Structural variant toolkit for VCFs
benchmarking data-science bioinformatics genomics sequencing vcf annotation-tool structural-variation vcf-comparison sv-merging
- Updated
Oct 7, 2025 - Python
Structural variant toolkit for VCFs
Pangenome structural variations (SV) merging and overlapping variant merging
A novel tool for accurately merging haplotype-based SV calls and comparing SVs across reference genomes
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