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Sniper: improved SNP discovery by multiply mapping deep sequenced reads

SNP (single nucleotide polymorphism) discovery using next-generation sequencing data remains difficult primarily because of redundant genomic regions, such as interspersed repetitive elements and paralogous genes, present in all eukaryotic genomes. To address this problem, we developed Sniper, a nov...

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Detalles Bibliográficos
Autores principales: Simola, Daniel F, Kim, Junhyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218843/
https://www.ncbi.nlm.nih.gov/pubmed/21689413
http://dx.doi.org/10.1186/gb-2011-12-6-r55
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author Simola, Daniel F
Kim, Junhyong
author_facet Simola, Daniel F
Kim, Junhyong
author_sort Simola, Daniel F
collection PubMed
description SNP (single nucleotide polymorphism) discovery using next-generation sequencing data remains difficult primarily because of redundant genomic regions, such as interspersed repetitive elements and paralogous genes, present in all eukaryotic genomes. To address this problem, we developed Sniper, a novel multi-locus Bayesian probabilistic model and a computationally efficient algorithm that explicitly incorporates sequence reads that map to multiple genomic loci. Our model fully accounts for sequencing error, template bias, and multi-locus SNP combinations, maintaining high sensitivity and specificity under a broad range of conditions. An implementation of Sniper is freely available at http://kim.bio.upenn.edu/software/sniper.shtml.
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spelling pubmed-32188432011-11-18 Sniper: improved SNP discovery by multiply mapping deep sequenced reads Simola, Daniel F Kim, Junhyong Genome Biol Method SNP (single nucleotide polymorphism) discovery using next-generation sequencing data remains difficult primarily because of redundant genomic regions, such as interspersed repetitive elements and paralogous genes, present in all eukaryotic genomes. To address this problem, we developed Sniper, a novel multi-locus Bayesian probabilistic model and a computationally efficient algorithm that explicitly incorporates sequence reads that map to multiple genomic loci. Our model fully accounts for sequencing error, template bias, and multi-locus SNP combinations, maintaining high sensitivity and specificity under a broad range of conditions. An implementation of Sniper is freely available at http://kim.bio.upenn.edu/software/sniper.shtml. BioMed Central 2011 2011-06-20 /pmc/articles/PMC3218843/ /pubmed/21689413 http://dx.doi.org/10.1186/gb-2011-12-6-r55 Text en Copyright ©2011 Simola and Kim; licensee BioMed Central Ltd http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited
spellingShingle Method
Simola, Daniel F
Kim, Junhyong
Sniper: improved SNP discovery by multiply mapping deep sequenced reads
title Sniper: improved SNP discovery by multiply mapping deep sequenced reads
title_full Sniper: improved SNP discovery by multiply mapping deep sequenced reads
title_fullStr Sniper: improved SNP discovery by multiply mapping deep sequenced reads
title_full_unstemmed Sniper: improved SNP discovery by multiply mapping deep sequenced reads
title_short Sniper: improved SNP discovery by multiply mapping deep sequenced reads
title_sort sniper: improved snp discovery by multiply mapping deep sequenced reads
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218843/
https://www.ncbi.nlm.nih.gov/pubmed/21689413
http://dx.doi.org/10.1186/gb-2011-12-6-r55
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