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SMaSH: a benchmarking toolkit for human genome variant calling

Motivation: Computational methods are essential to extract actionable information from raw sequencing data, and to thus fulfill the promise of next-generation sequencing technology. Unfortunately, computational tools developed to call variants from human sequencing data disagree on many of their pre...

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Detalhes bibliográficos
Main Authors: Talwalkar, Ameet, Liptrap, Jesse, Newcomb, Julie, Hartl, Christopher, Terhorst, Jonathan, Curtis, Kristal, Bresler, Ma’ayan, Song, Yun S., Jordan, Michael I., Patterson, David
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4173010/
https://ncbi.nlm.nih.gov/pubmed/24894505
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu345
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