Figure 1From: Assessment of clinical analytical sensitivity and specificity of next-generation sequencing for detection of simple and complex mutationsRepresentative mutation as detected on Sanger and SOLiD platforms. Panes 1A & 2A represent the SOLiD and Sanger data for ACADVL c.1504C > G (p.L502V) mutation. Panes 1B & 2B represent SOLiD and Sanger data for CFTR c.1521_1523delCTT mutation. Panes 1C & 2C represent SOLiD and Sanger data for CFTR c.2052_2053insA mutation. Panes 3 and 4 represent SOLiD and Sanger data for the GBA c.1265_1319del55 mutation.Back to article page