CAGI7_Annotate_All_Missense https://genomeinterpretation.org/cagi7-annotate-all-missense.html
-
Updated
Oct 18, 2025 - Python
CAGI7_Annotate_All_Missense https://genomeinterpretation.org/cagi7-annotate-all-missense.html
This script automates missense SNP extraction/counting from VCF files using BCFTools. Processes multiple samples, handles compressed formats, verifies dependencies, and generates standardized reports for genomic variant analysis
Add a description, image, and links to the missense-snp-extraction topic page so that developers can more easily learn about it.
To associate your repository with the missense-snp-extraction topic, visit your repo's landing page and select "manage topics."