Searching the RRID Resource Information Network

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

  • Register
X
Forgot Password

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

X

Leaving Community

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

No
Yes

Preparing word cloud

×

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

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Related Resources:gene ontology (facet)

Facets


Recent searches

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

256 Results - per page

Show More Columns | Download 256 Result(s)

Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
Pandora - Protein ANnotation Diagram ORiented Analysis
 
Resource Report
Resource Website
1+ mentions
Pandora - Protein ANnotation Diagram ORiented Analysis (RRID:SCR_005686) Pandora analysis service resource, data analysis service, data or information resource, database, production service resource, service resource With PANDORA, you can search for any non-uniform sets of proteins and detect subsets of proteins that share unique biological properties and the intersections of such sets. PANDORA supports GO annotations as well as additional keywords (from UniProt Knowledgebase, InterPro, ENZYME, SCOP etc). It is also integrated into the ProtoNet system, thus allowing testing of thousands of automatically generated protein families. Note that PANDORA replaces the ProtoGO browser developed by the same group. Platform: Online tool protein, annotation, mass spectrometry, ontology or annotation browser is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Hebrew University of Jerusalem; Jerusalem; Israel
Israeli Ministry of Defense ;
Hebrew University of Jerusalem; Jerusalem; Israel
PMID:14500825 Free for academic use nlx_149131 SCR_005686 Protein ANnotation Diagram ORiented Analysis 2026-09-05 06:25:40 2
GOfetcher
 
Resource Report
Resource Website
GOfetcher (RRID:SCR_005681) GOfetcher analysis service resource, data analysis service, data or information resource, database, production service resource, service resource THIS RESOURCE IS NO LONGER IN SERVICE, documented on June 29, 2012. We developed a web application, GOfetcher, with a very comprehensive search facility for the GO project and a variety of output formats for the results. GOfetcher has three different levels for searching the GO: Quick Search, Advanced Search, and Upload Files for searching. The application includes a unique search option which generates gene information given a nucleotide or protein accession number which can then be used in generating gene ontology information. The output data in GOfetcher can be saved into several different formats; including spreadsheet, comma-separated values, and the Extensible Markup Language (XML) format. Platform: Online tool gene, nucleotide, protein, ontology, ontology or annotation browser is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of Southern Mississippi; Mississippi; USA
NSF EPS-0556308;
U.S. Army ;
Environmental Quality Program contract #W912HZ-05-P-0145
PMID:18728045 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149124 http://mcbc.usm.edu/gofetcher/ SCR_005681 GOfetcher: a database with complex searching facility for gene ontology 2026-09-05 06:25:39 0
GoFish
 
Resource Report
Resource Website
1+ mentions
GoFish (RRID:SCR_005682) GoFish analysis service resource, data analysis service, production service resource, service resource, software resource, source code Software program, available as a Java applet online or to download, allows the user to select a subset of Gene Ontology (GO) attributes, and ranks genes according to the probability of having all those attributes., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, ontology or annotation browser, java, windows, mac os x, linux, unix, bio.tools is listed by: Gene Ontology Tools
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
has parent organization: University of Toronto; Ontario; Canada
has parent organization: Harvard Medical School; Massachusetts; USA
Aventis Pharmaceuticals ;
Howard Hughes Medical Institute ;
NHGRI
PMID:12691998 THIS RESOURCE IS NO LONGER IN SERVICE biotools:gofish, nlx_149126, OMICS_02272 http://llama.mshri.on.ca/Software.html, https://bio.tools/gofish SCR_005682 2026-09-05 06:25:40 1
GARBAN
 
Resource Report
Resource Website
GARBAN (RRID:SCR_005778) GARBAN analysis service resource, data analysis service, production service resource, service resource, software resource, source code 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 2026-09-05 06:25:41 0
FunCluster
 
Resource Report
Resource Website
1+ mentions
FunCluster (RRID:SCR_005774) FunCluster data analysis software, data processing software, software application, 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 2026-09-05 06:25:41 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 analysis service resource, data analysis service, production service resource, service resource, software resource, source code 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 2026-09-05 06:25:42 89
GOHyperGAll
 
Resource Report
Resource Website
1+ mentions
GOHyperGAll (RRID:SCR_005766) GOHyperGAll data analysis software, data processing software, software application, 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 2026-09-05 06:25:41 4
InterProScan
 
Resource Report
Resource Website
5000+ mentions
InterProScan (RRID:SCR_005829) analysis service resource, data access protocol, data analysis service, data analysis software, data processing software, production service resource, service resource, software application, software resource, web service Software package for functional analysis of sequences by classifying them into families and predicting presence of domains and sites. Scans sequences against InterPro's signatures. Characterizes nucleotide or protein function by matching it with models from several different databases. Used in large scale analysis of whole proteomes, genomes and metagenomes. Available as Web based version and standalone Perl version and SOAP Web Service. functional, analysis, sequence, protein, nucleotide, predict, presence, domain, site, proteome, genome, metagenome, bio.tools is listed by: Gene Ontology Tools
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
is related to: Gene Ontology
is related to: RARTF
is related to: InterPro
is related to: LegumeIP
is related to: UniProtKB
has parent organization: European Bioinformatics Institute
Biotechnology and Biological Sciences Research Council ;
EMBL ;
European Union
PMID:15980438
PMID:17202162
PMID:24451626
Free, Available for download, Freely available OMICS_01479, biotools:interproscan_4, nlx_149337 https://www.ebi.ac.uk/interpro/download.html, https://bio.tools/interproscan_4 SCR_005829 InterProScan Sequence Search, InterProScan 2, InterProScan 3, InterProScan 4, InterProScan 5 2026-09-05 06:25:42 7512
Whatizit
 
Resource Report
Resource Website
1+ mentions
Whatizit (RRID:SCR_005824) Whatizit analysis service resource, data access protocol, data analysis service, production service resource, service resource, software resource, web service A text processing system that allows you to do textmining tasks on text. It is great at identifying molecular biology terms and linking them to publicly available databases. Whatizit is also a Medline abstracts retrieval/search engine. Instead of providing the text by Copy&Paste, you can launch a Medline search. The abstracts that match your search criteria are retrieved and processed by a pipeline of your choice. Whatizit is also available as 1) a webservice and as 2) a streamed servlet. The webservice allows you to enrich content within your website in a similar way as in the wikipedia. The streamed servlet allows you to process large amounts of text. textual analysis, protein, gene, gene ontology, text-mining, annotation, literature analysis is listed by: Gene Ontology Tools
is listed by: OMICtools
is related to: Gene Ontology
is related to: UniProt
is related to: MEDLINE
is related to: NCBI Taxonomy
has parent organization: European Bioinformatics Institute
Free for academic use OMICS_01200, nlx_149329 http://www.ebi.ac.uk/webservices/whatizit SCR_005824 2026-09-05 06:25:42 8
GOEx - Gene Ontology Explorer
 
Resource Report
Resource Website
10+ mentions
GOEx - Gene Ontology Explorer (RRID:SCR_005779) GOEx software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented July 5, 2018. Gene Ontology Explorer (GOEx) combines data from protein fold changes with GO over-representation statistics to help draw conclusions in proteomic experiments. It is tightly integrated within the PatternLab for Proteomics project and, thus, lies within a complete computational environment that provides parsers and pattern recognition tools designed for spectral counting. GOEx offers three independent methods to query data: an interactive directed acyclic graph, a specialist mode where key words can be searched, and an automatic search. A recent hack included in GOEx is to load the sparse matrix index file directly into GOEx, instead of going through the report generation using the AC/T-fold methods. This makes it easy for GOEx to analyze any list of proteins as long as the list follows the index file format (described in manuscript) . Please note that if using this alternative strategy, there will be no protein fold information. Platform: Windows compatible proteomics, visualization, statistical analysis, gene ontology, parse, pattern recognition, spectral counting, analysis, protein fold is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Scripps Research Institute
CNPq ;
CAPES ;
FAPERJ BBP grant ;
PAPES ;
PDTIS ;
Ary Frauzino Foundation ;
NIAID ;
NIH ;
genesis molecular biology laboratory ;
Fiocruz-INCA collaboration ;
NIAID UCSD/MCB0237059;
NCRR P41RR011823;
NIMH 5R01 MH067880
PMID:19239707 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149249 http://pcarvalho.com/patternlab/goex.shtml SCR_005779 Gene Ontology Explorer, GO Explorer 2026-09-05 06:25:41 32
OWLTools
 
Resource Report
Resource Website
10+ mentions
OWLTools (RRID:SCR_005732) OWLTools software resource OWLTools (aka OWL2LS - OWL2 Life Sciences) is a java API for accessing ontologies in either OBO or OWL. OWLTools provides a bio-ontologies friendly wrapper on top of the Manchester OWL API. It provides many features, including: * convenience methods for OBO-like properties such as synonyms, textual definitions, obsoletion, replaced_by * simple graph-like operations over ontologies * visualization using the QuickGO graphs libraries Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible software library, ontology is listed by: Gene Ontology Tools
is related to: OBO
has parent organization: Gene Ontology
has parent organization: Google Project Hosting
is parent organization of: OwlSim
Open unspecified license - Free for academic use nlx_149192 SCR_005732 OWL2LS - OWL2 Life Sciences, OWL Tools 2026-09-05 06:25:41 18
Blip: Biomedical Logic Programming
 
Resource Report
Resource Website
1+ mentions
Blip: Biomedical Logic Programming (RRID:SCR_005733) Blip, blipkit software resource Biomedical Logical Programming (Blip) is a research-oriented deductive database and prolog application library for handling biological and biomedical data. It includes packages for advanced querying of ontologies and annotations. Blip underpins the Obol tool. Here are some distinguishing characteristics of Blip * Lightweight. Bloat-free: Blip only has as many modules as it needs to do its job. * Fast. * Declarative. Say what you want to do, not how you want to do it * Blip can be Query-oriented: specify your data sources and ask your query * Blip can be Application-oriented: it is designed to be used as an application library used by other bioinformatics tools * Mature and fully functional ontology module for handling both OBO-style ontologies and OWL ontologies. * Modules for handling biological sequences and sequence features. (currently limited functionality, added as needed) * A systems biology module for querying pathway and interaction data. (currently limited functionality, added as needed) * Relational database integration. SQL can be viewed as a highly restricted dialect of Prolog. Although the SWI-Prolog in-memory database is fast and scalable, sometimes it is nice to be able to fetch data from an external database. Blip contains a generic SQL utility module and predicate mappings for the GO database, Ensembl and Chado * Integration with a variety of bioinformatics file formats. SWI-Prolog has a variety of fast libraries for dealing with XML, RDF and tabular data files. Blip provides bridges from bio file formats encoded using these syntaxes into its native models. For other syntaxes, Blip seamlessly integrates other packages such as BioPerl and go-perl. Although these dependencies require extra installation, there is no point reinventing the wheel * Rapid development of web applications. Blip extends SWI-Prolog''''s excellent http support with a simple and powerful logical-functional-programming style application server, serval. This has been used to prototype a fully-featured next-generation replacement for the GO project amigo browser. * Scalable. Blip is not intended to be a toy system on toy data (although it is happy to be used as a toy if you like!). It is intended to be used as an application component and a tool operating on real-world biological and biomedical data Blip is written in SWI-Prolog, a fast, robust and scalable implementation of ISO Prolog. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible biology, biomedical, ontology, annotation, software library, bioinformatics, module is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Berkeley Bioinformatics Open-Source Projects
GNU Lesser General Public License nlx_149193 SCR_005733 Blip - Biomedical Logic Programming, Biomedical Logical Programming (Blip), Biomedical Logic Programming 2026-09-05 06:25:41 2
ClueGO
 
Resource Report
Resource Website
1000+ mentions
ClueGO (RRID:SCR_005748) ClueGO software resource A Cytoscape plug-in that visualizes the non-redundant biological terms for large clusters of genes in a functionally grouped network. It can be used in combination with GOlorize. The identifiers can be uploaded from a text file or interactively from a network of Cytoscape. The type of identifiers supported can be easily extended by the user. ClueGO performs single cluster analysis and comparison of clusters. From the ontology sources used, the terms are selected by different filter criteria. The related terms which share similar associated genes can be combined to reduce redundancy. The ClueGO network is created with kappa statistics and reflects the relationships between the terms based on the similarity of their associated genes. On the network, the node colour can be switched between functional groups and clusters distribution. ClueGO charts are underlying the specificity and the common aspects of the biological role. The significance of the terms and groups is automatically calculated. ClueGO is easy updatable with the newest files from Gene Ontology and KEGG. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible, THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. statistical analysis, function, gene ontology, pathway, annotation, network, plugin, gene is listed by: Gene Ontology Tools
is listed by: SoftCite
is related to: Gene Ontology
is related to: Cytoscape
is related to: KEGG
is related to: BioCarta Pathways
has parent organization: National Institute of Health and Medical Research; Rennes; France
National Institute of Health and Medical Research; Rennes; France ;
Ville de Paris ;
INCa ;
Austrian Ministry for Science and Research ;
BINII ;
European Union 7FP 202230
PMID:19237447 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149209 SCR_005748 2026-09-05 06:25:41 2951
CLENCH
 
Resource Report
Resource Website
1+ mentions
CLENCH (RRID:SCR_005735) CLENCH data processing software, software application, software resource, source code Cluster Enrichment (CLENCH) allows A. thaliana researchers to perform automated retrieval of GO annotations from TAIR and calculate enrichment of GO terms in gene group with respect to a reference set. Before calculating enrichment, CLENCH allows mapping of the returned annotations to arbitrary coarse levels using GO slim term lists (which can be edited by the user) and a local installation of GO. Platform: Windows compatible, Linux compatible, gene, microarray, function, functional categorization, statistical analysis, slimmer-type tool, gene ontology, annotation is listed by: Gene Ontology Tools
is related to: Gene Ontology
is related to: TAIR
has parent organization: Stanford Center for Biomedical Informatics Research
PMID:14764555 Free for academic use nlx_149216 http://www.personal.psu.edu/nhs109/Clench SCR_005735 CLENCH - Cluster Enrichment, CLENCH: A program for calculating cluster enrichment using the Gene Ontology, Cluster Enrichment, Cluster Enrichment (CLENCH) 2026-09-05 06:25:41 4
GreenPhylDB
 
Resource Report
Resource Website
10+ mentions
GreenPhylDB (RRID:SCR_002834) GreenPhylDB analysis service resource, data analysis service, data or information resource, database, production service resource, service resource A database designed for plant comparative and functional genomics based on complete genomes. It comprises complete proteome sequences from the major phylum of plant evolution. The clustering of these proteomes was performed to define a consistent and extensive set of homeomorphic plant families. Based on this, lists of gene families such as plant or species specific families and several tools are provided to facilitate comparative genomics within plant genomes. The analyses follow two main steps: gene family clustering and phylogenomic analysis of the generated families. Once a group of sequences (cluster) is validated, phylogenetic analyses are performed to predict homolog relationships such as orthologs and ultraparalogs. comparative genomics, genome, functional genomics, genomics, gene family, homolog, bio.tools uses: Gene Ontology
is listed by: bio.tools
is listed by: Debian
has parent organization: CIRAD
PMID:20864446 Free, Freely available, Available for download biotools:greenphyldb, nif-0000-02928 http://greenphyl.cirad.fr, http://www.greenphyl.org/v3/, https://bio.tools/greenphyldb SCR_002834 2026-09-05 06:24:54 20
Patterns of Gene Expression in Drosophila Embryogenesis
 
Resource Report
Resource Website
50+ mentions
Patterns of Gene Expression in Drosophila Embryogenesis (RRID:SCR_002868) BDGP insitu data or information resource, database, image collection, software resource, source code Database of embryonic expression patterns using a high throughput RNA in situ hybridization of the protein-coding genes identified in the Drosophila melanogaster genome with images and controlled vocabulary annotations. At the end of production pipeline gene expression patterns are documented by taking a large number of digital images of individual embryos. The quality and identity of the captured image data are verified by independently derived microarray time-course analysis of gene expression using Affymetrix GeneChip technology. Gene expression patterns are annotated with controlled vocabulary for developmental anatomy of Drosophila embryogenesis. Image, microarray and annotation data are stored in a modified version of Gene Ontology database and the entire dataset is available on the web in browsable and searchable form or MySQL dump can be downloaded. So far, they have examined expression of 7507 genes and documented them with 111184 digital photographs. embryo, embryogenesis, gene, anatomy, microarray, pattern, protocol, rna, gene expression, expression pattern, embryonic drosophila, in situ hybridization, annotation, est, FASEB list is related to: Gene Ontology
has parent organization: Berkeley Drosophila Genome Project
Howard Hughes Medical Institute ;
NIH ;
NIGMS R01 GM076655;
NHGRI HG00750;
NHGRI P41 HG00739
PMID:17645804
PMID:12537577
Free, Freely available, Available for download nif-0000-25550, r3d100011327 https://doi.org/10.17616/R32H0K http://www.fruitfly.org/cgi-bin/ex/insitu.pl SCR_002868 BDGP Embryonic Expression Patterns 2026-09-05 06:24:54 64
GOLEM An interactive, graphical gene-ontology visualization, navigation, and analysis tool
 
Resource Report
Resource Website
1+ mentions
GOLEM An interactive, graphical gene-ontology visualization, navigation, and analysis tool (RRID:SCR_003191) GOLEM analysis service resource, data analysis service, production service resource, service resource, software resource, source code THIS RESOURCE IS NO LONGER IN SERVICE, documented July 7, 2017. Welcome to the home of GOLEM: An interactive, graphical gene-ontology visualization, navigation,and analysis tool on the web. GOLEM is a useful tool which allows the viewer to navigate and explore a local portion of the Gene Ontology (GO) hierarchy. Users can also load annotations for various organisms into the ontology in order to search for particular genes, or to limit the display to show only GO terms relevant to a particular organism, or to quickly search for GO terms enriched in a set of query genes. GOLEM is implemented in Java, and is available both for use on the web as an applet, and for download as a JAR package. A brief tutorial on how to use GOLEM is available both online and in the instructions included in the program. We also have a list of links to libraries used to make GOLEM, as well as the various organizations that curate organism annotations to the ontology. GOLEM is available as a .jar package and a macintosh .app for use on- or off- line as a stand-alone package. You will need to have Java (v.1.5 or greater) installed on your system to run GOLEM. Source code (including Eclipse project files) are also available. GOLEM (Gene Ontology Local Exploration Map)is a visualization and analysis tool for focused exploration of the gene ontology graph. GOLEM allows the user to dynamically expand and focus the local graph structure of the gene ontology hierarchy in the neighborhood of any chosen term. It also supports rapid analysis of an input list of genes to find enriched gene ontology terms. The GOLEM application permits the user either to utilize local gene ontology and annotations files in the absence of an Internet connection, or to access the most recent ontology and annotation information from the gene ontology webpage. GOLEM supports global and organism-specific searches by gene ontology term name, gene ontology id and gene name. CONCLUSION: GOLEM is a useful software tool for biologists interested in visualizing the local directed acyclic graph structure of the gene ontology hierarchy and searching for gene ontology terms enriched in genes of interest. It is freely available both as an application and as an applet. gene ontology, ontology visualization, ontology analysis is related to: Gene Ontology
has parent organization: Princeton University; New Jersey; USA
NIGMS R01 GM071966;
NSF IIS-0513552;
NIGMS P50 GM071508
PMID:17032457 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-30620 https://lsi.princeton.edu/golem-interactive-graph-based-gene-ontology-navigation-and-analysis-tool SCR_003191 GOLEM An interactive graphical gene-ontology visualization navigation and analysis tool, GOLEM An interactive graphical gene-ontology visualization navigation analysis tool 2026-09-05 06:24:59 3
MouseNET
 
Resource Report
Resource Website
1+ mentions
MouseNET (RRID:SCR_003357) mouseNet analysis service resource, data analysis service, data or information resource, database, production service resource, service resource A functional network for laboratory mouse based on integration of diverse genetic and genomic data. It allows the users to accurately predict novel functional assignments and network components. MouseNET uses a probabilistic Bayesian algorithm to identify genes that are most likely to be in the same pathway/functional neighborhood as your genes of interest. It then displays biological network for the resulting genes as a graph. The nodes in the graph are genes (clicking on each node will bring up SGD page for that gene) and edges are interactions (clicking on each edge will show evidence used to predict this interaction). Most likely, the first results to load on the results page will be a list of significant Gene Ontology terms. This list is calculated for the genes in the biological network created by the mouseNET algorithm. If a gene ontology term appears on this list with a low p-value, it is statistically significantly overrepresented in this biological network. The graph may be explored further. As you move the mouse over genes in the network, interactions involving these genes are highlighted.If you click on any of the highlighted interactions graph, evidence pop-up window will appear. The Evidence pop-up lists all evidence for this interaction, with links to the papers that produced this evidence - clicking these links will bring up the relevant source citation(s) in PubMed. gene, network, mouse, protein function, visualization, open reading frame, graph is listed by: OMICtools
is related to: Gene Ontology
is related to: mouseMAP
has parent organization: Princeton University; New Jersey; USA
NSF DBI-0546275;
NIGMS R01 GM071966;
NSF IIS-0513552;
NIGMS P50 GM071508
PMID:18818725 Free, Freely available OMICS_01550, nif-0000-32003 SCR_003357 MouseNET 2026-09-05 06:25:02 3
GOlr
 
Resource Report
Resource Website
1+ mentions
GOlr (RRID:SCR_003939) GOlr software resource A public Solr index for the Gene Ontology. This index will replace some of the query functionality for GOOSE as well as become the new backend for AmiGO 2 and other services. solr is used by: AmiGO
has parent organization: Gene Ontology
Public nlx_158322 http://golr.berkeleybop.org/ SCR_003939 Gene Ontology Solr index 2026-09-05 06:25:11 4
Open PHACTS
 
Resource Report
Resource Website
10+ mentions
Open PHACTS (RRID:SCR_005050) OPS consortium, data or information resource, database, organization portal, portal, software 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 2026-09-05 06:25:28 11

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. Neuroscience Information Framework Resources

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