{"id":6222,"projects":[69],"description":"![build_status](https://img.shields.io/docker/build/weischenfeldt/bric-embl_delly_workflow.svg)\n![docker_pulls](https://img.shields.io/docker/pulls/weischenfeldt/bric-embl_delly_workflow.svg)\n![docker_builds](https://img.shields.io/docker/automated/weischenfeldt/bric-embl_delly_workflow.svg)\n\nA Dockstire version of the DELLY Structural Variant workflow used by the PPCG project.\nThis is an updated and improved version of the PCAWG DELLY Workflow\n\n### DELLY\n\n[DELLY](https://github.com/tobiasrausch/delly) is an integrated structural variant prediction method that can detect deletions, tandem duplications, inversions, insertions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data.\nIt uses paired-ends and split-reads to sensitively and accurately delineate genomic rearrangements throughout the genome.","image":"","tags":"","type":"","title":"bric-embl_delly_workflow","url":"https://dockstore.org/api/api/ga4gh/v2/tools/registry.hub.docker.com%2Fweischenfeldt%2Fbric-embl_delly_workflow","authors":[1],"rubrics":[25]}