|Study ID||Alternative Stable ID||Type|
Detection of SNV/indels in the germline of pediatric cancer patients with a focus on CHEK2 germline variants. Included in this EGA upload are the parents of the children in EGA uplodad EGAD00001008763.
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
This data set includes bam files (aligned to hg38) from the germline of parents whose children have CHEK2 germline mutations.
|Illumina HiSeq 2500,NextSeq 550||48|