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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Detalles Bibliográficos
Autores principales: Challis, Danny, Yu, Jin, Evani, Uday S, Jackson, Andrew R, Paithankar, Sameer, Coarfa, Cristian, Milosavljevic, Aleksandar, Gibbs, Richard A, Yu, Fuli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292476/
https://www.ncbi.nlm.nih.gov/pubmed/22239737
http://dx.doi.org/10.1186/1471-2105-13-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292476/
https://www.ncbi.nlm.nih.gov/pubmed/22239737
http://dx.doi.org/10.1186/1471-2105-13-8

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