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Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

Determination of copy number variants (CNVs) inferred in genome wide single nucleotide polymorphism arrays has shown increasing utility in genetic variant disease associations. Several CNV detection methods are available, but differences in CNV call thresholds and characteristics exist. We evaluated...

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Main Authors: Dellinger, Andrew E., Saw, Seang-Mei, Goh, Liang K., Seielstad, Mark, Young, Terri L., Li, Yi-Ju
格式: Artigo
語言:Inglês
出版: Oxford University Press 2010
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2875020/
https://ncbi.nlm.nih.gov/pubmed/20142258
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkq040
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