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CAPICE is a computational method for predicting the pathogenicity of SNVs and InDels. Repository description: 1) "paper_datasets.tar.gz" contains all datasets used in the CAPICE paper; 2) "CAPICE_v1.0_GRCh37_whole_genome_SNVs_InDels.tsv.gz" contains the precomputed scores for all possible SNVs and InDels in genome build 37. The gzip file contains two sub-directories, namely, "SNVs" and "InDels". Within each sub-directory, there are gzip files containing precomputed scores per chromosome. Commands: 1) To view the content: tar -tf /path/to/the/compressed/file 2) To de-compress: tar -C /path/to/store/decompressed/files --to-command='tar -xzvf -' -xzvf /path/to/the/compressed/file
Machine Learning, Clinical Genetics, Allele Frequency, Exome Sequencing, Variant Pathogenicity Prediction, Molecular Consequence, Genome Diagnostics
Machine Learning, Clinical Genetics, Allele Frequency, Exome Sequencing, Variant Pathogenicity Prediction, Molecular Consequence, Genome Diagnostics
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