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URL: http://aspiredb.msl.ubc.ca/
Proper Citation: AspireDB (RRID:SCR_016272)
Description: Web based software for analyzing genomic variants CNVs, SNVs, and Indels and phenotypes. It aims to represent the relationships between discovered variants and phenotypes.
Resource Type: data analysis software, data processing software, software application, software resource, web application
Keywords: gene, cnv, snv, indel, phenotype, analysis, variant
Funding: BC Knowledge Development Fund ; Canadian Foundation for Innovation
Availability: Account required, Freely available
Resource Name: AspireDB
Resource ID: SCR_016272
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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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