The whole-genome landscape of medulloblastoma subtypes
Displaying a heatmap of recurrent gene mutations found in 433 medulloblastoma patient samples from whole-genome and whole-exome sequencing data. Samples are grouped according to subtype (WNT, SHH, Group 3, Group 4). Ploidy, patient age group (infant, child, or adult), and gender are indicated. Visualization representative of Northcott, et al. 2017, Fig. 2a, 3a,b. Mousing over each instance of a mutation provides further information (sample, mutation type, amino acid change, and gene name). Clicking on each gene symbol opens a ProteinPaint view of mutations found within the gene for this cohort. Numbers next to each gene symbol in parentheses indicate the number of samples altered.