Figure 7From: Fast and scalable inference of multi-sample cancer lineagesLICHeE graphical user interface output for top lineage tree of ccRCC patient RK26 with node selection. Information is displayed about the SSNV members of the selected node. ccRCC, clear-cell renal cell carcinoma; SSNV, somatic single nucleotide variant; Stdev, standard deviation; VAF, variant allele frequency.Back to article page