DELLY is an integrated structural variant prediction method that can detect 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. |
hg clone https://toolshed.g2.bx.psu.edu/repos/jeremie/delly_
Name | Version | Type | |
---|---|---|---|
delly | 0.5.5 | package |
Name | Description | Version | Minimum Galaxy Version |
---|---|---|---|
structural variant prediction method | 1.0.0 | any |