delly | DELLY2: Structural variant discovery by integrated paired-end and split-read analysis | Genomics library

delly is a C++ library typically used in Artificial Intelligence, Genomics applications. delly has no bugs, it has no vulnerabilities, it has a Permissive License and it has low support. You can download it from GitHub.

Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data. It uses paired-ends, split-reads and read-depth to sensitively and accurately delineate genomic rearrangements throughout the genome. Structural variants can be annotated using Delly-sansa and visualized using Delly-maze or Delly-suave.