Figure 6
From: Identification of genomic indels and structural variations using split reads
The conceptual diagrams of the split-read analysis. SVs can be detected by sequence reads spanning their break points. The split-read analysis can directly identify deletions, small insertions, and the boundaries of large insertions. After the identification of SVs, duplications and translocations can be isolated out based on matching of insertions and deletions. Breakages in blue genomic lines denote different chromosomes.