Replaces traditional linear sequence alignment with pangenome graph mapping and generation. Constructs and aligns sequences to variation graphs to capture structural variants missed by linear references.
Tech Stack
CBiology & Biotechnology
Why minigraph?
• Fast graph construction
• Efficient mapping of long reads
• Captures large structural variations
Limitations
• Output format (GFA) requires specialized tools
• Not designed for short-read SNPs
• Complex graph visualization
3/5/2026
Last Update
40
Forks
60
Issues
MIT
License
Financial Leak Detected
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Competitor Cost
-$1,440
/ year (est. based on VG (Variation Graph toolkit))
