bric-embl_delly_workflow
   A Dockstire version of the DELLY Structural Variant workflow used by the PPCG project. This is an updated and improved version of the PCAWG DELLY Workflow ### DELLY [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. It uses paired-ends and split-reads to sensitively and accurately delineate genomic rearrangements throughout the genome.
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