CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics

BACKGROUND: Recent studies have shown that copy number variations (CNVs) are frequent in higher eukaryotes and associated with a substantial portion of inherited and acquired risk for various human diseases. The increasing availability of high-resolution genome surveillance platforms provides opport...

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Huvudupphovsmän: Gai, Xiaowu, Perin, Juan C, Murphy, Kevin, O'Hara, Ryan, D'arcy, Monica, Wenocur, Adam, Xie, Hongbo M, Rappaport, Eric F, Shaikh, Tamim H, White, Peter S
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2010
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Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2827374/
https://ncbi.nlm.nih.gov/pubmed/20132550
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-11-74
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