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URL: http://143.169.238.105/variantdb/index.php?page=variants
Proper Citation: VariantDB (RRID:SCR_018010)
Description: Web based interactive annotation and filtering platform that automatically annotates variants with allele frequencies, functional impact, pathogenicity predictions and pathway information. Allows filtering by all annotations, under dominant, recessive or de novo inheritance models. Flexible annotation and filtering portal for next generation sequencing data.
Resource Type: analysis service resource, data or information resource, portal, production service resource, service resource
Defining Citation: PMID:25352915
Keywords: Annotation, filtering, portal, next generation, sequencing data, variant, allele frequency, functional impact, pathogenicity prediction, pathway information
Funding: Belgian National Fund for Scientific Research-Flanders ; Fondation Leducq
Availability: Restricted
Resource Name: VariantDB
Resource ID: SCR_018010
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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
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