Cargando…
The impact of genetic structure on sequencing analysis
BACKGROUND: Genome-wide association studies have made substantial progress in identifying common variants associated with human diseases. Despite such success, a large portion of heritability remains unexplained. Evolutionary theory and empirical studies suggest that rare mutations could play an imp...
Autores principales: | Jadhav, Sneha, Vsevolozhskaya, Olga A., Tong, Xiaoran, Lu, Qing |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133514/ https://www.ncbi.nlm.nih.gov/pubmed/27980631 http://dx.doi.org/10.1186/s12919-016-0025-x |
Ejemplares similares
-
Genome-wide joint analysis of single-nucleotide variant sets and gene expression for hypertension and related phenotypes
por: Tong, Xiaoran, et al.
Publicado: (2016) -
Pathway-based joint effects analysis of rare genetic variants using Genetic Analysis Workshop 17 exon sequence data
por: Hu, Pingzhao, et al.
Publicado: (2011) -
Identification of functional genetic variation in exome sequence analysis
por: Jaffe, Andrew, et al.
Publicado: (2011) -
Genetic Analysis Workshop 18 single-nucleotide variant prioritization based on protein impact, sequence conservation, and gene annotation
por: Nalpathamkalam, Thomas, et al.
Publicado: (2014) -
Whole genome sequencing of 35 individuals provides insights into the genetic architecture of Korean population
por: Zhang, Wenqian, et al.
Publicado: (2014)