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URL: https://bioinformatics.csiro.au/variantspark/
Proper Citation: VariantSpark (RRID:SCR_018383)
Description: Software toolkit for genome wide association studies optimized for GWAS like datasets by CSIRO. Machine learning framework that creates insights from high dimensional data, including genomics and clinical data.
Resource Type: data processing software, software application, software resource, software toolkit
Keywords: Machine learning framework, high dimentional data, genomic data, clinical data, genome wide association, GWAS dataset, CSIRO
Availability: Free, Freely available
Resource Name: VariantSpark
Resource ID: SCR_018383
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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
