Genome-wide joint analysis of single-nucleotide variant sets and gene expression for hypertension and related phenotypes

BACKGROUND: With the advance of next-generation sequencing technologies, the study of rare variants in targeted genome regions or even the whole genome becomes feasible. Nevertheless, the massive amount of sequencing data brings great computational and statistical challenges for association analyses...

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Detalles Bibliográficos
Autores principales: Tong, Xiaoran, Wei, Changshuai, Lu, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133505/
https://www.ncbi.nlm.nih.gov/pubmed/27980623
http://dx.doi.org/10.1186/s12919-016-0017-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133505/
https://www.ncbi.nlm.nih.gov/pubmed/27980623
http://dx.doi.org/10.1186/s12919-016-0017-x

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