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Repository vcfallelicprimitives
Name: vcfallelicprimitives
Owner: anton
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.     
Link to this repository: https://toolshed.g2.bx.psu.edu/view/anton/vcfallelicprimitives/260173250dd2
Type: unrestricted
Revision: 3:260173250dd2
This revision can be installed: True
Times cloned / installed: 224
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Repository package_vcflib_8a5602bf07 revision bffe0495cd92 owned by anton

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Name Version Type
vcflib 8a5602bf07 package

Contents of this repository

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Name Description Version Minimum Galaxy Version
Split alleleic primitives (gaps or mismatches) into multiple VCF lines 0.0.2 any

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