Copy Number Variation Accuracy in Genome-Wide Association Studies

BACKGROUND/AIM: Copy number variations (CNVs) are a major source of alterations among individuals and are a potential risk factor in many diseases. Numerous diseases have been linked to deletions and duplications of these chromosomal segments. Data from genome-wide association studies and other micr...

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Detalhes bibliográficos
Main Authors: Lin, Peng, Hartz, Sarah M., Wang, Jen-Chyong, Krueger, Robert F., Foroud, Tatiana M., Edenberg, Howard J., Nurnberger, John I., Brooks, Andrew I., Tischfield, Jay A., Almasy, Laura, Webb, Bradley T., Hesselbrock, Victor M., Porjesz, Bernice, Goate, Alison M., Bierut, Laura J., Rice, John P.
Formato: Artigo
Idioma:Inglês
Publicado em: S. Karger AG 2011
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Original Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3153341/
https://ncbi.nlm.nih.gov/pubmed/21778733
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000324683
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