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Repository vcfflatten
Name: vcfflatten
Owner: devteam
Synopsis: Removes multi-allelic sites by picking the most common alternate
Removes multi-allelic sites by picking the most common alternate.
Requires allele frequency specification ''AF'' and use of ''G'' and ''A'' to specify
the fields which vary according to the Allele or Genotype.
Content homepage: https://github.com/ekg/vcflib
Development repository: https://github.com/galaxyproject/tools-iuc/tree/master/tool_collections/vcflib/vcfflatten
Link to this repository revision: https://toolshed.g2.bx.psu.edu/view/devteam/vcfflatten/1336a70f5c02
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/devteam/vcfflatten
Type: unrestricted
Revision: 1:1336a70f5c02
This revision can be installed: True
Times cloned / installed: 3078

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
Removes multi-allelic sites by picking the most common alternate 1.0.0_rc1.0 any

Categories
Sequence Analysis - Tools for performing Protein and DNA/RNA analysis
Variant Analysis - Tools for single nucleotide polymorphism data such as WGA