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Advantage of Using Allele-Specific Copy Numbers When Testing for Association in Regions with Common Copy Number Variants

Copy number variants (CNV) can be called from SNP-arrays; however, few studies have attempted to combine both CNV and SNP calls to test for association with complex diseases. Even when SNPs are located within CNVs, two separate association analyses are necessary, to compare the distribution of bi-al...

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Detalhes bibliográficos
Main Authors: Marenne, Gaëlle, Chanock, Stephen J., Malats, Núria, Génin, Emmanuelle
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3769257/
https://ncbi.nlm.nih.gov/pubmed/24040408
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0075350
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