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Updated: Nov 3, 2025

Simultaneous Mapping and Quantitation of Ribonucleotides in Human Mitochondrial DNA
Published on: November 14, 2017
The Isolation and Deep Sequencing of Mitochondrial DNA
Alexander G Bury1,2, Fiona M Robertson1,3, Angela Pyle1,3
1Wellcome Centre for Mitochondrial Research, Newcastle University, Newcastle-upon-Tyne, UK.
Abstract:
In recent years, next-generation sequencing (NGS) has become a powerful tool for studying both inherited and somatic heteroplasmic mitochondrial DNA (mtDNA) variation. NGS has proved particularly powerful when combined with single-cell isolation techniques, allowing the investigation of low-level heteroplasmic variants both between cells and within tissues. Nevertheless, there remain significant challenges, especially around the selective enrichment of mtDNA from total cellular DNA and the avoidance of nuclear pseudogenes. This chapter summarizes the techniques needed to enrich, amplify, sequence, and analyse mtDNA using NGS .
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