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Repository vcfcombine
Name: vcfcombine
Owner: devteam
Synopsis: Combine multiple VCF datasets
Combines VCF files positionally, combining samples when sites and
alleles are identical. Any number of VCF files may be combined. The INFO field and
other columns are taken from one of the files which are combined when records in
multiple files match. Alleles must have identical ordering to be combined into one
record. If they do not, multiple records will be emitted.
Content homepage: https://github.com/ekg/vcflib
Development repository: https://github.com/galaxyproject/tools-iuc/tree/master/tool_collections/vcflib/vcfcombine
Link to this repository: https://toolshed.g2.bx.psu.edu/view/devteam/vcfcombine/1f0ba67cc85a
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/devteam/vcfcombine
Type: unrestricted
Revision: 4:1f0ba67cc85a
This revision can be installed: True
Times cloned / installed: 3341

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
Combine multiple VCF datasets 1.0.0_rc3+galaxy0 16.01

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