famCNV: copy number variant association for quantitative traits in families

Summary: A program package to enable genome-wide association of copy number variants (CNVs) with quantitative phenotypes in families of arbitrary size and complexity. Intensity signals that act as proxies for the number of copies are modeled in a variance component framework and association with tra...

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Bibliografiska uppgifter
Huvudupphovsmän: Eleftherohorinou, Hariklia, Andersson-Assarsson, Johanna C., Walters, Robin G., El-Sayed Moustafa, Julia S., Coin, Lachlan, Jacobson, Peter, Carlsson, Lena M. S., Blakemore, Alexandra I. F., Froguel, Philippe, Walley, Andrew J., Falchi, Mario
Materialtyp: Artigo
Språk:Inglês
Publicerad: Oxford University Press 2011
Ämnen:
Applications Note
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3117380/
https://ncbi.nlm.nih.gov/pubmed/21546396
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr264
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