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Repository 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
Type: unrestricted
Revision: 1:f49b23b41a12
This revision can be installed: True
Times cloned / installed: 3358
Dependencies of this repository

Repository package_vcflib_8a5602bf07 revision 7e67466b033e owned by iuc

Name Version Type
vcflib 8a5602bf07 package

Contents of this repository

Name Description Version Minimum Galaxy Version
Split alleleic primitives (gaps or mismatches) into multiple VCF lines 0.0.3 any

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