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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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2011
Assuntos:
Applications Note
Acesso em linha: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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