The project’s sequencing cohort defines the largest, clinically annotated pediatric brain tumor cohort study to date and seeks to define the intersection of germline and somatic underpinnings of pediatric brain tumors across a shared developmental context of cancer and structural birth defects. Data includes tumor/normal whole genome sequencing pairs with matching RNASeq and paternal and maternal whole genome sequencing when available.
Get the Latest
news, articles, and resources sent to your inbox.