Published in
Oxford University Press (OUP), Bioinformatics, 13(27), p. 1873-1875
DOI: 10.1093/bioinformatics/btr264
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famCNV: copy number variant association for quantitative traits in families
Journal article published in 2011 by
Hariklia Eleftherohorinou,
Johanna C. Andersson-Assarsson,
Robin G. Walters,
Julia S. El-Sayed Moustafa 
,
Lachlan Coin ,
Peter Jacobson,
Lena M. S. Carlsson,
Alexandra I. F. Blakemore,
Philippe Froguel,
Andrew J. Walley ,
Mario Falchi
,
Lachlan Coin ,
Peter Jacobson,
Lena M. S. Carlsson,
Alexandra I. F. Blakemore,
Philippe Froguel,
Andrew J. Walley ,
Mario Falchi
This paper is made freely available by the publisher.
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Abstract
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 traits is assessed through formal likelihood testing.