Patent Application
20230178183
The present disclosure relates to the field of sequencing, and in particular to a sequencing method, an analysis method for sequencing results, an analysis system for sequencing results, a computer-readable storage medium, and an electronic device.
It is reported that single-molecule sequencing has been proposed as early as the 1980s. In 2003, the first single-molecule DNA sequencing experiment was successfully demonstrated by Dr. Stephen Quake, a professor in the Bioengineering Department of Stanford University. The first single-molecule sequencer (HeliScope) from Helicos was marketed in 2008. In 2009, Korlach and Turner published a paper in Science to introduce the principles of PacBio single-molecule sequencing technology. Thereafter, PacBio launched the PacBio RS sequencing system in 2010 and made it commercially available in 2011. Oxford Nanopore presented its MinION sequencing system at Advances in Genome Biology and Technology Conference (AGBT) in 2014. It is reported that Helicos, PacBio and MinION sequencing platforms all have high Single-Pass sequencing error rate up to 30%. Many studies have shown that the errors of the above sequencing platforms are mainly InDel and occur randomly, and the sequencing error rate can be reduced by repeated reading.
It has been reported in the literature that PacBio can overcome the high error rate problem of its Single Molecule Real-Time (SMRT) sequencing technology using Circular Consensus Sequence (CCS). In addition, MinION can significantly increase the sequencing accuracy up to 97% by the 2D and 1D2 sequencing methods.
It has been reported in literature that Helicos can reduce the error rate of deletion types in its sequencing to less than 1% by Two-Pass sequencing, but the procedures are tedious and complicated.
Thus, the existing sequencing methods are in need of further improvement.
Embodiments of the present disclosure seek to solve at least one of the problems existing in the related art to at least some extent. Accordingly, an embodiment of the present disclosure provides an effective sequencing method.
In a first aspect of the present disclosure, there is provided a sequencing method, comprising: (1) performing first sequencing on a sequencing template on a surface of a chip so as to obtain first sequencing data by forming a first newly generated sequencing strand, the sequencing template being ligated to the surface of the chip through a adapter; (2) performing first blocking on the 3′ end of at least a part of the first newly generated sequencing strand; and (3) performing second sequencing on the sequencing template so as to obtain second sequencing data by forming a second newly generated sequencing strand.
According to an embodiment, by performing two or more sequencing, mutual correction can be made subsequently to improve the accuracy of the sequencing results, and meanwhile, after a first run of sequencing, namely the first sequencing, by blocking the 3′ end of the newly generated sequencing strand remaining on the surface of the chip, the generation of interference signals can be effectively prevented in a second run of sequencing, namely the second sequencing. Thus, the accuracy of the sequencing results can be further improved.
In a second aspect of the present disclosure, provided is an analysis method for sequencing results. According to an embodiment of the present disclosure, the sequencing results include first sequencing data and second sequencing data, the first sequencing data and the second sequencing data both being composed of a plurality of reads, at least a part of the reads in the first sequencing data having corresponding reads in the second sequencing data, and the first sequencing data and the second sequencing data being obtained by the above method; and the analysis method for sequencing results comprises: (a) performing mutual correction based on at least a part of each of the first sequencing data and the second sequencing data so as to obtain final sequence information.
According to an embodiment, provided is an analysis method for sequencing results. The sequencing results include first sequencing data and second sequencing data, the first sequencing data and the second sequencing data both being composed of a plurality of reads, and at least a part of the reads in the first sequencing data having corresponding reads in the second sequencing data; and the analysis method for sequencing results comprises: (a) performing mutual correction based on at least a part of each of the first sequencing data and the second sequencing data so as to obtain final sequence information.
According to an embodiment, by performing mutual correction on the results of two runs of sequencing, the accuracy of the sequencing results can be improved. In addition, as described above, after a first run of sequencing, namely the first sequencing, by blocking the 3′ end of the newly generated sequencing strand remaining on the surface of the chip, the generation of interference signals can be effectively prevented in a second run of sequencing, namely the second sequencing. Thus, the accuracy of the sequencing results can be further improved.
In a third aspect of the present disclosure, also provided is an analysis system for sequencing results. According to an embodiment of the present disclosure, the system comprises: a sequencing device suitable for obtaining the sequencing results by the above method, which include first sequencing data and second sequencing data, the first sequencing data and the second sequencing data being both composed of a plurality of reads, and at least a part of the reads in the first sequencing data having corresponding reads in the second sequencing data; and an analysis device suitable for performing mutual correction based on at least a part of each of the first sequencing data and the second sequencing data so as to obtain final sequence information.
According to an embodiment, provided is an analysis system for sequencing results. The system comprises: a sequencing device used for obtaining the sequencing results, which include first sequencing data and second sequencing data, the first sequencing data and the second sequencing data being both composed of a plurality of reads, and at least a part of the reads in the first sequencing data having corresponding reads in the second sequencing data; and an analysis device suitable for performing mutual correction based on at least a part of each of the first sequencing data and the second sequencing data so as to obtain final sequence information.
The above analysis method for sequencing results can be effectively implemented by using any one of the above systems, so that the accuracy of the sequencing results can be improved by performing mutual correction on the results of multiple runs of sequencing. In addition, as described above, after a first run of sequencing, namely the first sequencing, by blocking the 3′ end of the newly generated sequencing strand remaining on the surface of the chip, the generation of interference signals can be effectively prevented in a second run of sequencing, namely the second sequencing. Thus, the accuracy of the sequencing results can be further improved.
Furthermore, the present disclosure provides a computer-readable storage medium having a computer program stored thereon. According to an embodiment, the program, when executed by a processor, implements the steps of any of the above methods.
The present disclosure also provides an electronic device, which comprises: the above computer-readable storage medium; and one or more processors to execute the program in the computer-readable storage medium.
Finally, the present disclosure provides a computer program product comprising instructions, which cause the computer to execute the sequencing method and/or the analysis method for sequencing results in any of the above embodiments when the program is executed by the computer.
The additional aspects and advantages of the present disclosure will be partially set forth in the following description, and will partially become apparent from the following description or be understood by practice of the present disclosure.
The aforementioned and/or additional aspects and advantages of the present disclosure will become apparent and easily understood from the description of the embodiments with reference to the following drawings, in which:
In the present disclosure, the terms “first” and “second” are used for description purpose only rather than being construed as indicating or implying relative importance or implicitly indicating the number or sequence of indicated technical features. Therefore, features defined with “first” and “second” may explicitly or implicitly include at least one of the features. In the description of the present disclosure, unless otherwise clearly and specifically defined, “a plurality of” means at least two, e.g., two or three.
Unless otherwise clearly specified and defined, the terms “mount”, “interconnect”, “connect”, “fix” and the like should be understood in their broad sense. For example, “connect” may be “fixedly connect”, “detachably connect” or “integrally connect”; “mechanically connect” and “electrically connect”; or “directly interconnect”, “indirectly interconnect through an intermediate”, “the communication between the interiors of two elements” or “the interaction between two elements”, unless otherwise clearly defined. For those of ordinary skill in the art, the specific meanings of the aforementioned terms in the present disclosure can be understood according to specific conditions.
The embodiments of the present disclosure are described in detail below, and the examples of the embodiments are shown in the drawings, throughout which identical or similar reference numerals represent identical or similar elements or elements having identical or similar functions. The embodiments described below with reference to the drawings are exemplary and are merely intended to explain the present disclosure rather than being construed as limiting the present disclosure.
In a first aspect of the present disclosure, provided is a sequencing method capable of reducing the output sequence noise and the error rate of a sequencing platform (e.g., the GenoCare™ single-molecule sequencing platform). The sequencing method according to an embodiment of the present disclosure is described with reference to
According to an embodiment, the method comprises the following steps.
S10: performing first sequencing to obtain first sequencing data.
In this step, first sequencing is performed on a sequencing template on a surface of a chip so as to obtain first sequencing data by forming a first newly generated sequencing strand, the sequencing template being ligated to the surface of the chip through a adapter thereon.
It should be noted that the term “chip” as used herein refers to a solid substrate having a surface, such as a planar surface, to which biomolecules to be detected are ligated, and is also known as flow cell. It is understood that the method is suitable for any sequencing platform that realizes nucleic acid sequence determination based on chip detection, such as the sequencing platforms based on the principle of the sequencing-by-synthesis currently being mainstream on the market, and is especially suitable for single-molecule sequencing platforms based on chip detection, such as GenoCare™, a single-molecule sequencing platform.
Referring to
S10a: hybridizing a library molecule in a sequencing library with the sequencing adapter on the surface of the chip;
S10b: forming the sequencing template by synthesizing a complementary strand with the library molecule as an initial template; and
S10c: removing the initial template, and performing a second blocking on the 3′ end of a nucleic acid molecule on the surface of the chip.
Thus, the influence of the remained active 3′ end on the subsequent reaction can be further eliminated by the second blocking. The “library” is a pool or a set of nucleic acid molecules or fragments of interest or under test derived from the nucleic acids of the sample under test. Generally, by processing fragments of interest or under test, e.g., adding known sequences, e.g., adapters, to one or both ends of fragments of interest, the fragments of interest (library molecules) can be ligated or immobilized onto (a surface of) a chip, and thus is suitable for loading onto a sequencing platform for sequencing.
Referring to
S20: performing first blocking on the 3′ end of at least a part of the first newly generated sequencing strand. In this step, the first blocking is performed on the 3′ end of at least a part of the first newly generated sequencing strand, by which the amount of valid data can be effectively increased and the interference of invalid data on information analysis can be reduced.
According to an embodiment, step S20 comprises: removing the first newly generated sequencing strand on the surface of the chip, and performing the first blocking on the 3′ end of the first newly generated sequencing strand remaining on the surface of the chip.
According to an embodiment, step S20 comprises: performing the first blocking on the 3′ end of the first newly generated sequencing strand, and removing the blocked first newly generated sequencing strand.
S30: performing second sequencing to obtain second sequencing data.
In this step, second sequencing is performed on the sequencing template so as to obtain second sequencing data by forming a second newly generated sequencing strand.
According to an embodiment, by performing two runs of sequencing, mutual correction can be made subsequently to improve the accuracy of the sequencing results, and meanwhile, after a first run of sequencing, namely the first sequencing, by blocking the 3′ end of the newly generated sequencing strand remaining on the surface of the chip, the generation of interference signals can be effectively prevented in a second run of sequencing, namely the second sequencing. Thus, the accuracy of the sequencing results can be further improved.
According to an embodiment, the first blocking, the second blocking, and the third blocking can be each independently performed by connecting the 3′ end hydroxyl group to an extension reaction blocker. Thus, the blocking effect can be further improved, so that the accuracy of sequencing can be further improved, and undesirable sequencing noise can be reduced.
According to an embodiment, the extension reaction blocker is ddNTP or a derivative thereof. Thus, the blocking effect can be further improved, so that the accuracy of sequencing can be further improved, and undesirable sequencing noise can be reduced.
According to an embodiment, the first blocking, the second blocking, and the third blocking are each independently performed using at least one of a DNA polymerase and a terminal transferase. Thus, the blocking effect can be further improved, so that the accuracy of sequencing can be further improved, and undesirable sequencing noise can be reduced.
According to an embodiment, the first blocking and the third blocking are each independently performed by connecting the 3′ end hydroxyl group to the ddNTP or the derivative thereof using a polymerase, and the second blocking is performed by connecting the 3′ end hydroxyl group to the ddNTP or the derivative thereof using the terminal transferase. Thus, the blocking effect can be further improved, so that the accuracy of sequencing can be further improved, and undesirable sequencing noise can be reduced.
In a second aspect of the present disclosure, provided is an analysis method for sequencing results, by which data of the two runs of sequencing generated by any of the above sequencing methods can be effectively analyzed, thereby further improving the accuracy of sequencing and avoiding sequencing errors.
Referring to
performing mutual correction based on at least a part of each of the first sequencing data and the second sequencing data so as to obtain final sequence information.
According to an embodiment, the mutual correction comprises the following steps:
selecting high-quality reads and corresponding reads of the high-quality reads in the first sequencing data and the second sequencing data, the lengths of the reads being not less than a predetermined length, and the sequencing quality of the reads being not less than a predetermined quality threshold; and
aligning the high-quality reads with the corresponding reads of the high-quality reads, and performing sequence information correction based on the results of the aligning.
According to an embodiment, by performing mutual correction on the results of two runs of sequencing, the accuracy of the sequencing results can be improved. In addition, as described above, after a first run of sequencing, namely the first sequencing, by blocking the 3′ end of the newly generated sequencing strand remaining on the surface of the chip, the generation of interference signals can be effectively prevented in a second run of sequencing, namely the second sequencing. Thus, the accuracy of the sequencing results can be further improved.
Referring to
S100: constructing a first read set.
In this step, a first read set is constructed based on the first sequencing data according to the lengths of the reads, the length of each read in the first read set being not less than a first predetermined length.
S200: constructing a second read set and a third read set.
In this step, a second read set and a third read set are constructed based on the first read set according to the lengths of the corresponding reads, the length of the corresponding read of each read in the second read set being not less than a second predetermined length, and the length of the corresponding read of each read in the third read set is within a predetermined length range.
S300: constructing a fourth read set and a fifth read set.
In this step, a fourth read set and a fifth read set are constructed based on the second read set and the corresponding reads thereof according to the sequencing quality of the reads in the second read set and the corresponding reads thereof.
According to an embodiment, the fourth read set and the fifth read set are each determined according to the following principles:
comparing the sequencing quality of the reads in the second read set with the sequencing quality of the corresponding reads thereof;
selecting the reads with higher sequencing quality as elements of the fourth read set, and selecting the reads with lower sequencing quality as elements of the fifth read set; and
in the case where the reads have the same sequencing quality, selecting the reads from the second read set as elements of the fourth read set, and selecting the corresponding reads as elements of the fifth read set.
S400: constructing a sixth read set.
In this step, the fourth read set is filtered according to the sequencing quality so as to construct a sixth read set, the sequencing quality of all of the reads in the sixth read set being not less than a first predetermined quality threshold.
S500: constructing a seventh read set.
In this step, the reads corresponding to the reads in the sixth read set are selected from the fifth read set according to the sixth read set so as to construct a seventh read set.
S600: aligning the sixth read set with the seventh read set to determine a first difference site.
In this step, the reads in the sixth read set are aligned with the reads in the seventh read set, and a first difference site is determined on the reads in the sixth read set.
S700: correcting the first difference site.
In this step, the first difference site is corrected using a predetermined sequencing error prediction model so as to determine first sequencing information, the sequencing error prediction model being used for determining the probability of an insertion or a deletion occurring at a difference site in a sequencing process.
Referring to
S400a: constructing an eighth read set.
In this step, the third read set is filtered according to the sequencing quality to construct an eighth read set, the sequencing quality of all of the reads in the eighth read set being not less than a second predetermined quality threshold.
S500a: constructing a ninth read set.
In this step, the reads corresponding to the reads in the seventh read set are selected from the second sequencing data according to the eighth read set so as to construct a ninth read set.
S600a: aligning the eighth read set with the ninth read set to determine a second difference site.
In this step, the reads in the eighth read set are aligned with the reads in the ninth read set, and a second difference site is determined on the reads in the eighth read set.
S700a: correcting the second difference site to determine second sequence information.
In this step, the second difference site is corrected using the sequencing error prediction model so as to determine second sequence information.
According to an embodiment, the sequencing error prediction model is obtained by training a naive Bayes model based on the results of aligning the first sequencing data and the second sequencing data with a reference genome.
According to an embodiment, for the first difference site and the second difference site:
if a read from the sixth read set has a base at the difference site, a corresponding read from the seventh read set has no base at the difference site, and the probability of a deletion occurring at the difference site is 50% or more, the base of the read from the sixth read set at the difference site is retained as a final sequencing result;
if a read from the sixth read set has no base at the difference site, a read from the seventh read set has a base at the difference site, and the probability of an insertion occurring at the difference site is 50% or more, the base of the read from the sixth read set at the difference site is retained as a final sequencing result; and
if a read from the sixth read set has a base at the difference site and a read from the seventh read set also has a base at the difference site, the base of the read from the sixth read set at the difference site is selected as a final sequencing result.
According to an embodiment, the first predetermined length and the second predetermined length are each independently not less than 20 bp, preferably not less than 25 bp; the predetermined length range is 10-25 bp; the first predetermined quality threshold and the second predetermined quality threshold are each independently not less than 50, preferably not less than 60.
Specifically, according to an embodiment, provided is a sequencing method for obtaining Reads1 and Reads2 by performing Two-Pass sequencing on a sequencing platform, e.g., the GenoCare™ single-molecule sequencing platform, using an adapter D7-S1-T/D9-S2 in combination with a sequencing primer D7S1T-R2P.
Embodiments of present disclosure provide an analysis method for analyzing the Reads1 and the Reads2 obtained by the above Two-Pass sequencing to obtain Consensus Reads. This analysis method can significantly reduce the noise sequences and the base error rate in the output Consensus Reads.
According to an embodiment, provided are an adapter and a sequencing primer for constructing a Two-Pass sequencing library, the adapter being obtained by annealing the oligonucleotide strand D7-S1-T and D9-S2 modified with a phosphate group at the 5′ end, and the sequencing primer being D7S1T-R2P. The D7-S1-T has a sequence of SEQ ID NO: 1, the D9-S2 has a sequence of SEQ ID NO: 2, and the D7S1T-R2P has a sequence of SEQ ID NO: 3.
According to an embodiment, there is provided a method for obtaining Reads1 and Reads2 by Two-Pass sequencing using the above adapter and the above sequencing primer, which comprises:
step 1: constructing a Two-Pass sequencing library, ligating an annealed adapter D7-S1-T/D9-S2 to a prepared fragmented human gDNA using a library preparation kit (VAHTS® Universal DNA Library Prep Kit for Illumina V2 (ND606-01)), and after the ligation, directly purifying the ligated gDNA without PCR amplification using a purification kit (VAHTS® DNA Clean Beads (N411-01)) to obtain a target library;
step 2: hybridizing the library obtained in the step 1 with an adapter on a surface of a sequencing chip;
step 3: synthesizing a complementary strand for an initial template hybridized on the surface of the chip in the step 2;
step 4 (optionally): blocking the 3′ end of a newly generated strand extended incompletely in the step 3 to reduce its interference with the sequencing;
step 5: performing denaturation to remove the initial template hybridized on the surface of the chip in the step 2;
step 6: blocking the 3′ end of the adapter remaining on the surface of the chip to reduce its interference with the sequencing;
step 7: hybridizing the sequencing primer D7S1T-R2P with the complementary strand synthesized in the step 3 as a template;
step 8: performing Read1 sequencing with the complementary strand synthesized in the step 3 as a template and the sequencing primer D7S1T-R2P hybridized in the step 7 as a primer;
step 9: performing denaturation to remove the newly generated sequencing strand in the step 8;
step 10: blocking the 3′ end of the newly generated sequencing strand in the step 8 that may be remained after the process in the step 9, to prevent the newly generated sequencing strand from continuing to extend during Read2 sequencing;
step 11: hybridizing the sequencing primer D7S1T-R2P with the complementary strand synthesized in the step 3 as a template;
step 12: performing the Read2 sequencing with the complementary strand synthesized in the step 3 as a template and the sequencing primer D7S1T-R2P hybridized in the step 11 as a primer;
step 13: dividing the sequencing data obtained in step 8 and step 12 to obtain sequences of Reads1 and Reads2 with coordinates corresponding in a one-to-one manner.
Further, the embodiment provides an analysis method for analyzing the Reads1 and the Reads2 obtained in any of the above embodiments to obtain Consensus Reads, which comprises:
step 14: constructing a correction model, which comprises: extracting, from the sequences of Reads1 and Reads2 obtained in the step 13, Reads with length ≥25 bp at the same coordinates/positions in both two runs of sequencing, outputting the extracted Reads as two files, T1 (from Reads1) and T2 (from Reads2), respectively, aligning the reads in T1 and T2 with a reference genome respectively, and calculating the probability of a Deletion or an Insertion occurring at middle bases under different combinations of preceding and following bases by a naive Bayes method. In the prediction process, for middle bases under different combinations of preceding and following bases, whether the middle base is retained is determined according to the probability of a Deletion or an Insertion occurring in the model. If the probability of a Deletion occurring in the model is more than 50%, the middle base is retained, otherwise, the middle base is discarded.
Step 15: filtering the Reads1 data obtained in the step 13 according to read length, and naming a set of sequences (reads) of the Reads1 with read length ≥25 bp as Fa1. By filtering out the sequences of short reads according to a read length of 25 bp, a part of noise sequences can be removed, and the mapping accuracy of the sequencing data is improved.
Step 16: dividing reads in the Fa1 obtained in the step 15 into two sets according to the lengths of their corresponding sequences (reads) in the Reads2 obtained in the step 13, in which the set of reads in the Fa1 with corresponding reads ≥25 bp in the Reads2 is named as Fa2, and a set of reads in the Fa1 with corresponding reads greater or equal to 10 bp and shorter than 25 bp is named as Fa3. Dividing the Fa1 into two parts for analysis here may reduce the loss of data throughput due to the filtering according to the length while improving the accuracy of Consensus Reads.
Step 17: comparing Q values of the reads in the Fa2 obtained in the step 16 with Q values of the reads in the Reads2 obtained in the step 13 with the coordinates corresponding thereto, naming a set of reads with higher Q values (selecting reads in the Fa2 when the Q values are equal) as Fa4, and naming a set of Reads with lower Q values (selecting reads in the Reads2 when the Q values are equal) as Fa5. The step divides the sequences (reads) of the Reads1 and the Reads2 into two sets with relative higher sequencing quality and lower sequencing quality, thereby may ensure the final output sequences of Consensus Reads are more accurate reads with higher sequencing quality in the two runs of sequencing.
Step 18: further filtering the Fa4 and the Fa5 obtained in the step 17, naming a set of the Reads in the Fa4 with Q values ≥a4 as Fa6, and naming a set of Reads in the Fa5 with coordinates corresponding to those of the Reads in the Fa6 as Fa7.
Step 19: aligning the Reads in the Fa6 and the Fa7 obtained in the step 18 in a one-to-one manner, grading the Reads according to the sequence similarity, correcting the Fa6 with the Fa7 as reference sequences, marking positions in the sequences of the Fa6 that are different from those in the sequences of the Fa7, and determining whether bases at the different positions are a Deletion or an Insertion one by one according to the correction model constructed in the step 14, so as to obtain Consensus Reads Part1 for output after the correction.
The expression of a different position in this step means that a base is detected only on one Read of either Fa6 or Fa7 at a certain position. In this case, whether the base should be retained is determined according to the correction model constructed in the step 14. If bases are detected in both of the Fa6 and the Fa7 at a certain position, but the types of the bases are not identical, the base in the Fa6 prevails, and this model does not correct for the above case.
Step 20: further filtering the Reads in the Fa3 obtained in the step 16, and naming a set of the Reads with Q values ≥a3 in the Fa3 as Fa8.
Step 21: extracting a set of the Reads in the Reads2 obtained in the step 13 with coordinates corresponding to those of the Reads in the Fa8, and naming the extracted set of the Reads as Fa9.
Step 22: aligning each Reads in the Fa9 with that in the Fa8, grading the Reads according to the sequence similarity, correcting the Fa8 with the Fa9 as reference sequences, marking positions in the Fa8 that are different from those in the Fa8, and determining whether bases at the different positions are a Deletion or an Insertion one by one according to the correction model constructed in the step 14, so as to obtain Consensus Reads Part2 for output after the correction.
Step 23: merging the Consensus Reads Part1 and the Consensus Reads Part2 with different similarity levels according to different application requirements to obtain the output Consensus Reads.
According to an embodiment, the process of hybridizing the library with an adapter on the surface of a sequencing chip described in the step 2 comprises (can be performed with conventional reagents):
1) denaturing the library for hybridization for 2-5 mins at 90-100° C.;
2) rapidly cooling the product obtained in the step 1) on an ice-water mixture for 2 mins or more to obtain a denatured hybridization library stock solution;
3) diluting the denatured hybridization library stock solution obtained in the step 2) to a suitable concentration, preferably 0.1-2 nM, with a hybridization solution (e.g., 3×SSC solution) to obtain a diluted hybridization library;
4) introducing 30-50 μL of the diluted hybridization library obtained in the step 3) into a sequencing chip channel pretreated with a dissolving reagent, and hybridizing the diluted hybridization library for 10-30 mins at 40-60° C.;
5) introducing 200-1000 μL of a cleaning solution 1 into the chip channel to remove the diluted hybridization library remained after the hybridization in the step 4); and
6) introducing 200-1000 μL of a cleaning solution 2 into the chip channel to remove the cleaning solution 1 in the step 5), so that the library is hybridized with an adapter on the surface of the sequencing chip.
According to an embodiment, the dissolving reagent comprises the following components: the cleaning solution 1 comprises the following components: 150 mM sodium chloride, 15 mM sodium citrate, 150 mM 4-hydroxyethylpiperazine ethanesulfonic acid, and 0.1% sodium dodecyl sulfate.
According to an embodiment, the cleaning solution 3 comprises the following components: 450 mM sodium chloride and 45 mM sodium citrate.
According to an embodiment, the cleaning solution 2 comprises the following components: 150 mM sodium chloride and 150 mM 4-hydroxyethylpiperazine ethanesulfonic acid.
According to an embodiment, the process of synthesizing a complementary strand for the initial template described in the step 3 comprises:
1) introducing 200-1000 μL of an extension reagent into the chip channel to perform a reaction at 50-70° C. for 5-10 mins;
2) introducing 200-1000 μL of the cleaning solution 1 into the chip channel to remove the extension reagent after the reaction in the step 1); and
3) introducing 200-1000 μL of the cleaning solution 2 into the chip channel to remove the cleaning solution 1 in the step 2), so that a complementary strand for the initial template is synthesized.
According to an embodiment, the extension reagent comprises the following components: 10-100 U/mL DNA polymerase, preferably Bst DNA polymerase, Bsu DNA polymerase, Klenow DNA polymerase, etc.; 0.2-2 mM dNTP; 0.5-2 M betaine, 20 mM tris(hydroxymethyl)aminomethane; 10 mM sodium chloride; 10 mM potassium chloride; 10 mM ammonium sulfate; 3 mM magnesium chloride; and 0.1% Triton X-100; pH 8.3.
According to an embodiment, the process of blocking the 3′ end of the strand extended incompletely described in the step 4 comprises:
1) introducing 200-1000 μL of a blocking reagent 1 into the chip channel to perform a reaction at 30-60° C. for 5-30 mins; and
2) introducing 200-1000 μL of the cleaning solution 1 into the chip channel to remove the blocking reagent 1 after the reaction in the step 1), so that the 3′ end of the strand extended incompletely is blocked.
According to an embodiment, the blocking reagent 1 comprises the following components: 10-100 U/mL DNA polymerase, preferably Klenow DNA polymerase, Bsu DNA polymerase, N9 DNA polymerase, etc.; 10-100 μM ddNTP; 5 mM manganese chloride; 20 mM tris(hydroxymethyl)aminomethane; 10 mM sodium chloride; 10 mM potassium chloride; 10 mM ammonium sulfate; 3 mM magnesium chloride; and 0.1% Triton X-100, pH 8.3.
According to an embodiment, the process of removing the initial template described in the step 5 comprises:
1) introducing 200-1000 μL of a denaturing reagent, which preferably may be formamide, 0.1 M NaOH, etc., into the chip channel to perform a reaction at 50-60° C. for 2-5 mins; and
2) introducing 200-1000 μL of the cleaning solution 1 into the chip channel to remove the denaturing reagent after the reaction in the step 1) and the initial template denatured and separated from the chip;
repeating the step 1) and the step 2) once, so that the initial template is removed.
According to an embodiment, the process of blocking the 3′ end of the adapter remaining on the surface of the chip described in the step 6 comprises:
1) introducing 200-1000 μL of the cleaning solution 2 into the chip channel;
2) introducing 200-1000 μL of a blocking reagent 2 into the chip channel to perform a reaction at 30-60° C. for 5-30 mins; and
3) introducing 200-1000 μL of the cleaning solution 1 into the chip channel to remove the blocking reagent 2 after the reaction in the step 2), so that the 3′ end of the adapter remaining on the surface of the chip is blocked.
According to an embodiment, the blocking reagent 2 comprises the following components: 100 U/mL terminal transferase (NEB, M0315L), 1×terminal transferase buffer, 0.25 mM cobalt chloride, and 10-100 μM ddNTP.
According to an embodiment, the process of hybridizing the sequencing primer D7S1T-R2P described in the step 7 comprises:
1) diluting a stock solution of the sequencing primer D7S1T-R2 to an appropriate concentration, preferably 0.1-1 μM, with a cleaning solution 3 to obtain a diluted sequencing primer hybridization solution;
2) introducing 200-1000 μL of the sequencing primer hybridization solution obtained in the step 1) into the chip channel to perform hybridization at 50-60° C. for 10-30 min;
3) introducing 200-1000 μL of the cleaning solution 1 into the chip channel to remove the sequencing primer remained after the hybridization in the step 2); and
According to an embodiment, the process of Read1 sequencing described in the step 8 can be performed with reference to the operation instructions in the GenoCare′ single-molecule two-color sequencing universal kit (filing number: YUESHEN XIEBEI 20190887).
According to an embodiment, the process of removing the newly generated sequencing strand described in the step 9 is performed with reference to step 5.
According to an embodiment, the process of blocking the 3′ end of the newly generated strand remained described in the step 10 can be performed with reference to step 4.
According to an embodiment, the process of hybridizing the sequencing primer D7S1T-R2P described in the step 11 is performed with reference to step 7.
According to an embodiment, the process of performing Read2 sequencing described in the step 12 is performed with reference to step 8.
According to an embodiment, the process of dividing the sequencing data to obtain sequences of Reads1 and Reads2 with coordinates corresponding in a one-to-one manner described in the step 13 comprises:
dividing each Read in the “.fa_” file output by BaseCalling into two parts evenly from the middle according to the number of sequencing cycles using python language, and outputting the two parts as two “.fa_” files, “Reads1.fa” and “Reads2.fa”, with identical sequence coordinates, respectively; and
removing the character “_” in Reads used in the files “Reads1.fa” and “Reads2.fa” obtained in the step 1) using python language, and outputting files “Reads1.fa” and “Reads2.fa”, so that sequences of Reads1 and Reads2 with coordinates corresponding in a one-to-one manner are obtained by dividing the sequencing data.
According to an embodiment, the process of constructing a correction model described in the step 14 comprises:
extracting, from the sequences of Reads1 and Reads2 obtained in the step 13, Reads with length ≥25 bp at the same coordinates in both two runs of sequencing, and outputting the extracted Reads as two fast files, T1 (from Reads1) and T2 (from Reads2), respectively;
aligning two corresponding Reads in the T1 and T2 files obtained in the step 1) in a sliding manner, and marking the same or different bases according to the results of the aligning, to obtain Common Reads;
mapping the T1 and T2 files obtained in the step 1) to reference sequences, to obtain Sam1 and Sam2 files;
finding the longest common substring Ref Reads in the reference sequences according to corresponding Reads in Sam1 and Sam2 obtained in the step 3) which are mapped to the same position; and
comparing bases that are different in two runs of sequencing in Common Reads obtained in the step 2) with Ref Reads obtained in the step 4), and calculating the probability of a Deletion or an Insertion occurring at middle bases under different combinations of preceding and following bases by a naive Bayes method, so that the correction model is constructed.
The method of any one of the above embodiments, in combination with the features of sequencing data, particularly single-molecule sequencing platform data, provides an optional sequencing method for obtaining Reads1 and Reads2 by performing Two-Pass sequencing using an adapter D7-S1-T/D9-S2 in combination with a sequencing primer D7S1T-R2P. In another aspect, the above related embodiments also provide an analysis method suitable for analyzing the data (Reads1 and Reads2) obtained by Two-Pass sequencing to obtain Consensus Reads. This analysis method can significantly reduce the noise sequences and the base error rate in the output Consensus Reads.
In a third aspect of the present disclosure, also provided is an analysis system for sequencing results capable of implementing the above analysis method for sequencing results. Referring to
The analysis method for sequencing results can be effectively implemented by using the system, so that the accuracy of the sequencing results can be improved by performing mutual correction on the results of two runs of sequencing. In addition, as described above, after a first run of sequencing, namely the first sequencing, by blocking the 3′ end of the newly generated sequencing strand remaining on the surface of the chip, the generation of interference signals can be effectively prevented in a second run of sequencing, namely the second sequencing. Thus, the accuracy of the sequencing results can be further improved.
Furthermore, the present disclosure provides a computer-readable storage medium having a computer program stored thereon, which, when executed by a processor, implements the steps of the above methods.
The present disclosure also provides an electronic device, which comprises: the above computer-readable storage medium; and one or more processors to execute the program in the computer-readable storage medium.
Embodiments of the present disclosure also provide a computer program product comprising instructions, which cause the computer to execute the sequencing method and/or the analysis method for sequencing results according to any one of the above embodiments when the program is executed by the computer.
The present disclosure will be described with reference to specific examples. It should be noted that these examples are only illustrative and not intended to limit the present disclosure in any way.
This example provides a set of sequencing and analysis methods for reducing the noise and error rate of the output sequence of a sequencing platform, particularly a single-molecule sequencing platform.
The set of sequencing and analysis methods provided by this example comprises:
a sequencing method for obtaining Reads1 and Reads2 by performing Two-Pass sequencing using an adapter D7-S1-T/D9-S2 in combination with a sequencing primer D7S1T-R2P. The adapter D7-S1-T/D9-S2 consists of an oligonucleotide strand D7-S1-T and D9-S2 modified with a phosphate group at the 5′ end. The D7-S1-T has a sequence of SEQ ID NO: 1, the D9-S2 has a sequence of SEQ ID NO: 2, and the sequencing primer D7S1T-R2P has a sequence of SEQ ID NO: 3. Specifically, the sequences and names of the primers involved in this example are summarized in Table 1.
The set of sequencing and analysis methods provided by this example also comprises an analysis method for analyzing the Reads1 and the Reads2 obtained by the above Two-Pass sequencing to obtain Consensus Reads. This analysis method can significantly reduce the noise sequences and the base error rate in the output Consensus Reads.
Further, the sequencing method for obtaining Reads1 and Reads2 by performing Two-Pass sequencing on a sequencing platform, e.g., the GenoCare™ single-molecule sequencing platform, using an adapter D7-S1-T/D9-S2 in combination with a sequencing primer D7S1T-R2P provided in this example comprises the following steps.
Step 1: constructing a Two-Pass sequencing library. An annealed D7-S1-T/D9-S2 adapter was ligated to a prepared fragmented human gDNA using a VAHTS® Universal DNA Library Prep Kit for Illumina V2 (ND606-01), and after the ligation, the ligated gDNA was directly purified without PCR amplification using VAHTS DNA Clean Beads (N411-01) to obtain a target library.
The specific steps of constructing a Two-Pass sequencing library in this example were as follows:
1) Fragmentation of human gDNAs: 0.1-1 μg of human gDNAs were fragmented ultrasonically to obtain DNA fragments of 100-300 bp, with the parameters of Covarisu set as follows: Peak Power, 75; Duty Factor, 25; Cycles/Burst, 50; Time(s), 250. Optionally, this step can be performed by an enzyme digestion method.
2) End-repair and A-tailing of the DNA fragments: the reaction system is shown in Table 2.
The reaction conditions: 20° C. for 15 min, followed by 65° C. for 10 min.
3) Ligation of the end-repaired and A-tailed product to an adapter: the reaction system is shown in Table 3.
The reaction conditions: left to stand at room temperature for 15 min after being well mixed.
4) Purification of the ligated product
The ligated product was purified using reagents of VAHTS® DNA Clean Beads (N411-01) according to the steps indicated in the instructions, and the operation instructions were slightly modified to recover 10 μL of products, so that a sequencing library was constructed. The specific steps were as follows:
a) the ligated PCR system was transferred into a 1.5 mL EP tube, followed by the addition of 0.8× (40 μL) magnetic beads, and the mixture was pipetted for 10 times to be well mixed and left to stand at room temperature for 3 min;
b) the 1.5 mL EP tube was placed on a magnetic rack and left to stand for 2-3 min, and the supernatant was removed;
c) the magnetic beads were rinsed with 200 μL of 80% ethanol and incubated at room temperature for 30 sec, and the supernatant was carefully removed;
d) the lid was opened, and the magnetic beads were dried for about 5-10 min until the residual ethanol was completely volatilized;
e) the tube was taken out of the rack and added with 22 μL of deionized water to elute the magnetic beads, after well mixing, the tube was left to stand at room temperature for 3 min and placed on the magnetic rack for 3 min until the solution was clarified, and 20 μL of the product was recovered, followed by the addition of 1.2× (24 μL) of magnetic beads, and the mixture was pipetted for 10 times to be well mixed and left to stand at room temperature for 3 min;
f) the 1.5 mL EP tube was placed on a magnetic rack and left to stand for 2-3 min, and the supernatant was removed;
g) steps c)-d) were repeated once; and
h) the tube was taken out of the rack and added with 11 μL of deionized water to elute the magnetic beads, after well mixing, the tube was left to stand at room temperature for 3 min and placed on the magnetic rack for 3 min until the solution was clarified, and 10 μL of the product was recovered, so that a sequencing library was constructed.
5) Quantification and detection
The constructed library was detected for concentration using Qubit 3.0 instrument and a Qubit dsDNA HS assay kit.
The constructed library was detected for fragment distribution using a LabChip DNA HS assay kit and a LabChip instrument.
Step 2: hybridizing the library obtained in the step 1 with a probe on the surface of a sequencing chip.
Chip Selection:
1) chip selection: the chip used was a chip modified with an epoxy group, and the probe was immobilized by the reaction of an amino group on the probe with the epoxy group on the surface of the chip, and the sequence is SEQ ID NO: 4. This example is not limiting as to the manner of surface modification and probe immobilization, which may be made, for example, with reference to published patent application CN109610006A, which is incorporated herein in its entirety.
The specific steps of hybridizing the library with a probe on the chip were as follows:
1) 3 μL of 20 nM sequencing library constructed in the step 1 was added with 3 μL of deionized water, and the mixture was mixed well and denatured at 95° C. for 5 min;
2) the denatured library obtained in the step 1) was rapidly cooled on an ice-water mixture for 2 min or more;
3) 24 μL of a hybridization solution was added to the product of the step 2) to dilute the library to a working concentration of 2 nM, where the hybridization solution was a 3×SSC buffer, and the 3×SSC buffer was prepared by diluting 20×SSC buffer (Sigma™, #56639-1L) with Rnase-free water.
4) 30 μL of the diluted hybridization library obtained in the step 3) was introduced into a channel of the chip, hybridized at 42° C. for 30 min, and cooled to room temperature;
5) 200 μL of a cleaning solution 1 was introduced into the hybridized channel obtained in the step 4), and the remaining library which was not hybridized to the surface of the chip was removed;
200 μL of a cleaning solution 2 was introduced into the hybridized channel of the chip to replace the cleaning solution 1 in the channel, so that the library was hybridized with the adapter on the surface of the sequencing chip.
The cleaning solution 1 comprises the following components: 150 mM sodium chloride, 15 mM sodium citrate, 150 mM 4-hydroxyethylpiperazine ethanesulfonic acid, and 0.1% sodium dodecyl sulfate.
The cleaning solution 2 comprises the following components: 150 mM sodium chloride and 150 mM 4-hydroxyethylpiperazine ethanesulfonic acid.
Step 3: synthesizing a complementary strand for an initial template.
The initial template was the library hybridized with the probe in the step 2. The specific steps of synthesizing a complementary strand for an initial template were as follows:
1) the chip hybridized with the library in the step 2 was placed in a sequencer;
2) 750 μL of an extension reagent was pumped into the hybridized channel of the chip, where the extension reagent comprises the following components: 120 U/mL Bst DNA polymerase (NEB, #M0275M), 0.2 mM dNTP (a mixture of dATP, dTTP, dCTP and dGTP, each at 0.2 μM), 1 M betaine, 20 mM tris(hydroxymethyl)aminomethane, 10 mM sodium chloride, 10 mM potassium chloride, 10 mM ammonium sulfate, 3 mM magnesium chloride, and 0.1% Triton X-100; pH 8.3;
3) the chip was heated to 60±0.5° C. and reacted for 10 min;
4) 220 μL of the cleaning solution 1 was pumped into the hybridized channel of the chip to remove the extension reagent; and
5) 440 μL of the cleaning solution 2 was pumped into the hybridized channel of the chip to remove the cleaning solution 1 in the step 4), so that a complementary strand for an initial template was synthesized.
Step 4 (optionally): blocking the 3′ end of the newly generated strand extended incompletely in the step 3. The specific steps of the blocking were as follows:
1) the chip was cooled to 37±0.5° C. and reacted for 90 s;
2) 750 μL of a blocking reagent 1 was pumped into the extended channel in the step 3 and reacted for 10 min, where the blocking reagent 1 comprises the following components: 100 U/mL Klenow fragment (3′→5′ exo−) (NEB, M0212M), 12.5 μM ddNTP mix (a mixture of ddATP, ddTTP, ddCTP and ddGTP, each at a concentration of 12.5 μM), 5 mM manganese chloride, 20 mM tris(hydroxymethyl)aminomethane, 10 mM sodium chloride, 10 mM potassium chloride, 10 mM ammonium sulfate, 3 mM magnesium chloride, and 0.1% Triton X-100; pH 8.3; and
3) 220 μL of the cleaning solution 1 was introduced into the blocked channel in the step 2) to remove the remaining blocking solution after the blocking reaction, so that the 3′ end of the newly generated strand extended incompletely was blocked.
Step 5: performing denaturation to remove the initial template. The specific steps of removing the initial template were as follows:
1) the chip was cooled to 55±0.5° C.;
2) 800 μL of formamide was introduced into the blocked channel in the step 4 to perform denaturation for 2 min;
3) 220 μL of the cleaning solution 1 was introduced into the blocked channel in the step 2) to remove the initial template after the denaturation; and
4) the step 2) and the step 3) were repeated once, so that the initial template was removed.
Step 6: blocking the 3′ end of the adapter remaining on the surface of the chip. The specific steps of blocking the 3′ end of the adapter remaining on the surface of the chip were as follows:
1) the chip was cooled to 37±0.5° C.;
2) 440 μL of the cleaning solution 2 was introduced into the blocked channel in the step 5 to replace the remaining cleaning solution 1 in the channel;
3) 750 μL of a blocking reagent 2 was introduced into the channel treated in the step 2) to perform a reaction for 15 min, where the blocking reagent 2 comprises the following components: 100 U/mL terminal transferase (NEB, M0315L), 1×terminal transferase buffer, 0.25 mM cobalt chloride, 100 μM ddNTP mix (a mixture of ddATP, ddTTP, ddCTP and ddGTP, each at a concentration of 100 μM); and 4) 220 μL of the cleaning solution 1 was introduced into the blocked channel in the step 3), so that the 3′ end of the adapter remaining on the surface of the chip was blocked.
Step 7: hybridization with the sequencing primer D7S1T-R2P. The specific steps of hybridization with the sequencing primer D7S1T-R2P were as follows:
1) the chip was heated to 55±0.5° C. and reacted for 1 min;
2) 800 μL of the diluted sequencing primer hybridization solution was introduced into the blocked channel in the step 6 for hybridization for 30 min, where the diluted sequencing primer hybridization solution is a cleaning solution 3 containing 0.1 μM of a primer D7S1T-R2P, and the cleaning solution 3 comprises the following components: 450 mM sodium chloride and 45 mM sodium citrate;
3) the chip was cooled to 37±0.5° C. and held for 90 s;
4) 220 μL of the cleaning solution 1 was introduced into the hybridized channel in the step 2) to remove the sequencing primer which was not hybridized in the channel;
5) 440 μL of the cleaning solution 2 was introduced into the channel treated in the step 4) to replace the cleaning solution 1 remaining in the channel, so that the sequencing primer was hybridized.
Step 8: performing Read1 sequencing. The specific steps of Read1 sequencing were as follows:
80 cycles of sequencing were performed, during which four nucleotides with two different fluorescent signals were adopted, and two nucleotides marked with different fluorescent signals were added in each cycle for signal detection.
Step 9: removing the newly generated sequencing strand.
The process of removing the newly generated sequencing strand was performed with reference to the procedures in the step 5.
Step 10: blocking the 3′ end of the remaining newly generated sequencing strand.
The process of blocking the 3′ end of the remaining newly generated sequencing strand was performed with reference to procedures in the step 4.
Step 11: hybridizing the sequencing primer D7S1T-R2P.
The process of hybridizing the sequencing primer D7S1T-R2P was performed with reference to procedures in the step 7.
Step 12: performing Read2 sequencing.
The process of Read2 sequencing was performed with reference to procedures in the step 8.
Step 13: dividing the sequencing data to obtain sequences of Reads1 and Reads2 with coordinates corresponding in a one-to-one manner.
The specific steps of dividing the sequencing data to obtain sequences of Reads1 and Reads2 with coordinates corresponding in a one-to-one manner in this example were as follows:
each Read in the “.fa_” file output by BaseCalling of 160 cycles of sequencing was divided, by python language, into two parts, i.e., first 80 cycles and last 80 cycles, the character “_” in all of the Reads was removed, and the two parts were output as two files with identical sequence coordinates, “Reads1.fa” and “Reads2. fa”, so that sequences of Reads1 and Reads2 with coordinates corresponding in a one-to-one manner were obtained by dividing the sequencing data.
Further, an analysis method for analyzing the Reads1 and the Reads2 obtained by the above Two-Pass sequencing to obtain Consensus Reads provided in this example comprises the following steps.
Step 14: constructing a correction model.
The specific steps of constructing the correction model in this example were as follows:
1) Reads with length ≥25 bp at the same coordinates in both two sequencing were extracted from the sequences of Reads1 and Reads2 obtained in the step 13 using python language, and the extracted Reads were then output as two fast files, T1 (from Reads1) and T2 (from Reads2), respectively, where the method for allowing the Reads at the same coordinates to be corresponding was to set the Reads IDs of Reads at the same coordinates to be identical in different Reads files when the files were generated;
2) the Reads in the T1 and the T2 were aligned with corresponding positions, and bases of the two Reads that were identical or not identical were marked in the alignment results to obtain Common Reads, where the corresponding of the positions was realized by determining whether the IDs of the two Reads were identical or not by comparison;
3) the T1 and T2 files were mapped to Reference to obtain Sam1 and Sam2 files, and the longest common substring Ref Reads were found in the Reference according to the Reads which were in corresponding positions in Sam1 and Sam2 and mapped to the same position, where the common substring refers to areas covered by two corresponding Reads after the mapping;
4) Common Reads in step 2) were compared with Ref Reads in step 3), where for Bases that were not identical in Common Reads, whether it was really present in the Reference was marked; if present, it was a Deletion for Reads in which this Base was not detected; if not present, it was a Insertion for Reads in which this Base was detected;
5) the Deletion and Insertion cases in the step 4) were counted, and meanwhile the types of bases preceding and following the positions where the bases were not identical were also counted. Thus, the probability of an Insertion or a Deletion occurring at the position preceding and following different types of bases was obtained.
Specifically, the naive Bayes model used in this example was as follows:
in which: P(D|XY) indicates the probability of Deletion occurring in a certain base when it is preceded and followed by X and Y bases, respectively, X,Y∈[A,C,G,T]; P(D) indicates the probability of Deletion occurring at a certain base; P(I) indicates the probability of Insertion occurring at a certain base.
P(XY|D) and P(XY|I) can be obtained by counting the frequency of the occurrence of the preceding and following bases when Deletion or Insertion occurs at different bases, and thus P(D|XY) and P(I|XY) can be calculated.
Step 15: filtering the reads according to a read length to obtain Fa1.
The specific steps of filtering the reads according to a read length in this example were as follows: all of the Reads in the Reads1 file were read line by line using Python language, and the Reads were output into a text file Fa1 if the length of the reads ≥25 bp.
Step 16: sorting the Reads in the Fa1 according to the read lengths of Reads2.
The specific steps of sorting the Reads in the Fa1 according to the read lengths of Reads2 described in this example were as follows:
all of the reads in the Fa1 corresponding to the reads in the Reads2 were read, and according to the lengths of the reads in the Reads2, if its corresponding reads in Reads2≥25 bp, then the reads in the Fa1 were saved in a Fa2 file; and if 10 bp≤Read2<25 bp, the corresponding Reads in the Fa1 were saved in a Fa3 file.
Step 17: outputting confidence reads according to a Q value.
The specific steps of outputting confidence Reads according to a Q value described in this example were as follows:
1) all of the Reads in Fa2 obtained in the step 16 were taken out, along with their corresponding Reads in the Reads2. The Reads ID was divided to obtain Quality Score values (abbreviated as Q value) of the Reads.
2) The Q values of the two corresponding Reads were compared, and the Reads with the larger Q value were output to the file Fa4, and the Reads with the smaller Q value were output to the file Fa5. If the Q values were equal, the Reads in the Reads1 were output to Fa4 and the Reads in the Reads2 were output to Fa5 by default.
Step 18: filtering the Reads in the Fa4 and the Fa5 according to Q values.
The specific steps of filtering the Reads in the Fa4 and the Fa5 according to Q values described in this example were as follows:
the Reads in the Fa4 were taken out, and if the Q value of the Reads in the Fa4≥60, the Reads were output to a file Fa6, and Reads in Fa5 corresponding to the Reads were output to a file Fa7.
Step 19: correcting the Reads in the Fa6 using the Reads in the Fa7 to obtain Consensus Reads Parts1 (abbreviated as CRP1).
The specific steps of the Reads in the Fa6 using the Reads in the Fa7 described in this example were as follows:
1) the Reads in the Fa6 and their corresponding Reads in the Fa7 were taken out, and the two corresponding Reads were aligned with each other to obtain a common consensus sequence portion, where the two sequences were aligned by a Smith-Waterman algorithm, and the consensus sequence refers to a local optimal matching sequence obtained by adding, deleting or modifying a part of Bases in the sequences after the alignment;
2) after the consensus sequence was obtained, positions where the bases were not identical in the consensus sequence were determined one by one according to the correction model constructed in the step 14, and the probability of a Deletion or an Insertion occurring at the Base position were calculated according to the types of the preceding and following bases of the Base position, where if the probability of a Deletion occurring at the position was more than 50%, it was determined that the Base detected at the position should not appear, and the Base at the position should be deleted, otherwise, the Base at the position should be retained;
3) after all Bases that were not identical were corrected, the corrected Reads were output, which was CRP1, where Base that were not identical here refers to a Base that is not detected in the two corresponding Reads at the same time, and if a Base is detected in both two Reads at the same position but the Base types are not identical and are not within the candidate range corrected in this example, the final Base type is based on the Base type of the Reads in the Fab.
Step 20: filtering the reads in the Fa3 according to Q values.
The specific steps of filtering the reads in the Fa3 according to Q values described in this example were as follows:
All of the Reads in the Fa3 were taken out, the Reads ID of the Reads in the Fa3 were divided to obtain the Q value of each of the Reads, and the Reads with the Q value ≥60 were output to the file Fa8.
Step 21: outputting the Reads of Reads2 corresponding to Reads in the Fa8 file.
The specific steps of outputting the Reads of Reads2 corresponding to Reads in the file Fa8 described in this example were as follows:
All of the Reads in the file Fa8 were taken out, and the corresponding Reads in the Reads2 were taken out and output to the file Fa9.
Step 22: correcting the Reads in the Fa8 using the Reads in the Fa9 to obtain Consensus Reads Parts2 (CRP2).
Specifically, the process of correcting the Reads in the Fa8 using the Reads in the Fa9 described in this example was performed with reference to procedures in the step 19.
Step 23: merging and outputting the Reads in the CRP1 and the CRP2 meeting the similarity threshold according to the requirements of different applications on the accuracy of the sequencing data to obtain Consensus Reads.
The specific steps of filtering and outputting the Reads in the Consensus Reads Parts according to the requirements of the different applications on the accuracy of the sequencing data described in this example were as follows:
1) the corresponding similarity threshold values were set according to the requirements of different applications on the accuracy of the sequencing data, where the similarity thresholds for the Part1 and the Part2 may be different;
2) the similarities of the Reads in CRP1 and CRP2 were calculated, where the similarity refers to the similarity between the corresponding Reads in the Reads1 and the Reads2; to calculate the similarities, the two corresponding Reads are aligned with each other; and then the ratio of the identical Base number in the consensus sequence obtained by the registration to the total Base number was calculated, where the alignment method, consensus sequence and Bases that are not identical are defined as in the step 19; and
3) the Reads in the CRP1 and the CRP2 meeting the requirement of the similarity threshold were output to a final file according to the requirements of different applications on the accuracy of the sequencing data to obtain Consensus Reads. The results are shown in Table 4.
Reference throughout this specification to “an embodiment”, “one embodiment”, “another embodiment”, “some embodiments”, “an example”, “a specific example”, “another example”, or “some examples”, means that a particular feature, structure, material, or characteristic described in connection with the embodiment or example is included in at least one embodiment or example of the present disclosure. Thus, the appearances of the phrases such as “in an embodiment”, “in one embodiment”, “in another embodiment”, “in some embodiments”, “in an example”, “in a specific example”, “in another example”, or “in some examples”, in various places throughout this specification are not necessarily referring to the same embodiment or example of the present disclosure. Furthermore, the particular features, structures, materials, or characteristics may be combined in any suitable manner in one or more embodiments or examples. In addition, in the absence of contradiction, those skilled in the art can combine the different embodiments or examples described in this specification, or combine the features of different embodiments or examples.
Although embodiments of the present disclosure have been shown and described above, it would be appreciated by those skilled in the art that the above embodiments are illustrative, cannot be construed to limit the present disclosure, and changes, alternatives, modifications and variants can be made in the embodiments within the scope of the present disclosure.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202010362587.6 | Apr 2020 | CN | national |
| 202010865293.5 | Aug 2020 | CN | national |
| 202010867569.3 | Aug 2020 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2021/091279 | 4/30/2021 | WO |
