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
L2L Microarray Analysis Tool
 
Resource Report
Resource Website
1+ mentions
L2L Microarray Analysis Tool (RRID:SCR_013440) L2L software application, data analysis service, data processing software, software resource, database, service resource, storage service resource, production service resource, data repository, data or information resource, analysis service resource, data analysis software THIS RESOURCE IS NO LONGER IN SERVICE, documented May 10, 2017. A pilot effort that has developed a centralized, web-based biospecimen locator that presents biospecimens collected and stored at participating Arizona hospitals and biospecimen banks, which are available for acquisition and use by researchers. Researchers may use this site to browse, search and request biospecimens to use in qualified studies. The development of the ABL was guided by the Arizona Biospecimen Consortium (ABC), a consortium of hospitals and medical centers in the Phoenix area, and is now being piloted by this Consortium under the direction of ABRC. You may browse by type (cells, fluid, molecular, tissue) or disease. Common data elements decided by the ABC Standards Committee, based on data elements on the National Cancer Institute''s (NCI''s) Common Biorepository Model (CBM), are displayed. These describe the minimum set of data elements that the NCI determined were most important for a researcher to see about a biospecimen. The ABL currently does not display information on whether or not clinical data is available to accompany the biospecimens. However, a requester has the ability to solicit clinical data in the request. Once a request is approved, the biospecimen provider will contact the requester to discuss the request (and the requester''s questions) before finalizing the invoice and shipment. The ABL is available to the public to browse. In order to request biospecimens from the ABL, the researcher will be required to submit the requested required information. Upon submission of the information, shipment of the requested biospecimen(s) will be dependent on the scientific and institutional review approval. Account required. Registration is open to everyone.. Documented on August 26, 2019.

Database of published microarray gene expression data, and a software tool for comparing that published data to a user''''s own microarray results. It is very simple to use - all you need is a web browser and a list of the probes that went up or down in your experiment. If you find L2L useful please consider contributing your published data to the L2L Microarray Database in the form of list files. L2L finds true biological patterns in gene expression data by systematically comparing your own list of genes to lists of genes that have been experimentally determined to be co-expressed in response to a particular stimulus - in other words, published lists of microarray results. The patterns it finds can point to the underlying disease process or affected molecular function that actually generated the observed changed in gene expression. Its insights are far more systematic than critical gene analyses, and more biologically relevant than pure Gene Ontology-based analyses. The publications included in the L2L MDB initially reflected topics thought to be related to Cockayne syndrome: aging, cancer, and DNA damage. Since then, the scope of the publications included has expanded considerably, to include chromatin structure, immune and inflammatory mediators, the hypoxic response, adipogenesis, growth factors, hormones, cell cycle regulators, and others. Despite the parochial origins of the database, the wide range of topics covered will make L2L of general interest to any investigator using microarrays to study human biology. In addition to the L2L Microarray Database, L2L contains three sets of lists derived from Gene Ontology categories: Biological Process, Cellular Component, and Molecular Function. As with the L2L MDB, each GO sub-category is represented by a text file that contains annotation information and a list of the HUGO symbols of the genes assigned to that sub-category or any of its descendants. You don''''t need to download L2L to use it to analyze your microarray data. There is an easy-to-use web-based analysis tool, and you have the option of downloading your results so you can view them at any time on your own computer, using any web browser. However, if you prefer, the entire L2L project, and all of its components, can be downloaded from the download page. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible
microarray, gene expression, adipogenesis, biological, biological process, cancer, cell cycle regulator, cellular component, chromatin, cockayne syndrome, dna damage, growth factor, hormone, human biology, hypoxic response, immune mediator, inflammatory mediator, molecular function, molecular neuroanatomy resource, adipocyte, development, hypoxia, immune, inflammation, metabolism, mitogen, neuro, rna, vascular, transcription, tissue, splicing, mouse, human, rat, source code, statistical analysis, gene, chromatin structure is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of Washington; Seattle; USA
Cockayne syndrome, DNA damage, Other, Aging, Cancer Cora May Poncin Foundation ;
NIGMS GM41624
PMID:16168088 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-10463 http://depts.washington.edu/l2l/about.html SCR_013440 L2L Microarray Database, L2L Microarray Analysis Tool: A simple tool for discovering the hidden biological significance in microarray expression data, L2L MDB 2026-02-15 09:20:28 1
PiGenome
 
Resource Report
Resource Website
PiGenome (RRID:SCR_013394) PiGenome data analysis service, database, service resource, production service resource, data or information resource, analysis service resource Database for ESTs (Expressed Sequence Tags), consensus sequences, bacterial artificial chromosome (BAC) clones, BES (BAC End Sequences). They have generated 69,545 ESTs from 6 full-length cDNA libraries (Porcine Abdominal Fat, Porcine Fat Cell, Porcine Loin Muscle, Liver and Pituitary gland). They have also identified a total of 182 BAC contigs from chromosome 6. It is very valuable resources to study porcine quantitative trait loci (QTL) mapping and genome study. Users can explore genomic alignment of various data types, including expressed sequence tags (ESTs), consensus sequences, singletons, QTL, Marker, UniGene and BAC clones by several options. To estimate the genomic location of sequence dataset, their data aligned BES (BAC End Sequences) instead of genomic sequence because Pig Genome has low-coverage sequencing data. Sus scrofa Genome Database mainly provide comparative map of four species (pig, cattle, dog and mouse) in chromosome 6. gene expression, genome, sequence, gene, expressed sequence tag, consensus sequence, bac clone, bac end sequence, bac contig, quantitative trait loci, singleton, marker, unigene, chromosome 6, blast, transcript, bacterial artificial chromosome, snp, alignment is related to: Gene Ontology
has parent organization: National Institute of Animal Science; Gyeonggi-do; South Korea
National Institute of Animal Science; Gyeonggi-do; Korea ;
Korean Rural Development Administration ;
Biogreen21 Project 20050301034467
PMID:19082661 nlx_153888 http://pigenome.nabc.go.kr/ SCR_013394 Sus scrofa Genome database, Pig Genome Database, Pigenome database 2026-02-15 09:20:43 0
PlantNATsDB - Plant Natural Antisense Transcripts DataBase
 
Resource Report
Resource Website
1+ mentions
PlantNATsDB - Plant Natural Antisense Transcripts DataBase (RRID:SCR_013278) PlantNATsDB data analysis service, database, service resource, production service resource, data or information resource, analysis service resource Natural Antisense Transcripts (NATs), a kind of regulatory RNAs, occur prevalently in plant genomes and play significant roles in physiological and/or pathological processes. PlantNATsDB (Plant Natural Antisense Transcripts DataBase) is a platform for annotating and discovering NATs by integrating various data sources involving approximately 2 million NAT pairs in 69 plant species. PlantNATsDB also provides an integrative, interactive and information-rich web graphical interface to display multidimensional data, and facilitate plant research community and the discovery of functional NATs. GO annotation and high-throughput small RNA sequencing data currently available were integrated to investigate the biological function of NATs. A ''''Gene Set Analysis'''' module based on GO annotation was designed to dig out the statistical significantly overrepresented GO categories from the specific NAT network. PlantNATsDB is currently the most comprehensive resource of NATs in the plant kingdom, which can serve as a reference database to investigate the regulatory function of NATs. natural antisense transcript, annotation, high-throughput, small rna sequencing, function, regulatory function, predict, sequence, small rna, blast, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
is related to: Gene Expression Omnibus
has parent organization: Zhejiang University; Zhejiang; China
National Natural Sciences Foundation of China 30971743;
National Natural Sciences Foundation of China 31050110121;
National Natural Sciences Foundation of China 31071659;
Ministry of Science and Technology of China 2009DFA32030;
Program for New Century Excellent Talents in University of China NCET-07-0740;
Huazhong Agricultural University Scientific and Technological Self-innovation Foundation 2010SC07
PMID:22058132 Free nlx_151492, biotools:plantnatsdb https://bio.tools/plantnatsdb SCR_013278 Plant Natural Antisense Transcripts DataBase 2026-02-15 09:20:26 9
GOnet
 
Resource Report
Resource Website
1+ mentions
GOnet (RRID:SCR_018977) software resource, data access protocol, web service, service resource, production service resource, analysis service resource Web tool for interactive Gene Ontology analysis of any biological data sources resulting in gene or protein lists. Gene Ontology, interactive analysis, data, gene, protein, gene list, protein list, analysis, bio.tools is listed by: Debian
is listed by: bio.tools
works with: Gene Ontology
NIH Common Fund ;
NIGMS ;
NHGRI R24 HG010032;
NIAID U19 AI118610;
NIAID U19 AI118626
PMID:30526489 biotools:GOnet https://github.com/mikpom/gonet
https://bio.tools/GOnet
SCR_018977 2026-02-15 09:22:25 3
SynGO
 
Resource Report
Resource Website
100+ mentions
SynGO (RRID:SCR_017330) data analysis service, ontology, service resource, production service resource, data or information resource, controlled vocabulary, analysis service resource Evidence based, expert curated knowledge base for synapse. Universal reference for synapse research and online analysis platform for interpretation of omics data. Interactive knowledge base that accumulates available research about synapse biology using Gene Ontology annotations to novel ontology terms. Synapse, evidence, curated, base, reference, analysis, omics, data, ontology, gene, annotation uses: Gene Ontology Stanley Center for Psychiatric Research at The Broad Institute of MIT and Harvard ;
European Union ;
CERCA Program/Generalitat de Catalunya ;
NINDS NS36251;
German Federal Ministry of Education and Research
PMID:31171447 Free, Freely available SCR_017330 Synaptic Gene Ontologies 2026-02-15 09:21:18 134
Gene Ontology Browsing Utility (GOBU)
 
Resource Report
Resource Website
Gene Ontology Browsing Utility (GOBU) (RRID:SCR_005662) GOBU source code, software resource Gene Ontology Browsing Utility (GOBU) (GOBU) is a Java-based software program for integrating biological annotation catalogs under an extendable software architecture. Users may interact with the Gene Ontology and user-defined hierarchy data of genes, and then use its plugins to (and not limited to) (1) browse the GO hierarchy with user defined data, (2) browse GO-oriented expression levels in the user data, (3) compute GO enrichment, and/or (4) customize data reporting. A set of classes and utility functions has been established so that a customized program can be made as a plugin or a command-line tool that programmically manipulate the Gene Ontology and specified user data. See the source code repository for examples. Reference Lin WD, Chen YC, Ho JM, Hsiao CD. GOBU: Toward an Integration Interface for Biological Objects. Journal of Information Science and Engineering. 2006 22(1):19-29. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible annotation, gene, browser, computation, visualization, software library, statistical analysis, term enrichment, ontology or annotation browser, ontology or annotation visualization is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Academia Sinica; Taipei; Taiwan
Open unspecified license - Free for academic use nlx_149098 SCR_005662 Gene Ontology Browsing Utility 2026-02-15 09:19:09 0
OWL API
 
Resource Report
Resource Website
10+ mentions
OWL API (RRID:SCR_005734) OWL API source code, software resource The OWL API is a Java API and reference implementation for creating, manipulating and serializing OWL Ontologies. The latest version of the API is focused towards OWL 2. The OWLAPI underpins ontology browsing and editing tools and platforms such as SWOOP and Protege4. Note that this API, or any other OWL-based API, can be used without an integrated OWL parser if you download a pre-converted OWL file generated from OBO. See OBO Ontologies List for all OBO ontologies converted to OWL (we do not list the full complement of OWL-based APIs here, only those of direct relevance to GO). The OWL API includes the following components: * An API for OWL 2 and an efficient in-memory reference implementation * RDF/XML parser and writer * OWL/XML parser and writer * OWL Functional Syntax parser and writer * Turtle parser and writer * KRSS parser * OBO Flat file format parser * Reasoner interfaces for working with reasoners such as FaCT++, HermiT, Pellet and Racer Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible ontology, owl, api, java, software library, parser, writer is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of Manchester; Manchester; United Kingdom
has parent organization: SourceForge
Open unspecified license - Free for academic use; available under either the LGPL or Apache Licenses nlx_149195 SCR_005734 The OWL API, OWLAPI 2026-02-15 09:19:02 15
Quantitative Enrichment of Sequence Tags
 
Resource Report
Resource Website
10+ mentions
Quantitative Enrichment of Sequence Tags (RRID:SCR_004065) QuEST software resource A Kernel Density Estimator-based package for analysis of massively parallel sequencing data from chromatin immunoprecipitation (ChIP-seq) experiments. genome-wide, transcription factor binding site, chip-seq, transcription factor, binding site, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
has parent organization: Stanford University; Stanford; California
PMID:19160518 OMICS_00458, biotools:quest https://bio.tools/quest SCR_004065 Quantitative Enrichment of Sequence Tags: QuEST 2026-02-14 02:00:40 49
Neural-Immune Gene Ontology
 
Resource Report
Resource Website
1+ mentions
Neural-Immune Gene Ontology (RRID:SCR_004120) NIGO data or information resource, ontology, controlled vocabulary Ontology that is a subset of GO directed for neurological and immunological systems. It was created by clipping those GO terms that are not associated to any gene in human, rat and mouse, and by clipping terms not found to be relevant to the neural and/or immune domains. obo is listed by: BioPortal
is related to: Gene Ontology
nlx_157506 SCR_004120 2026-02-14 02:00:37 1
SO
 
Resource Report
Resource Website
10+ mentions
SO (RRID:SCR_004374) SO data or information resource, ontology, controlled vocabulary A collaborative ontology for the definition of sequence features used in biological sequence annotation. SO was initially developed by the Gene Ontology Consortium. Contributors to SO include the GMOD community, model organism database groups such as WormBase, FlyBase, Mouse Genome Informatics group, and institutes such as the Sanger Institute and the EBI. Input to SO is welcomed from the sequence annotation community. The OBO revision is available here: http://sourceforge.net/p/song/svn/HEAD/tree/ SO includes different kinds of features which can be located on the sequence. Biological features are those which are defined by their disposition to be involved in a biological process. Biomaterial features are those which are intended for use in an experiment such as aptamer and PCR_product. There are also experimental features which are the result of an experiment. SO also provides a rich set of attributes to describe these features such as polycistronic and maternally imprinted. The Sequence Ontologies use the OBO flat file format specification version 1.2, developed by the Gene Ontology Consortium. The ontology is also available in OWL from Open Biomedical Ontologies. This is updated nightly and may be slightly out of sync with the current obo file. An OWL version of the ontology is also available. The resolvable URI for the current version of SO is http://purl.obolibrary.org/obo/so.owl. annotation, sequence, biological sequence, sequence variation, genome, genome annotation, owl, FASEB list is listed by: BioPortal
is related to: ASOoViR
is related to: VAGrENT
has parent organization: OBO
has parent organization: Gene Ontology
NHGRI HG02273 PMID:20796305
PMID:20226267
PMID:18629179
PMID:15892872
The community can contribute to this resource nlx_38918 SCR_004374 Sequence Ontology Project, Sequence Types and Features Ontology, Sequence Ontology 2026-02-14 02:00:58 44
Tk-GO
 
Resource Report
Resource Website
Tk-GO (RRID:SCR_008855) TkGO software resource Tk-GO is a GUI wrapping the basic functions of the GO AppHandle library from BDGP. GO terms are presented in an explorer-like browser, and behavior can be configured by altering Perl scripts. All available documentation is included in the download. Tk-GO uses the GO database (connects directly to the BDGP database by default) but is user-configurable. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible browser, gene, ontology or annotation browser is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Illumina
MIT License - Free for academic use nlx_149133 SCR_008855 2026-02-14 02:01:46 0
Spotfire
 
Resource Report
Resource Website
100+ mentions
Spotfire (RRID:SCR_008858) Spotfire software resource The Spotfire Gene Ontology Advantage Application integrates GO annotations with gene expression analysis in Spotfire DecisionSite for Functional Genomics. Researchers can select a subset of genes in DecisionSite visualizations and display their distribution in the Gene Ontology hierarchy. Similarly, selection of any process, function or cellular location in the Gene Ontology hierarchy automatically marks the corresponding genes in DecisionSite visualizations. Platform: Windows compatible analysis, predictive analytics, big data, visualization, gene ontology, annotation, gene expression, functional genomics, gene, function, cellular location, statistical analysis, genomics is listed by: Gene Ontology Tools
is listed by: Metabolomics Workbench
is related to: Gene Ontology
Commercial license. Spotfire is available for purchase (individual license / enterprise use) / Free trial. nlx_149169 SCR_008858 Tibco Spotfire, Spotfire Inc., Spotfire Gene Ontology Advantage Application, Spotfire - TIBCO Software 2026-02-14 02:01:47 474
DynGO
 
Resource Report
Resource Website
1+ mentions
DynGO (RRID:SCR_007009) DynGO software resource DynGO is a client-server application that provides several advanced functionalities in addition to the standard browsing capability. DynGO allows users to conduct batch retrieval of GO annotations for a list of genes and gene products, and semantic retrieval of genes and gene products sharing similar GO annotations (which requires more disk and memory to handle the semantic retrieval). The result are shown in an association tree organized according to GO hierarchies and supported with many dynamic display options such as sorting tree nodes or changing orientation of the tree. For GO curators and frequent GO users, DynGO provides fast and convenient access to GO annotation data. DynGO is generally applicable to any data set where the records are annotated with GO terms, as illustrated by two examples. Requirements: Java Platform: Windows compatible, Linux compatible, Unix compatible gene, annotation, browser, ontology or annotation browser is listed by: Gene Ontology Tools
is related to: Gene Ontology
NSF IIS-0430743 PMID:16091147 Free for academic use nlx_149118 http://gauss.dbb.georgetown.edu/liblab SCR_007009 DynGO: a tool for visualizing and mining of Gene Ontology and its associations 2026-02-14 02:01:26 6
OBO
 
Resource Report
Resource Website
100+ mentions
OBO (RRID:SCR_007083) OBO ontology, knowledge environment, data or information resource, controlled vocabulary, narrative resource, standard specification A collaboration involving developers of science-based ontologies who are establishing a set of principles for ontology development with the goal of creating a suite of orthogonal interoperable reference ontologies in the biomedical domain. In addition to a listing of OBO ontologies, this site provides a statement of the OBO Foundry principles, discussion fora, technical infrastructure, and other services to facilitate ontology development. Feedback is welcome and participation encouraged. biomedical, metadata standard, gold standard, FASEB list lists: CHEBI
lists: NCI Thesaurus
lists: Porifera Ontology
lists: Gazetteer
lists: Human Disease Ontology
lists: Information Artifact Ontology
lists: Teleost Anatomy Ontology
lists: Gene Ontology
lists: Spider Ontology
lists: Mental Functioning Ontology
lists: Ascomycete Phenotype Ontology
lists: Beta Cell Genomics Ontology
lists: Biological Collections Ontology
lists: Emotion Ontology
lists: Chemical Methods Ontology
lists: Chemical Information Ontology
lists: Clinical Measurement Ontology
lists: Common Anatomy Reference Ontology
lists: Experimental Conditions Ontology
lists: Dictyostelium Discoideum Anatomy Ontology
lists: Fission Yeast Phenotype Ontology
lists: Fly Taxonomy
lists: FlyBase Controlled Vocabulary
lists: Hymenoptera Anatomy Ontology
lists: Influenza Ontology
lists: Lipid Ontology
lists: Kinetic Simulation Algorithm Ontology
lists: Malaria Ontology
lists: Measurement Method Ontology
lists: Minimal Anatomical Terminology
lists: Ontology for Genetic Interval
lists: Ontology for Parasite LifeCycle
lists: Ontology of Adverse Events
lists: Ontology of Medically Related Social Entities
lists: Ontology of Vaccine Adverse Events
lists: Rat Strain Ontology
lists: Plant Environmental Conditions
lists: Plant Trait Ontology
lists: Population and Community Ontology
lists: RNA Ontology
lists: Rat Strain Ontology
lists: Subcellular Anatomy Ontology
lists: Software Ontology
lists: Suggested Ontology for Pharmacogenomics
lists: Vertebrate Taxonomy Ontology
lists: Physico-Chemical Process
lists: Adverse Event Reporting Ontology
lists: Xenopus Anatomy Ontology
lists: Cell Line Ontology
lists: Human Phenotype Ontology
lists: Neurobehavior Ontology
lists: Ontology for Biomedical Investigations
lists: Comparative Data Analysis Ontology
lists: Ontology for General Medical Science
lists: Physico-Chemical Methods and Properties
lists: Gene Regulation Ontology
is listed by: FORCE11
is related to: MeGO
is related to: Drosophila anatomy and development ontologies
is related to: Cell Type Ontology
is related to: OBO-Edit
is related to: go-perl
is related to: OWLTools
is related to: Zebrafish Anatomical Ontology
is related to: OBO Tracker: Plant Ontology (PO) TERM requests
is related to: eVOC
is related to: OnEx - Ontology Evolution Explorer
is related to: BioPerl
is related to: dkCOIN
is related to: Standards-based Infrastructure with Distributed Resources
is related to: OntoVisT
is related to: COBrA
is related to: Wandora
is related to: ONTO-PERL
is related to: Genomic Standards Consortium
is related to: Ontology Lookup Service
is related to: LexGrid
is related to: SBO
is related to: RIKEN integrated database of mammals
is related to: DOAF
is related to: Gene Ontology
is related to: African Population Ontology
has parent organization: Berkeley Bioinformatics Open-Source Projects
is parent organization of: OBO Relation Ontology
is parent organization of: SO
is parent organization of: PATO
is parent organization of: MPO
is parent organization of: AEO
is parent organization of: UBERON
PMID:17989687 nlx_22892 SCR_007083 The Open Biomedical Ontologies, OBO Foundry, Open Biological and Biomedical Ontologies, Open Biological and Biomedical Ontology Foundry 2026-02-14 02:01:27 169
go-db-perl
 
Resource Report
Resource Website
1+ mentions
go-db-perl (RRID:SCR_005721) go-db-perl software resource Software resource that extends the functionality of go-perl (on which it depends) with GO Database access functionality. go-db-perl comes bundled with various scripts and a shell command line interface that can be used as standalone tools. Installation is more involved than for go-perl; you will need a MySQL database plus the requisite DBI and DBD Perl modules. Full installation instructions are included in the download. go-db-perl is in use both to drive AmiGO and internally within Ensembl. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible software library, database, gene ontology, database or data warehouse is listed by: Gene Ontology Tools
is related to: AmiGO
is related to: go-moose
is related to: Ensembl
is related to: go-perl
has parent organization: Comprehensive Perl Archive Network
has parent organization: Gene Ontology
Free for academic use nlx_149180 SCR_005721 2026-02-14 02:01:10 1
Manatee
 
Resource Report
Resource Website
50+ mentions
Manatee (RRID:SCR_005685) Manatee software resource Manatee is a web-based gene evaluation and genome annotation tool; Manatee can store and view annotation for prokaryotic and eukaryotic genomes. The Manatee interface allows biologists to quickly identify genes and make high quality functional assignments, such as GO classifications, using search data, paralogous families, and annotation suggestions generated from automated analysis. Manatee can be downloaded and installed to run under the CGI area of a web server, such as Apache. Platform: Online tool, Linux compatible, Solaris gene, genome, annotation, ontology or annotation browser, ontology or annotation editor is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: J. Craig Venter Institute
has parent organization: University of Maryland School of Medicine; Maryland; USA
has parent organization: SourceForge
Open unspecified license - Free for academic use nlx_149128 SCR_005685 2026-02-14 02:01:10 64
go-perl
 
Resource Report
Resource Website
10+ mentions
go-perl (RRID:SCR_005730) go-perl software resource go-perl is a set of Perl modules for parsing, manipulating and exporting ontologies and annotations. It includes parsers for the OBO and GO gene association file formats. It has a graph-based object model with methods for graph traversal. For more details, see the documentation included with the modules. go-perl comes bundled with XSL (Extensible Stylesheet Language) transforms (which can also be used independently of Perl, provided you have files in OBO-XML format), as well as scripts that can be used as standalone tools. Installation should be simple, provided you have some experience with Perl and CPAN; see the INSTALL file for details. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible ontology, annotation, software library, slimmer-type tool, parser is listed by: Gene Ontology Tools
is related to: OBO
is related to: go-moose
is related to: go-db-perl
has parent organization: Comprehensive Perl Archive Network
has parent organization: Gene Ontology
Free for academic use nlx_149190 SCR_005730 2026-02-14 02:01:00 10
BiNGO: A Biological Networks Gene Ontology tool
 
Resource Report
Resource Website
500+ mentions
BiNGO: A Biological Networks Gene Ontology tool (RRID:SCR_005736) BiNGO software resource The Biological Networks Gene Ontology tool (BiNGO) is an open-source Java tool to determine which Gene Ontology (GO) terms are significantly overrepresented in a set of genes. BiNGO can be used either on a list of genes, pasted as text, or interactively on subgraphs of biological networks visualized in Cytoscape. BiNGO maps the predominant functional themes of the tested gene set on the GO hierarchy, and takes advantage of Cytoscape''''s versatile visualization environment to produce an intuitive and customizable visual representation of the results. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene ontology, gene, ontology, statistical analysis, term enrichment, biological network, plugin, bio.tools is listed by: Gene Ontology Tools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
is related to: Cytoscape
has parent organization: Ghent University; Ghent; Belgium
PMID:15972284 Open unspecified license - Free for academic use nlx_149196, biotools:bingo https://bio.tools/bingo SCR_005736 Biological Networks Gene Ontology 2026-02-14 02:01:00 790
Gene Ontology Extension
 
Resource Report
Resource Website
Gene Ontology Extension (RRID:SCR_010327) GO-EXT data or information resource, ontology, controlled vocabulary An extension of the Gene Ontology. obo is listed by: BioPortal
has parent organization: Gene Ontology
nlx_157414 SCR_010327 2026-02-14 02:01:57 0
CELDA Ontology
 
Resource Report
Resource Website
CELDA Ontology (RRID:SCR_001601) CELDA data or information resource, ontology, controlled vocabulary Structured vocabulary to organize cell-associated data and to place these data in clearly defined semantic relations to other biological facts. It describes cell types, their properties and origin and links this information to other existing ontologies like the Cell Ontology (CL), Foundational Model of Anatomy (FMA), Gene Ontology (GO), Mouse Anatomy and others using the top-level ontology BioTop. cell, expression, localization, development, anatomy, cell type, development, organ, kidney, liver, skin is related to: Cell Type Ontology
is related to: FMA
is related to: Gene Ontology
has parent organization: CellFinder
Seoul National University; Seoul; South Korea ;
Research Institute for Veterinary Science ;
DFG KU 851/3-1;
DFG LE 1428/3-1;
DFG JA 1904/2-1
PMID:23865855 THIS RESOURCE IS NO LONGER IN SERVICE nlx_153858 SCR_001601 Cell: Expression Localization Development Anatomy, CellFinder Ontology, CELDA Ontology 2026-02-14 02:00:06 0

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.