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Repository delly_merge
Name: delly_merge
Owner: iuc
Synopsis: Wrapper for Delly merge
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.
Type: unrestricted
Revision: 2:148389992630
This revision can be installed: True
Times cloned / installed: 165

Contents of this repository

Name Description Version Minimum Galaxy Version
structural variants across/within BCF/VCF file(s) 0.8.7+galaxy0 18.01

Categories
Variant Analysis - Tools for single nucleotide polymorphism data such as WGA