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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Detalles Bibliográficos
Autores principales: Forer, Lukas, Schönherr, Sebastian, Weissensteiner, Hansi, Haider, Florian, Kluckner, Thomas, Gieger, Christian, Wichmann, Heinz-Erich, Specht, Günther, Kronenberg, Florian, Kloss-Brandstätter, Anita
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2894823/
https://www.ncbi.nlm.nih.gov/pubmed/20546565
http://dx.doi.org/10.1186/1471-2105-11-318

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2894823/
https://www.ncbi.nlm.nih.gov/pubmed/20546565
http://dx.doi.org/10.1186/1471-2105-11-318

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