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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 Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
TREES toolbox
 
Resource Report
Resource Website
10+ mentions
TREES toolbox (RRID:SCR_010457) TREES toolbox software resource Software package, written in Matlab (Mathworks, Natick, MA), providing tools to automatically reconstruct neuronal branching from microscopy image stacks and to generate synthetic axonal and dendritic trees. It provides the basic tools to edit, visualize and analyze dendritic and axonal trees, methods for quantitatively comparing branching structures between neurons, and tools for exploring how dendritic and axonal branching depends on local optimization of total wiring and conduction distance. neuronal branching, microscopy, neuron, matlab, visualization, rendering, reconstruction, analysis, modeling, morphology, dendrite, axon, computational neuroanatomy, tree is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: University College London; London; United Kingdom
Max Planck Society ;
Wellcome Trust ;
Gatsby Charitable Foundation ;
Alexander von Humboldt-Stiftung ;
European Research Council
PMID:20700495 GNU General Public License v3, Creative Commons Attribution-NonCommercial-ShareAlike License v3, The community can contribute to this resource nlx_157723 http://www.nitrc.org/projects/treestoolbox SCR_010457 treestoolbox - A Matlab toolbox to generate edit visualize and analyze neuronal structure 2026-09-05 06:26:42 29
eVOC
 
Resource Report
Resource Website
1+ mentions
eVOC (RRID:SCR_010704) eVOC controlled vocabulary, data or information resource, ontology THIS RESOURCE IS NO LONGER IN SERVICE, documented May 10, 2017. A pilot effort that has developed a centralized, web-based biospecimen locator that presents biospecimens collected and stored at participating Arizona hospitals and biospecimen banks, which are available for acquisition and use by researchers. Researchers may use this site to browse, search and request biospecimens to use in qualified studies. The development of the ABL was guided by the Arizona Biospecimen Consortium (ABC), a consortium of hospitals and medical centers in the Phoenix area, and is now being piloted by this Consortium under the direction of ABRC. You may browse by type (cells, fluid, molecular, tissue) or disease. Common data elements decided by the ABC Standards Committee, based on data elements on the National Cancer Institute''s (NCI''s) Common Biorepository Model (CBM), are displayed. These describe the minimum set of data elements that the NCI determined were most important for a researcher to see about a biospecimen. The ABL currently does not display information on whether or not clinical data is available to accompany the biospecimens. However, a requester has the ability to solicit clinical data in the request. Once a request is approved, the biospecimen provider will contact the requester to discuss the request (and the requester''s questions) before finalizing the invoice and shipment. The ABL is available to the public to browse. In order to request biospecimens from the ABL, the researcher will be required to submit the requested required information. Upon submission of the information, shipment of the requested biospecimen(s) will be dependent on the scientific and institutional review approval. Account required. Registration is open to everyone., documented September 6, 2016. Set of orthogonal controlled vocabularies that unifies gene expression data by facilitating a link between the genome sequence and expression phenotype information. The system associates labelled target cDNAs for microarray experiments, or cDNA libraries and their associated transcripts with controlled terms in a set of hierarchical vocabularies. eVOC consists of four orthogonal controlled vocabularies suitable for describing the domains of human gene expression data including Anatomical System, Cell Type, Pathology and Developmental Stage. The four core eVOC ontologies provide an appropriate set of detailed human terms that describe the sample source of human experimental material such as cDNA and SAGE libraries. These expression terms are linked to libraries and transcripts allowing the assessment of tissue expression profiles, differential gene expression levels and the physical distribution of expression across the genome. Analysis is currently possible using EST and SAGE data, with microarray data being incorporated. The eVOC data is increasingly being accepted as a standard for describing gene expression and eVOC ontologies are integrated with the Ensembl EnsMart database, the Alternate Transcript Diversity Project and the UniProt Knowledgebase. Several groups are currently working to provide shared development of this resource such that it is of maximum use in unifying transcript expression information. mouse, mapping, cdna, development, microarray, expression, expressed sequence, anatomical system, cell type, developmental stage, experimental technique, microarray platform, pathology, pooling, tissue preparation, treatment, gene expression, genome sequence, expression phenotype, genome, sequence, phenotype, anatomical system, cell type, pathology, anatomy is related to: OBO
is related to: Bgee: dataBase for Gene Expression Evolution
has parent organization: University of the Western Cape; Bellville; South Africa
South African National Research Foundation ;
European Union ;
Wellcome Trust ;
South African Department of Arts Culture Science and Technology 32146
PMID:12799354 THIS RESOURCE IS NO LONGER IN SERVICE nlx_84448 SCR_010704 Expressed Sequence Annotation for Humans, eVOC (Expressed Sequence Annotation for Humans), eVOC Ontologies, eVOContology.org 2026-09-05 06:26:45 4
BioMart MartView
 
Resource Report
Resource Website
10+ mentions
BioMart MartView (RRID:SCR_010714) data access protocol, data or information resource, data set, software resource, web service A web server interface of BioMart software and provides a unified view over disparate data sources that enable bioscientists to retrieve data from one or multiple sources in a simple and efficient way. This MartView web server features seamless data federation making cross querying of data sources in a user friendly and unified way. Data sources include major biomolecular sequence, pathway and annotation databases such as Ensembl, Uniprot, Reactome, HGNC, Wormbase, etc. The web server not only provides access through a web interface, it also supports programmatic access through a Perl API as well as RESTful and SOAP oriented web services. gold standard is related to: biomaRt Ontario Institute for Cancer Research ;
Wellcome Trust ;
EMBL ;
European Union FP6 contract LHSG-CT-2004-512092
PMID:19420058
PMID:19144180
Free, Public nlx_89178 SCR_010714 MartView, BioMart Central Portal 2026-09-05 06:26:45 10
Gene3D
 
Resource Report
Resource Website
100+ mentions
Gene3D (RRID:SCR_007672) Gene3D data access protocol, data or information resource, data repository, database, service resource, software resource, storage service resource, web service A large database of CATH protein domain assignments for ENSEMBL genomes and Uniprot sequences. Gene3D is a resource of form studying proteins and the component domains. Gene3D takes CATH domains from Protein Databank (PDB) structures and assigns them to the millions of protein sequences with no PDB structures using Hidden Markov models. Assigning a CATH superfamily to a region of a protein sequence gives information on the gross 3D structure of that region of the protein. CATH superfamilies have a limited set of functions and so the domain assignment provides some functional insights. Furthermore most proteins have several different domains in a specific order, so looking for proteins with a similar domain organization provides further functional insights. Strict confidence cut-offs are used to ensure the reliability of the domain assignments. Gene3D imports functional information from sources such as UNIPROT, and KEGG. They also import experimental datasets on request to help researchers integrate there data with the corpus of the literature. The website allows users to view descriptions for both single proteins and genes and large protein sets, such as superfamilies or genomes. Subsets can then be selected for detailed investigation or associated functions and interactions can be used to expand explorations to new proteins. The Gene3D web services provide programmatic access to the CATH-Gene3D annotation resources and in-house software tools. These services include Gene3DScan for identifying structural domains within protein sequences, access to pre-calculated annotations for the major sequence databases, and linked functional annotation from UniProt, GO and KEGG., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. protein domain, protein, protein superfamily, hidden markov model, structural domain, genome, sequence, domain assignments, protein structure, bio.tools, FASEB list is listed by: bio.tools
is listed by: Debian
has parent organization: University College London; London; United Kingdom
NIH ;
Wellcome Trust ;
European Union FP6 ENFIN LSHG-CT-2003-503265;
European Union FP6 ENFIN LSHG-CT-2004-512092;
European Union FP6 ENFIN LSHG-CT-2005-518254;
DOE DE-AC02-065CH11357
PMID:19906693
PMID:18032434
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02877, biotools:gene3d https://bio.tools/gene3d SCR_007672 Gene3D - Structures assigned to Genomes 2026-09-05 06:26:14 272
Human Ageing Genomic Resources
 
Resource Report
Resource Website
100+ mentions
Human Ageing Genomic Resources (RRID:SCR_007700) HAGR data or information resource, database, software resource, software toolkit Collection of databases and tools designed to help researchers study the genetics of human ageing using modern approaches such as functional genomics, network analyses, systems biology and evolutionary analyses. A major resource in HAGR is GenAge, which includes a curated database of genes related to human aging and a database of ageing- and longevity-associated genes in model organisms. Another major database in HAGR is AnAge. Featuring over 4,000 species, AnAge provides a compilation of data on aging, longevity, and life history that is ideal for the comparative biology of aging. GenDR is a database of genes associated with dietary restriction based on genetic manipulation experiments and gene expression profiling. Other projects include evolutionary studies, genome sequencing, cancer genomics, and gene expression analyses. The latter allowed them to identify a set of genes commonly altered during mammalian aging which represents a conserved molecular signature of aging. Software, namely in the form of scripts for Perl and SPSS, is made available for users to perform a variety of bioinformatic analyses potentially relevant for studying aging. The Perl toolkit, entitled the Ageing Research Computational Tools (ARCT), provides modules for parsing files, data-mining, searching and downloading data from the Internet, etc. Also available is an SPSS script that can be used to determine the demographic rate of aging for a given population. An extensive list of links regarding computational biology, genomics, gerontology, and comparative biology is also available. gene, gerontology, human, model, senescence, genomics, longevity, genetics, perl, spss, demographic analysis, genome, evolution, gene expression, model organism, human aging, dietary restriction, genetic manipulation has parent organization: University of Liverpool; Liverpool; United Kingdom
is parent organization of: anage
is parent organization of: GenAge
Aging, Cancer Ellison Medical Foundation ;
Wellcome Trust ME050495MES;
European Union FP7 Health Research HEALTH-F4-2008-202047
PMID:23193293 GNU General Public License, Creative Commons Attribution v3 Unported License nif-0000-02938, r3d100011871 https://doi.org/10.17616/R34W81 SCR_007700 2026-09-05 06:26:14 107
CellML Model Repository
 
Resource Report
Resource Website
1+ mentions
CellML Model Repository (RRID:SCR_008113) CellML Repository data repository, service resource, software repository, software resource, storage service resource Repository of biological models created using CellML, a free, open-source, eXtensible markup language based standard for defining mathematical models of cellular function. Models may be browsed by category, which include: Calcium Dynamics, Cardiovascular Circulation, Cell Cycle, Cell Migration, Circadian Rhythms, Electrophysiology, Endocrine, Excitation-Contraction Coupling, Gene Regulation, Hepatology, Immunology, Ion Transport, Mechanical Constitutive Laws, Metabolism, Myofilament Mechanics, Neurobiology, pH Regulation, PKPD, Signal Transduction, Synthetic Biology. The community can contribute their models to this resource. cell function, cell model, model, cell, calcium dynamics, cardiovascularc circulation, cell cycle, cell migration, circadian rhythm, electrophysiology, endocrine, excitation-contraction coupling, gene regulation, hepatology, immunology, ion transport, mechanical constitutive law, metabolism, myofilament mechanics, neurobiology, ph regulation, pkpd, signal transduction, synthetic biology, image, exposure is used by: NIF Data Federation
is listed by: 3DVC
is listed by: Integrated Models
is related to: Integrated Manually Extracted Annotation
has parent organization: CellML
Wellcome Trust ;
Royal Society of New Zealand ;
Maurice Wilkins Centre for Molecular Biodiscovery
PMID:21216774
PMID:18658182
PMID:17947072
PMID:19162720
PMID:19380315
The community can contribute to this resource nif-0000-20828 SCR_008113 2026-09-05 06:26:18 6
CellML
 
Resource Report
Resource Website
100+ mentions
CellML (RRID:SCR_008061) CellML data or information resource, interchange format, markup language, narrative resource, standard specification The CellML language is an open standard based on the XML markup language. The purpose of CellML is to store and exchange computer-based mathematical models. CellML allows scientists to share models even if they are using different model-building software. It also enables them to reuse components from one model in another, thus accelerating model building. Although CellML was originally intended for the description of biological models; CellML includes information about model structure (how the parts of a model are organizationally related to one another), mathematics (equations describing the underlying processes) and metadata (additional information about the model that allows scientists to search for specific models or model components in a database or other repository). The CellML team is committed to providing freely available tools for creating, editing, and using CellML models. We provide information regarding tools we are developing internally and links to external projects developing tools which utilize the CellML format. Please let us know if you have an open source CellML tool looking for a home on the internet, as we are able to offer limited hosting services on cellml.org. biological model, cell, mathematical model, mathematics, metadata, model structure, model, xml, annotation, mark up language, FASEB list is listed by: 3DVC
is related to: PathGuide: the pathway resource list
is related to: Physiome Model Repository
has parent organization: University of Auckland; Auckland; New Zealand
is parent organization of: CellML Model Repository
VPH NoE ;
Maurice Wilkins Centre for Molecular Biodiscovery ;
International Union of Physiological Sciences: Physiome Project ;
aneurIST ;
NZIMA ;
Foundation for Research Science and Technology ;
Wellcome Trust
PMID:15142756
PMID:18658182
PMID:19564239
PMID:19380315
PMID:18579471
PMID:17947072
PMID:17271569
The CellML project is built by an open, Democratic community on an Open unspecified license / free ethic. nif-0000-10448 SCR_008061 CellML project, The CellML Project 2026-09-05 06:26:17 153
Wellcome Trust Sanger Institute; Hinxton; United Kingdom
 
Resource Report
Resource Website
500+ mentions
Wellcome Trust Sanger Institute; Hinxton; United Kingdom (RRID:SCR_011784) WTSI, Sanger institution Non profit research organization for genome sequences to advance understanding of biology of humans and pathogens in order to improve human health globally. Provides data which can be translated for diagnostics, treatments or therapies including over 100 finished genomes, which can be downloaded. Data are publicly available on limited basis, and provided more extensively upon request. research, genome, sequence, human, health, project, global, data, treatment, therapy is listed by: re3data.org
is affiliated with: Open Targets
is related to: Clonalframe
is related to: ClonalOrigin
is related to: TraCeR
is parent organization of: ILLUMINUS
is parent organization of: ARNIE
is parent organization of: Sequence Search and Alignment by Hashing Algorithm
is parent organization of: Sequencing of Idd regions in the NOD mouse genome
is parent organization of: CAROL
is parent organization of: DINDEL
is parent organization of: Wellcome Trust Case Control Consortium
is parent organization of: OLORIN
is parent organization of: Exomiser
is parent organization of: COSMIC - Catalogue Of Somatic Mutations In Cancer
is parent organization of: GeneDB
is parent organization of: Breast Cancer Somatic Genetics Study
is parent organization of: Artemis: Genome Browser and Annotation Tool
is parent organization of: ACT: Artemis Comparison Tool
is parent organization of: Alien hunter
is parent organization of: Pfam
is parent organization of: DNAPlotter
is parent organization of: VAGrENT
is parent organization of: SMALT
is parent organization of: LookSeq
is parent organization of: ZMP
is parent organization of: Deciphering Developmental Disorders
is parent organization of: Sanger Mouse Resources Portal
is parent organization of: SpliceDB
is parent organization of: DECIPHER
is parent organization of: 1000 Genomes: A Deep Catalog of Human Genetic Variation
is parent organization of: Genes to Cognition: Neuroscience Research Programme
is parent organization of: MEROPS
is parent organization of: Rfam
is parent organization of: VEGA
is parent organization of: Bacterial Genomes
is parent organization of: Caenorhabditis Genome Sequencing Projects
is parent organization of: D. rerio Blast Server
is parent organization of: Fungi Sequencing Projects
is parent organization of: PEER
is parent organization of: Alfresco - FRont-End for Sequence COmparison
is parent organization of: AutoCSA (Automatic Comparative Sequence Analysis)
is parent organization of: AceDB
is parent organization of: CnD
is parent organization of: Genomics of Drug Sensitivity in Cancer
is parent organization of: Zebrafish Genome Project
is parent organization of: Tree families database
is parent organization of: Ensembl
is parent organization of: BamView
is parent organization of: SVMerge
is parent organization of: RetroSeq
is parent organization of: Consensus CDS
is parent organization of: WormBase
is parent organization of: Belvu
is parent organization of: Bio-tradis
is parent organization of: Blixem
is parent organization of: Dotter
is parent organization of: Exonerate
is parent organization of: Fastaq
is parent organization of: Gubbins
is parent organization of: CellPhoneDB
is parent organization of: Ensembl Metazoa
is parent organization of: Scmap
is parent organization of: Scfind
is parent organization of: Recognition of Errors in Assemblies using Paired Reads
is parent organization of: SAMTOOLS
is parent organization of: Cell Model Passports
Wellcome Trust ISNI: 0000 0004 0606 5382, nlx_91258, grid.10306.34, Wikidata: Q1142544 https://ror.org/05cy4wa09 SCR_011784 Wellcome Trust Sanger Institute, Genome Research Limited, The Wellcome Sanger Institute, Sanger Institute, Wellcome Trust Sanger Institute Genome Research Limited 2026-09-05 06:27:12 543
IUPHAR/BPS Guide to Pharmacology
 
Resource Report
Resource Website
1000+ mentions
IUPHAR/BPS Guide to Pharmacology (RRID:SCR_013077) IUPHAR Database, IUPHAR-DB, IUPHAR GPCR, IUPHAR RECEPTOR data or information resource, database, narrative resource, portal, standard specification Portal and searchable database of pharmacological information. Information is presented at two levels, the initial view or landing pages for each target family provide expert-curated overviews of the key properties and the available selective ligands and tool compounds. For selected targets, more detailed introductory chapters for each family are available along with curated information on the pharmacological, physiological, structural, genetic and pathophysiogical properties of each target. pharmacology, drug discovery, portal, guide, physiology, molecular structure, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
has parent organization: NC-IUPHAR
Wellcome Trust PMID:21087994 nif-0000-03056, biotools:iuphar-db, r3d100013308 https://bio.tools/iuphar-db, https://doi.org/10.17616/R31NJMRG http://www.iuphar-db.org SCR_013077 International Union of Pharmacology Database, International Union of Basic and Clinical Pharmacology Database 2026-09-05 06:27:32 2375
Dietary Restriction Gene Database
 
Resource Report
Resource Website
1+ mentions
Dietary Restriction Gene Database (RRID:SCR_013720) GenDR Database of genes associated with dietary restriction. It includes genes inferred from experiments in model organisms in which genetic manipulations cancel out or disrupt the life-extending effects of dietary restriction and genes robustly altered due to dietary restriction, derived from a meta-analysis of microarray studies in mammals. gene, dietary restriction, microarray has parent organization: University of Liverpool; Liverpool; United Kingdom Wellcome Trust MEB050495MES;
Biotechnology and Biological Sciences Research Council H0084971
Free, Public SCR_013720 The GenDR Database of Dietary Restriction-Related Genes 2026-09-05 06:27:39 3
KymoButler
 
Resource Report
Resource Website
1+ mentions
KymoButler (RRID:SCR_021717) data analysis software, data processing software, software application, software resource Software tool as deep learning software for automated kymograph analysis. Uses artificial intelligence to trace lines in kymograph and extract information about particle movement. Speeds up analysis of kymographs by between 50 and 250 times, and comparisons show that it is as reliable as manual analysis. automated kymograph analysis, kymograph, particle movement Biotechnology and Biological Sciences Research Council ;
European Research Council ;
Herchel Smith Foundation ;
Isaac Newton Trust ;
Wellcome Trust
PMID:31405451 Free, Available for download, Freely available https://github.com/elifesciences-publications/KymoButler, https://gitlab.com/deepmirror/kymobutler, https://www.wolframcloud.com/objects/deepmirror/Projects/KymoButler/KymoButlerForm SCR_021717 2026-09-05 06:29:45 7
mRnd
 
Resource Report
Resource Website
100+ mentions
mRnd (RRID:SCR_022156) data access protocol, software resource, web service Web tool for calculations for Mendelian Randomization. Power calculations for Mendelian Randomization. Used to calculate statistical power for Mendelian Randomization study, using Non Centrality Parameter based approach. calculations for Mendelian Randomization, Mendelian Randomization, calculate statistical power, Mendelian Randomization study, Non Centrality Parameter Australian National Health and Medical Research Council ;
EU 7th Framework Programme ;
Leducq Foundation ;
Wellcome Trust
PMID:24159078 Free, Freely available https://github.com/kn3in/mRnd SCR_022156 2026-09-05 06:29:51 364
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 2026-09-05 06:29:56 295
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 2026-09-05 06:32:12 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 2026-09-05 06:32:14 135
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 2026-09-05 06:32:14 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 2026-09-05 06:32:19 1
PALM
 
Resource Report
Resource Website
50+ mentions
PALM (RRID:SCR_017029) PALM data analysis software, data processing software, software application, software resource Software tool for inference using permutation methods. Requires Matlab or Octave. Can be executed from inside either environment, or directly from the shell and can be called from scripts. For users who are familiar with statistics and willing to use experimental analysis tools. statistics, permutation, bootstrap, non parametric, combination, inference requires: MATLAB
is a plug in for: FSL
Brazilian National Research Council ;
GlaxoSmithKline ;
Marie Curie ITN ;
Medical Research Council ;
MRC G0900908;
NIBIB R01 EB015611;
Wellcome Trust
PMID:24530839
PMID:26074200
DOI:10.1002/hbm.23115
PMID:27288322
Free, Available for download, Freely available https://github.com/andersonwinkler/PALM SCR_017029 PALM, Permutation Analysis of Linear Models 2026-09-05 06:28:17 58
VasoTracker
 
Resource Report
Resource Website
1+ mentions
VasoTracker (RRID:SCR_017233) data acquisition software, data analysis software, data processing software, software application, software resource Open source and stand alone software for assessing vascular reactivity. Used in pressure myograph system. vascular, reactivity, pressure, myograph, system is related to: Durham University; Durham; England
has parent organization: University of Strathclyde; Glasgow; United Kingdom
British Heart Foundation ;
Wellcome Trust
PMID:30846942 Free, Available for download, Freely available https://github.com/VasoTracker/VasoTracker SCR_017233 2026-09-05 06:28:20 5
Physiome Model Repository
 
Resource Report
Resource Website
1+ mentions
Physiome Model Repository (RRID:SCR_017374) PMR data or information resource, data repository, dynamic model, model, service resource, storage service resource Repository of mainly CellML models powered by collection of software tools and libraries with PMR2 software suite as core power. Third party integration suites are RICORDO, Virtuoso, BiVeS/BudHat, OpenCOR, CombineArchive Web, WebCAT, Morre/MaSyMoS. Physiology, repository, CellML, cell, model, file, metadata, PMR2 is used by: SPARC Portal
is related to: CellML
is related to: International Union of Physiological Sciences: Physiome Project
Auckland Bioengineering Institute ;
British Heart Foundation ;
Maurice Wilkins Centre for Molecular Biodiscovery ;
Virtual Physiological Human Network of Excellence ;
Wellcome Trust
DOI:10.1093/bioinformatics/btq723 Free, Available for download, Freely available http://www.cellml.org/tools/pmr/, http://models.cellml.org/ SCR_017374 Physiome Repository, PMR2 2026-09-05 06:28:23 5

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  5. Collections

    If you are logged into NIF 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.