CONAN: copy number variation analysis software for genome-wide association studies

BACKGROUND: Genome-wide association studies (GWAS) based on single nucleotide polymorphisms (SNPs) revolutionized our perception of the genetic regulation of complex traits and diseases. Copy number variations (CNVs) promise to shed additional light on the genetic basis of monogenic as well as compl...

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Detaylı Bibliyografya
Asıl Yazarlar: Forer, Lukas, Schönherr, Sebastian, Weissensteiner, Hansi, Haider, Florian, Kluckner, Thomas, Gieger, Christian, Wichmann, Heinz-Erich, Specht, Günther, Kronenberg, Florian, Kloss-Brandstätter, Anita
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2010
Konular:
Software
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2894823/
https://ncbi.nlm.nih.gov/pubmed/20546565
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-11-318
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