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Repository vcfallelicprimitives
Name: vcfallelicprimitives
Owner: devteam
Synopsis: Splits alleleic primitives (gaps or mismatches) into multiple VCF lines
If multiple alleleic primitives (gaps or mismatches) are specified
in a single VCF record, this tools splits the record into multiple lines, but drops
all INFO fields.  "Pure" MNPs are split into multiple SNPs unless the -m flag is
provided.  Genotypes are phased where complex alleles have been decomposed, provided
genotypes in the input.
Content homepage: https://github.com/ekg/vcflib
Development repository: https://github.com/galaxyproject/tools-iuc/tree/master/tool_collections/vcflib/vcfallelicprimitives
Link to this repository revision: https://toolshed.g2.bx.psu.edu/view/devteam/vcfallelicprimitives/0a69cff7946e
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/devteam/vcfallelicprimitives
Type: unrestricted
Revision: 2:0a69cff7946e
This revision can be installed: True
Times cloned / installed: 3319

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
Split alleleic primitives (gaps or mismatches) into multiple VCF lines 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