Evaluation datasets and pre-computed scores for: "CAPICE: a computational method for Consequence-Agnostic Pathogenicity Interpretation of Clinical Exome variations"

CAPICE is a computational method for predicting the pathogenicity of SNVs and InDels.


This new repository added index for CAPICE v1.0 (build37) precomputed files.


Repository description:


1) "paper_datasets.tar.gz" contains all datasets used in the CAPICE paper;


2) "capice_v1.0_build37_indels.tsv.gz" contains the precomputed scores for InDels in genome build 37


3) "capice_v1.0_build37_indels.tsv.gz.tbi" contains the index for file"capice_v1.0_build37_indels.tsv.gz"


4) "capice_v1.0_build37_snvs.tsv.gz" contains the precomputed scores for all possible SNVs in genome build 37


5) "capice_v1.0_build37_snvs.tsv.gz.tbi" contains the index for file "capice_v1.0_build37_snvs.tsv.gz"