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dna-seq-varlociraptor\n\n[![Snakemake](https://img.shields.io/badge/snakemake-≥6.3.0-brightgreen.svg)](https://snakemake.github.io)\n[![GitHub actions status](https://github.com/snakemake-workflows/dna-seq-varlociraptor/workflows/Tests/badge.svg?branch=master)](https://github.com/snakemake-workflows/dna-seq-varlociraptor/actions?query=branch%3Amaster+workflow%3ATests)\n[![DOI](https://zenodo.org/badge/DOI/10.5281/zenodo.4675661.svg)](https://doi.org/10.5281/zenodo.4675661)\n\n\nA Snakemake workflow for calling small and structural variants under any kind of scenario (tumor/normal, tumor/normal/relapse, germline, pedigree, populations) via the unified statistical model of [Varlociraptor](https://varlociraptor.github.io).\n\n\n## Usage\n\nThe usage of this workflow is described in the [Snakemake Workflow Catalog](https://snakemake.github.io/snakemake-workflow-catalog/?usage=snakemake-workflows%2Fdna-seq-varlociraptor).\n\nIf you use this workflow in a paper, don't forget to give credits 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