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Repository vcfbreakcreatemulti
Name: vcfbreakcreatemulti
Owner: devteam
Synopsis: Break multiple alleles into multiple records, or combine overallpoing alleles into a single record
This tool breaks or creates multiallelic VCF records based on user
selection.

- Breaking = If multiple alleles are specified in a single record, break the record
into multiple lines, preserving allele-specific INFO fields.
- Creation = If overlapping alleles are represented across multiple records, merge
them into a single record.
Content homepage: https://github.com/ekg/vcflib
Development repository: https://github.com/galaxyproject/tools-iuc/tree/master/tool_collections/vcflib/vcfbreakcreatemulti
Link to this repository revision: https://toolshed.g2.bx.psu.edu/view/devteam/vcfbreakcreatemulti/3aa04b92957f
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/devteam/vcfbreakcreatemulti
Type: unrestricted
Revision: 1:3aa04b92957f
This revision can be installed: True
Times cloned / installed: 3149

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
Break multiple alleles into multiple records, or combine overallpoing alleles into a single record 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