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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Detalhes bibliográficos
Main Authors: Forer, Lukas, Schönherr, Sebastian, Weissensteiner, Hansi, Haider, Florian, Kluckner, Thomas, Gieger, Christian, Wichmann, Heinz-Erich, Specht, Günther, Kronenberg, Florian, Kloss-Brandstätter, Anita
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2010
Assuntos:
Software
Acesso em linha: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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