Identification of low frequency and rare variants for hypertension using sparse-data methods

Availability of genomic sequence data provides opportunities to study the role of low-frequency and rare variants in the etiology of complex disease. In this study, we conduct association analyses of hypertension status in the cohort of 1943 unrelated Mexican Americans provided by Genetic Analysis W...

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Detalles Bibliográficos
Autores principales: Shin, Ji-Hyung, Yi, Ruiyang, Bull, Shelley B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133522/
https://www.ncbi.nlm.nih.gov/pubmed/27980667
http://dx.doi.org/10.1186/s12919-016-0061-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133522/
https://www.ncbi.nlm.nih.gov/pubmed/27980667
http://dx.doi.org/10.1186/s12919-016-0061-6

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