Figure 2
From: A practical method to detect SNVs and indels from whole genome and exome sequencing data

Common indels identified by VCMM, GATK and SAMtools.
(a) SNV in WGS. SNVs in repeat regions and unknown contigs were not used for the comparison. (b) Indel in WGS. Indels in repeat regions and unknown contigs were not used for the comparison. (c) SNV in WES. (d) Coding indel in WES.