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URL: http://bioinformatics.research.nicta.com.au/software/is-rsnp/
Proper Citation: is-rSNP (RRID:SCR_000387)
Description: Software tool that predicts whether a single nucleotide polymorphism (SNP) is a regulatory SNP (rSNP). For a given SNP, and using a statistical framework, it can successfully predict the set of transcription factors (TFs) for which binding is affected. The algorithm provides the statistical power to scan large numbers of SNPs, making it suitable to use to screen all associated SNPs output by a typical genome-wide association studies (GWAS).
Abbreviations: is-rSNP
Synonyms: In silico regulatory SNP detection, is-rSNP: in silico regulatory SNP detection
Resource Type: software resource
Defining Citation: PMID:20823317
Keywords: genome-wide association study, single nucleotide polymorphism, transcription factor, regulatory single nucleotide polymorphism, in silico
Availability: THIS RESOURCE IS NO LONGER IN SERVICE
Resource Name: is-rSNP
Resource ID: SCR_000387
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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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