VCFTools is a Crystal shard for parsing VCF files. VCF is the main format used to store genomic variation in humans and other species.
Add this to your application's shard.yml:
dependencies:
VCF_tools:
github: diploidgenomics/vcftoolsrequire "VCF_tools"
VCFTools::Vcf.new(file_path).each_variant do |v|
puts "#{v.chromosome}:#{v.position}"
endTODO: Write development instructions here
- Fork it (https://github.com/diploidgenomics/vcftools/fork)
- Create your feature branch (git checkout -b my-new-feature)
- Commit your changes (git commit -am 'Add some feature')
- Push to the branch (git push origin my-new-feature)
- Create a new Pull Request
- diploidgenomics Peter Schols - creator, maintainer