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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
PubChem Substance
 
Resource Report
Resource Website
1000+ mentions
PubChem Substance (RRID:SCR_004742) PubChem Substance data repository, storage service resource, d spatial image, data or information resource, service resource, database As one of three primary databases of PubChem (Pcsubstance, Pccompound, and PCBioAssay), PubChem Substance Database contains descriptions of chemical samples, from a variety of sources, and links to PubMed citations, protein 3D structures, and biological screening results that are available in PubChem BioAssay. If the contents of a chemical sample are known, the description includes links to PubChem Compound. A PubChem FTP is available and new data is accepted into the repository. Pcsubstance contains more than 81 million records (2011). small molecule, biological activity, chemical substance, bioactivity, gold standard is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
has parent organization: PubChem
has parent organization: NCBI
PMID:26400175
PMID:26175801
nlx_74645 http://pubchem.ncbi.nlm.nih.gov/ SCR_004742 PubChem Substances Database, Pcsubstance, NCBI PubChem Substance, PubChem Substance Database 2026-02-13 10:55:30 2802
Organ Procurement and Transplantation Network
 
Resource Report
Resource Website
10+ mentions
Organ Procurement and Transplantation Network (RRID:SCR_004883) OPTN data or information resource, patient registry, people resource, database The only national patient waiting list and an online database system, called UNet, that links all of the professionals involved in the donation and transplantation system for the collection, storage, analysis, and publication of all OPTN data pertaining to the patient waiting list, organ matching, and transplants. The system contains data regarding every organ donation and transplant event occurring in the U.S. since October 1, 1987. UNet is a fail-safe, 24/7, secure Internet-based transplant information database created to enable the nation''''s organ transplant institutions to: * register patients for transplants * match donated organs to waiting patients * manage the time-sensitive, life-critical data of all patients, before and after their transplants Data reports are available by type: National Data, Regional Data, State Data, Center Data, Build Advanced Report, and Annual Report Data. UNet is being used right now by all of the nation''''s organ transplant programs, organ procurement organizations, and histocompatibility (tissue typing) laboratories working cooperatively to efficiently share a limited number of donated organs among thousands of patients. transplant, organ, kidney, pancreas, liver, heart, lung, intestine, adult, pediatric, adult human, young human, child, thoracic, waiting list, donation, transplantation, data set, medical data, FASEB list is listed by: NIDDK Research Resources
is listed by: NIDDK Information Network (dkNET)
has parent organization: UNOS - United Network for Organ Sharing
is parent organization of: LifeBanc
Health Resources and Services Administration nlx_143932 http://www.optn.org/ SCR_004883 Organ Procurement Transplantation Network 2026-02-13 10:55:31 43
NCBI Sequence Read Archive (SRA)
 
Resource Report
Resource Website
5000+ mentions
NCBI Sequence Read Archive (SRA) (RRID:SCR_004891) SRA data repository, storage service resource, data or information resource, service resource, database Repository of raw sequencing data from next generation of sequencing platforms including including Roche 454 GS System, Illumina Genome Analyzer, Applied Biosystems SOLiD System, Helicos Heliscope, Complete Genomics, and Pacific Biosciences SMRT. In addition to raw sequence data, SRA now stores alignment information in form of read placements on reference sequence. Data submissions are welcome. Archive of high throughput sequencing data,part of international partnership of archives (INSDC) at NCBI, European Bioinformatics Institute and DNA Database of Japan. Data submitted to any of this three organizations are shared among them. sequence, blast, next-generation sequence, alignment, read placement, reference sequence, roche 454 gs system, illumina genome analyzer, applied biosystems solid system, helicos heliscope, complete genomics, pacific biosciences smrt, high-throughput sequencing, data analysis service, gold standard is recommended by: National Library of Medicine
is recommended by: NIDDK Information Network (dkNET)
is listed by: OMICtools
is related to: European Nucleotide Archive (ENA)
is related to: RecountDB
is related to: SRAdb
is related to: DDBJ Sequence Read Archive
is related to: Bgee: dataBase for Gene Expression Evolution
is related to: NCBI BioSample
is related to: DDBJ Sequence Read Archive
is related to: METAGENOTE
has parent organization: NCBI
works with: SARS-CoV-2-Sequences
works with: Signaling Pathways Project
NLM PMID:22009675
PMID:21062823
Free, Available for download, Freely available OMICS_01031, nlx_86174, r3d100010775 https://doi.org/10.17616/R31S69 SCR_004891 Sequence Read Archive, , SRA, NCBI SRA 2026-02-13 10:55:31 6671
Nonhuman Primate Transplantation Tolerance Cooperative Study Group
 
Resource Report
Resource Website
Nonhuman Primate Transplantation Tolerance Cooperative Study Group (RRID:SCR_006847) NHPCSG portal, resource, data or information resource, research forum portal, disease-related portal, topical portal Cooperative program for research on nonhuman primate models of kidney, islet, heart, and lung transplantation evaluating the safety and efficacy of existing and new treatment regimens that promote the immune system''''s acceptance of a transplant and to understand why the immune system either rejects or does not reject a transplant. This program bridges the critical gap between small-animal research and human clinical trials. The program supports research into the immunological mechanisms of tolerance induction and development of surrogate markers for the induction, maintenance, and loss of tolerance. transplantation, clinical, kidney, islet, tolerance, heart, lung, treatment, immune system, tolerance induction is related to: NIDDK Information Network (dkNET) Kidney transplantation, Islet transplantation, Heart transplantation, Lung transplantation NIDDK ;
NIAID
nlx_152728 http://www.niddk.nih.gov/fund/diabetesspecialfunds/consortia/NHP.pdf SCR_006847 Non-human Primate Transplantation Tolerance Cooperative Study Group 2026-02-13 10:55:54 0
National Kidney and Urologic Diseases Information Clearinghouse
 
Resource Report
Resource Website
1+ mentions
National Kidney and Urologic Diseases Information Clearinghouse (RRID:SCR_006842) NKUDIC resource, data or information resource, service resource, narrative resource, training material Information dissemination service of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) established to increase knowledge and understanding about diseases of the kidneys and urologic system among people with these conditions and their families, health care professionals, and the general public: online, in booklets and fact sheets, by email, and over the phone. To carry out this mission, NKUDIC works closely with a coordinating panel of representatives from Federal agencies; voluntary organizations on the national level; professional groups; and State health departments to identify and respond to informational needs about kidney and urologic diseases. NKUDIC provides the following informational products and services: * Response to inquiries about kidney and urologic diseases-ranging from information about available patient and professional education materials to statistical data. By phone (8:30 a.m. to 5 p.m. eastern time, M-F), fax, mail, and email. * Publications about specific kidney and urologic diseases, provided free of copyright, in varying reading levels. Available online or as booklets and brochures. (See our Publications Catalog.) NKUDIC also sends publications to health fairs and community events. Please contact us for more information. * Referrals to health professionals through the National Library of Medicine''''s MEDLINEplus includes a consumer-friendly listing of organizations that will assist you in your search for physicians and other health professionals. * Exhibits at professional meetings specific to kidney and urologic diseases, as well as cross-cutting professional meetings. NKUDIC exhibits at 11 professional meetings, each year, including Society of Urologic Nurses and Associates, American Urologic Association, American Society of Nephrology, National Kidney Foundation, Polycystic Kidney Disease Research Foundation, American Academy of Family Physicians, American Academy of Physician Assistants, American Nurses Association, and the National Conference for Nurse Practitioners. statistics, publication, kidney, urologic system, bladder, renal health, renal disease is related to: NIDDK Information Network (dkNET)
has parent organization: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is parent organization of: Urologic Diseases in America
Kidney disease, Urologic disease NIDDK Free, Public nlx_152711 SCR_006842 National Kidney and Urologic Diseases Information Clearinghouse (NKUDIC) 2026-02-13 10:55:55 1
Center for Inherited Disease Research
 
Resource Report
Resource Website
100+ mentions
Center for Inherited Disease Research (RRID:SCR_007339) CIDR training service resource, analysis service resource, resource, material analysis service, production service resource, biomaterial analysis service, service resource, data computation service Next generation sequencing and genotyping services provided to investigators working to discover genes that contribute to disease. On-site statistical geneticists provide insight into analysis issues as they relate to study design, data production and quality control. In addition, CIDR has a consulting agreement with the University of Washington Genetics Coordinating Center (GCC) to provide statistical and analytical support, most predominantly in the areas of GWAS data cleaning and methods development. Completed studies encompass over 175 phenotypes across 530 projects and 620,000 samples. The impact is evidenced by over 380 peer-reviewed papers published in 100 journals. Three pathways exist to access the CIDR genotyping facility: * NIH CIDR Program: The CIDR contract is funded by 14 NIH Institutes and provides genotyping and statistical genetic services to investigators approved for access through competitive peer review. An application is required for projects supported by the NIH CIDR Program. * The HTS Facility: The High Throughput Sequencing Facility, part of the Johns Hopkins Genetic Resources Core Facility, provides next generation sequencing services to internal JHU investigators and external scientists on a fee-for-service basis. * The JHU SNP Center: The SNP Center, part of the Johns Hopkins Genetic Resources Core Facility, provides genotyping to internal JHU investigators and external scientists on a fee-for-service basis. Data computation service is included to cover the statistical genetics services provided for investigators seeking to identify genes that contribute to human disease. Human Genotyping Services include SNP Genome Wide Association Studies, SNP Linkage Scans, Custom SNP Studies, Cancer Panel, MHC Panels, and Methylation Profiling. Mouse Genotyping Services include SNP Scans and Custom SNP Studies. gene, genome, array, custom, dna, genome wide association study, genotyping, genotyping service, linkage scan, methylation profiling, hereditary disease, single gene disorder, snp, statistical genetics, whole genome, whole exome, exome sequencing, high throughput sequencing, single nucleotide polymorphism, sequencing, disease is listed by: NIDDK Information Network (dkNET)
has parent organization: Johns Hopkins University; Maryland; USA
Aging NHGRI ;
NCI ;
NEI ;
NIA ;
NIAAA ;
NIAMS ;
NICHD ;
NIDA ;
NIDCD ;
NIDCR ;
NIDDK ;
NIEHS ;
NIMH ;
NINDS ;
NHGRI N01-HG-65403;
US Department of Health and Human Services HHSN268200782096C;
S Department of Health and Human Services HHSN268201100011I;
S Department of Health and Human Services HHSN268201200008I;
NHGRI U01HG004438;
NHGRI U54HG006542
nif-0000-00223 SCR_007339 CIDR - Center for Inherited Disease Research 2026-02-13 10:56:04 206
T1DBase
 
Resource Report
Resource Website
100+ mentions
T1DBase (RRID:SCR_007959) data repository, storage service resource, resource, data or information resource, service resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 26,2019. In October 2016, T1DBase has merged with its sister site ImmunoBase (https://immunobase.org). Documented on March 2020, ImmunoBase ownership has been transferred to Open Targets (https://www.opentargets.org). Results for all studies can be explored using Open Targets Genetics (https://genetics.opentargets.org). Database focused on genetics and genomics of type 1 diabetes susceptibility providing a curated and integrated set of datasets and tools, across multiple species, to support and promote research in this area. The current data scope includes annotated genomic sequences for suspected T1D susceptibility regions; genetic data; microarray data; and global datasets, generally from the literature, that are useful for genetics and systems biology studies. The site also includes software tools for analyzing the data. genetics, beta cell, gene, variant, region, genomics, gene expression, genome-wide association study, data analysis service, bio.tools is used by: NIF Data Federation
is used by: NIDDK Information Network (dkNET)
is listed by: NIDDK Information Network (dkNET)
is listed by: Debian
is listed by: bio.tools
is related to: dkCOIN
has parent organization: University of Cambridge; Cambridge; United Kingdom
Type 1 diabetes. Diabetes Wellcome Trust ;
NIDDK ;
Juvenile Diabetes Research Foundation
PMID:20937630 THIS RESOURCE IS NO LONGER IN SERVICE. nif-0000-03531, biotools:t1dbase https://bio.tools/t1dbase SCR_007959 T1DBase - Type 1 Diabetes Database 2026-02-13 10:56:05 145
NCBI database of Genotypes and Phenotypes (dbGap)
 
Resource Report
Resource Website
500+ mentions
NCBI database of Genotypes and Phenotypes (dbGap) (RRID:SCR_002709) dbGaP data repository, storage service resource, data or information resource, service resource, database Database developed to archive and distribute clinical data and results from studies that have investigated interaction of genotype and phenotype in humans. Database to archive and distribute results of studies including genome-wide association studies, medical sequencing, molecular diagnostic assays, and association between genotype and non-clinical traits. clinical, trial, genotype, interaction, homology, cell, morphology, interaction, phenotype, molecular diagnosis, genetic recombination, gold standard, bio.tools is used by: International Genomics of Alzheimers Project
is used by: NIDDK Inflammatory Bowel Disease Genetics Consortium
is used by: NIH Heal Project
is used by: Genomic Data Commons Data Portal (GDC Data Portal)
is recommended by: National Library of Medicine
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: OMICtools
is listed by: re3data.org
is listed by: NIDDK Information Network (dkNET)
is listed by: bio.tools
is listed by: Debian
is related to: NIDDK Central Repository
is related to: eMERGE Network: electronic Medical Records and Genomics
is related to: Framingham Heart Study
is related to: PhenoExplorer
is related to: Chronic Renal Insufficiency Cohort Study
is related to: DbGaP Cleaner
is related to: Psychiatric Genomics Consortium
is related to: ISCA Consortium
is related to: Allen Institute for Brain Science
has parent organization: NCBI
is parent organization of: Resource for Genetic Epidemiology Research on Adult Health and Aging
NLM PMID:24297256
PMID:17898773
Restricted nif-0000-23342, OMICS_00263, biotools:dbgap, r3d100010788 http://www.ncbi.nlm.nih.gov/sites/entrez?db=gap
https://bio.tools/dbgap
https://doi.org/10.17616/R3GS4K
SCR_002709 database of Genotypes and Phenotypes (dbGaP), dbGaP, NCBI, Database of Genotypes and Phenotypes 2026-02-13 10:55:06 683
GenBank
 
Resource Report
Resource Website
10000+ mentions
GenBank (RRID:SCR_002760) GB data repository, storage service resource, data or information resource, service resource, database NIH genetic sequence database that provides annotated collection of all publicly available DNA sequences for almost 280 000 formally described species (Jan 2014) .These sequences are obtained primarily through submissions from individual laboratories and batch submissions from large-scale sequencing projects, including whole-genome shotgun (WGS) and environmental sampling projects. Most submissions are made using web-based BankIt or standalone Sequin programs, and GenBank staff assigns accession numbers upon data receipt. It is part of International Nucleotide Sequence Database Collaboration and daily data exchange with European Nucleotide Archive (ENA) and DNA Data Bank of Japan (DDBJ) ensures worldwide coverage. GenBank is accessible through NCBI Entrez retrieval system, which integrates data from major DNA and protein sequence databases along with taxonomy, genome, mapping, protein structure and domain information, and biomedical journal literature via PubMed. BLAST provides sequence similarity searches of GenBank and other sequence databases. Complete bimonthly releases and daily updates of GenBank database are available by FTP. genetic sequence, dna sequence, human genetics, human genome, nucleotide sequence, nucleotide, dna, dna data bank, gene mapping, genetics, gold standard is used by: Structural Genomics Consortium
is used by: xFITOM
is used by: Transcriptional Regulatory Element Database
is recommended by: National Library of Medicine
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: OMICtools
is listed by: re3data.org
is listed by: CINERGI
is related to: High Throughput Genomic Sequences Division
is related to: DNA DataBank of Japan (DDBJ)
is related to: HS3D - Homo Sapiens Splice Sites Dataset
is related to: Influenza Virus Resource
is related to: TPA
is related to: Anopheles gambiae (African malaria mosquito) genome view
is related to: Nucleotide database
is related to: NCBI BioSample
is related to: NCBI Nucleotide
is related to: SpliceDB
is related to: MaizeGDB
is related to: NCBI Assembly Archive Viewer
is related to: DNA DataBank of Japan (DDBJ)
is related to: European Molecular Biology Laboratory
is related to: INSDC
is related to: NCBI Protein Database
is related to: TrED
is related to: Xenopus Gene Collection
is related to: Mammalian Gene Collection
is related to: Zebrafish Gene Collection
is related to: INSDC
is related to: NCBI Virus
is related to: Codon and Codon-Pair Usage Tables
has parent organization: NCBI
is parent organization of: NCBI Genome Survey Sequences Database
is parent organization of: NCBI Genome Survey Sequences Database
works with: OGDraw
works with: A plasmid Editor
works with: Webcutter
works with: merge-gbk-records
works with: PremierBiosoft Proteo IQ Software
works with: SARS-CoV-2-Sequences
works with: rentrez
works with: MiMeDB
NLM PMID:24217914
PMID:23193287
PMID:21071399
Free, Freely available nif-0000-02873, r3d100010528, OMICS_01650 https://doi.org/10.17616/R3D31X SCR_002760 , Gen Bank, GenBank 2026-02-13 10:55:07 61478
SciCrunch
 
Resource Report
Resource Website
10+ mentions
SciCrunch (RRID:SCR_003115) SciCrunch data or information resource, portal, database, community building portal Community portal for researchers and content management system for data and databases. Intended to provide common source of data to research community and data about Research Resource Identifiers (RRIDs), which can be used in scientific publications. Central service where RRIDs can be searched and created. Designed to help communities of researchers create their own portals to provide access to resources, databases and tools of relevance to their research areas. Adds value to existing scientific resources by increasing their discoverability, accessibility, visibility, utility and interoperability, regardless of their current design or capabilities and without need for extensive redesign of their components or information models. Resources can be searched and discovered at multiple levels of integration, from superficial discovery based on limited description of resource at SciCrunch Registry, to deep content query at SciCrunch Data Federation. Data sharing, community, data, RRID, portal, data discovery, data accessibility, data visibility, data interoperability, scientific publication data, data access uses: NIF Data Federation
uses: SciBot
uses: SciGraph
is used by: SPARC Portal
is related to: Neuroscience Information Framework
is related to: SciScore
is related to: SciBot
is related to: SPARC Anatomy Working Group
is related to: PRECISE Traumatic Brain Injury Model Catalog
has parent organization: University of California at San Diego; California; USA
is parent organization of: Aging Portal
is parent organization of: NIDDK Information Network (dkNET)
is parent organization of: Resource Identification Portal
is parent organization of: Integrated Datasets
is parent organization of: Integrated
is parent organization of: InterLex
Free, Freely available nlx_156715 SCR_003115 2026-02-13 10:55:10 18
Mutant Mouse Resource and Research Center
 
Resource Report
Resource Website
1000+ mentions
Mutant Mouse Resource and Research Center (RRID:SCR_002953) MMRRC biomaterial supply resource, organism supplier, material resource National public repository system for mutant mice. Archives and distributes scientifically valuable spontaneous and induced mutant mouse strains and ES cell lines for use by biomedical research community. Includes breeding/distribution facilities and information coordinating center. Mice strains are cryopreserved, unless live colony must be established. Live mice are supplied from production colony, from colony recovered from cryopreservation, or via micro-injection of cell line into host blastocysts. MMRRC member facilities also develop technologies to improve handling of mutant mice, including advances in assisted reproductive techniques, cryobiology, genetic analysis, phenotyping and infectious disease diagnostics. RIN, Resource Information Network, stem cell, mouse strain, embryonic stem cell, embryonic stem cell line, cryopreserved, mutant mouse strain, mutant, transgenic, database, FASEB list, RRID Community Authority is used by: Integrated Animals
is listed by: One Mind Biospecimen Bank Listing
is listed by: Biositemaps
is listed by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: NIDDK Research Resources
is listed by: NIDDK Information Network (dkNET)
is listed by: Resource Information Network
is affiliated with: MUGA
is affiliated with: MegaMUGA
is related to: Federation of International Mouse Resources
is related to: Mouse Mutagenesis Center for Developmental Defects
is related to: MGI strains
has parent organization: Jackson Laboratory
has parent organization: University of California at Davis; California; USA
has parent organization: University of Missouri; Missouri; USA
has parent organization: University of North Carolina at Chapel Hill; North Carolina; USA
has parent organization: National Institutes of Health
is parent organization of: Deltagen and Lexicon Knockout Mice and Phenotypic Data Resource
provides: Knockout Mouse Project Repository
has organization facet: University of California at Davis Mutant Mouse Resource and Research Center
has organization facet: Mutant Mouse Resource and Research Center - University of North Carolina
has organization facet: Mutant Mouse Resource and Research Center - University of Missouri
has organization facet: Mutant Mouse Resource and Research Center - Jackson Laboratory
NIH Office of the Director U42 OD012210;
NIH Office of the Director U42 OD010918;
NIH Office of the Director U42 OD010924;
NIH Office of the Director U42 OD010921;
NCRR RR026296;
NIH Blueprint for Neuroscience Research
Restricted nif-0000-00045 SCR_002953 Mutant Mouse Regional Resource Center 2026-02-13 10:55:09 1025
Japanese Genotype-phenotype Archive (JGA)
 
Resource Report
Resource Website
10+ mentions
Japanese Genotype-phenotype Archive (JGA) (RRID:SCR_003118) JGA data repository, storage service resource, data or information resource, service resource, database A service for permanent archiving and sharing of all types of personally identifiable genetic and phenotypic data resulting from biomedical research projects. The JGA contains exclusive data collected from individuals whose consent agreements authorize data release only for specific research use or to bona fide researchers. Strict protocols govern how information is managed, stored and distributed by the JGA. Once processed, all data are encrypted. The JGA accepts only de-identified data approved by JST-NBDC. The JGA implements access-granting policy whereby the decisions of who will be granted access to the data resides with the JST-NBDC. After data submission the JGA team will process the data into databases and archive the original data files. The accepted data types include manufacturer-specific raw data formats from the array-based and new sequencing platforms. The processed data such as the genotype and structural variants or any summary level statistical analyses from the original study authors are stored in databases. The JGA also accepts and distributes any phenotype data associated with the samples. For other human biological data, please contact the NBDC human data ethical committee. biomedical, genetic, phenotype, gene, data sharing, genotype is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
has parent organization: DNA DataBank of Japan (DDBJ)
has parent organization: NBDC - National Bioscience Database Center
Free, Freely available nlx_156741, r3d100010818 https://doi.org/10.17616/R3861Q http://trace.ddbj.nig.ac.jp/jga/, http://trace.ddbj.nig.ac.jp/jga/index_e.html SCR_003118 JGA, Japanese Genotype-phenotype Archive (JGA), Japanese Genotype-phenotype Archive 2026-02-13 10:55:10 35
ArrayExpress
 
Resource Report
Resource Website
5000+ mentions
ArrayExpress (RRID:SCR_002964) ArrayExpress data repository, storage service resource, catalog, data or information resource, service resource, database International functional genomics data collection generated from microarray or next-generation sequencing (NGS) platforms. Repository of functional genomics data supporting publications. Provides genes expression data for reuse to the research community where they can be queried and downloaded. Integrated with the Gene Expression Atlas and the sequence databases at the European Bioinformatics Institute. Contains a subset of curated and re-annotated Archive data which can be queried for individual gene expression under different biological conditions across experiments. Data collected to MIAME and MINSEQE standards. Data are submitted by users or are imported directly from the NCBI Gene Expression Omnibus. gold, standard, functional, genomics, data, collection, microarray, next, generation, sequencing, NGS, repository uses: MIAME
uses: MINSEQE
uses: Gene Expression Omnibus
is used by: NIF Data Federation
is used by: BioSample Database at EBI
is used by: Integrated Datasets
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: DataCite
is listed by: OMICtools
is listed by: re3data.org
is related to: DDBJ Omics Archive
is related to: MIAME
is related to: Gene Expression Atlas
is related to: Experimental Factor Ontology
is related to: Bgee: dataBase for Gene Expression Evolution
is related to: ISA Infrastructure for Managing Experimental Metadata
is related to: FlyMine
is related to: MAGE-TAB
is related to: Experimental Factor Ontology
is related to: Magic
is related to: ArrayExpress (R)
is related to: CancerMIRNome
has parent organization: European Bioinformatics Institute
European Union ;
SLING 226073;
European Commission ;
Gen2Phen 200754;
NHGRI P41 HG003619
PMID:23193272
PMID:21071405
Available Public or Private, Free, Available for download, The community can contribute to this resource, Acknowledgement requested, to access private data registration required OMICS_01023, nif-0000-30123, r3d100010222 http://www.ebi.ac.uk/microarray-as/ae
https://doi.org/10.17616/R3302G
SCR_002964 , ArrayExpress, ArrayExpress - functional genomics data, ArrayExpress Archive 2026-02-13 10:55:09 7529
Database of Interacting Proteins (DIP)
 
Resource Report
Resource Website
100+ mentions
Database of Interacting Proteins (DIP) (RRID:SCR_003167) DIP data repository, storage service resource, data analysis service, analysis service resource, data or information resource, production service resource, service resource, database Database to catalog experimentally determined interactions between proteins combining information from a variety of sources to create a single, consistent set of protein-protein interactions that can be downloaded in a variety of formats. The data were curated, both, manually and also automatically using computational approaches that utilize the the knowledge about the protein-protein interaction networks extracted from the most reliable, core subset of the DIP data. Because the reliability of experimental evidence varies widely, methods of quality assessment have been developed and utilized to identify the most reliable subset of the interactions. This CORE set can be used as a reference when evaluating the reliability of high-throughput protein-protein interaction data sets, for development of prediction methods, as well as in the studies of the properties of protein interaction networks. Tools are available to analyze, visualize and integrate user's own experimental data with the information about protein-protein interactions available in the DIP database. The DIP database lists protein pairs that are known to interact with each other. By interact they mean that two amino acid chains were experimentally identified to bind to each other. The database lists such pairs to aid those studying a particular protein-protein interaction but also those investigating entire regulatory and signaling pathways as well as those studying the organization and complexity of the protein interaction network at the cellular level. Registration is required to gain access to most of the DIP features. Registration is free to the members of the academic community. Trial accounts for the commercial users are also available. blast, cellular network, ligand-receptor complex, ligand, network, protein, protein interaction, protein ligand, protein-protein interaction, protein receptor, receptor, sequence, interaction, regulatory pathway, signaling pathway, protein binding, bio.tools, FASEB list is recommended by: NIDDK Information Network (dkNET)
is recommended by: National Library of Medicine
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: OMICtools
is listed by: re3data.org
is listed by: NIH Data Sharing Repositories
is listed by: bio.tools
is listed by: Debian
is related to: IMEx - The International Molecular Exchange Consortium
is related to: IMEx - The International Molecular Exchange Consortium
is related to: MPIDB
is related to: TissueNet - The Database of Human Tissue Protein-Protein Interactions
is related to: InteroPorc
is related to: Interaction Reference Index
is related to: ConsensusPathDB
is related to: NIH Data Sharing Repositories
is related to: PSICQUIC Registry
is related to: Agile Protein Interactomes DataServer
has parent organization: University of California at Los Angeles; California; USA
NIGMS PMID:14681454 Free, Available for download, Freely available OMICS_01905, nif-0000-00569, r3d100010882, biotools:dip https://dip.doe-mbi.ucla.edu/dip/Main.cgi
https://bio.tools/dip
https://doi.org/10.17616/R3431F
SCR_003167 , Database of Interacting Proteins, DIP, Database of Interacting Proteins (DIP) 2026-02-13 10:55:11 153
Proteomics Identifications (PRIDE)
 
Resource Report
Resource Website
500+ mentions
Proteomics Identifications (PRIDE) (RRID:SCR_003411) PRIDE data repository, storage service resource, data or information resource, service resource, database Centralized, standards compliant, public data repository for proteomics data, including protein and peptide identifications, post-translational modifications and supporting spectral evidence. Originally it was developed to provide a common data exchange format and repository to support proteomics literature publications. This remit has grown with PRIDE, with the hope that PRIDE will provide a reference set of tissue-based identifications for use by the community. The future development of PRIDE has become closely linked to HUPO PSI. PRIDE encourages and welcomes direct user submissions of protein and peptide identification data to be published in peer-reviewed publications. Users may Browse public datasets, use PRIDE BioMart for custom queries, or download the data directly from the FTP site. PRIDE has been developed through a collaboration of the EMBL-EBI, Ghent University in Belgium, and the University of Manchester. proteomics, protein, peptide, mass spectrometry, annotation, standard, spectra, protein-protein interaction, amino acid, amino acid sequence, post-translational modification, biomart, bio.tools is used by: ProteomeXchange
is used by: BioSample Database at EBI
is recommended by: NIDDK Information Network (dkNET)
is listed by: Biositemaps
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: HUPO Proteomics Standards Initiative
is related to: ProteomeXchange
has parent organization: European Bioinformatics Institute
Wellcome Trust WT085949MA;
European Union FP7 LSHG-CT-2006-036814;
European Union FP7 260558;
European Union FP7 262067;
European Union FP7 202272;
BBSRC BB/I024204/1
PMID:23203882
PMID:19662629
Free, Available for download, Freely available nif-0000-03336, biotools:pride, r3d100011515 https://www.ebi.ac.uk/pride/archive/
https://bio.tools/pride
https://doi.org/10.17616/R3F330
SCR_003411 PRoteomics IDEntifications database, PRIDE Archive - proteomics data repository, PRIDE Archive, PRIDE, Proteomics Identifications, Proteomics Identifications (PRIDE), PRoteomics IDEntifications database (PRIDE) 2026-02-13 10:55:14 642
EMDataResource.org
 
Resource Report
Resource Website
100+ mentions
EMDataResource.org (RRID:SCR_003207) EMDB, EMDataResource data repository, storage service resource, portal, data or information resource, service resource, project portal Portal for deposition and retrieval of cryo electron microscopy (3DEM) density maps, atomic models, and associated metadata. Global resource for 3 Dimensional Electron Microscopy structure data archiving and retrieval, news, events, software tools, data standards, validation methods. deposition, retrival, cryo, electron, microscopy, 3DEM, density, maps, atomic, model, metadata, structure is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: 3DVC
is listed by: re3data.org
is affiliated with: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: Electron Microscopy Data Bank at PDBe (MSD-EBI)
is related to: PDBe - Protein Data Bank in Europe
is related to: National Center for Macromolecular Imaging
has parent organization: Rutgers University; New Jersey; USA
has parent organization: European Bioinformatics Institute
has parent organization: Baylor University; Texas; USA
NIGMS R01 GM079429;
BBSRC BBG022577
PMID:20935055
PMID:20888470
Free, Freely available r3d100010552, nif-0000-30776 https://doi.org/10.17616/R3T61P EMDataBank.org SCR_003207 EMDataResource, EMDResource, EMDB, EMDataBank.org, EMDataBank - Unified Data Resource for 3DEM, EMDataBank 2026-02-13 10:55:12 168
Type 1 Diabetes Resource
 
Resource Report
Resource Website
1+ mentions
Type 1 Diabetes Resource (RRID:SCR_001475) T1DR biomaterial supply resource, organism supplier, material resource International repository for importation, curation, genotypic and phenotypic validation, cryopreservation, and distribution of mouse stocks of value to the type 1 diabetes scientific community holding over 250 genetically modified or congenic mouse stocks that are being used to dissect genetic and biologic features of T1D. They provide extensive genotypic and phenotypic quality control and genetic stabilization for these strains, as well as incidence studies when available. An added value of T1DR stocks is their ability to propel advances in related areas of science, including research in non-T1D autoimmunity and infectious diseases. The staff provides information and technical assistance regarding selection and use of existing T1DR models, and will provide limited support for development of new models considered to be of high-value for the T1D community. The resource includes strains generated at the Jackson Laboratory as well as strains donated by external scientists. Investigators are highly encouraged to donate a strain to ensure its preservation and availability to other researchers. genotype, phenotype, animal model is listed by: One Mind Biospecimen Bank Listing
is listed by: NIDDK Information Network (dkNET)
has parent organization: Jackson Laboratory
Type 1 diabetes, Diabetes NIDDK UC4DK097610 Free, Freely Available nlx_152730 SCR_001475 2026-02-13 10:54:51 1
Type 1 Diabetes TrialNet
 
Resource Report
Resource Website
10+ mentions
Type 1 Diabetes TrialNet (RRID:SCR_001508) TrialNet portal, clinical trial, resource, data or information resource, disease-related portal, database, topical portal International network of researchers who are exploring ways to prevent, delay and reverse the progression of type 1 diabetes. It is conducting clinical trials with researchers from 18 Clinical Centers in the United States, Canada, Finland, United Kingdom, Italy, Germany, Australia and New Zealand. In addition, more than 150 medical centers and physician offices are participating in the TrialNet network. Studies are available for people newly diagnosed with type 1 diabetes, as well as for relatives of people with type 1 diabetes who are at greater risk of developing the disease. This NIH-sponsored clinical trials network conducts studies designed to evaluate new approaches to prevent or ameliorate type 1 diabetes specifically by interdicting the type 1 diabetes disease process. These include interventions designed to decrease beta-cell destruction and/or enhance beta-cell survival. Studies are conducted in non-diabetic persons at risk of type 1 diabetes in an effort to delay the development of type 1 diabetes as a clinical disease; or (if initiated prior to appearance of autoimmunity) in an effort to delay the appearance of autoimmunity; or in individuals with type 1 diabetes who are either newly diagnosed or have evidence of sustained beta cell function. Studies include long-term follow-up of subjects developing type 1 diabetes. The TrialNet network also supports natural history and genetics studies in populations screened for or enrolled in studies conducted by the TrialNet study group. In addition, TrialNet will evaluate methodologies that enhance the conduct of clinical trials interdicting the type 1 diabetes disease process. intervention, beta-cell, clinical, child, young human, natural history, genetics, prevention, delay is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Central Repository
has parent organization: University of South Florida; Florida; USA
is parent organization of: Living Biobank
Diabetes, Type 1 diabetes NIDDK U01DK061058 Available to the research community nlx_152812 SCR_001508 2026-02-13 10:54:52 22
CKID A Prospective Cohort Study of Kidney Disease in Children
 
Resource Report
Resource Website
10+ mentions
CKID A Prospective Cohort Study of Kidney Disease in Children (RRID:SCR_001500) CKID bibliography, portal, resource, data or information resource, research forum portal, disease-related portal, topical portal Prospective, observational cohort study of children with mild to moderate chronic kidney disease (CKD) to: (1) determine risk factors for progression of pediatric chronic kidney disease (CKD); (2) examine the impact of CKD on neurocognitive development; (3) examine the impact of CKD on risk factors for cardiovascular disease, and; (4) examine the impact of CKD on growth. The CKiD study population will include a cohort of 540 children, age 1 16 years, expected to be enrolled over a 24-month period. child, young human, pediatric, risk factor, kidney function, neurodevelopment, cognitive ability, behavior, kidney, urologic problem, glomerular disease, adverse effect, cognition, growth, adolescent, infant, clinical is listed by: NIDDK Information Network (dkNET)
has parent organization: Johns Hopkins University; Maryland; USA
Chronic kidney disease, Renal disease, Cardiovascular disease NIDDK U01DK066174;
NCRR M01RR000052
Free, Freely available nlx_152790 SCR_001500 CKID: A Prospective Cohort Study of Kidney Disease in Children, Chronic Kidney Disease in Children 2026-02-13 10:54:51 10
Collaborative Islet Transplant Registry
 
Resource Report
Resource Website
1+ mentions
Collaborative Islet Transplant Registry (RRID:SCR_001466) CITR data repository, storage service resource, resource, data or information resource, service resource, report, narrative resource, database Collect, analyze, and communicate on comprehensive and current data on all islet/beta cell transplants in human recipients performed in North America, as well as some European and Australian centers to expedite progress and promote safety in islet/beta cell transplantation. This site serves as a repository for general information concerning protocols, clinical transplantation sites, publications, and other information of interest to the general community. Annual Reports are available. Islet/beta cell transplantation is a complex procedure with many factors contributing to the outcome. Compiling and analyzing data from all transplant centers in the US, Canada, as well as some European and Australian centers will accelerate the identification of both critical risk factors and key determinants of success and thereby guide transplant centers in developing and refining islet/beta cell transplant protocols. The inclusion of the term collaborative in the name of the Registry emphasizes the importance of collaboration in fulfilling the CITR mission and goals. Close collaboration with the transplant centers will ensure that relevant questions are addressed, that data submitted are accurate and complete, and that the needs of the transplant community are served. Information on how to participate as a CITR Transplant Center and to receive a transplant center application is available through the website. Progress in islet transplantation depends entirely on complete, high-quality medical data, including the information patients consented to report to the Collaborative Islet Transplant Registry. To make it as easy as possible to provide updated information about patient's health, an on-line questionnaire is available or patients can mail it to their transplant center. This information is very important in the continuing search for a cure for Type 1 diabetes. transplant center, transplant, islet, beta cell, clinical, islet transplantation, beta cell transplantation, outcome, metadata standard, adverse event report, diabetes, data element, bibliography, questionnaire, protocol, risk factor, case report form, allograft, pancreatectomy, autograft, islet processing is listed by: NIDDK Information Network (dkNET) Type 1 diabetes, Diabetes NIDDK N01-DK6-2868;
NIDDK N01-DK1-2472
PMID:15387102 Free, Freely Available nlx_152693 SCR_001466 2026-02-13 10:54:52 9

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