Patent Grant
11549138
This invention relates to assays of biological molecules, and more particularly to assays for determining spatial distributions of a large number of biological molecules in a solid sample simultaneously.
In the following discussion certain articles and methods will be described for background and introductory purposes. Nothing contained herein is to be construed as an “admission” of prior art. Applicant expressly reserves the right to demonstrate, where appropriate, that the articles and methods referenced herein do not constitute prior art under the applicable statutory provisions.
Comprehensive gene expression analysis and protein analysis have been useful tools in understanding mechanisms of biology. Use of these tools has allowed the identification of genes and proteins involved in development and in various diseases such as cancer and autoimmune disease. Conventional methods such as in situ hybridization and other multiplexed detection of different transcripts have revealed spatial patterns of gene expression and have helped shed light on the molecular basis of development and disease. Other technologies that have enabled the quantitative analysis of many RNA sequences per sample include microarrays (see Shi, et al., Nature Biotechnology, 24(9):1151-61 (2006); and Slonim and Yanai, Plos Computational Biology, 5(10):e1000543 (2009)); serial analysis of gene expression (SAGE) (see Velculescu, et al, Science, 270(5235):484-87 (1995)), high-throughput implementations of qPCR (see Spurgeon, et al., Plos ONE, 3(2):e1662 (2008)) and in situ PCR (see Nuovo, Genome Res., 4:151-67 (1995)). As useful as these methods are, however, they do not enable simultaneous measurement of the expression of many genes or the presence and/or activity of multiple proteins at many spatial locations in a sample. Laser capture microdissection has permitted the analysis of many genes at a small number of locations, but it is very expensive, laborious, and does not scale well. Certain PCR assays in a 2D format preserve spatial information (see Armani, et al., Lab on a Chip, 9(24): 3526-34 (2009)), but these methods have low spatial resolution because they rely on physical transference of tissue into wells, which also prevents random access to tissue samples and high levels of multiplexing.
At present, no practical method exists to analyze at high resolution the spatial expression patterns of large numbers of genes, proteins, or other biologically active molecules simultaneously. There is thus a need for reproducible, high-resolution spatial maps of biological molecules in tissues. The present invention addresses this need.
This Summary is provided to introduce a selection of concepts in a simplified form that are further described below in the Detailed Description. This Summary is not intended to identify key or essential features of the claimed subject matter, nor is it intended to be used to limit the scope of the claimed subject matter. Other features, details, utilities, and advantages of the claimed subject matter will be apparent from the following written Detailed Description including those aspects illustrated in the accompanying drawings and defined in the appended claims.
The invention encompasses assay systems that provide high-resolution spatial maps of biological activity in tissues. The assay system comprises an assay capable of high levels of multiplexing where encoded probes are provided to a biological sample in defined spatial patterns; instrumentation capable of controlled delivery of reagents according to the spatial patterns; and a decoding scheme providing a readout that is digital in nature. In short, the present invention provides the ability to look at many biological targets in many locations, providing the resolution of in situ hybridization with the highly-parallel data analysis of sequencing.
Thus, in some embodiments, the invention provides an assay system to determine spatial patterns of abundance or activity or both of multiple biological targets at multiple sites in a sample, where the assay system performs the following steps: providing a sample affixed to a support; delivering encoded probes for the multiple biological targets to the multiple sites in the sample in a known spatial pattern, where each encoded probe comprises a probe region that may interact with the biological targets and a coding tag that identifies a location of the site to which the encoded probe was delivered; allowing the encoded probes to interact with the biological targets; separating encoded probes that interact with the biological targets from encoded probes that do not interact with the biological targets; determining all or a portion of a sequence of the encoded probes, and associating the abundance or activity or both of the multiple biological targets to the locations of the sites in the sample.
In particular aspects of the invention the biological targets comprise nucleic acids and the encoded probes are oligonucleotides, and in some aspects, there are two encoded probes for each of the multiple nucleic acid targets. In some aspects, the multiple biological targets comprise proteins, the probe regions of the encoding probes are proteins and the coding tags comprise oligonucleotides. In some aspects the multiple biological targets comprise enzymes. In some aspects the probe regions of the encoded probes comprise antibodies, aptamers or small molecules.
Some aspects of the assay system further comprise an amplification step between the separating step and the determining step. In some aspects, the determining step is performed by nucleic acid sequencing, and in preferred aspects, the sequencing is high-throughput digital nucleic acid sequencing.
In some aspects of the invention, the product of the multiple biological targets being assayed and the multiple sites in the sample is greater than 20, in some aspects product of the multiple biological targets being assayed and the multiple sites in the sample is greater than 50, in some aspects the product of the multiple biological targets being assayed and the multiple sites in the sample is greater than 75, 100, 150, 500, 750, 1,000, 5,000, 10,000, 25,000, 50,000, 100,000, 500,000, or 1,000,000 or more. In other aspects, the sequence of at least fifty thousand encoding probes are determined in parallel, in other aspects the sequence of at least one hundred thousand encoding probes are determined in parallel, in some aspects the sequence of at least five hundred thousand encoding probes are determined in parallel, and in some aspects the sequence of at least one million, ten million, one hundred million, one billion, ten billion, one hundred billion or more encoding probes are determined in parallel.
In some aspects, the known spatial pattern is determined by histological features of the sample. Also in some aspects, software programmed hardware performs at least two steps of the delivering step, the separation step, the determining step and the associating step.
In some aspects, the probe regions of the encoded probes are proteins and the separating step is accomplished by encoded probes that interact with the biological targets being captured by an affinity capture agent. In some aspects the probe regions of the encoding probes are nucleic acids and the separating step is accomplished by a washing of the sample.
In other embodiments there is provided an assay system to determine spatial patterns of abundance or activity or both of multiple nucleic acid targets at multiple sites in a sample, where the assay system performs the following steps: providing a sample affixed to a support; delivering oligonucleotide probes for multiple nucleic acid targets to the multiple sites in the sample in a known spatial pattern; allowing the oligonucleotide probes to hybridize with the nucleic acid targets; washing unhybridized encoded oligonucleotide probes from the sample; delivering one or more encoding agents to locations of the multiple sites in the sample according to a known spatial pattern, where the combination of encoding agents delivered to each site is different; coupling the encoding agents and the oligonucleotide probes to form encoded probes; determining all or a portion of a sequence of the encoded probes using high-throughput sequencing, and associating the abundance or activity or both of multiple biological targets to the locations of multiple sites in the sample.
Other embodiments of the invention provide an assay system to determine spatial patterns of abundance or activity or both of multiple protein targets at multiple sites in a sample, where the assay system performs the following steps: providing a sample affixed to a support; delivering encoded probes for the multiple protein targets to the multiple sites in the sample in a known spatial pattern, where each encoded probe comprises a protein probe region that may interact with the protein targets and a coding tag that identifies a location of the site to which the encoded probe was delivered and the protein probe region of the encoding probe of which the coding tag is part; allowing the encoded probes to interact with the protein targets; separating encoded probes that interact with the protein targets from encoded probes that do not interact with the protein targets; determining all or a portion of a sequence of the encoded probes by high throughput sequencing, and associating the abundance or activity or both of the multiple protein targets to the locations of the multiple sites in the sample.
Other embodiments provide an assay system to determine spatial patterns of abundance or activity or both of multiple biological targets at multiple sites in a sample, where the assay system performs the following steps: providing a sample affixed to a support; delivering encoded probes for the multiple biological targets to the multiple sites in the sample in a known spatial pattern, where each encoded probe comprises a probe region that may interact with the biological targets and a coding tag that identifies a location of the site to which the encoded probe was delivered and identifies the biological target; allowing the encoded probes to interact with the biological targets; determining all or a portion of a sequence of the encoded probes, and associating the abundance or activity or both of the multiple biological targets to the locations of the sites in the sample.
The assay system of the invention can utilize various detection mechanisms, based on the molecules to be detected and the reagents needed for such detection system. Exemplary methods that can be used with the assay systems of the invention are described in more detail below.
The terms used herein are intended to have the plain and ordinary meaning as understood by those of ordinary skill in the art. The following definitions are intended to aid the reader in understanding the present invention, but are not intended to vary or otherwise limit the meaning of such terms unless specifically indicated.
The term “antibody” as used herein is intended to refer to an entire immunoglobulin or antibody or any functional fragment of an immunoglobulin molecule which is capable of specific binding to an antigen (antibodies and antigens are “binding partners” as defined herein). “Antibody” as used herein is meant to include the entire antibody as well as any antibody fragments capable of binding the antigen or antigenic fragment of interest. Examples of such peptides include complete antibody molecules, antibody fragments, such as Fab, F(ab′)2, CDRS, VL, VH, and any other portion of an antibody which is capable of specifically binding to an antigen. Antibodies for assays of the invention are immunoreactive or immunospecific for, and therefore specifically and selectively bind to, proteins either detected (i.e., biological targets) or used for detection (i.e., probes) in the assays of the invention.
The term “binding agent” as used herein refers to any agent that specifically binds to a biological molecule of interest
“Complementary” or “substantially complementary” refers to the hybridization or base pairing or the formation of a duplex between nucleotides or nucleic acids, such as, for instance, between the two strands of a double-stranded DNA molecule or between an oligonucleotide primer and a primer binding site on a single-stranded nucleic acid. Complementary nucleotides are, generally, A and T (or A and U), or C and G. Two single-stranded RNA or DNA molecules are said to be substantially complementary when the nucleotides of one strand, optimally aligned and compared and with appropriate nucleotide insertions or deletions, pair with at least about 80% of the other strand, usually at least about 90% to about 95%, and even about 98% to about 100%).
“Hybridization” refers to the process in which two single-stranded polynucleotides bind non-covalently to form a stable double-stranded polynucleotide, The resulting (usually) double-stranded polynucleotide is a “hybrid” or “duplex,” “Hybridization conditions” will typically include salt concentrations of approximately less than 1M, often less than about 500 mM and may be less than about 200 mM. A “hybridization buffer” is a buffered salt solution such as 5% SSPE, or other such buffers known in the art. Hybridization temperatures can be as low as 5° C., but are typically greater than 22° C., and more typically greater than about 30° C., and typically in excess of 37° C. Hybridizations are often performed under stringent conditions, i.e., conditions under which a primer will hybridize to its target subsequence but will not hybridize to the other, non-complementary sequences. Stringent conditions are sequence-dependent and are different in different circumstances. For example, longer fragments may require higher hybridization temperatures for specific hybridization than short fragments. As other factors may affect the stringency of hybridization, including base composition and length of the complementary strands, presence of organic solvents, and the extent of base mismatching, the combination of parameters is more important than the absolute measure of any one parameter alone. Generally stringent conditions are selected to be about 5° C. lower than the Tm for the specific sequence at a defined ionic strength and pH. Exemplary stringent conditions include a salt concentration of at least 0.01M to no more than 1M sodium ion concentration (or other salt) at a pH of about 7.0 to about 8.3 and a temperature of at least 25° C. For example, conditions of 5×SSPE (750 mM NaCl, 50 mM sodium phosphate, 5 mM EDTA at pH 7.4) and a temperature of approximately 30° C. are suitable for allele-specific hybridizations, though a suitable temperature depends on the length and/or GC content of the region hybridized.
“Ligation” means to form a covalent bond or linkage between the termini of two or more nucleic acids, e.g., oligonucleotides and/or polynucleotides, in a template-driven reaction. The nature of the bond or linkage may vary widely and the ligation may be carried out enzymatically or chemically. As used herein, ligations are usually carried out enzymatically to form a phosphodiester linkage between a 5′ carbon terminal nucleotide of one oligonucleotide with a 3′ carbon of another nucleotide.
“Nucleic acid”, “oligonucleotide”, “oligo” or grammatical equivalents used herein refers generally to at least two nucleotides covalently linked together. A nucleic acid generally will contain phosphodiester bonds, although in some cases nucleic acid analogs may be included that have alternative backbones such as phosphoramidite, phosphorodithioate, or methylphophoroamidite linkages; or peptide nucleic acid backbones and linkages. Other analog nucleic acids include those with bicyclic structures including locked nucleic acids, positive backbones, non-ionic backbones and non-ribose backbones. Modifications of the ribose-phosphate backbone may be done to increase the stability of the molecules; for example, PNA:DNA hybrids can exhibit higher stability in some environments.
“Primer” means an oligonucleotide, either natural or synthetic, that is capable, upon forming a duplex with a polynucleotide template, of acting as a point of initiation of nucleic acid synthesis and being extended from its 3′ end along the template so that an extended duplex is formed. The sequence of nucleotides added during the extension process is determined by the sequence of the template polynucleotide. Primers usually are extended by a DNA polymerase.
The term “SNP” or “single nucleotide polymorphism” refers to a genetic variation between individuals; e.g., a single nitrogenous base position in the DNA of organisms that is variable. SNPs are found across the genome; much of the genetic variation between individuals is due to variation at SNP loci, and often this genetic variation results in phenotypic variation between individuals. SNPs for use in the present invention and their respective alleles may be derived from any number of sources, such as public databases (U.C. Santa Cruz Human Genome Browser Gateway website or the NCBI dbSNP website, or may be experimentally determined as described in U.S. Pat. No. 6,969,589; and US Pub. No. 2006/0188875 entitled “Human Genomic Polymorphisms.” Although the use of SNPs is described in some of the embodiments presented herein, it will be understood that other biallelic or multi-allelic genetic markers may also be used. A biallelic genetic marker is one that has two polymorphic forms, or alleles. As mentioned above, for a biallelic genetic marker that is associated with a trait, the allele that is more abundant in the genetic composition of a case group as compared to a control group is termed the “associated allele,” and the other allele may be referred to as the “unassociated allele.” Thus, for each biallelic polymorphism that is associated with a given trait (e.g., a disease or drug response), there is a corresponding associated allele. Other biallelic polymorphisms that may be used with the methods presented herein include, but are not limited to multinucleotide changes, insertions, deletions, and translocations. It will be further appreciated that references to DNA herein may include genomic DNA, mitochondrial DNA, episomal DNA, and/or derivatives of DNA such as amplicons, RNA transcripts, cDNA, DNA analogs, etc. The polymorphic loci that are screened in an association study may be in a diploid or a haploid state and, ideally, would be from sites across the genome.
The term “selectively binds”, “selective binding” and the like as used herein, when referring to a binding partner (e.g. protein, nucleic acid, antibody or other affinity capture agent, etc.), refers to a binding reaction of two or more binding partners with high affinity and/or complementarity to ensure selective hybridization under designated assay conditions. Typically, specific binding will be at least three times the standard deviation of the background signal. Thus, under designated conditions the binding partner binds to its particular “target” molecule and does not bind in a significant amount to other molecules present in the sample.
“Sequencing”, “sequence determination” and the like means determination of information relating to the nucleotide base sequence of a nucleic acid. Such information may include the identification or determination of partial as well as full sequence information of the nucleic acid. Sequence information may be determined “with varying degrees of statistical reliability or confidence. In one aspect, the term includes the determination of the identity and ordering of a plurality of contiguous nucleotides in a nucleic acid, “High throughput digital sequencing” or “next generation sequencing” means sequence determination using methods that determine many (typically thousands to billions) of nucleic acid sequences in an intrinsically parallel manner, i.e. where DNA templates are prepared for sequencing not one at a time, but in a bulk process, and where many sequences are read out preferably in parallel, or alternatively using an ultra-high throughput serial process that itself may be parallelized. Such methods include but are not limited to pyrosequencing (for example, as commercialized by 454 Life Sciences, Inc., Branford, Conn.); sequencing by ligation (for example, as commercialized in the SOLiD™ technology, Life Technology, Inc., Carlsbad, Calif.); sequencing by synthesis using modified nucleotides (such as commercialized in TruSeq™ and HiSeq™ technology by Illumina, Inc., San Diego, Calif., HeliScope™ by Helicos Biosciences Corporation, Cambridge, Mass., and PacBio RS by Pacific Biosciences of California, Inc., Menlo Park, Calif.), sequencing by ion detection technologies (Ion Torrent, Inc., South San Francisco, Calif.); sequencing of DNA nanoballs (Complete Genomics, Inc., Mountain View, Calif.); nanopore-based sequencing technologies (for example, as developed by Oxford Nanopore Technologies, LTD, Oxford, UK), and like highly parallelized sequencing methods.
The term “Tm” is used in reference to the “melting temperature.” The melting temperature is the temperature at which a population of double-stranded nucleic acid molecules becomes half dissociated into single strands. Several equations for calculating the Tm of nucleic acids are well known in the art. As indicated by standard references, a simple estimate of the Tm value may be calculated by the equation, Tm=81.5+0.41 (% G+C), when a nucleic acid is in aqueous solution at 1M NaCl (see e.g., Anderson and Young, Quantitative Filter Hybridization, in Nucleic Acid Hybridization (1985)). Other references (e.g., Allawi and SantaLucia, Jr., Biochemistry, 36:10581-94 (1997)) include alternative methods of computation which take structural and environmental, as well as sequence characteristics into account for the calculation of Tm.
The practice of the techniques described herein may employ, unless otherwise indicated, conventional techniques and descriptions of organic chemistry, polymer technology, molecular biology (including recombinant techniques), cell biology, biochemistry, and sequencing technology, which are within the skill of those who practice in the art. Such conventional techniques include polymer array synthesis, hybridization and ligation of polynucleotides, and detection of hybridization using a label. Specific illustrations of suitable techniques can be had by reference to the examples herein. However, other equivalent conventional procedures can, of course, also be used. Such conventional techniques and descriptions can be found in standard laboratory manuals such as Green, et al., Eds., Genome Analysis: A Laboratory Manual Series (Vols. I-IV) (1999); Weiner, Gabriel, Stephens, Eds., Genetic Variation: A Laboratory Manual (2007); Dieffenbach, Dveksler, Eds., PCR Primer: A Laboratory Manual (2003); Bowtell and Sambrook, DNA Microarrays: A Molecular Cloning Manual (2003); Mount, Bioinformatics: Sequence and Genome Analysis (2004); Sambrook and Russell, Condensed Protocols from Molecular Cloning: A Laboratory Manual (2006); and Sambrook and Russell, Molecular Cloning: A Laboratory Manual (2002) (all from Cold Spring Harbor Laboratory Press); Stryer, Biochemistry (4th Ed.) (1995) W.H, Freeman, New York N.Y.; Gait, “Oligonucleotide Synthesis: A Practical Approach” (2002) IRL Press, London; Nelson and Cox, Lehninger, Principles of Biochemistry (2000) 3rd Ed., W. H. Freeman Pub., New York, N.Y.; and Berg, et al., Biochemistry (2002) 5th Ed., W. H. Freeman Pub., New York, N.Y., all of which are herein incorporated in their entirety by reference for all purposes.
Note that as used herein and in the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a nucleic acid” refers to one or more nucleic acids, and reference to “the assay” includes reference to equivalent steps and methods known to those skilled in the art, and so forth.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. All publications mentioned herein are incorporated by reference for the purpose of describing and disclosing devices, formulations and methodologies that may be used in connection with the presently described invention.
Where a range of values is provided, it is understood that each intervening value, between the upper and lower limit of that range and any other stated or intervening value in that stated range is encompassed within the invention. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges, and are also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either both of those included limits are also included in the invention,
In the following description, numerous specific details are set forth to provide a more thorough understanding of the present invention. However, it will be apparent to one of skill in the art that the present invention may be practiced without one or more of these specific details. In other instances, well-known features and procedures well known to those skilled in the art have not been described in order to avoid obscuring the invention.
The assay systems of the invention provide spatially-encoded, multiplexed assays comprising 1) an assay capable of high levels of multiplexing with an efficient spatial encoding scheme; 2) instrumentation capable of delivering reagents according to a spatial pattern; and 3) decoding determined by a readout that is digital in nature. The assay systems of the invention detect the presence or absence and relative amount of a biological target or biological activity indicative of a biological target, as well as the location of the biological target or activity in a biological sample, e.g., a tissue section or other biological structure disposed upon a support such as a microscope slide or culture dish.
The assay system further provides instrumentation with an ability to deliver reagents in a spatially-defined pattern. This instrumentation, together “with software, reagents and protocols, provides a key component of the highly innovative assay system of the invention, allowing for measurement of numerous biological targets or activities in a meaningful spatial environment, including gene expression and peptide localization, An encoding scheme used in these assay systems allows one to determine the location of biological targets or activity (or lack thereof) in the biological samples after the products of the multiplexed assay are removed from the biological sample and pooled for analysis. Decoding of the encoding scheme can be performed by, e.g., next-generation sequencing, which easily provides millions to trillions of data points at low cost. The assay results such as the amount or activity of biological targets can then be mapped back to specific location in the biological sample. The assay systems open a new analytical window into the complex spatial patterns of cellular function and regulation in biological samples.
A simplified overview of the assay system 100 of the present invention is provided at
In some embodiments, the probe and coding tag portions of the encoded probe are pre-coupled before being delivered to the biological sample, For example, in the case where the encoded probes are oligonucleotides, both the probe and coding tag sequence can be synthesized as a single oligonucleotide. Alternatively, the probe and coding tag portions of the encoding probes can be synthesized or obtained separately and combined before delivery to the biological sample (e.g., two separate oligonucleotides can be synthesized and coupled by, e.g., ligation; or an antibody and an oligonucleotide can be prepared separately and conjugated before delivery to the biological sample). Also, as is described in
At step 130, the encoded probes are allowed to react or interact with the biological targets, i.e., conditions are provided to allow e.g., oligonucleotides to hybridize to nucleic acid targets, enzymes to catalyze reactions with protein targets, antibodies to bind epitopes, etc. In the case where the biological targets are nucleic acids, the encoded probes are typically oligonucleotides and hybridize to the target nucleic acids. In the case that the biological targets are proteins, the encoded probes typically are aptamers, small molecules, or oligonucleotide-conjugated proteins that interact with target proteins by binding to them or by reacting with them (that is, one of the proteins is a substrate for the other). Encoding oligonucleotides may be coupled to the probes (proteins) by conjugation, chemical or photo-crosslinking via suitable groups and the like.
Once encoded probes interact with the biological targets, the encoded probes that interacted with the biological targets must be separated from the encoded probes that did not interact with the biological targets at step 140. In the case where the biological targets are nucleic acids and the encoded probes are oligonucleotides, the separation can be accomplished by, e.g., washing the unhybridized encoded probes from the sample. Similarly, for other assays that are based on affinity binding, including those using aptamer, small molecule, and protein probes, washing steps can be used to remove low affinity binders. In the case where the probe is transformed via interaction with the target, e.g., in the case of a peptide, e.g., via cleavage by a protease or phosphorylation by a kinase, it is convenient to collect, all encoded probes 13 both encoded probes that interacted with the biological targets and were transformed and encoded probes that were not transformed. After collection or pooling, an antibody or other affinity capture agent can be used to capture probes that were transformed by addition of a moiety (e.g., a phosphate group). In cases where probes have been transformed via cleavage, the transformed probes can be separated, e.g., by capturing the non-transformed probes via a tag that is removed from the transformed probes during the transformation (e.g., by cleavage), or by adding a new tag at the site of cleavage.
Once the reacted (transformed) or interacted encoded probes are separated from the unreacted or un-interacted encoded probes, the sequence of the reacted and/or interacted encoded probes is determined at step 150 by, preferably, sequencing. The sequence of the encoded probes allows the mapping of the assay results at step 160 back to locations in the biological sample.
In step 240, the oligonucleotide probes that did not hybridize to target nucleic acids are removed, and thereby separated from oligonucleotide probes that did hybridize to target nucleic acids. In this embodiment, separation can be accomplished by, e.g., washing the sample to remove unhybridized oligonucleotide probes. Next, in step 250, encoding oligonucleotides (the encoding agents) are delivered to the biological sample according to a chosen spatial pattern, where the encoding oligonucleotides comprise coding tags that are used to encode the location of biological targets in the biological sample. Note that in contrast to the assay system of
In step 270, the sequence of the coding tags in the encoded probes as well as the sequence or a portion of the sequence of the probe itself is determined, and in step 280, the target nucleic acids are mapped back to the biological sample. In some embodiments, the abundance of sequences reveals the relative quantity of biological targets at the location. Although this embodiment shows the individual steps in a particular order, so as to better explain the invention, the precise order of the steps can be varied. For example, steps 220 and 250 can be combined, so that a mixture of the probes and encoding oligonucleotides is delivered according to a chosen spatial pattern. Coupling step 260 can then be carried out immediately after the combined steps 220 and 250, or concomitantly with them. In this case, step 240 would then occur after step 260. It can therefore be appreciated that the two key results of this series of steps, i.e., the location-specific encoding of probe molecules and the separation of probe molecules based on their ability to interact with corresponding target molecules, can be accomplished with some flexibility in the implementation of the particular steps. Similarly, there is considerable flexibility in the design of the coding scheme. As described infra, the assays of the invention are particularly amenable to combinatorial methods.
Thus, the present invention provides an ability to look at many different biological targets in many locations, providing the resolution of in situ hybridization with the highly-parallel data analysis of sequencing. In some embodiments, the sum of the multiple biological targets being assayed and the multiple sites in the biological sample is greater than 20, in other embodiments, the sum of the multiple biological targets being assayed and the multiple sites in the biological sample is greater than 50, in other embodiments, the sum of the multiple biological targets being assayed and the multiple sites in the biological sample is greater than 100, greater than 500, 1,000, 10,000, 25,000, 100,000, 500,000, 1,000,000. It will be appreciated that, due to the spatial encoding dimension of the invention, even much larger numbers can be contemplated. For example, assaying 10,000 targets per location×10,000 locations would generate 108 different assays, and even larger numbers than these can easily be contemplated, particularly if spatial locations with resolution on the order of that of single cells are utilized. Further, in embodiments where high-throughput digital sequencing is employed, the sequences of at least 1,000 encoding probes are typically determined in parallel. More typically, using a digital readout, it is desirable to obtain multiple sequence reads for each assay (defined by a probe and a spatial location code). It is desirable to obtain an average of at least 3 copies per assay, and more typically at least 10 or at least 30 copies per assay, depending on the design of the experiment and requirements of the assay. For a quantitative readout with suitable dynamic range, it may be desirable to obtain at least 1,000 reads per assay. Therefore, if 1,000,000 assays are carried out, the number of sequence reads may be 1 billion or more. With high-throughput digital sequencing, and allowing for redundancy, the sequence of at least 10,000 encoding probes are determined in parallel, or the sequence of at least 100,000, 500,000, 1,000,000, 10,000,000, 100,000,000, 1,000,000,000 or more encoding probes are determined in parallel.
Assays
The assay portion of the assay systems of the present invention comprise the following general steps: delivering probes and encoding agents where the encoding agents (in some embodiments pre-coupled to the probes) are delivered to the sample according to a known spatial pattern, allowing the probes to interact or react with biological targets in the sample, and, if the probes and encoding agents have not been pre-coupled, coupling the encoding agents to probes.
The samples of the present invention include virtually any biological sample or samples that can be affixed to a support or provided essentially in a two-dimensional manner, where the ability to tie an assayed biological target or activity back to the location within the biological sample is important. Exemplary biological samples include tissue sections (e.g., including whole animal sectioning and tissue biopsies), cell populations on slides or culture dishes, and the like. The assay systems of the invention are particularly advantageous in that they are compatible with numerous biological sample types, including fresh samples, such as primary tissue sections, and preserved samples including but not limited to frozen samples and paraformalin-fixed, paraffin-embedded (FFPE) samples. An important aspect of the assay systems of the invention is that the biological samples are immobilized on a substrate surface having discrete, independently measurable areas.
The biological targets to be detected can be any biological molecules including but not limited to proteins, nucleic acids, lipids, carbohydrates, ions, or multicomponent complexes containing any of the above. Examples of subcellular targets include organelles, e.g., mitochondria, Golgi apparatus, endoplasmic reticulum, chloroplasts, endocytic vesicles, exocytic vesicles, vacuoles, lysosomes, etc.
In some particular embodiments, the assay system is used to analyze nucleic acids, e.g., by genotyping, quantitation of DNA copy number or RNA transcripts, localization of particular transcripts within samples, and the like.
Two encoding agents, both comprising a coding tag (seen at 315 and 317), a ligation region (seen at 311 and 313), and a primer region (seen at 319 and 321) are combined with and ligated to the extended probe at step 304 to form an encoded target-specific oligonucleotide. Again, in contrast with
Following ligation, the encoded probes are eluted, pooled, and, optionally, sequencing adapters are added to the encoded probes via PCR. In alternative embodiments, sequencing primers may be ligated to the encoding oligonucleotides, or sequencing primer sequences can be included as part of the encoding oligonucleotide. As seen in
A combination of extension and ligation reactions are exemplified in
In other embodiments, the assay system of the invention also can be used to analyze peptides or proteins, the presence of antibodies, enzymatic and other protein activities, posttranslational modifications, active and non-active forms of peptides, as well as peptide isoforms in a biological sample. Accordingly, the probes may comprise an active region of an enzyme, a binding domain of an immunoglobulin, defined domains of proteins, whole proteins, synthetic peptides, peptides with introduced mutations, aptamers and the like.
In certain aspects, the probes are substrates for enzymes or proenzymes, e.g., kinases, phosphatases, zymogens, proteases, or fragments thereof. In certain aspects, the probes are phosphorylation substrates used to detect proteins involved in one or more signal transduction pathways, e.g., a kinase or a phosphatase. In another specific aspect of the invention, the probes are specific protease substrates that associate only with individual proteases or classes of proteases. In other aspects, the probes are different processed forms, isoforms and/or domains of an enzyme. Protein-based probes are typically conjugated or otherwise linked to oligonucleotide encoding agents. The oligonucleotide encoding agents in this case would also include a nucleotide sequence component that allows for identification of the protein probe.
In certain aspects, the present invention provides assays for evaluating differences in the amount and/or activity of biological targets between different locations in a sample and/or between samples. The method includes determining a plurality of encoded results from the biological sample and evaluating the differences in quantity of the biological targets at each location in the biological sample.
To maximize the efficiency of encoding, a combinatorial approach using pairs of coding tags in the encoding oligonucleotides can be used. By de-coupling the target-specific information and the coding tags, the number of oligonucleotides required is dramatically reduced, with a concomitant decrease in cost.
The target-specific oligonucleotides are delivered to the biological sample, where the target-specific oligonucleotides hybridize to target nucleic acids in the biological sample if target nucleic acids are present. Unhybridized target-specific oligonucleotides are then removed, e.g., by washing. The encoding oligonucleotides are then delivered to the biological sample according to the spatial pattern shown at 530. The encoding oligonucleotides are ligated (or, e.g., extended and ligated) to any target-specific oligonucleotides that hybridized to the target nucleic acid in the biological sample, the ligated constructs are then eluted from the biological sample, pooled, and sequencing adapters are added through, e.g., PCR or ligation, if the sequences were not previously included in the encoding oligonucleotides. The ligated constructs are sequenced by, e.g., high throughput or “next generation” sequencing.
The pool of resulting sequences is shown at 540. A sequence readout was obtained for target-specific oligonucleotide 1 only at a4b1, a4b2, a1b3, a2b3, a3b3, a4b3 and a4b4 (positions shown with horizontal lines). A sequence readout was obtained for target-specific oligonucleotide 2 only at a1b1 (position shown with vertical lines). A sequence readout was obtained for both target-specific oligonucleotides 1 and 2 at positions a2b1, a3b1, a1b2, a2b2, and a3b2 (positions shown with cross-hatching). No sequence readout was obtained for either target-specific oligonucleotides at a1b4, a2b4 or a3b4 (positions shown without shading). Thus, in the biological sample on which the assay took place the first target nucleic acid was detected in a large portion of the left side and at the bottom of the biological sample, the second target nucleic acid was detected only in the upper left portion of the biological sample, and neither target nucleic acid was detected in the upper right portion of the biological sample. The differential expression of the two target nucleic acids now can be mapped back to the biological sample and to the biological structures or cell types in these locations in the biological sample, as shown in 550.
In addition to location information, information relating to relative abundance of the encoded tags can be obtained. For example, if it is found that there are ten times as many a4T1b1 sequences occurring in the data set as compared to a4T1b2 sequences, this would indicate that target nucleic acid sequence 1 is ten times more abundant at the a4T1b1 location than at the a4T1b2 location.
In the case of nucleotide analysis as shown in
Due to the spatial encoding aspect of the assay system of the invention, a large amount of information can be generated with even a modest number of assays. For example, five or more biological targets assayed at five or more positions in the sample generates 25 or more combinations. Using digital sequencing as a readout, the optimum number of sequence reads per combination depends on the sensitivity and dynamic range required, and can be adjusted, For example, if for each combination on average 100 reads are sampled, the total for 25 combination is 25,000 reads. If 1,000 targets are assayed at 1,000 locations with an average sampling depth of 1,000, then 109 reads are required. These numbers, although large, are within the capacity of intrinsically parallel digital sequencing methods, which can generate datasets of billions or even trillions of reads in a reasonable timeframe and at a very low cost per read. Therefore, by varying the numbers of positions interrogated or biological targets assayed, or both, and using digital sequencing, large amounts of information can be obtained. In specific aspects, multiple locations are interrogated for two or more biological molecules.
Reagent Delivery Systems
The reagent delivery system of the invention includes instrumentation that allows the delivery of reagents to discrete portions of the biological sample, maintaining the integrity of the spatial patterns of the encoding scheme. Reagent delivery systems of the assay systems of the invention comprise optional imaging means, reagent delivery hardware and control software. Reagent delivery can be achieved in a number of different ways. It should be noted that reagent delivery may be to many different biological samples at one time. A single tissue section has been exemplified herein; however, multiple biological samples may be affixed and analyzed simultaneously. For example, pions of a tissue sample can be analyzed in parallel and the data combined to build a 3D map.
Integral to the assay system of the invention is instrumentation that allows for spatial patterning of reagents onto the biological sample. Technologies for formulating and delivering both biological molecules (e.g. oligonucleotides or antibodies) and chemical reagents (e.g., small molecules or dNTPs) are known in the art, and uses of these instrument systems are known to one skilled in the art and easily adaptable to the assay systems of the invention. One example of a suitable reagent delivery system is the Labcyte™ Echo acoustic liquid handier, which can be used to deliver nanoliter scale droplets containing biological molecules with high precision and reproducibility. One skilled in the art could incorporate this reagent delivery device into the overall system, using software to specify the locations to which reagents should be delivered.
Other instruments that can be used for the deposition of agents and/or coding identifiers onto biological samples include, but are not limited to, ink jet spotting; mechanical spotting by means of pin, pen or capillary; micro contact printing; photochemical or photolithographic methods; and the like. For several applications, it may be preferred to segment or sequester certain areas of the biological samples into one or more assay areas for different reagent distributions and/or biological target determination. The assay areas may be physically separated using barriers or channels.
In one exemplary aspect, the reagent delivery system may be a flow-based system. The flow-based systems for reagent delivery in the present invention can include instrumentation such as one or more pumps, valves, fluid reservoirs, channels, and/or reagent storage cells. Reagent delivery systems are configured to move fluid to contact a discrete section of the biological sample. Movement of the reagents can be driven by a pump disposed, for example, downstream of the fluid reagents. The pump can drive each fluid reagent to (and past) the reaction compartment. Alternatively, reagents may be driven through the fluid by gravity. US Pub. Nos. 20070166725 and 20050239192 disclose certain general-purpose fluidics tools that can be used with the assay systems of the invention, allowing for the precise manipulation of gases, liquids and solids to accomplish very complex analytical manipulations with relatively simple hardware.
In a more specific example, one or more flow-cells can be attached to the substrate-affixed biological sample from above. The flow-cell can include inlet and outlet tubes connected thereto and optionally an external pump is used to deliver reagents to the flow-cell and across the biological sample. The flow cells are configured to deliver reagents only to certain portions of the biological sample, restricting the amount and type of reagent delivered to any specific section of the biological sample.
In another aspect, a microfluidic system can be integrated into the substrate upon which the biological sample is disposed or externally attached on top of the substrate. Microfluidic passages for holding and carrying fluid may be formed on and/or above the planar substrate by a fluidics layer abutted to the substrate. Fluid reagents can be selected and delivered according to selective opening and closing of valves disposed between reagent reservoirs.
Pumps generally include any mechanism for moving fluid and/or reagents disposed in fluid. In some examples, the pump can be configured to move fluid and/or reagents through passages with small volumes (i.e., microfluidic structures). The pump can operate mechanically by exerting a positive or negative pressure on fluid and/or on a structure carrying fluid, electrically by appropriate application of an electric field(s), or both, among other means. Exemplary mechanical pumps may include syringe pumps, peristaltic pumps, rotary pumps, pressurized gas, pipettors, etc. Mechanical pumps may be micromachined, molded, etc. Exemplary electrical pumps may include electrodes and may operate by electrophoresis, electroendoosmosis, electrocapillarity, dielectrophoresis (including traveling wave forms thereof), and/or the like.
Valves generally include any mechanism for regulating the passage of fluid through a channel. Valves can include, for example, deformable members that can be selectively deformed to partially or completely close a channel, a movable projection that can be selectively extended into a channel to partially or completely block a channel, an electrocapillary structure, and/or the like.
An open gasket can be attached to the top of the biological sample and the sample and reagents can be injected into the gasket. Suitable gasket materials include, but are not limited to, neoprene, nitrile, and silicone rubber. Alternatively, a watertight reaction chamber may be formed by a gasket sandwiched between the biological sample on the substrate and a chemically inert, water resistant material such as, but not limited to, black-anodized aluminum, thermoplastics (e.g., polystyrene, polycarbonate, etc), glass, etc.
In an optional embodiment, the assay system comprises imaging means to determine features and organization of the biological sample of interest. The images obtained, e.g., may be used to design the deposition pattern of the reagents, Imaging means are optional, as an individual can instead view the biological sample using, e.g., a microscope, analyze the organization of the biological sample, and specify a spatial pattern for delivery assay reagents. If included, the delivery system can comprise a microcircuit arrangement including an imager, such as a CCD or IGFET-based (e.g., CMOS-based) imager and an ultrasonic sprayer for reagent delivery such as described in US Pub. No. 20090197326, which is incorporated herein by reference. Also, it should be noted that although
In yet another alternative, the reagent delivery system controls the delivery of reagents to specific patterns on a biological sample surface using semiconductor techniques such as masking and spraying. Specific areas of a biological sample can be protected from exposure to reagents through use of a mask to protect specific areas from exposure. The reagents may be introduced to the biological sample using conventional techniques such as spraying or fluid flow. The use of masked delivery results in a patterned delivery scheme on the substrate surface.
In a preferred aspect of the invention, the reagent delivery instrumentation is based on inkjet printing technology. There are a variety of different ink-jetting mechanisms (e.g., thermal, piezoelectric) and compatibility has been shown with aqueous and organic ink formulations. Sets of independently actuated nozzles can be used to deliver multiple reagents at the same time, and very high resolutions are be achieved.
In order to target specific sites of interest, an informative image of the biological sample to be assayed may be used to assist in the reagent delivery methods and associated encoding scheme. Sample regions of the biological sample can be identified using image processing (e.g., images of cell types differentiated by immunohistochemistry or other staining chemistries) integrated with other features of the assay system. In some aspects, software is used to automatically translate image information into a reagent delivery pattern. A mechanism to register and align very precisely the biological sample for reagent delivery is thus an important component of the assay systems of the invention. Mechanisms such as the use of fiducial markers on slides and/or other very accurate physical positioning systems can be adapted to this purpose.
The invention preferably comprises a complete suite of software tailored to the assay system. Optionally, oligonucleotide design software is used to design the encoding nucleotides (and in embodiments where nucleic acids are assayed, the target-specific oligonucleotides) for the specific assay to be run, and may be integrated as a part of the system. Also optionally, algorithms and software for reagent delivery and data analysis (i.e., sequence analysis) may be integrated to determine assay results. Integrated data analysis is particularly useful, as the type of dataset that is generated may be massive as a consequence of scale. Algorithms and software tools that are specifically designed for analysis of the spatially-associated data generated by the assay systems, including pattern-analysis software and visualization tools, enhance the value of the data generated by the assay systems.
In certain aspects, the assay system comprises processes for making and carrying out the quality control of reagents, e.g., the integrity and sequence fidelity of oligonucleotide pools. In particular, reagents are formulated according to factors such as volatility, stability at key temperatures, and chemical compatibility for compatibility with the reagent delivery instrumentation and may be analyzed by instrumentation integrated within the assay system.
Sequencing
Numerous methods can be used to identify the coding tags and probe sequences in the encoded probes of the assay systems of the invention. The coding tags can be detected using techniques such as mass spectroscopy (e.g., Maldi-T of, LC-MS/MS), nuclear magnetic resonance imaging, or, preferably, nucleic acid sequencing. Examples of techniques for decoding the coding tags of the present invention can be found, for example, in US Pub. No. 20080220434, which is incorporated herein by reference. For example, the coding tags may be oligonucleotide mass tags (OMTs or massTags). Such tags are described, e.g., in US Pub. No. 20090305237, which is incorporated by reference in its entirety. In yet another alternative, the encoded probes can be amplified and hybridized to a microarray. This would require separate amplification reactions to be carried out, in which each amplification is specific to a particular spatial code or subset of codes, accomplished by using code-specific primers. Each amplification would also incorporate a different resolvable label (e.g. fluorophor). Following hybridization, the relative amounts of a particular target mapping to different spatial locations in the sample can be determined by the relative abundances of the resolvable labels.
In one particularly preferred aspect, the resulting coding tags according to the assay system are substrates for high-throughput, next-generation sequencing, and highly parallel next-generation sequencing methods are used to confirm the sequence of the coding tags, for example, with SOLiD™ technology (Life Technologies, Inc.) or Genome Ananlyzer (Illumina, Inc.). Such next-generation sequencing methods can be carried out, for example, using a one pass sequencing method or using paired-end sequencing. Next generation sequencing methods include, but are not limited to, hybridization-based methods, such as disclosed in e.g., Drmanac, U.S. Pat. Nos. 6,864,052; 6,309,824; and 6,401,267; and Drmanac et al, U.S. patent publication 2005/0191656; sequencing-by-synthesis methods, e.g., U.S. Pat. Nos. 6,210,891; 6,828,100; 6,969,488; 6,897,023; 6,833,246; 6,911,345; 6,787,308; 7,297,518; 7,462,449 and 7,501,245; US Publication Application Nos. 20110059436; 20040106110; 20030064398; and 20030022207; Ronaghi, et al, Science, 281: 363-365 (1998); and Li, et al, Proc. Natl. Acad. Sci., 100: 414-419 (2003); ligation-based methods, e.g., U.S. Pat. Nos. 5,912,148 and 6,130,073; and U.S. Pat. Appln Nos. 20100105052, 20070207482 and 20090018024; nanopore sequencing e.g., U.S. Pat. Appln Nos. 20070036511; 20080032301; 20080128627; 20090082212; and Soni and Meller, Clin Chem 53: 1996-2001 (2007)), as well as other methods, e.g., U.S. Pat. Appln Nos. 20110033854; 20090264299; 20090155781; and 20090005252; also, see, McKernan, et al., Genome Res., 19:1527-41 (2009) and Bentley, et al., Nature 456:53-59 (2008), all of which are incorporated herein in their entirety for all purposes.
Applications of Assay System
It will be apparent to one skilled in the art upon reading the present disclosure that there are numerous important areas of biological research, diagnostics, and drug development that will benefit from a high throughput multiplexed assay system that can measure simultaneously the amount and spatial location of a biological target in a biological sample. For example, combining the ability to estimate the relative abundance of different RNA transcripts with the ability to reconstruct an image of spatial patterns of abundance across many locations, which may be as small as or even smaller than individual cells, in a tissue enables many different areas of basic research. The following are exemplary uses and are by no means meant to be limiting in scope.
In one example, 3-dimensional patterns of gene expression are determined by analyzing a series of tissue sections, in a manner analogous to image reconstruction in CT scanning, Such a method can be used to measure changes in gene expression in disease pathology, e.g., in cancerous tissue and/or a tissue upon injury, inflammation or infection. With the assay systems of the invention, more detailed information on gene expression and protein localization in complex tissues is obtained, leading to new insights into the function and regulation both in normal and diseased states, and provides new hypotheses that can be tested. For example, an assay system of the invention may enable some of the insights gained from many individual studies and larger programs like ENCODE (Birney, et al., Nature, 447:799-816 (2007)) and modENCODE to be integrated at the tissue level. The assay systems also aid computational efforts to model interacting networks of gene expression in the field of systems biology.
The assay systems also provide a novel approach to analysis of somatic variation, e.g., somatic mutations in cancer or variability in response to infectious organisms. For example, tumors are typically highly heterogeneous, containing cancer cells as well as genetically normal cells in an abnormal local environment. Cancer cells undergo mutation and selection, and in this process it is not unusual for local clones to develop. Identifying relatively rare somatic mutations in the context of tumors may enable the study of the role of key mutations in the selection of clonal variants. Transcriptional patterns associated with angiogenesis, inflammation, or other cancer-related processes in both cancer and genetically normal cells can be analyzed for insights into cancer biology and assist in the development of new therapeutic agents for the treatment of cancers. In another example, individuals have varying susceptibility to infectious organisms, and the assay systems of the invention can be used to study the interaction between microbes and tissues or the various cell types within the tissue.
Importantly, in addition to providing spatially-associated information, the invention allows a great increase in the sensitivity of detecting rare mutations, as signal to noise can be dramatically increased since only a small location is assayed in any given reaction. In a typical assay for rare mutations in a mixed sample, the sample is treated in bulk, i.e., nucleic acids are extracted from many cells into a single pool. Thus, if a mutation is present in one cell in 10,000, it must be detected against a background of normal DNA from 10,000 cells. In contrast, with the assay systems of the invention many cells can be analyzed, but individual cells or small groups of cells would be identified by the spatial coding system. Therefore, in the assay systems of the present invention, background is reduced by orders of magnitude, greatly increasing sensitivity. Furthermore, the spatial organization of mutant cells can be observed, which may be particularly important in detecting key mutations in tissue sections in cancer. Already molecular histological analyses are yielding insights into cancer biology and may have potential for use in diagnostics. The technology of the invention promises to greatly increase the power of such approaches.
The present invention provides assays, assay systems, and methods of using such assays in spatially encoded biological assays. The invention provides an assay system comprising one or more agents provided in defined spatial patterns on a substrate surface, and a detection system for identifying the presence or absence, relative amount, and location of a biological molecule. Such biological molecules include, but are not limited to, nucleic acids, peptides, carbohydrates, cellular components, and the like. The assay system is a novel multiplexing approach, as it allows multiple molecules and their respective multiple locations to be identified in a single system using a unique encoding scheme. This encoding scheme uses both molecule-specific binding agents and coding identifiers to provide a practical and cost-effective determination of information on multiple biological molecules, including specific positional information of such molecules in a biological sample, e.g., a tissue section. The single molecule detection analysis using the encoding system also allows relative amounts of biological molecules to be detected, thus providing information on expression levels, sequestering in specific locales, and the like.
The assay systems detect the presence or absence, and relative amount, of a biological molecule at more than one spatial location in a sample. In addition, the assays provide methods for doing this for multiple biological molecules simultaneously. The assay systems utilize one or more binding agents that specifically bind to the biological molecule of interest and unique coding identifiers associated with specific binding agents. The detection system utilizes a method for identifying the presence and spatial address of the agent binding based on the positive and/or negative results that are obtained using detection of the agent and identifier and the encoding scheme of the spatial patterns on the substrate surface. In a specific aspect, the encoding scheme employs limited reagent delivery to the spatial patterns on the substrate surface, and access of the coding identifiers and/or binding agents to portions of the sample is controlled through such limited delivery.
In one aspect, the assay system detects the presence or absence and spatial location of a biological molecule based on the positive and/or negative results that are obtained using limited reagent delivery and the encoding scheme of the spatial patterns on the substrate surface.
The assay system and methods of the invention are based on relational, solid-state substrates with positions that represent specific spatial locations within a biological sample, e.g., a cell, organelle or tissue. The ability to use encoding features to represent locations allows high-throughput analysis of the presence or absence, and relative amount, of a biological molecule at more than one spatial location in a sample. The encoding features also allow provide assaying of multiple biological molecules at these multiple locations simultaneously.
A primary feature of the invention is the preservation of the spatial organization of elements in a sample of interest through the use of an encoding scheme. For example, the assay may be designed to preserve the relative position of cells in a tissue, and the assay may interrogate the individual cells for genomic DNA variation (including epigenetic modifications), and RNA and protein expression.
In one specific aspect, the encoding scheme of the assay system comprises the use of two or more coding patterns, each comprising regions defined by spatial patterns on the substrate surface. For example, the assay system can utilize an encoding scheme that comprises a 2-dimensional grid format based on the discrete positioning of the binding agents in the substrate surfaces. In another example, the spatial patterns may be based on more randomized cell locations, e.g., the patterns on the substrate surface follow an underlying biological structure rather than a strict, x,y grid pattern. This aspect includes systems with two or more substantially identical spatial patterns using different binding agents and/or coding identifiers, as well as systems having different patterns for different agents and/or coding identifiers. The encoding scheme of the systems can be controlled by delivery of different reagents to discrete regions on the substrate surfaces, which allows different reactions to take place on substantially similar agents of known location on the substrate surfaces.
In one specific aspect, the invention provides high resolution, high-throughput analysis of nucleic acids and/or expression levels that provides both detection and spatial identification of large numbers of nucleic acids, e.g., DNA or RNA.
In another specific aspect, the invention provides high resolution, high-throughput analysis of proteins that provides both detection and spatial identification of large numbers of such proteins, e.g., kinases or proteases.
Numerous reagent delivery systems can be used with the assay system of the invention. The primary criteria of such reagent delivery systems is the ability to direct delivery of specific agents based on spatial patterns on the substrate surface.
In one preferred aspect, the encoding scheme utilizes a reagent delivery system based on printing and informatics technologies to implement the spatial patterns used for identification and localization of the biological materials. For example, the patterns found in the encoding scheme may be created using ink jet printing technology to provide reagents at specific locations on one or more substrate surfaces. The desired patterns are set out in specific coding patterns on the substrate surface.
In certain aspects of the invention, the binding agents are immobilized directly to the substrate surface, and the location of the binding agents is known or determined prior to use of the substrate surface in the assay system. In another aspect, the binding agents are immobilized onto beads or other separate structural elements that are then provided in known locations on the substrate surface. In yet another aspect, the binding agents may be provided in or on features of the substrate surface, e.g., provided in wells or channels.
In specific aspects of the invention, the binding agents are nucleic acids immobilized directly or indirectly to the substrate surface, e.g., directly through the use of amino groups on the substrate surface or indirectly through the use of a linker. The location of the nucleic acid sequences is known or determined prior to use of the substrate surface in the assay system. In another specific aspect, the nucleic acids may be immobilized directly or indirectly onto beads that are then provided in known locations on the substrate surface. In yet another aspect, the nucleic acids may be provided in or on features of the substrate surface, e.g., provided in wells.
In these aspects involving nucleic acid agents, any methods of sequence determination can be used, e.g., sequencing, hybridization and the like. In a preferred aspect, nucleic acid sequencing, and preferably next-generation sequencing, is used to decode the spatial encoding scheme in the assay system of the invention. This provides a very wide dynamic range for very large numbers of assays, allowing for efficient multiplexing.
In some aspects, the assay utilizes two or more oligonucleotides, the oligonucleotides comprising a universal primer region and a region that correlates specifically to a single spatial pattern within the spatial encoding scheme. In a specific aspect, the assay comprises two allele specific oligonucleotides and one locus specific oligonucleotides. These oligonucleotides allow the identification of specific SNPs, indels or mutations within an allele. This is useful in the identification of genetic changes in somatic cells, genotyping of tissues, and the like.
In other specific aspects of the invention, the binding agents are peptides. In one aspect, these peptides are associated directly or indirectly to known locations on a substrate surface, e.g., using binding protein pairs or through oligonucleotide linkers complementary to oligonucleotides on the substrate surface. In another aspect, the binding agents are peptides are immobilized directly or indirectly onto beads or other separate structural elements that are then provided in known locations on the substrate surface. In yet another aspect, the peptides may be provided in or on features of the substrate surface, e.g., provided in wells.
In yet other specific aspects of the invention, the binding agents are chemical entities (e.g., small molecules) that are coded, e.g. using sequence tags or mass spectroscopy tags as coding identifiers. In one aspect, these chemical entities can be are immobilized directly to the substrate surface. In another aspect, the binding agents are immobilized onto beads or other separate structural elements that are then provided in known locations on the substrate surface. In yet another aspect, the binding agents may be provided in or on features of the substrate surface, e.g., provided in wells.
The assay system of the invention can utilize various detection mechanisms, based on the molecules to be detected and the reagents needed for such detection system. Exemplary methods that can be used with the assay systems of the invention are described in more detail below.
The assay system and methods of the invention are based on relational methods that allow extraction of data to detect the presence or absence and relative amount of a biological molecule, and the location of this molecule in a sample having a distinct structure, e.g., a tissue section or other biological structure with distinct locations of specific biological molecules. The encoding scheme used in these systems corresponds to the structural elements of the sample, and the information obtained using a two-dimensional coding system is indicative of the spatial addresses of these molecules in a sample of interest.
Integral to the assay system of the invention is a method for spatial patterning of reagents. Technologies for formulating and delivering both biological molecules (e.g. DNA or antibodies) and chemical reagents (e.g., small molecules or dNTPs) have already been demonstrated, and use of these systems will be available to one skilled in the art and easily adaptable upon reading this specification.
The assay design of the invention provides an accurate and easily scalable spatial encoding system. The ability to deliver reagents in a spatially defined pattern together with software, reagents and protocols comprises a novel and highly innovative assay system for spatial analysis of various biological molecules and activities. This allows the assays to measure numerous biological functions in a meaningful spatial environment, including functions such as gene expression and peptide localization. The systems provide the potential to open a new analytical window into the complex spatial patterns of cellular function and regulation in biological systems.
The biological molecules to be detected can be any biological molecules such as proteins, nucleic acids, lipids, carbohydrates, ions, or multicomponent complexes containing any of the above. Further examples of subcellular objects include organelles, e.g., mitochondria, Golgi apparatus, endoplasmic reticulum, chloroplast, endocytic vesicle, exocytic vesicles, vacuole, lysosome, etc.
The assay systems of the invention are particularly advantageous in that they are compatible with numerous samples types, such as fresh samples, such as primary tissue sections, and preserved samples including but not limited to frozen samples and paraformalin-fixed, paraffin-embedded (FFPE) samples. An important aspect of the assay systems of the invention is that the binding agents are immobilized on a substrate surface in discrete, independently measureable areas. These discrete areas can be formed by spatially selective deposition of the binding agents on the substrate surface. Numerous methods can be used for the deposition of the agent and the coding identifiers associates with the agent. For example, the coding identifiers can be delivered together or separately from the agent. If delivered together they can be attached (e.g., synthesized as a single molecule or attached through ligation or a chemical coupling mechanism) or simply mixed together to be attached after delivery to the substrate. In a preferred aspect, the agent and the coding identifier are made separately, mixed together for attachment, and delivered either attached or as a mixture to be attached on the surface. In a specific aspect the binding agents are delivered generally over the substrate surface and the coding identifiers are delivered in a pattern-specific manner.
Examples of methods that can be used for deposition of agents and/or coding identifiers onto the substrate surface include, but are not limited to, ink jet spotting, mechanical spotting by means of pin, pen or capillary, micro contact printing, fluidically contacting the measurement areas with the biological or biochemical or synthetic recognition elements upon their supply in parallel or crossed micro channels, upon exposure to pressure differences or to electric or electromagnetic potentials, and photochemical or photolithographic immobilization methods.
For several applications, it may be preferred to arrange the substrates into segments of one or more measurement areas for reagent distribution and agent determination. These regions may be physically separated using barriers or channels. They may still comprise several additional discrete measurement areas with agents that are different or in different combination from each other.
In certain aspects, the present invention provides a method, e.g., a machine-based method, for evaluating changes in the presence and/or location of a biological molecule over time. The method includes providing a plurality of encoded array results representative of the biological molecule over time and evaluating the differences in detection and/or localization of the biological molecules.
Nucleic Acid Detection and Localization
In a particular aspect, the assay system is used to analyze nucleic acids, e.g genotyping, gene expression analysis, localization of particular transcripts within samples, and the like.
Genotyping may be performed using any technique known to those of skill in the art. Preferred techniques permit rapid, accurate determination of multiple variations with a minimum of sample handling. Some examples of suitable techniques involve but are not limited to direct DNA sequencing, capillary electrophoresis, hybridization, allele-specific probes or primers, single-strand conformation polymorphism analysis, nucleic acid arrays, bead arrays, restriction fragment length polymorphism analysis, cleavage fragment length polymorphism analysis, random amplified polymorphic DNA, ligase detection reaction, heteroduplex or fragment analysis, differential sequencing with mass spectrometry, atomic force microscopy, pyrosequencing, FRET (e.g., TaqMan (Applied Biosystems, Inc., Foster City, Calif.) and Molecular Beacon (Stratagene, La Jolla, Calif.) assays), and other related techniques. Several methods for DNA sequencing are well known and generally available in the art. See, for example, Sambrook, et al., Molecular Cloning: A Laboratory Manual (Cold Spring Harbor Laboratory, New York) (2001); Ausubel, et al., Current Protocols in Molecular Biology (John Wiley and Sons, New York) (1997), Twyman, et al. (2003) “Techniques Patents for SNP Genotyping”, Pharmacogenomics 4(1):67-79; and Kristensen, et al. (2001) “High-Throughput Methods for Detection of Genetic Variation”, BioTechniques 30(2):318-332. For details on the use of nucleic acid arrays (DNA chips) for the detection of, for example, SNPs, see U.S. Pat. No. 6,300,063 issued to Lipshultz, et al., and U.S. Pat. No. 5,837,832 to Chee, et al., HuSNP Mapping Assay, reagent kit and user manual, Affymetrix Part No. 90094 (Affymetrix, Santa Clara, Calif.). The molecular inversion probe (MIP) assay format (Hardenbol et al., 2003) is another example of a highly multiplexable assay that may be used with the assay systems of the invention.
In one exemplary and preferred method for analyzing nucleic acids using the assay system of the invention, the detection of nucleic acids uses two allele-specific oligonucleotides and a locus specific oligonucleotide. The assay methods are carried out according to the strategy outlined in
In
In one preferred aspect, the final construct created from the assay method is a substrate for next-generation sequencing, and highly parallel next-generation sequencing methods are used to confirm the sequence of constructs. Such sequencing methods can be carried out, for example, using a one pass sequencing method or using paired-end sequencing. Next generation sequencing methods include, but are not limited to, hybridization-based methods, such as disclosed in Drmanac, U.S. Pat. Nos. 6,864,052; 6,309,824; and 6,401,267; and Drmanac et al, U.S. patent publication 2005/0191656, and sequencing by synthesis methods, e.g., Nyren et al, U.S. Pat. No. 6,210,891; Ronaghi, U.S. Pat. No. 6,828,100; Ronaghi et al (1998), Science, 281: 363-365; Balasubramanian, U.S. Pat. No. 6,833,246; Quake, U.S. Pat. No. 6,911,345; Li et al, Proc. Natl. Acad. Sci., 100: 414-419 (2003); Smith et al, PCT publication WO 2006/074351; use of reversible extension terminators, e.g., Turner, U.S. Pat. No. 6,833,246 and Turner, U.S. Pat. No. 6,833,246 and ligation-based methods, e.g., Shendure et al (2005), Science, 309: 1728-1739, Macevicz, U.S. Pat. No. 6,306,597; which references are incorporated by reference. Soddart et al., PNAS USA. 2009 Apr. 20; Xiao et al., Nat Methods. 2009 March; 6(3):199-201. Epub 2009 Feb. 8.
To maximize the efficiency of encoding, a combinatorial approach using pairs of oligonucleotides can be used. For example, with only two sets of 100 codes, a substrate can theoretically encode up to 10,000 locations. The number of assay oligonucleotides required is dramatically reduced, the cost decreased, and the robustness of the approach increased by decoupling the coding sequences from the genome-specific sequences. Alternative assay formats can also be used (e.g. ligation or primer extension followed by ligation).
By ligating the codes on separately, only 2n target-specific assay oligonucleotides are needed for n targets. For example, assaying 100 different targets at 10,000 spatial locations would require 2×100 targeting oligonucleotides and 2×100 encoding oligonucleotides, using a combinatorial approach outlined in
Due to the matrix system of the invention, a large amount of information can be obtained even using five or more positions interrogated for five or more biological molecules. By varying one or the other of these, large amounts of information can be obtained, both in terms of locations and/or specific biological In specific aspects, multiple locations are interrogated for two or more biological molecules. As an example, for each datapoint˜1,000 reads may be sampled, for a total of −10E9 reads for 10E6 datapoints.
Peptide Detection Systems
The assay system of the invention can be used to analyze biological molecules using peptide agents that are associated with the substrate surface in a spatial pattern. Such peptides may comprise an active region of an enzyme, a binding domain of an immunoglobulin, defined domains of proteins, whole proteins, synthetic peptides, peptides with introduced mutations, etc.
The assay system of the invention allows the identification and spatial location of various forms of peptides, including isoforms and peptides that have undergone posttranslational modification. Importantly, certain aspects of the invention allow the identification of active versus non-active forms of such peptides in a sample. This allows the identification of the presence or absence of specific peptide isoforms, and also acts as a proxy for identification of peptide activity in a sample.
In certain aspects of the invention, the binding agents associated with the substrate surfaces of the assay system include substrates for enzymes or proenzymes, e.g., a kinase, a phosphatase, a zymogen, a protease, or a fragment thereof. In certain aspects, the binding agents associated with the substrate surfaces are phosphorylation substrates used to detect proteins involved with one or more signal transduction pathways, e.g., a kinase or a phosphatase. In another specific aspect of the invention, the binding agents are specific protease substrates that associate only with individual or classes of proteases. In other aspects, the binding agents on the substrate surface are different processed forms, isoforms and/or domains of an enzyme.
Reagent Delivery
The reagent delivery system of the invention can be any system that allows the delivery of reagents to discrete portions of the array in order to keep the integrity of the defined spatial patterns of the encoding scheme. Such discrete delivery can be achieved in a number of different ways.
In one exemplary aspect, the reagent delivery system can be a flow-based system. The flow-based systems for reagent delivery in the present invention can include one or more pumps, valves, fluid reservoirs, channels, and/or reagent storage cells. Such a reagent delivery system is configured to move fluid in contact with a discrete section of the substrate surface. Movement of the reagents can be driven through a fluid by a pump disposed, for example, downstream of the fluid reagents. The pump can drive each fluid reagent to (and past) the reaction compartment. Alternatively, the reagents may be driven through the fluid by gravity.
US Appln Nos. 20070166725 and 20050239192 disclose certain general purpose fluidics tools that can be used with the assay systems of the invention. These allow the precise manipulation of gases, liquids and solids to accomplish very complex analytical manipulations with relatively simple hardware.
In a more specific example, one or more flow-cells can be attached to the substrate from above. The flow-cell can include inlet and outlet tubes connected thereto and optionally an external pump can be used to deliver the sample or reagents to the flow-cell and across the substrate. The flow cell is configured to deliver reagents only to certain portions of the array, restricting the amount and type of reagent delivered to any specific section of the array.
In another aspect, a microfluidic system can be integrated into the substrate or externally attached on top of the substrate. Microfluidic passages for holding and carrying fluid can be formed on and/or above the planar substrate by a fluidics layer abutted to the substrate. Fluid reagents can be selected according to selective opening and closing of valves disposed between reagent reservoirs.
Pumps generally include any mechanism for moving fluid and/or reagents disposed in fluid. In some examples, the pump can be configured to move fluid and/or reagents through passages with small volumes (i.e., microfluidic structures). The pump can operate mechanically by exerting a positive or negative pressure on fluid and/or on a structure carrying fluid, electrically by appropriate application of an electric field(s), or both, among others. Exemplary mechanical pumps may include syringe pumps, peristaltic pumps, rotary pumps, pressurized gas, pipettors, etc. The mechanical pumps may be micromachined, molded, etc. Exemplary electrical pumps can include electrodes and may operate by electrophoresis, electroendoosmosis, electrocapillarity, dielectrophoresis (including traveling wave forms thereof), and/or the like.
Valves generally include any mechanism for regulating the passage of fluid through a channel. The valves can include, for example, deformable members that can be selectively deformed to partially or completely close a channel, a movable projection that can be selectively extended into the channel to partially or completely block the channel, an electrocapillary structure, and/or the like.
In yet another aspect, an open gasket can be attached to the top of the substrate and the sample and reagents can be injected into the gasket. Suitable gasket materials include, but are not limited to, neoprene, nitrile, and silicone rubber. Alternatively, a watertight reaction chamber formed by a gasket sandwiched between the substrate and a chemically inert, water resistant material such as, but not limited to, black-anodized aluminum, thermoplastics (e.g., polystyrene, polycarbonate, etc), glass, etc.
In a specific aspect of the present invention, the delivery system can compnse a microcircuit arrangement including an imager, such as a CCD or IGFET-based (e.g., CMOS-based) imager and an ultrasonic sprayer for reagent delivery such as described in US Appln No. 20090197326, which is incorporated herein by reference.
In yet another aspect of the invention, the reagent delivery system controls the delivery of reagents to specific patterns on a substrate surface using semiconductor techniques such as masking and spraying. Specific areas of a substrate surface can be protected from exposure to reagents through use of a mask to protect specific areas from exposure. The reagents may be introduced to the substrate using conventional techniques such as spraying or fluid flow. The use of the masked substrate delivery results in a patterned delivery scheme on the substrate surface.
In a preferred aspect of the invention, the reagent delivery instrumentation is based on inkjet printing technology. There are a variety of different ink-jetting mechanisms (e.g., thermal, piezoelectric) and compatibility has been shown with aqueous and organic ink formulations. Sets of independently actuated nozzles can be used to deliver multiple reagents at the same time, and very high resolutions can be achieved.
Software for Use in the Assay System
In order to target specific sites of interest, an informative image of the biological section to be analyzed can be used to assist in the reagent delivery methods and associated encoding scheme. Sample regions can be identified using image processing (e.g., images of cell types differentiated by immunohistochemistry or other staining chemistries) integrated with the other features of the assay system. In some aspects, software is used to automatically translate this information into a reagent delivery pattern. A mechanism to register and align very precisely the biological sample in a targeting system is thus a preferred component of the assay systems of the invention. Mechanisms such as the use of fiducial markers on slides and other very accurate physical positioning systems can be adapted to this purpose.
Additional software components will also be key components that will be part of a complete assay system. The invention thus preferably comprises a complete suite of software tailored to the assay system. Optionally, oligonucleotide design software will be customized for the specific assay to be run, and may be integrated as a part of the system. Also optionally, algorithms and software for data analysis may be integrated to assist in determination of results of the assays. This can be especially useful, as the type of dataset that will be generated will be novel, particularly as a consequence of scale. The ability to provide algorithms and software tools that are specifically designed for analysis of spatially-associated data for significant patterns, including pattern-analysis software and visualization tools, is a novel feature that will enhance the value of the data generated by the assay systems.
In certain aspects, the assay system will comprise processes for making and carrying out quality control of reagents, e.g., the integrity and sequence fidelity of oligonucleotide pools. In particular, reagents will need to be formulated for compatibility with the reagent delivery instrumentation. Factors such as volatility, stability at key temperatures, and chemical compatibility can be optimized by those skilled in the art upon reading the present disclosure.
Applications of Assay System
It will be apparent to one skilled in the art upon reading the present disclosure that there are numerous very important areas of biological research, diagnostics, and drug development that will benefit from a high throughput means to simultaneously measure the presence or absence and spatial location of a biological molecule in a sample. For example, this technology combining the ability to analyze semi-quantitatively the expression of many different genes with the ability to image the spatial organization of expression across many cells in a tissue is enabling for many different areas of basic research. The following are exemplary uses and are by no means meant to be limiting in scope.
In one example, 3-dimensional patterns of expression can be determined by analyzing a series of tissue sections, in a manner analogous to image reconstruction in CT scanning. This can be used to measure changes in gene expression in disease pathology, e.g., in cancerous tissue and/or a tissue upon injury, inflammation or infection. With the assay systems of the invention, more detailed information on gene expression and protein localization in complex tissues can be obtained. This may lead to new insights into the function and regulation both in normal and diseased states, and is likely to provide new hypotheses that can be tested. For example, a system of the invention may enable some of the insights gained from many individual studies and larger programs like ENCODE (Birney et al., 2007) and modENCODE to be integrated at the tissue level. The assay systems will also aid in computational efforts to model interacting networks of gene expression in the field of systems biology.
The assay systems also provide a novel approach that enables the analysis of somatic variation, e.g., somatic mutations in cancer or variability in response to infectious organisms. For example, tumors are typically highly heterogeneous, containing cancer cells as well as genetically normal cells in an abnormal local environment. Cancer cells undergo mutation and selection, and in this process it is not unusual for local clones to develop. Identifying relatively rare somatic mutations in the context of tumors may enable the study of the role of key mutations in the selection of clonal variants. Transcriptional patterns associated with angiogenesis, inflammation, or other cancer related processes in both cancer and genetically normal cells can be analyzed for insights into cancer biology and assist in the development of new therapeutic agents for the treatment of cancers.
In another example, different people have varying susceptibility to infectious organisms, and much of this may be to underlying genetic differences in individuals and/or populations. Identifying these differences will aid in an understanding of the underlying disease pathologies and assist in the development of vaccines or therapeutics to prevent or ameliorate these disease states.
Importantly, in addition to providing spatially associated information, the technology of the invention will allow a great increase in the sensitivity of detecting rare mutations. The reason is that signal to noise can be dramatically increased because the approach of the invention assays a small location in any given reaction. In a typical assay for rare mutations in a mixed sample, the sample is treated in bulk, i.e. nucleic acids are extracted from many cells into a single pool. Thus, if a mutation is present in 1 cell in 10,000, it must be detected against a background of normal DNA from ˜10,000 cells. In contrast, with the systems of the invention many cells can be analyzed, but individual cells or small groups of cells would be identified by the spatial coding system. Therefore, the background can be reduced by orders of magnitude, greatly increasing sensitivity. Furthermore, the spatial organization of mutant cells can be observed. This may be particularly important in detecting key mutations in tissue sections in cancer. Already, molecular histological analyses are yielding insights into cancer biology and may have potential for use in diagnostics (Choe et al., 2003). The technology of the invention promises to greatly increase the power of such approaches.
The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how to make and use the present invention, and are not intended to limit the scope of what the inventor regards as his invention, nor are they intended to represent or imply that the experiments below are all of or the only experiments performed. It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in the specific embodiments without departing from the spirit or scope of the invention as broadly described. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive.
Efforts have been made to ensure accuracy with respect to numbers used (e.g., amounts, temperature, etc.) but some experimental errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, molecular weight is weight average molecular weight, temperature is in degrees centigrade, and pressure is at or near atmospheric.
As an initial proof of concept, a model system is developed using a microarray to demonstrate a working single-plex assay. The basic design validates the concept of the assay, and establishes a working assay prior to addressing issues related to the analysis of a more complicated biological sample. Conventional sequencing is used as a readout for this proof of concept.
A microarray is used as a proxy for a tissue section. The target sequences of the microarray are fully specified, so that the composition of the targets are known and can be varied systematically. Synthetic oligonucleotide templates are attached to a glass slide via a 5′ amino modification. Each slide has a single oligonucleotide template sequence, and the assays that are carried out may employ either ligation, or extension followed by ligation as this may be useful in determining certain polymorphisms.
Once the in situ part of the assay is complete, the reaction products are eluted and analyzed by qPCR to determined presence or absence of a product and estimate yield, and by conventional sequencing to determine the structure of the assay products. The single plex assays that are tested include appropriate positive and negative controls, and a single nucleotide variant (SNV) to check ability to discriminate single base variants.
The complexity of the assay system is increased to establish scalability of the assay for use in high throughput studies. Scalability of both the spatial encoding and assay systems is demonstrated by carrying out a 24-plex×24-site assay using a microarray model system.
The amount of biological target, here a DNA target sequence, at each assay location is systematically varied on microarray substrate. For example, in a microarray with 50 micron spot size (center to center), a 1 mm2 area contains˜400 spots. The region around each site is optionally occupied by a region that is devoid of these spots to allow individual resolvability of the target sequences. Alternatively, the spots may be clustered, with two or more directly adjacent spots surrounded by or adjacent to a region that is devoid of target sequences.
In order to demonstrate that spatial encoding is accurate, the sites comprise different target compositions to show that the assay readout matches the expected composition of each site. With 24 target sequences, a simple digital pattern is made with each site having a different set of 12 targets present and 12 targets absent, to make a binary code (0=absent, 1=present). The assay readout is then determined to show that the detected regions match the expected signal after spatial decoding. In this particular example, the code space is large enough (224) so that even a few errors would not result in different codes being mixed up. Moreover, this design allows identification of errors and allows an estimation not only of accuracy of spatial encoding but also of accuracy calling the presence or absence of target sequences.
In an exemplary aspect, a 4×4 arrangement of 16 sequences is used for the array configuration. A white square indicates that the sequence is absent and a black square that it is present, i.e. 8 of the 16 possible sequences are present in this sample. In a different sample, a different pattern of absent and present sequences can be constructed. In this way, unique patterns are associated with spatial locations so that the accuracy of spatial encoding can be measured.
The ability to detect quantitative differences is evaluated by generating dose-response curves for each of the 24 assays that are carried out at each site in a 24-site assay. This allows estimation of the limit of detection, dynamic range, and power to detect a given fold-change across the range.
In one aspect, a latin square design is used to represent individual targets at different ratios by varying the number of features for each target. In other words, with multiple spots in a site, the number of spots allocated to each of the 24 target sequences can be varied and each of the 24 sites can have a different composition. A 1×3 inch microarray is sufficiently large to permit multiple replicates. This larger set of 24 sequences will require deconvolution, and this is accomplished using high throughput techniques such as next-generation sequencing technologies (e.g., SOLiD™ technology (Life Technologies, Inc., Carlsbad, Calif.) or Genome Analyzer (Illumina, Inc., San Diego, Calif.)). The use of the 24-plex assay demonstrates both the accuracy of spatial encoding and decoding, and the quantitative response of the assay system.
Genomic DNA is assayed as a proof of concept for assaying RNA, as it provides a way to establish a single-copy reference signal. Once a working assay is developed for FFPE samples, it is adapted to an RNA assay. To this end, assay oligonucleotide concentrations are assayed to ensure compatibility with high multiplexing. Assuming a cell diameter of 10 microns, and delivery of a 10 micron diameter reagent droplet to an individual cell, the volume of the droplet will be ˜500 μl and can contain˜3×1011 molecules at a concentration. To assay 1,000 target sequences in 10,000 cells, ˜2,000 targeting oligonucleotides would be required in a droplet. Therefore, each droplet could contain˜160 million copies of each assay oligo, a vast excess over the few thousand target sequences in a cell.
The handling of small absolute numbers of product molecules generated from very small or compromised samples are enhanced to counter the issue of low recovery efficiency; that is, elution is efficient and losses resulting from adsorption of molecules to surfaces are prevented. An approach to addressing the latter issue is to include a carrier material, such as glycogen or carrier nucleic acids.
A control RNA template is immobilized to a solid support in order to create an artificial system. The assay is performed using T4 DNA ligase, which can repair nicks in DNA/RNA hybrids. Assays are carried out on matched slides, or different sections of the same slide, where in one case gDNA is assayed and in the other RNA is assayed. When assaying gDNA the slide can be pretreated with RNase, and when assaying RNA the slide is pretreated with DNase. Results of the assay are confirmed by extracting gDNA or RNA and quantitating the relative amounts by qPCR or RT-qPCR respectively.
In order make the tissue section RNA assays as informative as possible, pre-existing information on expression levels in specific tissues to target transcripts across a range of abundances are used in the assay design. Both high abundance transcripts, as well as some medium and low abundance transcripts, are targeted to enable an initial assessment of the quantitative performance characteristics of the assay.
The preceding merely illustrates the principles of the invention. It will be appreciated that those skilled in the art will be able to devise various arrangements which, although not explicitly described or shown herein, embody the principles of the invention and are included within its spirit and scope. Furthermore, all examples and conditional language recited herein are principally intended to aid the reader in understanding the principles of the invention and the concepts contributed by the inventors to furthering the art, and are to be construed as being without limitation to such specifically recited examples and conditions. Moreover, all statements herein reciting principles, aspects, and embodiments of the invention as well as specific examples thereof, are intended to encompass both structural and functional equivalents thereof. Additionally, it is intended that such equivalents include both currently known equivalents and equivalents developed in the future, i.e., any elements developed that perform the same function, regardless of structure. The scope of the present invention, therefore, is not intended to be limited to the exemplary embodiments shown and described herein. Rather, the scope and spirit of present invention is embodied by the appended claims. In the claims that follow, unless the term “means” is used, none of the features or elements recited therein should be construed as means-plus-function limitations pursuant to 35 U.S.C. § 112, ¶6.
This application is a continuation of U.S. patent application Ser. No. 17/030,230, filed Sep. 23, 2020, which is a continuation of U.S. patent application Ser. No. 16/988,284, filed Aug. 7, 2020, now U.S. Pat. No. 10,961,566, which is a continuation of U.S. patent application Ser. No. 16/414,213, filed May 16, 2019, now U.S. Pat. No. 10,787,701, which is a continuation of U.S. patent application Ser. No. 16/402,098, filed May 2, 2019, now U.S. Pat. No. 10,472,669, which is a continuation of U.S. patent application Ser. No. 16/276,235 filed Feb. 14, 2019, now U.S. Pat. No. 10,480,022, which is a continuation application of U.S. patent application Ser. No. 15/187,661, filed Jun. 20, 2016, now U.S. Pat. No. 10,308,982, which is a continuation of Ser. No. 13/080,616 filed Apr. 5, 2011, now U.S. Pat. No. 9,371,598, which claims the benefit of U.S. Provisional Patent Application No. 61/321,124, filed Apr. 5, 2010 and is incorporated herein by reference.
| Number | Name | Date | Kind |
|---|---|---|---|
| 4514388 | Psaledakis | Apr 1985 | A |
| 4574729 | Wells | Mar 1986 | A |
| 4683195 | Mullis | Jul 1987 | A |
| 4683202 | Mullis | Jul 1987 | A |
| 4800159 | Mullis | Jan 1989 | A |
| 4883867 | Lee | Nov 1989 | A |
| 4965188 | Mullis | Oct 1990 | A |
| 4968601 | Jacobson et al. | Nov 1990 | A |
| 4988617 | Landegren et al. | Jan 1991 | A |
| 5002882 | Lunnen | Mar 1991 | A |
| 5130238 | Malek | Jul 1992 | A |
| 5183053 | Yeh et al. | Feb 1993 | A |
| 5308751 | Ohkawa | May 1994 | A |
| 5321130 | Yue | Jun 1994 | A |
| 5410030 | Yue | Apr 1995 | A |
| 5436134 | Haugland | Jul 1995 | A |
| 5455166 | Walker | Oct 1995 | A |
| 5472881 | Beebe et al. | Dec 1995 | A |
| 5494810 | Barany et al. | Feb 1996 | A |
| 5503980 | Cantor | Apr 1996 | A |
| 5512439 | Homes | Apr 1996 | A |
| 5512462 | Cheng | Apr 1996 | A |
| 5559032 | Porneroy | Sep 1996 | A |
| 5582977 | Yue | Dec 1996 | A |
| 5589173 | O'Brien | Dec 1996 | A |
| 5599675 | Brenner | Feb 1997 | A |
| 5610287 | Nikiforov et al. | Mar 1997 | A |
| 5641658 | Adams | Jun 1997 | A |
| 5648245 | Fire et al. | Jul 1997 | A |
| 5658751 | Yue | Aug 1997 | A |
| 5716825 | Hancock et al. | Feb 1998 | A |
| 5750341 | Macevicz | May 1998 | A |
| 5763175 | Brenner | Jun 1998 | A |
| 5807522 | Brown et al. | Sep 1998 | A |
| 5830711 | Barany et al. | Nov 1998 | A |
| 5837832 | Chee et al. | Nov 1998 | A |
| 5837860 | Anderson et al. | Nov 1998 | A |
| 5854033 | Lizardi | Dec 1998 | A |
| 5863753 | Haugland | Jan 1999 | A |
| 5866377 | Kim et al. | Feb 1999 | A |
| 5871921 | Landegren et al. | Feb 1999 | A |
| 5912148 | Eggerding | Jun 1999 | A |
| 5919626 | Shi et al. | Jul 1999 | A |
| 5925545 | Reznikoff et al. | Jul 1999 | A |
| 5958775 | Wickstrom et al. | Sep 1999 | A |
| 5965443 | Reznikoff et al. | Oct 1999 | A |
| 6013440 | Lipshutz | Jan 2000 | A |
| 6027889 | Barany et al. | Feb 2000 | A |
| 6060240 | Kamb et al. | May 2000 | A |
| 6083761 | Kedar et al. | Jul 2000 | A |
| 6130073 | Eggerding | Oct 2000 | A |
| 6136592 | Leighton | Oct 2000 | A |
| 6143496 | Brown | Nov 2000 | A |
| 6153389 | Haarer | Nov 2000 | A |
| 6159736 | Reznikoff et al. | Dec 2000 | A |
| 6165714 | Lane et al. | Dec 2000 | A |
| 6172218 | Brenner | Jan 2001 | B1 |
| 6210891 | Nyren | Apr 2001 | B1 |
| 6210894 | Brennan | Apr 2001 | B1 |
| 6214587 | Dattagupta | Apr 2001 | B1 |
| 6221591 | Aerts | Apr 2001 | B1 |
| 6251639 | Kum | Jun 2001 | B1 |
| 6258558 | Szostak | Jul 2001 | B1 |
| 6258568 | Nyren | Jul 2001 | B1 |
| 6261804 | Szostak | Jul 2001 | B1 |
| 6265552 | Schatz | Jul 2001 | B1 |
| 6266459 | Walt | Jul 2001 | B1 |
| 6268148 | Barany et al. | Jul 2001 | B1 |
| 6274320 | Rothberg | Aug 2001 | B1 |
| 6281804 | Haller | Aug 2001 | B1 |
| 6291180 | Chu | Sep 2001 | B1 |
| 6300063 | Lipshutz et al. | Oct 2001 | B1 |
| 6306597 | Macevicz | Oct 2001 | B1 |
| 6309824 | Drmanac | Oct 2001 | B1 |
| 6337472 | Garner et al. | Jan 2002 | B1 |
| 6344316 | Lockhart | Feb 2002 | B1 |
| 6355431 | Chee | Mar 2002 | B1 |
| 6368801 | Faruqi | Apr 2002 | B1 |
| 6391937 | Beuhler et al. | May 2002 | B1 |
| 6401267 | Drmanac | Jun 2002 | B1 |
| 6404907 | Gilchrist | Jun 2002 | B1 |
| 6416950 | Lohse | Jul 2002 | B1 |
| 6432360 | Church et al. | Aug 2002 | B1 |
| 6485982 | Charlton | Nov 2002 | B1 |
| 6503713 | Rana | Jan 2003 | B1 |
| 6506561 | Cheval et al. | Jan 2003 | B1 |
| 6518018 | Szostak | Feb 2003 | B1 |
| 6544732 | Chee | Apr 2003 | B1 |
| 6544790 | Sabatini | Apr 2003 | B1 |
| 6565727 | Shenderov | May 2003 | B1 |
| 6573043 | Cohen et al. | Jun 2003 | B1 |
| 6579695 | Lambalot | Jun 2003 | B1 |
| 6620584 | Chee | Sep 2003 | B1 |
| 6632641 | Brennan | Oct 2003 | B1 |
| 6673620 | Loeffler | Jan 2004 | B1 |
| 6677160 | Stockman et al. | Jan 2004 | B1 |
| 6699710 | Kononen | Mar 2004 | B1 |
| 6737236 | Pieken et al. | May 2004 | B1 |
| 6770441 | Dickinson | Aug 2004 | B2 |
| 6773566 | Shenderov | Aug 2004 | B2 |
| 6773886 | Kaufman | Aug 2004 | B2 |
| 6787308 | Balasubramanian | Sep 2004 | B2 |
| 6797470 | Barany et al. | Sep 2004 | B2 |
| 6800453 | Labaer | Oct 2004 | B2 |
| 6812005 | Fan et al. | Nov 2004 | B2 |
| 6828100 | Ronaghi | Dec 2004 | B1 |
| 6833246 | Balasubramanian | Dec 2004 | B2 |
| 6852487 | Barany et al. | Feb 2005 | B1 |
| 6859570 | Walt | Feb 2005 | B2 |
| 6864052 | Drmanac | Mar 2005 | B1 |
| 6867028 | Janulaitis | Mar 2005 | B2 |
| 6872816 | Hall et al. | Mar 2005 | B1 |
| 6875572 | Pradent et al. | Apr 2005 | B2 |
| 6878515 | Landegren | Apr 2005 | B1 |
| 6890741 | Fan et al. | May 2005 | B2 |
| 6897023 | Fu | May 2005 | B2 |
| 6911132 | Pamula | Jun 2005 | B2 |
| 6911345 | Quake | Jun 2005 | B2 |
| 6913881 | Aizenstein et al. | Jul 2005 | B1 |
| 6913921 | Fischer | Jul 2005 | B2 |
| 6942968 | Dickinson et al. | Sep 2005 | B1 |
| 6969488 | Bridgham | Nov 2005 | B2 |
| 6969589 | Patil | Nov 2005 | B2 |
| 6977033 | Becker | Dec 2005 | B2 |
| 7001792 | Sauer et al. | Feb 2006 | B2 |
| 7011944 | Prudent et al. | Mar 2006 | B2 |
| 7052244 | Fouillet | May 2006 | B2 |
| 7057026 | Barnes | Jun 2006 | B2 |
| 7083980 | Reznikoff et al. | Aug 2006 | B2 |
| 7098041 | Kaylor et al. | Aug 2006 | B2 |
| 7115400 | Adessi | Oct 2006 | B1 |
| 7118883 | Inoue | Oct 2006 | B2 |
| 7128893 | Leamon et al. | Oct 2006 | B2 |
| 7163612 | Sterling | Jan 2007 | B2 |
| 7166431 | Chee et al. | Jan 2007 | B2 |
| 7192735 | Lanibalot | Mar 2007 | B2 |
| 7211414 | Hardin | May 2007 | B2 |
| 7223371 | Hayenga et al. | May 2007 | B2 |
| 7229769 | Kozlov | Jun 2007 | B2 |
| 7244559 | Rothberg | Jul 2007 | B2 |
| 7255994 | Lao | Aug 2007 | B2 |
| 7258976 | Mitsuhashi | Aug 2007 | B2 |
| 7259258 | Kozlov et al. | Aug 2007 | B2 |
| 7264929 | Rothberg | Sep 2007 | B2 |
| 7270950 | Szostak | Sep 2007 | B2 |
| 7282328 | Kong et al. | Oct 2007 | B2 |
| 7297518 | Quake | Nov 2007 | B2 |
| 7315019 | Turner | Jan 2008 | B2 |
| 7328979 | Decre | Feb 2008 | B2 |
| 7329492 | Hardin | Feb 2008 | B2 |
| 7358047 | Hafner et al. | Apr 2008 | B2 |
| 7361488 | Fan et al. | Apr 2008 | B2 |
| 7375234 | Sharpless et al. | May 2008 | B2 |
| 7378242 | Hurt | May 2008 | B2 |
| 7393665 | Brenner | Jul 2008 | B2 |
| 7405281 | Xu | Jul 2008 | B2 |
| 7407757 | Brenner | Aug 2008 | B2 |
| 7427678 | Pieken et al. | Sep 2008 | B2 |
| 7462449 | Quake | Dec 2008 | B2 |
| 7499806 | Kermani et al. | Mar 2009 | B2 |
| 7501245 | Quake | Mar 2009 | B2 |
| 7537897 | Brenner | May 2009 | B2 |
| 7544473 | Brennan | Jun 2009 | B2 |
| 7547380 | Velev | Jun 2009 | B2 |
| 7563576 | Chee | Jul 2009 | B2 |
| 7579153 | Brenner | Aug 2009 | B2 |
| 7582420 | Oliphant et al. | Sep 2009 | B2 |
| 7595883 | El Gamal | Sep 2009 | B1 |
| 7601492 | Fu et al. | Oct 2009 | B2 |
| 7601498 | Mao | Oct 2009 | B2 |
| 7608434 | Reznikoff et al. | Oct 2009 | B2 |
| 7611869 | Fan | Nov 2009 | B2 |
| 7635566 | Brenner | Dec 2009 | B2 |
| 7641779 | Becker | Jan 2010 | B2 |
| 7666612 | Johnsson | Feb 2010 | B2 |
| 7674589 | Cohen et al. | Mar 2010 | B2 |
| 7674752 | He | Mar 2010 | B2 |
| 7700286 | Stroun et al. | Apr 2010 | B2 |
| 7709198 | Luo et al. | May 2010 | B2 |
| 7754429 | Rigatti | Jul 2010 | B2 |
| 7776547 | Roth | Aug 2010 | B2 |
| 7776567 | Mao | Aug 2010 | B2 |
| 7785869 | Belgrader et al. | Aug 2010 | B2 |
| 7803943 | Mao | Sep 2010 | B2 |
| 7844940 | Shin et al. | Nov 2010 | B2 |
| 7848553 | Hertel et al. | Dec 2010 | B2 |
| 7858321 | Glezer | Dec 2010 | B2 |
| 7888009 | Barany et al. | Feb 2011 | B2 |
| 7892747 | Barany et al. | Feb 2011 | B2 |
| 7914981 | Barany et al. | Mar 2011 | B2 |
| 7955794 | Shen et al. | Jun 2011 | B2 |
| 7960119 | Chee | Jun 2011 | B2 |
| 7960120 | Rigatti | Jun 2011 | B2 |
| 8003354 | Shen et al. | Aug 2011 | B2 |
| 8030477 | Cerrina et al. | Oct 2011 | B2 |
| 8076063 | Fan | Dec 2011 | B2 |
| 8092784 | Mao | Jan 2012 | B2 |
| 8148068 | Brenner | Apr 2012 | B2 |
| 8148518 | Buchanan | Apr 2012 | B2 |
| 8198028 | Rigatti et al. | Jun 2012 | B2 |
| 8206917 | Chee | Jun 2012 | B2 |
| 8207093 | Szostak | Jun 2012 | B2 |
| 8278034 | Muraca | Oct 2012 | B2 |
| 8288103 | Oliphant | Oct 2012 | B2 |
| 8288122 | O'Leary et al. | Oct 2012 | B2 |
| 8337851 | Aukerman | Dec 2012 | B2 |
| 8343500 | Wraith | Jan 2013 | B2 |
| 8383338 | Kitzman | Feb 2013 | B2 |
| 8460865 | Chee | Jun 2013 | B2 |
| 8481257 | Van Eijk | Jul 2013 | B2 |
| 8481292 | Casbon | Jul 2013 | B2 |
| 8481698 | Lieberman et al. | Jul 2013 | B2 |
| 8486625 | Gunderson | Jul 2013 | B2 |
| 8507204 | Pierce et al. | Aug 2013 | B2 |
| 8551710 | Bernitz et al. | Oct 2013 | B2 |
| 8568979 | Stuelpnagel et al. | Oct 2013 | B2 |
| RE44596 | Stroun et al. | Nov 2013 | E |
| 8586310 | Mitra | Nov 2013 | B2 |
| 8597891 | Barany et al. | Dec 2013 | B2 |
| 8603743 | Liu et al. | Dec 2013 | B2 |
| 8604182 | Luo et al. | Dec 2013 | B2 |
| 8614073 | Van Eijk | Dec 2013 | B2 |
| 8624016 | Barany et al. | Jan 2014 | B2 |
| 8637242 | Shen | Jan 2014 | B2 |
| 8685889 | Van Eijk | Apr 2014 | B2 |
| 8741564 | Seligmann | Jun 2014 | B2 |
| 8741606 | Casbon | Jun 2014 | B2 |
| 8748103 | Faham et al. | Jun 2014 | B2 |
| 8778849 | Bowen | Jul 2014 | B2 |
| 8785353 | Van Eijk | Jul 2014 | B2 |
| 8790873 | Namsaraev et al. | Jul 2014 | B2 |
| 8809238 | Livak et al. | Aug 2014 | B2 |
| 8815512 | Van Eijk | Aug 2014 | B2 |
| 8835358 | Fodor | Sep 2014 | B2 |
| 8865410 | Shendure | Oct 2014 | B2 |
| 8906626 | Oliphant et al. | Dec 2014 | B2 |
| 8911945 | Van Eijk | Dec 2014 | B2 |
| 8936912 | Mitra | Jan 2015 | B2 |
| 8951726 | Luo et al. | Feb 2015 | B2 |
| 8951728 | Rasmussen | Feb 2015 | B2 |
| 8951781 | Reed | Feb 2015 | B2 |
| 9005891 | Sinicropi et al. | Apr 2015 | B2 |
| 9005935 | Belyaev | Apr 2015 | B2 |
| 9023768 | Van Eijk | May 2015 | B2 |
| 9062348 | Van Eijk | Jun 2015 | B1 |
| 9080210 | Van Eijk | Jul 2015 | B2 |
| 9085798 | Chee | Jul 2015 | B2 |
| 9121069 | Lo | Sep 2015 | B2 |
| 9163283 | Chee et al. | Oct 2015 | B2 |
| 9194001 | Brenner | Nov 2015 | B2 |
| 9217176 | Faham et al. | Dec 2015 | B2 |
| 9290808 | Fodor | Mar 2016 | B2 |
| 9290809 | Fodor | Mar 2016 | B2 |
| 9309556 | Myllykangas et al. | Apr 2016 | B2 |
| 9328383 | Van Eijk | May 2016 | B2 |
| 9334536 | Van Eijk | May 2016 | B2 |
| 9340830 | Lipson | May 2016 | B2 |
| 9371598 | Chee | Jun 2016 | B2 |
| 9376716 | Van Eijk | Jun 2016 | B2 |
| 9376719 | Van Eijk | Jun 2016 | B2 |
| 9404156 | Hicks | Aug 2016 | B2 |
| 9416409 | Hayden | Aug 2016 | B2 |
| 9447459 | Van Eijk | Sep 2016 | B2 |
| 9453256 | Van Eijk | Sep 2016 | B2 |
| 9493820 | Van Eijk | Nov 2016 | B2 |
| 9506061 | Brown | Nov 2016 | B2 |
| 9512487 | Faham et al. | Dec 2016 | B2 |
| 9557330 | Siciliano et al. | Jan 2017 | B2 |
| 9574230 | Van Eijk | Feb 2017 | B2 |
| 9593365 | Frisen et al. | Mar 2017 | B2 |
| 9598728 | Barany et al. | Mar 2017 | B2 |
| 9657335 | Van Eijk | May 2017 | B2 |
| 9670542 | Van Eijk | Jun 2017 | B2 |
| 9702004 | Van Eijk | Jul 2017 | B2 |
| 9745627 | Van Eijk | Aug 2017 | B2 |
| 9777324 | Van Eijk | Oct 2017 | B2 |
| 9816134 | Namsaraev | Nov 2017 | B2 |
| 9850536 | Oliphant et al. | Dec 2017 | B2 |
| 9868979 | Chee et al. | Jan 2018 | B2 |
| 9879313 | Chee et al. | Jan 2018 | B2 |
| 9889422 | Smith et al. | Feb 2018 | B2 |
| 9896721 | Van Eijk | Feb 2018 | B2 |
| 9898576 | Van Eijk | Feb 2018 | B2 |
| 9898577 | Van Eijk | Feb 2018 | B2 |
| 9902950 | Church et al. | Feb 2018 | B2 |
| 9902991 | Sinicropi et al. | Feb 2018 | B2 |
| 9958454 | Kozlov et al. | May 2018 | B2 |
| 10023907 | Van Eijk | Jul 2018 | B2 |
| 10030261 | Frisen et al. | Jul 2018 | B2 |
| 10072104 | Winnik et al. | Sep 2018 | B2 |
| 10095832 | Van Eijk | Oct 2018 | B2 |
| 10144966 | Cantor | Dec 2018 | B2 |
| 10196691 | Harkin et al. | Feb 2019 | B2 |
| 10246752 | Faham et al. | Apr 2019 | B2 |
| 10266876 | Cai et al. | Apr 2019 | B2 |
| 10633648 | Seelig et al. | Apr 2020 | B2 |
| 10697013 | Brenner et al. | Jun 2020 | B1 |
| 10767223 | Brenner et al. | Sep 2020 | B1 |
| 10774372 | Chee et al. | Sep 2020 | B2 |
| 10774374 | Frisen et al. | Sep 2020 | B2 |
| 10829803 | Terbrueggen et al. | Nov 2020 | B2 |
| 10927403 | Chee et al. | Feb 2021 | B2 |
| 11046996 | Chee et al. | Jun 2021 | B1 |
| 11162132 | Frisen et al. | Nov 2021 | B2 |
| 11286515 | Chee et al. | Mar 2022 | B2 |
| 11299774 | Frisen et al. | Apr 2022 | B2 |
| 11332790 | Chell et al. | May 2022 | B2 |
| 11352659 | Frisen et al. | Jun 2022 | B2 |
| 11359228 | Chee et al. | Jun 2022 | B2 |
| 11390912 | Frisen et al. | Jul 2022 | B2 |
| 11407992 | Dadhwal | Aug 2022 | B2 |
| 11408029 | Katiraee et al. | Aug 2022 | B2 |
| 11434524 | Ramachandran Iyer et al. | Sep 2022 | B2 |
| 11479809 | Frisen et al. | Oct 2022 | B2 |
| 20010039029 | Nemori et al. | Nov 2001 | A1 |
| 20010055764 | Empendocles et al. | Dec 2001 | A1 |
| 20020006477 | Shishido et al. | Jan 2002 | A1 |
| 20020040275 | Cravatt | Apr 2002 | A1 |
| 20020045169 | Shoemaker et al. | Apr 2002 | A1 |
| 20020045272 | McDevitt et al. | Apr 2002 | A1 |
| 20020048766 | Doyle et al. | Apr 2002 | A1 |
| 20020055100 | Kawashima | May 2002 | A1 |
| 20020058250 | Firth | May 2002 | A1 |
| 20020064779 | Landegren | May 2002 | A1 |
| 20020086441 | Baranov et al. | Jul 2002 | A1 |
| 20020132246 | Kallioniemi et al. | Sep 2002 | A1 |
| 20020137031 | Wolber | Sep 2002 | A1 |
| 20020150909 | Stuelpnagel | Oct 2002 | A1 |
| 20020164611 | Bamdad | Nov 2002 | A1 |
| 20020168645 | Taylor | Nov 2002 | A1 |
| 20030017451 | Wang et al. | Jan 2003 | A1 |
| 20030022207 | Balasubramanian | Jan 2003 | A1 |
| 20030040035 | Slamon | Feb 2003 | A1 |
| 20030064398 | Barnes | Apr 2003 | A1 |
| 20030073086 | Guire et al. | Apr 2003 | A1 |
| 20030087232 | Christians | May 2003 | A1 |
| 20030096323 | James | May 2003 | A1 |
| 20030113713 | Glezer | Jun 2003 | A1 |
| 20030001342 | Isola et al. | Jul 2003 | A1 |
| 20030124595 | Lizardi | Jul 2003 | A1 |
| 20030138879 | Lambalot | Jul 2003 | A1 |
| 20030148335 | Shen et al. | Aug 2003 | A1 |
| 20030153850 | Davis et al. | Aug 2003 | A1 |
| 20030162216 | Gold | Aug 2003 | A1 |
| 20030165948 | Alsmadi et al. | Sep 2003 | A1 |
| 20030170637 | Pirrung et al. | Sep 2003 | A1 |
| 20030175947 | Liu et al. | Sep 2003 | A1 |
| 20030190744 | McGarry et al. | Oct 2003 | A1 |
| 20030205632 | Kira et al. | Nov 2003 | A1 |
| 20030215936 | Kallioniemi et al. | Nov 2003 | A1 |
| 20030224419 | Corcoran | Dec 2003 | A1 |
| 20030232348 | Jones et al. | Dec 2003 | A1 |
| 20030232382 | Brennan | Dec 2003 | A1 |
| 20030235535 | Zhou | Dec 2003 | A1 |
| 20030235852 | Roberts | Dec 2003 | A1 |
| 20040002090 | Mayer et al. | Jan 2004 | A1 |
| 20040019005 | Van Ness | Jan 2004 | A1 |
| 20040023320 | Steiner et al. | Feb 2004 | A1 |
| 20040033499 | Ilsley et al. | Feb 2004 | A1 |
| 20040050699 | Goncalves | Mar 2004 | A1 |
| 20040067492 | Peng et al. | Apr 2004 | A1 |
| 20040067493 | Matsuzaki | Apr 2004 | A1 |
| 20040082059 | Webb | Apr 2004 | A1 |
| 20040096853 | Mayer | May 2004 | A1 |
| 20040106110 | Balasubramanian | Jun 2004 | A1 |
| 20040112442 | Maerkl | Jun 2004 | A1 |
| 20040121456 | Fischer | Jun 2004 | A1 |
| 20040175822 | Timperman et al. | Sep 2004 | A1 |
| 20040219588 | Furuta | Nov 2004 | A1 |
| 20040224326 | Kim et al. | Nov 2004 | A1 |
| 20040235103 | Reznikoff et al. | Nov 2004 | A1 |
| 20040248325 | Bukusoglu | Dec 2004 | A1 |
| 20040259105 | Fan et al. | Dec 2004 | A1 |
| 20050003431 | Wucherpfennig | Jan 2005 | A1 |
| 20050014203 | Darfler et al. | Jan 2005 | A1 |
| 20050019776 | Callow et al. | Jan 2005 | A1 |
| 20050019842 | Prober et al. | Jan 2005 | A1 |
| 20050026188 | Van Kessel | Feb 2005 | A1 |
| 20050037362 | Remacle et al. | Feb 2005 | A1 |
| 20050037393 | Gunderson et al. | Feb 2005 | A1 |
| 20050042695 | Meares et al. | Feb 2005 | A1 |
| 20050048580 | Labaer | Mar 2005 | A1 |
| 20050064460 | Holliger et al. | Mar 2005 | A1 |
| 20050079520 | Wu | Apr 2005 | A1 |
| 20050100900 | Kawashima et al. | May 2005 | A1 |
| 20050130173 | Leamon et al. | Jun 2005 | A1 |
| 20050130188 | Walt | Jun 2005 | A1 |
| 20050136414 | Gunderson et al. | Jun 2005 | A1 |
| 20050164292 | Farooqui | Jul 2005 | A1 |
| 20050179746 | Roux et al. | Aug 2005 | A1 |
| 20050191656 | Drmanac et al. | Sep 2005 | A1 |
| 20050191698 | Chee et al. | Sep 2005 | A1 |
| 20050196786 | Levy | Sep 2005 | A1 |
| 20050202433 | Van Beuningen | Sep 2005 | A1 |
| 20050227271 | Kwon | Oct 2005 | A1 |
| 20050239192 | Nasarabadi et al. | Oct 2005 | A1 |
| 20050244850 | Huang | Nov 2005 | A1 |
| 20050255548 | Lipovsek et al. | Nov 2005 | A1 |
| 20050257284 | Nakajima et al. | Nov 2005 | A1 |
| 20050260653 | LaBaer | Nov 2005 | A1 |
| 20050266417 | Barany et al. | Dec 2005 | A1 |
| 20060003394 | Song | Jan 2006 | A1 |
| 20060039823 | Yamakawa et al. | Feb 2006 | A1 |
| 20060046313 | Roth | Mar 2006 | A1 |
| 20060063160 | West et al. | Mar 2006 | A1 |
| 20060079453 | Sidney et al. | Apr 2006 | A1 |
| 20060084078 | Zhao | Apr 2006 | A1 |
| 20060105352 | Qiao et al. | May 2006 | A1 |
| 20060110739 | Heyduk | May 2006 | A1 |
| 20060134669 | Casasanta | Jun 2006 | A1 |
| 20060164490 | Kim et al. | Jul 2006 | A1 |
| 20060183150 | Cohen et al. | Aug 2006 | A1 |
| 20060188875 | Cox et al. | Aug 2006 | A1 |
| 20060188901 | Barnes et al. | Aug 2006 | A1 |
| 20060194331 | Pamula et al. | Aug 2006 | A1 |
| 20060199183 | Valat et al. | Sep 2006 | A1 |
| 20060199207 | Matysiak | Sep 2006 | A1 |
| 20060211001 | Yu et al. | Sep 2006 | A1 |
| 20060216721 | Kozlov et al. | Sep 2006 | A1 |
| 20060216775 | Burkart et al. | Sep 2006 | A1 |
| 20060228758 | Muchhal et al. | Oct 2006 | A1 |
| 20060240439 | Smith et al. | Oct 2006 | A1 |
| 20060263789 | Kincaid | Nov 2006 | A1 |
| 20060275782 | Gunderson et al. | Dec 2006 | A1 |
| 20060275799 | Banerjee et al. | Dec 2006 | A1 |
| 20060281109 | Barr Ost et al. | Dec 2006 | A1 |
| 20070003954 | Kodadek et al. | Jan 2007 | A1 |
| 20070014810 | Baker et al. | Jan 2007 | A1 |
| 20070020625 | Duchaud et al. | Jan 2007 | A1 |
| 20070020640 | McCloskey et al. | Jan 2007 | A1 |
| 20070020669 | Ericsson | Jan 2007 | A1 |
| 20070023292 | Kim et al. | Feb 2007 | A1 |
| 20070026430 | Andersen et al. | Feb 2007 | A1 |
| 20070036511 | Lundquist et al. | Feb 2007 | A1 |
| 20070048812 | Moravec et al. | Mar 2007 | A1 |
| 20070054288 | Su et al. | Mar 2007 | A1 |
| 20070087360 | Boyd | Apr 2007 | A1 |
| 20070099208 | Drmanac et al. | May 2007 | A1 |
| 20070116612 | Williamson | May 2007 | A1 |
| 20070128624 | Gormley et al. | Jun 2007 | A1 |
| 20070128656 | Agrawal | Jun 2007 | A1 |
| 20070134723 | Kozlov et al. | Jun 2007 | A1 |
| 20070141718 | Bui et al. | Jun 2007 | A1 |
| 20070161020 | Luo et al. | Jul 2007 | A1 |
| 20070161029 | Li et al. | Jul 2007 | A1 |
| 20070166705 | Milton et al. | Jul 2007 | A1 |
| 20070166725 | McBride et al. | Jul 2007 | A1 |
| 20070172873 | Brenner et al. | Jul 2007 | A1 |
| 20070178503 | Jiang | Aug 2007 | A1 |
| 20070207482 | Church et al. | Sep 2007 | A1 |
| 20070231823 | McKernan | Oct 2007 | A1 |
| 20070251824 | Patton | Nov 2007 | A1 |
| 20070254305 | Paik et al. | Nov 2007 | A1 |
| 20070264656 | Kawamura | Nov 2007 | A1 |
| 20070269805 | Hogers | Nov 2007 | A1 |
| 20070280517 | De La Torre-Bueno et al. | Dec 2007 | A1 |
| 20080003586 | Hyde et al. | Jan 2008 | A1 |
| 20080009420 | Schroth et al. | Jan 2008 | A1 |
| 20080032301 | Rank et al. | Feb 2008 | A1 |
| 20080038734 | Sorge et al. | Feb 2008 | A1 |
| 20080047835 | MacConnell | Feb 2008 | A1 |
| 20080071071 | LaBaer et al. | Mar 2008 | A1 |
| 20080108082 | Rank et al. | May 2008 | A1 |
| 20080108804 | Hayashizaki et al. | May 2008 | A1 |
| 20080124252 | Marchand et al. | May 2008 | A1 |
| 20080124810 | Terbrueggen et al. | May 2008 | A1 |
| 20080128627 | Lundquist et al. | Jun 2008 | A1 |
| 20080132429 | Perov et al. | Jun 2008 | A1 |
| 20080145616 | Gharib et al. | Jun 2008 | A1 |
| 20080153086 | Wong | Jun 2008 | A1 |
| 20080160580 | Adessi et al. | Jul 2008 | A1 |
| 20080199929 | Yeung et al. | Aug 2008 | A1 |
| 20080220434 | Thomas | Sep 2008 | A1 |
| 20080220981 | McGregor | Sep 2008 | A1 |
| 20080261204 | Lexow | Oct 2008 | A1 |
| 20080280773 | Fedurco et al. | Nov 2008 | A1 |
| 20080286795 | Kawashima et al. | Nov 2008 | A1 |
| 20080293046 | Allawi et al. | Nov 2008 | A1 |
| 20080293591 | Taussig et al. | Nov 2008 | A1 |
| 20080312103 | Nemoto et al. | Dec 2008 | A1 |
| 20090005252 | Drmanac et al. | Jan 2009 | A1 |
| 20090006002 | Honisch et al. | Jan 2009 | A1 |
| 20090018024 | Church | Jan 2009 | A1 |
| 20090026082 | Rothbeig et al. | Jan 2009 | A1 |
| 20090036323 | van Eijk et al. | Feb 2009 | A1 |
| 20090062148 | Goldberg | Mar 2009 | A1 |
| 20090082212 | Williams | Mar 2009 | A1 |
| 20090099041 | Church et al. | Apr 2009 | A1 |
| 20090105959 | Braverman et al. | Apr 2009 | A1 |
| 20090117573 | Fu et al. | May 2009 | A1 |
| 20090127589 | Rothberg et al. | May 2009 | A1 |
| 20090155781 | Drmanac et al. | Jun 2009 | A1 |
| 20090169089 | Hunt et al. | Jul 2009 | A1 |
| 20090170713 | van Eijk et al. | Jul 2009 | A1 |
| 20090192044 | Fouillet | Jul 2009 | A1 |
| 20090197326 | El Gamal et al. | Aug 2009 | A1 |
| 20090202998 | Schlumpberger et al. | Aug 2009 | A1 |
| 20090215633 | van Eijk et al. | Aug 2009 | A1 |
| 20090233802 | Bignell et al. | Sep 2009 | A1 |
| 20090239232 | Kurn | Sep 2009 | A1 |
| 20090253163 | Xie et al. | Oct 2009 | A1 |
| 20090253581 | van Eijk et al. | Oct 2009 | A1 |
| 20090253582 | Pena et al. | Oct 2009 | A1 |
| 20090264299 | Drmanac et al. | Oct 2009 | A1 |
| 20090280487 | Hung et al. | Nov 2009 | A1 |
| 20090283407 | Van Eijk | Nov 2009 | A1 |
| 20090289184 | Deininger | Nov 2009 | A1 |
| 20090291854 | Weisinger-Mayr et al. | Nov 2009 | A1 |
| 20090003052 | Cantor et al. | Dec 2009 | A1 |
| 20090312193 | Kim et al. | Dec 2009 | A1 |
| 20090321262 | Adachi et al. | Dec 2009 | A1 |
| 20100009871 | Reed et al. | Jan 2010 | A1 |
| 20100014537 | Jacquet et al. | Jan 2010 | A1 |
| 20100035249 | Hayashizaki | Feb 2010 | A1 |
| 20100055733 | Lutolf et al. | Mar 2010 | A1 |
| 20100069263 | Shendure et al. | Mar 2010 | A1 |
| 20100096266 | Kim et al. | Apr 2010 | A1 |
| 20100099103 | Hsieh et al. | Apr 2010 | A1 |
| 20100105052 | Drmanac et al. | Apr 2010 | A1 |
| 20100105112 | Heltze et al. | Apr 2010 | A1 |
| 20100111768 | Banerjee et al. | May 2010 | A1 |
| 20100113302 | Williams | May 2010 | A1 |
| 20100120043 | Sood et al. | May 2010 | A1 |
| 20100120097 | Matz et al. | May 2010 | A1 |
| 20100120098 | Grunenwald et al. | May 2010 | A1 |
| 20100126862 | Sabin et al. | May 2010 | A1 |
| 20100129874 | Mitra et al. | May 2010 | A1 |
| 20100137143 | Rothberg et al. | Jun 2010 | A1 |
| 20100145037 | Makarov et al. | Jun 2010 | A1 |
| 20100151464 | Stuelpnagel et al. | Jun 2010 | A1 |
| 20100151511 | Gereenizer et al. | Jun 2010 | A1 |
| 20100159446 | Haff et al. | Jun 2010 | A1 |
| 20100173384 | Johnsson et al. | Jul 2010 | A1 |
| 20100184614 | Ye et al. | Jul 2010 | A1 |
| 20100184618 | Namsaraev et al. | Jul 2010 | A1 |
| 20100210475 | Lee et al. | Aug 2010 | A1 |
| 20100227329 | Cuppens | Sep 2010 | A1 |
| 20100267590 | Grudzien et al. | Oct 2010 | A1 |
| 20100273219 | May et al. | Oct 2010 | A1 |
| 20100282617 | Rothberg et al. | Nov 2010 | A1 |
| 20100303722 | Jin et al. | Dec 2010 | A1 |
| 20110024511 | Rietzler et al. | Feb 2011 | A1 |
| 20110027772 | Ahn et al. | Feb 2011 | A1 |
| 20110028685 | Purkayastha et al. | Feb 2011 | A1 |
| 20110033854 | Drmanac et al. | Feb 2011 | A1 |
| 20110045462 | Fu et al. | Feb 2011 | A1 |
| 20110048951 | Wu | Mar 2011 | A1 |
| 20110059436 | Hardin et al. | Mar 2011 | A1 |
| 20110059865 | Smith et al. | Mar 2011 | A1 |
| 20110086774 | Dunaway | Apr 2011 | A1 |
| 20110111409 | Sinicropi et al. | May 2011 | A1 |
| 20110151451 | Lemaire et al. | Jun 2011 | A1 |
| 20110152111 | Fan et al. | Jun 2011 | A1 |
| 20110172115 | Thompson et al. | Jul 2011 | A1 |
| 20110177518 | Kartalov et al. | Jul 2011 | A1 |
| 20110201515 | Webster et al. | Aug 2011 | A1 |
| 20110207134 | Faham et al. | Aug 2011 | A1 |
| 20110223613 | Gut | Sep 2011 | A1 |
| 20110244448 | Shirai et al. | Oct 2011 | A1 |
| 20110245101 | Chee et al. | Oct 2011 | A1 |
| 20110245111 | Chee | Oct 2011 | A1 |
| 20110275077 | James | Nov 2011 | A1 |
| 20110287435 | Grunenwald et al. | Nov 2011 | A1 |
| 20120021930 | Schoen et al. | Jan 2012 | A1 |
| 20120046175 | Rodesch et al. | Feb 2012 | A1 |
| 20120046178 | Van Den Boom et al. | Feb 2012 | A1 |
| 20120065081 | Chee | Mar 2012 | A1 |
| 20120077693 | Cazalis et al. | Mar 2012 | A1 |
| 20120129248 | Chee et al. | May 2012 | A1 |
| 20120135871 | van Eijk et al. | May 2012 | A1 |
| 20120142014 | Cai | Jun 2012 | A1 |
| 20120157322 | Myllykangas | Jun 2012 | A1 |
| 20120160683 | Ye et al. | Jun 2012 | A1 |
| 20120195810 | Cohen et al. | Aug 2012 | A1 |
| 20120196297 | Yost et al. | Aug 2012 | A1 |
| 20120202698 | van Eijk et al. | Aug 2012 | A1 |
| 20120202704 | Fan et al. | Aug 2012 | A1 |
| 20120220479 | Ericsson et al. | Aug 2012 | A1 |
| 20120245053 | Shirai et al. | Sep 2012 | A1 |
| 20120252702 | Muratani et al. | Oct 2012 | A1 |
| 20120258871 | Kozlov et al. | Oct 2012 | A1 |
| 20120270305 | Reed et al. | Oct 2012 | A1 |
| 20120270748 | Chee et al. | Oct 2012 | A1 |
| 20120279954 | Ceremony et al. | Nov 2012 | A1 |
| 20120289414 | Mitra et al. | Nov 2012 | A1 |
| 20120301925 | Belyaev | Nov 2012 | A1 |
| 20130005594 | Terbrueggen et al. | Jan 2013 | A1 |
| 20130005600 | Olek | Jan 2013 | A1 |
| 20130035239 | Kong et al. | Feb 2013 | A1 |
| 20130052331 | Kram et al. | Feb 2013 | A1 |
| 20130065768 | Zheng et al. | Mar 2013 | A1 |
| 20130079232 | Kain et al. | Mar 2013 | A1 |
| 20130096033 | Routenberg | Apr 2013 | A1 |
| 20130109595 | Routenberg | May 2013 | A1 |
| 20130122516 | Hong et al. | May 2013 | A1 |
| 20130171621 | Luo et al. | Jul 2013 | A1 |
| 20130202718 | Pepin et al. | Aug 2013 | A1 |
| 20130211249 | Barnett et al. | Aug 2013 | A1 |
| 20130244884 | Jacobson et al. | Sep 2013 | A1 |
| 20130260372 | Buermann et al. | Oct 2013 | A1 |
| 20130261019 | Lin et al. | Oct 2013 | A1 |
| 20130302801 | Asbury et al. | Nov 2013 | A1 |
| 20140065609 | Hicks et al. | Mar 2014 | A1 |
| 20140066318 | Frisen et al. | Mar 2014 | A1 |
| 20140121118 | Warner | May 2014 | A1 |
| 20140155274 | Xie et al. | Jun 2014 | A1 |
| 20140227705 | Vogelstein et al. | Aug 2014 | A1 |
| 20140342921 | Weiner | Nov 2014 | A1 |
| 20150051085 | Vogelstein et al. | Feb 2015 | A1 |
| 20150072867 | Soldatov | Mar 2015 | A1 |
| 20150087027 | Makarov et al. | Mar 2015 | A1 |
| 20150344942 | Frisen et al. | Dec 2015 | A1 |
| 20160003812 | Porreca et al. | Jan 2016 | A1 |
| 20160024576 | Chee | Jan 2016 | A1 |
| 20160138091 | Chee et al. | May 2016 | A1 |
| 20160145677 | Chee et al. | May 2016 | A1 |
| 20160298180 | Chee | Oct 2016 | A1 |
| 20160304952 | Boyden et al. | Oct 2016 | A1 |
| 20160333403 | Chee | Nov 2016 | A1 |
| 20170058339 | Chee | Mar 2017 | A1 |
| 20170058340 | Chee | Mar 2017 | A1 |
| 20170058345 | Chee | Mar 2017 | A1 |
| 20170088881 | Chee | Mar 2017 | A1 |
| 20170166962 | van Eijk et al. | Jun 2017 | A1 |
| 20180094316 | Scott et al. | Apr 2018 | A1 |
| 20180112209 | Eshoo | Apr 2018 | A1 |
| 20180201980 | Chee et al. | Jul 2018 | A1 |
| 20180247017 | van Eijk et al. | Aug 2018 | A1 |
| 20180291439 | van Eijk et al. | Oct 2018 | A1 |
| 20190017106 | Frisen et al. | Jan 2019 | A1 |
| 20190024153 | Frisen et al. | Jan 2019 | A1 |
| 20190024154 | Frisen et al. | Jan 2019 | A1 |
| 20190203275 | Friesen et al. | Jul 2019 | A1 |
| 20190264268 | Frisen et al. | Aug 2019 | A1 |
| 20200109443 | Chee | Apr 2020 | A1 |
| 20200277663 | Ramachandran Iyer et al. | Sep 2020 | A1 |
| 20200277664 | Frenz | Sep 2020 | A1 |
| 20200283852 | Oliphant et al. | Sep 2020 | A1 |
| 20200354774 | Church et al. | Nov 2020 | A1 |
| 20200399687 | Frisen et al. | Dec 2020 | A1 |
| 20200407781 | Schnall-Levin et al. | Dec 2020 | A1 |
| 20210010068 | Chee et al. | Jan 2021 | A1 |
| 20210010070 | Schnall-Levin et al. | Jan 2021 | A1 |
| 20210017583 | Chee et al. | Jan 2021 | A1 |
| 20210140982 | Uytingco | May 2021 | A1 |
| 20210172007 | Chee et al. | Jun 2021 | A1 |
| 20210189475 | Tentori et al. | Jun 2021 | A1 |
| 20210198741 | Williams | Jul 2021 | A1 |
| 20210199660 | Williams et al. | Jul 2021 | A1 |
| 20210214785 | Stoeckius | Jul 2021 | A1 |
| 20210222241 | Bharadwaj | Jul 2021 | A1 |
| 20210222242 | Ramachandran Iyer | Jul 2021 | A1 |
| 20210222253 | Uytingco | Jul 2021 | A1 |
| 20210223227 | Stoeckius | Jul 2021 | A1 |
| 20210230681 | Patterson et al. | Jul 2021 | A1 |
| 20210230692 | Daugharthy et al. | Jul 2021 | A1 |
| 20210238664 | Bava | Aug 2021 | A1 |
| 20210238675 | Bava | Aug 2021 | A1 |
| 20210238680 | Bava | Aug 2021 | A1 |
| 20210247316 | Bava | Aug 2021 | A1 |
| 20210262019 | Alvarado Martinez et al. | Aug 2021 | A1 |
| 20210285036 | Yin et al. | Sep 2021 | A1 |
| 20210285046 | Chell | Sep 2021 | A1 |
| 20210292748 | Frisen et al. | Sep 2021 | A1 |
| 20210292822 | Frisen et al. | Sep 2021 | A1 |
| 20210317510 | Chee et al. | Oct 2021 | A1 |
| 20210317524 | Lucero | Oct 2021 | A1 |
| 20210324457 | Ramachandran Iyer et al. | Oct 2021 | A1 |
| 20210332424 | Schnall-Levin | Oct 2021 | A1 |
| 20210332425 | Pfeiffer et al. | Oct 2021 | A1 |
| 20210348221 | Chell et al. | Nov 2021 | A1 |
| 20220002791 | Frisen et al. | Jan 2022 | A1 |
| 20220010367 | Ramachandran Iyer et al. | Jan 2022 | A1 |
| 20220017951 | Ramachandran Iyer et al. | Jan 2022 | A1 |
| 20220025446 | Shah | Jan 2022 | A1 |
| 20220025447 | Tentori et al. | Jan 2022 | A1 |
| 20220033888 | Schnall-Levin et al. | Feb 2022 | A1 |
| 20220049293 | Frenz et al. | Feb 2022 | A1 |
| 20220049294 | Uytingco et al. | Feb 2022 | A1 |
| 20220064630 | Bent et al. | Mar 2022 | A1 |
| 20220081728 | Williams | Mar 2022 | A1 |
| 20220090058 | Frisen et al. | Mar 2022 | A1 |
| 20220090175 | Uytingco et al. | Mar 2022 | A1 |
| 20220090181 | Gallant et al. | Mar 2022 | A1 |
| 20220098576 | Dadhwal | Mar 2022 | A1 |
| 20220098661 | Chew et al. | Mar 2022 | A1 |
| 20220106632 | Galonska et al. | Apr 2022 | A1 |
| 20220106633 | Engblom et al. | Apr 2022 | A1 |
| 20220112486 | Ramachandran Iyer et al. | Apr 2022 | A1 |
| 20220119869 | Ramachandran Iyer et al. | Apr 2022 | A1 |
| 20220127659 | Frisen et al. | Apr 2022 | A1 |
| 20220127666 | Katiraee et al. | Apr 2022 | A1 |
| 20220127672 | Stoeckius | Apr 2022 | A1 |
| 20220145361 | Frenz et al. | May 2022 | A1 |
| 20220154255 | Chee et al. | May 2022 | A1 |
| 20220170083 | Khaled et al. | Jun 2022 | A1 |
| 20220195422 | Gallant et al. | Jun 2022 | A1 |
| 20220195505 | Frisen et al. | Jun 2022 | A1 |
| 20220213526 | Frisen et al. | Jul 2022 | A1 |
| 20220241780 | Tentori et al. | Aug 2022 | A1 |
| 20220267844 | Ramachandran Iyer et al. | Aug 2022 | A1 |
| 20220282329 | Chell et al. | Sep 2022 | A1 |
| 20220290217 | Frenz et al. | Sep 2022 | A1 |
| 20220298560 | Frisen et al. | Sep 2022 | A1 |
| 20220325325 | Chee et al. | Oct 2022 | A1 |
| 20220326251 | Uytingco et al. | Oct 2022 | A1 |
| 20220333192 | Uytingco | Oct 2022 | A1 |
| 20220333195 | Schnall-Levin et al. | Oct 2022 | A1 |
| 20220348905 | Dadhwal | Nov 2022 | A1 |
| 20220348992 | Stoeckius et al. | Nov 2022 | A1 |
| Number | Date | Country |
|---|---|---|
| 1680604 | Oct 2005 | CN |
| 1981188 | Jun 2007 | CN |
| 101221182 | Jul 2008 | CN |
| 0901631 | Mar 1999 | EP |
| 0961110 | Dec 1999 | EP |
| 1782737 | May 2007 | EP |
| 1878502 | Jan 2008 | EP |
| 1910562 | Apr 2008 | EP |
| 1923471 | May 2008 | EP |
| 1929039 | Jun 2008 | EP |
| 1966393 | Sep 2008 | EP |
| 2002017 | Dec 2008 | EP |
| 2292788 | Mar 2011 | EP |
| 2302070 | Mar 2011 | EP |
| 2350648 | Aug 2011 | EP |
| 2363504 | Sep 2011 | EP |
| 2580351 | Apr 2013 | EP |
| 2789696 | Oct 2014 | EP |
| 2963127 | Jan 2016 | EP |
| 3045544 | Jul 2016 | EP |
| 3239304 | Nov 2017 | EP |
| 2007-014297 | Jan 2007 | JP |
| 2007-074967 | Mar 2007 | JP |
| 2009-036694 | Feb 2009 | JP |
| 2011-182702 | Sep 2011 | JP |
| 2013-544498 | Dec 2013 | JP |
| 2014-217381 | Nov 2014 | JP |
| 10-2009-0000812 | Jan 2009 | KR |
| 10-2009-0081260 | Jul 2009 | KR |
| 2145635 | Feb 2000 | RU |
| 2270254 | Feb 2006 | RU |
| 2410439 | Jan 2011 | RU |
| WO 1989010977 | Nov 1989 | WO |
| WO 1991006678 | May 1991 | WO |
| WO 1995023875 | Sep 1995 | WO |
| WO 1995025116 | Sep 1995 | WO |
| WO 1995035505 | Dec 1995 | WO |
| WO 1997031256 | Aug 1997 | WO |
| WO 1998044151 | Oct 1998 | WO |
| WO 1999032654 | Jul 1999 | WO |
| WO 1999044062 | Sep 1999 | WO |
| WO 1999044063 | Sep 1999 | WO |
| WO 1999063385 | Dec 1999 | WO |
| WO 1999067641 | Dec 1999 | WO |
| WO 200017390 | Mar 2000 | WO |
| WO 2000018957 | Apr 2000 | WO |
| WO 2000024940 | May 2000 | WO |
| WO 200106012 | Jan 2001 | WO |
| WO 2001007915 | Feb 2001 | WO |
| WO 2001009363 | Feb 2001 | WO |
| WO 2001042796 | Jun 2001 | WO |
| WO 2001046402 | Jun 2001 | WO |
| WO 2001059161 | Aug 2001 | WO |
| WO 2001090415 | Nov 2001 | WO |
| WO 2001096608 | Dec 2001 | WO |
| WO 2002024952 | Mar 2002 | WO |
| WO 2002040874 | May 2002 | WO |
| WO 2002059355 | Aug 2002 | WO |
| WO 2002059364 | Aug 2002 | WO |
| WO 2002077283 | Oct 2002 | WO |
| WO 2002088396 | Nov 2002 | WO |
| WO 2003002979 | Jan 2003 | WO |
| WO 2003003810 | Jan 2003 | WO |
| WO 2003008538 | Jan 2003 | WO |
| WO 2003010176 | Feb 2003 | WO |
| WO 2003102233 | Dec 2003 | WO |
| WO 2003106973 | Dec 2003 | WO |
| WO 2004015080 | Feb 2004 | WO |
| WO 2004028955 | Apr 2004 | WO |
| WO 2004055159 | Jul 2004 | WO |
| WO 2004067759 | Aug 2004 | WO |
| WO 2004108268 | Dec 2004 | WO |
| WO 2005007814 | Jan 2005 | WO |
| WO 2005010145 | Feb 2005 | WO |
| WO 2005026387 | Mar 2005 | WO |
| WO 2005042759 | May 2005 | WO |
| WO 2005067648 | Jul 2005 | WO |
| WO 2005113804 | Dec 2005 | WO |
| WO 2006020515 | Feb 2006 | WO |
| WO 2006056861 | Jun 2006 | WO |
| WO 2006064199 | Jun 2006 | WO |
| WO 2006065597 | Jun 2006 | WO |
| WO 2006074351 | Jul 2006 | WO |
| WO 2006084130 | Aug 2006 | WO |
| WO 2006117541 | Nov 2006 | WO |
| WO 2006124771 | Nov 2006 | WO |
| WO 2006137733 | Dec 2006 | WO |
| WO 2007000669 | Jan 2007 | WO |
| WO 2007010251 | Jan 2007 | WO |
| WO 2007030373 | Mar 2007 | WO |
| WO 2007037678 | Apr 2007 | WO |
| WO 2007041689 | Apr 2007 | WO |
| WO 2007060599 | May 2007 | WO |
| WO 2007073165 | Jun 2007 | WO |
| WO 2007073171 | Jun 2007 | WO |
| WO 2007073271 | Jun 2007 | WO |
| WO 2007076128 | Jul 2007 | WO |
| WO 2007076726 | Jul 2007 | WO |
| WO 2007114693 | Oct 2007 | WO |
| WO 2007120241 | Oct 2007 | WO |
| WO 2007139766 | Dec 2007 | WO |
| WO 2007145612 | Dec 2007 | WO |
| WO 2008022332 | Feb 2008 | WO |
| WO 2008069906 | Jun 2008 | WO |
| WO 2008157801 | Dec 2008 | WO |
| WO 2009032167 | Mar 2009 | WO |
| WO 2009036525 | Mar 2009 | WO |
| WO 2009152928 | Dec 2009 | WO |
| WO 2009156725 | Dec 2009 | WO |
| WO 2010019826 | Feb 2010 | WO |
| WO 2010027870 | Mar 2010 | WO |
| WO 2010053587 | May 2010 | WO |
| WO 2010126614 | Nov 2010 | WO |
| WO 2010127186 | Nov 2010 | WO |
| WO 2011008502 | Jan 2011 | WO |
| WO 2011014879 | Feb 2011 | WO |
| WO 2011062933 | May 2011 | WO |
| WO 2011071943 | Jun 2011 | WO |
| WO 2011094669 | Aug 2011 | WO |
| WO 2011102903 | Aug 2011 | WO |
| WO 2011127006 | Oct 2011 | WO |
| WO 2011127099 | Oct 2011 | WO |
| WO 2011143583 | Nov 2011 | WO |
| WO 2011155833 | Dec 2011 | WO |
| WO 2012022975 | Feb 2012 | WO |
| WO 2012049316 | Apr 2012 | WO |
| WO 2012058096 | May 2012 | WO |
| WO 2012071428 | May 2012 | WO |
| WO 2012083225 | Jun 2012 | WO |
| WO 2012129242 | Sep 2012 | WO |
| WO 2012139110 | Oct 2012 | WO |
| WO 2012140224 | Oct 2012 | WO |
| WO 2012142213 | Oct 2012 | WO |
| WO 2012148477 | Nov 2012 | WO |
| WO 2012159089 | Nov 2012 | WO |
| WO 2012168003 | Dec 2012 | WO |
| WO 2013033271 | Mar 2013 | WO |
| WO 2013090390 | Jun 2013 | WO |
| WO 2013123442 | Aug 2013 | WO |
| WO 2013138510 | Sep 2013 | WO |
| WO 2013142389 | Sep 2013 | WO |
| WO 2013150083 | Oct 2013 | WO |
| WO 2014060483 | Apr 2014 | WO |
| WO 2014210223 | Dec 2014 | WO |
| WO 2014210225 | Dec 2014 | WO |
| WO 2020076979 | Apr 2020 | WO |
| WO 2020123305 | Jun 2020 | WO |
| WO 2020123309 | Jun 2020 | WO |
| WO 2020123311 | Jun 2020 | WO |
| WO 2020123316 | Jun 2020 | WO |
| WO 2020123317 | Jun 2020 | WO |
| WO 2020123318 | Jun 2020 | WO |
| WO 2020123319 | Jun 2020 | WO |
| WO 2020190509 | Sep 2020 | WO |
| WO 2020198071 | Oct 2020 | WO |
| WO 2020219901 | Oct 2020 | WO |
| WO 2021091611 | May 2021 | WO |
| WO 2021092433 | May 2021 | WO |
| WO 2021097255 | May 2021 | WO |
| WO 2021133849 | Jul 2021 | WO |
| WO 2021142233 | Jul 2021 | WO |
| WO 2021168261 | Aug 2021 | WO |
| WO 2021168278 | Aug 2021 | WO |
| WO 2021216708 | Oct 2021 | WO |
| WO 2021225900 | Nov 2021 | WO |
| WO 2021236625 | Nov 2021 | WO |
| WO 2021236929 | Nov 2021 | WO |
| WO 2021237056 | Nov 2021 | WO |
| WO 2021237087 | Nov 2021 | WO |
| WO 2021242834 | Dec 2021 | WO |
| WO 2021247543 | Dec 2021 | WO |
| WO 2021247568 | Dec 2021 | WO |
| WO 2021252499 | Dec 2021 | WO |
| WO 2021252576 | Dec 2021 | WO |
| WO 2021252591 | Dec 2021 | WO |
| WO 2021263111 | Dec 2021 | WO |
| WO 2022025965 | Feb 2022 | WO |
| WO 2022060798 | Mar 2022 | WO |
| WO 20220606953 | Mar 2022 | WO |
| WO 2022087273 | Apr 2022 | WO |
| WO 2022098810 | May 2022 | WO |
| WO 2022099037 | May 2022 | WO |
| WO 2022109181 | May 2022 | WO |
| WO 2022140028 | Jun 2022 | WO |
| WO 2022147005 | Jul 2022 | WO |
| WO 2022147296 | Jul 2022 | WO |
| WO 2022164615 | Aug 2022 | WO |
| WO 2022178267 | Aug 2022 | WO |
| WO 2022198068 | Sep 2022 | WO |
| WO 2022221425 | Oct 2022 | WO |
| Entry |
|---|
| U.S. Appl. No. 60/416,118, filed Oct. 3, 2002, Fan et al. |
| U.S. Appl. No. 62/839,575, filed Apr. 26, 2019, Bent et al. |
| [No Author Listed], “HuSNP Mapping Assay User's Manual,” Affymetrix Part No. 90094 (Affymetrix, Santa Clara, Calif), GeneChip, 2000, 104 pages. |
| [No Author Listed], “Microarray technologies have excellent possibilities in genomics-related researches,” Science Tools From Amersham Pharmacia Biotech, 1998, 3(4): 8 pages (with English Translation). |
| Adessi et al., “Solid phase DNA amplification: characterisation of primer attachment and amplification mechanisms,” Nucl. Acids Res., Oct. 2000, 28(20):E87, 8 pages. |
| Affymetrix, “GeneChip Human Genome U133 Set,” retrieved from the Internet: on the World Wide Web at affymetrix.com/support/technical/datasheets/hgu133_datasheet.pdf, retrieved on Feb. 26, 2003. |
| Affymetrix, “Human Genome U95Av2,” Internet Citation, retrieved from the internet: on the World Wide Web affymetrix.com, retrieved on Oct. 2, 2002. |
| Agbavwe et al., “Efficiency, error and yield in light-directed maskless synthesis of DNA microarrays,” Journal of Nanobiotechnology, Dec. 2011, 9:57, 17 pages. |
| Ahern et al., “Biochemical, Reagents Kits Offer Scientists Good Return on Investment,” The Scientist, 1995, 9(15):20, 7 pages. |
| Akeroyd, “Click chemistry for the preparation of advanced macromolecular architectures,” Stellenbosch University, PhD Dissertation, Mar. 2010, 138 pages. |
| Albretsen et al., “Applications of magnetic beads with covalently attached oligonucleotides in hybridization: Isolation and detection of specific measles virus mRNA from a crude cell lysate”, Anal. Biochem. 189:40-50, 1990. |
| Albretsen et al., “Optimal conditions for hybridization with oligonucleotides: a study with myc-oncogene DNA probes,” Anal Biochem., Apr. 1988. 170(1): 193-202. |
| Allawi and SantaLucia, “Thermodynamics and NMR of Internal GâT Mismatches in DNA,” Biochemistry, 1996, 36:10581-10594. |
| Altaras et al., “Production and formulation of adenovirus vectors,” Adv Biochem Eng Biotechnol., Nov. 2005, 99:193-260. |
| Anderson et al., “Microarrayed Compound Screening to Identify Activators and Inhibitors of AMP-Activated Protein Kinase,” J. of Biomolecular Screening, 2004, 9:112. |
| Andersson et al., “Analysis of protein expression in cell microarrays: a tool for antibody-based proteomics.,” J Histochem Cytochem., 4(12): 1413-1423, 2006. |
| Andresen et al., “Deciphering the Antibodyome—Peptide Arrays for Serum Antibody Biomarker Diagnostics,” Current Proteomics, 6(1), 1-12, 2009. |
| Andresen et al., “Helicase-dependent amplification: use in OnChip amplification and potential for point-of-care diagnostics,” Expert Rev Mol Diagn., Oct. 2009, 9(7):645-650. |
| Angenendt et al., “Cell-free Protein expression and functional assay in a nanowell chip format,” Analytical Chemistry, 2004, 76(7):1844-49. |
| Angenendt et al., “Generation of High Density Protein Microarrays by Cell-free in Situ Expression of Unpurified PCR Products,” Molecular and Cellular Proteomics, (2006) Ch. 5.9, pp. 1658-1666. |
| Armani et al, “2D-PCR: a method of mapping DNA in tissue sections.” Lab on a Chip, 2009, 9(24):3526-34. |
| Atkinson, Overview of Translation: Lecture Manuscript, U of Texas (2000) DD. 6.1-6.8. |
| Azioune et al., “Simple and rapid process for single cell micro-patterning,” Lab Chip, Jun. 2009, 9(11):1640-1642. |
| Bains et al, “A Novel Method for Nucleic Acid Sequence Determination”, Journal of Theoretical Biology, 1988, 135(3), 303-7. |
| Baird et al., “Rapid SNP Discovery and Genetic Mapping Using Sequenced RAD markers,” PLOS One, 2008, 3(10):e3376. |
| Barbie et al., “Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1,” Nature, Nov. 2009, 462(7269): 108-12. |
| Barnes, “PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates.,” Proc. Natl. Acad. Sci USA, 91: 2216-2220, 1994. |
| Baugh et al, “Quantitative analysis of mRNA amplification by in vitro transcription,” Nucleic Acids Res., 2001, 29:5:e29. |
| Beattie et al., “Advances in genosensor research,” Clin Chem., May 1995, 41(5):700-6. |
| Beier et al., “Versatile derivatisation of solid support media for covalent bonding on DNA-microchips,” Nucleic Acids Res., May 1999, 27(9):1970-7. |
| Bell, “A Simple Way to Treat PCR Products Prior to Sequencing Using ExoSAP-IT,” Biotechniques, 2008, vol. 44, No. 6. |
| Bentley et al, “Accurate whole human genome sequencing using reversible terminator chemistry”, Nature, 2008, 456:53-59. |
| Berger et al., “Universal bases for hybridization, replication and chain termination,” Nucleic Acid Res., Aug. 2000, 28(15):2911-2914. |
| Bielas et al., “Human cancers express a mutator phenotype,” Proc. Natl. Acad. Sci. USA, 2006, 103(48): 18238-18242. |
| Bielas et al., “Quantification of random genomic mutations,” Nat. Methods, 2005, 2(4):285-290. |
| Biol.wwu.edu [online], “Principles of Di-Base Sequencing and the Advantages of Color Space Analysis in the SOLiD System,” 2008, retrieved on Mar. 11, 2022, retrieved from URL<https://biol.wwu.edu//young/470/stuff/abi-solid.pdf>, 4 pages. |
| Birney, et al, “Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project,” Nature, 2007, 447:799-816. |
| Blair et al., “Microarray temperature optimization using hybridization kinetics,” Methods Mol Biol., 2009, 529:171-96. |
| Blanchard et al., “High-density oligonucleotide arrays,” Biosensors & Bioelectronics, 1996, 11(6-7):687-690. |
| Blanco et al., “A practical approach to FRET-based PNA fluorescence in situ hybridization,” Methods, Dec. 2010, 52(4):343-51. |
| Biandini et al., “Animal models of Parkinson's disease,” FEBS J., Apr. 2012, 279(7):1156-66. |
| Blokzijl et al., “Profiling protein expression and interactions: proximity ligation as a tool for personalized medicine,” J Intern. Med., 2010, 268:232-245. |
| Blow, “Tissue Issues,” Nature, 448(23), 959-962, 2007. |
| Boeke et al., “Transcription and reverse transcription of retrotransposons,” Annu Rev Microbiol, 1989, 43:403-34. |
| Bonfield et al., “The application of numerical estimates of base calling accuracy to DNA sequencing projects,” Nucleic Acids Research, 1995, 23(8): 1406-1410. |
| Bos et al., “In Vitro Evaluation of DNA-DNA Hybridization as a Two-Step Approach in Radioimmunotherapy of Cancer,” Cancer Res., Jul. 1, 1994, 54(13):3479-3486. |
| Boutros et al., “The art and design of genetic screens: RNA interference,” Nat Rev Genet., Jul. 2008, 9(7):554-66. |
| Bowtell, “The genesis and evolution of high-grade serous ovarian cancer,” Nat. Rev. Cancer, 2010, (11 ):803-808 ABSTRACT. |
| Brandon et al., “Mitochondrial mutations in cancer,” Oncogene, 2006, 25(34):4647-4662. |
| Brenner et al, “In vitro cloning of complex mixtures of DNA on microbeads: physical separation of differentially expressed cDNAs,” Proc. Natl. Acad. Sci. USA, 2000, 97, 1665-1670. |
| Brenner et al., “Gene expression analysis bv massively parallel signature sequencing (MPSS) on microbead arrays”, Nat. Biotech. 18: 630-634, 2000. |
| Brockman et al., “Quality scores and SNP detection in sequencing-by-synthesis systems,” Methods, 2008, 18:763-770. |
| Brow, “35—The Cleavase I enzyme for mutation and polymorphism scanning,” PCR Applications Protocols for Functional Genomics, 1999, pp. 537-550. |
| Brown et al., “Retroviral integration: structure of the initial covalent product and its precursor, and a role for the viral IN protein,” Proc Natl Acad Sci USA, Apr. 1989, 86(8):2525-9. |
| Bullard et al., “Direct comparison of nick-joining activity of the nucleic acid ligases front bacteriophage T4,” Biochem. J. 2006, 398:135-144. |
| Burns et al., “Well-less, gel-permeation formats for ultra-HTS,” DDT, 2001, 6(12):S40-S47. |
| Burton et al., “Coverslip Mounted-Immersion Cycled in Situ RT-PCR for the Localization of mRNA in Tissue Sections,” Biotechniques, 1998, 24; pp. 92-100. |
| Calvert, “Materials science. Printing cells,” Science, Oct. 2007, 318(5848):208-209. |
| Carlson et al., “Function and Structure of a Prokaryotic Formylglycine-generating Enzyme,” J. of Biological Chemistry, 2008, 283(29):20117-125. |
| Carter et al., “Stabilization of an optical microscope to 0.1 nm in three dimensions,” Applied Optics, 2007, 46:421-427. |
| Cerritelli et al., “Ribonuclease H: the enzymes in eukaryotes,” FEBS Journal, Mar. 2009, 276(6):1494-505. |
| Cerutti et al., “Generation of sequence-specific, high affinity anti-DNA antibodies,” Journal of Biological Chemistry, 2001, 276(16):12769-12773. |
| Cha et al., “Specificity, Efficiency and Fidelity of PCR,” Genome Res., 1993, 3:518-29. |
| Chandra et al., “Cell-free synthesis-based protein microarrays and their applications,” Proteomics, 2009, 5(6):717-30. |
| Chatterjee et al., “Protein Microarray On-Demand: A Novel Protein Microarray System,” PLos One, 2008, 3(9):e3265. |
| Chatterjee, et al., “Mitochondrial DNA mutations in human cancer. Oncogene,” 2006, 25(34):4663-4674. |
| Chen et al., “A Homogeneous, Ligase-mediated DNA diagnostic test,” Genome research, 1998, 8(5):549-556. |
| Chen et al., “DNA hybridization detection in a microfluidic Channel using two fluorescently labelled nucleic acid probes,” Biosensors and Bioelectronics, 2008, 23:1878-1882. |
| Chen et al., “Geometric control of cell life and death,” Science, May 1997, 276(5317):1425-1428. |
| Chen et al., “Parallel single nucleotide polymorphism genotyping by surface invasive cleavage with universal detection,” Anal Chem., Apr. 2005, 77(8):2400-5. |
| Cheng et al., “Sensitive Detection of Small Molecules by Competitive Immunomagnetic-Proximity Ligation Assay,” Anal Chem, 2012, 84:2129-2132. |
| Cheng, “The Contrast Formation in Optical Microscopy,” Handbook of Biological Confocal Microscopy, 2006, Chapter 8, pp. 162-206. |
| Chester et al. “Dimethyl sulfoxide-mediated primer Tm reduction: a method for analyzing the role of renaturation temperature in the polymerase chain reaction,” Anal Biochem, Mar. 1993, 209(2):284-90. |
| Chial, “DNA Sequencing Technologies Key to the Human Genome Project,” Nature Education, 2008, 1(1):219, 7 pages. |
| Chiang et al., “NFkappaB translocation in human microvessel endothelial cells using a four-compartment subcellular protein redistribution assay,” J Biochem Biophys Methods, Nov. 2000, 46(1-2):53-68. |
| Chrisey et al., “Covalent attachment of synthetic DNA to self-assembled monolayer films,” Nucleic Acids Res., Aug. 1996, 24(15):3031-9. |
| Chung et al., “Imaging single-cell signaling dynamics with a deterministic high-density single-cell trap array,” Anal Chem, Sep. 2011, 83(18):7044-7052. |
| Ciaccio et al., “Systems analysis of EGF receptor signaling dynamics with microwestern arrays,” Nat Methods, Feb. 2010, 7(2):148-55. |
| Cockroft et al., “A single-molecule nanopore device detects DNA polymerase activity with single-nucleotide resolution,” J Am Chem Soc., Jan. 2008, 130(3):818-20. |
| Colegio et al., “In vitro transposition system for efficient generation of random mutants of Campylobacter jejuni,” J Bacteriol., Apr. 2001, 183(7):2384-8. |
| Condina et al., “A sensitive magnetic bead method for the detection and identification of tyrosine phosphorylation in proteins by MALDI-TOF/TOF MS,” Proteomics, 2009, 9:3047-3057. |
| Constantine et al., “Use of genechip high-density oligonucleotide arrays for gene expression monitoring,” Life Sceience News, Amersham Life Science; 11-14, 1998. |
| Cook et al., “The effects of secondare structure and O2 on the formation of direct strand breaks upon UV irradiation of 5-bromodeoxyuridine-containing oligonucleotides,” Chem Biol., Jul. 1999, 6(7):451-9. |
| Copeland et al., “Mitochondrial DNA Alterations in Cancer,” Cancer Invest., 2002, 557-569 |
| Cornett et al., “MALDI imaging mass spectrometry: molecular snapshots of biochemical systems,” Nature Methods, 2007, 4(10):828-833. |
| Cox et al., “Tissue subcellular fractionation and protein extraction for use in mass-spectrometry-based proteomics,” Nat Protoc., 2006, 1(4):1872-8. |
| Craig, “Transposon Tn7,” Curr Top Microbiol Immunol., 1996, 204:27-48. |
| Craig, “V(D)J recombination and transposition: closer than expected,” Science, Mar. 1996, 271(5255):1512, 1 page. |
| Cujec et al. “Selection of v-abl tyrosine kinase substate sequences from randomized peptide and cellular proteomic libraries using mRNA display,” Chemistry and Biology, 2002, 9:253-264. |
| Curtis et al., “Adhesion of cells to polystyrene surfaces,” J Cell Biol., Nov. 1983, 97(5):1500-1506. |
| Czarnik, “Encoding methods for combinatorial chemistry,” Curr Opin Chem Biol., Jun. 1997, 1(1):60-6. |
| Dahl et al., “Circle-to-cirle amplification for precise and sensitive DNA analysis,” Proc. Natl. Acad. Sci., 2004, 101:4548-4553. |
| Darmanis, et al., “ProteinSeq: High-Performance Proteomic Analyses by Proximity, Ligation and Next Generation Sequencing,” PLos One, 2011, 6(9):e25583. |
| Daubendiek et al., “Rolling-Circle RNA Synthesis: Circular Oligonucleotides as Efficient Substrates for T7 RNA Polymerase,” J. Am. Chem. Soc., 1995, 117:77818-7819. |
| Dawson et al., “Genetic animal models of Parkinson's disease,” Neuron, Jun. 2010, 66(5):646-661 |
| De Clercq, “A 40-year journey in search of selective antiviral chemotherapy,” Annu Rev Pharmacol Toxicol., 2011, 51:1-24. |
| Deamer et al., “Characterization of nucleic acids bv nanopore analysis,” Acc Chem Res., Oct. 2002, 35(10):817-25. |
| Deamer et al., “Nanopores and nucleic acids: prospects for ultrarapid sequencing,” Trends Biotechnol., Apr. 2000, 18(4):147-51. |
| Dean et al., “Comprehensive human genome amplification using multiple displacement amplification,” Proc Natl. Acad. Sci. USA 99:5261-66, 2002. |
| Deibel et al., “Biochemical properties of purified human terminal deoxynucleotidyltransferase,” J Biol Chem., May 1980, 255(9):4206-12. |
| Devine et al., “Efficient integration of artificial transposons into plasmid targets in vitro: a useful tool for DNA mapping, sequencing and genetic analysis,” Nucleic Acids Res., Sep. 1994, 22(18):3765-72. |
| Dhindsa et al., “Virtual Electrowetting Channels: Electronic Liquid Transport with Continuous Channel Functionality,” Lab Chip, 2010, 10:832-836. |
| Diez-Roux et al., “A high-resolution anatomical atlas of the transcriptome in the mouse embryo,” PLoS Biol., Jan. 2011, 9(1):e1000582, 14 pages. |
| Doddridge et al., “UV-induced strand break damage in single stranded bromodeoxyuridine-containing DNA oligonucleotides,” Chem Commun., 1998, p. 1997-1998. |
| Dressman et al., “Transforming single DNA molecules into fluorescent magnetic particles for detection and enumeration of genetic variations,” Proc. Natl. Acad. Sci. USA, 2003, 100:8817-8822. |
| Drmanac et al., “Accurate sequencing by hybridization for DNA diagnostics and individual genomics,” Nature Biotechnology, 16:54-58, 1998. |
| Druley et al., “Quantification of rare allelic variants from pooled genomic DNA,” Nat. Methods 6: 263-65, 2009. |
| Duhr et al., “Why molecules move along a temperature gradient,” Proc Natl Acad Sci USA, Dec. 2006, 103(52): 19678-19682. |
| Duncan et al., “Affinity chromatography of a sequence-specific DNA binding protein using teflon-linked oligonucleotides”, Anal. Biochem. 169: 104-108, 1988. |
| Eberwine et al., “Analysis of gene expression in single live neurons,” Proc. Natl. Acad. Sci., USA 89, 3010-3014, 1992. |
| Eberwine, “Amplification of mRNA Populations Using aRNA Generated from Immobilized Oligo(dT)-T7 Primed cDNA,” BioTechniques 20 (4), 584, 1996. |
| Ebihara et al., “Molecular detection of dermatophytes and nondermatophytes in onychomycosis by nested polymerase chain reaction based on 28S ribosomal RNA gene sequences,” Br J Dermatol., Nov. 2009, 161(5):1038-44. |
| Eguiluz et al., “Multitissue array review: A chronological description of tissue array techniques, applications and procedures,” Pathology Research and Practice, 2006, 202:561-568. |
| Ekins et al., “Microarrays: their origins and applications,” Trends in Biotechnology, Jun. 1999, 17(6):217-218. |
| Eldridge et al. “An in vitro selection strategy for conferring protease resistance to ligand binding peptides,” Protein Eng Des Sel., 22(11): 691-698, 2009. |
| Ellington et al., “Antibody-based protein multiplex platforms: technical and operational challenges,” Clin Chem 56(2): 186-193, 2010. |
| Emmert-Buck et al., “Laser capture microdissection,” Science, Nov. 1996, 274(5289):998-1001. |
| Espina et al., “Laser-capture microdissection,” Nat Protoc, 2006, 1(2):586-603. |
| Extended European Search Report in European Appln. No. 11766613.1, dated Jan. 15, 2014, 4 pages. |
| Fahy et al., “Design and synthesis of polycrylamide-based oligonucleotide supports for use in nucleic acid diagnostics,” Nucleic Acids Res., Apr. 1993, 21(8):1819-26. |
| Falconnet et al., “Surface engineering approaches to micropattern surfaces for cell-based assays,” Biomaterials, Jun. 2006, 27(16):3044-3063. |
| Fan et al., “Highly parallel SNP genotyping,” Cold Spring Symp. Quant. Biol., 68: 69-78, 2003. |
| Fang et al., “Fluoride-cleavable biotinylation phosphoramidite for 5′-end-labeling and affinity purification of synthetic oligonucleotides,” Nucleic Acids Res., Jan. 2003, 31(2):708-715. |
| Ferreira et al., “Photocrosslinkable Polymers for Biomedical Applications,” Biomedical Engineering—Frontiers and Challenges, Prof. Reza, 2011, 22 pages. |
| Fire and Xu, “Rolling replication of short DNA circles,” Proc. Natl. Acad. Sci., 92: 4641-4645, 1995. |
| Fodor et al., “Light-Directed, Spatially Addressable Parallel Chemical Synthesis,” Science, 251(4995), 767-773, 1995. |
| Folch et al., “Microfabricated elastomeric stencils for micropatterning cell cultures,” J Biomed Mater Res, November 2000, 52(2):346-353. |
| Fredriksson et al., “Multiplexed protein detection by proximity ligation for cancer detection,” Nature Methods, 4(4): 327-29, 2007. |
| Fredriksson et al., “Multiplexed proximity ligation assays to profile putative plasma biomarkers relevant to pancreatic and ovarian cancer,” Clin. Chem., 5(3): 582-89, 2008. |
| Fredriksson et al., “Protein detection using proximity-dependent DNA ligation assays,” Nature Biotech., 20: 473-77, 2002. |
| Frese et al., “Formylglycine Aldehyde Tag-Protein Engineering through a Novel Posttranslational Modification,” ChemBioChem., 10: 425-27, 2009. |
| Fu et al., “Counting individual DNA molecules by the stochastic attachment of diverse labels,” PNAS, 108: 9026-9031, 2011. |
| Fu et al., “Repeat subtraction-mediated sequence capture from a complex genome,” Plant J., Jun. 2010, 62(5): 898-909. |
| Fullwood et al., “Next-generation DNA sequencing of paired-end tags (PET) for transcriptome and genome analyses,” Genome Res., 19: 521-532, 2009. |
| Galon et al., “The immune score as a new possible approach for the classification of cancer,” J Transl Med., Jan. 2012, 10:1, 4 pages. |
| Gans et al., “Inkjet Printing of Polymers: State of the Art and Future Developments,” Advanced Materials, Feb. 2004, 16(3):203-213. |
| Gao et al., “High density peptide microarrays. In situ synthesis and applications,” Molecular Diversity, 8, 177-187, 2004. |
| Geiss et al., “Direct multiplexed measurement of gene expression with color-coded probe pairs,” nature biotechnology, 2008, 26(3):317-325. |
| Genbank Accession No. AC009495.1, “Homo sapiens clone NH0490I02, *** Sequencing in Progress ***, 12 unordered pieces,” Aug. 24, 1999, 53 pages. |
| Genbank Accession No. AC009495.5, “Homo sapiens BAC clone RP11-490I2 from 2, complete sequence,” Apr. 21, 2005, 32 pages. |
| Genbank Accession No. AC037198.2, “Homo sapiens chromosome 15 clone CTD-2033D15 map 15q14, *** Sequencing in Progress ***, 62 unordered pieces,” Apr. 25, 2000, 39 pages. |
| Genbank Accession No. AC087379.2, “Homo sapiens chromosome 11 clone RP11-396O20 map 11, *** Sequencing in Progress ***, 5 ordered pieces,” Jul. 6, 2002, 47 pages. |
| Genbank Accession No. AC087741.1, “Homo sapiens chromosome 17 clone RP11-334C17 map 17, Low-Pass Sequence Sampling,” Jan. 22, 2001, 18 pages. |
| Genbank Accession No. AC100826.1, “Homo sapiens chromosome 15 clone RP11-279F6 map 15, Low-Pass Sequence Sampling,” Nov. 22, 2001, 21 pages. |
| Genbank Accession No. AL445524.1, “Homo sapiens chromosome 1 clone RP11-295G20, Working Draft Sequence, 19 unordered pieces,” Oct. 14, 2000, 47 pages. |
| Genome.ucsc.edu, [online], “Genome Browser Gateway,” 2000, retrieved on Jun. 11, 2021, retrieved from URL<https://genome.ucsc.edu/cgi-bin/hgGateway>, 3 pages. |
| Gerard et al. “Excess dNTPs minimize RNA hydrolysis during reverse transcription,” Biotechniques, Nov. 2002, 33(5): 984, 986, 988, 990. |
| Giam et al., “Scanning probe-enabled nanocombinatorics define the relationship between fibronectin feature size and stem cell fate,” PNAS, Mar. 2012, 109(12):4377-4382. |
| Gibson et al., “Enzymatic assembly of DNA molecules up to several hundred kilobases,” Nat Methods., May 2009, 6(5):343-5. |
| Gill et al., “Nucleic acid isothermal amplification technologies: a review,” Nucleosides Nucleotides Nucleic Acids, Mar. 2008, 27(3):224-43. |
| Gilles et al., “Single nucleotide polymorphic discrimination by an electronic dot blot assay on semiconductor microchips,” Nat Biotechnol, Apr. 1999, 17(4):365-70. |
| Glass et al., “SIMPLE: a sequential immunoperoxidase labeling and erasing method,” J. Histochem. Cytochem., Oct. 2009, 57(10):899-905. |
| Gloor, “Gene targeting in Drosophila,” Methods Mol Biol., 2004, 260:97-114. |
| Gnanapragasam, “Unlocking the molecular archive: the emerging use of formalin-fixed paraffin-embedded tissue for biomarker research in urological cancer,” BJU International, 105, 274-278, 2009. |
| Goebl et al., “Development of a sensitive and specific in situ hybridization technique for the cellular localization of antisense oligodeoxynucleotide drags in tissue sections,” Toxicologic Pathology, Jun. 2007, 35(4):541-548. |
| Goldkom and Prockop, “A simple and efficient enzymatic method for covalent attachment of DNA to cellulose. Application for hybridization-restriction analysis and for in vitro synthesis of DNA probes.”, Nucleic Acids Res. 14:9171-9191, 1986. |
| Goryshin et al., “Tn5 in vitro transposition,” J Biol Chem., Mar. 1998, 273(13):7367-74. |
| Gotz et al., “Animal models of Alzheimer's disease and frontotemporal dementia,” Nat Rev Neurosci., Jul. 2008, 9(7):532-44. |
| Grant et al., “Pathways and mechanisms of endocytic recycling,” Nat. Rev. Mol. Cell Biol., Sep. 2009, 10(9):597-608. |
| Grokhovsky, “Specificity of DNA cleavage by ultrasound,” Molecular Biology, 2006, 40(2):276-283. |
| Gudjonsson et al., “Myoepithelial cells: their origin and function in breast morphogenesis and neoplasia,” J Mammary Gland Biol Neoplasia, Jul. 2005, 10(3):261-72. |
| Gunderson et al., “Decoding Randomly Ordered DNA Arrays,” Genome Research 14: 870-877, 2004. |
| Guo et al., “Direct fluorescence analysis of genetic polymorphisms by hybridization with oligonucleotide arrays on glass supports,” Nucleic Acids Res., Dec. 1994, 22(24):5456-65. |
| Hahnke et al., “Striptease on glass: validation of an improved stripping procedure for in situ microarrays,” J Biotechnol., Jan. 2007, 128(1):1-13. |
| Hajduk et al., “Drug discovery: A question of library design,” Nature, Feb. 2011, 470(7332):42-43. |
| Hamaguchi et al., “Direct reverse transcription-PCR on oligo(dT)-immobilized polypropylene microplates after capturing total mRNA from crude cell lysates.” Clin Chem., Nov. 1998. 44(11):2256-63. |
| Hammond et al. “Profiling cellular protein complexes by proximity ligation with dual tag microarray readout,” PLoS ONE, 2012, 7(7):e40405. |
| Han et al., “3C and 3C-based techniques: the powerful tools for spatial genome organization deciphering”, Molecular Cytogenetics (2018) 11:21, 10 pages, 2018. |
| Hardenbol et al., “Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay,” Genome Res., Feb. 2005, 15(2):269-75. |
| Hardenbol et al., “Multiplexed genotyping with sequence-tagged molecular inversion probes,” Nature Biotechnol, Jun. 2003, 21(6):673-678. |
| Harris et al., “The design and application of target-focused compound libraries,” Comb Chem High Throughput Screen, Jul. 2011, 14(6):521-531. |
| Hayes et al., “Electrophoresis of proteins and nucleic acids: I-Theory,” BMJ, Sep. 1989, 299(6703):843-6. |
| He et al.. “In situ synthesis of protein arrays,” Current Opinion in Biotechnology, 19:4-9, 2008. |
| He et al., “Printing protein arrays from DNA arrays,” Nature Methods, 5:175-77, 2008. |
| He, “Cell-free protein synthesis: applications in proteomics and biotechnology,” New Biotechnology 25: 126-132, 2008. |
| Healy, “Nanopore-based single-molecule DNA analysis,” Nanomedicine (Lond), Aug. 2007, 2(4):459-81. |
| Hedskog et al., “Dynamics of HIV-1 Quasispecies during Antiviral Treatment Dissected using Ultra-Deep Pyrosequencing,” PLoS One, 5(7):e11345, 2010. |
| Hein et al., “Click Chemistry, A Powerful Tool for Pharmaceutical Sciences”, Pharm Res., 25(10):2216-2230, 2008. |
| Hejatko et al., “In Situ Hybridization Techniques for mRNA Detection in Whole Mount Arabidopsis Samples,” Nature Protocols, 2006, 1(4): 1939-1946. |
| Hendrickson et al., “High sensitivity multianalyte immunoassay using covalent DNA-labeled antibodies and polymerase chain reaction,” Nucleic Acid Research, Feb. 11, 1995, 23(3):522-529. |
| Hessner et al., “Genotyping of factor V G1691A (Leiden) without the use of PCR by invasive cleavage of oligonucleotide probes,” Clin Chem., Aug. 2000, 46(8 Pt 1): 1051-6. |
| Hiatt et al., “Parallel, tag-directed assembly of locally-derived short sequence reads,” Nature Methods 7(2): 119-25, 2010. |
| Hlubek et al., “Heterogeneous expression of Wnt/beta-catenin target genes within colorectal cancer,” Int J Cancer., Nov. 2007, 121(9):1941-8. |
| Ho et al., “Bacteriophage T4 RNA ligase 2 (gp24.1) exemplifies a family of RNA ligases found in all phylogenetic domains,” PNAS, Oct. 2002, 99(20):12709-14. |
| Hober et al., “Human protein atlas and the use of microarray technologies,” Curr Opin Biotechnol., Feb. 2008, 19(1):30-35. |
| Holmstrøm et al., “A highly sensitive and fast nonradioactive method for detection of polymerase chain reaction products,” Anal Biochem, Mar. 1993, 209(2):278-83. |
| Hoyer et al., “Electrostatic spraying: a novel technique for preparation of polymer coatings on electrodes,” Anal Chem, Nov. 1996, 68(21):3840-4. |
| Hu et al., “High reproducibility using sodium hydroxide-stripped long oligonucleotide DNA microarrays,” Biotechniques, Jan. 2005, 38(1):121-4. |
| Hycultbiotech.com, [online], “Immunohistochemistry, Paraffin” Apr. 2010, retrieved on Apr. 16, 2020, retrieved from URL<https://www.hycultbiotech.com/media/wysiwyg/Protocol_Immunohistochemistry_Paraffin_2.pdf>, 3 pages. |
| Hytönen et al., “Design and construction of highly stable, protease-resistant chimeric avidins,” J Biol Chem., Mar. 2005, 280(11): 10228-33. |
| Ichikawa et al., “In vitro transposition of transposon Tn3,” J Biol. Chem., Nov. 1990, 265(31):18829-32, Abstract. |
| Illumina.com [online], “Array-Based Gene Expression Analysis,” 2011, retrieved on Dec. 13, 2021, retrieved from URL<https://www.illumina.com/documents/products/datasheets/datasheet_gene_exp_analysis.pdf, 5 pages. |
| Imbeaud et al., “Towards standardization of RNA quality assessment using user-independent classifiers of microcapillary electrophoresis traces,” Nucleic Acids Res., Mar. 2005, 33(6):e56, 12 pages. |
| Inoue and Wittbrodt, “One for All—A Highly Efficient and Versatile Method for Fluorescent Immunostaining in Fish Embryos,” PLoS One 6, e19713, 2011. |
| Invitrogen, Immune Response Biomarker Profiling Service Report, Invitrogen, 2009, 1-33. |
| Jabara et al., Accurate sampling and deep sequencing of the HIV-1 protease gene using a Primer ID. PNAS 108(50); 20166-20171, 2011. |
| Jain, “Transport of molecules, particles, and cells in solid tumors,” Annu. Rev. Biomed. Eng., 1999, 1:241-263. |
| Jamurand Oliver, “Permeabilization of cell membranes.,” Method Mal. Biol., 588: 63-66, 2010. |
| Jawhar et al., “Tissue Microarray: A rapidly evolving diagnostic and research tool,” Annals of Saudi Medicine, Mar. 2009, 29(2):123-7. |
| Jensen et al., “Zinc fixation preserves flow cytometry scatter and fluorescence parameters and allows simultaneous analysis of DNA content and synthesis, and intracellular and surface epitopes,” Cytometry A., Aug. 2010, 77(8):798-804. |
| Jones et al., Comparative lesion sequencing provides insights into tumor evolution. Proc. Natl. Acad. Sci. USA 105(11): 4283-4288, 2008. |
| Joos et al., “Covalent attachment of hybridizable oligonucleotides to glass supports,” Anal Biochem., Apr. 1997, 247(1):96-101. |
| Jucá et al., “Effect of dimethyl sulfoxide on reverse transcriptase activity,” Braz. J. Med. Biol. Res., Mar. 1995, 28(3):285-90. |
| Kainkaryam et al., “Pooling in high-throughput drug screening” Curr Opin Drug Discov Devel., May 2009, 12(3):339-50. |
| Kanehisa, “Use of statistical criteria for screening potential homologies in nucleic acid sequences ”, Nucleic Acids Res. 12: 203-213, 1984. |
| Kap et al., “Histological Assessment of PAXgene Tissue Fixation and Stabilization Reagents,” PLoS One 6, e27704, 10 pages, 2011. |
| Kapteyn et al., “Incorporation of Non-Natural Nucleotides Into Template-Switching Oligonucleotides Reduces Background and Improves cDNA Synthesis From Very Small RNA Samples,” BMC Genomics, 2010, 11(413): 1-9. |
| Kibbe, “OligoCalc: an online oligonucleotide properties calculator,” Nucleic Acids Res., Jul. 2007, 35:W43-6. |
| Kirby et al., “Cryptic plasmids of Mycobacterium avium: Tn552 to the rescue,” Mol Microbiol., Jan. 2002, 43(1): 173-86. |
| Kleckner et al., “Tn10 and IS10 transposition and chromosome rearrangements: mechanism and regulation in vivo and in vitro,” Curr Top Microbiol Immunol., 1996, 204:49-82. |
| Koch et al., “Photochemical immobilization of anthraquinone conjugated oligonucleotides and PCR amplicons on solid surfaces,” Bioconjugate Chem., Jul. 2000, 11(4):474-483. |
| Kolb et al., “Click Chemistry: Diverse Chemical Function from a Few Good Reactions,” Angew. Chem. Int. Ed., 40(11): 2004-2021, 2001. |
| Kolbert et al., “Ribosomal DNA sequencing as a tool for identification of bacterial pathogens,” Curr Opin Microbiol, Jun. 1999, 2(3):299-305. |
| König et al., “iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution,” Nat Struct Mol Biol., Jul. 2010, 17(7):909-915. |
| Korbel et al., “Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome,” Science, 318(5849): 420-426, 2007. |
| Korlach et al., “Selective aluminum passivation for targeted immobilization of single DNA polymerase molecules in zero-mode waveguide nanostructures,” Proc. Natl. Acad. Sci. USA 105, 1176-1181, 2008. |
| Kozlov et al., “A High-Complexity Multiplexed Solution-Phase Assay for Profiling Protease Activity on Microarrays,” Comb Chem High Throughput Screen, 11: 24-35, 2008. |
| Kozlov et al., “A Highly Scalable Peptide-Based Assay System for Proteomics,” PLoS ONE, 7(6): e37441, 2012. |
| Kozlov et al., “A Method for Rapid Protease Substrate Evaluation and Optimization,” Comb Chem High Throughput Screen, 9: 481-87, 2006. |
| Kristensen et al., “High-Throughput Methods for Detection of Genetic Variation,” BioTechniques, Feb. 2001, 30(2):318-332. |
| Kuijpers et al. “Specific recognition of antibody-oligonucleotide conjugates by radiolabeled antisense nucleotides: a novel approach for two-step radioimmunotherapy of cancer,” Bioconjugate Chem., Jan. 1, 1993, 4(1):94-102. |
| Kurz et al., “cDNA-Protein Fusions: Covalent Protein-Gene Conjugates for the In Vitro Selection of Peptides and Proteins,” ChemBioChem, 2: 666-72, 2001. |
| Kwok, “High-throughput genotyping assay approaches,” Pharmocogenomics, Feb. 2000, 1(1):95-100. |
| Lage et al., “Whole Genome Analysis of Genetic Alterations in Small DNA Samples Using Hyperbranched Strand Displacement Amplification and Array-CGH,” Genome Research 13: 294-307, 2003. |
| Lampe et al., “A purified mariner transposase is sufficient to mediate transposition in vitro,” EMBO J., Oct. 1996, 15(19):5470-9. |
| Lamture et al., “Direct detection of nucleic acid hybridization on the surface of a charge coupled device,” Nucleic Acid Res., Jun. 1994, 22(11):2121-5. |
| Landegren et al., “Reading bits of genetic information: methods for single-nucleotide polymorphism analysis,” Genome Res., Aug. 1998, 8(8):769-76. |
| Langdale et al., “A rapid method of gene detection using DNA bound to Sephacryl”, Gene 36: 201-210, 1985. |
| Larman et al., “Autoantigen discovery with a synthetic human peptidome,” Nature Biotechnology, doi:1 0.1038/nbt.1856, vol. 29, No. 6, pp. 535-541, 2011. |
| Larsen et al., “Characterization of a recombinantly expressed proteinase K-like enzy me from a psychrotropbic Serratia sp,” FEBS J., Jan. 2006, 273(1):47-60. |
| Larsson et al., “In situ detection and genotyping of individual mRNA molecules,” Nat Methods, May 2010, 7(5):395-7. |
| Larsson et al., “In situ genotyping individual DNA molecules by target-primed rolling-circle amplification of padlock probes,” Nat Methods, Dec. 2004, 1(3):227-32. |
| Lassmann el al., A Novel Approach For Reliable Microarray Analysis of Microdissected Tumor Cells From Formalin-Fixed and Paraffin-Embedded Colorectal Cancer Resection Specimens, J Mol Med, 87, 211-224, 2009. |
| Laurell et al., “Chip integrated strategies for acoustic separation and manipulation of cells and particles,” Chem. Soc. Rev., Mar. 2007, 36(3):492-506. |
| Lee et al., “A novel COL3A1 gene mutation in patient with aortic dissected aneurysm and cervical artery dissections,” Heart Vessels, Mar. 2008, 23(2):144-8. |
| Lee et al., “Cytokines in cancer immunotherapy,” Cancers (Basel), Oct. 2011, 3(4):3856-3893. |
| Lee et al., “Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing,” BMC Genomics, Dec. 2009, 10:646, 12 pages. |
| Lee et al., “Protein nanoarravs generated by dip-pen nanolithography,” Science, Mar. 2002, 295(5560):1702-1705. |
| Lenard, “Viral Membranes,” Encyclopedia of Virology, Jul. 2008, pp. 308-314. |
| Leriche et al., “Cleavable linkers in chemical biology.”, Bioorganic & Medicinal Chemistry, 20: 571-582, 2012. |
| Levene et al., “Zero-Mode Waveguides for Single-Molecule Analysis at High Concentrations,” Science 299, 682-686, 2003. |
| Li et al., “A photocleavable fluorescent nucleotide for DNA sequencing and analysis,” Proc. Natl. Acad. Sci., 100: 414-419, 2003. |
| Li et al., “DNA molecules and configurations in a solid-state nanopore microscope,” Nat Mater., Sep. 2003, 2(9):611-5. |
| Li et al., “RASL-seq for Massively Parallel and Quantitative Analysis of Gene Expression,” Curr Protoc Mol Biol., Apr. 2012, 4(13):1-10. |
| Linnarsson, “Recent advances in DNA sequencing methods—general principles of sample preparation,” Experimental Cell Research, 316: 1339-1343, 2010. |
| Liu et al., “Method for Quantitative Proteomics Research by Using Metal Element Chelated Tags Coupled with Mass Spectrometry,” Analytical Chemistry, 2006, 78:6614-6621. |
| Liu et al., “Surface and interface control on photochernically initiated immobilization,” J Am Chem Soc., Nov. 2006, 128(43):14067-72. |
| Liu et al., An integrated and sensitive detection platform for biosensing application based on Fe@Au magnetic nanoparticles as bead array carries Biosensors and Bioelectronics, 2010, 26(4):1442-1448. |
| Lizardi et al., “Mutation detection and single-molecule counting using isothermal rolling-circle amplification,” Nat. Genet. 19: 225-232, 1998. |
| Lu et al., “A microfluidic electroporation device for cell lysis,” Lab Chip., Jan. 2005, 5(1):23-29. |
| Lund et al., “Assessment of methods for covalent binding of nucleic acids to magnetic beads, Dynabeads, and the characteristics of the bound nucleic acids in hybridization reactions.”, Nucleic Acids Res., 16: 10861-80, 1988. |
| Lundberg et al., “High-fidelity amplification using a thermostable DNA polymerase isolated from Pyrococcus furiosus.,” Gene., 108(1): 1-6, 1991. |
| Lundberg et al., “Homogeneous antibody-based proximity extension assays provide sensitive and specific detection of low-abundant proteins inhuman blood,” Nucleic Acids Res., 39(15): e102, 2011. |
| Lundberg et al., “Multiplexed homogeneous proximity ligation assays for high-throughput protein biomarker research in serological material,” Mol Cell Proteomics, 10(4): M110.004978, 2011. |
| Lundin et al., “Increased throughput by parallelization of library preparation for massive sequencing,” PLoS One, Apr. 2010, 5(4):e10029, 7 pages. |
| Lundquist et al., “Parallel confocal detection of single molecules in real time,” Opt. Lett. 33, 1026-1028, 2008. |
| Lyamichev et al., “Invader assay for SNP genotyping,” Methods Mol Biol., 2003, 212:229-40. |
| Lyamichev et al., “Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes,” NatBiotechnol., Mar. 1999, 17(3):292-6. |
| Lyck, et al., “Immunohistochemical Markers for Quantitative Studies of Neurons and Glia in Human Neocortex,” J Histochem Cytochem 56, 201-21, 2008. |
| Lykidis et al., “Novel zinc-based fixative for liigh quality DNA, RNA and protein analysis,” Nucleic Acids Res., Jun. 2007, 35(12):e85, 10 pages. |
| MacBeath et al., “Printing proteins as microarrays for high-throughput function determination,” Science, Sep. 2000, 289(5485): 1760-1763. |
| MacIntyre, “Unmasking antigens for immunohistochemistry.,” Br J Biomed Sci. 58, 190-6, 2001. |
| Malkov et al., “Multiplexed measurements of gene signatures in different analytes using the Nanostring nCounter™ Assay System.” BMC research notes., 2009, 2:80. |
| Marras, “Selection of fluorophore and quencher pairs for fluorescent nucleic acid hybridization probes,” Methods Mol Biol., 2006, 335:3-16. |
| Martin, “Cutadapt removes adapter sequences from high-throughput sequencing reads,” EMBnet Journal, 2011, 17(1):10-12. |
| Massey et al., “Fluorescence resonance energy transfer (FRET) for DNA biosensors: FRET pairs and Förster distances for various dye-DNA conjugates,” Anal Chim Acta., May 2006, 568(1-2):181-9. |
| Masuda et al., “Analysis of chemical modification of RNA from formalin-fixed samples and optimization of molecular biology applications for such samples,” Nucleic Acids Research, Nov. 1999, 27(22):4436-4443. |
| Materna et al., “High accuracy, high-resolution prevalence measurement for the majority of locally expressed regulatory genes in early sea urchin development,” Gene Expr Patterns., 2010, 10(4-5):177-184. |
| Mattheyses et al., “Imaging with total internal reflection fluorescence microscopy for the cell biologist,” J Cell Sci., Nov. 2010, 123(Pt 21):3621-3628. |
| McCloskey et al., “Encoding PCR Products with Batch-stamps and Barcodes,” Biochem. Genet. 45: 761-767, 2007. |
| Mcgee, “Structure and Analysis of Affymetrix Arrays,” UTSW Microarray Analysis Course, Oct. 28, 2005, 68 pages. |
| Mckernan et al., “Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding,” Genome Res., 19: 1527-41, 2009. |
| Metzker “Sequencing technologies—the next generation,” Nature Reviews Genetics, 11:31-46, 2010. |
| Meyer et al., “Fast evolving 18S rRNA sequences from Solenogastres (Mollusca) resist standard PCR amplification and give new insights into mollusk substitution rate heterogeneity,” BMC Evol. Biol., Mar. 2010, 10:70, 12 pages. |
| Micke et al., “Biobanking of fresh frozen tissue: RNA is stable in nonfixed surgical specimens,” Lab Invest., Feb. 2006, 86(2):202-11. |
| Miele et al., “Mapping cis- and trans- chromatin interaction networks using chromosome conformation capture (3C),” Methods Mol Biol., 2009, 464:105-21. |
| Miller et al., “Basic Concepts of Microarrays and Potential Applications in Clinical Microbiology,” Clinical Microbiology Reviews, vol. 22, No. 4, pp. 611-633, 2009. |
| Miner et al., “Molecular barcodes detect redundancy and contamination in hairpin-bisulfite PCR,” Nucleic Acids Res., Sep. 2004, 32(17):e135, 4 pages. |
| Mir et al., “Sequencing by cyclic ligation and cleavage (CycliC) directly on a microarray captured template,” Nucleic Acids Research, 37(1):e5, 8 pages, 2009. |
| Mitra et al., “Digital genotyping and haplotyping with polymerase colonies,” Proc. Natl. Acad. Sci. USA, May 2003, 100(10):5926-5931. |
| Mitra et al., “Fluorescent in situ sequencing on polymerase colonies,” Anal Biochem, Sep. 2003, 320(1):55-65. |
| Mitra et al., “In situ localized amplification and contact replication of many individual DNA molecules,” Nucleic Acids Res., Dec. 1999, 27(24):e34, 6 pages. |
| Mitsuhashi et al., “Gene manipulationonplastic plates,” Nature 357: 519-520, 1992. |
| Mizusawa et al., “A bacteriophage lambda vector for cloning with BamHI and Sau3A,” Gene, 20: 317-322, 1982. |
| Mlecinik et al., “Histopathologic-based prognostic factors of colorectal cancers are associated with the state of the local immune reaction,” J Clin Oncol., Feb. 2011, 29(6):610-8. |
| Mortazavi et al., “Mapping and quantifying mammalian transcriptomes by RNA-Seq,” Nature Methods, 5(7): 621-8, 2008. |
| Moshrefzadeh et al., “Nonuniform photobleaching of dyed polymers for optical waveguides,” Applied Physics Letters, 1993, 62:16-18. |
| Motea et al., “Terminal deoxynucleotidyl transferase: the storv of a misguided DNA polymerase,” Biochim Biophys Acta., May 2010, 1804(5): 1151-66. |
| Mueller et al., “RNA Integrity Number (RIN)—Standardization of RNA Quality Control,” Agilent Technologies, 2004, 8 pages. |
| Nadji et al., “Immunohistochemistry of tissue prepared by a molecular-friendly fixation and processing system,” Appl Immunohistochem Mol Morphol., Sep. 2005, 13(3):277-82. |
| Nagahara et al., “Neuroprotective effects of brain-derived neurotrophic factor in rodent and primate models of Alzheimer's disease,” Nat Med., Mar. 2009, 15(3):331-337. |
| Nagai et al., “Site-specific DNA cleavage by antisense oligonucleotides covalently linked to phenazine di-N-oxide,” J Biol. Chem., Dec. 1991, 266(35):23994-4002. |
| Nakamura et al., “Biocompatible inkjet printing technique for designed seeding of individual living cells,” Tissue Eng, Nov. 2005, 11(11-12):1658-1666. |
| Nakao et al., “Myosin heavy chain gene expression in human heart failure,” J Clin Invest., Nov. 1997, 100(9):2362-70. |
| Nam et al., “Nanoparticle-Based Bio-Bar Codes for the Ultrasensitive Detection of Proteins,” Science, Sep. 26, 2003, 301(5641):1884-1886. |
| Nandakumar et al., “How an RNA Ligase Discriminates RNA versus DNA Damage,” Molecular Cell, 2004, 16(2):211-221. |
| Ng et al., “Gene identification signature (GIS) analvsis for transcriptome characterization and genome annotation,” Nature Methods, 2(2): 105-111, 2005. |
| Ng et al., “Massively parallel sequencing and rare disease,” Human Malec. Genetics, 19(2): R119-R24, 2010. |
| Ng et al., “Multiplex sequencing of paired-end ditags (MS-PET): a strategy for the ultra-high-throughput analysis of transcriptomes and genomes,” Nucleic Acids Research, Jul. 2006, 34(12): e84, 10 pages. |
| Nichols et al., “RNA Ligases,” Curr Protoc Mol Biol., October 2008, 84(1):3.15.1-3.15.4. |
| Nicholson, “Diffusion and related tomsport mechanisms in brain tissue,” Rep. Prog. Phys., Jun. 2001, 64(7):815-884. |
| Niedringhaus et al., “Landscape of next-generation sequencing technologies,” Anal Chem., Jun. 2011, 83(12):4327-41. |
| Niemeyer, “The developments of semisynthetic DNA-protein conjugates,” Trends Biotechnol, Sep. 2002, 20(9): 395-401. |
| Nikiforov et al., “The use of 96-well polystyrene plates for DNA hybridization-based assays: an evaluation of different approaches to oligonucleotide immobilization,” Anal Biochem, May 1995, 227(1):201-9. |
| Niklas et al., “Selective permeabilization for the high-throughput measurement of compartmented enzyme activities in mammalian cells,” Anal Biochem, Sep. 2011, 416(2):218-27. |
| Nilsson et al., “RNA-templated DNA ligation for transcript analysis,” Nucleic Acids Res., Jan. 2001, 29(2):578-81. |
| Nuovo, “In situ PCR: protocols and applications.,” Genome Res, Feb. 1995, 4 (4): 151-167. |
| Ohtsubo et al., “Bacterial insertion sequences,” Curr Top Microbiol Immunol., 1996, 204:1-26. |
| Oleinikov et al., “Self-assembling protein arrays using electronic semiconductor microchips and in vitro translation,” J Proteome Res, May-Jun. 2003, 2(3): 313-319. |
| Olivier, “The Invader assay for SNP genotyping,” Mutat. Res., Jun. 2005, 573(1-2):103-110. |
| Oren et al., “Selective lysis of bacteria but not mammalian cells by diastereomers of melittin: structure-function study,” Biochemistry, Feb. 1997, 36(7):1826-35. |
| Osada et al., “Epitope mapping using ribosome display in a resconstituted cell-free protein synthesis system,” J Biochem, May 2009, 145(5): 693-700. |
| O-Shannessy et al., “Detection and quantitation of hexa-histidine-tagged recombinant proteins on western blots and by a surface plasmon resonance biosensor technique,” Anal Biochem, 229(1): 119-124, 1995. |
| Ostuni et al., “Patternine Mammalian Cells Using Elastomeric Membranes,” Langmuir, Aug. 2000, 16(20):7811-7819. |
| Palamanda et al., “Evaluation of CYP1A1 and CYP2B1/2 m-RNA Induction in Rat Liver Slices Using the NanoString® Technology: A Novel Tool for Drug Discovery Lead Optimization,” Drug metabolism letters, Nov. 3, 2009, 3(3): 171-175. |
| Pandey et al., “Inhibition of terminal deoxynucleotidyl transferase by adenine dinucleotides. Unique inhibitory action of Ap5A,” FEBS Lett., Mar. 1987, 213(1):204-8. |
| Park et al., “Cancer gene therapy using adeno-associated virus vectors,” Front Biosci., Jan. 2008, 13:2653-59. |
| Park et al., “The Estimation of Breast Cancer Disease-Probability by Difference of Individual Susceptibility,” Cancer Res. Treat., Feb. 2003, 35(1):35-51, Abstract. |
| Patil et al., “DNA-based therapeutics and DNA delivery svstems: a comprehensive review,” AAPS J. Apr. 2005, 7(1):E61-77. |
| Patton et al., “Rainbow's end: the quest for multiplexed fluorescence quantitative analysis in proteomics.” Current Opinion to Chemical Biology, Feb. 1, 2002, 6(1):63-69. |
| PCT International Preliminary Report on Patentability in International Appln. No. PCT/US2011/031308, dated Oct. 9, 2012, 7 pages. |
| PCT International Search Report and Written Opinion in International Appln. No. PCT/US2011/031308, dated May 25, 2011, 8 pages. |
| Pellestor et al., “The peptide nucleic acids (PNAs), powerful tools for molecular genetics and cytogenetics,” Eur J Hum Genet., Sep. 2004, 12(9):694-700. |
| Pemov et al., “DNA analysis with multiplex microarray-enhanced PCR,” Nucl. Acids Res., Jan. 2005, 33(2):e11, 9 pages. |
| Penland et al., “RNA expression analysis of formalin-fixed paraffin-embedded tumors,” Laboratory Investigation, Apr. 2007, 87(4):383-391. |
| Perler et al., “Intervening sequences in an Archaea DNA polymerase gene,” PNAS USA, Jun. 1992, 89(12): 5577-5581. |
| Perocchi et al., “Antisense artifacts in transcriptome microarray experiments are resolved by actinomycin D,” Nucleic Acids Res., 2007, 35(19):e128, 7 pages. |
| Petterson et al., “Generations of sequencing technologies,” Genomics, 2009, 105-111. |
| Pipenburg et al., “DNA detection using recombination proteins,” PLoS Biol., Jul. 2006. 4(7):e204, 7 pages. |
| Pirici et al., “Antibody elution method for multiple immunohistochemistry on primary antibodies raised in the same species and of the same subtypem,” J. Histochem. Cytochem., Jun. 2009, 57(6):567-75. |
| Piston et al., “Fluorescent protein FRET: the good, the bad and the ugly,” Trends Biochem Sci., Sep. 2007, 32(9):407-14. |
| Plasterk, “The Tcl/mariner transposon family,” Curr Top Microbiol Immunol., 1996, 204:125-43. |
| Pluen et al., “Diffusion of macromolecules in agarose gels: comparison of linear and globular configurations,” Biophys J., Jul. 1999, 77(1):542-552. |
| Polsky-Cynkin et al., “Use of DNA Immobilizedon Plastic and Agarose Supports to Detect DNA by Sandwich Hybridization,” Clin. Chem. 31: 1438-1443, 1985. |
| Porreca et al., “Polony DNA sequencing,” Curr Protoc Mol Biol., Nov. 2006, Chapter 7, Unit 7.8, pp. 7.8.1-7.8.22. |
| U.S. Appl. No. 61/267,363, filed Dec. 7, 2009 (Year: 2009). |
| Punwaney et al., “Human papillomavirus may be common within nasopharyngeal carcinoma of Caucasian Americans: investigation of Epstein-Barr virus and human papillomavirus in eastern and western nasopharyngeal carcinoma using ligation-dependent polymerase chain reaction,” Head & Neck, Jan. 1999, 21(1):21-29. |
| Raab et al., “Human tRNA genes function as chromatin insulators,” EMBO J., Jan. 2012, 31(2):330-50. |
| Ramachandran et al., “Next-generation high-density self-assembling functional protein arrays,” Nature Methods, Jun. 2008, 5(6):535-538. |
| Ramanujan et al., “Diffusion and convection in collagen gels: implications for transport in the tumor interstitium,” Biophys. J., Sep. 2002, 83(3): 1650-1660. |
| Ranki et al., “Sandwich hybridization as a convenient method for the detection of nucleic acids in crude samples”, Gene 21: 77-85, cellulose, 1983. |
| Razonable, “Antiviral drugs for viruses other than human immunodeficiency virus,” Mayo Clinic Proceedings, Oct. 2011, 86(10):1009-26. |
| Reinartz et al., “Massively parallel signature sequencing (MPSS) as a tool for in-depth quantitative gene expression profiling in all organisms,” Brief Funct Genomic Proteomic, Feb. 2002, 1(1):95-104. |
| Rettig et al., “Large-scale single-cell trapping and imaging using microweil arrays,” Anal Chem, Sep. 2005, 77(17):5628-5634. |
| Reznikoff, “Tn5 as a model for understanding DNA transposition,” Mol Microbiol., Mar. 2003, 47(5):1199-206. |
| Ristova et al., “Study of hydrogenated amorphous silicon thin films as a potential sensor for He—Ne laser light detection,” Applied Surface Science, Sep. 2003, 218(1-4):44-53. |
| Roberts et al., “RNA-peptide fusions for the in vitro selection of peptides and proteins,” PNAS USA, Nov. 1997, 94: 12297-122302. |
| Robinson et al., “Small-sample estimation of negative binomial dispersion, with applications to SAGE data,” Biostatistics, Apr. 2008, 9(2):321-332. |
| Rogers et al., “Immobilization of oligonucleotides onto a glass support, via disulfide bonds: A method for preparation of DNA microarrays.” Anal Biochem., Jan. 1999, 266(1):23-30. |
| Rogers et al., “Use of a novel cross-linking method to modify adenovirus tropism,” Gene Ther., Dec. 1997, 4(12):1387-92. |
| Ronaghi et al., “A sequencing method based on real-time pyrophosphate,” Science, Jul. 1998, 281(5375): 363-365. |
| Ronaghi et al., “Real-time DNA sequencing using detection of pyrophosphate release,” Analytical Biochemistry, Nov. 1996, 242(1): 84-89. |
| Ronaghi, “Pyrosequencing sheds light on DNA sequencing,” Genome Res, Jan. 2001, 11(1):3-11. |
| Rosenthal et al., “Cell patterning chip for controlling the stem cell microenvironment,” Biomaterials, Jul. 2007, 28(21):3208-3216. |
| Rouillard et al., “OligoArray 2.0: design of oligonucleotide probes for DNA microarrays using a thermodynamic approach,” Nuc. Acid Research, Jun. 2003, 31(12): 3057-3062. |
| Rountenberg et al., “Microfluidic probe: a new tool for integrating microfluidic environments and electronic wafer-probing,” Lab Chip, Oct. 2009, 10(1):123-127. |
| Rubin et al., “Whole-genome resequencing reveals loci under selection during chicken domestication.,” Nature, Mar. 2010, 464: 587-591. |
| Rubina et al., “Hydrogel-based protein microchips: manufacturing, properties, and applications,” Biotechniques, May 2003, 34(5):1008-14. |
| Rush et al., “New Aldehyde Tag Sequences Identified by Screening Formylglycine Generating Enzymes in Vitro and in Vivo,” J. of American Chemical Society, Aug. 2008. 130(37): 12240-12241. |
| Russell et al., “Molecular mechanisms of late endosome morphology, identity and sorting,” Curr. Opin. Cell Bio., Aug. 2006, 18(4):422-428. |
| San Paulo et al., “High-resolution imaging of antibodies by tapping-mode atomic force microscopy: attractive and repulsive tip-sample interaction regimes,” Biophys J., Mar. 2000, 78(3):1599-1605. |
| Sano et al., “Immuno-PCR: Very Sensitive Antigen Detection by Means of Specific Antibody-DNA Conjugates,” Science, Oct. 2, 1992, 258(5079):120-122. |
| Schellings et al., “Absence of SPARC results in increased cardiac rupture and dysfunction after acute myocardial infarction,” J Exp Med., Jan. 2009, 206(1):113-23. |
| Schena et al., “Quantitative monitoring of gene expression patterns with a complementary DNA microarray,” Science, Oct. 1995, 270(5235):467-470. |
| Schena et al., “Entering the Postgenome Era,” Science, 1995, 270:368-9, 371. |
| Schlapak et al., “Glass surfaces grafted with high-density poly (ethylene glycol) as substrates for DNA oligonucleotide microarrays,” Langinuir, Jan. 2006, 22: 277-285. |
| Schmitt et al., “Detection of ultra-rare mutations by next-generation sequencing,” PNAS (2012) 109:14508-14523. |
| Scholz et al., “The Molecular Chaperone Hsp90 Is Required for Signal Transduction by Wild-Type Hck and Maintenance of Its Constitutively Active Counterpart1,” Cell Growth Differ., Aug. 2001, 12(8):409-417. |
| Schouten et al., “Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification,” Nucleic Acids Res., Jun. 2002, 30(12):e57, 13 pages. |
| Schroeder et al., “The RIN: an RNA integrity No. for assigning integrity values to RNA measurements,” BMC Molecular Biology, Jan. 2006, 7:3, 14 pages. |
| Schweitzer et al., “Multiplexed protein profiling on microarrays by rolling-circle amplification,” Nature Biotechnology, Apr. 2002, 20(4):359-365. |
| Schwers et al., “A high-sensitivity, medium-density, and target amplification-free planar waveguide microarray system for gene expression analysis of formalin-fixed and paraffin-embedded tissue,” Clin. Chem., Nov. 2009, 55(11): 1995-2003. |
| ScienceDirect.com [online], “Plant Fibers,” Definition, 2011, retrieved on Apr. 13, 2022, retrieved from URL<https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/plant-fibers>, 9 pages. |
| Sekar et al., “Fluorescence resonance energy transfer (FRET) microscopy imaging of live cell protein localizations,” J Cell Biol., Mar. 2003, 160(5):629-33. |
| Sergeeva et al., “Display technologies: Application for the discovery of drug and gene delivery aaents,” Advanced Drug Delivery Reviews (2006) 58(15):1622-I654. |
| Seurynck-Servoss et al., “Evaluation of Surface Chemistries for Antibody Microanays”, Anal Biochem., 371(1): 105-115, 2007. |
| Shalon et al., “A DNA microarray system for analyzing complex DNA samples using two-color fluorescent probe hybridization,” Genome Res., Jul. 1996, 6(7):639-45. |
| Shelbourne et al., “Fast copper-free click DNA ligation by the ring-strain promoted alkyne-azide cycloaddition reaction.”, Chem. Commun., 47: 6257-6259, 2011. |
| Shendure et al., “Accurate Multiplex Polony Sequencing of an Evolved Bacterial Genome,” Science, 2005, 309:1728-1732. |
| Shi et al., “The Micro Array Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements,” Nature Biotechnology, 2006, 24(9):1151-61. |
| Shi, “Enabling large-scale pharmacogenetic studies by high-throughput mutation detection and genotyping technologies,” Clin. Chem., Feb. 2001, 47(2):164-172. |
| Shirai et al., “Novel Tools for Analyzing Gene Expressions in Single Cells,” The 5th International Workshop on Approaches to Single-Cell Analysis, The University of Tokyo, Mar. 3-4, 2011, 1 page. |
| Shoemaker et al., “Quantitative phenotypic analysis of yeast deletion mutants using a highly parallel molecular bar-coding strategy,” Nature genetics (1996) 14:450-456. |
| Shults et al., “A multiplexed protein kinase assay,” Chem Bio Chem (2007) 8:93 3-942. |
| Sievertzon et al., “Transcriptome analysis in primary neural stem cells using a tag cDNA amplification method,” BMC Neuroscience, Dec. 2005, 6: 28. |
| Simonis et al., “Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture-on-chip (4C),” Nat Genet., Nov. 2006, 38(11):1348-54. |
| Slonim and Yanai, “Getting started in gene expression microarray analysis,” Plos Computational Biology, 2009, 5(10):e1000543. |
| Soderberg et al. “Characterizing proteins and their interactions in cells and tissues using the in situ proximity ligation assay,” Methods, Jul. 2008, 45(3):227-232. |
| Soderberg et al., “Direct observation of individual endogenous protein complexes in situ by proximity ligation,” Nature Methods, 2006, 3:995-1000. |
| Son et al., “A platform for ultrasensitive and selective multiplexed marker protein assay toward early-stage cancer diagnosis,” Nanomedicine, Feb. 7, 2007, 2(1):79-82. |
| Soni and Meller, “Progress toward ultrafast DNA sequencing using solid-state nanopores,” Clin Chem., 2007, 53: 1996-2001. |
| Spiess et al., “A highly efficient method for long-chain cDNA synthesis using trehalose and betaine,” Anal. Biochem., Feb. 2002, 301(2): 168-74. |
| Spurgeon et al., “High Throughput Gene Expression Measurement with Real Time PCR in a Microfluidic Dynamic Array,” Plos ONE, 2008, 3(2):e1662. |
| Stevens Jr. et al., “Enhancement of phosphoprotein analysis using a fluorescent affinity tag and mass spectrometry,” Rapid Commun Mass Spectrom, 2005, 19(15):2157-62. |
| Stimpson et al., “Real-time detection of DNA hybridization and melting on oligonucleotide arrays by using optical wave guides,” Proc Natl Acad Sci USA, Jul. 1995, 92(14):6379-83. |
| Stoddart et al., “Single-nucleotide discrimination in immobilized DNA oligonucleotides with a biological nanopore,” PNAS U S A., May 2009, 106(19):7702-7707. |
| Stroh et al., “Quantum dots spectrally distinguish multiple species within the tumor milieu in vivo,” Nat Med., Jun. 2005, 11(6):678-82. |
| Subramanian et al., “Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles,” PNAS, Oct. 2005, 102(43):15545-15550. |
| Suh et al., “A simple soft lithographic route to fabrication of poly(ethylene glycol) microstructures for protein and cell patterning,” Biomaterials, Feb. 2004, 25(3):557-563. |
| Sumitomo et al., “Ca2+ ion transport through channels formed by -hemolysin analyzed using a microwell array on a Si substrate,” Biosensors and Bioelectronics. 2012, 31(1):445-450. |
| Summersgill et al., “Fluorescence In Situ Hybridization Analysis of Formalin Fixed Paraffin Embedded Tissues, Including Tissue Microarrays,” Chapter 4, Bridger, J. Ed., Methods in Molecular Biology 659, 2010, 51-70, 2010. |
| Sun et al., “Direct immobilization of DNA probes on non-modified plastics by UV irradiation and integration in microfluidic devices for rapid bioassay,” Anal. Bio. Chem., 402: 741-748, 2012. |
| Surzhik et al., “Template-dependent biosynthesis of polv(G) x poly (C) and its antiviral activity in vitro and in vivo,” Antiviral Res., May 1988, 38(2):131-40. |
| Sutherland et al., “Utility of formaldehyde cross-linking and mass spectrometry in the study of protein-protein interactions,” J. Mass Spectrom., Jun. 2008, 43(6):699-715. |
| Swartz et al., “Interstitial flow and its effects in soft tissues,” Annu Rev Biomed Eng., 2007, 9:229-56. |
| Syková et al., “Diffusion in brain extracellular space,” Physiol Rev., Oct. 2008, 88(4):1277-340. |
| Tai et al., “Replication-competent retrovirus vectors for cancer gene therapy,” Front Biosci., Jan. 2008, 13:3083-95. |
| Takahashi et al., “In Vitro Selection of Protein and Peptide Libraries Using mRNA Display,” Nucleic Acid and Peptide Aptamers: Methods and Protocols (2009) 535:293-314 (Ch. 17). |
| Tan et al., “Parylene peel-off arrays to probe the role of cell-cell interactions in tumour angiogenesis,” Integr Biol (Camb), Oct. 2009, 1(10):587-594. |
| Tang et al., “RNA-Seq analysis to capture the transcriptome landscape of a single cell.,” Nat Protoc., 5: 516-35, 2010. |
| Taniguchi et al., “Quantitative analysis of gene expression in a single cell by qPCR,” Nature Methods, 6, pp. 503-506, 2009. |
| Tawfik et al., “Man-made cell-like compartments for molecular evolution,” Nat Biotechnol., Jul. 1998, 16(7):652-6. |
| Taylor et al., “Mitochondrial DNA mutations in human disease.” Nature Reviews Genetics. May 2005, 6(5):389-402. |
| Tegtmeyer et al., “Alternative Interactions of the SV40 A Protein with DNA,” Virology, 1981, 115:75-87. |
| Thacker et al., “Alkaline Hydrolysis—Carcass Disposal: A Comprehensive Review,” National Agriculture Biosecurity Center, Aug. 2004, Chapter 6, pp. 1-12. |
| Thiery et al., “Multiplex target protein imaging in tissue sections by mass spectrometry—TAMSIM,” Rapid Commun. Mass Spectrom., 2007, 21:823-829. |
| Thorne et al., “In vivo diffusion analysis with quantum dots and dextrans predicts the width of brain extracellular space,” Proc Natl Acad Sci USA, Apr. 2006, 103(14):5567-5572. |
| Thornton, “High rate thick film growth.” Annual review of materials science, Aug. 1977, 7(1):239-60. |
| Tian et al., “Antigen peptide-based immunosensors for rapid detection of antibodies and antigens,” Anal Chem May 26, 2009, 81 (13):5218-5225. |
| Tijssen et al., “Overview of principles of hybridization and the strategy of nucleic acid assays” in Techniques in Biochemistry and Molecular Biology—Hybridization with Nucleic Acid Probes, 1993, 24(Chapter 2), 65 pages. |
| Timofeev et al., “Regioselective immobilization of short oligonucleotides to acrylic copolymer gels,” Nucleic Acids Res., Aug. 1996, 24(16):3142-8. |
| Tolbert et al., “New Methods for Proteomic Research: Preparation of Proteins with N-Terminal Cysteines for Labeling and Conjugation,” Angewandte Chemie International Edition. Jun. 17, 2002, 41(12):2171-4. |
| Totet et al., “Immunocompetent infants as a human reservoir for Pneumocystis jirovecii: rapid screening by non-invasive sampling and real-time PCR at the mitochondrial large subunit rRNA gene,” J Eukaryot Microbiol., 2003, pp. 668-669. |
| Toubanaki et al., “Dry-reagent disposable biosensor for visual genotyping of single nucleotide polymorphisms by oligonucleotide ligation reaction: application to pharmacogenetic analysis,” Hum Mutat., Aug. 2008, 29(8):1071-8. |
| Twyman et al., “Techniques Patents for SNP Genotyping,” Pharmacogenomics, Jan. 2003, 4(1):67-79. |
| U.S. Appl. No. 60/416,118 Fan et al., Multiplex Nucleic Acid Analysis Using Archived or Fixed Samples, filed Oct. 3, 2002, 22 pages. |
| Valencia et al., “mRNA-Display-Based Selections for Proteins with Desired Functions: A Protease-Substrate Case Study.” Biotechnology progress, May 2008, 24(3):561-9. |
| Valley et al., “Optoelectronic tweezers as a tool for parallel single-cell manipulation and stimulation,” IEEE Trans Biomed Circuits Syst., Dec. 2009, 3(6):424-31. |
| Van Gelder et al., “Amplified RNA synthesized from limited quantities of heterogeneous cDNA.” Proc. Natl. Acad. Sci. USA 87, 1663-1667, 1990. |
| Van Ness et al., “A versatile solid support system for oligodeoxy nucleotide probe-based hybridization assays”, Nucleic Acids Res. 19: 3345-3350, 1991. |
| Vasiliskov et al., “Fabrication of microarray of gel-immobilized compounds on a chip by copolymerization,” Biotechniques, Sep. 1999, 27(3):592-606. |
| Velculescu et al., “Serial analysis of gene expression.” Science, Oct. 20, 1995, 270(5235):484-7. |
| Vermesh et al., “High-density, multiplexed patterning of cells at single-cell resolution for tissue engineering and other applications,” Angew Chem Int Ed Engl, Aug. 2011, 50(32):7378-7380. |
| Vincent et al., “Helicase-dependent isothermal DNA amplification,” EMBO Rep., Aug. 2004, 5(8):795-800. |
| Viollet et al., “T4 RNA ligase 2 truncated active site mutants: improved tools for RNA analysis,” BMC Biotechnol., Jul. 2011, 11:72, 14 pages. |
| Vogelstein et al., “Digital PCR,” Proceedings of the National Academy of Sciences, Aug. 3, 1999, 96:9236-9241. |
| Wade et al., “Genome sequence, comparative analysis, and population genetics of the domestic horse.,” Science., 326: 865-7, 2009. |
| Waichman et al., “Functional immobilization and patterning of proteins by an enzymatic transfer reaction,” Analytical chemistry, Jan. 21, 2010, 82(4):1478-85. |
| Walker et al., “Strand displacement amplification—an isothermal in vitro DNA amplification technique,” Nucleic acids research, Apr. 11, 1992, 20(7):1691-1696. |
| Wang et al., “Mutations in NEXN, a Z-disc gene, are associated with hypertrophic cardiomyopathy,” Am J Hum Genet., Nov. 2010, 87(5):687-93. |
| Wang et al., “Single cell analysis: the new frontier in ‘omics’” Trends Biotechnol., 28: 281-90, 2010. |
| Wang et al., “High-fidelity mRNA amplification for gene profiling.” Nature biotechnology. Apr. 2000, 18(4):457-459. |
| Wang, “RNA amplification for successful gene profiling analysis,” J Transl Med., Jul. 2005, 3:28, 11 pages. |
| Watanabe et al., “Cellular networks involved in the influenza virus life cycle,” Cell Host & Microbe, Jun. 2010, 7(6):427-39. |
| Waxman et al., “De-regulation of common housekeeping genes in hepatocellular carcinoma,” BMC Genomics, 2007, 1-9. |
| Weichhart et al., “Functional selection of vaccine candidate peptides from Staphylococcus aureus whole-genome expression libraries in vitro,” Infection and Immunity, 2003, 71 (8):4333-4641. |
| Weinreich et al., “Evidence that the cis Preference of the Tn5 Transposase is Caused by Nonproductive Multimerization,” Genes and Development, Oct. 1994, 8(19):2363-2374. |
| Wheeler et al., “Microfluidic device for single-cell analysis,” Analytical Chemistry, Jul. 2003, 75(14):3581-3586. |
| Wiedmann et al., “Ligase chain reaction (LCR)—overview and applications,” PCR Methods Appl., Feb. 1994, 3(4):851-64. |
| Wikipedia.org [online], “Random hexamer,” Jan. 2012, Retrieved on Jan. 21, 2022, retrieved from URL<https://en.wikipedia.org/w/index.php?title=Random_hexamer&oldid=473042236>, 1 page. |
| Williams, “RAC reviews serious adverse event associated with AAV therapy trial,” Mol Ther., Dec. 2007, 15(12):2053-54. |
| Willi-Monnerat et al., “Comprehensive spatiotemporal transcriptomic analyses of the ganglionic eminences demonstrate the uniqueness of its caudal subdivision,” Molecular and Cellular Nueorsciences 37(4):845-856, 2008. |
| Wilson et al., “New transposon delivery plasmids for insertional mutagenesis in Bacillus anthracis,” J Microbiol Methods, Dec. 2007, 71(3):332-5. |
| Wolf et al., “Rapid hybridization kinetics of DNA attached to submicron latex particles”, Nucleic Acids Res. 15: 2911-2926, 1987. |
| Wong et al., “Direct Site-Selective Covalent Protein Immobilization Catalyzed by a Phosphopantetheinyl Transferase,” J. Am. Chem Soc., 2008, 130:12456-64. |
| Woo et al., “A Comparison of cDNA, Oligonucleotide, and Affymetrix GeneChip Gene Expression Microarray Platforms,” Journal of Biomolecular Techniques, 2004, 15(4), 276-284. |
| Wood et al., “Single cell trapping and DNA damage analysis using microwell arrays,” PNAS, Jun. 2010, 107(22):10008-10013. |
| Worthington et al., “Cloning of random oligonucleotides to create single-insert plasmid libraries,” Analyt. Biochem, 2001, 294:169-175. |
| Wright et al., “Reusable, reversibly sealable parylene membranes for cell and protein patterning,” J Biomed Mater Res A., May 2008, 85(2):530-538. |
| Wu et al., “Detection DNA Point Mutation with Rolling-Circle Amplification Chip,” Bioinformatics and Biomedical Engineering (ICBBE), 2010 4th International Conference on IEEE, Piscatway, NJ, USA, Jun. 18, 2010, 14 pages. |
| Xiao et al., “Direct determination of haplotypes from single DNA molecules,” Nature Methods, 2009, 6(3):199-201. |
| Xie et al. “CryoFISH: Fluorescence In Situ Hybridization on Ultrathin Cryosections,” Fluorescence in situ Hybridization (FISH), Jul. 2010, pp. 221-230. |
| Yan et al., “Decorin gene delivery inhibits cardiac fibrosis in spontaneously hypertensive rats by modulation of transforming growth factor-beta/Smad and p38 mitogen-activated protein kinase signaling pathways,” Hum Gene Ther., Oct. 2009, 20(10):1190-200. |
| Yasukawa et al., “Effects of organic solvents on the reverse transcription reaction catalyzed by reverse transcriptases from avian mycloblastosis virus and Moloney murine leukemia virus,” Biosci Biotechnol Biochem., 2010, 74(9):1925-30. |
| Yeakley et al., “Profiling alternative splicing on fiber-optic arrays,” Nature Biotechnology, Apr. 2002, 20(4):353-358. |
| Yershov et al., “DNA analysis and diagnostics on oligonucleotide microchips,” Proc. Natl. Acad. Sci. USA, May 1996, 93(10):4913-4918. |
| Yet et al., “Cardiac-specific expression of heme oxygenase-1 protects against ischemia and reperfusion injury in transgenic mice,” Circ Res., Jul. 2001, 89(2):168-73. |
| Yin et al., “Genetically encoded short peptide tag for versatile protein labeling by Sfp phosphopantetheinyl transferase,” PNAS, 2005, 102(44):15815-20. |
| Yonezawa et al., “DNA display for in vitro selection of diverse peptide libraries,” Nucleic Acids Research, 2003, 31 (19):e118. |
| Yusof et al., “Inkjet-like printing of single-cells,” Lab Chip, Jul. 2011, 11(14):2447-2454. |
| Zhang et al., “A novel mechanism of transposon-mediated gene activation,” PLoS Genet., Oct. 2009, 5(10):e1000689, 10 pages. |
| Zhang et al., “Binding-induced DNA assembly and its application to yoctomole detection of proteins,” Anal Chem (2012) 84(2):877-884. |
| Zhang et al., “Single-base mutational analysis of cancer and genetic diseases using membrane bound modified oligonucleotides,” Nucleic Acids Res., Jul. 1991, 19(14):3929-33. |
| Zhang et al., “Stripping custom microRNA microarrays and the lessons learned about probe-slide interactions,” Anal Biochem. Mar. 2009, 386(2):222-7. |
| Zheng et al., Origins of human mitochondrial point mutations as DNA polymerase mediated errors. Mutat. Res. 599(1-2): 11-20, 2006. |
| Zheng, “Spectroscopy-based quantitative fluorescence resonance energy transfer analysis,” Methods Mol Biol., 2006, 337:65-77. |
| Zhou et al., “Genetically encoded short peptide tags for orthogonal protein labeling by Sfp and AcpS phosphopantetheinyl transferases,” ACS Chemical Biol., 2007 25:337-346. |
| Zhu et al., “Reverse Transcriptase Template Switching: A Smart Approach for Full-Length cDNA Library Construction,” BioTechniques, 2001, 30(4):892-897. |
| Zieba et al., “Bright-field microscopy visualization of proteins and protein complexes by in situ proximity ligation with peroxidase detection,” Clin Chem, Jan. 2010, 56(1):99-110. |
| Zilberman et al., “Genome-wide analysis of DNA methylation patterns,” Development (2007) 134: 3959-3965. |
| Zuker, “Mfold web server for nucleic acid folding and hybridization prediction,” Nucleic Acids Res., Jul. 2003, 31(13):3406-15. |
| U.S. Appl. No. 16/353,937, filed Mar. 14, 2019, Frisen et al. |
| Ahern, “Biochemical, Reagents Kits Offer Scientists Good Return on Investment,” The Scientist, Jul. 1995, 9(15):20, 7 pages. |
| Ahlfen et al., “Determinants of RNA quality from FFPE samples,” PLoS One, Dec. 2007, 2(12):e1261, 7 pages. |
| Boulé et al., “Terminal deoxynucleotidyl transferase indiscriminately incorporates ribonucleotides and deoxyribonucleotides,” J Biol Chem., Aug. 2001, 276(33):31388-93. |
| Cardona et al., “TrakEM2 0.9a User Manual,” Sep. 8, 2011, retrieved on Jul. 29, 2022, retrieved from URL <https://www.ini.uzh.ch/˜acardona/trakem2_manual.html>, 38 pages. |
| Chen et al., “Gray-scale photolithography using microfluidic photomasks,” PNAS, Feb. 2003, 100(4):1499-1504. |
| Dalma-Weiszhausz et al., “The affymetrix GeneChip platform: an overview,” Methods Enzymol., 2006, 410:3-28. |
| Deo et al., “Detection of mammalian microRNA expression by in situ hybridization with RNA oligonucleotides,” Dev Dyn., Sep. 2006, 235(9):2538-48. |
| Escholarship.org [online], “Methods and devices for fabricating and assembling DNA and protein arrays for high-throughput analyses [electronic resource],” 2010, retrieved on Jun. 8, 2022, retrieved from URL<https://escholarship.org/uc/item/6tf7p46s>, 155 pages. |
| Evers et al., “The effect of formaldehyde fixation on RNA: optimization of formaldehyde adduct removal,” J Mol Diagn., May 2011, 13(3):282-8. |
| Fischer et al., “Hematoxylin and eosin staining of tissue and cell sections,” CSH Protoc., May 2008, 3(5):1-3. |
| Hafner et al., “Identification of microRNAs and other small regulatory RNAs using cDNA library sequencing,” Methods, Jan. 2008, 44(1):3-12. |
| Hanauer et al., “Separation of nanoparticles by gel electrophoresis according to size and shape,” Nano Lett., Sep. 2007, 7(9):2881-5. |
| Hattersley et al., “Development of a microfluidic device for the maintenance and interrogation of viable tissue biopsies,” Lab Chip., Nov. 2008, 8(11):1842-6. |
| Ho et al., “Characterization of an ATP-Dependent DNA Ligase Encoded by Chlorella Virus PBCV-1,” Journal of Virology, Mar. 1997, 71(3):1931-1937. |
| Hsuih et al., “Novel, Ligation-Dependent PCR Assay for Detection of Hepatitis C Virus in Serum,” Journal of Clinical Microbiology, Mar. 1996, 34(3):501-507. |
| Im et al., “An Introduction to Performing Immunofluorescence Staining,” Biobanking: Methods and Protocols, Method in Molecular Biology, Yong (ed.), 2019, 1897, Chapter 26, 299-311. |
| Jennane et al., “Photolithography of self-assembled monolayers: optimization of protecting groups by an electroanalytical method,” Can, J Chem., Dec. 1996, 74(12):2509-2517. |
| Kumar et al., “Template-directed oligonucleotide strand ligation, covalent intramolecular DNA circularization and catenation using click chemistry,” J Am Chem Soc., May 2007, 129(21):6859-64. |
| Lopez-Otín et al., “Protease degradomics: a new challenge for proteomics,” Nat Rev Mol Cell Biol., Jul. 2002, 3(7):509-19. |
| Magaki et al., “An introduction to Performance of Immunohistochemistry,” Biobanking: Methods and Protocols, Method in Molecular Biology, Yong (ed.), 2019, 1897, Chapter 25, 289-298. |
| Nandakumar et al., “RNA Substrate Specificity and Structure-guided Mutational Analysis of Bacteriophage T4 RNA Ligase 2,” Journal of Biological Chemistry, Jul. 2004, 279(30):31337-31347. |
| Ozsolak et al., “Digital transcriptome profiling from attomole-level RNA samples,” Genome Res., Apr. 2010, 20(4):519-25. |
| Shibata et al., “Detection of human papilloma vims in paraffin-embedded tissue using the polymerase chain reaction,” J Exp Med., Jan. 1988, 167(1):225-30. |
| Slomovic et al., “Addition of poly(A) and poly(A)-rich tails during RNA degradation in the cytoplasm of human cells,” Proc Natl Acad Sci USA, Apr. 2010, 107(16):7407-12. |
| Taylor et al., “Microfluidic local perfusion chambers for the visualization and manipulation of synapses,” Neuron., Apr. 2010, 66(1):57-68, 25 pages. |
| Toy et al., “A Simple Plastic Perfusion Chamber for Continuous Maintenance and Cinematography of Tissue Cultures,” Experimental Cell Research, 1958, 14:97-103. |
| Ulery et al., “Biomedical Applications of Biodegradable Polymers,” J Polym Sci B Polym Phys., Jun. 2011, 49(12):832-864. |
| Vandenbroucke et al., “Quantification of splice variants using real-time PCR,” Nucleic Acids Research, 2001, 29(13):e68, 7 pages. |
| Wang et al., “Paramagnetic microspheres with core-shell-ed structures,” Journal of Materials Science, Apr. 2012, 47(16):5946-54. |
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