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Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation
BACKGROUND: The recent discovery of widespread copy number variation in humans has forced a shift away from the assumption of two copies per locus per cell throughout the autosomal genome. In particular, a SNP site can no longer always be accurately assigned one of three genotypes in an individual....
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1934372/ https://ncbi.nlm.nih.gov/pubmed/17608949 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-8-211 |
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