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URL: http://chgv.org/GenicIntolerance/
Proper Citation: Residual Variation Intolerance Score (RVIS) (RRID:SCR_013850)
Description: A gene-based score intended to help in the interpretation of human sequence data. The score is designed to rank genes in terms of whether they have more or less common functional genetic variation relative to the genome wide expectation given the amount of apparently neutral variation the gene has. A gene with a positive score has more common functional variation, and a gene with a negative score has less and is referred to as intolerant.
Abbreviations: RVIS
Synonyms: Residual Variation Intolerance Score
Resource Type: data or information resource, narrative resource, standard specification
Defining Citation: DOI:10.1371/journal.pgen.1003709
Keywords: gene, score, sequence, interpretation, rank, functional genetic variation
Funding: NIH Epi4K Sequencing ; Bioinformatics and Biostatistics Core U01NS077303
Resource Name: Residual Variation Intolerance Score (RVIS)
Resource ID: SCR_013850
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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