Mity is a bioinformatic analysis pipeline designed to call mitochondrial SNV and INDEL variants from Whole Genome Sequencing (WGS) data.
Mity can: - identify very low-heteroplasmy variants, even <1% heteroplasmy when there is sufficient read-depth (eg >1000x) - filter out common artefacts that arise from high-depth sequencing - easily integrate with existing nuclear DNA analysis pipelines (mity merge) - provide an annotated report, designed for clinicians and researchers to interrogate
