Figure 2 | Scientific Reports

Figure 2

From: A simple method for sequencing the whole human mitochondrial genome directly from samples and its application to genetic testing

Figure 2

Mapping and coverage results for sequencing the mtDNA in two pediatric patients with mitochondrial disease, indicating deletion-type mutations. (A,B) Sequencing results for mtDNA indicating a deletion-type mutation between mtDNA nucleotides 8581 and 13990 in sample M132 (A) and a deletion-type mutation between mtDNA nucleotides 9822 and 14559 in sample Hep575 (B). The sequencing coverage is indicated in red. Additional information for both samples is provided in Supplemental Table 1.

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