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famCNV: copy number variant association for quantitative traits in families
Summary: A program package to enable genome-wide association of copy number variants (CNVs) with quantitative phenotypes in families of arbitrary size and complexity. Intensity signals that act as proxies for the number of copies are modeled in a variance component framework and association with tra...
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| Autori principali: | , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3117380/ https://ncbi.nlm.nih.gov/pubmed/21546396 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr264 |
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