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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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書目詳細資料
Main Authors: Marenne, Gaëlle, Chanock, Stephen J., Malats, Núria, Génin, Emmanuelle
格式: Artigo
語言:Inglês
出版: Public Library of Science 2013
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在線閱讀: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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