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

Internet

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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