Exome sequencing of Fibromyalgia patients
Fibromyalgia is a complex disorder characterized by increased sensitivity to pain and extreme tiredness. It affects mostly women, and its causes are unknown. In this study we have performed exome sequencing of 87 fibromyalgia cases, including some sibling pairs, to perform rare variant association analysis and identify fibromyalgia risk factors. A few of the included samples have been also included in a previous GWAS study.
- Type: Other
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
| Dataset ID | Description | Technology | Samples |
|---|---|---|---|
| EGAD00001005288 | Illumina HiSeq 2500 | 87 |
| Publications | Citations |
|---|---|
|
Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation.
PLoS Comput Biol 17: 2021 e1007784 |
3 |