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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 processing software, web application, software application, data analysis software, software resource
Keywords: gene, cnv, snv, indel, phenotype, analysis, variant
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Source: SciCrunch Registry
