| 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. |
hg clone https://toolshed.g2.bx.psu.edu/repos/iuc/delly_merge
| Name | Description | Version | Minimum Galaxy Version |
|---|---|---|---|
| structural variants across/within BCF/VCF file(s) | 0.9.1+galaxy1 | 18.01 | |