Skip to main content
Figure 3 | BMC Bioinformatics

Figure 3

From: SeqGene: a comprehensive software solution for mining exome- and transcriptome- sequencing data

Figure 3

Distribution of short indels across the trio using VarScan, SAMtools and SeqGene. In the Venn diagrams, the numbers shown in the overlap indicate shared mutations between the family members. Numbers not in parentheses are the number of indels that passed genotype pedigree check; numbers in parentheses are the number of indels that failed genotype pedigree check, i.e., Mendelian errors.

Back to article page