URL: http://wiki.chasmsoftware.org/index.php/Main_Page
Proper Citation: CHASM/SNV-Box (RRID:SCR_006445)
Description: CHASM is a method that predicts the functional significance of somatic missense mutations observed in the genomes of cancer cells, allowing mutations to be prioritized in subsequent functional studies, based on the probability that they give the cells a selective survival advantage. SNV-Box is a database of pre-computed features of all possible amino acid substitutions at every position of the annotated human exome. Users can rapidly retrieve features for a given protein amino acid substitution for use in machine learning.
Abbreviations: CHASM/SNV-Box
Synonyms: CHASM / SNV-Box, Cancer-specific High-throughput Annotation of Somatic Mutations
Resource Type: database, data or information resource, software resource
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