Structural variant toolkit for VCFs
benchmarking data-science bioinformatics genomics sequencing vcf annotation-tool structural-variation vcf-comparison sv-merging
-
Updated
Sep 8, 2026 - Python
Structural variant toolkit for VCFs
Structural variant VCF annotation, filtering, duplicate removal and comparison
Pangenome structural variation (SV) merging and deduplication
A novel tool for accurately merging haplotype-based SV calls and comparing SVs across reference genomes
To associate your repository with the sv-merging topic, visit your repo's landing page and select "manage topics."