Figure 5
From: Open-access synthetic spike-in mRNA-seq data for cancer gene fusions
To independently verify the presence of fusion reads (true positives) in the sequencing data, data was aligned using GSNAP to a combined reference sequence consisting of the human genome GRCh37 build and nine fusion transcripts. For each fusion, the number of fusions supporting reads identified by GSNAP (blue squares), THF (purple triangle), CHS (red triangle), and SSH (inverted green triangle) are plotted for replicates R1 and R2.