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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
Sybil
 
Resource Report
Resource Website
10+ mentions
Sybil (RRID:SCR_005593) Sybil data or information resource, database, software resource A web-based software package for comparative genomics. comparative genomics, genome, synteny, protein cluster, protein, gene, genomic region, synteny gradient, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:22121156 OMICS_00945, biotools:sybil https://bio.tools/sybil SCR_005593 Sybil: Web-based software for comparative genomics 2026-08-15 11:23:09 37
LookSeq
 
Resource Report
Resource Website
1+ mentions
LookSeq (RRID:SCR_005625) LookSeq software resource A web-based application for alignment visualization, browsing and analysis of genome sequence data. alignment, visualization, browsing, analysis, genome, sequence is listed by: OMICtools
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
OMICS_00886 SCR_005625 2026-08-15 11:23:10 5
NIMH Image Library
 
Resource Report
Resource Website
1+ mentions
NIMH Image Library (RRID:SCR_005588) NIMH Image Library image collection, data or information resource Database of photographs and illustrations of general biomedical research and research tools, mental health specific research, and treatment related images that are available, copyright free, to the public at no cost. Many images are available in low, medium, and high resolutions. Formats include jpg, gif, and png. NIMH images may not be used to state or imply the endorsement by NIMH or by an NIMH employee of a commercial product, service, or activity, or use in any other manner that might mislead. No fee is charged for using the images. However, credit must be given to the National Institute of Mental Health, National Institutes of Health, Department of Health and Human Services unless otherwise instructed to give credit to the photographer or other source., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. database, biomedical, mental health, treatment, brain, research, imaging, genetics, research lab, tool, therapy, medical care has parent organization: National Institute of Mental Health NIMH THIS RESOURCE IS NO LONGER IN SERVICE nlx_146221 SCR_005588 National Institute of Mental Health Image Library 2026-08-15 11:23:16 4
tranSMART
 
Resource Report
Resource Website
10+ mentions
tranSMART (RRID:SCR_005586) tranSMART software resource tranSMART is a knowledge management platform that enables scientists to develop and refine research hypotheses by investigating correlations between genetic and phenotypic data, and assessing their analytical results in the context of published literature and other work. tranSMART is licensed through GPL 3. The integration, normalization, and alignment of data in tranSMART permits users to explore data very efficiently to formulate new research strategies. Some of tranSMART''s specific applications include: * Revalidating previous hypotheses * Testing and refining novel hypotheses * Conducting cross-study meta-analysis * Searching across multiple data sources to find associations of concepts, such as a gene''s involvement in biological processes or experimental results * Comparing biological processes and pathways among multiple data sets from related diseases or even across multiple therapeutic areas Data Repository The tranSMART Data Repository combines a data warehouse with access to federated sources of open and commercial databases. tranSMART accommodates: * Phenotypic data, such as demographics, clinical observations, clinical trial outcomes, and adverse events * High content biomarker data, such as gene expression, genotyping, pharmacokinetic and pharmaco-dynamics markers, metabolomics data, and proteomics data * Unstructured text-data, such as published journal articles, conference abstracts and proceedings, and internal studies and white papers * Reference data from sources such as MeSH, UMLS, Entrez, GeneGo, Ingenuity, etc. * Metadata providing context about datasets, allowing users to assess the relevance of results delivered by tranSMART Data in tranSMART is aligned to allow identification and analysis of associations between phenotypic and biomarker data, and it is normalized to conform with CDISC and other standards to facilitate search and analysis across different data sources. tranSMART also enables investigators to search published literature and other text sources to evaluate their analysis in the context of the broader universe of reported research. External data can also be integrated into the tranSMART data repository, either from open data projects like GEO, EBI Array Express, GCOD, or GO, or from commercially available data sources. Making data accessible in tranSMART enables organizations to leverage investments in manual curation, development costs of automated ETL tools, or commercial subscription fees across multiple research groups. Dataset Explorer tranSMART''s Dataset Explorer provides flexible, powerful search and analysis capabilities. The core of the Dataset Explorer integrates and extends the open source i2b2 application, Lucene text indexing, and GenePattern analytical tools. Connections to other open source and commercial analytical tools such as Galaxy, Integrative Genomics Viewer, Plink, Pathway Studio, GeneGo, Spotfire, R, and SAS can be established to expand tranSMART''s capabilities. tranSMART''s design allows organizations flexibility in selecting analytical tools accessible through the Dataset Explorer, and provides file export capabilities to enable researchers to use tools not accessible in the tranSMART portal. source code, genetic, phenotype, gene, data storage repository, data analysis service is used by: eTRIKS
is used by: RanchoBiosciences
nlx_146211 http://www.transmartproject.org/ SCR_005586 2026-08-15 11:23:09 13
Childrens Hospital Oakland Research Institute
 
Resource Report
Resource Website
10+ mentions
Childrens Hospital Oakland Research Institute (RRID:SCR_005582) CHORI organization portal, data or information resource, training resource, portal CHORI is the internationally renowned biomedical research institute of Children''s Hospital and Research Center at Oakland. With world-class scientists and research centers known both nationally and internationally in multiple fields, CHORI is 5th in the nation for National Institutes of Health pediatric research funding. Bridging basic science and clinical research in the treatment and prevention of human disease, CHORI is a leader in translational research, providing cures for blood diseases, developing new vaccines for infectious diseases, and discovering new treatment protocols for previously fatal or debilitating conditions. Striving to provide the highest standard of excellence and innovation, CHORI brings together a multidisciplinary collaborative of distinguished investigators in six different Centers of Research: The Center for Cancer Research, The Center for Genetics, The Center for Immunobiology & Vaccine Development, The Center for Nutrition & Metabolism, The Center for Prevention of Obesity, Cardiovascular Disease & Diabetes, and The Center for Sickle Cell Disease & Thalassemia. Within these major areas of focus, CHORI pushes the frontiers of science and of excellence beyond their borders. Among the leading biotech enterprises in the Bay Area, CHORI produced 25 patents in the last 5 years alone. In addition to providing world-class research, CHORI is also a teaching institute, offering unique educational opportunities to high school, college, doctoral and post-doctoral students. pediatric, research, young human, cancer, genetics, immunobiology, vaccine, nutrition, metabolism, obesity, cardiovascular disease, diabetes, sickle cell disease, thalassemia is parent organization of: BacPac Resources Center
is parent organization of: Knockout Mouse Project Repository
NIH nlx_146206 SCR_005582 Children''s Hospital Oakland Research Institute, Children''s Hospital Oakland Research Institute (CHORI) 2026-08-15 11:23:16 13
OLego
 
Resource Report
Resource Website
10+ mentions
OLego (RRID:SCR_005811) OLego software resource A program specifically designed for de novo spliced mapping of mRNA-seq reads. It adopts a multiple-seed-and-extend scheme, and does not rely on a separate external mapper. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Columbia University; New York; USA
biotools:olego, OMICS_01244 https://bio.tools/olego SCR_005811 2026-08-15 11:23:18 15
XuvTools
 
Resource Report
Resource Website
10+ mentions
XuvTools (RRID:SCR_005894) XuvTools data processing software, software application, image processing software, software resource XuvTools (pronounced ex-you-vee-tools) is a fully automated 3D stitching software for biomedical image data, typically confocal microscopy images. XuvTools runs on Microsoft Windows XP and Vista, Linux and Apple Mac computers. It supports 32 and 64bit operating systems (with 64bit highly preferred). The goal of XuvTools is to provide tools, that combine multiple microscopic recordings to obtain a larger field of view (stitching) and a higher dynamic range (HDR recombination), or better resolution (multi view reconstruction), and to make these tools publicly available. What XuvTools can do: * Full 3D Stitching * Scaling, if the voxel sizes are known from image data * Fully automatic stitching modes * Manual pre-alignment modes * Arbitrary large datasets * Reads stage coordinates if available * free, no hidden costs * Reads many many input formats via LOCI Bio-Formats and Dmitry Fedorov''s BioImage. Limitations of XuvTools: (current limitations, we are working on it!) * No 2D Stitching: stacks need 4 Z-slices or more * No memory management: You need lots of RAM * No rotational alignment * The only supported output formats are: Imaris, HDF5 (No TIFF output support) 3d microscopy, image stitching, bleaching, correlation, large scale microscopy, mosaic, virtual microscopy, 3d, confocal microscopy, microscopy has parent organization: Friedrich Miescher Institute
has parent organization: University of Freiburg; Baden-Wurttemberg; Germany
Landesforschungsschwerpunktprogramm des Landes Baden-W??rttemberg ;
German Federal and State Governments ;
DFG
PMID:19196411 Free and Open unspecified license software, GNU GENERAL PUBLIC LICENSE nlx_149464 SCR_005894 www.XuvTools.org, XuvTools - the eXtend yoUr View Toolkit 2026-08-15 11:23:18 22
Ontologizer
 
Resource Report
Resource Website
100+ mentions
Ontologizer (RRID:SCR_005801) Ontologizer production service resource, data processing software, data analysis service, software application, software resource, source code, service resource, analysis service resource The Ontologizer is a Java webstart application for GO term enrichment analysis that provides browsing and graph visualization capabilities. The Ontologizer allows users to analyze data with the standard Fisher exact test and also the parent-child method and topology methods. The tool can be started directly from the web using Java webstart. For graph visualizations, users need to install the GraphViz library. The tool is freely available to all, and source code is available at SourceForge. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible high-throughput, biological data, gene ontology, statistical analysis, fisher exact test, visualization, graph, java, annotation, parent-child, topology is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Charite - Universitatsmedizin Berlin; Berlin; Germany
DFG SFB 760 PMID:18511468
PMID:17848398
Free for academic use nlx_149289 SCR_005801 The Ontologizer 2026-08-15 11:23:14 124
Zebrafish Anatomical Ontology
 
Resource Report
Resource Website
1+ mentions
Zebrafish Anatomical Ontology (RRID:SCR_005887) ZFA ontology, data or information resource, controlled vocabulary A structured controlled vocabulary of the anatomy and development of the Zebrafish (Danio rerio). It includes a list of structures, organized hierarchically into an ontology, with descriptions of each structure. The current version is being written by a consortium of researchers, each serving as an expert for a particular set of anatomical structures. Additional anatomical information derived from the current literature is provided by the ZFIN curation group. Development of a complete and uniform anatomical ontology for the zebrafish is vital to the success of zebrafish science. The anatomical ontology is necessary for: * Effective data dissemination and informatics. * A reference framework. * Interoperability. anatomy, structure, anatomical structure, obo is used by: Teleost Anatomy Ontology
is recommended by: Zebrafish Brain Atlas
is listed by: BioPortal
is related to: OBO
is related to: Bgee: dataBase for Gene Expression Evolution
has parent organization: Zebrafish Information Network (ZFIN)
nlx_149454 SCR_005887 Zebrafish Anatomy and Development Ontology, ZFIN - Zebrafish Anatomical Ontology 2026-08-15 11:23:18 4
University of Nevada at Reno; Nevada; USA
 
Resource Report
Resource Website
1+ mentions
University of Nevada at Reno; Nevada; USA (RRID:SCR_005882) university Public land-grant research university in Reno, Nevada. is parent organization of: University of Nevada Reno Labs and Facilities
is parent organization of: Nevada Proteomics Center
is parent organization of: NeoCortical Simulator
is parent organization of: GazeMetrics
is parent organization of: Nevada University at Reno Nevada Bioinformatics Center Core Facility
is parent organization of: University of Nevada Reno School of Medicine High Spatial and Temporal Resolution Imaging Core Facility
is parent organization of: University of Nevada at Reno Nevada Proteomics Center Core Facility
is parent organization of: University of Nevada at Reno Nevada Genomics Center Core Facility
is parent organization of: University of Nevada Reno Transgenic Animal Genotyping and Phenotyping Core Facility
Wikidata:Q1185955, grid.266818.3, nlx_153964, ISNI:0000 0004 1936 914X https://ror.org/01keh0577 SCR_005882 University of Nevada at Reno, University of Nevada Reno 2026-08-15 11:23:18 1
PeptideMapper
 
Resource Report
Resource Website
1+ mentions
PeptideMapper (RRID:SCR_005763) PeptideMapper data access protocol, software resource, web service The PeptideMapper Web-Service provides alignments of peptide sequence alignments to proteins, mRNA, EST, and HTC sequences from Genbank, RefSeq, UniProt, IPI, VEGA, EMBL, and HInvDb. This mapping infrastructure is supported, in part, by the compressed peptide sequence database infrastructure (Edwards, 2007) which enables a fast, suffix-tree based mapping of peptide sequences to gene identifiers and a gene-focused detailed mapping of peptide sequences to source sequence evidence. The PeptideMapper Web-Service can be used interactively or as a web-service using either HTTP or SOAP requests. Results of HTTP requests can be returned in a variety of formats, including XML, JSON, CSV, TSV, or XLS, and in some cases, GFF or BED; results of SOAP requests are returned as SOAP responses. The PeptideMapper Web-Service maps at most 20 peptides with length between 5 and 30 amino-acids in each request. The number of alignments returned, per peptide, gene, and sequence type, is set to 10 by default. The default can be changed on the interactive alignments search form or by using the max web-service parameter. peptide, sequence, protein, alignment, expressed sequence tag, mrna, est, htc, genbank, refseq, uniprot, ipi, vega, embl, hinvdb has parent organization: Edwards Lab NCI CA126189 PMID:17437027 nlx_149229 SCR_005763 PeptideMapper Web-Service, Peptide Mapper 2026-08-15 11:23:17 4
The Mouse: Genetics meets Behavior
 
Resource Report
Resource Website
1+ mentions
The Mouse: Genetics meets Behavior (RRID:SCR_005884) data or information resource, portal, topical portal This file describes a selection of the behavioral paradigms that have been useful in behaviorally phenotyping mouse mutants. anxiety, behavior, behavioral, impulse, learning, memory, mouse, mutant, neurobehavioral, phenotype nif-0000-10370, nlx_66823 SCR_005884 2026-08-15 11:23:15 2
NESCent - National Evolutionary Synthesis Center
 
Resource Report
Resource Website
1+ mentions
NESCent - National Evolutionary Synthesis Center (RRID:SCR_005911) NESCent institution The National Evolutionary Synthesis Center (NESCent) is a nonprofit science center dedicated to cross-disciplinary research in evolution. NESCent promotes the synthesis of information, concepts and knowledge to address significant, emerging, or novel questions in evolutionary science and its applications. NESCent achieves this by supporting research and education across disciplinary, institutional, geographic, and demographic boundaries. Synthetic research in evolutionary science takes many forms but includes integrating novel data sets and models to address important problems within a discipline, developing new analytical approaches and tools, and combining methods and perspectives from multiple disciplines to answer and even create new fundamental scientific questions. NESCent facilitates such synthetic research by providing an environment for fertile interactions among scientists. Our Science and Synthesis program sponsors postdoctoral fellows and sabbatical scholars as resident scientists, and two kinds of meetings, working groups and catalysis meetings. Catalysis meetings provide a novel mechanism for bringing together diverse research communities and cultures to identify common interests, while working groups provide an opportunity for scientists to work together intensively on fundamental synthetic questions over a several-year period. These activities are community driven through our application process and evaluated by an external advisory board. Our Informatics program provides state of the art informatics tools to visiting and in-house scientists and aims to take the lead in assembling novel databases and developing new analytical tools for evolutionary biology. Finally it is sponsoring a major initiative to provide a digital data repository for work in evolutionary biology. NESCent''s Education and Outreach group communicates the results of evolutionary biology research to the general public and scientific community, provides outreach to groups who are underrepresented in evolutionary biology and works to improve evolution education. evolution, evolutionary biology has parent organization: Duke University; North Carolina; USA
has parent organization: University of North Carolina at Chapel Hill; North Carolina; USA
has parent organization: North Carolina State University; North Carolina; USA
is parent organization of: FEED
is parent organization of: Phenoscape Knowledgebase
is parent organization of: TreeBASE
is parent organization of: Dryad Digital Repository
NSF EF-0905606 Wikidata: Q6972505, ISNI: 0000 0000 9027 3547, nlx_149487, grid.419343.8, Crossref funder ID: 100007514 https://ror.org/001ykb961 SCR_005911 National Evolutionary Synthesis Center 2026-08-15 11:23:19 7
TOPSAN
 
Resource Report
Resource Website
10+ mentions
TOPSAN (RRID:SCR_005758) TOPSAN database, data repository, storage service resource, data or information resource, image collection, service resource Collect, share, and distribute information about protein three-dimensional structures. It serves as a portal for the scientific community to learn about protein structures solved by SG centers, and also to contribute their expertise in annotating protein function. The premise of the TOPSAN project is that, no matter how much any individual knows about a particular protein, there are other members of the scientific community who know more about certain aspects of the same protein, and that the collective analyses from experts will be far more informative than any local group, let alone individual, could contribute. They believe that, if the members of the biological community are given the opportunity, authorship incentives, and an easy way to contribute their knowledge to the structure annotation, they would do so. Therefore, borrowing elements from successful, distributed, collaborative projects, such as Wikipedia (the free encyclopedia anyone can edit) and from other open source software development projects, TOPSAN will be a broad, collaborative effort to annotate protein structures, initially, those determined at the JCSG. They believe that the annotation of proteins solved by structural genomics consortia offers a unique opportunity to challenge the extant paradigm of how biological data is collected and distributed, and to connect structural genomics and structural biology to the entire biological research community. TOPSAN is designed to be scalable, modular and extensible. Furthermore, it is intended to be immediately useful in a simplistic way and will accommodate incremental improvements to functionality as usage becomes more sophisticated. Their annotation pages will offer the end user a combination of automatically generated as well as expert-curated annotations of protein structures. They will use available technology to increase the speed and granularity of the exchange of scientific ideas, and use incentive mechanisms that will encourage collaborative participation. protein, structure, 3d, protein structure, protein function, annotate, crowd sourcing, image, annotation, genomics, collaboration has parent organization: Sanford Burnham Prebys Medical Discovery Institute
has parent organization: University of California at San Diego; California; USA
NIGMS U54 GM074898;
NIGMS P20 GM076221
PMID:20961957
PMID:20716366
PMID:20944203
PMID:20961957
Creative Commons Attribution v3 License, The community can contribute to this resource nlx_149221 SCR_005758 he Open Protein Structure Annotation Network, TOPSAN Project, TOPSAN - The Open Protein Structure Annotation Network 2026-08-15 11:23:17 10
PePr
 
Resource Report
Resource Website
50+ mentions
PePr (RRID:SCR_005759) PePr software resource A ChIP-Seq peak calling or differential binding analysis tool that is primarily designed for data with biological replicates. It uses a negative binomial distribution to model the read counts among the samples in the same group, and look for consistent differences between ChIP and control group or two ChIP groups run under different conditions. python, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Google Code
PMID:24894502 GNU General Public License, v3 OMICS_04058, biotools:pepr https://bio.tools/pepr SCR_005759 pepr-chip-seq, Peak Prioritization Pipeline, pepr-chip-seq: A ChIP-Seq analyzing program for biological replicates 2026-08-15 11:23:13 55
dna-bison
 
Resource Report
Resource Website
1+ mentions
dna-bison (RRID:SCR_005913) dna-bison software resource Allows users with access to a computer cluster to rapidly align whole-genome bisulfite sequencing or RRBS reads. is listed by: OMICtools
has parent organization: SourceForge
OMICS_00582 SCR_005913 2026-08-15 11:23:15 1
PubSearch
 
Resource Report
Resource Website
1+ mentions
PubSearch (RRID:SCR_005830) PubSearch data or information resource, service resource, database, software resource THIS RESOURCE IS NO LONGER IN SERVCE, documented September 2, 2016. PubSearch is a web-based literature curation tool, allowing curators to search and annotate genes to keywords from articles. It has a simple mySQL database backend and uses a set of Java Servlets and JSPs for querying, modifying, and adding gene, gene-annotation, and literature information. PubSearch can be downloaded from GMOD. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene, annotate, editor, literature curation tool, literature, ontology or annotation editor is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: TAIR
has parent organization: Stanford University; Stanford; California
NHGRI R01HG02728 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149338 SCR_005830 2026-08-15 11:23:18 1
MAPPFinder
 
Resource Report
Resource Website
10+ mentions
MAPPFinder (RRID:SCR_005791) MAPPFinder data processing software, software application, data analysis software, software resource MAPPFinder is an accessory program for GenMAPP. This program allows users to query any existing GenMAPP Expression Dataset Criterion against GO gene associations and GenMAPP MAPPs (microarray pathway profiles). The resulting analysis provides the user with results that can be viewed directly upon the Gene Ontology hierarchy and within GenMAPP, by selecting terms or MAPPs of interest. Platform: Windows compatible gene, gene ontology, gene association, gene expression, profile, microarray, pathway, statistical analysis is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of California at San Francisco; California; USA
has parent organization: Gene Map Annotator and Pathway Profiler
University of California at San Francisco; California; USA ;
San Francisco General Hospital; California; USA ;
NHLBI ;
NCRR MO1RR00083
PMID:12540299 Free for academic use nlx_149270 SCR_005791 2026-08-15 11:23:14 26
GOArray
 
Resource Report
Resource Website
1+ mentions
GOArray (RRID:SCR_005785) GOArray data processing software, software application, data analysis software, software resource GOArray is a Perl program which inputs a lists of genes annotated as of interest (GOI) or not, and determines if any associated GO terms have an overrepresentation of GOI. A permutation test is optionally used to assess confidence in the results. Output includes multiple visualizations and supplementary information and, for future reference, a summary of the statistical methods used. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible perl, gene, visualization, gene ontology, statistical analysis is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Yale School of Medicine; Connecticut; USA
Free for academic use nlx_149259 http://goarray.med.yale.edu/GOArray/ SCR_005785 2026-08-15 11:23:18 1
American Liver Foundation
 
Resource Report
Resource Website
1+ mentions
American Liver Foundation (RRID:SCR_005855) ALF institution The mission of the American Liver Foundation (ALF) is to facilitate, advocate and promote education, support and research for the prevention, treatment and cure of liver disease. These values guide our work as volunteers and staff of the American Liver Foundation as we move toward our ultimate goal of a world without liver disease. By living these values every day, we offer hope to all those affected by liver disease. * Research: Research is integral to the work of American Liver Foundation and is essential to improving treatment and finding cures. * Education: Many forms of liver disease are preventable, and many more can be cured if detected early. Yet tens of thousands of people in the U.S. are living with liver disease and don''t even know it. * Advocacy: American Liver Foundation takes a leadership role in advocating on behalf of the millions of Americans living with liver disease and their families. liver, hepatitis has parent organization: AASLD - American Association for the Study of Liver Diseases Liver disease nlx_149392, Crossref funder ID: 100001424, ISNI: 0000 0001 0140 6051, grid.453776.4 https://ror.org/02dfyb978 SCR_005855 2026-08-15 11:23:18 6

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