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
X
Forgot Password

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

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

  • Related Resources:gene ontology (facet)

Facets


Recent searches

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

255 Results - per page

Show More Columns | Download 255 Result(s)

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
Gemma
 
Resource Report
Resource Website
1000+ mentions
Gemma (RRID:SCR_008007) Gemma data or information resource, database Resource for reuse, sharing and meta-analysis of expression profiling data. Database and set of tools for meta analysis, reuse and sharing of genomics data. Targeted at analysis of gene expression profiles. Users can search, access and visualize coexpression and differential expression results. chip, microarray, functional genomics, gene expression, coexpression, differential expression, FASEB list is used by: NIF Data Federation
is used by: Integrated Data Annotation
is listed by: Debian
is listed by: SoftCite
is related to: Gene Ontology
is related to: Gene Expression Omnibus
is related to: Phenocarta
has parent organization: University of British Columbia; British Columbia; Canada
is parent organization of: Neurocarta
NIGMS GM076990;
Canadian Foundation for Innovation ;
Michael Smith Foundation for Health Research ;
Canadian Institutes for Health Research
PMID:22782548 Free, Freely available nif-0000-08127, r3d100012747 https://sources.debian.org/src/gemma/
https://doi.org/10.17616/R36R54
https://doi.org/10.17616/R36R54
SCR_008007 2026-02-14 02:06:41 1112
OncoboxPD
 
Resource Report
Resource Website
1+ mentions
OncoboxPD (RRID:SCR_023723) data or information resource, database Structured curated collection of protein based and of metabolic human molecular pathways. Human molecular pathways database with tools for activity calculating and visualization.All pathways are functionally classified according to GO terms enrichment patterns. All pathway participants, their interactions and reactions are uniformly processed and annotated, and are ready for numeric analysis of experimental expression data.For every comparison graph is generated summarizing top up and down regulated pathways. Gene Ontology terms enrichment patterns, human molecular pathways, curated collection, GO terms enrichment patterns, experimental expression data analysis, is related to: oncoboxlib
is related to: Gene Ontology
Russian Science Foundation ;
National Natural Science Foundation of China ;
Qingdao Key Research Project ;
Qingdao Key Health Discipline Development Fund
PMID:35615022 Free, Freely available SCR_023723 Oncobox Pathway Databank 2026-02-14 02:06:35 3
ECO
 
Resource Report
Resource Website
10+ mentions
ECO (RRID:SCR_002477) ECO data or information resource, ontology, controlled vocabulary A controlled vocabulary that describes types of scientific evidence within the realm of biological research that can arise from laboratory experiments, computational methods, manual literature curation, and other means. Researchers can use these types of evidence to support assertions about research subjects that result from scientific research, such as scientific conclusions, gene annotations, or other statements of fact. ECO comprises two high-level classes, evidence and assertion method, where evidence is defined as a type of information that is used to support an assertion, and assertion method is defined as a means by which a statement is made about an entity. Together evidence and assertion method can be combined to describe both the support for an assertion and whether that assertion was made by a human being or a computer. However, ECO can not be used to make the assertion itself; for that, one would use another ontology, free text description, or other means. ECO was originally created around the year 2000 to support gene product annotation by the Gene Ontology. Today ECO is used by many groups concerned with provenance in scientific research. ECO is used in AmiGO 2 evidence, assertion, assertion method, gene product, obo, evidence code, experiment, similarity, provenance is listed by: BioPortal
is related to: AmiGO
is related to: Gene Ontology
has parent organization: University of Maryland School of Medicine; Maryland; USA
has parent organization: Google Code
NIGMS GM089636 Free, Available for download, Freely available nlx_155860 http://code.google.com/p/evidenceontology/
http://bioportal.bioontology.org/ontologies/ECO
SCR_002477 Evidence Codes Ontology, Evidence Ontology, evidenceontology, The Evidence Ontology 2026-02-14 02:05:01 19
PhenoGO
 
Resource Report
Resource Website
1+ mentions
PhenoGO (RRID:SCR_013646) data or information resource, database PhenoGO is a computed database designed for high throughput mining that provides phenotypic and experimental context - such as the cell type, disease, tissue, and organ - to existing annotations between gene products and Gene Ontology (GO) terms, as specified in the Gene Ontology Annotations (GOA) for multiple model organisms. Phenotypic and Experimental (P&E) contexts to identifiers are computationally mapped to general biological ontologies, including: the Cell Ontology (CO), phenotypes from the Unified Medical Language System (UMLS), species from Taxonomy of the National Center for Biotechnology Information (NCBI) taxonomy, and specialized ontologies such as Mammalian Phenotype Ontology (MP) and Mouse Anatomy (MA). uses: WormBase
uses: SGD
uses: Gene Ontology
uses: Mouse Genome Informatics (MGI)
uses: FlyBase
is related to: WormBase
is related to: SGD
is related to: Gene Ontology
is related to: Mouse Genome Informatics (MGI)
is related to: FlyBase
has parent organization: University of Arizona; Arizona; USA
Available to the research community, Acknowledgement requested nlx_152722 www.phenogo.org SCR_013646 Phenotype Context Database for Gene Ontology Annotations 2026-02-14 02:06:20 2
dcGO
 
Resource Report
Resource Website
10+ mentions
dcGO (RRID:SCR_014392) data or information resource, database A database of domain-centric ontologies on functions, phenotypes, diseases and more. As a biomedical ontology resource, dcGO integrates functional, phenotypic, disease, and drug information. As a protein domain resource, it includes annotations to both the individual domains and supra-domains. Domain classifications and ontologies are organized in hierarchies, and dcGO includes the facility to browse the hierarchies: SCOP Hierarchy for browsing domains, GO Hierarchy for browsing GO terms, and BO Hierarchy for browsing other terms (mostly phenotypes). Users can mine and browse through resources. database, mining, domain centric ontology, phenotype, human disease, drug, biomedical ontology, protein domain, hierarchy uses: Gene Ontology
has parent organization: University of Bristol; Bristol; United Kingdom
PMID:23161684 Acknowledgement required, Both flat files and MySQL tables are available for download SCR_014392 2026-02-14 02:06:21 27
Semantic Measures Library
 
Resource Report
Resource Website
Semantic Measures Library (RRID:SCR_001383) SML software library, software toolkit, software resource Open source Java library dedicated to semantic measures computation and analysis. Tools based on the SML are also provided through the SML-Toolkit, a command line software giving access to some of the functionalities of the library. The SML and the toolkit can be used to compute semantic similarity and semantic relatedness between semantic elements (e.g. concepts, terms) or entities semantically characterized (e.g. entities defined in a semantic graph, documents annotated by concepts defined in an ontology). semantic measure, semantic similarity, semantic relatedness, functional similarity, gene ontology, annotation, parse, gene, disease ontology, mesh, rdf, owl, umls, snomed-ct, java, semantic, command line is listed by: FORCE11
is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Ecole des Mines d'Ales; Ales; France
Ecole des Mines d'Ales; Ales; France ;
LGI2P Research Center
PMID:24108186 Free, Available for download, Freely available nlx_152555 http://www.semantic-measures-library.org SCR_001383 SML-Toolkit, Semantic Measures Library and ToolKit, Semantic Measures Library & ToolKit 2026-02-15 09:18:05 0
MEME Suite - Motif-based sequence analysis tools
 
Resource Report
Resource Website
1000+ mentions
MEME Suite - Motif-based sequence analysis tools (RRID:SCR_001783) MEME Suite software application, source code, data analysis service, data processing software, software resource, database, service resource, production service resource, data or information resource, analysis service resource, data analysis software Suite of motif-based sequence analysis tools to discover motifs using MEME, DREME (DNA only) or GLAM2 on groups of related DNA or protein sequences; search sequence databases with motifs using MAST, FIMO, MCAST or GLAM2SCAN; compare a motif to all motifs in a database of motifs; associate motifs with Gene Ontology terms via their putative target genes, and analyze motif enrichment using SpaMo or CentriMo. Source code, binaries and a web server are freely available for noncommercial use. gene ontology, motif, comparative genomics, dna regulatory motif, dna sequence, dna, gene, transcription factor, genome, protein, analysis, function analysis, comparison, cluster, enrichment analysis, sequence analysis, bio.tools, FASEB list lists: DREME
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
is related to: Glam2
is related to: ANNOgesic
is related to: memesuite-lite
has parent organization: National Biomedical Computation Resource
is parent organization of: GOMO - Gene Ontology for Motifs
NCRR R01 RR021692 PMID:19458158
DOI:10.1093/nar/gkl198
Free, Freely available nif-0000-10298, biotools:meme_suite, OMICS_08103 https://bio.tools/meme_suite http://meme.sdsc.edu/meme4_6_1/intro.html, http://meme.nbcr.net/meme/, https://sources.debian.org/src/meme/ SCR_001783 The MEME Suite 2026-02-15 09:18:10 2091
AmiGO
 
Resource Report
Resource Website
1000+ mentions
AmiGO (RRID:SCR_002143) AmiGO data analysis service, database, service resource, production service resource, data or information resource, analysis service resource Web tool to search, sort, analyze, visualize and download data of interest. Along with providing details of the ontologies, gene products and annotations, features a BLAST search, Term Enrichment and GO Slimmer tools, the GO Online SQL Environment and a user help guide.Used at the Gene Ontology (GO) website to access the data provided by the GO Consortium. Developed and maintained by the GO Consortium. search, sort, analyze, visualize, data, ontology, gene, annotation, FASEB list uses: GOlr
is used by: NIF Data Federation
is listed by: OMICtools
is listed by: Gene Ontology Tools
is related to: ASAP
is related to: Candida Genome Database
is related to: Berkeley Bioinformatics Open-Source Projects
is related to: ECO
is related to: Zebrafish Information Network (ZFIN)
is related to: Gramene
is related to: WormBase
is related to: NCBI Protein Database
is related to: UniProtKB
is related to: GeneDB Lmajor
is related to: TAIR
is related to: SGD
is related to: GeneDB Tbrucei
is related to: VMD
is related to: JCVI CMR
is related to: go-db-perl
is related to: Mouse Genome Informatics (MGI)
is related to: NCBI
is related to: FlyBase
is related to: GeneDB Pfalciparum
is related to: PomBase
is related to: Pseudomonas Genome Database
is related to: Dictyostelium discoideum genome database
is related to: Plant Ontology
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: MeGO
is related to: ASPGD
is related to: EcoCyc
is related to: Reactome
is related to: SGN
is related to: GO-Module
is related to: Songbird Brain Transcriptome Database
is related to: Rat Genome Database (RGD)
is related to: RamiGO
has parent organization: Gene Ontology
NHGRI P41 HG002273 PMID:19033274 Free, Available for download, Freely available nif-0000-20935, OMICS_02266 http://sourceforge.net/projects/geneontology/ SCR_002143 GO Consortium, AmiGO, AmiGO 2, AmiGene Ontology, Gene Ontology Database, Gene Ontology Consortium, GO Database, The Gene Ontology Consortium 2026-02-15 09:18:14 1242
High-Throughput GoMiner
 
Resource Report
Resource Website
1+ mentions
High-Throughput GoMiner (RRID:SCR_000173) web application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. A web program that organizes lists of genes of interest (for example, under- and overexpressed genes from a microarray experiment) for biological interpretation in the context of the Gene Ontology and automates the analysis of multiple microarrays then integrates the results across all of them in exportable output files and visualizations. High-Throughput GoMiner is an enhancement of GoMiner and is implemented with both a command line interface and a web interface. The program can also: efficiently perform automated batch processing of an arbitrary number of microarrays; produce a human- or computer-readable report that rank-orders the multiple microarray results according to the number of significant GO categories; integrate the multiple microarray results by providing organized, global clustered image map visualizations of the relationships of significant GO categories; provide a fast form of false discovery rate multiple comparisons calculation; and provide annotations and visualizations for relating transcription factor binding sites to genes and GO categories. term enrichment, gene ontology, gene, microarray, common variable immune deficiency, high-throughput, visualization, database is listed by: Gene Ontology Tools
is related to: Gene Ontology
is related to: GoMiner
has parent organization: National Cancer Institute
has parent organization: National Cancer Institute
NCI 1Z01BC010842-01 PMID:15998470 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149300 SCR_000173 2026-02-15 09:17:53 2
GONUTS
 
Resource Report
Resource Website
1+ mentions
GONUTS (RRID:SCR_000653) GONUTS database, data or information resource, narrative resource, wiki A wiki where users of the Gene Ontology can contribute and view notes about how specific GO terms are used. GONUTS can also be used as a GO term browser, or to search for GO annotations of specific genes from included organisms. The rationale for this wiki is based on helping new users of the gene ontology understand and use it. The GONUTS wiki is not an official product of the the Gene Ontology consortium. The GO consortium has a public wiki at their website, http://wiki.geneontology.org/. Maintaining the ontology involves many decisions to carefully choose terms and relationships. These decisions are currently made at GO meetings and via online discussion using the GO mailing lists and the Sourceforge curator request tracker. However, it is difficult for someone starting to use GO to understand these decisions. Some insight can be obtained by mining the tracker, the listservs and the minutes of GO meetings, but this is difficult, as these discussions are often dispersed and sometimes don't contain the GO accessions in the relevant messages. Wikis provide a way to create collaboratively written documentation for each GO term to explain how it should be used, how to satisfy the true path requirement, and whether an annotation should be placed at a different level. In addition, the wiki pages provide a discussion space, where users can post questions and discuss possible changes to the ontology. GONUTS is currently set up so anyone can view or search, but only registered users can edit or add pages. Currently registered users can create new users, and we are working to add at least one registered user for each participating database (So far we have registered users at EcoliHub, EcoCyc, GOA, BeeBase, SGD, dictyBase, FlyBase, WormBase, TAIR, Rat Genome Database, ZFIN, MGI, UCL and AgBase... ontology or annotation browser, ontology or annotation search engine, ontology or annotation editor, protein is listed by: Gene Ontology Tools
is listed by: OMICtools
is related to: Gene Ontology
has parent organization: EcoliHub
NIGMS 1U24 GM077905-01;
NIGMS U24 GM088849
PMID:22110029 Free for academic use, The community can contribute to this resource OMICS_02268, nlx_30164 SCR_000653 Gene Ontology Normal Usage Tracking System, GONUTS wiki 2026-02-15 09:17:58 1
Aging Portal
 
Resource Report
Resource Website
Aging Portal (RRID:SCR_000496) Aging portal, database, catalog, data or information resource, topical portal Portal devoted to aging relevant scientific data and resources. late adult human, senescence uses: Aging Genes and Interventions Database
uses: anage
uses: Human Life-Table Database
uses: Gene Ontology
uses: Grants.gov
uses: Integrated Blogs
uses: Integrated Clinical Trials
uses: Integrated Videos
uses: Integrated Grants
uses: Lifespan Observations Database
uses: One Mind Biospecimen Bank Listing
uses: Gait in Parkinson's Disease
uses: SciCrunch Registry
has parent organization: SciCrunch
Aging NIA 1R03AG043018-01 Restricted nlx_158366 SCR_000496 2026-02-15 09:17:56 0
NCBI BioSystems Database
 
Resource Report
Resource Website
100+ mentions
NCBI BioSystems Database (RRID:SCR_004690) BioSystems data analysis service, database, service resource, storage service resource, production service resource, data repository, data or information resource, analysis service resource Database that provides access to biological systems and their component genes, proteins, and small molecules, as well as literature describing those biosystems and other related data throughout Entrez. A biosystem, or biological system, is a group of molecules that interact directly or indirectly, where the grouping is relevant to the characterization of living matter. BioSystem records list and categorize components, such as the genes, proteins, and small molecules involved in a biological system. The companion FLink tool, in turn, allows you to input a list of proteins, genes, or small molecules and retrieve a ranked list of biosystems. A number of databases provide diagrams showing the components and products of biological pathways along with corresponding annotations and links to literature. This database was developed as a complementary project to (1) serve as a centralized repository of data; (2) connect the biosystem records with associated literature, molecular, and chemical data throughout the Entrez system; and (3) facilitate computation on biosystems data. The NCBI BioSystems Database currently contains records from several source databases: KEGG, BioCyc (including its Tier 1 EcoCyc and MetaCyc databases, and its Tier 2 databases), Reactome, the National Cancer Institute's Pathway Interaction Database, WikiPathways, and Gene Ontology (GO). It includes several types of records such as pathways, structural complexes, and functional sets, and is desiged to accomodate other record types, such as diseases, as data become available. Through these collaborations, the BioSystems database facilitates access to, and provides the ability to compute on, a wide range of biosystems data. If you are interested in depositing data into the BioSystems database, please contact them. pathway, disease, gene, protein, small molecule, literature, computation, image, biomarker, drug, structural complex, functional set, biological system, molecule, gold standard, bio.tools is listed by: re3data.org
is listed by: Debian
is listed by: bio.tools
is related to: KEGG
is related to: NCBI Structure
is related to: BioCyc
is related to: EcoCyc
is related to: MetaCyc
is related to: Reactome
is related to: Pathway Interaction Database
is related to: WikiPathways
is related to: Gene Ontology
has parent organization: NCBI
NIH PMID:19854944 r3d100011033, biotools:biosystems, nlx_69646 https://bio.tools/biosystems
https://doi.org/10.17616/R31K80
SCR_004690 BioSystems Database, NCBI BioSystems 2026-02-15 09:18:47 118
QuickGO
 
Resource Report
Resource Website
500+ mentions
QuickGO (RRID:SCR_004608) QuickGO database, ontology, software resource, data access protocol, web service, data or information resource, controlled vocabulary A web-based browser for Gene Ontology terms and annotations, which is provided by the UniProtKB-GOA group at the EBI. It is able to offer a range of facilities including bulk downloads of GO annotation data which can be extensively filtered by a range of different parameters and GO slim set generation. The software for QuickGO is freely available under the Apache 2 license. QuickGO can supply GO term information and GO annotation data via REST web services. gene, ontology, annotation, browser, visualization, search engine, slimmer-type tool, ontology or annotation browser, ontology or annotation search engine, ontology or annotation visualization, database or data warehouse, windows, mac os x, linux, unix, gold standard, bio.tools is listed by: OMICtools
is listed by: Gene Ontology Tools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
is related to: STRAP
has parent organization: European Bioinformatics Institute
BBSRC BB/E023541/1 PMID:19744993
PMID:20157483
Apache License, v2, Free for academic use biotools:quickgo, nlx_60318, OMICS_02276 https://bio.tools/quickgo SCR_004608 Quick GO 2026-02-15 09:18:51 523
Open PHACTS
 
Resource Report
Resource Website
10+ mentions
Open PHACTS (RRID:SCR_005050) OPS organization portal, portal, database, software resource, consortium, data or information resource Project that developed an open access discovery platform, called Open Pharmacological Space (OPS), via a semantic web approach, integrating pharmacological data from a variety of information resources and tools and services to question this integrated data to support pharmacological research. The project is based upon the assimilation of data already stored as triples, in the form subject-predicate-object. The software and data are available for download and local installation, under an open source and open access model. Tools and services are provided to query and visualize this data, and a sustainability plan will be in place, continuing the operation of the Open PHACTS Discovery Platform after the project funding ends. Throughout the project, a series of recommendations will be developed in conjunction with the community, building on open standards, to ensure wide applicability of the approaches used for integration of data. drug, enzyme family, structure, receptor, target, ki, pathway, pharmacology, enzyme, small molecule, data mining, annotation, drug discovery, drug development, pharmacological profile, pharmacokinetic, admet data, biological target, chemical, linked data, rdf, nanopublication, platform, semantic technology, text mining, bioinformatics, cheminformatics, interoperability, chemistry, data provenance, compound, small molecule, semantic integration, drug discovery uses: CHEBI
uses: ChemSpider
uses: ConceptWiki
uses: DrugBank
uses: ENZYME
uses: UniProt
uses: Gene Ontology
uses: WikiPathways
is listed by: Consortia-pedia
is listed by: FORCE11
is related to: Nanopub.org
is related to: eTRIKS
is related to: Janssen Research and Development
is related to: Almirall
is related to: ESTEVE
is related to: Merck
is related to: Pfizer Animal Genetics
is related to: VU University; Amsterdam; Netherlands
is related to: European Bioinformatics Institute
is related to: Maastricht University; Maastricht; Netherlands
is related to: University of Bonn; Bonn; Germany
is related to: Royal Society of Chemistry
is related to: Spanish National Cancer Research Center
is related to: Netherlands Bioinformatics Centre
is related to: SIB Swiss Institute of Bioinformatics
is related to: Technical University of Denmark; Lyngby; Denmark
is related to: University of Santiago de Compostela; Santiago de Compostela; Spain
is related to: University of Vienna; Vienna; Austria
is related to: University of Hamburg; Hamburg; Germany
is related to: University of Manchester; Manchester; United Kingdom
is related to: BioSolveIT
is related to: ConnectedDiscovery
is related to: OpenLink Software
is related to: SciBite
is related to: Open PHACTS Foundation
has parent organization: University of Vienna; Vienna; Austria
Innovative Medicines Initiative grant 115191;
EFPIA ;
Open PHACTS Foundation
PMID:22683805 Open unspecified license, Registration required, Non-commercial r3d100011550, nlx_144033 https://www.force11.org/node/4684
http://www.imi.europa.eu/content/open-phacts
https://doi.org/10.17616/R3T63F
SCR_005050 Open PHACTS - Open Pharmacological Space, OpenPhacts.org, Open Pharmacological Space, Open Pharmacological Concepts Triple Store, OpenPHACTS, Open PHACTS: Open Pharmacological Space 2026-02-15 09:18:53 11
CoPub
 
Resource Report
Resource Website
1+ mentions
CoPub (RRID:SCR_005327) CoPub web service, data access protocol, service resource, software resource Text mining tool that detects co-occuring biomedical concepts in abstracts from the MedLine literature database. It allows batch input of multiple human, mouse or rat genes and produces lists of keywords from several biomedical thesauri that are significantly correlated with the set of input genes. These lists link to Medline abstracts in which the co-occurring input genes and correlated keywords are highlighted. Furthermore, CoPub can graphically visualize differentially expressed genes and over-represented keywords in a network, providing detailed insight in the relationships between genes and keywords, and revealing the most influential genes as highly connected hubs. microarray, gene, literature, enrich, annotate, network, database, differential expression, bio.tools uses: MEDLINE
uses: Gene Ontology
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Netherlands Bioinformatics Centre
Netherlands Bioinformatics Centre PMID:18442992 Free, Public, Acknowledgement requested OMICS_01178, biotools:copub https://bio.tools/copub http://services.nbic.nl/cgi-bin/copub/CoPub.pl SCR_005327 2026-02-15 09:18:56 5
GARBAN
 
Resource Report
Resource Website
GARBAN (RRID:SCR_005778) GARBAN source code, data analysis service, software resource, service resource, production service resource, analysis service resource THIS RESOURCE IS NO LONGER IN SERVICE, documented on July 12, 2012. GARBAN is a tool for analysis and rapid functional annotation of data arising from cDNA microarrays and proteomics techniques. GARBAN has been implemented with bioinformatic tools to rapidly compare, classify, and graphically represent multiple sets of data (genes/ESTs, or proteins), with the specific aim of facilitating the identification of molecular markers in pathological and pharmacological studies. GARBAN has links to the major genomic and proteomic databases (Ensembl, GeneBank, UniProt Knowledgebase, InterPro, etc.), and follows the criteria of the Gene Ontology Consortium (GO) for ontological classifications. Source may be shared: e-mail garban (at) ceit.es. Platform: Online tool cdna microarray, proteomics, cdna, microarray, statistical analysis, gene, est, protein, genomic, gene ontology is listed by: Gene Ontology Tools
is related to: Gene Ontology
PMID:14594726 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149247 http://garban.tecnun.es SCR_005778 Genomic Analysis and Rapid Biological ANnotation, University of Navarra; Pamplona; Spain 2026-02-15 09:19:11 0
FunCluster
 
Resource Report
Resource Website
1+ mentions
FunCluster (RRID:SCR_005774) FunCluster software application, data processing software, data analysis software, software resource FunCluster is a genomic data analysis algorithm which performs functional analysis of gene expression data obtained from cDNA microarray experiments. Besides automated functional annotation of gene expression data, FunCluster functional analysis aims to detect co-regulated biological processes through a specially designed clustering procedure involving biological annotations and gene expression data. FunCluster''''s functional analysis relies on Gene Ontology and KEGG annotations and is currently available for three organisms: Homo Sapiens, Mus Musculus and Saccharomyces Cerevisiae. FunCluster is provided as a standalone R package, which can be run on any operating system for which an R environment implementation is available (Windows, Mac OS, various flavors of Linux and Unix). Download it from the FunCluster website, or from the worldwide mirrors of CRAN. FunCluster is provided freely under the GNU General Public License 2.0. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible genomic, gene, functional analysis, gene expression, cdna microarray, cdna, microarray, function, cluster, annotation, biological process, statistical analysis, bio.tools is listed by: Gene Ontology Tools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
has parent organization: Cordelier Research Center
PMID:17007070
PMID:16506959
PMID:16046292
Free for academic use, GNU General Public License, v2 nlx_149242, biotools:funcluster https://bio.tools/funcluster SCR_005774 FunCluster R Package, FunCluster Algorithm 2026-02-15 09:19:03 2
GREAT: Genomic Regions Enrichment of Annotations Tool
 
Resource Report
Resource Website
50+ mentions
GREAT: Genomic Regions Enrichment of Annotations Tool (RRID:SCR_005807) GREAT source code, data analysis service, software resource, service resource, production service resource, analysis service resource Data analysis service that predicts functions of cis-regulatory regions identified by localized measurements of DNA binding events across an entire genome. Whereas previous methods took into account only binding proximal to genes, GREAT is able to properly incorporate distal binding sites and control for false positives using a binomial test over the input genomic regions. GREAT incorporates annotations from 20 ontologies and is available as a web application. The utility of GREAT extends to data generated for transcription-associated factors, open chromatin, localized epigenomic markers and similar functional data sets, and comparative genomics sets. Platform: Online tool term enrichment, cis-regulatory region, function, gene, genomic, annotation, ontology, chromatin immunoprecipitation, sequencing, chip-seq, comparative genomics, transcription factor binding is listed by: Gene Ontology Tools
is listed by: OMICtools
is related to: PRISM (Stanford database)
is related to: Gene Ontology
has parent organization: Stanford University School of Medicine; California; USA
Bio-X ;
Howard Hughes Medical Institute ;
Stanford University; California; USA ;
Packard ;
Searle Scholar ;
Microsoft Research ;
Alfred P. Sloan Foundation ;
Edward Mallinckrodt Jr. Foundation ;
NIH ;
Human Frontier Science Program fellowship LT000896/2009-l;
NICHD 1R01HD059862;
NHGRI R01HG005058;
NSF CCF-0939370;
DFG Hi 1423/2-1
PMID:20436461
PMID:23814184
Free for academic use, Acknowledgement requested nlx_149295, OMICS_00635 SCR_005807 Genomic Regions Enrichment of Annotations Tool (GREAT), Genomic Regions Enrichment of Annotations Tool 2026-02-15 09:19:03 82
GOHyperGAll
 
Resource Report
Resource Website
1+ mentions
GOHyperGAll (RRID:SCR_005766) GOHyperGAll software application, data processing software, data analysis software, software resource To test a sample population of genes for overrepresentation of GO terms, the R/BioC function GOHyperGAll computes for all GO nodes a hypergeometric distribution test and returns the corresponding p-values. A subsequent filter function performs a GO Slim analysis using default or custom GO Slim categories. Basic knowledge about R and BioConductor is required for using this tool. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible, THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, gene ontology, annotation, statistical analysis, slimmer-type tool is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of California at Riverside; California; USA
PMID:18354039 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149267 SCR_005766 2026-02-15 09:19:11 4
FastSemSim
 
Resource Report
Resource Website
1+ mentions
FastSemSim (RRID:SCR_006919) FastSemSim software library, software toolkit, software resource A package that implements several semantic similarity measures. It is both a library and an end-user application, featuring an intuitive graphical user interface (GUI). It has been implemented with the aim of being fast, expandable, and easy to use. It allows the user to work with the most updated version of GO database and customizable annotation corpora. It provides a set of logically-organized classes that can be easily exploited to both integrate semantic similarity into different analysis pipelines and extend the library with new measures. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible software library, functional similarity, semantic similarity, graphical user interface, gene ontology, annotation, parse, gene, protein is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of Padua; Padua; Italy
has parent organization: SourceForge
Open unspecified license - Free for academic use. GNU GPL license. However, This software is currently unpublished work. You must contact us before using it or its results or any work/app. based on top of it in any published work. nlx_149309 SCR_006919 2026-02-15 09:19:24 6

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. NIDM Terminology Resources

    Welcome to the nidm-terms Resources search. From here you can search through a compilation of resources used by nidm-terms 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 nidm-terms 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 nidm-terms then you can log in from here to get additional features in nidm-terms 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 nidm-terms 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.