Command-line toolkit for genomic datasets.
A Haskell script for selecting variants from a variant calling format (vcf) file based on variants present in a mgibed file.
A Haskell script that prepares .tsv files generated from sequencing data analysis for manual review.
A Haskell script for creating input files for bam-readcount from ensembl-vep output and variant-calling format (vcf) files.
A Haskell script that performs basic filtration, using a filtration string, on somatic variant data.
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