URL: https://cadd.gs.washington.edu/
Proper Citation: Combined Annotation Dependent Depletion (RRID:SCR_018393)
Description: Web tool for predicting deleteriousness of variants throughout human genome. Software tool for scoring deleteriousness of single nucleotide variants as well as insertion and deletions variants in human genome.
Abbreviations: CADD
Synonyms: Combined Annotation Dependent Depletion
Resource Type: data access protocol, data analysis software, data processing software, sequence analysis software, service resource, software application, software resource, web service
Defining Citation: PMID:30371827, PMID:24487276
Keywords: Human genome, disease, prediction, injurious variant, single nucleotide variant, insertion variant, deletion variant, deleteriousness scoring
Funding: Berlin Institute of Health ; Brotman Baty Institute for Precision Medicine ; Charite University Medicine Berlin ; German Research Foundation ; Howard Hughes Medical Institute ; NCI R01 CA197139; NHGRI U54 HG006493
Availability: Restricted
Resource Name: Combined Annotation Dependent Depletion
Resource ID: SCR_018393
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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
