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URL: http://www.sanger.ac.uk/science/tools/carol
Proper Citation: CAROL (RRID:SCR_001800)
Description: Software application that is a combined functional annotation score of non-synonymous coding variants. A major challenge in interpreting whole-exome data is predicting which of the discovered variants are deleterious or neutral. To address this question in silico, they have developed a score called Combined Annotation scoRing toOL (CAROL), which combines information from two bioinformatics tools: PolyPhen-2 and SIFT, in order to improve the prediction of the effect of non-synonymous coding variants. The combination of annotation tools can help improve automated prediction of whole-genome/exome non-synonymous variant functional consequences. (entry from Genetic Analysis Software) The software should run on any UNIX or GNU/Linux system.
Abbreviations: CAROL
Synonyms: Combined Annotation scoRing toOL
Resource Type: software application, software resource
Defining Citation: PMID:22261837
Keywords: gene, genetic, genomic, r, prediction, non-synonymous coding variant
Availability: Free, Available for download, Freely available
Resource Name: CAROL
Resource ID: SCR_001800
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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