delly 0.7.9 Integrated structural variant prediction method
Delly is an integrated structural variant prediction method that can discover and genotype deletions, tandem duplications, inversions 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.
- Website: https://github.com/dellytools/delly
- License: GPL 3+
- Package source: bioinformatics.scm
- Patches: snippet
- Builds: x86_64-linux, i686-linux