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Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets

Imputation allows the inference of unobserved genotypes in low-density data sets, and is often used to test for disease association at variants that are poorly captured by standard genotyping chips (such as low-frequency variants). Although much effort has gone into developing the best imputation al...

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Detalhes bibliográficos
Main Authors: Jostins, Luke, Morley, Katherine I, Barrett, Jeffrey C
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3110048/
https://ncbi.nlm.nih.gov/pubmed/21364697
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.10
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