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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2011
Témata:
Applications Note
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky