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Repository delly_cnv
Name: delly_cnv
Owner: iuc
Synopsis: Wrapper for Delly cnv
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.
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/iuc/delly_cnv
Type: unrestricted
Revision: 0:d402af96808e
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Contents of this repository

Name Description Version Minimum Galaxy Version
discover and genotype copy-number variants 0.8.7+galaxy0 18.01

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