Cargando…
Identification of multiple rare variants associated with a disease
Identifying rare variants that are responsible for complex disease has been promoted by advances in sequencing technologies. However, statistical methods that can handle the vast amount of data generated and that can interpret the complicated relationship between disease and these variants have lagg...
Autores principales: | Jung, Jeesun, Dantzer, Jessica, Liu, Yunlong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287826/ https://www.ncbi.nlm.nih.gov/pubmed/22373445 http://dx.doi.org/10.1186/1753-6561-5-S9-S103 |
Ejemplares similares
-
Evaluation of pooled association tests for rare variant identification
por: Lin, Wan-Yu, et al.
Publicado: (2011) -
Prioritizing single-nucleotide variations that potentially regulate alternative splicing
por: Teng, Mingxiang, et al.
Publicado: (2011) -
Identification of rare variants for hypertension with incorporation of linkage information
por: Chiu, Yen-Feng, et al.
Publicado: (2014) -
Association screening for genes with multiple potentially rare variants: an inverse-probability weighted clustering approach
por: Liu, Ying, et al.
Publicado: (2011) -
Addition of multiple rare SNPs to known common variants improves the association between disease and gene in the Genetic Analysis Workshop 17 data
por: Sykes, Jenna, et al.
Publicado: (2011)