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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Detalles Bibliográficos
Autores principales: Mägi, Reedik, Kumar, Ashish, Morris, Andrew P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287830/
https://www.ncbi.nlm.nih.gov/pubmed/22373025
http://dx.doi.org/10.1186/1753-6561-5-S9-S107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287830/
https://www.ncbi.nlm.nih.gov/pubmed/22373025
http://dx.doi.org/10.1186/1753-6561-5-S9-S107

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