Manta
Rapid structural variant caller tailored specifically for high-throughput clinical sequencing pipelines.
Key Info
- URL: https://github.com/Illumina/manta
- Category: CNV Analysis
- API: Yes
- Free: Free
- ACMG Relevance: N/A
- Link Status: ARCHIVED 2026-04-09 — repo archived by Illumina (★462, last push Oct 2025). Still functional, widely used in pipelines.
Why It Matters
Exceptional at discovering break-end structural variants and medium-sized indels that read-depth alone cannot accurately resolve.
How to Use
See https://github.com/Illumina/manta for documentation and access.
STRC Research Usage
Not directly applicable to E1659A via API. Requires local installation or web interface. See documentation for manual usage.
Next Steps
- Test with STRC E1659A variant
- Verify API access
- Document specific results
Connections
- STRC Variant c.4976A>C — Misha [see-also]
- STRC Gene [about]