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Copy Number Variation detection from 1000 Genomes project exon capture sequencing data

BACKGROUND: DNA capture technologies combined with high-throughput sequencing now enable cost-effective, deep-coverage, targeted sequencing of complete exomes. This is well suited for SNP discovery and genotyping. However there has been little attention devoted to Copy Number Variation (CNV) detecti...

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Detalles Bibliográficos
Autores principales:	Wu, Jiantao, Grzeda, Krzysztof R, Stewart, Chip, Grubert, Fabian, Urban, Alexander E, Snyder, Michael P, Marth, Gabor T
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Methodology Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563612/ https://www.ncbi.nlm.nih.gov/pubmed/23157288 http://dx.doi.org/10.1186/1471-2105-13-305

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