nf-CBRA-snvs
Workflow optimized for the analysis of rare diseases, designed to detect SNVs and INDELs in targeted sequencing data (CES/WES) and whole genome sequencing (WGS), built on Nextflow.
Topics
Collections
Details
- License:
- MIT
- Maturity:
- Emerging
- Cost:
- Free of charge
- Tool Type:
- workflow
- Operating Systems:
- Linux
- Added:
- 8/12/2025
- Last Updated:
- 8/12/2025
Operations
Documentation
User manual
https://github.com/CIBERER/nf-CBRA-snvsLinks
Repository
https://github.com/CIBERER/nf-CBRA-snvs