Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes

Motivation: The development of cost-effective next-generation sequencing methods has spurred the development of high-throughput bioinformatics tools for detection of sequence variation. With many disparate variant-calling algorithms available, investigators must ask, ‘Which method is best for my dat...

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Detalhes bibliográficos
Publicado no:Bioinformatics
Main Authors: Trubetskoy, Vassily, Rodriguez, Alex, Dave, Uptal, Campbell, Nicholas, Crawford, Emily L., Cook, Edwin H., Sutcliffe, James S., Foster, Ian, Madduri, Ravi, Cox, Nancy J., Davis, Lea K.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2015
Assuntos:
Original Papers
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4287941/
https://ncbi.nlm.nih.gov/pubmed/25270638
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu591
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