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URL: https://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg38&g=snp151
Proper Citation: dbSNP151 (RRID:SCR_028814)
Description: Database containing common germline alterations. dbSNP build 151 contains a subset of common germline variants (such as single nucleotide polymorphisms) defined by a minor allele frequency (MAF) of 1% or greater in major population groups.Database is used as a reference for various applications, such as measuring non-synonymous mutations in tumor mutation burden calculations.
Resource Type: data or information resource, database
Keywords: common germline alterations, subset of common germline variants, minor allele frequency,
Availability: Free, Freely available
Resource Name: dbSNP151
Resource ID: SCR_028814
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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
The NIDDK Information Network (dkNET) serves the needs of basic and clinical investigators by providing seamless access to large pools of data and research resources relevant to the mission of The National Institute of Diabetes Digestive and Kidney Diseases (NIDDK). dkNET is hosted at University of California San Diego, and is supported by NIH NIDDK grant U24DK097771.
Email: info_at_ dknet.org
