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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Bibliografiske detaljer
Main Authors: Forer, Lukas, Schönherr, Sebastian, Weissensteiner, Hansi, Haider, Florian, Kluckner, Thomas, Gieger, Christian, Wichmann, Heinz-Erich, Specht, Günther, Kronenberg, Florian, Kloss-Brandstätter, Anita
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2010
Fag:
Software
Online adgang: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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