Fig. 1
From: Sequencing and curation strategies for identifying candidate glioblastoma treatments
Somatic alterations associated to potential therapy in NY-GGC study. a Distribution of therapeutic associations with single nucleotide variants (SNV), copy number variations (CNV), insertions/deletions (Indel) and structural variations (SV) discovered from whole genome sequencing (WGS) data in the NY-GGC study 33 sample data set. b Matrix outlining the types of variants per gene discovered by WGS across the cohort. Blue boxes indicate copy number losses, orange boxes indicate copy number gains, grey circle represents a somatic nucleotide variant, and open circle is specific to the EGFR vIII SV.