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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: | , , , , , |
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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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