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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2010
Assuntos:
Software
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados