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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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| Main Authors: | , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Oxford University Press
2011
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| נושאים: | |
| גישה מקוונת: | 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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