Cargando…
Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation
Cohort-wide very low-depth whole-genome sequencing (WGS) can comprehensively capture low-frequency sequence variation for the cost of a dense genome-wide genotyping array. Here, we analyse 1x sequence data across the APOC3 gene in a founder population from the island of Crete in Greece (n = 1239) an...
Autores principales: | Gilly, Arthur, Ritchie, Graham Rs, Southam, Lorraine, Farmaki, Aliki-Eleni, Tsafantakis, Emmanouil, Dedoussis, George, Zeggini, Eleftheria |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5081052/ https://www.ncbi.nlm.nih.gov/pubmed/27146844 http://dx.doi.org/10.1093/hmg/ddw088 |
Ejemplares similares
-
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits
por: Southam, Lorraine, et al.
Publicado: (2017) -
A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates
por: Tachmazidou, Ioanna, et al.
Publicado: (2013) -
Very low-depth whole-genome sequencing in complex trait association studies
por: Gilly, Arthur, et al.
Publicado: (2019) -
Insights into the genetic architecture of haematological traits from deep phenotyping and whole-genome sequencing for two Mediterranean isolated populations
por: Kuchenbaecker, Karoline, et al.
Publicado: (2022) -
Genome-wide meta-analysis of 92 cardiometabolic protein serum levels
por: Gilly, Arthur, et al.
Publicado: (2023)