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
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.

Who archives the data?

There are no publications available