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Documentation

Take in a VCFs of known variants and observed variants and output a report
Take in a reference genome and evolve it.
VCF comparison script from VCFTools

Modules

Comparative assesment of variant calling (CAVar)
Take in a reference genome and evolve it.
Take in a reference genome and evolve it multiple times to produce multiple FASTA files and VCF files containing the differences to the original reference.
Create a VCF with the differences between a reference and a single evolved genome. Outputs a gzipped VCF file and a tabix file.
Take in a set of input parameters for the evalute pipeline functionality, validate them, then manipulate them into a usable set.
Aggregate together the results of multiple VCF comparisons
Take in the output of VCF compare and return details about intersection of variants.
Moose types to use for validation
Validates the executable is available in the path before running it
FaSlice.pm from VCFTools
Vcf
Vcf.pm from VCFTools

Provides

in lib/Vcf.pm
in lib/Vcf.pm
in lib/Vcf.pm
in lib/Vcf.pm
in lib/Vcf.pm