Rare variant analysis of blood pressure phenotypes in the Genetic Analysis Workshop 18 whole genome sequencing data using sequence kernel association test

Sequence kernel association test (SKAT) has become one of the most commonly used nonburden tests for analyzing rare variants. Performance of burden tests depends on the weighting of rare and common variants when collapsing them in a genomic region. Using the systolic and diastolic blood pressure phe...

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Detalles Bibliográficos
Autores principales: Mallaney, Cates, Sung, Yun Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143707/
https://www.ncbi.nlm.nih.gov/pubmed/25519353
http://dx.doi.org/10.1186/1753-6561-8-S1-S10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143707/
https://www.ncbi.nlm.nih.gov/pubmed/25519353
http://dx.doi.org/10.1186/1753-6561-8-S1-S10

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