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 (Type)
Description
Pattern
Path to folder containing the vcf files with precomputed CADD scores.
This folder contains the uncompressed files that would otherwise be in data/annotation folder as described in https://github.com/kircherlab/CADD-scripts/#manual-installation.
*.{vcf,vcf.gz}
