Figure 3From: Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathyOverlap of SNVs identified in four targeted exome sequencing replicates of the same individual's DNA in the Illumina platform. (a) Comparison of identified coding SNPs (cSNPs) within and between sequencing technologies (GAII vs. HiSeq). There is a high percentage of shared identified SNPs both within and between the different technologies. (b) Comparison of identified InDels within and between sequencing technologies. We observe less overlap between the two technologies probably due to a higher rate of false positive InDels.Back to article page