Description

CADD is a tool for scoring the deleteriousness of single nucleotide variants as well as insertion/deletions variants in the human genome.

Input

Name
Description
Pattern

0 ()

1 ()

0 ()

Output

Name
Description
Pattern

tsv ()

versions ()

Tools

cadd Documentation

CADD scripts release for offline scoring

https://github.com/kircherlab/CADD-scripts/doi: 10.1093/nar/gky1016License: Restricted. Free for non-commercial users.