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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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Autores principales: Marenne, Gaëlle, Chanock, Stephen J., Malats, Núria, Génin, Emmanuelle
Formato: Artigo
Lenguaje:Inglês
Publicado: Public Library of Science 2013
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Acceso en línea: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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