Cargando…
PyroHMMsnp: an SNP caller for Ion Torrent and 454 sequencing data
Both 454 and Ion Torrent sequencers are capable of producing large amounts of long high-quality sequencing reads. However, as both methods sequence homopolymers in one cycle, they both suffer from homopolymer uncertainty and incorporation asynchronization. In mapping, such sequencing errors could sh...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711422/ https://www.ncbi.nlm.nih.gov/pubmed/23700313 http://dx.doi.org/10.1093/nar/gkt372 |
_version_ | 1782276945978851328 |
---|---|
author | Zeng, Feng Jiang, Rui Chen, Ting |
author_facet | Zeng, Feng Jiang, Rui Chen, Ting |
author_sort | Zeng, Feng |
collection | PubMed |
description | Both 454 and Ion Torrent sequencers are capable of producing large amounts of long high-quality sequencing reads. However, as both methods sequence homopolymers in one cycle, they both suffer from homopolymer uncertainty and incorporation asynchronization. In mapping, such sequencing errors could shift alignments around homopolymers and thus induce incorrect mismatches, which have become a critical barrier against the accurate detection of single nucleotide polymorphisms (SNPs). In this article, we propose a hidden Markov model (HMM) to statistically and explicitly formulate homopolymer sequencing errors by the overcall, undercall, insertion and deletion. We use a hierarchical model to describe the sequencing and base-calling processes, and we estimate parameters of the HMM from resequencing data by an expectation-maximization algorithm. Based on the HMM, we develop a realignment-based SNP-calling program, termed PyroHMMsnp, which realigns read sequences around homopolymers according to the error model and then infers the underlying genotype by using a Bayesian approach. Simulation experiments show that the performance of PyroHMMsnp is exceptional across various sequencing coverages in terms of sensitivity, specificity and F(1) measure, compared with other tools. Analysis of the human resequencing data shows that PyroHMMsnp predicts 12.9% more SNPs than Samtools while achieving a higher specificity. (http://code.google.com/p/pyrohmmsnp/). |
format | Online Article Text |
id | pubmed-3711422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37114222013-07-15 PyroHMMsnp: an SNP caller for Ion Torrent and 454 sequencing data Zeng, Feng Jiang, Rui Chen, Ting Nucleic Acids Res Methods Online Both 454 and Ion Torrent sequencers are capable of producing large amounts of long high-quality sequencing reads. However, as both methods sequence homopolymers in one cycle, they both suffer from homopolymer uncertainty and incorporation asynchronization. In mapping, such sequencing errors could shift alignments around homopolymers and thus induce incorrect mismatches, which have become a critical barrier against the accurate detection of single nucleotide polymorphisms (SNPs). In this article, we propose a hidden Markov model (HMM) to statistically and explicitly formulate homopolymer sequencing errors by the overcall, undercall, insertion and deletion. We use a hierarchical model to describe the sequencing and base-calling processes, and we estimate parameters of the HMM from resequencing data by an expectation-maximization algorithm. Based on the HMM, we develop a realignment-based SNP-calling program, termed PyroHMMsnp, which realigns read sequences around homopolymers according to the error model and then infers the underlying genotype by using a Bayesian approach. Simulation experiments show that the performance of PyroHMMsnp is exceptional across various sequencing coverages in terms of sensitivity, specificity and F(1) measure, compared with other tools. Analysis of the human resequencing data shows that PyroHMMsnp predicts 12.9% more SNPs than Samtools while achieving a higher specificity. (http://code.google.com/p/pyrohmmsnp/). Oxford University Press 2013-07 2013-05-21 /pmc/articles/PMC3711422/ /pubmed/23700313 http://dx.doi.org/10.1093/nar/gkt372 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online Zeng, Feng Jiang, Rui Chen, Ting PyroHMMsnp: an SNP caller for Ion Torrent and 454 sequencing data |
title | PyroHMMsnp: an SNP caller for Ion Torrent and 454 sequencing data |
title_full | PyroHMMsnp: an SNP caller for Ion Torrent and 454 sequencing data |
title_fullStr | PyroHMMsnp: an SNP caller for Ion Torrent and 454 sequencing data |
title_full_unstemmed | PyroHMMsnp: an SNP caller for Ion Torrent and 454 sequencing data |
title_short | PyroHMMsnp: an SNP caller for Ion Torrent and 454 sequencing data |
title_sort | pyrohmmsnp: an snp caller for ion torrent and 454 sequencing data |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711422/ https://www.ncbi.nlm.nih.gov/pubmed/23700313 http://dx.doi.org/10.1093/nar/gkt372 |
work_keys_str_mv | AT zengfeng pyrohmmsnpansnpcallerforiontorrentand454sequencingdata AT jiangrui pyrohmmsnpansnpcallerforiontorrentand454sequencingdata AT chenting pyrohmmsnpansnpcallerforiontorrentand454sequencingdata |