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URL: http://www2.hu-berlin.de/wikizbnutztier/software/CandiSNPer/
Proper Citation: CandiSNPer (RRID:SCR_005173)
Description: A webtool which helps in characterizing Single Nucleotide Polymorphisms (SNPs) that are located in the vicinity of an SNP of interest (start SNP). Along with the computation of the maximal Linkage Disequilibrium (LD) region around the start SNP. CandiSNPer provides additional information with respect to the molecular consequences of the SNPs and the genes located in the LD region.
Abbreviations: CandiSNPer
Resource Type: service resource, software resource, source code
Defining Citation: PMID:20172942
Keywords: single nucleotide polymorphism, gene, plot, linkage disequilibrium, variant, genome-wide association study, genotyping, perl, r
Availability: Free for academic use
Resource Name: CandiSNPer
Resource ID: SCR_005173
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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