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Mity is a bioinformatic analysis pipeline designed to call mitochondrial SNV and INDEL variants from Whole Genome Sequencing (WGS) data.

Installers

  • noarch v1.1.0

conda install

To install this package run one of the following:
conda install bioconda::mity

Description

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

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