The variant call format and VCFtools

Summary: The variant call format (VCF) is a generic format for storing DNA polymorphism data such as SNPs, insertions, deletions and structural variants, together with rich annotations. VCF is usually stored in a compressed manner and can be indexed for fast data retrieval of variants from a range o...

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Detalhes bibliográficos
Main Authors: Danecek, Petr, Auton, Adam, Abecasis, Goncalo, Albers, Cornelis A., Banks, Eric, DePristo, Mark A., Handsaker, Robert E., Lunter, Gerton, Marth, Gabor T., Sherry, Stephen T., McVean, Gilean, Durbin, Richard
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2011
Assuntos:
Applications Note
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3137218/
https://ncbi.nlm.nih.gov/pubmed/21653522
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr330
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