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

<p>CAPICE is a computational method for predicting the pathogenicity of SNVs and InDels.</p> <p>This new repository added index for CAPICE v1.0 (build37) precomputed files.</p> <p><strong>Repository description:</strong></p> <p>1) &quot;paper_datasets.tar.gz&quot; contains all datasets used in the CAPICE paper;</p> <p>2) &quot;capice_v1.0_build37_indels.tsv.gz&quot; contains the precomputed scores for InDels in genome build 37</p> <p>3) &quot;capice_v1.0_build37_indels.tsv.gz.tbi&quot; contains the index for file&quot;capice_v1.0_build37_indels.tsv.gz&quot;</p> <p>4)&nbsp;&quot;capice_v1.0_build37_snvs.tsv.gz&quot; contains the precomputed scores for all possible SNVs in genome build 37</p> <p>5) &quot;capice_v1.0_build37_snvs.tsv.gz.tbi&quot; contains the index for file &quot;capice_v1.0_build37_snvs.tsv.gz&quot;</p> <p>&nbsp;</p>