Study
Germline sequencing
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001006705 | Other |
Study Description
Detection of SNVs/ indels in the germline of pediatric cancer patients with a focus on CHEK2 germline variants
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 |
|---|---|---|---|
| EGAD00001009678 |
This dataset contains germline variants (in .vcf format) from six pediatric cancer patients (sample IDs D1 - D6). WES data of the children and their parents was mapped to hg38. A consensus of four variant callers was used to obtain germline variants of the children.
|
6 |
Who archives the data?
