Family-based tests applied to extended pedigrees identify rare variants related to hypertension

The application of family-based tests to whole-genome sequenced data provides a new window on the role of rare variant alleles in the etiology of disease. By applying family-based tests to these data, we can now identify rare variants associated with disease. Approaches for common variants, by contr...

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Detalles Bibliográficos
Autores principales: Xu, Mengyuan, Wang, Harold Z, Guo, Wei, Qin, Haide, Shugart, Yin Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143699/
https://www.ncbi.nlm.nih.gov/pubmed/25519318
http://dx.doi.org/10.1186/1753-6561-8-S1-S31

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143699/
https://www.ncbi.nlm.nih.gov/pubmed/25519318
http://dx.doi.org/10.1186/1753-6561-8-S1-S31

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