Extended Data Fig. 10: Multi-platform approach in ZERO increases reportable events.

a, The number of reportable events identified in each individual patient, coloured by the source of the data, whether from WGS only, RNAseq only, both WGS and RNA, germline WGS or by methylation array. The x-axis is each patient in the cohort. The y-axis is the number of reportable findings in each patient. b, The total number of reportable variants separated by type of event and coloured by the platform identifying the event. SNV: Single Nucleotide Variant, CNV: Copy Number Variant, SV: Structural Variant, EXP: Gene Expression, GL: Germline, METH: Methylation, TMB: Tumour Mutation Burden.