An integrative variant analysis suite for whole exome next-generation sequencing data

BACKGROUND: Whole exome capture sequencing allows researchers to cost-effectively sequence the coding regions of the genome. Although the exome capture sequencing methods have become routine and well established, there is currently a lack of tools specialized for variant calling in this type of data...

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Détails bibliographiques
Auteurs principaux: Challis, Danny, Yu, Jin, Evani, Uday S, Jackson, Andrew R, Paithankar, Sameer, Coarfa, Cristian, Milosavljevic, Aleksandar, Gibbs, Richard A, Yu, Fuli
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2012
Sujets:
Software
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3292476/
https://ncbi.nlm.nih.gov/pubmed/22239737
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-13-8
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