1.90	up
		BINDING
		PROTEIN
T2BP	235971_at		1.47	up	1.27	up
T2BP	238858_at		1.32	up	1.21	up
TBC1D8	204526_s_at	TBC1 DOMAIN	1.55	up	1.40	up
		FAMILY,
		MEMBER 8
TCTEL1	201999_s_at	T-COMPLEX-	1.46	up	1.22	up
		ASSOCIATED-
		TESTIS-
		EXPRESSED 1
TGFBI	201506_at	TRANSFORMING	1.38	down	1.41	down
		GROWTH
		FACTOR,
		BETA-1
TTYH2	223741_s_at	TWEETY,	1.28	down	1.24	down
		DROSOPHILA,
		HOMOLOG OF, 2
WDFY3	212598_at	WD REPEAT	1.77	up	1.35	up
		AND FYVE
		DOMAIN
		CONTAINING 3
WDFY3	212606_at		1.56	up	1.35	up
WSB1	201296_s_at	WD REPEAT	1.74	up	1.52	up
		AND SOCS
		BOX-
		CONTAINING 1
ZDHHC19	231122_x_at	ZINC FINGER,	2.08	up	2.13	up
		DHHC
		DOMAIN
		CONTAINING
		19 (ZDHHC19
ZDHHC19	1553952_at		1.37	up	1.38	up
ZFP36L2	201367_s_at	ZINC FINGER	1.23	down	1.28	down
		PROTEIN 36,
		C3H TYPE-
		LIKE 2; ZFP36L2

Each of the sequences, genes, proteins, and probesets identified in Table 31 is hereby incorporated by reference herein in its entirety.

Table 31, above, provides a list of select biomarkers of the present invention. Where known, gene names are provided. Column two of Table 32, below, provides the GenBank@ database accession numbers for the human nucleotide sequences of the biomarkers listed in Table 31, where known. Column three of Table 32 further provides the GenBank® database accession numbers for the corresponding amino acid sequences of the biomarkers of Table 31, where known. The biomarkers of the present invention include, but are not limited to, the genes and proteins identified by the accession numbers of Table 32, splicing variants thereof, discriminating fragments of mRNA, cDNA or other nucleic acids and/or peptides corresponding to all or a discriminating portion of such genes and proteins, etc.

These gene and protein accession numbers are provided in order to identify some of the biomarkers of the present invention. GenBank* is the publicly available genetic sequence database of the National Institutes of Health (NIH), and is an annotated collection of all publicly available DNA sequences (see, e.g., Nucleic Acids Research 2004 Jan 1;32(1):23-26, which is incorporated by reference herein in its entirety). GenBank* is part of the International Nucleotide Sequence Database Collaboration, which comprises the DNA DataBank of Japan (DDBJ), the European Molecular Biology Laboratory (EMBL), and GenBank at the National Center for Biotechnology Information (NCBI).

TABLE 32
Gene and protein accession numbers for exemplary biomarkers
that discriminate between converters and non-converters
			Gene	Protein
Gene	Affymetrix		Accession	Accession
Symbol	Probeset name	Gene Name	Number	Number
Column 1	Column 2	Column 3	Column 4	Column 5
	1555785_a_at	EST
<NA>	227150_at	EST
<NA>	238973_s_at	EST
<NA>	239893_at	EST
<NA>	237563_s_at	EST
<NA>	244313_at	EST
<NA>	237071_at	EST
<NA>	229934_at	EST
<NA>	1555311_at	EST
<NA>	233264_at	EST
<NA>	239780_at	EST
<NA>	238405_at	EST
3′HEXO	226416_at	HISTONE MRNA 3′ END	NM_153332	NP_699163
		EXORIBONUCLEASE
3′HEXO	231852_at
ADORA2A	205013_s_at	ADENOSINE A2 RECEPTOR	NM_000675	NP_000666
ANXA3	209369_at	ANNEXIN A3	NM_005139	NP_005130
ASAHL	214765_s_at	N-ACYLSPHINGOSINE	NM_014435	NP_055250
		AMIDOHYDROLASE-LIKE
		PROTEIN
ASAHL	232072_at
ASAHL	227135_at
ATP11B	1554557_at	ATPASE, CLASS VI, TYPE 11B	XM_087254	XP_087254
ATP6V1C1	202872_at	ATPASE, H+ TRANSPORTING,	NM_001695	NP_001686
		LYSOSOMAL, 42-KD, V1	NM_001007254	NP_001007255
		SUBUNIT C, ISOFORM 1
B4GALT5	221485_at	BETA-1,4-	NM_004776	NP_004767
		GALACTOSYLTRANSFERASE
BASP1	202391_at	BRAIN-ABUNDANT SIGNAL	NM_006317	NP_006308
		PROTEIN
BAZ1A	217986_s_at	BROMODOMAIN ADJACENT	NM_013448	NP_038476
		TO ZINC FINGER DOMAIN,	NM_182648	NP_872589
		1A
BCL6	203140_at	B-CELL LYMPHOMA 6	NM_001706	NP_001697
			NM_138931	NP_620309
BMX	206464_at	BONE MARROW KINASE, X-	NM_001721	NP_001712
		LINKED	NM_203281	NP_975010
C16orf7	205781_at	CHROMOSOME 16 OPEN-	NM_004913	NP_004904
		READING FRAME 7
C20orf32	1554786_at	CHROMOSOME 20 OPEN-	NM_020356	NP_065089
		READING FRAME 32
C3F	203547_at	COMPLEMENT COMPONENT	NM_005768	NP_005759
		3
C8FW	202241_at	C8FW GENE;	NM_025195	NP_079471
		PHOSPHOPROTEIN.
CEACAM1	209498_at	CARCINOEMBRYONIC	NM_001712	NP_001703
		ANTIGEN-RELATED CELL
		ADHESION MOLECULE 1
CEACAM1	211883_x_at
CECR1	219505_at	CAT EYE SYNDROME	NM_017424	NP_059120
		CHROMOSOME REGION,	NM_177405	NP_803124
		CANDIDATE 1
CHCHD7	222701_s_at	COILED-COIL-HELIX	NM_001011667	NP_001011667
		DOMAIN-CONTAINING	NM_001011668	NP_001011668
		PROTEIN 7	NM_001011669	NP_001011669
			NM_001011670	NP_001011670
			NM_001011671	NP_001011671
			NM_024300	NP_077276
CHSY1	203044_at	CARBOHYDRATE	NM_014918	NP_055733
		SYNTHASE 1
CKLF	223451_s_at	CHEMOKINE-LIKE FACTOR	NM_016326	NP_057410
			NM_016951	NP_058647
			NM_181640	NP_857591
			NM_181641	NP_857592
CKLF	219161_s_at
CL25022	217883_at	C2ORF25	NM_015702	NP_056517
CPD	201940_at	CARBOXYPEPTIDASE D	NM_001304	NP_001295
CPD	201941_at
CRTAP	1554464_a_at	CARTILAGE-ASSOCIATED	NM_006371	NP_006362
		PROTEIN
DHRS9	219799_s_at	MEMBRANE PROTEIN,	NM_005771	NP_005762
		PALMITOYLATED 3; MPP3	NM_199204	NP_954674
EIF4G3	201936_s_at	EUKARYOTIC	NM_003760	NP_003751
		TRANSLATION INITIATION
		FACTOR 4-GAMMA, 3
FAD104	218618_s_at	FIBRONECTIN TYPE III	NM_022763	NP_073600
		DOMAIN CONTAINING 3B
		(FNDC3B)
FAD104	225032_at
FAD104	222692_s_at
FAD104	222693_at
FCGR1A	214511_x_at	FC FRAGMENT OF IGG, HIGH	NM_000566	NP_000557
		AFFINITY IA
FCGR1A	216950_s_at
FLJ11175	229005_at		NM_018349	NP_060819
FLJ11175	220603_s_at
FLJ11259	218627_at		NM_018370	NP_060840
FLJ11795	220112_at		NM_024669	NP_078945
FLJ22833	219334_s_at	HYPOTHETICAL PROTEIN	NM_022837
		FLJ22833
G0S2	213524_s_at		NM_015714	NP_056529
GADD45B	207574_s_at	GROWTH ARREST- AND DNA	NM_015675	NP_056490
		DAMAGE-INDUCIBLE GENE
		GADD45
GADD45B	209304_x_at
GK	214681_at	GLYCEROL KINASE	NM_000167	NP_000158
			NM_203391	NP_976325
GPR160	223423_at	G PROTEIN-COUPLED	NM_014373	NP_055188
		RECEPTOR 160
HLA-DMA	217478_s_at	HLA-D	NM_006120	NP_006111
		HISTOCOMPATIBILITY TYPE
HLA-DMB	203932_at		NM_002118	NP_002109
HLA-DPA1	211991_s_at		NM_033554	NP_291032
HLA-DQB1	209823_x_at		NM_002123	NP_002114
HLA-DRA	210982_s_at		NM_002123	NP_002114
HLA-DRA	208894_at
HLA-DRB1	215193_x_at		NM_002124	NP_002115
HLA-DRB1	209312_x_at
HLA-DRB4	204670_x_at		NM_021983	NP_068818
HLA-DRB4	208306_x_at
HPGD	203913_s_at	15-	NM_000860	NP_000851
		HYDROXYPROSTAGLANDIN
		DEHYDROGENASE
		HYDROXYPROSTAGLANDIN
		DEHYDROGENASE 15-(NAD)
HRPT2	218578_at	HYPERPARATHYROIDISM 2	NM_024529	NP_078805
HSPC163	228437_at	HSPC163 PROTEIN	NM_014184	NP_054903
HSPC163	218728_s_at
IDI1	204615_x_at	ISOPENTENYL-	NM_004508	NP_004499
		DIPHOSPHATE DELTA-
		ISOMERASE
IL18R1	206618_at	INTERLEUKIN 18 RECEPTOR	NM_003855	NP_003846
		1
KCNE1	236407_at	POTASSIUM CHANNEL,	NM_000219	NP_000210
		VOLTAGE-GATED, ISK-
		RELATED SUBFAMILY
KIF1B	225878_at	KINESIN FAMILY MEMBER	NM_015074	NP_055889
		1B	NM_183416	NP_904325
KREMEN1	227250_at	KRINGLE CONTAINING	NM_032045	NP_114434
		TRANSMEMBRANE PROTEIN	NM_153379	NP_700358
		1
LDLR	202068_s_at	LOW DENSITY LIPOPROTEIN	NM_000527	NP_000518
		RECEPTOR
LIMK2	202193_at	LIM DOMAIN KINASE 2	NM_005569	NP_005560
			NM_016733	NP_057952
LOC199675	235568_at	HYPOTHETICAL PROTEIN	NM_174918	NP_777578
		LOC199675
LOC284829	225669_at
LOC285771	237870_at	HYPOTHETICAL PROTEIN
		LOC285771)
LRG1	228648_at	LEUCINE-RICH ALPHA-2-	NM_052972	NP_443204
		GLYCOPROTEIN 1
MGC22805	239196_at	NOVEL GENE (MGC22805),
MGC22805	238439_at
MPEG1	226841_at	MACROPHAGE EXPRESSED	XM_166227	XP_166227
		GENE 1
OAT	201599_at	ORNITHINE	NM_000274	NP_000265
		AMINOTRANSFERASE
		DEFICIENCY
ORF1-FL49	224707_at	PUTATIVE NUCLEAR	NM_032412	NP_115788
		PROTEIN ORF1-FL49
PDCD1LG1	227458_at	PROGRAMMED CELL DEATH	NM_014143	NP_054862
		1 LIGAND 1
PFKFB2	226733_at	6-PHOSPHOFRUCTO-2-	NM_006212	NP_006203
		KINASE
PFKFB2	209992_at
PFKFB3	202464_s_at	6-PHOSPHOFRUCTO-2-	NM_004566	NP_004557
		KINASE/FRUCTOSE-2,6-
		BISPHOSPHATASE 3
PGS1	219394_at	PHOSPHATIDYLGLYCERO-	NM_024419	NP_077733
		PHOSPHATE SYNTHASE
PHTF1	205702_at	PUTATIVE HOMEODOMAIN	NM_006608	NP_006599
		TRANSCRIPTION FACTOR 1
PIK3AP1	226459_at	PHOSPHOINOSITIDE 3-	NM_152309	NP_689522
		KINASE ADAPTOR PROTEIN
		1
PLSCR1	241916_at	PHOSPHOLIPID	NM_021105	NP_066928
		SCRAMBLASE 1
PRO2852	223797_at	HYPOTHETICAL PROTEIN
		PRO2852
PRV1	219669_at	NEUTROPHIL-SPECIFIC	NM_020406	NP_065139
		ANTIGEN 1 (POLYCYTHEMIA
		RUBRA VERA 1)
PSTPIP2	219938_s_at	PROLINE/SERINE/THREONINE	NM_024430	NP_077748
		PHOSPHATASE-
		INTERACTING PROTEIN 1
		(PROLINE-SERINE-
		THREONINE PHOSPHATASE
		INTERACTING PROTEIN 2)
PTDSR	212723_at	CHROMOSOME 17 GENOMIC	NM_015167	NP_055982
		CONTIG, ALTERNATE
		ASSEMBLY
		(PHOSPHATIDYLSERINE
		RECEPTOR)
RABGEF1	218310_at	RAB GUANINE NUCLEOTIDE	NM_014504	NP_055319
		EXCHANGE FACTOR (RAB
		GUANINE NUCLEOTIDE
		EXCHANGE FACTOR (GEF)
		1)
RARA	228037_at	RETINOIC ACID RECEPTOR,	NM_000964	NP_000955
		ALPHA
RNASEL	229285_at	RIBONUCLEASE L	NM_021133	NP_066956
SAMSN1	1555638_a_at	SAM DOMAIN, SH3 DOMAIN,	NM_022136	NP_071419
		AND NUCLEAR
		LOCALIZATION SIGNALS 1
SAMSN1	220330_s_at
SEC15L1	226259_at	SEC15-LIKE 1	NM_019053	NP_061926
		(S. CEREVISIAE) (SEC15L1),
		MRNA
SIPA1L2	225056_at	SIGNAL-INDUCED	NM_020808	NP_065859
		PROLIFERATION-
		ASSOCIATED GENE 1
		(SIGNAL-INDUCED
		PROLIFERATION-
		ASSOCIATED 1 LIKE 2)
SLC26A8	237340_at	SOLUTE CARRIER FAMILY	NM_052961	NP_443193
		26, MEMBER 8	NM_138718	NP_619732
SLC2A3	202499_s_at	SOLUTE CARRIER FAMILY 2	NM_006931	NP_008862
		(FACILITATED GLUCOSE
		TRANSPORTER), MEMBER 3
SOCS3	227697_at	SUPPRESSOR OF CYTOKINE	NM_003955	NP_003946
		SIGNALING 3
SOD2	216841_s_at	SUPEROXIDE DISMUTASE 2	NM_000636	NP_000627
SPPL2A	226353_at	SIGNAL PEPTIDE	NM_032802	NP_116191
		PEPTIDASE-LIKE 2A
SRPK1	202200_s_at	PROTEIN KINASE,	NM_003137	NP_003128
		SERINE/ARGININE-SPECIFIC,
		1 (SFRS PROTEIN KINASE 1)
STK3	204068_at	SERINE/THREONINE	NM_006281	NP_006272
		PROTEIN KINASE 3
SULF2	224724_at	SULFATASE 2 (SULF2),	NM_198596	NP_940998
		TRANSCRIPT VARIANT 2
SULF2	233555_s_at
T2BP	226117_at	TRAF-2 BINDING PROTEIN	NM_052864	NP_443096
		(TRAF-INTERACTING
		PROTEIN WITH A
		FORKHEAD-ASSOCIATED
		DOMAIN)
T2BP	235971_at
T2BP	238858_at
TBC1D8	204526_s_at	TBC1 DOMAIN FAMILY,	NM_007063	NP_008994
		MEMBER 8
TCTEL1	201999_s_at	T-COMPLEX-ASSOCIATED-	NM_006519	NP_006510
		TESTIS-EXPRESSED 1
TGFBI	201506_at	TRANSFORMING GROWTH	NM_000358	NP_000349
		FACTOR, BETA-1
TTYH2	223741_s_at	TWEETY, DROSOPHILA,	NM_032646	NP_116035
		HOMOLOG OF, 2	NM_052869	NP_443101
WDFY3	212598_at	WD REPEAT AND FYVE	NM_014991	NP_055806
		DOMAIN CONTAINING 3	NM_178583	NP_848698
			NM_178585	NP_848700
WDFY3	212606_at
WSB1	201296_s_at	WD REPEAT AND SOCS BOX-	NM_015626	NP_056441
		CONTAINING 1	NM_134264	NP_599026
			NM_134265	NP_599027
ZDHHC19	231122_x_at	ZINC FINGER, DHHC	NM_144637	NP_653238
		DOMAIN CONTAINING 19
		(ZDHHC19)
ZDHHC19	1553952_at
ZFP36L2	201367_s_at	ZINC FINGER PROTEIN 36,	NM_006887	NP_008818
		C3H TYPE-LIKE 2; ZFP36L2

Each of the sequences, genes, proteins, and probesets identified in Table 32 is hereby incorporated by reference herein in its entirety.

6.8 Biomarker Combinations Based on Additional Filtering Criteria

Section 6.6 describes exemplary biomarkers that discriminate between converters and nonconverters. Section 6.7 describes one exemplary combination of the biomarkers of Section 6.6. The biomarkers of Section 6.7 were identified by the application of an additional filtering criterion to the biomarkers of Section 6.6. This section describes additional combinations of the biomarkers identified in Section 6.7. The subsections identified in this section discriminate between converters and nonconverters.

Table 33 lists biomarkers in one exemplary combination. The combination detailed in Table 33 was identified by taking the list of biomarkers in Table 31 and imposing additional filtering criteria. These additional criteria include a requirement that each respective biomarker under consideration exhibit at least a 1.2× fold change between the median feature value for the respective biomarker among the subjects that acquired sepsis during a defined time period (sepsis subjects) and the median value for the respective biomarker among subjects that do not acquire sepsis during the defined time period (SIRS subjects) in the T₋₁₂ baseline data described in Section 6.5. Furthermore, the summation of the PAM score, CART score, and RF score for the biomarker in the T₋₁₂ baseline data time period had to exceed unity. Application of these additional filtering criteria reduced the biomarkers from the 130 found in Table 31, to ten biomarkers.

TABLE 33
Exemplary combination of biomarkers that discriminate between
converters and non-converters
	Affymetrix		T−12 Values	T−36 Values
Gene	Probeset	Gene	Median		Median
Symbol	name	Name	FC	Direction	FC	Direction
Column	Column	Column	Column	Column	Column	Column
1	2	3	4	5	6	7
	1555785_a_at	EST	1.34	up	1.31	up
CL25022	217883_at		1.36	up	1.31	up
IDI1	204615_x_at	ISOPENTENYL-	1.51	up	1.31	up
		DIPHOSPHATE
		DELTA-
		ISOMERASE
MGC22805	239196_at	NOVEL GENE	2.30	up	1.86	up
		(MGC22805)
ORF1-	224707_at		1.75	up	1.65	up
FL49
ZDHHC19	1553952_at		1.37	up	1.38	up
CHSY1	203044_at	CARBOHYDRATE	1.78	up	1.24	up
		SYNTHASE 1
SLC2A3	202499_s_at	SOLUTE	1.87	up	1.71	up
		CARRIER
		FAMILY 2
		(FACILITATED
		GLUCOSE
		TRANSPORTER),
		MEMBER 3
FAD104	225032_at		1.63	up	1.41	up
T2BP	235971_at		1.47	up	1.27	up

Each of the sequences, genes, proteins, and probesets identified in Table 33 is hereby incorporated by reference.

Table 34 lists biomarkers in yet another exemplary combination of biomarkers. The combination detailed in Table 34 was identified by taking the list of biomarkers in Table 31 and imposing the additional requirement that each biomarker is annotated with a corresponding known gene and that such a gene has a known biological function. Methods, tables, software and other resources for addressing this latter question are available from the Gene Ontology Consortium, (www.geneontology.org), which is hereby incorporated by reference in its entirety. Application of these additional filtering criteria reduced the biomarkers from the 130 found in the set of Table 31, to 52 biomarkers, representing 42 unique gene sequences (see FIG. 30).

TABLE 34
Exemplary combination of biomarkers that discriminate
between converters and non-converters
Gene Symbol      Corresponding Gene Name
(BCL6 na)        (B-cell CLL/lymphoma 6 (zinc finger protein 51) LOC389185)
(HLA-DRB1,3,4,5) (major histocompatibility complex class II DR beta 1 3, 4, 5)
(RABGEF1 na)     (LOC401368 LOC402538 RAB guanine nucleotide exchange factor
                 (GEF) 1)
3HEXO            3 exoribonuclease
ADORA2A          adenosine A2a receptor
ANKRD22          ankyrin repeat domain 22
ANXA3            annexin A3
ATP11B           ATPase Class VI type 11B
ATP6V1C1         ATPase H+ transporting lysosomal 42 kDa V1 subunit C isoform 1
BASP1            brain abundant membrane attached signal protein 1
BAZ1A            bromodomain adjacent to zinc finger domain 1A
C16orf7          chromosome 16 open reading frame 7
CD4              CD4 antigen (p55)
CEACAM1          carcinoembryonic antigen-related cell adhesion molecule 1 (biliary
                 glycoprotein)
CECR1            cat eye syndrome chromosome region candidate 1
CKLF             chemokine-like factor
CPD              carboxypeptidase D
EIF4G3           eukaryotic translation initiation factor 4 gamma 3
FCGR1A           Fc fragment of IgG high affinity Ia receptor for (CD64)
G0S2             putative lymphocyte G0/G1 switch gene
GADD45B          growth arrest and DNA-damage-inducible beta
HLA-DMB          major histocompatibility complex class II DM beta
HLA-DPA1         major histocompatibility complex class II DP alpha 1
HLA-DQB1         major histocompatibility complex class II DQ beta 1
HLA-DRA          major histocompatibility complex class II DR alpha
HPGD             hydroxyprostaglandin dehydrogenase 15-(NAD)
IL18R1           interleukin 18 receptor 1
KCNE1            potassium voltage-gated channel Isk-related family member 1
LDLR             low density lipoprotein receptor (familial hypercholesterolemia)
PDCD1LG1         programmed cell death 1 ligand 1
PHTF1            putative homeodomain transcription factor 1
PRV1             polycythemia rubra vera 1
PTDSR            phosphatidylserine receptor
RARA             retinoic acid receptor alpha
RNASEL           ribonuclease L (25-oligoisoadenylate synthetase-dependent)
SEC15L1          SEC 15-like 1 (S. cerevisiae)
SLC26A8          solute carrier family 26 member 8
SLC2A3           solute carrier family 2 (facilitated glucose transporter) member 3
STK3             serine/threonine kinase 3 (STE20 homolog yeast)
TGFBI            transforming growth factor beta-induced 68 kDa
XRN1             5-3 exoribonuclease 1
ZFP36L2          zinc finger protein 36 C3H type-like 2

Each of the sequences, genes, proteins, and probesets identified in Table 34 is hereby incorporated by reference.

In one embodiment, the biomarker profile comprises a plurality of biomarkers that collectively contain at least five, at least ten at least fifteen, at least twenty, at least thirty, between 2 and 5, between 3 and 7, or less than 15 of the sequences of the probesets of Table 32, or complements thereof, or genes including one of at least five of the sequences or complements thereof, or a discriminating fragment thereof, or an amino acid sequence encoded by any of the foregoing nucleic acid sequences, or any discriminating fragment of such an amino acid sequence. Such biomarkers can be mRNA transcripts, cDNA or some other form of amplified nucleic acid or proteins.

In one embodiment, the biomarker profile comprises a plurality of biomarkers that collectively contain at least five, at least ten at least fifteen, at least twenty, at least thirty, between 2 and 5, between 3 and 7, or less than 15 of the sequences of the probesets of Table 33, or complements thereof, or genes including one of at least five of the sequences or complements thereof, or a discriminating fragment thereof, or an amino acid sequence encoded by any of the foregoing nucleic acid sequences, or any discriminating fragment of such an amino acid sequence. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example amplified nucleic acid, or proteins.

In one embodiment, the biomarker profile comprises a plurality of biomarkers that collectively contain at least five, at least ten at least fifteen, at least twenty, at least thirty, between 2 and 5, between 3 and 7, or less than 15 of the sequences of the probesets of Table 34, or complements thereof, or genes including one of at least five of the sequences or complements thereof, or a discriminating fragment thereof, or an amino acid sequence encoded by any of the foregoing nucleic acid sequences, or any discriminating fragment of such an amino acid sequence. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example amplified nucleic acid, or proteins.

In one embodiment, the biomarker profile comprises a plurality of biomarkers that collectively contain at least five, at least ten at least fifteen, at least twenty, at least thirty, between 2 and 5, between 3 and 7, or less than 15 of the sequences of the probesets of Table 33 or Table 34, or complements thereof, or genes including one of at least five of the sequences or complements thereof, or a discriminating fragment thereof, or an amino acid sequence encoded by any of the foregoing nucleic acid sequences, or any discriminating fragment of such an amino acid sequence. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example amplified nucleic acid, or proteins.

In one embodiment, the biomarker profile comprises a biomarker that has the sequence of U133 plus 2.0 probeset SLC2A3 or a complement thereof, or a gene including the sequence of the probeset SLC2A3 or a complement thereof, or a discriminating fragment thereof, or an amino acid sequence encoded by any of the foregoing nucleic acid sequences, or any discriminating fragment of such an amino acid sequence. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example amplified nucleic acid, or proteins.

In the case where a biomarker is based upon a gene that includes the sequence of a probeset listed in Table 30, 31, 32, 33, or 34 or a complement thereof, the biomarker can be, for example, a transcript made by the gene, a complement thereof, or a discriminating fragment or complement thereof, or a cDNA thereof, or a discriminating fragment of the cDNA, or a discriminating amplified nucleic acid molecule corresponding to all or a portion of the transcript or its complement, or a protein encoded by the gene, or a discriminating fragment of the protein, or an indication of any of the above. Further still. the biomarker can be, for example, a protein encoded by a gene that includes a probeset sequence described in Table 30, 31, 32, 33 or 34, or a discriminating fragment of the protein, or an indication of the above. Here, a discriminating molecule or fragment is a molecule or fragment that, when detected, indicates presence or abundance of the above-identified transcript, cDNA, amplified nucleic acid, or protein.

6.9 Differential Gene Expression in the Th1/Th2 Pathway in Sirs and Sepsis Patients

This section describes methods used to identify a set of biomarkers that discriminate between converters and nonconverters, using the methods described, e.g., in Section 5.10, supra. Briefly, 97 SIRS subject were admitted to critical care units of a major university trauma center were evaluated using the methods described in Section 6.1. Comparisons were made using T₋₃₆ and T₋₁₂ static data described in Sections 6.3 and 6.4, respectively. The subjects were divided into two classes: converters (47) and nonconverters (50). Blood samples drawn from converters were time matched to samples from nonconverters in order to perform comparisons, as described in Sections 6.3 and 6.4, respectively. The blood samples were collected and analyzed as described in Section 6.2.

Biomarkers that discriminated between converters and nonconverters with (i) a Wilcoxon (adjusted) p value of 0.05 or less and (ii) an exhibited a mean fold differential expression value between converters and nonconverters of 1.2 or greater in either the T₋₃ or the T₋₁₂ static test were selected as the set of discriminating biomarkers. This set of discriminating biomarkers was then filtered using an annotation data based filtering rule imposed by DAVID 2.0, which is available from the National Institutes of Health (see, http://apps1.niaid.nih.gov/david/, the contents of which are incorporated by reference herein in their entirety). Specifically, that annotation data based filtering rule imposed by David 2.0 had the form of annotation rule 4 in Section 5.10, reproduce below

Annotation rule 4.Select all biomarkers that are in biological pathway X.The specific form of this annotation data based filtering rule in this example wasSelect all biomarkers that are in the Th1/Th2 biological pathway (cell differentiation pathway).Table 35 below lists the Affymetrix U133 plus 2.0 probesets that are in genes known to be involved in this Th1/Th2 cell differentiation pathway.

TABLE 35
U133 plus 2.0 Probesets in genes involved in
the Th1/Th2 cell differentiation pathway.
		U133 + 2.0	P value
	Symbol	probeset	(adjusted)
	CD28	211856_x_at	0.018
	CD28	211861_x_at
	CD28	206545_at
	CD86	205685_at	0.0034
	CD86	205685_at	0.0187
	CD86	210895_s_at	0.0034
	CD86	210895_s_at	0.0187
	CD86	205686_s_at	0.0114
	HLA-DRA	210982_s_at	0.0034
	HLA-DRA	210982_s_at	0.0187
	HLA-DRA	208894_at	0.0034
	HLA-DRA	208894_at	0.0187
	HLA-DRB1	221491_x_at
	HLA-DRB1	217323_at
	HLA-DRB1	217362_x_at	0.0034
	HLA-DRB1	217362_x_at	0.0472
	HLA-DRB1	215193_x_at	0.0034
	HLA-DRB1	215193_x_at	0.0187
	HLA-DRB1	209728_at
	HLA-DRB1	204670_x_at	0.0034
	HLA-DRB1	204670_x_at	0.0187
	HLA-DRB1	208306_x_at	0.0034
	HLA-DRB1	208306_x_at	0.0187
	HLA-DRB1	209312_x_at	0.0034
	HLA-DRB1	209312_x_at	0.0187
	HLA-DRB1	215666_at
	HLA-DRB1	215669_at
	HLA-DRB3	221491_x_at
	HLA-DRB3	217323_at
	HLA-DRB3	217362_x_at	0.0034
	HLA-DRB3	217362_x_at	0.0472
	HLA-DRB3	215193_x_at	0.0034
	HLA-DRB3	215193_x_at	0.0187
	HLA-DRB3	209728_at
	HLA-DRB3	204670_x_at	0.0034
	HLA-DRB3	204670_x_at	0.0187
	HLA-DRB3	208306_x_at	0.0034
	HLA-DRB3	208306_x_at	0.0187
	HLA-DRB3	209312_x_at	0.0034
	HLA-DRB3	209312_x_at	0.0187
	HLA-DRB3	215666_at
	HLA-DRB3	215669_at
	HLA-DRB4	221491_x_at
	HLA-DRB4	217323_at
	HLA-DRB4	217362_x_at	0.0034
	HLA-DRB4	217362_x_at	0.0472
	HLA-DRB4	215193_x_at	0.0034
	HLA-DRB4	215193_x_at	0.0187
	HLA-DRB4	209728_at
	HLA-DRB4	204670_x_at	0.0034
	HLA-DRB4	204670_x_at	0.0187
	HLA-DRB4	208306_x_at	0.0034
	HLA-DRB4	208306_x_at	0.0187
	HLA-DRB4	209312_x_at	0.0034
	HLA-DRB4	209312_x_at	0.0187
	HLA-DRB4	215666_at
	HLA-DRB4	215669_at
	HLA-DRB5	221491_x at
	HLA-DRB5	217323_at
	HLA-DRB5	217362_x_at	0.0034
	HLA-DRB5	217362_x_at	0.0472
	HLA-DRB5	215193_x_at	0.0034
	HLA-DRB5	215193_x_at	0.0187
	HLA-DRB5	209728_at
	HLA-DRB5	204670_x_at	0.0034
	HLA-DRB5	204670_x_at	0.0187
	HLA-DRB5	208306_x_at	0.0034
	HLA-DRB5	208306_x_at	0.0187
	HLA-DRB5	209312_x_at	0.0034
	HLA-DRB5	209312_x_at	0.0187
	HLA-DRB5	215666_at
	HLA-DRB5	215669_at
	IFNG	210354_at
	IFNGR1	211676_s_at	0.00342
	IFNGR1	242903_at	0.0034
	IFNGR1	202727_s_at	0.0054
	IFNGR2	231696_x_at
	IFNGR2	201642_at	0.0034
	IL12A	207160_at
	IL12B	207901_at
	IL12RB1	239522_at
	IL12RB1	206890_at
	IL12RB2	206999_at
	IL18	206295_at
	IL18R1	206618_at	0.0034
	IL18R1	206618_at	0.0187
	IL2	207849_at
	IL2RA	211269_s_at
	IL2RA	206341_at	0.0247
	IL4	207538_at
	IL4	207539_s_at
	IL4R	203233_at	0.0034
	IL4R	203233_at	0.0187
	TNFRSF5	222292_at	0.0126
	TNFRSF5	215346_at
	TNFRSF5	205153_s_at
	TNFRSF5	35150_at	0.0086
	TNFSF5	207892_at	0.0034

Table 36 below identifies the genes that contain the probesets that remained in the set of discriminating biomarkers upon application of the annotation data based filtering rule.

TABLE 36
Identified genes.
	Data		Fold-change
	source	Adjusted	(Median sepsis vs.	Relative
Gene name	(static)	p value	Median SIRS)	regulation
CD86	T−12	0.003	1.56	Down
	T−36	0.019	1.23	Down
HLA-DRA	T−12	0.003	1.29	Down
	T−36	0.019	1.23	Down
HLA-DRB1,3,4,5	T−12	0.003	1.25	Down
	T−36	0.019	1.27	Down
IFNGR1	T−12	0.003	1.39	Up
IFNGR2	T−12	0.003	1.25	Up
IL18R1	T−12	0.003	3.17	Up
	T−36	0.019	2.37	Up
IL4R	T−12	0.003	1.61	Up
	T−36	0.019	1.39	Up

The genes in Table 36 represent biomarkers that discriminate between converters and converters. Further, these genes are in the Th1/Th2 cell differentiation pathway. The results in the table show that, although clinically similar, SIRS patients who subsequently developed sepsis expressed genes related to Th1/Th2 Cells differently than SIRS patients who remained uninfected. These differences occurred prior to the onset of clinical sepsis. For a discussion of Th1/Th2 cell differentiation pathway genes and related genes, see, e.g., Abbas et al., 1996, Functional diversity of helper T lymphocytes, Nature 383:787-793; Fearon and Locksley, 1996, Science 272:50-53; and Mossman and Sad, 1996, Immunol. Today 17:138-146; each of which is hereby incorporated by reference in its entirety.

6.10 RT-PCR

In Section 6.1, it was noted that two Paxgene (RNA) tubes were drawn from each subject in the study on each day of the study. One tube was used for microarray analysis as described in Section 6.2. The other tube was used for RT-PCR analysis. In this section, the correlation between the gene expression values obtained by RT-PCR and the gene expression values obtained by microarray is presented for three of the genes listed in Table 30, IL18R1, FCGR1A, and MMP9. In this comparison, static expression data from both assays (RT-PCR and microarray) for all time points measured in the subject were correlated to obtain a correlation coefficient. The correlations were computed within ‘R’, a public domain statistical computing language (http://www.r-project.org/, which is hereby incorporated by reference), using the following code:

corCalc <- function(x,y){
n <- length(x)
## if there are any missing values in the data
if(any(is.na(x)) ∥ any(is.na(y))){
## index where missing values occur
rm.idx <- which(is.na(x))
rm.idx <- c(rm.idx, which(is.na(y)))
## remove missing values
x <- x[-rm.idx]
y <- y[-rm.idx]
## update length
n <- length(x)
}
R <- (n*sum(x*y)-sum(x)*sum(y))/(sqrt((n*sum(x{circumflex over ( )}2)-
(sum(x)){circumflex over ( )}2)*(n*sum(y{circumflex over ( )}2) - (sum(y)){circumflex over ( )}2)))
return(R)
}

FIG. 31 shows the correlation between IL18R1 expression, as determined by RT-PCR, and the intensity of the X206618_at probeset, as determined using the techniques described in Section 6.2, using all available time points across the training population. Each point in FIG. 31 is the gene expression value for a given subject in the training population from the RT-PCR data and the microarray data. Substantial correlation between the RT-PCR and the microarray data was found. In particular, the overall correlation between expression of IL18R1 as determined by RT-PCR and microarray data for X206618_at was 0.85.

FIG. 32 shows the correlation between FCGR1A expression, as determined by RT-PCR, and the intensity of the X214511_x_at, X216950_s_at and X216951_at probesets, as determined using the techniques described in Section 6.2, using all available time points in the training population. Each point in FIG. 32 is the gene expression value for a given subject in the training population from the RT-PCR data and the microarray data. As is evident in FIG. 32, the overall correlation between expression of FCGR1A and each of the two FCGR1A probesets that are found in Table 30, X21451 1_x_at and X216950_s_at, was significant. In particular the correlation coefficient between FCGR1A and X214511_x_at was 0.88. Likewise, the correlation coefficient between and FCGR1A and X216950_s_at was 0.88. The overall correlation between expression of FCGR1A and the FCGR1A probeset not found in Table 30, X216951_at, was 0.53, which was not as significant as the other two probesets.

FIG. 33 shows the correlation between MMP9 expression, as determined by RT-PCR, and the intensity of the X203936_s_at probeset, as determined using the techniques described in Section 6.2, using all available time points in the training population. Each point in FIG. 32 is the gene expression value for a given subject in the study from the RT-PCR data and the microarray data. Substantial correlation between the RT-PCR and the microarray data was found. In particular, the overall correlation between expression of MMP9 as determined by RT-PCR and microarray data for X203936_s_at was 0.87.

FIG. 34 shows the correlation between CD86 expression, as determined by RT-PCR, and the intensity of the X205685_at, X205686_s_at, and X210895_s_at probesets, as determined using the techniques described in Section 6.2, using all available time points. Each point in FIG. 34 is the gene expression value for a given subject in the study from the RT-PCR data and the microarray data. As is evident in FIG. 34, the overall correlation between expression of CD86 and CD86 probeset that is found in Table 30, 210895_s_at, was significant (correlation coefficient of 0.71). The overall correlation between expression of CD86 and the probesets not found in Table 30, X205685_at, X205686_s_at, was not as significant (correlation coefficient of 0.66 and 0.56, respectively).

In one embodiment, a biomarker profile of the present invention comprises a plurality of biomarkers selected from Table 30, including at least one sequence of a probeset in the set of: {X206618_at, X214511_x_at, X216950_s_at, X203936_s_at, and 210895_s_at} or complements thereof, or genes including the sequence or a complement of the sequence thereof, or a discriminating fragment thereof, or an amino acid sequence encoded by any of the foregoing nucleic acid sequences, or any discriminating fragment of such an amino acid sequence. Such biomarkers can be, for example, mRNA transcripts, cDNA or some other nucleic acid, for example, amplified nucleic acid or proteins. In one embodiment, a biomarker profile the of the present invention comprises a nucleic acid that codes for TGFB1, IL18R1, or FCGR1A, a discriminating portion of TGFB1, IL18R1, or FCGR1A, complements of such nucleic acids, proteins encoded by such nucleic acids, or antibodies that selectively bind to any of the foregoing.

6.11 Discovery of Select Nucleic Acid Biomarkers

The experiments described above identified a number of biomarkers that discriminate between sepsis and SIRS. In this example, a discovery process was performed in order to confirm which biomarkers differentiate between patients who subsequently develop sepsis (“sepsis patients”) and patients who do not (“SIRS patients”). In the discovery process, samples from SIRS patients and sepsis patients taken at: (i) date of entry, (ii) T₋₆₀, (iii) T₋₃₆, and (iv) T₋₁₂ data points were studied by RT-PCR, as described in Section 6.11.1 and by Affymetrix gene chip analysis, as described in Section 6.11.2.

6.11.1 RT-PCR Analysis

Biomarkers in multiple samples were measured by RT-PCR at multiple time points and analyzed in several different ways: static time of entry, static T₋₆₀, static T₋₃& baseline T₋₆₀, baseline T₋₃₆, and baseline T₋₁₂ data points. RT-PCR is described in Section 5.4.1.2, and 6.10, above. Representative of these analyses is the static T₋₁₂ data analysis which is described in detail below. In the T₋₁₂ static analysis, biomarkers features were measured using a specific blood sample, designated the T₋₂ blood sample, as defined in Section 6.4, above.

For the T₁₂ static analysis, there were 72 biomarkers measured on 96 samples. Each sample was collected from a different member the population. Of these features, 15 were transformed by log transformations. 5 by square root transformations and the remaining 52 were not transformed.

The 96 member population was initially split into a training set (n=73) and a validation set (n=23). The training set was used to estimate the appropriate classification algorithm parameters while the trained algorithm was applied to the validation set to independently assess performance. Of the 73 training samples, 36 were labeled Sepsis, meaning that the subjects developed sepsis at some point during the observation time period, and 37 were SIRS, meaning that they did not develop sepsis during the observation time period. Table 37 provides distributions of the race, gender and age for these samples.

TABLE 37
Distributions of the race, gender, and age for the training data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	10	14	1
	Female	0	10	1
SIRS	Male	5	22	0
	Female	0	10	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	43.2	40	80
SIRS	18	44.6	40	90

For the 23 validation samples, 12 were labeled Sepsis and 11 were labeled SIRS. Table 38 provides distributions of the race, gender and age for these samples.

TABLE 38
Distributions of the race, gender, and age for the validation data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	0	7	0
	Female	0	4	0
SIRS	Male	2	6	0
	Female	0	4	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	43.4	43	81
SIRS	19	51.9	51.5	85

Each sample in the training data was randomly assigned to one of ten groups used for cross-validation. The number of training samples in these groups ranged from 6 to 8. The samples were assigned in way that attempted to balance the number of sepsis and SIRS samples across folds. As described in more detail below, several different methods were used to judge whether select biomarkers discriminate between the Sepsis and SIRS groups.

Wilcoxon and Q-value tests. The first method used to identify discriminating biomarkers was a Wilcoxon test (unadjusted). The abundance value for a given biomarker across the samples in the training data was subjected to the Wilcoxon test. The Wilcoxon test considers both group classification (sepsis versus SIRS) and abundance value in order to compute a p value for the given biomarker. The p value provides an indication of how well the abundance value for the given biomarker across the samples collected in the training set discriminates between the sepsis and SIRS state. The lower the p value, the better the discrimination. When the p value is less than a specific confidence level, such as 0.05, an inference is made that the biomarker discriminates between the sepsis and SIRS phenotype. There were 33 significant biomarkers using this method (see Table 39).

The second method used to identify discriminating biomarkers was the Wilcoxon Test (adjusted). Due to the large number of biomarkers, 72, and the relatively small number of samples, 96, there was a high risk of finding falsely significant biomarkers. An adjusted p-value was used to counter this risk. In particular, the method of Benjamini and Hochberg, 1995, J. R. Statist. Soc. B 57, pp 289-300, which is hereby incorporated herein by reference in its entirety, was used to control the false discovery rate. Here, the false discovery rate is defined as the number of biomarkers truly significant divided by the number of biomarkers declared significant. For example, if the adjusted p-value is less than 0.05, there is a 5% chance that the biomarker is a false discovery. Results using this test are reported in Table 39. There were 11851 significant biomarkers using this method (see Table 39). As used, herein, a biomarker is considered significant if it has a p-value of less than 0.05 as determined by the Wilcoxon test (adjusted).

The third method used to identify discriminating biomarkers was the use of Q values. In such an approach, the biomarkers are ordered by their q-values and if a respective biomarker has a Q value of X. then respective biomarker and all others more significant have a combined false discovery rate of X. However, the false discovery rate for any one biomarker may be much larger. There were 27 significant biomarkers using this method (see Table 39).

TABLE 39
Cumulative number of significant calls for the three methods.
Note that all samples (training and validation)
were used to compare Sepsis and SIRS groups. Missing
biomarker feature values were not included in the analyses.
	≤1e−04	≤0.001	≤0.01	≤0.025	≤0.05	≤0.1	≤1
p-value	0	22	25	29	33	38	72
(unadjusted)
p-value	0	16	25	25	27	33	72
(adjusted)
q-value	0	0	28	38	47	59	72

CART. In addition to analyzing the microarray data using Wilcoxon and Q-value tests in order to identify biomarkers that discriminate between the sepsis and SIRS subpopulations in the training set, classification and regression tree (CART) analysis was used. CART is described in Section 5.5.1, above. Specifically, the data summarized above was used to predict the disease state by iteratively partitioning the data based on the best single-variable split of the data. In other words, at each stage of the tree building process, the biomarker whose expression values across the training population best discriminate between the sepsis and SIRS population was invoked as a decision branch. Cross-validation was carried out, with the optimal number of splits estimated independently in each of the 10 iterations. The final tree is depicted in FIG. 36, and uses seven biomarkers: TNFSF13B, FCGR1A, HMOX1, MMP9, APAF1, APAF1.1, and CCL3.

FIG. 37 shows the distribution of the seven biomarkers used in the decision tree between the sepsis and SIRS groups in the training data set. In FIG. 37, the top of each box denotes the 75^th percentile of the data across the training set and the bottom of each box denotes the 25^th percentile, and the median value for each biomarker across the training set is drawn as a line within each box. The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 40. From this confusion matrix, the overall accuracy was estimated to be 68.5% with a 95% confidence interval of 56.6% to 78.9%. The estimated sensitivity was 72.2% and the estimated specificity was 64.9%.

TABLE 40
Confusion matrix for training samples using
the cross-validated CART algorithm of FIG. 36
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	26	13
	SIRS	10	24

For the 23 validation samples held back from training data set, the overall accuracy was estimated to be 78.3% with a 95% confidence interval of 56.3% to 92.5%, sensitivity 66.7% and specificity 90.9%. Table 41 shows the confusion matrix for the validation samples.

TABLE 41
Confusion matrix for validation samples
using the cross-validated CART algorithm
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	8	1
	SIRS	4	10

Random Forests. Another decision rule that can be developed using biomarkers of the present invention is a Random Forests decision tree. Random Forests is a tree based method that uses bootstrapping instead of cross-validation. For each iteration, a random sample (with replacement) is drawn and the largest tree possible is grown. Each tree receives a vote in the final class prediction. To fit a random forest, the number of trees (e.g. bootstrap iterations) is specified. No more than 500 were used in this example, but at least 50 are needed for a burn-in period. The number of trees was chosen based on the accuracy of the training data. For this data, 462 trees were used to train the algorithm (see FIG. 38). In FIG. 38, curve 3202 is a smoothed estimate of overall accuracy as a function of tree number. Curve 3804 is a smoothed curve of tree sensitivity as a function of tree number. Curve 3806 is a smoothed curve of tree specificity as a function of tree number. Using this algorithm, 49 biomarkers had non-zero importance and were used in the model. The random forest algorithm gauges biomarker importance by the average reduction in the training accuracy. The biomarkers were ranked by this method and are shown in FIG. 39. The random forest method uses a number of different decision trees. A biomarker is considered to have discriminating significance if it served as a decision branch of a decision tree from a significant random forest analysis. As used herein, a significant random forest analysis is one where the lower 95% confidence interval on accuracy by cross validation on a training data set is greater than 50% and the point estimate for accuracy on a validation set is greater than 65%.

The predicted confusion matrix for the training dataset using the decision tree developed using the Random Forest method is given in Table 42. From this confusion matrix, the overall accuracy was estimated to be 76.7% (confidence intervals cannot be computed when using the bootstrap accuracy estimate). The estimated sensitivity was 77.8% and the estimated specificity was 75.7%.

TABLE 42
Confusion matrix for training samples
against the decision tree developed
using the Random Forest method.
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	28	8
	SIRS	9	28

For the 23 validation samples held back from training, the overall accuracy was estimated to be 78.3% with a 95% confidence interval of 56.3% to 92.5%, sensitivity 75% and specificity 81.8%. Table 43 shows the confusion matrix for the validation samples.

TABLE 43
Confusion matrix for the validation samples
against the decision tree developed
using the Random Forest method.
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	9	2
	SIRS	3	9

MART. Multiple Additive Regression Trees (MART), also known as “gradient boosting machines,” was used to simultaneously assess the importance of biomarkers and classify the subject samples. Several fitting parameters are specified in this approach including (i) number of trees, (ii) step size (commonly referred to as “shrinkage”), and (iii) degree of interaction (related to the number of splits for each tree). More information on MART is described in Section 5.5.4 above. The degree of interaction was set to 1 to enforce an additive model (e.g. each tree has one split and only uses one biomarker).

Estimating interactions may require more data to function well. The step size was set to 0.05 so that the model complexity was dictated by the number of trees. The optimal number of trees was estimated by leaving out a random subset of cases at each fitting iteration, then assessing quality of prediction on that subset. After fitting more trees than were warranted, the point at which prediction performance stopped improving was estimated as the optimal point.

The estimated model used 15 trees and 6 biomarkers across all trees. The MART algorithm also provides a calculation of biomarker importance (summing to 100%), which are given in FIG. 40. Biomarkers with zero importance were excluded. FIG. 41 shows the distribution of the selected biomarkers between the Sepsis and SIRS groups.

Cross-validation was carried out, with the optimal number of trees estimated independently in each of the 10 iterations. The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 44. From this confusion matrix, the overall accuracy was estimated to be 75.3% with a 95% confidence interval of 63.9% to 84.7%. The estimated sensitivity was 72.2% and the estimated specificity was 78.4%.

TABLE 44
Confusion matrix for the training samples
using the cross-validated MART algorithm.
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	26	8
	SIRS	10	29

For the 23 validation samples held back from training, the overall accuracy was estimated to be 78.3% with a 95% confidence interval of 56.3% to 92.5%, sensitivity 81.8% and specificity 75%. Table 45 shows the confusion matrix for the validation samples.

TABLE 45
Confusion matrix for the validation
samples using the MART algorithm.
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	9	3
	SIRS	2	9

PAM. Yet another decision rule developed using biomarkers of the present invention is predictive analysis of microarrays (PAM), which is described in Section 5.5.2, above. In this method, a shrinkage parameter that determines the number of biomarkers used to classify samples is specified. This parameter was chosen via cross-validation. There were no biomarkers with missing values. Based on cross-validation, the optimal threshold value was 2.12, corresponding to 5 biomarkers. FIG. 42 shows the accuracy across different thresholds. In FIG. 42, curve 4202 is the overall accuracy (with 95% confidence interval bars). Curve 4204 shows decision rule sensitivity as a function of threshold value. Curve 4206 shows decision rule specificity as a function of threshold value. Using the threshold of 2.12, the overall accuracy for the training samples was estimated to be 80.8% with a 95% confidence interval of 70.9% to 87.9%. The estimated sensitivity was 89.2% and the estimated specificity was 72.2%. Table 46 shows the confusion matrix for the training data where the predicted classifications were made from the cross-validated models.

TABLE 46
Confusion matrix for training samples
using cross-validated PAM algorithm
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	33	10
	SIRS	4	26

For the 23 validation samples held back from training, the overall accuracy was estimated to be 82.6% with a 95% confidence interval of 61.2% to 95%, sensitivity 91.7% and specificity 72.7%. Table 47 shows the confusion matrix for the validation samples.

TABLE 47
Confusion matrix for validation samples
using cross-validated PAM algorithm
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	11	3
	SIRS	1	8

FIG. 43 shows the selected biomarkers, ranked by their relative discriminatory power, and the irrelative importance in the model.

FIG. 44 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals. Fifty distinct biomarkers were selected from across all the algorithms illustrated in FIG. 44. The identity of these fifty selected features is found in FIG. 45, which further illustrates an overall ranking of these biomarkers for the T₋₁₂ data set. For the selected biomarkers. the x-axis depicts the percentage of times that it was selected. Within the percentage of times that biomarkers were selected, the biomarkers are ranked.

From the analysis of the T₋₁₂ data set and the other data sets, biomarkers were ranked according to how often they were included in the CART, MART, PAM. random forests. The results of this ranking is summarized in Table 48 below:

TABLE 48
Top ranked biomarkers as determined by RT-PCR
		Gene	Protein
Gene		Accession	Accession	T−12	T−36
symbol	Gene Name	Number	Number	Hours	Hours
FCGR1A	FC FRAGMENT OF IGG, HIGH	NM_000566	NP_000557	1	1
	AFFINITY IA
MMP9	MATRIX	NM_004994	NP_004985	2	5
	METALLOPROTEINASE 9
	(GELATINASE B, 92 KDA
	GELATINASE, 92 KDA TYPE IV
	COLLAGENASE)
IL18R1	INTERLEUKIN 18 RECEPTOR 1	NM_003855	NP_003846	3	2
ARG2	ARGINASE TYPE II	NM_001172	CAG38787	4	3
IL1RN	INTERLEUKIN-1 RECEPTOR	NM_000577,	AAN87150	4	4
	ANTAGONIST GENE	NM_173841,
		NM_173842,
		NM_173843
TNFSF13B	TUMOR NECROSIS FACTOR	NM_006573	NP_006564	4	5
	(LIGAND) SUPERFAMILY,
	MEMBER 13B
ITGAM	INTEGRIN, ALPHA M	NM_000632	NP_000623	5	7
	(COMPLEMENT COMPONENT
	RECEPTOR 3, ALPHA; ALSO
	KNOWN AS CD11B (P170),
	MACROPHAGE ANTIGEN
	ALPHA POLYPEPTIDE)
CD4	CD4 ANTIGEN (P55)	NM_000616	NP_000607	6	7
TGFBI	TRANSFORMING GROWTH	NM_000358	NP_000349	6	9
	FACTOR, BETA-1
	(TRANSFORMING GROWTH
	FACTOR, BETA-INDUCED,
	68 KDA)
CD86	CD86 ANTIGEN (CD28	NM_006889	NP_008820	6	6
	ANTIGEN LIGAND 2, B7-2	NM_175862	NP_787058
	ANTIGEN)
TLR4	TOLL-LIKE RECEPTOR 4	AH009665	AAF05316	6	6
IFI16	INTERFRON, GAMMA-	NM_005531	AAH17059	6	9
	INDUCIBLE PROTEIN 16
ICAM1	INTERCELLULAR ADHESION	NM_010493	NP_000192,	6	10
	MOLECULE 1		AAQ14902,
			AAQ14901
TGFBR2	TRANSFORMING GROWTH	NM_003242	AAF27281	6	8
	FACTOR, BETA RECEPTOR II
PLA2G7	PLATELET-ACTIVATING	NM_005084	CAH73907	7	6
	FACTOR ACETYLHYDROLASE
IL-10	INTERLEUKIN 10	NM_000572	CAH73907	8	7

As Table 48 indicates, in general, important biomarkers at T₋₁ were also important biomarkers at earlier time points. The ten biomarkers that are italicized in Table 48 were carried forward to confirmation as described in Section 6.12.1, below. CD4 was excluded in this embodiment because it was found to be different on day of entry. 6.11.2 Discovery Affymetrix Gene Chip Analysis

The patients were also analyzed using Affymetrix gene chip analysis. Such an analysis is described in Section 6.2 Biomarkers in multiple samples were measured by Affymetrix gene chip analysis at multiple time points and analyzed in several different ways: static time of entry, static T₋₆₀, static T₋₃₆, baseline T₋₆₀, baseline T₋₃₆, and baseline T₋₁₂ data points. The Affymetrix gene chip assay is described in Section 6.2, above. Representative of these analyses is the static T₋₁ data analysis described in detail below. In the T₋₁₂ static analysis, biomarkers features were measured using a specific blood sample, designated the T₋₁₂ blood sample, as defined in Section 6.4, above.

For the T₋₁₂ static analysis, there were 54,613 biomarkers measured on 90 samples. Each sample was collected from a different member the population. Of these features, 31,047 were transformed by log transformations, 2518 by square root transformations and the remaining 21,048 were not transformed.

The 90 member population was initially split into a training set (n=69) and a validation set (n=21). The training set was used to estimate the appropriate classification algorithm parameters while the trained algorithm was applied to the validation set to independently assess performance. Of the 69 training samples, 34 were labeled Sepsis, meaning that the subjects developed sepsis at some point during the observation time period, and 35 were SIRS, meaning that they did not develop sepsis during the observation time period. Table 49 provides distributions of the race, gender and age for these samples.

TABLE 49
Distributions of the race, gender, and age for the training data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	9	13	1
	Female	0	10	1
SIRS	Male	5	20	0
	Female	0	10	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	44.1	39	80
SIRS	18	44.1	40	90

For the 21 validation samples, 11 were labeled Sepsis and 10 were labeled SIRS. Table 50 provides distributions of the race, gender and age for these samples.

TABLE 50
Distributions of the race, gender, and age for the validation data
	Group	Gender	Black	Caucasian	Other
	Sepsis	Male	0	7	0
		Female	0	3	0
	SIRS	Male	2	6	0
		Female	0	3	0
	Group	Minimum	Mean	Median	Maximum
	Sepsis	18	43.4	40	81
	SIRS	19	53	52	85

Each sample in the training data was randomly assigned to one of ten groups used for cross-validation. The number of training samples in these groups ranged from 6 to 8. The samples were assigned in way that attempted to balance the number of sepsis and SIRS samples across folds. As described in more detail below, several different methods were used to judge whether select biomarkers discriminate between the Sepsis and SIRS groups.

Wilcoxon and Q-value tests. The first method used to identify discriminating biomarkers was a Wilcoxon test (unadjusted). The abundance value for a given biomarker across the samples in the training data was subjected to the Wilcoxon test. The Wilcoxon test considers both group classification (sepsis versus SIRS) and abundance value in order to compute a p value for the given biomarker. The p value provides an indication of how well the abundance value for the given biomarker across the samples collected in the training set discriminates between the sepsis and SIRS state. The lower the p value, the better the discrimination. When the p value is less than a specific confidence level, such as 0.05, an inference is made that the biomarker discriminates between the sepsis and SIRS phenotype. There were 19791 significant biomarkers using this method (see Table 51).

The second method used to identify discriminating biomarkers was the Wilcoxon Test (adjusted). Due to the large number of biomarkers, 54613, and the relatively small number of samples, 90, there was a high risk of finding falsely significant biomarkers. An adjusted p-value was used to counter this risk. In particular, the method of Benjamini and Hochberg, 1995, J. R. Statist. Soc. B 57, pp 289-300, which is hereby incorporated herein by reference in its entirety, was used to control the false discovery rate. Here, the false discovery rate is defined as the number of biomarkers truly significant divided by the number of biomarkers declared significant. For example, if the adjusted p value is less than 0.05, there is a 5% chance that the biomarker is a false discovery. Results using this test are reported in Table 51. There were 11851 significant biomarkers using this method (see Table 51). As used, herein, a biomarker is considered significant if it has a p-value of less than 0.05 as determined by the Wilcoxon test (adjusted).

The third method used to identify discriminating biomarkers was the use of Q values. In such an approach, the biomarkers are ordered by their q-values and if a respective biomarker has a Q value of X, then respective biomarker and all others more significant have a combined false discovery rate of X. However, the false discovery rate for any one biomarker may be much larger. There were 11581 significant biomarkers using this method (see Table 51).

TABLE 51
Cumulative number of significant calls for the three methods.
Note that all 96 samples (training and validation)
were used to compare Sepsis and SIRS groups. Missing
biomarker feature values were not included in the analyses.
	≤1e−04	≤0.001	≤0.01	≤0.025	≤0.05	≤0.1	≤1
p-value	0	5417	11537	15769	19791	24809	54613
(unadjusted)
p-value	0	0	5043	8374	11851	16973	54613
(adjusted)
q-value	0	0	7734	12478	17820	24890	54613

CART. In addition to analyzing the microarray data using Wilcoxon and Q-value tests in order to identify biomarkers that discriminate between the sepsis and SIRS subpopulations in the training set, classification and regression tree (CART) analysis was used. CART is described in Section 5.5.1, above. Specifically, the data summarized above was used to predict the disease state by iteratively partitioning the data based on the best single-variable split of the data. In other words, at each stage of the tree building process, the biomarker whose expression values across the training population best discriminate between the sepsis and SIRS population was invoked as a decision branch. Cross-validation was carried out, with the optimal number of splits estimated independently in each of the 10 iterations. The final tree uses four probesets: X214681_at, X230281_at, X1007_s_at, and X1560432_at, where each given probeset is the U133 plus 2.0 Affymetrix probe set name. The confusion matrix for the training data, based on the final tree from the cross-validated CART algorithm is given in Table 52. From this confusion matrix, the overall accuracy was estimated to be 65.2% with a 95% confidence interval of 52.8% to 76.3%. The estimated sensitivity was 61.8% and the estimated specificity was 68.6%.

TABLE 52
Confusion matrix for training samples using the cross-validated
CART algorithm
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	21	11
	SIRS	13	24

For the 21 validation samples held back from training data set, the overall accuracy was estimated to be 71.4% with a 95% confidence interval of 47.8% to 88.7%, sensitivity 90.9% and specificity 50%. The confusion matrix for the validation samples was predicted Sepsis/true Sepsis 10, predicted SIRS/true Sepis 1, predicted Sepsis/true SIRS 5, predicted SIRS/true SIRS 5.

Random Forests. Another decision rule that can be developed using biomarkers of the present invention is a Random Forests decision tree. Random Forests is a tree based method that uses bootstrapping instead of cross-validation. For each iteration, a random sample (with replacement) is drawn and the largest tree possible is grown. Each tree receives a vote in the final class prediction. To fit a random forest, the number of trees (e.g. bootstrap iterations) is specified. No more than 500 were used in this example, but at least 50 are needed for a burn-in period. The number of trees was chosen based on the accuracy of the training data. For this data, 439 trees were used to train the algorithm. Using this algorithm, 845 biomarkers had non-zero importance and were used in the model. The random forest algorithm gauges biomarker importance by the average reduction in the training accuracy.

The random forest method uses a number of different decision trees. A biomarker is considered to have discriminating significance if it served as a decision branch of a decision tree from a significant random forest analysis. As used herein, a significant random forest analysis is one where the lower 95% confidence interval on accuracy by cross validation on a training data set is greater than 50% and the point estimate for accuracy on a validation set is greater than 65%.

The predicted confusion matrix for the training dataset using the decision tree developed using the Random Forest method is given in Table 53. From this confusion matrix, the overall accuracy was estimated to be 75.4% (confidence intervals cannot be computed when using the bootstrap accuracy estimate). The estimated sensitivity was 73.5% and the estimated specificity was 77.1%.

TABLE 53
Confusion matrix for training samples against the decision tree
developed using the Random Forest method.
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	27	9
	SIRS	8	25

For the 21 validation samples held back from training, the overall accuracy was estimated to be 76.2% with a 95% confidence interval of 76.2% to 99.9%, sensitivity 100% and specificity 90%. Table 54 shows the confusion matrix for the validation samples.

TABLE 54
Confusion matrix for the validation samples against the decision
tree developed using the Random Forest method.
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	11	1
	SIRS	0	9

MART. Multiple Additive Regression Trees (MART), also known as “gradient boosting machines,” was used to simultaneously assess the importance of biomarkers and classify the subject samples. Several fitting parameters are specified in this approach including (i) number of trees, (ii) step size (commonly referred to as “shrinkage”), and (iii) degree of interaction (related to the number of splits for each tree). More information on MART is described in Section 5.5.4 above. The degree of interaction was set to 1 to enforce an additive model (e.g. each tree has one split and only uses one biomarker).

Estimating interactions may require more data to function well. The step size was set to 0.05 so that the model complexity was dictated by the number of trees. The optimal number of trees was estimated by leaving out a random subset of cases at each fitting iteration, then assessing quality of prediction on that subset. After fitting more trees than were warranted, the point at which prediction performance stopped improving was estimated as the optimal point.

The estimated model used 28 trees and 17 biomarkers across all trees. The MART algorithm also provides a calculation of biomarker importance (summing to 100%). Biomarkers ranked in decreasing order of importance to the model, with the most important biomarker first were: X206513_at, X214681_at, X235359_at, X221850_x_at, X213524_s_at, X225656_a, X200881_s_at, X229743_at, X215178_x_at, X215178_x_at, X216841_s_at, X216841_at, X244158_at, X238858_at, X205287_s_at, X233651_s_at, X229572_at, X214765_s_at.

Cross-validation was carried out, with the optimal number of trees estimated independently in each of the 10 iterations. The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 55. From this confusion matrix, the overall accuracy was estimated to be 76.8% with a 95% confidence interval of 65.1% to 86.1%. The estimated sensitivity was 76.5% and the estimated specificity was 77.1%.

TABLE 55
Confusion matrix for the training samples using the cross-validated
MART algorithm.
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	26	8
	SIRS	8	27

For the 21 validation samples held back from training, the overall accuracy was estimated to be 85.7% with a 95% confidence interval of 63.7% to 97%, sensitivity 80% and specificity 90.9%. Table 56 shows the confusion matrix for the validation samples.

TABLE 56
Confusion matrix for the validation samples using the MART algorithm.
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	8	1
	SIRS	2	10

PAM. Yet another decision rule developed using biomarkers of the present invention is predictive analysis of microarrays (PAM), which is described in Section 5.5.2, above. In this method, a shrinkage parameter that determines the number of biomarkers used to classify samples is specified. This parameter was chosen via cross-validation. There were no biomarkers with missing values. Based on cross-validation, the optimal threshold value was 2.1, corresponding to 820 biomarkers.

Using the threshold of 2.1, the overall accuracy for the training samples was estimated to be 80.9% with a 95% confidence interval of 73.4% to 86.7%. The estimated sensitivity was 85.7% and the estimated specificity was 76.5%. Table 57 shows the confusion matrix for the training data where the predicted classifications were made from the cross-validated models.

TABLE 57
Confusion matrix for training samples using cross-validated PAM
algorithm
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	11	1
	SIRS	0	9

For the 21 validation samples held back from training, the overall accuracy was estimated to be 95.2% with a 95% confidence interval of 76.2% to 99.9%, sensitivity 100% and specificity 90%. Table 58 shows the confusion matrix for the validation samples.

TABLE 58
Confusion matrix for validation samples using cross-validated
PAM algorithm
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	11	1
	SIRS	0	9

The top ten biomarkers identified by PAM, ranked from most important to least important were: X206513_at, X213524_s_at, X200881_s_at, X218992_at, X238858_at, X221123_x_at, X228402_at, X230585_at, X209304_x_at, X214681_at.

FIG. 46 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals using T₋₁ static data obtained from an Affymetrix gene chip discovery training population. Fifty distinct biomarkers were selected from across all the algorithms illustrated in FIG. 46. The identity of the top 50 biomarkers, ranked from most to least significant is: X204102_s_at, X236013_at, X213668_s_at, X1556639_at, X218220_at, X207860_at, X232422_at, X218578_at, X205875_s_at, X226043_at, X225879_at, X224618_at, X216316_x_at, X243159_x_at, X202200_s_at, X201936_s_at, X242492_at, X216609_at, X214328_s_at, X228648_at, X223797_at, X225622_at, X205988_at, X201978_s_at, X200874_s_at, X210105_s_at, X203913_s_at, X204225_at, X227587_at, X220865_s_at, X206682_at, X222664_at, X212264_s_at, X219669_at, X221971_x_at, X1554464_a_at, X242590_at, X227925_at, X221916_s_at, X202101_s_at, X211078_s_at, X44563_at, X206513_at, X215178_x_at, X235359_at, X225656_at, X244158_at, X214765_s_at, X229743_at, X214681.

From the analysis of the T₋₁ data set and the other data sets, the 34 biomarkers indicated in Table 59 below were selected for confirmation. As indicated in Table 59, biomarkers were selected based on the Affymetrix gene chip analysis for one of three criteria, biological relevance (BR), high fold change (HF), or statistical importance (SI) in the Affymetrix gene chip analysis.

TABLE 59
Nucleic acid based biomarkers selected for confirmation from Affymetrix Assay
		Gene	Protein
Gene		Accession	Accession	Selection
Symbol	Gene Name	Number	Number	Criterion
BCL2A1	BCL2-RELATED PROTEIN A1	NM_004049	NP_004040	BR
CCL5	CHEMOKINE (C-C MOTIF)	NM_002985	NP_002976	BR
	LIGAND 5
CSF1R	COLONY STIMULATING	NM_005211	NP_005202	BR
	FACTOR 1 RECEPTOR,
	FORMERLY MCDONOUGH
	FELINE SARCOMA VIRAL
	(V-FMS) ONCOGENE
	HOMOLOG
GADD45A	GROWTH ARREST AND	NM_001924	NP_001915	BR
	DNA-DAMAGE-
	INDUCIBLE, ALPHA
GADD45B	GROWTH ARREST- AND	NM_015675	NP_056490	BR
	DNA DAMAGE-
	INDUCIBLE GENE GADD45
IFNGR1	INTERFERON GAMMA	NM_000416	NP_000407	BR
	RECEPTOR 1
IL10RA	INTERLEUKIN 10	NM_001558	NP_001549	BR
	RECEPTOR, ALPHA
IRAK2	INTERLEUKIN-1	NM_001570	NP_001561	BR
	RECEPTOR-ASSOCIATED
	KINASE 2
IRAK4	INTERLEUKIN-1	NM_016123	NP_057207	BR
	RECEPTOR-ASSOCIATED
	KINASE 4
JAK2	JANUS KINASE 2 (A	NM_004972	NP_004963	BR
	PROTEIN TYROSINE KINASE)
LY96	LYMPHOCYTE ANTIGEN 96	NM_015364	NP_056179	BR
MAP2K6	MITOGEN-ACTIVATED	NM_002758	NP_002749	BR
	PROTEIN KINASE KINASE 6	NM_031988	NP_114365
MAPK14	MAPK14 MITOGEN-	NM_001315	NP_001306	BR
	ACTIVATED PROTEIN	NM_139012	NP_620581
	KINASE 14	NM_139013	NP_620582
		NM_139014	NP_620583
MKNK1	MAP KINASE	NM_003684	NP_003675	BR
	INTERACTING	NM_198973	NP_945324
	SERINE/THREONINE
	KINASE 1
OSM	ONCOSTATIN M	NM_020530	NP_065391	BR
SOCS3	SUPPRESSOR OF	NM_003955	NP_003946	BR
	CYTOKINE SIGNALING 3
TDRD9	TUDOR DOMAIN	NM_153046	NP_694591	BR
	CONTAINING 9
TNFRSF6	TUMOR NECROSIS	NM_152877	NP_000034	BR
	FACTOR RECEPTOR
	SUPERFAMILY, MEMBER 6
TNFSF10	TUMOR NECROSIS	NM_003810	NP_003801	BR
	FACTOR (LIGAND)
	SUPERFAMILY, MEMBER 10
ANKRD22	ANKYRIN REPEAT	NM_144590	NP_653191	HF
	DOMAIN 22
ANXA3	ANNEXIN A3	NM_005139	NP_005130	HF
CEACAM1	CARCINOEMBRYONIC	NM_001712	NP_001703	HF
	ANTIGEN-RELATED CELL
	ADHESION MOLECULE 1
LDLR	LOW DENSITY	NM_000527	NP_000518	HF
	LIPOPROTEIN RECEPTOR
PFKFB3	6-PHOSPHOFRUCTO-2-	NM_004566	NP_004557	HF
	KINASE/FRUCTOSE-2,6-
	BISPHOSPHATASE 3
PRV1	NEUTROPHIL-SPECIFIC	NM_020406	NP_065139	HF
	ANTIGEN 1
	(POLYCYTHEMIA RUBRA
	VERA 1)
PSTPIP2	PROLINE/SERINE/THREONINE	NM_024430	NP_077748	HF
	PHOSPHATASE-
	INTERACTING PROTEIN 1
	(PROLINE-SERINE-
	THREONINE
	PHOSPHATASE
	INTERACTING PROTEIN 2)
TIFA	TRAF-INTERACTING	NM_052864	NP_443096	HF
	PROTEIN WITH A
	FORKHEAD-ASSOCIATED
	DOMAIN
VNN1	VANIN 1	NM_004666	NP004657	HF
NCR1	NATURAL	NM_004829	NP_004820	SI
	CYTOTOXICITY
	TRIGGERING RECEPTOR 1
FAD104	FIBRONECTIN TYPE III	NM_022763	NP_073600	SI
	DOMAIN CONTAINING 3B
	(FNDC3B)
INSL3	INSULIN-LIKE 3 (LEYDIG	NM_005543	NP_005534	SI
	CELL)
CRTAP	CARTILAGE-ASSOCIATED	NM_006371	NP_006362	SI
	PROTEIN
HLA-DRA	MAJOR	NM_002123	NP_002114	SI
	HISTOCOMPATIBILITY
	COMPLEX, CLASS II, DR
	ALPHA
SOD2	SUPEROXIDE DISMUTASE	NM_000636	NP_000627	SI
	2, MITOCHONDRIAL

6.12 Confirmation of Select Nucleic Acid Biomarkers

In this example, a confirmatory process was performed in order to confirm which biomarkers differentiate between patients who subsequently develop sepsis (“sepsis patients”) and patients who do not (“SIRS patients”).

6.12.1 Confirmatory Analysis of Biomarkers Identified by RT-PCR

The biomarkers identified by italicizes in Table 48 of Section 6.11.1, namely FCGR1A, MMP9, IL18R1, ARG2, IL1RN, TNFSF13B, ITGAM, TGFB1, CD86, and TLR4, were analyzed using RT-PCR at multiple time points and analyzed in several different ways: static time of entry, static T₋₆₀, static T₋₃₆ baseline T₋₆₀, baseline T₋₃₆ and baseline T₋₁₂ data points. RT-PCR is described in Section 5.4.1.2, above. Representative of these analyses is the static T₋₁₂ data analysis described in detail below. In the T₋₁₂ static analysis, biomarkers features were measured using a specific blood sample, designated the T₋₁₂ blood sample, as defined in Section 6.4, above.

For the T₋₁₂ static analysis, the biomarkers FCGR1A, MMP9, IL18R1, ARG2, IL1RN, TNFSF13B, ITGAM, TGFB1, CD86, and TLR4, were measured from 50 samples. Each sample was collected from a different member of the population. Of these biomarkers, seven were transformed by log transformations, and three by square root transformations.

The 50 member population was initially split into a training set (n=39) and a validation set (n=11). The training set was used to estimate the appropriate classification algorithm parameters while the trained algorithm was applied to the validation set to independently assess performance. Of the 50 training samples, 23 were labeled Sepsis, meaning that the subjects developed sepsis at some point during the observation time period, and 16 were SIRS, meaning that they did not develop sepsis during the observation time period. Table 60 provides distributions of the race, gender and age for these samples.

TABLE 60
Distributions of the race, gender, and age for the training data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	3	13	0
	Female	0	7	0
SIRS	Male	5	7	1
	Female	0	2	0
Group	Minimum	Mean	Median	Maximum
Sepsis	20	52.3	56	80
SIRS	20	39.9	32.5	79

For the 11 validation samples, five were labeled Sepsis and six were labeled SIRS. Table 61 provides distributions of the race, gender and age for these samples.

TABLE 61
Distributions of the race, gender, and age for the validation data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	2	1	0
	Female	0	3	0
SIRS	Male	0	3	0
	Female	0	2	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	51.7	59.5	76
SIRS	24	47.2	43	76

Each sample in the training data was randomly assigned to one of ten groups used for cross-validation. The number of training samples in these groups ranged from three to five. The samples were assigned in way that attempted to balance the number of sepsis and SIRS samples across folds. As described in more detail below, several different methods were used to judge whether select biomarkers discriminate between the Sepsis and SIRS groups.

Wilcoxon and Q-value tests. The first method used to identify discriminating biomarkers was a Wilcoxon test (unadjusted). The abundance value for a given biomarker across the samples in the training data was subjected to the Wilcoxon test. The Wilcoxon test considers both group classification (sepsis versus SIRS) and abundance value in order to compute a p value for the given biomarker. The p value provides an indication of how well the abundance value for the given biomarker across the samples collected in the training set discriminates between the sepsis and SIRS state. The lower the p value, the better the discrimination. When the p value is less than a specific confidence level, such as 0.05, an inference is made that the biomarker discriminates between the sepsis and SIRS phenotype. There were nine significant biomarkers using this method (see Table 62).

The second method used to identify discriminating biomarkers was the Wilcoxon Test (adjusted). Due to the large number of biomarkers, 10, and the relatively small number of samples, 50, there was a high risk of finding falsely significant biomarkers. An adjusted p value was used to counter this risk. In particular, the method of Benjamini and Hochberg, 1995, J. R. Statist. Soc. B 57, pp 289-300, which is hereby incorporated herein by reference in its entirety, was used to control the false discovery rate. Here, the false discovery rate is defined as the number of biomarkers truly significant divided by the number of biomarkers declared significant. For example, if the adjusted p value is less than 0.05, there is a 5% chance that the biomarker is a false discovery. Results using this test are reported in Table 62. There were nine significant biomarkers using this method (see Table 62). As used, herein, a biomarker is considered significant if it has a p value of less than 0.05 as determined by the Wilcoxon test (adjusted).

The third method used to identify discriminating biomarkers was the use of Q values. In such an approach, the biomarkers are ordered by their Q values and if a respective biomarker has a Q value of X. then respective biomarker and all others more significant have a combined false discovery rate of X. However, the false discovery rate for any one biomarker may be much larger. There were nine significant biomarkers using this method (see Table 62).

TABLE 62
Cumulative number of significant calls for the three methods.
Note that all samples (training and validation)
were used to compare Sepsis and SIRS groups. Missing
biomarker feature values were not included in the analyses.
	≤1e−04	≤0.001	≤0.01	≤0.025	≤0.05	≤0.1	≤1
p-value	0	7	9	9	9	9	10
(unadjusted)
p-value	0	7	9	9	9	9	10
(adjusted)
q-value	0	0	0	0	0	0	10

CART. In addition to analyzing the microarray data using Wilcoxon and Q-value tests in order to identify biomarkers that discriminate between the sepsis and SIRS subpopulations in the training set, classification and regression tree (CART) analysis was used. CART is described in Section 5.5.1, above. Specifically, the data summarized above was used to predict the disease state by iteratively partitioning the data based on the best single-variable split of the data. In other words, at each stage of the tree building process, the biomarker whose expression values across the training population best discriminate between the sepsis and SIRS population was invoked as a decision branch. Cross-validation was carried out, with the optimal number of splits estimated independently in each of the 10 iterations. The final tree uses three biomarkers which are listed in order of importance IL18R1, ARG2, and FCGR1A, where IL18R1 was the most important. The confusion matrix for the training data, based on the final tree from the cross-validated CART algorithm is given in Table 63. From this confusion matrix, the overall accuracy was estimated to be 82.1% with a 95% confidence interval of 66.5% to 92.5%. The estimated sensitivity was 82.6% and the estimated specificity was 81.2%.

TABLE 63
Confusion matrix for training samples using the cross-validated
CART algorithm
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	19	3
	SIRS	4	13

For the 11 validation samples held back from training data set, the overall accuracy was estimated to be 100% with a 95% confidence interval of 71.5% to 100%, sensitivity 100% and specificity 100%. Table 64 shows the confusion matrix for the validation samples.

TABLE 64
Confusion matrix for validation samples using the cross-validated
CART algorithm
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	5	0
	SIRS	0	6

Random Forests. Another decision rule that can be developed using biomarkers of the present invention is a Random Forests decision tree. Random Forests is a tree based method that uses bootstrapping instead of cross-validation. For each iteration, a random sample (with replacement) is drawn and the largest tree possible is grown. Each tree receives a vote in the final class prediction. To fit a random forest, the number of trees (e.g. bootstrap iterations) is specified. For this data, 1000 trees were used to train the algorithm. Using this algorithm, 9 of the 10 biomarkers had non-zero importance and were used in the model. Biomarker importance, from greatest to smallest, was: TGFB1. MMP9, TLR4, IL1RN, TNFSF, ARG2, FCGR1A, and IL18R1.

The random forest method uses a number of different decision trees. A biomarker is considered to have discriminating significance if it served as a decision branch of a decision tree from a significant random forest analysis. As used herein, a significant random forest analysis is one where the lower 95% confidence interval on accuracy by cross validation on a training data set is greater than 50% and the point estimate for accuracy on a validation set is greater than 65%.

The predicted confusion matrix for the training dataset using the decision tree developed using the Random Forest method is given in Table 65. From this confusion matrix, the overall accuracy was estimated to be 79.5% with a 95% confidence interval between 63.5% and 90.7%. The estimated sensitivity was 87% and the estimated specificity was 68.8%.

TABLE 65
Confusion matrix for training samples against the decision tree
developed using the Random Forest method.
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	20	5
	SIRS	3	11

For the 11 validation samples held back from training, the overall accuracy was estimated to be 81.8% with a 95% confidence interval of 48.2% to 97.7%, sensitivity 60% and specificity 100%. Table 66 shows the confusion matrix for the validation samples.

TABLE 66
Confusion matrix for the 11 validation samples against the decision
tree developed using the Random Forest method.
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	6	0
	SIRS	2	3

MART. Multiple Additive Regression Trees (MART), also known as “gradient boosting machines,” was used to simultaneously assess the importance of biomarkers and classify the subject samples. Several fitting parameters are specified in this approach including (i) number of trees, (ii) step size (commonly referred to as “shrinkage”), and (iii) degree of interaction (related to the number of splits for each tree). More information on MART is described in Section 5.5.4 above. The degree of interaction was set to 1 to enforce an additive model (e.g. each tree has one split and only uses one biomarker).

Estimating interactions may require more data to function well. The step size was set to 0.05 so that the model complexity was dictated by the number of trees. The optimal number of trees was estimated by leaving out a random subset of cases at each fitting iteration, then assessing quality of prediction on that subset. After fitting more trees than were warranted, the point at which prediction performance stopped improving was estimated as the optimal point.

The estimated model used 30 trees and 7 biomarkers across all trees. The MART algorithm also provides a calculation of biomarker importance (summing to 100%). Biomarkers ranked in decreasing order of importance to the model, with the most important biomarker first were: ITGAM, TGFB1, TLR4, TNFSF, FCGR1A, IL18R1, and ARG2.

Cross-validation was carried out, with the optimal number of trees estimated independently in each of the 10 iterations. The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 67. From this confusion matrix, the overall accuracy was estimated to be 74.4% with a 95% confidence interval of 57.9% to 87%. The estimated sensitivity was 73.8% and the estimated specificity was 68.8%.

TABLE 67
Confusion matrix for the training samples using the cross-validated
MART algorithm.
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	18	5
	SIRS	5	11

For the 11 validation samples held back from training, the overall accuracy was estimated to be 74.4% with a 95% confidence interval of 57.9% to 87%, sensitivity 78.3% and specificity 68.8%. Table 68 shows the confusion matrix for the validation samples.

TABLE 68
Confusion matrix for the validation samples using the MART algorithm.
	True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	6	2
	SIRS	0	3

PAM. Yet another decision rule developed using biomarkers of the present invention is predictive analysis of microarrays (PAM), which is described in Section 5.5.2. above. In this method, a shrinkage parameter that determines the number of biomarkers used to classify samples is specified. This parameter was chosen via cross-validation. There were no biomarkers with missing values. Based on cross-validation, the optimal threshold value was 0.55, corresponding to 9 biomarkers.

Using the threshold of 0.55, the overall accuracy for the training samples was estimated to be 82.3% with a 95% confidence interval of 68.8% to 90.7%. The estimated sensitivity was 68.8% and the estimated specificity was 91.3%. Table 69 shows the confusion matrix for the training data where the predicted classifications were made from the cross-validated models.

TABLE 69
Confusion matrix for training samples
using cross-validated PAM algorithm
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	11	2
	SIRS	5	21

For the 11 validation samples held back from training, the overall accuracy was estimated to be 72.67% with a 95% confidence interval of 39% to 94%, sensitivity 40% and specificity 100%. Table 70 shows the confusion matrix for the validation samples.

TABLE 70
Confusion matrix for validation samples
using cross-validated PAM algorithm
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	2	0
	SIRS	3	6

The top nine biomarkers identified by PAM, ranked from most important to least important were: ARG2, TGFB1, MMP9, TLR4, ITGAM, IL18R1, TNFSF, IL1RN, and FCGR1A. FIG. 47 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals using T₋₁₂ static data obtained from an Affymetrix gene chip confirmatory training population. Based on the results of the RT-PCR analysis summarized in FIG. 47 and at other time points, all ten biomarkers under study in this confirmation process were significant. Some of the biomarkers discriminated as early as T₋₆₀.

6.12.2 Confirmatory Analysis of Biomarkers Identified by Affymetrix Gene Chip Analysis

The biomarkers identified in Table 59 of Section 6.11.2 and the ten biomarkers identified in Table 48 of Section 6.11.1 (FCGR1A, MMP9, IL18RI, ARG2, IL1RN, TNFSF13B, ITGAM, TGFB1, CD86, and TLR4), a total of 44 biomarkers, were analyzed using RT-PCR at multiple time points and analyzed in several different ways: static time of entry, static T₋₆₀, static T₋₃₆, baseline T₋₃₆, baseline T₋₃₆, and baseline T₋₁₂ data points. RT-PCR is described in Section 5.4.1.2, above. Representative of these analyses is the static T₋₁₂ data analysis described in detail below. In the T₋₁₂ static analysis, biomarkers features were measured using a specific blood sample, designated the T₋₁₂ blood sample, as defined in Section 6.4, above.

For the T₋₁₂ static analysis, the 44 biomarkers were measured from 37 samples. Each sample was collected from a different member of the population. Of these biomarkers, 23 were transformed by log transformations, and 21 by square root transformations.

The 37 member population was initially split into a training set (n=28) and a validation set (n=9). The training set was used to estimate the appropriate classification algorithm parameters while the trained algorithm was applied to the validation set to independently assess performance. Of the 28 training samples, 14 were labeled Sepsis, meaning that the subjects developed sepsis at some point during the observation time period, and 14 were SIRS, meaning that they did not develop sepsis during the observation time period. Table 71 provides distributions of the race, gender and age for these samples.

TABLE 71
Distributions of the race, gender, and age for the training data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	1	7	0
	Female	0	6	0
SIRS	Male	4	6	1
	Female	0	2	0
Group	Minimum	Mean	Median	Maximum
Sepsis	28	58	56	76
SIRS	20	42.5	39.5	79

For the 9 validation samples, five were labeled Sepsis and four were labeled SIRS. Table 72 provides distributions of the race, gender and age for these samples.

TABLE 72
Distributions of the race, gender, and age for the validation data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	2	0	0
	Female	0	3	0
SIRS	Male	0	2	0
	Female	0	2	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	49.8	58	76
SIRS	24	45.8	41.5	76

Each sample in the training data was randomly assigned to one of ten groups used for cross-validation. The number of training samples in these groups ranged from two to four. The samples were assigned in way that attempted to balance the number of sepsis and SIRS samples across folds. As described in more detail below, several different methods were used to judge whether select biomarkers discriminate between the Sepsis and SIRS groups.

Wilcoxon and Q-value tests. The first method used to identify discriminating biomarkers was a Wilcoxon test (unadjusted). The abundance value for a given biomarker across the samples in the training data was subjected to the Wilcoxon test. The Wilcoxon test considers both group classification (sepsis versus SIRS) and abundance value in order to compute a p value for the given biomarker. The p value provides an indication of how well the abundance value for the given biomarker across the samples collected in the training set discriminates between the sepsis and SIRS state. The lower the p value, the better the discrimination. When the p value is less than a specific confidence level, such as 0.05, an inference is made that the biomarker discriminates between the sepsis and SIRS phenotype. There were 38 significant biomarkers using this method (see Table 73).

The second method used to identify discriminating biomarkers was the Wilcoxon Test (adjusted). Due to the large number of biomarkers, 44, and the relatively small number of samples, 37, there was a high risk of finding falsely significant biomarkers. An adjusted p value was used to counter this risk. In particular, the method of Benjamini and Hochberg, 1995, J. R. Statist. Soc. B 57, pp 289-300, which is hereby incorporated herein by reference in its entirety, was used to control the false discovery rate. Here, the false discovery rate is defined as the number of biomarkers truly significant divided by the number of biomarkers declared significant. For example, if the adjusted p value is less than 0.05, there is a five percent chance that the biomarker is a false discovery. Results using this test are reported in Table 73. There were 38 significant biomarkers using this method (see Table 73). As used, herein, a biomarker is considered significant if it has a p value of less than 0.05 as determined by the Wilcoxon test (adjusted).

The third method used to identify discriminating biomarkers was Q values. In this third approach, the biomarkers were ordered by their Q values and if a respective biomarker has a Q value of X, then respective biomarker and all others more significant have a combined false discovery rate of X. However, the false discovery rate for any one biomarker may be much larger. There were 38 significant biomarkers using this method (see Table 73).

TABLE 73
Cumulative number of significant calls for the three methods.
Note that all samples (training and validation)
were used to compare sepsis and SIRS groups. Missing
biomarker feature values were not included in the analyses.
	≤1e−04	≤0.001	≤0.01	≤0.025	≤0.05	≤0.1	≤1
p-value	0	27	38	38	38	38	44
(unadjusted)
p-value	0	23	38	38	38	38	44
(adjusted)
q-value	0	36	38	39	39	39	44

CART. In addition to analyzing the microarray data using Wilcoxon and Q-value tests in order to identify biomarkers that discriminate between the sepsis and SIRS subpopulations in the training set, classification and regression tree (CART) analysis was used. CART is described in Section 5.5.1, above. Specifically, the data summarized above was used to predict the disease state by iteratively partitioning the data based on the best single-variable split of the data. In other words, at each stage of the tree building process, the biomarker whose expression values across the training population best discriminate between the sepsis and SIRS population was invoked as a decision branch. Cross-validation was carried out with the optimal number of splits estimated independently in each of the 10 iterations. The final tree uses three biomarkers which are listed in order of importance OSM, HLA-DRA, and IL-18, where OSM was the most important. The confusion matrix for the training data, based on the final tree from the cross-validated CART algorithm is given in Table 74. From this confusion matrix, the overall accuracy was estimated to be 67.9% with a 95% confidence interval of 47.6% to 84.1%. The estimated sensitivity was 64.3% and the estimated specificity was 71.4%.

TABLE 74
Confusion matrix for training samples
using the cross-validated CART algorithm
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	9	4
	SIRS	5	10

For the 9 validation samples held back from training data set, the overall accuracy was estimated to be 88.9% with a 95% confidence interval of 51.8% to 99.7%, sensitivity 75% and specificity 100%. Table 75 shows the confusion matrix for the validation samples.

TABLE 75
Confusion matrix for validation samples
using the cross-validated CART algorithm
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	3	0
	SIRS	1	5

Random Forests. Another decision rule that can be developed using biomarkers of the present invention is a Random Forests decision tree. Random Forests is a tree based method that uses bootstrapping instead of cross-validation. For each iteration, a random sample (with replacement) is drawn and the largest tree possible is grown. Each tree receives a vote in the final class prediction. To fit a random forest, the number of trees (e.g. bootstrap iterations) is specified. For this data, 1000 trees were used to train the algorithm. Using this algorithm, 35 of the 44 biomarkers had non-zero importance and were used in the model. Biomarker importance, from greatest to smallest, was: OSM, GADD45B, ARG2, IL18R1, TDRD9, PFKFB3, MAPK14, PRV1, MAP2K6, TNFRSF6, FCGR1A, INSL3, LY96, PSTPIP2, ANKRD22, TNFSF10, HLA-DRA, FNDC3B, TIFA, GADD45A, VNN1, ITGAM, BCL2A1, TLR4, TNFSF13B, SOCS3, IL1RN, CEACAM1, and SOD2.

The random forest method uses a number of different decision trees. A biomarker is considered to have discriminating significance if it served as a decision branch of a decision tree from a significant random forest analysis. As used herein, a significant random forest analysis is one where the lower 95% confidence interval on accuracy by cross validation on a training data set is greater than 50% and the point estimate for accuracy on a validation set is greater than 65%.

The predicted confusion matrix for the training dataset using the decision tree developed using the Random Forest method is given in Table 76. From this confusion matrix, the overall accuracy was estimated to be 78.6%. The estimated sensitivity was 78.6% and the estimated specificity was also 78.6%.

TABLE 76
Confusion matrix for training samples
against the decision tree developed
using the Random Forest method.
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	11	3
	SIRS	3	11

For the 9 validation samples held back from training, the overall accuracy was estimated to be 77.8% with a 95% confidence interval of 40.0% to 97.2%, sensitivity 50% and specificity 100%. Table 77 shows the confusion matrix for the validation samples.

TABLE 77
Confusion matrix for validation samples
against the decision tree developed
using the Random Forest method.
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	5	0
	SIRS	2	2

MART. Multiple Additive Regression Trees (MART), also known as “gradient boosting machines,” was used to simultaneously assess the importance of biomarkers and classify the subject samples. Several fitting parameters are specified in this approach including (i) number of trees, (ii) step size (commonly referred to as “shrinkage”), and (iii) degree of interaction (related to the number of splits for each tree). More information on MART is described in Section 5.5.4 above. The degree of interaction was set to 1 to enforce an additive model (e.g. each tree has one split and only uses one biomarker).

Estimating interactions may require more data to function well. The step size was set to 0.05 so that the model complexity was dictated by the number of trees. The optimal number of trees was estimated by leaving out a random subset of cases at each fitting iteration, then assessing quality of prediction on that subset. After fitting more trees than were warranted, the point at which prediction performance stopped improving was estimated as the optimal point.

The estimated model used 21 trees and 9 biomarkers across all trees. The MART algorithm also provides a calculation of biomarker importance (summing to 100%). Biomarkers ranked in decreasing order of importance to the model, with the most important biomarker first were: ARG2, GADD45B, OSM, LY96. INSL3, ANKRD22, MAP2K6, PSTPIP2, and TGFB1.

Cross-validation was carried out, with the optimal number of trees estimated independently in each of the 10 iterations. The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 78. From this confusion matrix, the overall accuracy was estimated to be 75% with a 95% confidence interval of 55.1 to 89.3%. The estimated sensitivity was 71.4% and the estimated specificity was 78.6%.

TABLE 78
Confusion matrix for the training samples
using the cross-validated MART algorithm.
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	10	3
	SIRS	4	11

For the 9 validation samples held back from training, the overall accuracy was estimated to be 88.9% with a 95% confidence interval of 51.8% to 99.7%, sensitivity 100% and specificity 75%. Table 79 shows the confusion matrix for the validation samples.

TABLE 79
Confusion matrix for the validation
samples using the MART algorithm.
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	5	1
	SIRS	0	3

PAM. Yet another decision rule developed using biomarkers of the present invention is predictive analysis of microarrays (PAM), which is described in Section 5.5.2, above. In this method, a shrinkage parameter that determines the number of biomarkers used to classify samples is specified. This parameter was chosen via cross-validation. There were no biomarkers with missing values. Based on cross-validation, the optimal threshold value was 2.05, corresponding to 6 biomarkers.

Using the threshold of 2.05, the overall accuracy for the training samples was estimated to be 82.5% with a 95% confidence interval of 68.7% to 91%. The estimated sensitivity was 78.6% and the estimated specificity was 85.7%. Table 80 shows the confusion matrix for the training data where the predicted classifications were made from the cross-validated models.

TABLE 80
Confusion matrix for training samples
using cross-validated PAM algorithm
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	11	2
	SIRS	3	12

For the 9 validation samples held back from training, the overall accuracy was estimated to be 77.8% with a 95% confidence interval of 40% to 97.2%, sensitivity 50% and specificity 100%. Table 81 shows the confusion matrix for the validation samples.

TABLE 81
Confusion matrix for validation samples
using cross-validated PAM algorithm
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	2	0
	SIRS	2	5

The top six biomarkers identified by PAM, ranked from most important to least important were: GADD45B. TDRD9, MAP2K6, OSM, TNFSF10, and ANKRD22. FIG. 48 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals using T₋₁₂ static data for the 44 biomarkers analyzed in this Section. Based on the results of the RT-PCR analysis summarized in FIG. 48 and at other time points, all forty-four biomarkers under study in this confirmation process were significant. Some of the biomarkers discriminated as early as T₋₆₀.

6.13 Select Protein Biomarkers

In this example, experiments were performed in order to confirm which protein based biomarkers differentiate between patients who subsequently develop sepsis (“sepsis patients) and patients who do not (“SIRS patients). In the discovery process, samples were analyzed by a bead based protein immunoassay, as described in Section 6.13.1.

6.13.1 Discovery of Protein Biomarkers Using a Head Based Protein Immunoassay

Multiplex Analysis. A set of biomarkers was analyzed simultaneously in real time, using a multiplex analysis method described in U.S. Pat. No. 5,981,180 (“the '180 patent”), herein incorporated by reference in its entirety, and in particular for its teachings of the general methodology, bead technology, system hardware and antibody detection. For this analysis, a matrix of microparticles was synthesized, where the matrix consisted of different sets of microparticles. Each set of microparticles had thousands of molecules of a distinct antibody capture reagent immobilized on the micro particle surface and was color-coded by incorporation of varying amounts of two fluorescent dyes. The ratio of the two fluorescent dyes provided a distinct emission spectrum for each set of microparticles, allowing the identification of a microparticle within a set following the pooling of the various sets of microparticles. U.S. Pat. Nos. 6,268,222 and 6,599,331 also are incorporated herein by reference in their entirety, and in particular for their teachings of various methods of labeling microparticles for multiplex analysis.

The sets of labeled beads were pooled and combined with a plasma sample from individuals. The labeled beads were identified by passing them single file through a flow device that interrogated each microparticle with a laser beam that excited the fluorophore labels. An optical detector then measured the emission spectrum of each bead to classify the beads into the appropriate set. Because the identity of each antibody capture reagent was known for each set of microparticles, each antibody specificity was matched with an individual microparticle that passes through the flow device. U.S. Pat. No. 6,592,822 is also incorporated herein by reference in its entirety, and in particular for its teachings of multi-analyte diagnostic system that can be used in this type of multiplex analysis.

To determine the amount of analyte that bound a given set of microparticles, a reporter molecule was added such that it formed a complex with the antibodies bound to their respective analyte. In the present example, the reporter molecule was a fluorophore-labeled secondary antibody. The fluorophore on the reporter was excited by a second laser having a different excitation wavelength, allowing the fluorophore label on the secondary antibody to be distinguished from the fluorophores used to label the microparticles. A second optical detector measured the emission from the fluorophore label on the secondary antibody to determine the amount of secondary antibody complexed with the analyte bound by the capture antibody. In this manner, the amount of multiple analytes captured to beads could be measured in a single reaction.

Data Analysis and Results. For each sample, the concentrations of analytes that bound several different antibodies were measured. Each analyte is a biomarker, and the concentration of each analyte in the sample can be a feature of that biomarker. The biomarkers were analyzed with select antibody reagents listed in Table 14 of United States Patent Publication Number U.S. 2004/0096917 A1, which is hereby incorporated herein by reference in its entirety. These antibody reagents are commercially available from Rules Based Medicine (Austin, Texas). The antibody reagents are categorized as specifically binding either (1) circulating protein biomarker components of blood, (2) circulating antibodies that normally bind molecules associated with various pathogens (identified by the pathogen that each biomarker is associated with, where indicated), or (3) autoantibody biomarkers that are associated with various disease states. Various approaches may be used to identify features that can inform a decision rule to classify individuals into the SIRS or sepsis groups. The methods chosen were CART, MART, PAM and random forests.

Biomarkers in multiple samples were measured using the above described assay at multiple time points and analyzed in several different ways: static time of entry, static T₋₆₀, static T₋₃₆, baseline T₋₆₀, baseline T₋₃₆, and baseline T₁₂ data points. Representative of these analyses is the static T₁₂ data analysis which is described in detail below. In the T₋₁₂ static analysis, biomarkers features were measured using a specific blood sample, designated the T₋₁₂ blood sample, as defined in Section 6.4, above.

For the T₋₁ static analysis, there were 60 biomarkers measured on 97 samples. Each sample was collected from a different member the population. Of these features, 53 were transformed by log transformations, 11 by square root transformations and the remaining 2 were not transformed.

The 97 member population was initially split into a training set (n=74) and a validation set (n=23). The training set was used to estimate the appropriate classification algorithm parameters while the trained algorithm was applied to the validation set to independently assess performance. Of the 74 training samples, 36 were labeled Sepsis, meaning that the subjects developed sepsis at some point during the observation time period, and 38 were labeled SIRS, meaning that they did not develop sepsis during the observation time period. Table 82 provides distributions of the race, gender and age for these samples.

TABLE 82
Distributions of the race, gender, and age for the training data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	10	14	1
	Female	0	10	1
SIRS	Male	5	24	0
	Female	0	9	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	43.2	40	80
SIRS	18	44.9	40	90

For the 23 validation samples, 12 were labeled Sepsis and 11 were labeled SIRS. Table 83 provides distributions of the race, gender and age for these samples.

TABLE 83
Distributions of the race, gender, and age for the validation data
Group	Gender	Black	Caucasian	Other
Sepsis	Male	0	7	0
	Female	0	4	0
SIRS	Male	2	6	0
	Female	0	4	0
Group	Minimum	Mean	Median	Maximum
Sepsis	18	43.4	43	81
SIRS	19	51.9	51.5	85

Each sample in the training data was randomly assigned to one of ten groups used for cross-validation. The number of training samples in these groups ranged from 6 to 8. The samples were assigned in way that attempted to balance the number of sepsis and SIRS samples across folds. As described in more detail below, several different methods were used to judge whether select biomarkers discriminate between the Sepsis and SIRS groups.

Wilcoxon and Q-value tests. The first method used to identify discriminating biomarkers was a Wilcoxon test (unadjusted). The abundance value for a given biomarker across the samples in the training data was subjected to the Wilcoxon test. The Wilcoxon test considers both group classification (sepsis versus SIRS) and abundance value in order to compute a p value for the given biomarker. The p value provides an indication of how well the abundance value for the given biomarker across the samples collected in the training set discriminates between the sepsis and SIRS state. The lower the p value, the better the discrimination. When the p value is less than a specific confidence level, such as 0.05, an inference is made that the biomarker discriminates between the sepsis and SIRS phenotype. There were 24 significant biomarkers using this method (see Table 84).

The second method used to identify discriminating biomarkers was the Wilcoxon Test (adjusted). Due to the large number of biomarkers, 60, in combination with the relatively small number of samples, 97, there was a high risk of finding falsely significant biomarkers. An adjusted p-value was used to counter this risk. In particular, the method of Benjamini and Hochberg, 1995, J. R. Statist. Soc. B 57, pp 289-300, which is hereby incorporated herein by reference in its entirety, was used to control the false discovery rate. Here, the false discovery rate is defined as the number of biomarkers truly significant divided by the number of biomarkers declared significant. For example, if the adjusted p-value is less than 0.05, there is a 5% chance that the biomarker is a false discovery. Results using this test are reported in Table 84. There were 16 significant biomarkers using this method (see Table 84). As used, herein, a biomarker is considered significant if it has a p-value of less than 0.05 as determined by the Wilcoxon test (adjusted).

The third method used to identify discriminating biomarkers was the use of Q values. In such an approach, the biomarkers are ordered by their q-values and if a respective biomarker has a q-value of X, then respective biomarker and all others more significant have a combined false discovery rate of X. However, the false discovery rate for any one biomarker may be much larger. There were 16 significant biomarkers using this method (see Table 84).

TABLE 84
Cumulative number of significant calls for the three methods.
Note that all samples (training and validation)
were used to compare Sepsis and SIRS groups. Missing
biomarker feature values were not included in the analyses.
	≤1e−04	≤0.001	≤0.01	≤0.025	≤0.05	≤0.1	≤1
p-value	0	6	14	20	24	25	60
(unadjusted)
p-value	0	0	6	13	16	24	60
(adjusted)
q-value	0	0	13	20	25	31	60

CART. In addition to analyzing the microarray data using Wilcoxon and Q-value tests in order to identify biomarkers that discriminate between the sepsis and SIRS subpopulations in the training set, classification and regression tree (CART) analysis was used. CART is described in Section 5.5.1, above. Specifically, the data summarized above was used to predict the disease state by iteratively partitioning the data based on the best single-variable split of the data. In other words, at each stage of the tree building process, the biomarker whose expression values across the training population best discriminate between the sepsis and SIRS population was invoked as a decision branch. Cross-validation was carried out, with the optimal number of splits estimated independently in each of the 10 iterations. The final tree is depicted in FIG. 49, and uses ten biomarkers: MIP1beta, thrombopoietin, C reactive protein, IL-10, IL-16, beta-2 microglobulin, alpha fetoprotein, IL-6, adiponectin, and ICAM.

FIG. 50 shows the distribution of the ten biomarkers used in the decision tree between the sepsis and SIRS groups in the training data set. In FIG. 50, the top of each box denotes the 75^th percentile of the data across the training set and the bottom of each box denotes the 25^th percentile, and the median value for each biomarker across the training set is drawn as a line within each box. The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 85. From this confusion matrix, the overall accuracy was estimated to be 63.5% with a 95% confidence interval of 51.5% to 74.4%. The estimated sensitivity was 66.7% and the estimated specificity was 60.5%.

TABLE 85
Confusion matrix for training
samples using cross-validated CART
		True Diagnosis
	Predicted	Sepsis	SIRS
	Sepsis	24	15
	SIRS	12	23

For the 23 validation samples held back from training data set, the overall accuracy was estimated to be 65.2% with a 95% confidence interval of 42.7% to 83.6%, sensitivity 66.7% and specificity 63.6%. Table 86 shows the confusion matrix for the validation samples.

TABLE 86
Confusion matrix for validation samples
using cross-validated CART
		True Diagnosis
		Predicted	Sepsis	SIRS
		Sepsis	8	1
		SIRS	4	10

Random Forests. Another decision rule that can be developed using biomarkers of the present invention is a Random Forests decision tree. Random Forests is a tree based method that uses bootstrapping instead of cross-validation. For each iteration, a random sample (with replacement) is drawn and the largest tree possible is grown. Each tree receives a vote in the final class prediction. To fit a random forest, the number of trees (e.g. bootstrap iterations) is specified. No more than 500 were used in this example, but at least 50 are needed for a burn-in period. The number of trees was chosen based on the accuracy of the training data. For this data, 64 trees were used to train the algorithm (see FIG. 51). In FIG. 51, curve 4802 is a smoothed estimate of overall accuracy as a function of tree number. Curve 4804 is a smoothed curve of tree sensitivity as a function of tree number. Curve 4806 is a smoothed curve of tree specificity as a function of tree number. Using this algorithm, 34 biomarkers had non-zero importance and were used in the model. The random forest algorithm gauges biomarker importance by the average reduction in the training accuracy. The biomarkers were ranked by this method and are shown in FIG. 52. The random forest method uses a number of different decision trees. A biomarker is considered to have discriminating significance if it served as a decision branch of a decision tree from a significant random forest analysis. As used herein, a significant random forest analysis is one where the lower 95% confidence interval on accuracy by cross validation on a training data set is greater than 50% and the point estimate for accuracy on a validation set is greater than 65%.

The predicted confusion matrix for the training dataset using the decision tree developed using the Random Forest method is given in Table 87. From this confusion matrix, the overall accuracy was estimated to be 70.3% (confidence intervals cannot be computed when using the bootstrap accuracy estimate). The estimated sensitivity was 69.4% and the estimated specificity was 71.1%.

TABLE 87
Confusion matrix for training samples against the decision
tree developed using the Random Forest method.
		True Diagnosis
		Predicted	Sepsis	SIRS
		Sepsis	27	11
		SIRS	11	25

For the 23 validation samples held back from training, the overall accuracy was estimated to be 60.9% with a 95% confidence interval of 38.5% to 80.3%, sensitivity 83.3% and specificity 36.4%. Table 88 shows the confusion matrix for the validation samples.

TABLE 88
Confusion matrix for the 23 validation samples against the
decision tree developed using the Random Forest method.
		True Diagnosis
		Predicted	Sepsis	SIRS
		Sepsis	10	7
		SIRS	2	4

MART. MART was used to simultaneously assess the importance of biomarkers and classify the subject samples. Several fitting parameters are specified in this approach including (i) number of trees, (ii) step size (commonly referred to as “shrinkage”), and (iii) degree of interaction (related to the number of splits for each tree). More information on MART is described in Section 5.5.4 above. The degree of interaction was set to 1 to enforce an additive model (e.g. each tree has one split and only uses one biomarker).

The degree of interaction was set to 1 to enforce an additive model (e.g. each tree has one split and only uses one feature), because this often works well even when a weak interaction is present. Moreover, estimating interactions may require more data to function well. The step size was set to 0.05 so that the model complexity was dictated by the number of trees. The optimal number of trees was estimated by leaving out a random subset of cases at each fitting iteration, then assessing quality of prediction on that subset. After fitting more trees than were warranted, the point at which prediction performance stopped improving was estimated as the optimal point.

The estimated model used 11 trees and 4 biomarkers across all trees. The MART algorithm also provides a calculation of biomarker importance (summing to 100%), which are given in FIG. 53. Biomarkers with zero importance were excluded. FIG. 54 shows the distribution of the selected biomarkers between the Sepsis and SIRS groups.

Cross-validation was carried out, with the optimal number of trees estimated independently in each of the 10 iterations. The confusion matrix for the training data where the predicted classifications were made from the cross-validated model is given in Table 89. From this confusion matrix, the overall accuracy was estimated to be 70.3% with a 95% confidence interval of 58.5% to 80.3%. The estimated sensitivity was 63.9% and the estimated specificity was 76.3%.

TABLE 89
Confusion matrix for the training samples
using the cross-validated MART algorithm.
		True Diagnosis
		Predicted	Sepsis	SIRS
		Sepsis	23	9
		SIRS	13	29

For the 23 validation samples held back from training, the overall accuracy was estimated to be 73.9% with a 95% confidence interval of 51.6% to 89.8%, sensitivity 63.6% and specificity 83.3%. Table 90 shows the confusion matrix for the validation

TABLE 90
Confusion matrix for the validation
samples using the MART algorithm.
		True Diagnosis
		Predicted	Sepsis	SIRS
		Sepsis	7	2
		SIRS	4	10

PAM. Yet another decision rule developed using biomarkers of the present invention is predictive analysis of microarrays (PAM), which is described in Section 5.5.2, above. In this method, a shrinkage parameter that determines the number of biomarkers used to classify samples is specified. This parameter was chosen via cross-validation. There were no biomarkers with missing values. Based on cross-validation, the optimal threshold value was 0.08, corresponding to 59 biomarkers. FIG. 55 shows the accuracy across different thresholds. In FIG. 55, curve 5202 is the overall accuracy (with 95% confidence interval bars). Curve 5204 shows decision rule sensitivity as a function of threshold value. Curve 5206 shows decision rule specificity as a function of threshold value. Using the threshold of 0.08, the overall accuracy for the training samples was estimated to be 74.9 with a 95% confidence interval of 65.3% to 82.5%. The estimated sensitivity was 78.9% and the estimated specificity was 69.4%. Table 91 shows the confusion matrix for the training data where the predicted classifications were made from the cross-validated models.

TABLE 91
Confusion matrix for training samples
using cross-validated PAM algorithm
		True Diagnosis
		Predicted	Sepsis	SIRS
		Sepsis	30	11
		SIRS	8	25

For the 23 validation samples held back from training, the overall accuracy was estimated to be 65.2% with a 95% confidence interval of 42.7% to 83.6%, sensitivity 91.7% and specificity 36.4%. Table 92 shows the confusion matrix for the validation samples.

TABLE 92
Confusion matrix for validation samples
using cross-validated PAM algorithm
		True Diagnosis
		Predicted	Sepsis	SIRS
		Sepsis	11	7
		SIRS	1	4

FIG. 56 shows the selected biomarkers, ranked by their relative discriminatory power, and their relative importance in the model.

FIG. 57 provides a summary of the CART, MART, PAM, and random forests (RF) classification algorithm (decision rule) performance and associated 95% confidence intervals. Fifty distinct biomarkers were selected from across all the algorithms illustrated in FIG. 58. The identity of these fifty selected features is found in FIG. 58. FIG. 58 illustrates an overall ranking of biomarkers for the T₋₁₂ data set. For the selected biomarkers, the x-axis depicts the percentage of times that it was selected. Within the percentage of times that biomarkers were selected, the biomarkers are ranked.

From the analysis of the T₁₂ data set and the other data sets, ten protein based biomarkers were selected for confirmation using the methodology described in Section 16.3.2. These biomarkers are listed in Table 93, below. Table 93: Protein based biomarkers selected for confirmation from immunoassay

TABLE 93
Protein based biomarkers selected
for confirmation from immunoassay
		Gene	Protein
Gene		Accession	Accession
Symbol	Gene Name	Number	Number
IL-6	INTERLEUKIN 6	NM_000600	NP_000591
IL-8	INTERLEUKIN 8	M28130	AAA59158
CRP	C Reactive protein	CAA39671	NM_000567
IL-10	INTERLEUKIN 10	NM_000572	CAH73907
APOC3	APOLIPOPROTEIN CIII	NM_000040	CAA25648
MMP9	MATRIX	NM_004994	NP_004985
	METALLOPROTEINASE 9
	(GELATINASE B, 92 KDA
	GELATINASE, 92 KDA
	TYPE IV COLLAGENASE)
TIMP1	TISSUE INHIBITOR OF	NM_003254	AAA75558
	METALLOPROTEINASE 1
MCP1	MONOCYTE	AF493698,	AAQ75526
	CHEMOATTRACTANT	AF493697
	PROTEIN 1
AFP	ALPHA-FETOPROTEIN	NM_001134	CAA79592
B2M	BETA-2 MICROGLOBULIN	NM_004048	AAA51811

Each of the sequences, genes, proteins, and probesets identified in Table 93 is hereby incorporated by reference.

6.13.2 Confirmation of Protein Biomarkers Using a Bead Based Protein Immunoassay

Confirmation of the biomarkers identified in Table 93 was performed using the same assay described in Section 6.13.1 at multiple time points and analyzed in several different ways: static time of entry, static T₋₆₀, static T₋₃₆, baseline T₋₆₀, baseline T₋₃₆, and baseline T₋₁₂ data points. Representative of these analyses is the static T₋₁₂ data analysis which is described in detail below. In the T₋₁₂ static analysis, biomarkers features were measured using a specific blood sample, designated the T₋₁₂ blood sample, as defined in Section 6.4, above. FIG. 59 illustrates the results of the analysis of static T₋₁₂ bead based protein assay, using CART, MART, PAM and random forests, where the static T₋₁₂ time point is as described in Section 6.4. The best decision tree in both the training and validation datasets for CART used six biomarkers. For both the training data and the validation data, the estimated model for MART used 4 biomarkers across all trees. A total of 7 biomarkers were of significance in both the training and the validation sets using PAM. Using random forest. 4 biomarkers under study were actually found to have discriminating significance in both the training and validation data sets. Based on the results of the analysis of the bead based protein immunoassay summarized in FIG. 59, each of the ten protein based biomarkers identified in Section 6.13.1 were confirmed by this experiment.

6.13.3 Confirmation of Protein Biomarkers Using BD Cytometric Bead Array Assay

IL-6, IL-8, and IL-10 proteins were confirmed using the BD™ Cytometric Bead Array (CBA) assay as embodied in the BD™ CBA Human Inflammation Kit. Flow cytometry is an analysis tool that allows for the discrimination of different particles on the basis of size and color. Multiplexing is the simultaneous assay of many analytes in a single sample. CBA employs a series of particles with discrete fluorescence intensities to simultaneously detect multiple soluble analytes. CBA is combined with flow cytometry to create a multiplexed assay. The BD CBA system uses the sensitivity of amplified fluorescence detection by flow cytometry to measure soluble analytes in a particle-based immunoassay. Each bead in a CBA provides a capture surface for a specific protein and is analogous to an individually coated well in an ELISA plate. The BD CBA capture bead mixture is in suspension to allow for the detection of multiple analytes in a small volume sample.

The combined advantages of the broad dynamic range of fluorescent detection via flow cytometry and the efficient capturing of analytes via suspended particles enable CBA to use fewer sample dilutions and to obtain the value of an unknown in substantially less time (compared to conventional ELISA). The BD™ CBA Human Inflammation Kit can be used to quantitatively measure Interleukin-8 (IL-8), Interleukin-1p (IL-10), Interleukin-6 (IL-6), Interleukin-10 (IL-10). Tumor Necrosis Factor (TNF), and Interleukin-12p70 (IL-12p70) protein levels in a single sample. The kit performance has been optimized for analysis of specific proteins in tissue culture supernatants, EDTA plasma, and serum samples.

Six bead populations with distinct fluorescence intensities have been coated with capture antibodies specific for IL-8, IL-1p, IL-6, IL-10, TNF, and IL-12p70 proteins. The six bead populations are mixed together to form the BD™ CBA which is resolved in the FL3 channel of a flow cytometer such as the BD FACScan™ or BD FACSCalibur™ flow cytometer. The capture beads. PE-conjugated detection antibodies, and recombinant standards or test samples are incubated together to form sandwich complexes. Following acquisition of sample data using the flow cytometer, the sample results are generated in graphical and tabular format using the BD™ CBA Analysis Software. More details about the BD™ CBA Human Inflammation Kit are described in the BD™ CBA Human Inflammation Kit Instruction Manual, catalog number 551811, available from BD biosciences, which is hereby incorporated by reference herein in its entirety. Using the BD™ CBA Human Inflammation Kit, the biomarkers IL-6, IL-8, and IL-10 were confirmed as discriminating between sepsis and SIRS.

6.14 Assessing Subcombinations of the Biomarkers Identified in Table I

One embodiment of the present invention encompasses any 2 or more of the 53 biomarkers listed in Table I as predictors for classifying a subject as sepsis or SIRS. One embodiment of the present invention encompasses any 3 or more of the 53 biomarkers listed in Table I as predictors for classifying a subject as sepsis or SIRS. As such, the present invention further encompasses any subcombination of the 53 biomarkers listed in Table I as predictors for classifying a subject as sepsis or SIRS provided that there are at least 2 or 3 biomarkers in the subcombination. This section discloses experiments that demonstrate the predictive power of exemplary subcombinations of the 53 biomarkers listed in Table I. Several thousand subcombinations were tested and the vast majority of those subcombinations had an accuracy of at least seventy percent. This indicates that the vast majority of the possible subcombinations of the 53 biomarkers listed in Table I will discriminate between sepsis and SIRS subjects.

6.14.1 Subcombinations of Nucleic Acid Biomarkers at T₋₁₂

There are a total of 44 biomarkers for which RT-PCR nucleic acid data is available as reported in Table J. A total of 4800 different subcombinations of this set of biomarkers were constructed using the T₁₂ time point data described in Section 6.12. Each different subcombination was then tested for its ability to discriminate between sepsis subjects and SIRS subjects. The 4800 subcombinations represent a random sampling of the total number of possible subcombinations possible for the 44 biomarkers of the present invention reported in Table J. Randomness of the 4800 subcombinations was ensured using the following algorithm:

CONSIDER 2 to 25 biomarkers from Table J
{
LET the current number be k;
DO the following 200 times
{
SELECT k biomarkers at random from Table J;
LET the current set of biomarkers be S;
}
DO the following 10 times
{
FOR biomarker set S, randomly set aside 10% of patients as a
validation population and 90% as a training population;
FIT a model to the training population using Random Forest with
T−12 time point data;
PREDICT results for the validation population;
CALCULATE agreement with the known status of the validation
population;
}
AVERAGE the ten agreement rates and report;
SET k = k+1;
IF k > 10 then END; ELSE return to top;
}
END

There were a total of 152 patients for which T₋₁₂ data was available from a combination of discovery and confirmatory data described above. Of these 152 patients, 80 were sepsis and 72 were SIRs. The calculations described above test 200 subcombinations at each interval 2 through 25. In other words, 200 subcombinations each consisting of two biomarkers randomly selected from Table J were tested, 200 subcombinations each consisting of three biomarkers randomly selected from Table J were tested, and so forth, through 200 subcombinations each consisting of twenty-five biomarkers randomly selected from Table J for a total of 24 families of subcombinations, where each family of subcombinations consists of 200 subcombinations of biomarkers each having k biomarkers, where k is a number in the set 2 through 25.

The data set with assay results for all biomarkers under consideration was maintained in memory, as were a list of unique biomarker names. To evaluate subsets of a specific size (say, k=three), then that many (three) biomarker names were selected randomly from the set of unique biomarker names, using a pseudorandom number generators provided in the R software package. See Venables and Smith, An Introduction to R, ISBN 0-9541617-4-2, which is hereby incorporated by reference in its entirety. A matrix of assay results for the selected biomarker names was constructed. This matrix could have more columns than the number of selected biomarker names, since some biomarkers have more than one assay result. An estimate of true predictive accuracy, when using the modeling technique “Random Forest,” was then constructed for this matrix. The Random Forest algorithm was implemented as described in Breiman, 2001, “Random Forests,” Machine Learning 45(1), pp. 5-32, which is hereby incorporated by reference in its entirety.

For a given data matrix, the prediction of true predictive accuracy was calculated as follows: 10% of patients were randomly selected in a balanced manner, i.e., 10% of septic patients and 10% of SIRS patients were selected. Selected patients were set aside for the validation population, and a random forest model was fitted to the remaining data (the training population). If there were any missing values in the training data or the set-aside data, a recursive partitioning model was fitted to other assay results as well as the Sepsis/SIRS information in order to predict assay values. The recursive partitioning model is described in Breiman et al., 1984, Classification and Regression Trees. Wadsworth, which is hereby incorporated by reference in its entirety. Missing values were then replaced with their predicted values. Missing values in the set-aside data were replaced with predictions from the recursive-partition model fitted to the training data, so that knowledge of the SIRS/Sepsis status for the validation population was not used in any way to classify validation patients.

By comparing the true status of the 10% set aside (the validation population) with the predicted status according to the random forest model fitted to the other 90% (the training population), sensitivity, specificity, and agreement were calculated. This process was repeated 10 times, and the final sensitivity, specificity, and agreement estimates (also termed accuracy, also termed performance) for the given marker subset were those values averaged across the 10 iterations. This process was applied to every subset. For each size considered (k value, i.e., number of biomarkers), 200 random subsets were selected and evaluated. These 200 performance (accuracy) estimates form an estimate of the distribution of performances of all subsets of biomarkers of a given size (k value).

FIG. 60 plots the accuracy of each of these 24 families of subcombinations as bar graphs. FIG. 61 plots the accuracy (performance) of each individual subcombination in each of the 24 families of subcombinations. Thus, FIG. 61 plots the accuracy (performance) of a total of 4800 subcombinations of the set of biomarkers listed in Table J.

FIGS. 60 and 61 indicate that for k>5, the distributions are Gaussian, (bell-shaped), indicating that each respective family (k=5, . . . , 24) is an accurate depiction of the subcombination space represented by the family. For k<=5, a handful of subsets give lower accuracy (performance) estimates. However, the results available for k<=5 indicate that this class of biomarker subcombinations discriminate between sepsis and SIRS as well. The results reported in FIGS. 60 and 61 show that, with as few as two biomarkers randomly selected from Table J, an accuracy (performance) estimate above 50% was virtually always obtained. Table 94 contains the number of subcombinations in each family (k=2, 4, . . . , 25) that performed with a threshold accuracy of greater than 60% (column 2), greater than 70% (column 3), greater than 80% (column 4), greater than 90% (column 5), or an accuracy of less than 60% (column 6). The data summarized in FIGS. 60 and 61. as well as Table 94, demonstrates that, for time T-j₂ data almost all subcombinations of biomarkers comprising between 2 and 25 biomarkers from Table J will discriminate between sepsis and SIRs subjects.

TABLE 94
Number of subcombinations from Table J that performed with
a given threshold accuracy using T−12 nucleic acid data
Column 1	Column 2	Column 3	Column 4	Column 5	Column 6
Number of	Greater	Greater	Greater	Greater	Less than
Biomarkers	than 60%	than 70%	than 80%	than 90%	60%
2	197	145	17	0	3
3	199	160	25	0	1
4	199	174	38	0	1
5	200	186	51	0	0
6	200	194	50	0	0
7	200	195	48	0	0
8	200	194	64	0	0
9	200	200	61	1	0
10	200	196	64	0	0
11	200	196	70	0	0
12	200	199	70	0	0
13	200	199	73	0	0
14	200	198	67	0	0
15	200	198	79	0	0
16	200	198	70	0	0
17	200	198	64	0	0
18	200	199	84	0	0
19	200	197	83	0	0
20	200	199	82	0	0
21	200	199	85	0	0
22	200	198	80	0	0
23	200	200	83	0	0
24	200	198	83	0	0
25	200	198	81	0	0

6.14.2 Subcombinations of Protein Biomarkers at T₋₁₂

There are a total of 10 biomarkers for which protein abundance data is available as reported in Table K. A total of 1600 different subcombinations of this set of biomarkers were constructed using the T₁₂ time point data described in Section 6.13. Each different subcombination was then tested for its ability to discriminate between sepsis and SIRS subjects. The 1600 subcombinations represent a random sampling of the total number of possible subcombinations possible for the 10 biomarkers of the present invention reported in Table K. Randomness of the 1600 subcombinations was ensured using the following algorithm:

CONSIDER 3 to 10 biomarkers from Table K
{
LET the current number be k;
DO the following 200 times
{
SELECT k biomarkers at random from Table K;
LET the current set of biomarkers be S;
}
DO the following 10 times
{
FOR biomarker set S, randomly set aside 10% of patients as a
validation population and 90% as a training population;
FIT a model to the training population using Random Forest with
T−12 time point data;
PREDICT results for the validation population;
CALCULATE agreement with the known status of the validation
population;
}
AVERAGE the ten agreement rates and report;
SET k = k+1;
IF k > 10 then END; ELSE return to top;
}
END

Computations were performed as described in further detail in Section 6.14.1. There were a total of 152 patients for which T₋₁₂ data was available from a combination of discovery and confirmatory data described above. Of these 152 patients, 80 were sepsis and 72 were SIRs. For some biomarkers in Table K, there were multiple data sources. For instance, there is IL-6, IL-8, and IL-10 protein data from three different labs. Thus, there is a complex pattern of incidence among patients. Some patients may be tested by one lab, others by two, etc. This was determined by how the project evolved and what samples were available (some patient samples were exhausted before they could be tested with assays developed later). To handle this complex incidence, the following strategy was used. In any given iteration, if a protein that was tested in multiple labs was selected, all assay results for the protein were selected. A missing-value imputation scheme was then used to fill out missing values, making it look like all patients were tested with all assays. This data was then fed into the Random Forest model as correlated inputs that measure the same underlying compound. Thus, consider the case where k is equal to 3 and one of the randomly chosen proteins from Table K is IL-8, from 3 different laboratories, and the other 2 proteins are unique meaning that they are each from only one laboratory. The data from all three TL-8 sources are selected, plus the other two unique assays for the other two proteins, for a total of five assays. The missing-value imputation scheme is then used to fill out missing values, making it look like all patients had results from three different sources for a total of nine assays.

The calculations described above test 200 subcombinations at each interval 3 through 10. In other words, 200 subcombinations each consisting of three randomly selected biomarkers from Table K were tested, 200 subcombinations each consisting of four biomarkers randomly selected from Table K were tested, and so forth, through 200 subcombinations each consisting of ten biomarkers randomly selected from Table K for a total of 8 families of subcombinations, where each family of subcombinations consists of 200 subcombinations of biomarkers all having k biomarkers, where k is a number in the set 3 through 10. FIG. 62 plots the accuracy of each of these eight families of subcombinations as bar graphs. FIG. 63 plots the accuracy (performance) of each individual subcombination in each of the eight families of subcombinations. Thus, FIG. 63 plots the accuracy (performance) of a total of 1600 subcombinations of the set of biomarkers listed in Table K.

FIGS. 62 and 63 show that the distribution for each family of subcombinations is Gaussian (bell-shaped), indicating that each respective family (k=3, 4, . . . , 10) is an accurate depiction of the subcombination space represented by the family. The results reported in FIGS. 62 and 63 show that, with as few as three biomarkers randomly selected from Table K, an accuracy (performance) estimate above 50% was virtually always obtained. Table 95 contains the number of subcombinations in each family (k=3, 4, . . . , 10) that performed with a threshold accuracy of greater than 60% (column 2), greater than 70% (column 3), greater than 80% (column 4). greater than 90% (column 5), or an accuracy of less than 60% (column 6). The data summarized in FIGS. 62 and 63, as well as Table 95, demonstrates that, for time T₋₁₂ data, almost all subcombinations of biomarkers comprising between 3 and 10 biomarkers from Table K will discriminate between sepsis and SIRs subjects.

TABLE 95
Number of subcombinations from Table K that performed
with a given threshold accuracy using T−12 protein data
Column 1	Column 2	Column 3	Column 4	Column 5	Column 6
Number of	Greater	Greater	Greater	Greater	Less than
Biomarkers	than 60%	than 70%	than 80%	than 90%	60%
3	192	58	0	0	8
4	196	106	1	0	4
5	200	117	1	0	0
6	200	136	0	0	0
7	200	151	1	0	0
8	200	172	1	0	0
9	200	188	1	0	0
10	200	187	0	0	0

6.14.3 Subcombinations of Protein Biomarkers at T₋₃₆

A total of 1600 different subcombinations of the set of biomarkers of Table K were constructed for the T₋₃6 time point using the protein based data described in Section 6.13. Each different subcombination was then tested for its ability to discriminate between sepsis and SIRS subjects. There were a total of 142 patients for which T₋₃₆data was available from a combination of discovery and confirmatory data described above. Of these 142 patients, 79 were sepsis and 63 were SIRs. The 1600 subcombinations represent a random sampling of the total number of possible subcombinations possible for the 10 biomarkers of the present invention reported in Table K. Randomness of the 1600 subcombinations was ensured using the algorithm identified in Section 6.14.2, the only difference being that T₋₃₆ data rather than T₋₂ data was used. Computations were performed as described in further detail in Section 6.14.1. FIG. 64 plots the accuracy of each of these eight families of subcombinations as bar graphs. FIG. 65 plots the accuracy (performance) of each individual subcombination in each of the eight families of subcombinations. Thus, FIG. 65 plots the accuracy (performance) of a total of 1600 subcombinations of the set of biomarkers listed in Table K.

The results reported in FIGS. 64 and 65 show that, with as few as three biomarkers randomly selected from Table K, an accuracy (performance) estimate above 60% was typically obtained. Table 95 contains the number of subcombinations in each family (k=3, 4, . . . , 10) that performed with a threshold accuracy of greater than 60% (column 2). greater than 70% (column 3), greater than 80% (column 4). greater than 90% (column 5), or an accuracy of less than 60% (column 6). The data summarized in FIGS. 64 and 65, as well as Table 95, demonstrates that, for time T₋₃₆ data, most subcombinations of biomarkers comprising between 3 and 10 biomarkers from Table K will discriminate between sepsis and SIRs subjects.

TABLE 96
Number of subcombinations from Table K that performed
with a given threshold accuracy using T−36 protein data
Column 1	Column 2	Column 3	Column 4	Column 5	Column 6
Number of	Greater	Greater	Greater	Greater	Less than
Biomarkers	than 60%	than 70%	than 80%	than 90%	60%
3	138	23	0	0	62
4	152	25	0	0	48
5	171	32	0	0	29
6	180	30	0	0	20
7	188	37	0	0	12
8	194	40	0	0	6
9	194	27	0	0	6
10	199	20	0	0	1

6.14.4 Subcombinations of Nucleic Acid Biomarkers at T₋₃₆

A total of 4600 different subcombinations of the set of biomarkers of Table J were constructed for the T₋₃₆ time point using the nucleic acid based data described in Section 6.13. Each different subcombination was then tested for its ability to discriminate between sepsis and SIRS subjects. There were a total of 142 patients for which T₋₃₆ data was available from a combination of discovery and confirmatory data described above. Of these 142 patients, 79 were sepsis and 63 were SIRs. The 4600 subcombinations represent a random sampling of the total number of possible subcombinations possible for the 44 biomarkers of the present invention reported in Table J at the T₋₃₆ time point. Randomness of the 4600 subcombinations was ensured using the algorithm identified in Section 6.14.1. the only difference being that T₋₃₆ data rather than T₋₂ data was used and that the minimum k value was 3. Computations were performed as described in further detail in Section 6.14.1. FIG. 66 plots the accuracy of each of these 23 families of subcombinations as bar graphs. FIG. 67 plots the accuracy (performance) of each individual subcombination in each of the 23 families of subcombinations. Thus, FIG. 67 plots the accuracy (performance) of a total of 4600 subcombinations of the set of biomarkers listed in Table J.

The results reported in FIGS. 66 and 67 show that, with as few as three biomarkers randomly selected from Table J, an accuracy (performance) estimate above 60% was typically obtained. Table 97 contains the number of subcombinations in each family (k=3, 4, . . . , 25) that performed with a threshold accuracy of greater than 60% (column 2), greater than 70% (column 3), greater than 80% (column 4), greater than 90% (column 5), or an accuracy of less than 60% (column 6). The data summarized in FIGS. 66 and 67, as well as Table 97, demonstrate that, for time T₋₃₆ data, most subcombinations of biomarkers comprising between 3 and 25 biomarkers from Table J will discriminate between sepsis and SIRs subjects.

TABLE 97
Number of subcombinations from Table J that performed with
a given threshold accuracy using T−36 nucleic acid data
Column 1	Column 2	Column 3	Column 4	Column 5	Column 6
Number of	Greater	Greater	Greater	Greater	Less than
Biomarkers	than 60%	than 70%	than 80%	than 90%	60%
3	194	115	4	0	6
4	196	128	8	0	4
5	200	159	6	0	0
6	200	161	6	0	0
7	200	173	10	0	0
8	200	182	10	0	0
9	200	189	8	0	0
10	200	188	10	0	0
11	200	194	10	0	0
12	200	193	13	0	0
13	200	190	19	0	0
14	200	192	24	0	0
15	200	196	20	0	0
16	200	195	16	0	0
17	200	196	22	0	0
18	200	195	18	0	0
19	200	196	14	0	0
20	200	194	14	0	0
21	200	197	14	0	0
22	200	197	11	0	0
23	200	200	15	0	0
24	200	199	20	0	0
25	200	199	19	0	0

6.14.5 Subcombinations of Combined Nucleic Acid and Protein Biomarker Data at T₋₁₂

There are a total of 53 biomarkers listed Table I. A total of 4600 different subcombinations of this set of biomarkers were constructed using all available T₋₁₂ time point data. For the subset of biomarkers in Table I that are listed in Table J, the T₋₁₂ time point data consisted of RT-PCR data described above. For the subset of biomarkers that are listed in Table K, the T₋₁₂ Lime point data consisted of bead based data described above. The one exception to this was “MMP9” for which both protein and gene-expression data was available. Therefore, MMP9 gene and protein abundance data was treated as separate biomarkers. To accomplish this, MMP9 nucleic data was termed “MMP9.GE” and MMP9 protein abundance data from the bead based assays was termed MMIP9.Protein.

Each different subcombination was tested for its ability to discriminate between sepsis subjects and SIRS subject %. The 4600 subcombinations represent a random sampling of the total number of possible subcombinations possible for the 53 biomarkers of the present invention reported in Table 1. Randomness of the 4600 subcombinations was ensured using the following algorithm:

CONSIDER 3 to 25 biomarkers from Table I
{
LET the current number be k;
DO the following 200 times
{
SELECT k biomarkers at random from Table I;
LET the current set of biomarkers be S;
}
DO the following 10 times
{
FOR biomarker set S, randomly set aside 10% of patients as a
validation population and 90% as a training population;
FIT a model to the training population using Random Forest with
T−12 time point data;
PREDICT results for the validation population;
CALCULATE agreement with the known status of the validation
population;
}
AVERAGE the ten agreement rates and report;
SET k = k+1;
IF k > 10 then END; ELSE return to top;
}
END

There were a total of 152 patients for which T₋₁₂ data was available from a combination of discovery and confirmatory data described above. Of these 152 patients, 80 were sepsis and 72 were SIRs. Computations were performed as described in further detail in Section 6.14.1. The calculations described above test 200 subcombinations at each interval 2 through 25. In other words, 200 subcombinations each consisting of three biomarkers randomly selected from Table I were tested, 200 subcombinations each consisting of four biomarkers randomly selected from Table I were tested, and so forth, through 200 subcombinations each consisting of twenty-five biomarkers randomly selected from Table I for a total of 23 families of subcombinations, where each family of subcombinations consists of 200 subcombinations of biomarkers each having k biomarkers, where k is a number in the set 3 through 25. FIG. 68 plots the accuracy of each of these 23 families of subcombinations as bar graphs. FIG. 69 plots the accuracy (performance) of each individual subcombination in each of the 23 families of subcombinations. Thus, FIG. 69 plots the accuracy (performance) of a total of 4600 subcombinations of the set of biomarkers listed in Table 1.

FIGS. 68 and 69 indicate that for k>5, the distributions are Gaussian, (bell-shaped), indicating that each respective family (k=5, . . . , 25) is an accurate depiction of the subcombination space represented by the family. For k<=5, a handful of subsets give lower accuracy (performance) estimates. The results reported in FIGS. 68 and 69 show that, with as few as three biomarkers randomly selected from Table I, an accuracy (performance) estimate above 50% r was virtually always obtained. Table 98 contains the number of subcombinations in each family (k=3, 4, . . . , 25) that performed with a threshold accuracy of greater than 60% (column 2), greater than 70% (column 3), greater than 80% (column 4), greater than 90% (column 5), or an accuracy of less than 60% (column 6). The data summarized in FIGS. 68 and 69, as well as Table 98, demonstrate that, for time T₋₁₂ data, almost all subcombinations of biomarkers comprising between 3 and 25 biomarkers from Table I will discriminate between sepsis and SIRs subjects.

TABLE 98
Number of subcombinations from Table I that performed
with a given threshold accuracy using T−12 combined
nucleic acid and protein data
Column 1	Column 2	Column 3	Column 4	Column 5	Column 6
Number of	Greater	Greater	Greater	Greater	Less than
Biomarkers	than 60%	than 70%	than 80%	than 90%	60%
3	200	157	11	0	0
4	200	166	12	0	0
5	200	191	25	0	0
6	200	191	30	0	0
7	200	195	33	0	0
8	200	198	44	0	0
9	200	200	49	0	0
10	200	198	63	0	0
11	200	199	65	0	0
12	200	200	71	0	0
13	200	200	64	0	0
14	200	200	66	0	0
15	200	200	74	0	0
16	200	199	74	0	0
17	200	200	73	0	0
18	200	200	76	0	0
19	200	200	87	0	0
20	200	199	94	0	0
21	200	200	77	0	0
22	200	200	84	0	0
23	200	200	81	0	0
24	200	200	93	0	0
25	200	200	85	0	0

6.14.6 Subcombinations of Combined Nucleic Acid and Protein Biomarker Data at T₋₃₆

Subcombinations of biomarkers were selected as described in Section 6.14.5, the only difference being that T₋₃₆ data rather than T₋₁₂ data was used. A total of 4600 different subcombinations of Table I were constructed using all available T₋₃₆ time point data. There were a total of 142 patients for which T₋₃₆data was available from a combination of discovery and confirmatory data described above. Of these 142 patients, 79 were sepsis and 63 were SIRs. Computations were performed as described in further detail in Section 6.14.1. The calculations described above test 200 subcombinations at each interval 3 through 25. In other words, 200 subcombinations each consisting of three biomarkers randomly selected from Table I were tested, 200 subcombinations each consisting of four biomarkers randomly selected from Table I were tested, and so forth. through 200 subcombinations each consisting of twenty-five biomarkers randomly selected from Table I for a total of 23 families of subcombinations, where each family of subcombinations consists of 200 subcombinations of biomarkers each having k biomarkers, where k is a number in the set 3 through 25. FIG. 70 plots the accuracy of each of these 23 families of subcombinations as bar graphs. FIG. 71 plots the accuracy (performance) of each individual subcombination in each of the 23 families of subcombinations. Thus, FIG. 71 plots the accuracy (performance) of a total of 4600 subcombinations of the set of biomarkers listed in Table I.

FIGS. 70 and 71 indicate that for k>5, the distributions are Gaussian, (bell-shaped), indicating that each respective family (k=5, . . . , 25) is an accurate depiction of the subcombination space represented by the family. For k<=5, a handful of subsets give lower accuracy (performance) estimates. The results reported in FIGS. 70 and 71 show that, with as few as three biomarkers randomly selected from Table 1, an accuracy (performance) estimate above 50% was virtually always obtained. Table 99 contains the number of subcombinations in each family (k=3, 4, . . . , 25) that performed with a threshold accuracy of greater than 60% (column 2), greater than 70% (column 3), greater than 80% (column 4), greater than 90% (column 5), or an accuracy of less than 60% (column 6). The data summarized in FIGS. 70 and 71, as well as Table 99, demonstrate that, for time T₋₃ data, almost all subcombinations of biomarkers comprising between 3 and 25 biomarkers from Table I will discriminate between sepsis and SIRs subjects.

TABLE 99
Number of subcombinations from Table I that performed
with a given threshold accuracy using T−36 combined
nucleic acid and protein data
Column 1	Column 2	Column 3	Column 4	Column 5	Column 6
Number of	Greater	Greater	Greater	Greater	Less than
Biomarkers	than 60%	than 70%	than 80%	than 90%	60%
3	187	96	4	0	13
4	199	127	5	0	1
5	200	145	7	0	0
6	200	149	9	0	0
7	200	148	9	0	0
8	200	157	8	0	0
9	200	175	13	0	0
10	199	179	7	0	1
11	200	180	11	0	0
12	200	175	11	0	0
13	200	184	15	0	0
14	200	184	10	0	0
15	200	180	5	0	0
16	200	190	17	0	0
17	200	191	16	0	0
18	200	190	15	0	0
19	200	191	8	0	0
20	200	196	13	0	0
21	200	198	15	0	0
22	200	195	9	0	0
23	200	195	14	0	0
24	200	195	10	0	0
25	200	196	18	0	0

6.15 Mean Expression Value of Biomarkers in Sepsis and Sirs Patients Identified in Table I

The mean expression values of the biomarkers of Table I were determined for subjects that acquired sepsis (Sepis subjects) and subjects that did not acquire sepsis (SIRS subjects) in the populations described in Sections 6.11.2, 6.12.2 (Affymetrix data), 611.1. 6.12.1 (RT-PCR data), 6.13.3 (bead data),. and 6.13.1 and 6.13.2 (bead data) at the T₋₁₂, T₋₃₆, and T₋₆₀ Lime points. This data is set forth in Table 100 below. In Table 100, a biomarker with the _Affy extension represents the combined data of Sections 6.11.2 and 6.11.2 (Affymetrix data). a biomarker with the 0.185 extension represents the combined data of Sections 6.11.1 and 6.12.1 (RT-PCR data), a biomarker with the BDB extension represents the data of Section 6.13.3. and a biomarker with the RBM extension represents the data of Sections 6.13.1 and 6.13.2.

For nucleic acid biomarkers in Table 100 that were identified by gene arrays (.Affy), the values in Table 100 represent mean relative fluorescence intensity units obtained for the specific probe sequences examined. As such, they are not actual units of measure, just relative quantity of one group to another. Additionally, as part of the data analysis, some of these values may have undergone a log transformation or other adjustment, prior to being reported. The expression values for the nucleic acid biomarkers (0.18S) found in Table 100 are defined by the relative “cycle-time to threshold.” As such, they do not cite actual units of measure, just relative quantity of one group to another. A sample with a higher amount of nucleic acid will become positive sooner (fewer cycles) than one with less nucleic acid, which will require more cycles before the resultant signal crosses a positivity threshold. For the protein biomarkers in Table 101, the units were as follows alphafetoprotein (AFP) μg/mL (micrograms per milliliter of plasma), Beta-2-Microglobulin B2M) μg/mL, Interleukin-6 (IL-6) μg/mL (picograms/milliliter), Interleukin-8 (IL-8) μg/mL, Interleukin-10 (IL-10) μg/mL, Monocyte Chemoatractant Protein 1 (MCP) μg/mL, Matrix Metalloproteinase 9 (MMP9) ng/mL (nanogram/milliliter), Tissue Inhibitor of Metalloproteinase 1 (TIMPI) ng/mL (nanogram/mL), C Reactive protein (CRP) μg/mL, and Apoliprotein CIII μg/mL.

TABLE 100
Mean expression values for the biomarkers of Table I as measured in the
experimental Affymetrix, RT-PCR, and bead data of Section 6.
	SIRS	Sepsis	SIRS	Sepsis	SIRS	Sepsis
Marker	T−12	T−12	T−36	T−36	T−60	T−60
ANKRD22_Affy	8.33	9.72	8.28	9.27	8.51	9.17
ANXA3_Affy	10.06	11.28	10.19	11.197	10.49	11.14
BCL2A1_Affy	8.55	9.87	8.73	9.48	9.01	9.60
CCL5_Affy	11.69	11.30	11.73	11.22	11.49	11.29
CD86_Affy	8.59	8.10	8.68	8.13	8.57	8.20
CEACAM1_Affy	7.81	8.74	7.83	8.43	7.91	8.43
CRTAP_Affy	9.30	8.81	9.31	8.87	9.31	8.96
CSF1R_Affy	9.36	8.79	9.34	8.93	9.40	8.89
FAD104_Affy	7.89	8.63	8.04	8.39	8.18	8.36
FCGR1A_Affy	7.38	8.10	7.34	7.90	7.53	7.76
GADD45A_Affy	8.26	9.03	8.36	8.95	8.53	9.01
GADD45B_Affy	8.81	9.40	8.80	9.21	8.91	9.20
HLA.DRA_Affy	11.91	11.22	11.80	11.13	11.78	11.28
IFNGR1_Affy	11.20	11.51	11.25	11.53	11.38	11.52
IL18Rl_Affy	6.65	8.23	6.81	7.90	7.00	7.95
INSL3_Affy	6.93	7.37	7.01	7.31	7.10	7.23
IRAK2_Affy	7.13	7.66	7.20	7.52	7.19	7.50
IRAK4_Affy	7.76	8.052	7.90	7.90	7.88	7.96
ITGAM_Affy	11.26	11.80	11.36	11.78	11.53	11.78
JAK2_Affy	6.85	7.523	7.02	7.35	7.08	7.38
LDLR_Affy	7.05	7.788	7.09	7.76	7.12	7.75
LY96_Affy	9.50	10.26	9.65	10.03	9.76	10.02
MAP2K6_Affy	8.261	9.17	8.49	9.02	8.59	9.05
MAPK14_Affy	8.75	9.75	8.99	9.51	9.16	9.48
MKNKl_Affy	10.02	10.59	10.07	10.50	10.30	10.60
Gene_MMP9_Affy	12.05	13.03	12.28	12.95	12.41	12.93
NCR1_Affy	5.64	5.94	5.645	5.90	5.77	5.91
OSM_Affy	6.70	7.51	6.79	7.25	7.00	7.32
PFKFB3_Affy	9.60	10.92	9.78	10.83	10.18	10.82
PRV1_Affy	9.79	11.99	9.89	11.81	10.58	11.72
PSTPIP2_Affv	8.63	9.64	8.68	9.45	8.90	9.44
SOCS3_Affy	7.26	8.43	7.31	8.10	7.69	8.12
SOD2_Affy	9.94	10.66	10.07	10.69	10.27	10.59
TDRD9_Affy	6.84	8.30	7.02	8.30	7.43	8.18
TGFBI_Affy	10.17	9.31	10.27	9.45	10.37	9.63
TIFA_Affy	5.99	6.51	5.94	6.31	6.01	6.27
TNFSF10_Affy	10.38	10.77	10.51	10.56	10.47	10.52
TNFSF13B_Affy	10.23	10.70	10.24	10.56	10.48	10.58
IL10alpha_Affy	9.91	9.53	9.87	9.56	9.91	9.63
ANKRD22.18S	20.35	18.33	20.31	18.65	20.01	18.70
ANXA3.18S	17.29	15.52	17.00	15.50	16.78	15.68
ARG2.18S	20.36	19.09	20.12	19.26	19.93	19.13
BCL2A1.18S	18.58	17.00	18.20	17.05	17.84	17.04
CD86.18S	19.81	20.19	19.70	20.15	19.68	20.10
CEACAM1.18S	19.98	18.34	19.84	18.39	19.73	18.36
FCGR1A.18S	16.78	15.03	16.51	15.32	16.329	15.59
GADD45A.18S	19.73	18.46	19.69	18.45	19.38	18.53
GADD45B.18S	16.72	15.52	16.61	15.65	16.50	15.86
IFNGR1.18S	16.00	15.23	15.77	15.20	15.68	15.23
IL1RN.18S	17.24	16.01	17.03	16.05	16.95	16.27
IL18R1.18S	20.56	18.71	20.15	18.72	20.04	18.72
INSL3.18S	21.41	20.03	21.22	20.01	21.00	20.22
IRAK2.18S	20.45	19.20	20.28	19.29	20.32	19.49
IRAK4.18S	18.25	17.74	18.06	17.65	17.98	17.71
ITGAM.18S	15.45	14.51	15.27	14.57	15.12	14.60
JAK2.18S	17.77	16.90	17.56	16.97	17.50	17.06
LDLR.18S	20.34	19.31	20.19	19.10	20.28	19.24
LY96.18S	19.24	18.20	18.95	18.27	18.75	18.35
MAP2K6.18S	18.11	16.78	17.86	16.62	17.73	16.74
MKNK1.18S	17.61	16.48	17.37	16.48	17.22	16.58
Gene_MMP9.18S	14.89	13.40	14.70	13.27	14.53	13.15
NCR1.18S	21.89	21.06	21.79	20.99	21.82	21.11
OSM.18S	19.98	18.41	19.71	18.51	19.49	18.57
PFKFB3.18S	17.83	15.86	17.53	15.85	17.IS	16.00
PRV1.18S	16.87	13.49	16.28	13.08	15.42	13.34
PSTP1P2.18S	17.45	16.18	17.24	16.31	17.13	16.37
SOCS3.18S	16.83	15.09	16.57	15.12	16.20	15.30
SOD2.18S	13.62	12.83	13.50	12.87	13.41	13.12
TDRD9.18S	22.65	20.64	22.32	20.45	21.95	20.57
TIFA.18S	19.02	17.40	18.89	17.69	18.70	17.97
TLR4.18S	17.93	17.03	17.83	17.24	17.73	17.33
TNFRSF6.18S	17.31	16.51	17.02	16.74	17.05	16.88
TNFSF10.18S	16.21	15.32	15.98	15.49	16.00	15.68
TNFSF13B.18S	16.32	15.43	16.16	15.72	16.01	15.71
VNN1.18S	17.16	15.39	16.70	15.19	16.51	15.12
AlphaFetoprotein_RBM	3.77	4.22	3.70	4.34	3.34	4.01
ApolipoproteinCIII_RBM	59.72	38.05	53.84	38.34	53.38	40.03
Beta2Microglobulin_RBM	2.83	3.63	2.57	3.02	2.43	2.89
CReactiveProtein_RBM	146.95	261.16	206.21	258.20	171.76	245.76
IL6_RBM	82.87	4858.72	99.21	308.50	98.28	341.38
IL8_RBM	31.03	121.58	36.78	78.93	30.15	69.30
IL10_RBM	21.92	64.45	33.16	38.60	21.12	37.43
MCP1_RBM	237.84	796.87	259.82	505.33	229.04	558.73
Protein_MMP9_RBM	1143.25	1809.30	992.84	1390.05	961.12	1364.40
TIMP1_RBM	226.68	406.90	237.22	351.29	235.05	344.12
ARG2_SPM	21.34	20.25	21.30	20.43	21.32	20.56
CD86_SPM	17.31	17.95	17.47	17.90	17.53	17.87
FCGR1A_SPM	16.16	14.48	15.98	14.85	15.80	15.13
IL1RN_SPM	15.75	14.81	15.59	14.95	15.55	15.10
IL6_SPM	23.58	23.55	23.71	23.67	23.70	23.58
IL8_SPM	21.97	21.99	22.46	22.48	22.68	22.41
IL10_SPM	21.15	20.02	21.10	20.26	20.96	20.24
IL18R1_SPM	18.33	16.54	18.06	16.75	18.04	16.83
ITGAM_SPM	14.66	13.82	14.37	13.84	14.37	13.96
Gene_MMP9_SPM	13.14	11.71	12.90	11.82	13.01	11.95
TIMP1_SPM	13.57	13.00	13.38	12.95	13.47	13.02
TLR4_SPM	14.86	14.22	14.80	14.35	14.71	14.41
TNFSF13B_SPM	14.63	13.91	14.56	14.13	14.52	14.21
CReactiveProtein_SPM	23.19	23.00	23.26	23.20	23.27	23.25
IL6_BDB	−0.15	0.59	−0.25	−0.02	−0.19	0.147
IL8_BDB	−0.24	0.74	−0.30	0.24	−0.32	0.20
IL10_BDB	−0.18	0.57	−0.27	0.35	−0.20	0.10
MCP1_BDB	−0.18	0.58	−0.18	0.01	−0.25	0.20

The range of expression values of the biomarkers of Table I were determined for subjects that acquired sepsis (Sepis subjects) and subjects that did not acquire sepsis (SIRS subjects) in the populations described in Sections 6.11.2, 6.12.2 (Affymetrix data), 611.1, 6.12.1 (RT-PCR data), 6.13.3 (bead data), and 6.13.1 and 6.13.2 (bead data) at the T₋₁₂. and T₋₆ time points. This data is set forth in Table 101 below. In Table 101, a biomarker with the _Affy extension represents the combined data of Sections 6.11.2 and 6.11.2 (Affymetrix data), a biomarker with the 0.18S extension represents the combined data of Sections 6.11.1 and 6.12.1 (RT-PCR data), a biomarker with the BDB extension represents the data of Section 6.13.3. and a biomarker with the RBM extension represents the data of Sections 6.13.1 and 6.13.2. Time points are given in column 6, where T₋₁₂ represents the T₋₁₂ time point, and T₋₃₆ represents the T₋₃₆ time point. Units in Table 101 are as described for Table 100.

TABLE 101
Expression value ranges for the biomarkers of Table I as measured
in the experimental Affymetrix, RT-PCR, and bead data of Section 6.
	Minimum value	Maximum value	Minimum value	Maximum value
Biomarker	in sepsis subjects	in sepsis subjects	in SIRS subjects	in SIRS subjects	Time
1	2	3	4	5	6
ANKRD22_Affy	7.953749641	12.12893617	7.152671629	11.15686619	T-12
ANXA3_Affy	8.694223626	12.60070358	7.888396707	11.77082747	T-12
BCL2A1_Affy	7.44669819	11.98497181	6.831314584	10.15766376	T-12
CCL5_Affy	8.898803629	12.84470384	10.18676932	12.76079187	T-12
CD86_Affy	7.053070944	9.279967603	7.868508261	9.428684419	T-12
CEACAM1_Affy	7.392836443	10.11429986	6.897178024	8.990696622	T-12
CRTAP_Affy	7.96569575	10.04792044	8.402744052	10.11557268	T-12
CSF1R_Affy	8.12973354	9.802040206	8.308888545	10.10429638	T-12
FAD104_Affy	7.670795141	10.63246961	5.857923276	9.290926038	T-12
FCGR1A_Affy	6.796282224	9.51719797	6.335911956	9.135545399	T-12
GADD45A_Affy	7.874842459	10.63426409	6.244572007	9.859106279	T-12
GADD45B_Affy	8.479965651	10.29001883	7.992247915	9.49903678	T-12
HLA.DRA_Affy	9.174921757	12.40164437	10.91664573	12.59721891	T-12
IFNGR1_Affy	9.881934243	12.20352664	10.20622485	12.04433802	T-12
IL18R1_Affy	5.617961135	10.58599306	5.401354816	8.680200674	T-12
INSL3_Affy	6.498476621	8.453102101	6.380834209	7.658960107	T-12
IRAK2_Affy	6.875497116	9.68130844	6.749722992	8.274075293	T-12
IRAK4_Affy	7.433778424	8.878566727	7.144224029	8.232236692	T-12
ITGAM_Affy	10.49945783	12.40537329	10.40124379	12.02696288	T-12
JAK2_Affy	5.855248527	8.799277378	5.832795685	7.719583127	T-12
LDLR_Affy	6.257275326	9.674292614	6.131286337	7.912581783	T-12
LY96_Affy	8.415332968	11.70570487	8.133946247	10.62910735	T-12
MAP2K6_Affy	7.596722579	10.56652274	7.340508485	9.871737402	T-12
MAPK14_Affy	8.070466208	10.92164826	7.114917424	10.02925699	T-12
MKNK1_Affy	9.279266935	11.72051891	8.987912062	11.32996284	T-12
Gene_MMP9_Affy	11.53180146	14.23119077	10.53501559	13.54148736	T-12
NCR1_Affy	5.317900783	6.518234278	5.112152822	6.108537679	T-12
OSM_Affy	6.711016689	8.50414686	5.914544406	7.870308905	T-12
PFKFB3_Affy	8.872516729	12.35520872	8.119052014	11.65471067	T-12
PRV1_Affy	8.247231438	14.06000214	7.787420639	12.82213193	T-12
PSTPIP2_Affy	7.917121337	10.93727651	7.633999161	10.56933315	T-12
SOCS3_Affy	6.800978821	10.18734767	6.095547925	8.999643638	T-12
SOD2_Affy	9.638778614	11.7873112	8.477270195	11.33496413	T-12
TDRD9_Affy	5.982800228	10.55761021	5.394035579	9.208195372	T-12
TGFBI_Affy	7.954609344	11.19226116	8.973848308	11.1560402	T-12
TIFA_Affy	5.620694754	8.03295421	5.430693745	7.140866404	T-12
TNFSF10_Affy	9.847323138	11.63713214	9.035999538	11.33035464	T-12
TNFSF13B_Affy	8.585414556	11.79818987	8.90534601	11.34212616	T-12
IL10alpha_Affy	8.690880784	10.54878771	9.024669305	10.52469989	T-12
ANKRD22.18S	14.554	20.607	18.026	22.621	T-12
ANXA3.18S	12.994	18.89	14.989	20.069	T-12
ARG2.18S	16.703	22.511	17.729	23.054	T-12
BCL2A1.18S	14.219	19.664	15.565	20.206	T-12
CD86.18S	18.391	22.429	18.245	21.426	T-12
CEACAM1.18S	15.174	20.37	16.808	21.929	T-12
FCGR1A.18S	12.273	17.502	14.289	19.097	T-12
GADD45A.18S	15.697	20.631	18.602	21.118	T-12
GADD45B.18S	14.214	17.599	15.52	18.143	T-12
IFNGR1.18S	13.746	17.418	14.233	17.389	T-12
IL1RN.18S	13.7	18.656	14.995	19.231	T-12
IL18R1.18S	15.6	21.649	16.63	23.144	T-12
INSL3.18S	18.077	22.515	19.735	23.106	T-12
IRAK2.18S	16.851	21.205	17.775	22.286	T-12
IRAK4.18S	16.637	19.164	17.001	19.648	T-12
ITGAM.18S	12.6	17.346	13.709	17.172	T-12
JAK2.18S	15.292	19.228	16.431	19.001	T-12
LDLR.18S	16.909	21.4	18.195	22.081	T-12
LY96.18S	16.811	20.726	17.543	20.956	T-12
MAP2K6.18S	14.062	18.942	16.2005	20.678	T-12
MKNK1.18S	14.677	18.261	15.589	19.195	T-12
Gene_MMP9.18S	10.128	16.281	12.644	17.265	T-12
NCR1.18S	18.175	23.462	19.544	23.756	T-12
OSM.18S	16.6	20.544	17.835	22.174	T-12
PFKFB3.18S	12.897	18.994	14.446	20.982	T-12
PRV1.18S	9.4745	19.6	11.749	23.823	T-12
PSTPIP2.18S	14.243	18.013	16.098	18.792	T-12
SOCS3.18S	13.312	18.094	14.603	18.51	T-12
SOD2.18S	10.822	14.875	11.836	15.269	T-12
TDRD9.18S	17.069	23.9	20.012	25.404	T-12
TIFA.18S	14.66	20.607	16.122	20.522	T-12
TLR4.18S	15.013	19.366	15.452	19.347	T-12
TNFRSF6.18S	14.771	18.42	16.046	18.633	T-12
TNFSF10.18S	14.175	16.71	14.913	18.005	T-12
TNFSF13B.18S	13.296	17.2755	14.113	18.23	T-12
VNN1.18S	12.363	19.695	14.788	20.209	T-12
AlphaFetoprotein_RBM	0.465	28.9	0.862	15	T-12
ApolipoproteinCIII_RBM	9.1	104	14	170	T-12
Beta2Microglobulin_RBM	0.912	17	0.815	14.2	T-12
CReactiveProtein_RBM	5.2	743	9.3	435	T-12
IL6_RBM	11.9	350000	5.85	1090	T-12
IL8_RBM	5.7	2430	4.6	136	T-12
IL10_RBM	9.4	1080	6.73	115	T-12
MCP1_RBM	68	20100	54	1860	T-12
Protein_MMP9_RBM	82.7	6100	37	5500	T-12
TIMP1_RBM	99.6	1670	91.7	777	T-12
ARG2_SPM	18.19	22.88	19.11	23.53	T-12
CD86_SPM	16.51	20.02	15.83	18.57	T-12
FCGR1A_SPM	11.78	16.69	13.448	18.43	T-12
IL1RN_SPM	12.82	17.055	12.92	17.13	T-12
IL6_SPM	22.71	24.493	22.61	24.22	T-12
IL8_SPM	17.728	23.645	19.218	24.27	T-12
IL10_SPM	16.905	22.09	17.41	23.38	T-12
IL18R1_SPM	13.69	19.36	13.628	20.7	T-12
ITGAM_SPM	12.33	16.26	12.21	16.24	T-12
Gene_MMP9_SPM	8.53	14.62	9.58	15.92	T-12
TIMP1_SPM	11.63	15.048	11.71	14.93	T-12
TLR4_SPM	12.5	16.64	13.61	16.06	T-12
TNFSF13B_SPM	12.29	15.86	12.37	15.998	T-12
CReactiveProtein_SPM	16.23	24.313	18.803	24.245	T-12
IL6_BDB	−0.158501071	12.45941145	−0.166932601	−0.076083727	T-12
IL8_BDB	−0.260734671	10.31273265	−0.284430649	−0.128681359	T-12
IL10_BDB	−0.317504403	4.487381808	−0.541755786	0.071431589	T-12
MCP1_BDB	−0.215354271	11.61107183	−0.231122309	−0.10084064	T-12
IL6_CBA	−0.674647421	5.170323126	−0.825867097	−0.022530263	T-12
IL8_CBA	−0.620553789	5.923519248	−0.821374574	2.902006709	T-12
IL10_CBA	−0.661588916	4.74196577	−0.730146126	6.047793474	T-12
ANKRD22_Affy	7.396771628	11.57062629	7.129021339	9.443944368	T-36
ANXA3_Affy	8.70013622	12.54023119	8.331913923	12.10925762	T-36
BCL2A1_Affy	7.183882918	11.76715511	6.405590222	10.37097944	T-36
CCL5_Affy	9.328902305	12.61675161	10.40637568	12.86027708	T-36
CD86_Affy	6.732706362	9.538835708	7.716006192	9.498278669	T-36
CEACAM1_Affy	7.13157116	9.873881135	7.032079139	9.080997559	T-36
CRTAP_Affy	7.558590076	9.700256103	8.59265066	10.03618173	T-36
CSF1R_Affy	7.837660302	9.949036275	8.464494614	10.30550413	T-36
FAD104_Affy	7.014972123	10.15391937	6.239710352	8.845757597	T-36
FCGR1A_Affy	6.911908197	9.049485977	6.738241369	8.397213121	T-36
GADD45A_Affy	7.56337487	10.85396197	6.589642416	9.749741171	T-36
GADD45B_Affy	8.51689696	10.06660743	8.254872004	9.532337644	T-36
HLA.DRA_Affy	9.633249373	12.27644605	10.46875169	12.67263889	T-36
IFNGR1_Affy	10.57959732	12.27228887	9.808984607	11.81736908	T-36
IL18R1_Affy	5.49992437	10.36284472	5.348365647	9.056683263	T-36
INSL3_Affy	6.751235769	8.470974618	6.354223568	7.671828775	T-36
IRAK2_Affy	6.667783945	8.746281062	6.803703241	7.823003239	T-36
IRAK4_Affy	7.263029682	8.81320843	7.431560803	8.530795242	T-36
ITGAM_Affy	10.78220173	12.65177246	10.81608481	11.95316198	T-36
JAK2_Affy	6.39933742	8.609398755	6.113876348	7.761009287	T-36
LDLR_Affy	6.592115082	9.576882573	6.429539125	7.875471828	T-36
LY96_Affy	8.653718448	11.10873698	7.823465941	10.99470657	T-36
MAP2K6_Affy	7.76590836	10.96462704	7.656234297	9.824692325	T-36
MAPK14_Affy	8.115337243	10.65189637	8.035017587	10.2553217	T-36
MKNK1_Affy	9.648189763	11.7078247	9.01371136	10.87910413	T-36
Gene_MMP9_Affy	11.11827617	14.10554558	11.20801397	13.49402871	T-36
NCR1_Affy	5.193987983	6.909045684	5.005834897	6.207479976	T-36
OSM_Affy	6.580322029	7.935265514	6.196973735	7.452713795	T-36
PFKFB3_Affy	9.424977102	12.34048574	8.499191685	11.18985748	T-36
PRV1_Affy	8.075175165	13.89885359	7.885024966	13.11270704	T-36
PSTPIP2_Affy	8.014852906	10.87208092	7.546671853	9.463070109	T-36
SOCS3_Affy	7.377913606	9.55384035	6.2535144	8.311473326	T-36
SOD2_Affy	9.246088148	11.68031375	9.036280605	11.01924042	T-36
TDRD9_Affy	6.248252454	11.18511333	5.639880173	9.344436192	T-36
TGFBI_Affy	7.994695342	11.02064264	9.079527674	11.18636937	T-36
TIFA_Affy	5.521978531	7.303421302	5.384514217	6.593248984	T-36
TNFSF10_Affy	9.60197872	11.18227009	9.614398352	11.21902779	T-36
TNFSF13B_Affy	9.376572388	11.47004606	8.423154647	11.14896209	T-36
IL10alpha_Affy	8.838180931	10.20810676	9.056040579	10.61188847	T-36
ANKRD22.18S	16.059	21.635	18.344	22.188	T-36
ANXA3.18S	13.508	18.565	14.637	19.196	T-36
ARG2.18S	16.7215	22.085	16.452	23.1025	T-36
BCL2A1.18S	14.892	20.169	15.558	21.208	T-36
CD86.18S	18.109	22.671	17.734	21.408	T-36
CEACAM1.18S	15.864	20.381	17.141	21.711	T-36
FCGR1A.18S	12.919	17.238	13.773	18.616	T-36
GADD45A.18S	16.021	20.468	17.567	21.221	T-36
GADD45B.18S	14.051	16.799	15.43	18.189	T-36
IFNGR1.18S	13.89	16.44	14.532	17.1035	T-36
IL1RN.18S	14.2965	18.584	14.569	18.818	T-36
IL18R1.18S	15.6475	21.683	17.068	21.9465	T-36
INSL3.18S	18.708	21.952	19.775	23.714	T-36
IRAK2.18S	17.563	20.591	18.878	21.765	T-36
IRAK4.18S	16.688	18.592	16.633	19.467	T-36
ITGAM.18S	12.974	16.862	12.696	16.597	T-36
JAK2.18S	15.659	18.42	16.185	18.67	T-36
LDLR.18S	16.925	20.765	18.764	21.351	T-36
LY96.18S	17.018	20.384	17.293	21.37	T-36
MAP2K6.18S	14.375	19.44	15.5485	20.507	T-36
MKNK1.18S	15.064	17.922	15.281	19.103	T-36
Gene_MMP9.18S	10.4315	16.075	12.673	16.9025	T-36
NCR1.18S	18.189	22.531	20.01	23.281	T-36
OSM.18S	16.79	20.311	18.219	21.612	T-36
PFKFB3.18S	13.095	18.678	14.042	19.647	T-36
PRV1.18S	9.732	18.921	10.63	20.57	T-36
PSTPIP2.18S	14.568	17.943	15.363	18.848	T-36
SOCS3.18S	13.309	16.962	14.629	18.503	T-36
SOD2.18S	11.004	15.117	12.246	14.872	T-36
TDRD9.18S	17.108	22.863	19.203	24.013	T-36
TIFA.18S	15.498	20.069	16.808	20.769	T-36
TLR4.18S	15.77	19.352	15.578	19.604	T-36
TNFRSF6.18S	14.782	17.867	15.952	18.014	T-36
TNFSF10.18S	14.049	16.332	14.388	17.196	T-36
TNFSF13B.18S	13.898	16.896	13.276	18.038	T-36
VNN1.18S	12.406	18.076	13.061	20.4895	T-36
AlphaFetoprotein_RBM	0.0878	45.2	0.399	14	T-36
ApolipoproteinCIII_RBM	8.1	105	17	143	T-36
Beta2Microglobulin_RBM	0.857	13.4	0.953	10.6	T-36
CReactiveProtein_RBM	9.3	548	45	735	T-36
IL6_RBM	8.93	6140	5.85	1480	T-36
IL8_RBM	2.4	977	2.5	429	T-36
IL10_RBM	2.68	397	4.4	760	T-36
MCP1_RBM	77	4280	60	2170	T-36
Protein_MMP9_RBM	59	9000	73	3840	T-36
TIMP1_RBM	89.9	1130	85.2	1050	T-36
ARG2_SPM	17.868	23.15	17.68	23.42	T-36
CD86_SPM	16.15	20.528	16.36	18.78	T-36
FCGR1A_SPM	12.53	17.43	13.633	17.868	T-36
IL1RN_SPM	13.375	17.043	13.98	17.695	T-36
IL6_SPM	23.12	24.378	23.17	24.46	T-36
IL8_SPM	20.33	23.78	19.38	24.24	T-36
IL10_SPM	16.785	23.34	18.648	23.63	T-36
IL18R1_SPM	14.16	19.13	15.98	19.68	T-36
ITGAM_SPM	12.55	15.84	12.683	15.79	T-36
Gene_MMP9_SPM	9.163	15	10.66	14.91	T-36
TIMP1_SPM	11.53	14.895	11.77	15.08	T-36
TLR4_SPM	13.2	15.91	13.52	16	T-36
TNFSF13B_SPM	12.56	15.415	13.19	16.725	T-36
CReactiveProtein_SPM	19.6	23.97	20.8	24	T-36
IL6_BDB	−0.684465464	2.880494108	−0.730942369	1.994658691	T-36
IL8_BDB	−0.825836521	3.74397758	−1.025991342	0.789180774	T-36
IL10_BDB	−1.371058252	8.324182809	−1.079489666	2.72772331	T-36
MCP1_BDB	−0.80163532	2.625526703	−0.828696306	2.820125749	T-36

7. REFERENCES CITED

The present invention can be implemented as a computer program product that comprises a computer program mechanism embedded in a computer readable storage medium. For instance, the computer program product could contain the program modules shown in FIG. 35. These program modules can be stored on a CD-ROM, DVD, magnetic disk storage product, or any other computer readable data or program storage product. The program modules can also be embedded in permanent storage, such as ROM, one or more programmable chip, or one or more application specific integrated circuits (ASICs). Such permanent storage can be localized in a server, 802.11 access point, 802.11 wireless bridge/station, repeater, router, mobile phone, or other electronic devices. The software modules in the computer program product can also be distributed electronically, via the Internet or otherwise, by transmission of a computer data signal (in which the software modules are embedded) either digitally or on a carrier wave.

Having now fully described the invention with reference to certain representative embodiments and details, it will be apparent to one of ordinary skill in the art that changes and modifications can be made thereto without departing from the spirit or scope of the invention as set forth herein. The specific embodiments described herein are offered by way of example only, and the invention is to be limited only by the terms of the appended claims, along with the full scope of equivalents to which such claims are entitled.

Claims

1. A method of predicting the development of sepsis or diagnosing sepsis in a test subject at risk for developing sepsis, the method comprising: evaluating whether a plurality of features in a biomarker profile of the test subject satisfies a first value set, wherein satisfying the first value set predicts that the test subject is likely to develop sepsis or has developed sepsis, and wherein the plurality of features correspond to, or are measurable aspects of, a plurality of biomarkers, the plurality of biomarkers comprising at least three biomarkers listed in Table I, wherein the plurality of biomarkers comprises at least six biomarkers listed in Table I when the plurality of biomarkers comprises both IL-6 and IL-8.

2. The method of claim 1, the method further comprising: evaluating whether the plurality of features in the biomarker profile of the test subject satisfies a second value set, wherein satisfying the second value set predicts that the test subject is not likely to develop sepsis.

3. The method of claim 1, wherein said plurality of biomarkers consists of between 3 and 54 biomarkers listed in Table I.

4-14. (canceled)

15. The method of claim 1, wherein each biomarker in said plurality of biomarkers is a biomarker listed in Table J.

16. (canceled)

17. The method of claim 1, wherein each biomarker in said plurality of biomarkers is a biomarker listed in Table K.

18-19. (canceled)

20. The method of claim 49, wherein each biomarker is a DNA, a cDNA, an amplified DNA, an RNA, or an mRNA.

21. (canceled)

22. The method of claim 1, wherein a first biomarker in said plurality of biomarkers is a nucleic acid biomarker listed in Table J and a second biomarker in said plurality of biomarkers is a protein biomarker listed in Table K.

23. The method of claim 1, wherein a feature in said plurality of features is a measurable aspect of a biomarker and a feature value for said feature is determined using a biological sample taken from said test subject at a single point in time.

24-26. (canceled)

27. The method of claim 23, wherein said biological sample is whole blood.

28. The method of claim 23, wherein said biological sample is plasma, serum, saliva, sputum, urine, cerebral spinal fluid, a tissue specimen, a tissue biopsy, or a stool specimen.

29. (canceled)

30. The method of claim 1, wherein a feature in said plurality of features is a measurable aspect of a biomarker in said biomarker profile and a feature value for said feature is determined using a plurality of samples taken from said test subject at different points in time.

31-35. (canceled)

36. The method of claim 1, the method further comprising constructing, prior to the evaluating step, said biomarker profile.

37-40. (canceled)

41. The method of claim 36, wherein the constructing step comprises applying a data analysis algorithm to features corresponding to biomarkers listed in Table I that are obtained from members of a population.

42. The method of claim 41, wherein said population comprises subjects that subsequently develop sepsis (sepsis subjects) and subjects that do not subsequently develop sepsis (SIRS subjects).

43. (canceled)

44. The method of claim 41, wherein said data analysis algorithm is a decision tree, predictive analysis of microarrays, a multiple additive regression tree, a neural network, a clustering algorithm, principal component analysis, a nearest neighbor analysis, a linear discriminant analysis, a quadratic discriminant analysis, a support vector machine, an evolutionary method, a projection pursuit, or weighted voting.

45-74. (canceled)

75. A microarray comprising a plurality of probe spots, wherein at least twenty percent of the probe spots in the plurality of probe spots correspond to a plurality of biomarkers listed in Table I, wherein the plurality of biomarkers comprises at least six biomarkers listed in Table I when the plurality of biomarkers comprises both IL-6 and IL-8.

76-80. (canceled)

81. A kit for predicting the development of sepsis in a test subject, the kit comprising a plurality of antibodies that, collectively, specifically bind at least three biomarkers listed in Table I or at least three biomarkers listed in Table K.

82-88. (canceled)

89. A computer comprising: a central processing unit;a memory coupled to the central processing unit, the memory storing:instructions for performing the method of claim 1.

90-113. (canceled)