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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Библиографические подробности
Главные авторы: 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
Формат: Artigo
Язык:Inglês
Опубликовано: Oxford University Press 2011
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Applications Note
Online-ссылка: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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