Delly is a structural variant detection method for the discovery of germline and somatic genomic rearrangements. Delly can detect deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data.
Homepage
https://github.com/dellytools/delly
Contact
rausch (at) embl (dot) de
Funding
Neither development nor maintenance funded by de.NBI.