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R-Gada: a fast and flexible pipeline for copy number analysis in association studies
BACKGROUND: Genome-wide association studies (GWAS) using Copy Number Variation (CNV) are becoming a central focus of genetic research. CNVs have successfully provided target genome regions for some disease conditions where simple genetic variation (i.e., SNPs) has previously failed to provide a clea...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2915992/ https://ncbi.nlm.nih.gov/pubmed/20637081 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-11-380 |
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