Structural variant toolkit for VCFs
-
Updated
Oct 11, 2025 - Python
Structural variant toolkit for VCFs
Structural variant VCF annotation, duplicate removal and comparison
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
Add a description, image, and links to the sv-merging topic page so that developers can more easily learn about it.
To associate your repository with the sv-merging topic, visit your repo's landing page and select "manage topics."