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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.
Content homepage: https://github.com/dellytools/delly
Development repository: https://github.com/galaxyproject/tools-iuc/tree/master/tools/delly
Link to this repository revision: https://toolshed.g2.bx.psu.edu/view/iuc/delly_cnv/d402af96808e
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/iuc/delly_cnv
Type: unrestricted
Revision: 0:d402af96808e
This revision can be installed: True
Times cloned / installed: 351

Contents of this repository

Valid tools - click the name to preview the tool and use the pop-up menu to inspect all metadata
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