Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Preparing word cloud

×

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.

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Funding Agency:wellcome trust (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

168 Results - per page

Show More Columns | Download 168 Result(s)

Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
MEROPS
 
Resource Report
Resource Website
500+ mentions
MEROPS (RRID:SCR_007777) MEROPS, MEROPS fam data or information resource, database An information resource for peptidases (also termed proteases, proteinases and proteolytic enzymes) and the proteins that inhibit them. The MEROPS database uses an hierarchical, structure-based classification of the peptidases. In this, each peptidase is assigned to a Family on the basis of statistically significant similarities in amino acid sequence, and families that are thought to be homologous are grouped together in a Clan. There is a Summary page for each family and clan, and these have indexes. Each of the Summary pages offers links to supplementary pages. About 3000 individual peptidases and inhibitors are included in the database, and there is a Summary page describing each one. You can navigate to this by any of several routes. There are indexes of Name, MEROPS Identifier and source Organism on the menu bar. Each Summary page describes the classification and nomenclature of the peptidase or inhibitor, and provides links to supplementary pages showing sequence identifiers, the structure if known, literature references and more. peptidase, protease, proteinase, proteolytic enzyme, protein, inhibitor, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
is related to: TopFIND
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
Wellcome Trust WT077044/Z/05/Z PMID:19892822 biotools:merops, r3d100012783, nif-0000-03112 https://bio.tools/merops, https://doi.org/10.17616/R33225, https://doi.org/10.17616/R33225 SCR_007777 MEROPS- the Peptidase Database, MEROPS - the Peptidase Database, MEROPS database, MEROPS fam 2026-09-19 12:57:10 762
Genes to Cognition Database
 
Resource Report
Resource Website
Genes to Cognition Database (RRID:SCR_002735) G2Cdb data or information resource, database Database of protein complexes, protocols, mouse lines, and other research products generated from the Genes to Cognition project, a project focused on understanding molecular complexes involved in synaptic transmission in the brain. allele, gene list, mouse line, human disease, phenotyping, plasticity, behavior, proteonomics, brain, cognition, cognition disorder, learning, memory, neuroscience, experimental protocol, synapse proteomics, synapse Wellcome Trust ;
MRC ;
BBSRC ;
Gatsby Charitable Foundation ;
Human Frontiers Science Programme ;
European Union ;
Framework Programme ;
EPSRC ;
NSF
PMID:18984621 Free, Freely available nif-0000-02864 http://www.genes2cognition.org/cgi-bin/SearchView SCR_002735 Genes-to-Cognition Database 2026-09-19 12:56:37 0
MLST
 
Resource Report
Resource Website
1000+ mentions
MLST (RRID:SCR_010245) data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on March 17, 2022. A nucleotide sequence based approach for the unambiguous characterisation of isolates of bacteria and other organisms via the internet. The aim of MLST is to provide a portable, accurate, and highly discriminating typing system that can be used for most bacteria and some other organisms. It is envisaged that this approach will be particularly helpful for the typing of bacterial pathogens. To achieve this aim we have taken the proven concepts of multilocus enzyme electrophoresis (MLEE) and have adapted them so that alleles at each locus are defined directly, by nucleotide sequencing, rather than indirectly from the electrophoretic moblity of their gene products. MLST was developed in the laboratories of Martin Maiden, Dominique Caugant, Ian Feavers, Mark Achtman and Brian Spratt. This site is hosted at Imperial College with funding from the Wellcome Trust. The location of the subsites for the individual species are shown on their respective front pages. has parent organization: Imperial College London; London; United Kingdom Wellcome Trust THIS RESOURCE IS NO LONGER IN SERVICE. nlx_156883 SCR_010245 2026-09-19 12:57:21 1242
Human Developmental Biology Resource
 
Resource Report
Resource Website
100+ mentions
Human Developmental Biology Resource (RRID:SCR_006326) HDBR biomaterial supply resource, material resource Collection of human embryonic and fetal material (Tissue and RNA) ranging from 3 to 20 weeks of development available to the international scientific community. Material can either be sent to registered users or our In House Gene Expression Service (IHGES) can carry out projects on user''''s behalf, providing high quality images and interpretation of gene expression patterns. Gene expression data emerging from HDBR material is added to our gene expression database which is accessible via our HUDSEN (Human Developmental Studies Network) website. A significant proportion of the material has been cytogenetically karyotyped, and normal karyotyped material is provided for research. development, fetal material, fetus, embryonic human, fetus human, karyotype, gene expression, image, imaging, FASEB list is listed by: One Mind Biospecimen Bank Listing
is related to: HUDSEN Human Gene Expression Spatial Database
has parent organization: Newcastle University; Newcastle upon Tyne; United Kingdom
has parent organization: University College London; London; United Kingdom
Normal MRC ;
Wellcome Trust
Public: Intended for use primarily by academic researchers. Every effort is made to ensure that optimal use is made of donated tissue, Both in terms of the aims and quality of the research for which it is used and avoidance of duplication/wastage. Applications by pharmaceutical or biotechnology companies for access to the Resource are considered, Provided that the tissue itself is not used directly for financial gain. nlx_152030 SCR_006326 MRC-Wellcome Trust Human Developmental Biology Resource 2026-09-19 12:57:53 316
Open Trials
 
Resource Report
Resource Website
1+ mentions
Open Trials (RRID:SCR_015570) data or information resource, database Database that contains data such as registry entries, portions of regulatory documents describing individual trials, structured data on methods and results, and researchers and papers from and/or related to clinical trials. The initiative aims to locate, match, and share all publicly accessible data and documents, on all trials conducted, on all medicines and other treatments, globally. clinical trial, clinical trial database, clinical trial data, open database, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: University of Oxford; Oxford; United Kingdom
Laura and John Arnold Foundation ;
Wellcome Trust ;
World Health Organisation ;
West of England Academic Health Science Network
Open source biotools:opentrials https://bio.tools/opentrials SCR_015570 2026-09-19 12:57:35 3
mousebrain.org
 
Resource Report
Resource Website
100+ mentions
mousebrain.org (RRID:SCR_016999) atlas, data or information resource Atlas of brain cell types, derived from single cell RNA-Seq data from Linnarsson Lab. Can be browsed by taxon, cell type, tissue, and gene, with information on enriched genes, specific markers, anatomical location and more. Single cell gene expression atlas of mouse nervous system. Atlas, brain cell, cell type, single cell RNA seq data, taxon, tissue, gene, marker, anatomical location, data has parent organization: Karolinska Institute; Stockholm; Sweden Åke Wiberg Foundation ;
Cancerfonden ;
European Research Council ;
EU ;
Hjärnfonden ;
Knut and Alice Wallenberg Foundation ;
Ollie and Elof Ericssons Foundation ;
SFO Strat Regen ;
SSF ;
Swedish Foundation for Strategic Research ;
Swedish Research Council ;
Wellcome Trust
PMID:30096314 Free, Available for download, Freely available SCR_018356 SCR_016999 Linnarsson lab Mouse Brain Atlas 2026-09-19 12:57:36 135
GEROprotectors
 
Resource Report
Resource Website
10+ mentions
GEROprotectors (RRID:SCR_016737) data or information resource, database Collection of structured and manually curated data of current therapeutic interventions in aging and age-related disease. Describes compounds and mechanisms using multiple chemical and biological databases. geroprotector, data, collection, current, thearpeutic, prevention, aging, disease, geriatic uses: PubChem
uses: ChemSpider
uses: DrugBank
uses: ChEMBL
uses: CHEBI
uses: UniProt
uses: GenAge
Fund in Memory of Dr. Amir Abramovich ;
Israel Ministry of Science and Technology ;
Wellcome Trust
PMID:26342919 Public, Free, Freely available SCR_016737 Geroprotectors 2026-09-19 12:57:36 13
BIGSdb
 
Resource Report
Resource Website
1+ mentions
BIGSdb (RRID:SCR_023551) data or information resource, database Platform for gene-by-gene bacterial population annotation and analysis. Designed to store and analyse sequence data for bacterial isolates. Used for scalable analysis of bacterial genome variation at population level. sequence data, bacterial isolates, gene-by-gene bacterial population, annotation and analysis, bacterial genome variation, Wellcome Trust PMID:21143983 Free, Freely available https://bigsdb.readthedocs.io/en/latest/ SCR_023551 Bacterial Isolate Genome Sequence Database 2026-09-19 12:57:39 1
Pavlovia
 
Resource Report
Resource Website
100+ mentions
Pavlovia (RRID:SCR_023320) software resource, web application Web application as repository and launch platform for Psychopy experiments and other open-source tools. Open Science Tools Limited, Psychopy experiments, repository and launch platform, behavioural sciences, University of Nottingham; Nottingham; United Kingdom ;
Wellcome Trust
Restricted SCR_023320 2026-09-19 12:55:33 282
Eagle
 
Resource Report
Resource Website
50+ mentions
Eagle (RRID:SCR_015991) software resource, software toolkit Software package for statistical estimation of haplotype phase either within a genotyped cohort or using a phased reference panel in large scale sequencing. The package includes Eagle1 (to harness identity-by-descent among distant relatives to rapidly call phase using a fast scoring approach) and Eagle2 (to analyze a full probabilistic model similar to the diploid Li-Stephens model used by previous HMM-based methods. hmm, hidden markov model, statistic, estimation, haplotype, phase, reference, panel, sequencing, algorithm, analysis, probability is listed by: Debian
is listed by: OMICtools
has parent organization: Broad Institute
Austrian Science Fund J-3401;
Dutch Brain Foundation ;
Fannie and John Hertz Foundation ;
NCRR S10 RR028832;
NHGRI F32HG007805;
NHGRI HG007022;
NHGRI R01 HG006399;
NHLBI HL117626;
NIMH R01 MH101244;
NWO 480-05-003;
Wellcome Trust WT098051
PMID:27694958
PMID:27270109
Free, Available for download, Freely available OMICS_14099, SCR_017262 https://sources.debian.org/src/bio-eagle/, https://github.com/poruloh/Eagle, https://data.broadinstitute.org/alkesgroup/Eagle/downloads/ SCR_015991 Bio-eagle, Eagle1, Eagle2 2026-09-19 12:58:14 57
fragon
 
Resource Report
Resource Website
fragon (RRID:SCR_019158) software resource, software toolkit Software tool for rapid high resolution structure determination from ideal protein fragments. Pipeline to determine crystal structures using molecular replacement with small fragments followed by density modification. It is available through CCP4. Density modification, molecular replacement, protein fragments, crystal structure determination is related to: CCP4 Wellcome Trust PMID:29533228 Free, Freely available SCR_019158 2026-09-19 12:58:18 0
Wellcome-CTC Mouse Strain SNP Genotype Set
 
Resource Report
Resource Website
1+ mentions
Wellcome-CTC Mouse Strain SNP Genotype Set (RRID:SCR_003216) Wellcome-CTC Mouse Strain SNP Genotype Set data or information resource, data set THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 19,2025. Data set of genotypes available for 480 strains and 13370 successful SNP assays that are mapped to build34 of the mouse genome, including 107 SNPs that are mapped to random unanchored sequence 13374 SNPs are mapped onto Build 33 of the mouse genome. You can access the data relative to Build 33 or Build 34. genome, genotype, snp, chromosome, haplotype, haplotype structure, recombinant inbred mouse strain has parent organization: Wellcome Trust Centre for Human Genetics Wellcome Trust ;
NCRR R24RR015116;
NIGMS R01GM072863;
NIAAA U01AA014425;
NINDS R01NS049445;
NIMH P20-MH 62009;
NIAAA U24AA13513
THIS RESOURCE IS NO LONGER IN SERVICE nlx_156947 SCR_003216 2026-09-19 12:58:35 3
GENCODE
 
Resource Report
Resource Website
5000+ mentions
Rating or validation data
GENCODE (RRID:SCR_014966) data or information resource, dataset, portal, project portal Human and mouse genome annotation project which aims to identify all gene features in the human genome using computational analysis, manual annotation, and experimental validation. human, mouse, genome, annotation, sequence, gene features, bio.tools is listed by: Debian
is listed by: bio.tools
is affiliated with: ENCODE
NHGRI 5U54HG004555;
Wellcome Trust WT098051
PMID:22955987 Free biotools:GENCODE https://bio.tools/GENCODE SCR_014966 ENCODE 2026-09-19 12:56:04 8811
NS-Forest
 
Resource Report
Resource Website
1+ mentions
NS-Forest (RRID:SCR_018348) data processing software, software application, software resource Software tool as method that takes cluster results from single cell nuclei RNAseq experiments and generates lists of minimal markers needed to define each cell type cluster. Utilizes random forest of decision trees machine learning approach. Used to determine minimum set of marker genes whose combined expression identified cells of given type with maximum classification accuracy. Single cell, RNAseq experiment, generated gene list, minimum set, marker gene, define cell type cluster, random forest, decision tree, machine learning, identify cell, cell clasyfication is related to: Allen Institute for Brain Science Allen Institute for Brain Science ;
California Institute for Regenerative Medicine ;
Chan Zuckerberg Initiative DAF ;
JCVI Innovation Fund ;
NIAID R21 AI122100;
NIAID U19 AI118626;
Wellcome Trust
PMID:29590361 Free, Available for download, Freely available SCR_018348 Necessary and Sufficient Forest, NS-Forestversion 1.3, NS-Forest v2.0, NS-Forest version 1.0 2026-09-19 12:56:09 2
BioMart Project
 
Resource Report
Resource Website
100+ mentions
BioMart Project (RRID:SCR_002987) data access protocol, data or information resource, portal, project portal, software resource, web service THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 4,2023.Platform provides free software and data services to international scientific community in order to foster scientific collaboration and facilitate scientific discovery process. Project adheres to open source philosophy that promotes collaboration and code reuse. biology, data, management, data mining, search, descriptive, graphical, application, perl, java, gold standard is used by: Blueprint Epigenome
is related to: Mouse Genome Informatics (MGI)
is related to: biomaRt
has parent organization: Ontario Institute for Cancer Research
has parent organization: European Bioinformatics Institute
Breast Cancer Campaign Tissue Bank ;
Center for Genome Regulation ;
Center for Mathematical Modelling ;
European Molecular Biology Laboratory ;
NSF NRF 2013M3A6A4043695;
Sandra Ibarra Foundation for Cancer ;
Spanish Government ;
U.S. Department of Energy ;
Wellcome Trust
PMID:21930506
PMID:19144180
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-30184 SCR_002987 BioMart software 2026-09-19 12:55:06 295
Roary
 
Resource Report
Resource Website
500+ mentions
Roary (RRID:SCR_018172) data analysis software, data processing software, sequence analysis software, software application, software resource Software tool for rapid large scale prokaryote pan genome analysis. Builds large scale pan genomes, identifying core and accessory genes. Makes construction of pan genome of thousands of prokaryote samples on standard desktop without compromising on accuracy of results. Not intended for meta genomics or for comparing extremely diverse sets of genomes. Genome analysis, prokaryote pan genome, pan genome, gene identification, analysis, bio.tools is listed by: Debian
is listed by: bio.tools
is listed by: OMICtools
works with: Scoary
Wellcome Trust PMID:26198102 Free, Available for download, Freely available OMICS_09491, biotools:roary https://github.com/sanger-pathogens/Roary, https://bio.tools/roary, https://sources.debian.org/src/roary/ SCR_018172 2026-09-19 12:55:17 710
ClonalOrigin
 
Resource Report
Resource Website
1+ mentions
ClonalOrigin (RRID:SCR_016061) data analysis software, data processing software, sequence analysis software, software application, software resource Software package for comparative analysis of the sequences of a sample of bacterial genomes in order to reconstruct the recombination events that have taken place in their ancestry. comparative, analysis, sequence, bacteria, genome, reconstruct, recombination, events, ancestry, bayesian is listed by: Debian
is listed by: OMICtools
is related to: Imperial College London; London; United Kingdom
is related to: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
National Science Foundation DBI-0630765;
Science Foundation of Ireland 05/FE1/B882;
Wellcome Trust WT082930MA
PMID:20923983
DOI:10.1534/genetics.110.120121
Free, Available for download OMICS_18881 https://sources.debian.org/src/clonalorigin/ SCR_016061 2026-09-19 12:55:15 8
Cytograph
 
Resource Report
Resource Website
1+ mentions
Cytograph (RRID:SCR_023101) data analysis software, data processing software, software application, software resource Software multistage analysis pipeline which progressively discovers cell types or states while mitigating impact of technical artifacts.Used for single cell analysis. cell types discovery, cell states discovery, single cell analysis Ake Wiberg Foundation ;
European Research Council ;
Knut and Alice Wallenberg Foundation ;
Ollie and Elof Ericssons Foundation ;
Swedish Foundation for Strategic Research ;
Swedish Research Council ;
Wellcome Trust
PMID:30096314 Free, Freely available SCR_023101 2026-09-19 12:55:28 3
NWB Explorer
 
Resource Report
Resource Website
1+ mentions
NWB Explorer (RRID:SCR_021151) data access protocol, software application, software resource, standalone software, web service Web application and standalone application to read, visualize and explore content of NWB:N 2 files.Used to share neurophysiological data in Neurodata Without Borders format. Read NWB files, visualize NWB files, explore NWB files, NWB, neurophysiology data sharing, Neurodata Without Borders format, neurophysiology data uses: Jupyter Notebook
uses: PyNWB
is listed by: Neurodata Without Borders
is related to: Metacell
is related to: Open Source Brain
Wellcome Trust Free, Available for download, Freely available https://www.nwb.org/tools/ SCR_021151 2026-09-19 12:54:49 1
SpikeInterface
 
Resource Report
Resource Website
1+ mentions
SpikeInterface (RRID:SCR_021150) data analysis software, data processing software, data visualization software, software application, software resource Software tool as unified framework for spike sorting. Python framework to unify preexisting spike sorting technologies into single codebase and to facilitate straightforward comparison and adoption of different approaches.Used to reproducibly run, compare, and benchmark most modern spike sorting algorithms; pre-process, post-process, and visualize extracellular datasets; validate, curate, and export sorting outputs. Spike sorting, Python framework, unify preexisting spike sorting, single codebase, spike sorting algorithms is listed by: Neurodata Without Borders ETH Zurich Postdoctoral Fellowship ;
Norwegian Ministry of Education ;
Research and Church Affairs ;
University of Edinburgh ;
University of Oslo ;
Wellcome Trust
PMID:33170122 Free, Available for download, Freely available https://www.nwb.org/tools/, https://github.com/SpikeInterface/spikeinterface/blob/master/doc/index.rst SCR_021150 2026-09-19 12:54:49 4

Can't find your Tool?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.

Can't find the RRID you're searching for? X
X
  1. RRID Portal Resources

    Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that RRID has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on RRID then you can log in from here to get additional features in RRID such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.