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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...
Autores principales: | Challis, Danny, Yu, Jin, Evani, Uday S, Jackson, Andrew R, Paithankar, Sameer, Coarfa, Cristian, Milosavljevic, Aleksandar, Gibbs, Richard A, Yu, Fuli |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
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 |
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