Publications
Whole Exome Sequencing in Atrial Fibrillation.
Lubitz SA, et al.
PLoS Genet. 2016 Sep 2;12(9):e1006284. doi: 10.1371/journal.pgen.1006284
Dataset phenotypes
- atrial fibrillation
Dataset subjects
| Cases | Controls | Cohort | Ancestry |
|---|---|---|---|
| 246 | 1,000 | Atherosclerosis Risk in Communities Study (ARIC) | African American |
| 730 | 4,000 | Atherosclerosis Risk in Communities Study (ARIC) | European |
| 251 | 500 | Cardiovascular Health Study (CHS) | European |
| 100 | 1,155 | ESP | African American |
| 233 | 1,686 | ESP | European |
| 174 | 1,082 | Framingham Heart Study (FHS) | European |
Dataset subjects by ancestry
| Cases | Controls | Ancestry |
|---|---|---|
| 346 | 2,155 | African American |
| 1,388 | 7,268 | European |
| 1,734 | 9,423 | All |
Project
Atrial Fibrillation Consortium
The Atrial Fibrillation Consortium (AFGen) seeks to identify the genetic basis of atrial fibrillation using a wide variety of genetic analyses.
Experiment summary
AFGen exome sequence analysis is a meta-analysis of exome sequencing results from 1,734 individuals with atrial fibrillation and 9,423 controls.
Dataset ID
ExSeq_RSNG