Study
Whole genome sequencing of AVM endothelial and non-endothelial cell fractions
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001006719 | Other |
Study Description
We previously identified somatic activating KRAS mutations in a majority of human arteriovenous malformations (AVMs), using whole exome sequencing, which were enhanced in AVM endothelial cell fractions. We have now performed whole genome sequencing on AVM endothelial and non-endothelial cell fractions, as well as paired blood samples, in order to identify further somatic mutations.
Study Datasets 1 dataset.
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 |
|---|---|---|---|
| EGAD00001009696 |
Whole genome sequencing data of brain AVM endothelial and non-endothelial cell fractions, as well as paired blood samples
|
unspecified | 31 |
Who archives the data?
