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Assessing the impact of missing genotype data in rare variant association analysis

Human genome resequencing technologies are becoming ever more affordable and provide a valuable source of data about rare genetic variants in the human genome. Such rare variation may play an important role in explaining the missing heritability of complex human traits. We implement an existing meth...

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Detalhes bibliográficos
Main Authors: Mägi, Reedik, Kumar, Ashish, Morris, Andrew P
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3287830/
https://ncbi.nlm.nih.gov/pubmed/22373025
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1753-6561-5-S9-S107
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