Figure 2From: SeqGene: a comprehensive software solution for mining exome- and transcriptome- sequencing dataDistribution of SNP positions 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 SNP positions that passed genotype pedigree check; numbers in parentheses are the number of SNPs positions that failed genotype pedigree check, i.e., Mendelian errors.Back to article page