Cargando…
Rare Variants Association Analysis in Large-Scale Sequencing Studies at the Single Locus Level
Genetic association analyses of rare variants in next-generation sequencing (NGS) studies are fundamentally challenging due to the presence of a very large number of candidate variants at extremely low minor allele frequencies. Recent developments often focus on pooling multiple variants to provide...
Autores principales: | Jeng, Xinge Jessie, Daye, Zhongyin John, Lu, Wenbin, Tzeng, Jung-Ying |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927097/ https://www.ncbi.nlm.nih.gov/pubmed/27355347 http://dx.doi.org/10.1371/journal.pcbi.1004993 |
Ejemplares similares
-
Efficient identification of rare variants in large populations: deep re-sequencing the CRP locus in the CARDIA study
por: Chen, Christina T. L., et al.
Publicado: (2013) -
A powerful test for multiple rare variants association studies that incorporates sequencing qualities
por: Daye, Z. John, et al.
Publicado: (2012) -
Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels
por: Tin, Adrienne, et al.
Publicado: (2018) -
Gene expression variability and the analysis of large-scale RNA-seq studies with the MDSeq
por: Ran, Di, et al.
Publicado: (2017) -
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies
por: Li, Xihao, et al.
Publicado: (2023)