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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Detaylı Bibliyografya
Asıl Yazarlar: 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.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: S. Karger AG 2011
Konular:
Original Paper
Online Erişim: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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