Mitochondrial point heteroplasmy: insights from deep-sequencing of human replicate samples.
Marina KorolijaViktorija SukserKristian VlahovičekPublished in: BMC genomics (2024)
Our findings reliably show different mutational loads between tissues at sub-1% allele frequencies, which may serve as an informative medical biomarker of time-dependent, tissue-specific mutational burden, or help discriminate forensically relevant tissues in a single person, close maternal relatives or unrelated individuals of similar phylogenetic background.