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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: data or information resource, database, software resource
Related Condition: Cancer
Funding: NCI CA152432; NCI CA135866; NSF DBI0845275
Availability: Acknowledgement requested, Free, Non-commercial
Resource Name: CHASM/SNV-Box
Resource ID: SCR_006445
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
