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URL: https://gemini.readthedocs.io/en/latest/
Proper Citation: GEMINI (RRID:SCR_014819)
Description: Framework for exploring genetic variation in the context of the genome annotations available for the human genome. Users can load a VCF file into a database and each variant is automatically annotated by comparing it to several genome annotations from source such as ENCODE tracks, UCSC tracks, OMIM, dbSNP, KEGG, and HPRD.
Synonyms: GEnome MINIng (GEMINI), GEMINI - a flexible framework for exploring genome variation, Genome Mining, GEnome MINIng
Resource Type: software resource
Defining Citation: DOI:10.1371/journal.pcbi.1003153
Keywords: framework, genetic variation, annotation, human, genome, vcf, database, , bio.tools, FASEB list
Availability: Freely available
Resource Name: GEMINI
Resource ID: SCR_014819
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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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