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
CharProtDB: Characterized Protein Database
 
Resource Report
Resource Website
CharProtDB: Characterized Protein Database (RRID:SCR_005872) CharProtDB data or information resource, database The Characterized Protein Database, CharProtDB, is designed and being developed as a resource of expertly curated, experimentally characterized proteins described in published literature. For each protein record in CharProtDB, storage of several data types is supported. It includes functional annotation (several instances of protein names and gene symbols) taxonomic classification, literature links, specific Gene Ontology (GO) terms and GO evidence codes, EC (Enzyme Commisssion) and TC (Transport Classification) numbers and protein sequence. Additionally, each protein record is associated with cross links to all public accessions in major protein databases as ��synonymous accessions��. Each of the above data types can be linked to as many literature references as possible. Every CharProtDB entry requires minimum data types to be furnished. They are protein name, GO terms and supporting reference(s) associated to GO evidence codes. Annotating using the GO system is of importance for several reasons; the GO system captures defined concepts (the GO terms) with unique ids, which can be attached to specific genes and the three controlled vocabularies of the GO allow for the capture of much more annotation information than is traditionally captured in protein common names, including, for example, not just the function of the protein, but its location as well. GO evidence codes implemented in CharProtDB directly correlate with the GO consortium definitions of experimental codes. CharProtDB tools link characterization data from multiple input streams through synonymous accessions or direct sequence identity. CharProtDB can represent multiple characterizations of the same protein, with proper attribution and links to database sources. Users can use a variety of search terms including protein name, gene symbol, EC number, organism name, accessions or any text to search the database. Following the search, a display page lists all the proteins that match the search term. Click on the protein name to view more detailed annotated information for each protein. Additionally, each protein record can be annotated. protein, annotation, functional annotation, taxonomic classification, literature, gene ontology, evidence code, enzyme commission, transport classification, protein sequence, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
has parent organization: J. Craig Venter Institute
NHGRI R01 HG004881;
NIAID contract HHSN266200100038C
PMID:22140108 biotools:charprotdb, nlx_149421 https://bio.tools/charprotdb SCR_005872 Characterized Protein Database 2026-02-14 02:06:25 0
VirHostNet: Virus-Host Network
 
Resource Report
Resource Website
1+ mentions
VirHostNet: Virus-Host Network (RRID:SCR_005978) VirHostNet data or information resource, database Public knowledge base specialized in the management and analysis of integrated virus-virus, virus-host and host-host interaction networks coupled to their functional annotations. It contains high quality and up-to-date information gathered and curated from public databases (VirusMint, Intact, HIV-1 database). It allows users to search by host gene, host/viral protein, gene ontology function, KEGG pathway, Interpro domain, and publication information. It also allows users to browse viral taxonomy. interaction, protein, virus, protein-protein interaction, protein interaction, infectious disease, antiviral drug design, proteome, interactome, molecular function, cellular pathway, protein domain, virus-virus, virus-host, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
is related to: VirusMINT
is related to: IntAct
is related to: HIV-1 Human Protein Interaction Database
is related to: PSICQUIC Registry
has parent organization: Claude Bernard University Lyon 1; Lyon; France
PMID:18984613 Acknowledgement requested, Public nif-0000-03634, OMICS_01910, biotools:virhostnet https://bio.tools/virhostnet SCR_005978 Virus-Host Network 2026-02-14 02:05:53 6
HPRD - Human Protein Reference Database
 
Resource Report
Resource Website
1000+ mentions
HPRD - Human Protein Reference Database (RRID:SCR_007027) HPRD data or information resource, database Database that represents a centralized platform to visually depict and integrate information pertaining to domain architecture, post-translational modifications, interaction networks and disease association for each protein in the human proteome. All the information in HPRD has been manually extracted from the literature by expert biologists who read, interpret and analyze the published data. protein, disease, network, post-translational, proteome, protein binding, protein s, protein c, pathway, protein-protein interaction, protein expression, subcellular localization, phosphorylation motif, signaling pathway, protein sequence, blast, molecule, domain, motif, post-translational modification, protein isoform, FASEB list is used by: Mutation Annotation and Genomic Interpretation
is used by: Pathway Analysis Tool for Integration and Knowledge Acquisition
is used by: GEMINI
is listed by: re3data.org
is related to: Human Proteinpedia
is related to: MatrixDB
is related to: Interaction Reference Index
is related to: Pathway Commons
is related to: ConsensusPathDB
is related to: Gene Ontology
is related to: Agile Protein Interactomes DataServer
has parent organization: Johns Hopkins University; Maryland; USA
has parent organization: Institute of Bioinformatics; Bangalore; India
PMID:18988627
PMID:16381900
PMID:14525934
Acknowledgement requested, Free, Non-commercial, Commercial requires license nif-0000-00137, r3d100010978 https://doi.org/10.17616/R3MK9N SCR_007027 Human Protein Reference Database 2026-02-14 02:05:57 1266
ECgene: Gene Modeling with Alternative Splicing
 
Resource Report
Resource Website
10+ mentions
ECgene: Gene Modeling with Alternative Splicing (RRID:SCR_007634) ECgene data or information resource, database Database of functional annotation for alternatively spliced genes. It uses a gene-modeling algorithm that combines the genome-based expressed sequence tag (EST) clustering and graph-theoretic transcript assembly procedures. It contains genome, mRNA, and EST sequence data, as well as a genome browser application. Organisms included in the database are human, dog, chicken, fruit fly, mouse, rhesus, rat, worm, and zebrafish. Annotation is provided for the whole transcriptome, not just the alternatively spliced genes. Several viewers and applications are provided that are useful for the analysis of the transcript structure and gene expression. The summary viewer shows the gene summary and the essence of other annotation programs. The genome browser and the transcript viewer are available for comparing the gene structure of splice variants. Changes in the functional domains by alternative splicing can be seen at a glance in the transcript viewer. Two unique ways of analyzing gene expression is also provided. The SAGE tags deduced from the assembled transcripts are used to delineate quantitative expression patterns from SAGE libraries available publicly. The cDNA libraries of EST sequences in each cluster are used to infer qualitative expression patterns. est cluster, genome, alternative splicing, splice, gene, mrna, est, annotation, gene modeling, structure, function, gene expression, transcript, genome browser, differential expression, snp is listed by: OMICtools
is related to: Gene Ontology
has parent organization: Ewha Womans University; Seoul; South Korea
PMID:17132829
PMID:15805497
PMID:15608289
nif-0000-02780, OMICS_01884 http://genome.ewha.ac.kr/ECgene/ SCR_007634 ECgene - Genome Annotation for Alternative Splicing 2026-02-14 02:06:00 12
Functional Annotation
 
Resource Report
Resource Website
1+ mentions
Functional Annotation (RRID:SCR_017519) service resource MGI GO project provides functional annotations for mouse gene products using Gene Ontology. Functional annotation using Gene Ontology (GO). MGI, GO, functional, annotation, mouse, gene, product, Gene Ontology uses: Gene Ontology
has parent organization: Mouse Genome Informatics (MGI)
Free, Freely available SCR_017519 2026-02-14 02:03:13 4
Integrated Manually Extracted Annotation
 
Resource Report
Resource Website
Integrated Manually Extracted Annotation (RRID:SCR_008876) Integrated MEA, Integrated LinkOut, Manually Extracted Annotation, data or information resource, database A virtual database of annotations made by 50 database providers (April 2014) - and growing (see below), that map data to publication information. All NIF Data Federation sources can be part of this virtual database as long as they indicate the publications that correspond to data records. The format that NIF accepts is the PubMed Identifier, category or type of data that is being linked to, and a data record identifier. A subset of this data is passed to NCBI, as LinkOuts (links at the bottom of PubMed abstracts), however due to NCBI policies the full data records are not currently associated with PubMed records. Database providers can use this mechanism to link to other NCBI databases including gene and protein, however these are not included in the current data set at this time. (To view databases available for linking see, http://www.ncbi.nlm.nih.gov/books/NBK3807/#files.Databases_Available_for_Linking ) The categories that NIF uses have been standardized to the following types: * Resource: Registry * Resource: Software * Reagent: Plasmid * Reagent: Antibodies * Data: Clinical Trials * Data: Gene Expression * Data: Drugs * Data: Taxonomy * Data: Images * Data: Animal Model * Data: Microarray * Data: Brain connectivity * Data: Volumetric observation * Data: Value observation * Data: Activation Foci * Data: Neuronal properties * Data: Neuronal reconstruction * Data: Chemosensory receptor * Data: Electrophysiology * Data: Computational model * Data: Brain anatomy * Data: Gene annotation * Data: Disease annotation * Data: Cell Model * Data: Chemical * Data: Pathways For more information refer to Create a LinkOut file, http://neuinfo.org/nif_components/disco/interoperation.shtm Participating resources ( http://disco.neuinfo.org/webportal/discoLinkoutServiceSummary.do?id=4 ): * Addgene http://www.addgene.org/pgvec1 * Animal Imaging Database http://aidb.crbs.ucsd.edu * Antibody Registry http://www.neuinfo.org/products/antibodyregistry/ * Avian Brain Circuitry Database http://www.behav.org/abcd/abcd.php * BAMS Connectivity http://brancusi.usc.edu/ * Beta Cell Biology Consortium http://www.betacell.org/ * bioDBcore http://biodbcore.org/ * BioGRID http://thebiogrid.org/ * BioNumbers http://bionumbers.hms.harvard.edu/ * Brain Architecture Management System http://brancusi.usc.edu/bkms/ * Brede Database http://hendrix.imm.dtu.dk/services/jerne/brede/ * Cell Centered Database http://ccdb.ucsd.edu * CellML Model Repository http://www.cellml.org/models * CHEBI http://www.ebi.ac.uk/chebi/ * Clinical Trials Network (CTN) Data Share http://www.ctndatashare.org/ * Comparative Toxicogenomics Database http://ctdbase.org/ * Coriell Cell Repositories http://ccr.coriell.org/ * CRCNS - Collaborative Research in Computational Neuroscience - Data sharing http://crcns.org * Drug Related Gene Database https://confluence.crbs.ucsd.edu/display/NIF/DRG * DrugBank http://www.drugbank.ca/ * FLYBASE http://flybase.org/ * Gene Expression Omnibus http://www.ncbi.nlm.nih.gov/geo/ * Gene Ontology Tools http://www.geneontology.org/GO.tools.shtml * Gene Weaver http://www.GeneWeaver.org * GeneDB http://www.genedb.org/Homepage * Glomerular Activity Response Archive http://gara.bio.uci.edu * GO http://www.geneontology.org/ * Internet Brain Volume Database http://www.cma.mgh.harvard.edu/ibvd/ * ModelDB http://senselab.med.yale.edu/modeldb/ * Mouse Genome Informatics Transgenes ftp://ftp.informatics.jax.org/pub/reports/MGI_PhenotypicAllele.rpt * NCBI Taxonomy Browser http://www.ncbi.nlm.nih.gov/Taxonomy/taxonomyhome.html * NeuroMorpho.Org http://neuromorpho.org/neuroMorpho * NeuronDB http://senselab.med.yale.edu/neurondb * SciCrunch Registry http://neuinfo.org/nif/nifgwt.html?tab=registry * NIF Registry Automated Crawl Data http://lucene1.neuinfo.org/nif_resource/current/ * NITRC http://www.nitrc.org/ * Nuclear Receptor Signaling Atlas http://www.nursa.org * Olfactory Receptor DataBase http://senselab.med.yale.edu/ordb/ * OMIM http://omim.org * OpenfMRI http://openfmri.org * PeptideAtlas http://www.peptideatlas.org * RGD http://rgd.mcw.edu * SFARI Gene: AutDB https://gene.sfari.org/autdb/Welcome.do * SumsDB http://sumsdb.wustl.edu/sums/ * Temporal-Lobe: Hippocampal - Parahippocampal Neuroanatomy of the Rat http://www.temporal-lobe.com/ * The Cell: An Image Library http://www.cellimagelibrary.org/ * Visiome Platform http://platform.visiome.neuroinf.jp/ * WormBase http://www.wormbase.org * YPED http://medicine.yale.edu/keck/nida/yped.aspx * ZFIN http://zfin.org biomedical, bibliographic, linkout, literature is used by: NIF Data Federation
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Gene Ontology Tools
is related to: BAMS Connectivity
is related to: Biological General Repository for Interaction Datasets (BioGRID)
is related to: BioNumbers
is related to: PubMed
is related to: Brain Architecture Management System
is related to: CellML Model Repository
is related to: CHEBI
is related to: Comparative Toxicogenomics Database (CTD)
is related to: Coriell Cell Repositories
is related to: Drug Related Gene Database
is related to: DrugBank
is related to: Gene Weaver
is related to: Internet Brain Volume Database
is related to: Cell Centered Database
is related to: Brede Database
is related to: ModelDB
is related to: NeuronDB
is related to: NeuroMorpho.Org
is related to: Nuclear Receptor Signaling Atlas
is related to: Cell Image Library (CIL)
is related to: Animal Imaging Database
is related to: Olfactory Receptor DataBase
is related to: Glomerular Activity Response Archive
is related to: CRCNS
is related to: OMIM
is related to: Rat Genome Database (RGD)
is related to: Visiome Platform
is related to: NIDA Data Share
is related to: bioDBcore
is related to: Addgene
is related to: Antibody Registry
is related to: Beta Cell Biology Consortium
is related to: FlyBase
is related to: SumsDB
is related to: SciCrunch Registry
is related to: Mouse Genome Informatics Transgenes
is related to: NCBI Taxonomy
is related to: OpenNeuro
is related to: PeptideAtlas
is related to: Temporal-Lobe: Hippocampal - Parahippocampal Neuroanatomy of the Rat
is related to: NIF Registry Automated Crawl Data
is related to: AutDB
is related to: Gene Expression Omnibus
is related to: Gene Ontology
is related to: Avian Brain Circuitry Database
is related to: Zebrafish Information Network (ZFIN)
is related to: GeneDB
is related to: WormBase
is related to: YPED
has parent organization: Integrated
PMID:20387131
PMID:18975149
Data are licensed by their respective owners. Use and distribution is subject to the Terms of Use by the original resource as well as the, Creative Commons Attribution License nlx_149407 http://neuinfo.org/nif/nifgwt.html?query=nlx_149407, https://neuinfo.org/mynif/search.php?q=*&t=indexable&list=cover&nif=nlx_149407-1 SCR_008876 Integrated Manually Extracted Annotation View, NIF Integrated LinkOut, NIF Integrated Manually Extracted Annotation, NIF LinkOut 2026-02-14 02:06:10 0
SynaptomeDB
 
Resource Report
Resource Website
SynaptomeDB (RRID:SCR_000157) SynaptomeDB data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. Ontology-based knowledgebase for synaptic genes. These genes encode components of the synapse including neurotransmitters and their receptors, adhesion / cytoskeletal proteins, scaffold proteins, transporters, and others. It integrates various and complex data sources for synaptic genes and proteins., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, protein, pathway, synaptome, protein-protein interaction, synaptic gene, synapse, motif, presynaptic, postsynaptic, vesicle is related to: Gene Ontology
has parent organization: Johns Hopkins University; Maryland; USA
PMID:22285564 THIS RESOURCE IS NO LONGER IN SERVICE nlx_157656 SCR_000157 2026-02-14 02:05:31 0
MitoMiner
 
Resource Report
Resource Website
50+ mentions
MitoMiner (RRID:SCR_001368) data or information resource, database A database of mitochondrial proteomics data. It includes two sets of proteins: the MitoMiner Reference Set, which has 10477 proteins from 12 species; and MitoCarta, which has 2909 proteins from mouse and human mitochondrial proteins. MitoMiner provides annotation from the Gene Ontology (GO) and UniProt databases. This reference set contains all proteins that are annotated by either of these resources as mitochondrial in any of the species included in MitoMiner. MitoMiner data via is available via Application Programming Interface (API). The client libraries are provided in Perl, Python, Ruby and Java. mitochondrion, proteomics, function, homolog, proteome, protein expression, mass-spectrometry, protein, metabolism, green fluorescent protein tag, ortholog, FASEB list uses: HomoloGene
uses: UniProt
uses: KEGG
uses: OMIM
uses: The Human Protein Atlas
uses: Gene Ontology
MRC PMID:22121219
PMID:19208617
Public, Acknowledgement requested, Code: nlx_152504 SCR_001368 MitoMiner - A database of the mitochondrial proteome 2026-02-14 02:06:04 76
LIPID MAPS Proteome Database
 
Resource Report
Resource Website
1+ mentions
LIPID MAPS Proteome Database (RRID:SCR_003062) LMPD data or information resource, database Database of lipid related proteins representing human and mouse proteins involved in lipid metabolism. Collection of lipid related genes and proteins contains data for genes and proteins from Homo sapiens, Mus musculus, Rattus norvegicus, Saccharomyces cerevisiae, Caenorhabditis elegans, Escherichia coli, Macaca mulata, Drosophila melanogaster, Arabidopsis thaliana and Danio rerio. gene, protein, lipid, metabolism, metabolomics uses: Gene Ontology
uses: KEGG
uses: UniProt
uses: Entrez Gene
uses: ENZYME
has parent organization: LIPID Metabolites And Pathways Strategy
NIGMS PMID:16381922 Free, Freely available nif-0000-03085 http://www.lipidmaps.org/data/proteome/index.cgi SCR_003062 LIPID MAPS Proteome Database (LMPD) 2026-02-14 02:06:13 3
Integrated Molecular Interaction Database
 
Resource Report
Resource Website
1+ mentions
Integrated Molecular Interaction Database (RRID:SCR_003546) IMID data or information resource, database Database for molecular interaction information integrated with various other bio-entity information, including pathways, diseases, gene ontology (GO) terms, species and molecular types. The information is obtained from several manually curated databases and automatic extraction from literature. There are protein-protein interaction, gene/protein regulation and protein-small molecule interaction information stored in the database. The interaction information is linked with relevant GO terms, pathway, disease and species names. Interactions are also linked to the PubMed IDs of the corresponding abstracts the interactions were obtained from. Manually curated molecular interaction information was obtained from BioGRID, IntAct, NCBI Gene, and STITCH database. Pathway related information was obtained from KEGG database, Pathway Interaction database and Reactome. Disease information was obtained from PharmGKB and KEGG database. Gene ontology terms and related information was obtained from Gene Ontology database and GOA database. pathway, disease, gene ontology, specie, interaction, molecular, protein-protein interaction, gene/protein regulation, protein-small molecule interaction, gene, protein, regulation is related to: Gene Ontology
is related to: Entrez Gene
is related to: Pathway Commons
is related to: Biological General Repository for Interaction Datasets (BioGRID)
is related to: IntAct
is related to: Search Tool for Interactions of Chemicals
is related to: KEGG
is related to: Pathway Interaction Database
is related to: Reactome
is related to: PharmGKB
has parent organization: Florida State University; Florida; USA
PMID:22238258 nlx_157667 SCR_003546 2026-02-14 02:05:44 1
Cotton EST Database
 
Resource Report
Resource Website
10+ mentions
Cotton EST Database (RRID:SCR_003301) Cotton EST Database data or information resource, database Database platform for cotton expressed sequence tag (EST)-related information, covering assembled contigs, function annotation, analysis of GO and KEGG, SNP, miRNA, SSR-related marker information. expressed sequence tag, contig, indel mutant, single nucleotide polymorphism, transcription factor, protein kinase, gene, mirna, blast, est-simple sequence repeat, simple sequence repeat, pathway, function is related to: Gene Ontology
is related to: KEGG
has parent organization: East Carolina University; Carolina; USA
PMID:22087239 THIS RESOURCE IS NO LONGER IN SERVICE r3d100011232 https://doi.org/10.17616/R3X63C http://www.leonxie.com/ SCR_003301 2026-02-14 02:05:43 10
SwissLipids
 
Resource Report
Resource Website
10+ mentions
SwissLipids (RRID:SCR_019074) data or information resource, database Expert curated resource that provides framework for integration of lipid and lipidomic data with biological knowledge and models. Provides curated knowledge of lipid structures and metabolism which is used to generate in silico library of feasible lipid structures. These are arranged in hierarchical classification that links mass spectrometry analytical outputs to all possible lipid structures, metabolic reactions and enzymes. Provides reference namespace for lipidomic data publication, data exploration and hypothesis generation. Lipid, lipidomic data, curated lipid data, lipid structure, lipid metabolism, mass spectrometry analytical output, refernce namespace, lipidomic data publication, hypothesis generation uses: UniProt
uses: CHEBI
uses: RHEA
uses: Gene Ontology
Swiss Federal Government ;
SystemsX.ch
DOI:10.1093/bioinformatics/btv285 Free, Freely available r3d100012603 https://doi.org/10.17616/R3TZ18 SCR_019074 2026-02-14 02:06:49 16
ErmineJ
 
Resource Report
Resource Website
50+ mentions
ErmineJ (RRID:SCR_006450) ermineJ software application, data processing software, data analysis software, software resource Data analysis software for gene sets in expression microarray data or other genome-wide data that results in rankings of genes. A typical goal is to determine whether particular biological pathways are doing something interesting in the data. The software is designed to be used by biologists with little or no informatics background. A command-line interface is available for users who wish to script the use of ermineJ. Major features include: * Implementation of multiple methods for gene set analysis: ** Over-representation analysis ** A resampling-based method that uses gene scores ** A rank-based method that uses gene scores ** A resampling-based method that uses correlation between gene expression profiles (a type of cluster-enrichment analysis). * Gene sets receive statistical scores (p-values), and multiple test correction is supported. * Support of the Gene Ontology terminology; users can choose which aspects to analyze. * User files use simple text formats. * Users can modify gene sets or create new ones. * The results can be visualized within the software. * It is simple to compare multiple analyses of the same data set with different settings. * User-definable hyperlinks are provided to external sites to allow more efficient browsing of the results. * For programmers, there is a command line interface as well as a simple application programming interface that can be used to plug ermineJ functionality into your own code Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible microarray, gene ontology, analysis, high-throughput, gene, gene expression, statistical analysis, term enrichment, genome is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of British Columbia; British Columbia; Canada
has parent organization: Columbia University; New York; USA
PMID:16280084 Free for academic use nif-0000-07758 SCR_006450 ermineJ: Gene Ontology analysis for high-throughput data 2026-02-15 09:19:16 50
StRAnGER
 
Resource Report
Resource Website
10+ mentions
StRAnGER (RRID:SCR_004247) StRAnGER software application, data processing software, data analysis software, software resource StRAnGER (Statistical Ranking of ANotated Genomic Experimental Results) is a web application for the automated statistical analysis of annotated gene profiling experiments, exploiting controlled biological vocabularies, like the Gene Ontology or the KEGG pathways terms. Starting from annotated lists of differentially expressed genes StRAnGER repartitions and reorders the initial distribution of terms to define a new distribution of elements where each element pools terms holding the same enrichment score. The elements are then prioritized according to StRAnGER''''s algorithm and, by applying bootstrapping techniques, a corrected measure of the statistical significance of these elements is derived, enabling the selection of terms mapped to these elements, unambiguously associated with respective significant gene sets. Besides their high statistical score, another selection criterion for the terms is the number of their members, something that incurs a biological prioritization in line with a Systems Biology context. Platform: Online tool controlled vocabulary, functional analysis, genomics, annotation, visualization, statistical analysis, term enrichment, ontology or annotation visualization is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: National Hellenic Research Foundation
PMID:21293737 Free for academic use nlx_25932 SCR_004247 Statistical Ranking of ANotated Genomic Experimental Results 2026-02-15 09:18:43 18
EGAN: Exploratory Gene Association Networks
 
Resource Report
Resource Website
1+ mentions
EGAN: Exploratory Gene Association Networks (RRID:SCR_008856) EGAN software application, data processing software, data analysis software, software resource Exploratory Gene Association Networks (EGAN) is a software tool that allows a bench biologist to visualize and interpret the results of high-throughput exploratory assays in an interactive hypergraph of genes, relationships (protein-protein interactions, literature co-occurrence, etc.) and meta-data (annotation, signaling pathways, etc.). EGAN provides comprehensive, automated calculation of meta-data coincidence (over-representation, enrichment) for user- and assay-defined gene lists, and provides direct links to web resources and literature (NCBI Entrez Gene, PubMed, KEGG, Gene Ontology, iHOP, Google, etc.). EGAN functions as a module for exploratory investigation of analysis results from multiple high-throughput assay technologies, including but not limited to: * Transcriptomics via expression microarrays or RNA-Seq * Genomics via SNP GWAS or array CGH * Proteomics via MS/MS peptide identifications * Epigenomics via DNA methylation, ChIP-on-Chip or ChIP-Seq * In-silico analysis of sequences or literature EGAN has been built using Cytoscape libraries for graph visualization and layout, and is comparable to DAVID, GSEA, Ingenuity IPA and Ariadne Pathway Studio. There are pre-collated EGAN networks available for human (Homo sapiens), mouse (Mus musculus), rat (Rattus norvegicus), chicken (Gallus gallus), zebrafish (Danio rerio), fruit fly (Drosophila melanogaster), nematode (Caenorhabditis elegans), mouse-ear cress (Arabidopsis thaliana), rice (Oryza sativa) and brewer's yeast (Saccharomyces cerevisiae). There is now an EGAN module available for GenePattern (human-only). Platform: Windows compatible, Mac OS X compatible, Linux compatible gene, gene association, network, protein-protein interaction, pathway, interaction, annotation, signaling pathway, enrichment, cytoscape, visualization is listed by: 3DVC
is listed by: Gene Ontology Tools
is related to: Gene Ontology
is related to: Cytoscape
has parent organization: UCSF Helen Diller Family Comprehensive Cancer Center Biostatistics Core
NCI P30 CA92103 PMID:19933825 Free for academic use nlx_149222 SCR_008856 Exploratory Gene Association Networks, Exploratory Gene Association Networks (EGAN) 2026-02-15 09:19:58 8
GOdist
 
Resource Report
Resource Website
GOdist (RRID:SCR_005770) GOdist software application, data processing software, data analysis software, software resource GOdist is a Matlab program that analyzes Affymetrix microarray expression data implementing Kolmogorov-Smirnov (KS) continuous statistics approach. It also implements the discrete approach using Fisher exact test employing a two-tailed hypergeometric distribution. GOdist enables detection of both kinds of changes within specific GO terms represented on the array in relation to different populations: the global array population, the direct parents of the analyzed GO term and the global parent of it (e.g. biological process, molecular function or cellular component). Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible statistical analysis, function, gene, gene expression, gene ontology, matlab, affymetrix, microarray, biological process, molecular function, cellular component, fisher exact test, kolmogorov-smirnov is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Hebrew University of Jerusalem; Jerusalem; Israel
PMID:15550480 Free for academic use nlx_149260 SCR_005770 2026-02-15 09:19:02 0
THEA - Tools for High-throughput Experiments Analysis
 
Resource Report
Resource Website
THEA - Tools for High-throughput Experiments Analysis (RRID:SCR_005802) THEA software application, data processing software, data analysis software, software resource THIS RESOURCE IS NO LONGER IN SERVICE, on documented July 16, 2012. An integrated information processing system dedicated to the analysis of post-genomic data. It allows automatic annotation of data issued from classification systems with selected biological information (including the Gene Ontology). Users can either manually search and browse through these annotations, or automatically generate meaningful generalizations according to statistical criteria (data mining). Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible high-throughput, analysis, ontology, microarray, genomic, annotation, gene ontology, data mining, statistical analysis is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Virtual Biology Lab
French Ministry of Higher Education and Research ;
Bioinformatic Program
PMID:15130932 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149290 SCR_005802 Tools for High-throughput Experiments Analysis 2026-02-15 09:19:12 0
MAPPFinder
 
Resource Report
Resource Website
10+ mentions
MAPPFinder (RRID:SCR_005791) MAPPFinder software application, data processing software, data analysis software, software resource MAPPFinder is an accessory program for GenMAPP. This program allows users to query any existing GenMAPP Expression Dataset Criterion against GO gene associations and GenMAPP MAPPs (microarray pathway profiles). The resulting analysis provides the user with results that can be viewed directly upon the Gene Ontology hierarchy and within GenMAPP, by selecting terms or MAPPs of interest. Platform: Windows compatible gene, gene ontology, gene association, gene expression, profile, microarray, pathway, statistical analysis is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of California at San Francisco; California; USA
has parent organization: Gene Map Annotator and Pathway Profiler
University of California at San Francisco; California; USA ;
San Francisco General Hospital; California; USA ;
NHLBI ;
NCRR MO1RR00083
PMID:12540299 Free for academic use nlx_149270 SCR_005791 2026-02-15 09:19:03 26
GOArray
 
Resource Report
Resource Website
1+ mentions
GOArray (RRID:SCR_005785) GOArray software application, data processing software, data analysis software, software resource GOArray is a Perl program which inputs a lists of genes annotated as of interest (GOI) or not, and determines if any associated GO terms have an overrepresentation of GOI. A permutation test is optionally used to assess confidence in the results. Output includes multiple visualizations and supplementary information and, for future reference, a summary of the statistical methods used. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible perl, gene, visualization, gene ontology, statistical analysis is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Yale School of Medicine; Connecticut; USA
Free for academic use nlx_149259 http://goarray.med.yale.edu/GOArray/ SCR_005785 2026-02-15 09:19:03 1
OnEx - Ontology Evolution Explorer
 
Resource Report
Resource Website
1+ mentions
OnEx - Ontology Evolution Explorer (RRID:SCR_000602) OnEx web application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 6,2023. Web-based application that integrates versions of 16 life science ontologies including the Gene Ontology, NCI Thesaurus and selected OBO ontologies with data leading back to 2002 in a common repository to explore ontology changes. It allows to study and apply the evolution of these integrated ontologies on three different levels. It provides global ontology evolution statistics and ontology-specific evolution trends for concepts and relationships and it allows the migration of annotations in case a new ontology version was released ontology, gene, protein, function, process, component, ontology or annotation browser, evolution, trend, annotation, version is listed by: OMICtools
is listed by: Gene Ontology Tools
is related to: Gene Ontology
is related to: NCI Thesaurus
is related to: OBO
has parent organization: University of Leipzig; Saxony; Germany
BMBF 01AK803E;
DFG
PMID:19678926 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02273, nlx_149129 http://www.izbi.de/onex, http://aprilia.izbi.uni-leipzig.de:8080/onex/ SCR_000602 Ontology Evolution Explorer (OnEx), Ontology Evolution Explorer 2026-02-15 09:17:57 1

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.