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famCNV: copy number variant association for quantitative traits in families.

Abstract:
UNLABELLED: 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. AVAILABILITY AND IMPLEMENTATION: The Java package is made available at www.imperial.ac.uk/medicine/people/m.falchi/. CONTACT: m.falchi@imperial.ac.uk.
Publication status:
Published

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Authors


Eleftherohorinou, H More by this author
Andersson-Assarsson, JC More by this author
Walters, RG More by this author
El-Sayed Moustafa, JS More by this author
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Journal:
Bioinformatics (Oxford, England)
Volume:
27
Issue:
13
Pages:
1873-1875
Publication date:
2011-07-05
DOI:
EISSN:
1367-4811
ISSN:
1367-4803
URN:
uuid:4f509333-cee8-4762-bda4-0ad35d066904
Source identifiers:
375244
Local pid:
pubs:375244

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