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URL: http://sherlock.ucsf.edu/
Proper Citation: Sherlock (RRID:SCR_001628)
Description: Service to discover disease genes in GWAS using eQTL signature matching by simply submitting your list of GWAS associations (SNPs and p-values). It is important to upload all SNPs in your association study, not just the top hits. Sherlock may be able to group multiple lower-confidence SNPs to discover functionally-important genes.
Abbreviations: Sherlock
Resource Type: data or information resource, service resource
Defining Citation: PMID:23643380
Keywords: genome-wide association study, expression quantitative trait locus, disease gene, snp, gene expression, gene, disease, association, p-value, cis, trans, genetic variation, mapping, phenotype, FASEB list
Funding: NIGMS R01GM070808; NIGMS U19GM61390; NIGMS P50 GM081879
Availability: Free, Freely available
Resource Name: Sherlock
Resource ID: SCR_001628
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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