Fig. 3
From: SMuRF: a novel tool to identify regulatory elements enriched for somatic point mutations
Assessing the sample specificity of SMuRF. SMuRF was run on matched chromatin accessibility data from seven other tissue types. Each peak set was randomly sampled 5 times and SMuRF was run on each iteration. SK-N-SH_RA had the lowest peak number and was not sampled. The selected peak sets were also matched to the HepG2 dataset for peak length. The number of significantly mutated CREs identified by SMuRF in each run are shown as green diamonds, with the height of the bar for each tissue corresponding to the average CRE number