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SCAN: SNP and copy number annotation
Motivation: Genome-wide association studies (GWAS) generate relationships between hundreds of thousands of single nucleotide polymorphisms (SNPs) and complex phenotypes. The contribution of the traditionally overlooked copy number variations (CNVs) to complex traits is also being actively studied. T...
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| 主要な著者: | , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2010
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2852202/ https://ncbi.nlm.nih.gov/pubmed/19933162 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btp644 |
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