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Repository exomedepth
Name: exomedepth
Owner: crs4
Synopsis: ExomeDepth: Calls copy number variants (CNVs) from targeted sequence data
Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing
experiments designed to identify the genetic basis of Mendelian disorders.
Content homepage: https://cran.r-project.org/package=ExomeDepth
Development repository: https://github.com/galaxyproject/tools-iuc/tree/master/tools/exomedepth
Link to this repository: https://toolshed.g2.bx.psu.edu/view/crs4/exomedepth/5d60331757d3
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/crs4/exomedepth
Type: unrestricted
Revision: 8:5d60331757d3
This revision can be installed: True
Times cloned / installed: 473

Contents of this repository

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Name Description Version Minimum Galaxy Version
Calls copy number variants (CNVs) from targeted sequence data 1.1.0 16.01

Categories
Sequence Analysis - Tools for performing Protein and DNA/RNA analysis