Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data

MOTIVATION: Variant calling from next-generation sequencing (NGS) data is susceptible to false positive calls due to sequencing, mapping and other errors. To better distinguish true from false positive calls, we present a method that uses genotype array data from the sequenced samples, rather than p...

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Publicado en:Bioinformatics
Autores principales: Shringarpure, Suyash S, Mathias, Rasika A, Hernandez, Ryan D, O’Connor, Timothy D, Szpiech, Zachary A, Torres, Raul, De La Vega, Francisco M, Bustamante, Carlos D, Barnes, Kathleen C, Taub, Margaret A
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2017
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Original Papers
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5408850/
https://ncbi.nlm.nih.gov/pubmed/28035032
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btw786
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