Fig. 2. Integrative analysis of cancer panel analysis of 20 patients. Each grey column represents specific data for 1 of the 20 patients in order. Genomic polymorphism of SNP/Indel mutation by truncating, in the frame, missense is noted by a color dot in a grey column with black, brown, and green. Structural variation was found in 5 patients annotated by purple color; the most common finding was ERG: TMPRSS2 fusion. No CNV amplification was found by our targeted next-generation sequencing (NGS) panel. This oncoprint was obtained by use of The cBioPortal for Cancer Genomics (http://cbioportal.org) graphic visualization Genetic alteration tool.
