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
LegumeIP
 
Resource Report
Resource Website
10+ mentions
LegumeIP (RRID:SCR_008906) LegumeIP service resource, data or information resource, data analysis service, database, production service resource, analysis service resource LegumeIP is an integrative database and bioinformatics platform for comparative genomics and transcriptomics to facilitate the study of gene function and genome evolution in legumes, and ultimately to generate molecular based breeding tools to improve quality of crop legumes. LegumeIP currently hosts large-scale genomics and transcriptomics data, including: * Genomic sequences of three model legumes, i.e. Medicago truncatula, Glycine max (soybean) and Lotus japonicus, including two reference plant species, Arabidopsis thaliana and Poplar trichocarpa, with the annotation based on UniProt TrEMBL, InterProScan, Gene Ontology and KEGG databases. LegumeIP covers a total 222,217 protein-coding gene sequences. * Large-scale gene expression data compiled from 104 array hybridizations from L. japonicas, 156 array hybridizations from M. truncatula gene atlas database, and 14 RNA-Seq-based gene expression profiles from G. max on different tissues including four common tissues: Nodule, Flower, Root and Leaf. * Systematic synteny analysis among M. truncatula, G. max, L. japonicus and A. thaliana. * Reconstruction of gene family and gene family-wide phylogenetic analysis across the five hosted species. LegumeIP features comprehensive search and visualization tools to enable the flexible query on gene annotation, gene family, synteny, relative abundance of gene expression. gene function, genome evolution, legume, gene, genome, plant, genomics, transcriptomic, gene annotation, gene family, synteny, gene expression, blast, genomic sequence, microarray, rna-seq, comparative genomics, bio.tools is listed by: 3DVC
is listed by: Debian
is listed by: bio.tools
is related to: UniProt
is related to: InterProScan
is related to: Gene Ontology
is related to: KEGG
has parent organization: Samuel Roberts Noble Foundation
Samuel Roberts Noble Foundation ;
NSF ABI-0960897
PMID:22110036 biotools:legumeip, nlx_151455 https://bio.tools/legumeip SCR_008906 LegumeIP: an integrative database for comparative genomics and transcriptomics of model legumes, LegumeIP - An Integrative Platform to Study Gene Function and Genome Evolution in Legumes 2026-07-28 09:42:18 19
GOMO - Gene Ontology for Motifs
 
Resource Report
Resource Website
1+ mentions
GOMO - Gene Ontology for Motifs (RRID:SCR_008864) GOMO software application, service resource, data analysis service, software resource, data processing software, production service resource, analysis service resource Gene Ontology for Motifs (GOMO) is an alignment- and threshold-free comparative genomics approach for assigning functional roles to DNA regulatory motifs from DNA sequence. The algorithm detects associations between a user-specified DNA regulatory motif (expressed as a position weight matrix; PWM) and Gene Ontology terms. The original method for predicting the roles of transcription factors (TFs starts with a PWM motif describing the DNA-binding affinity of the TF. GOMO uses the PWM to score the promoter region of each gene in the genome for its likelihood to be bound by the TF. The resulting ''''affinity'''' scores are then used to test each term in the Gene Ontology for association with high-scoring genes. The algorithm was subsequently extended to leverage conserved signals using multiple, related species in a comparative approach, which greatly improves the resulting annotations. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene, motif, genomics, gene ontology, function, compare, ontology or annotation editor, statistical analysis, dna binding motif, dna binding, dna, transcription factor, sequence is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of Queensland; Brisbane; Australia
has parent organization: MEME Suite - Motif-based sequence analysis tools
Australian Research Council ;
University of Queensland; Brisbane; Australia ;
International Research Tuition Award ;
NCRR R01 RR021692
PMID:20147307
PMID:18544606
Free for academic use nlx_149250 SCR_008864 Gene Ontology for Motifs 2026-07-28 09:42:24 3
Onto-Express To Go (OE2GO)
 
Resource Report
Resource Website
Onto-Express To Go (OE2GO) (RRID:SCR_008854) OE2GO software application, service resource, data analysis service, software resource, text-mining software, production service resource, analysis service resource Onto-Express is a web-based tool in the Onto-Tools suite that performs automated function profiling for a list of differentially expressed genes. However, Onto-Express does not support functional profiling for the organisms that do not have annotations in public domain, or use of custom (i.e. user-defined) ontologies. This limitation is also true for most of the other existing tools for functional profiling, which means that researchers working with uncommon organisms and/or new annotations or ontologies may be forced to construct such profiles manually. Onto-Express To Go (OE2GO) is a new tool added to the Onto-Tools ensemble to address these issues. OE2GO is built on top of OE to leverage its existing functionality. In OE2GO, the users now have an option to use either the Onto-Tools database as a source of functional annotations or provide their own annotations in a separate file. Currently, OE2GO supports annotation file in the Gene Ontology format. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene, gene expression, annotation, data mining, ontology browser, annotation browser, ontology search engine, annotation search engine, ontology visualization, annotation visualization, statistical analysis, term enrichment, browser, visualization, search engine is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Wayne State University; Michigan; USA
PMID:17584796 Free for academic use nlx_149112 SCR_008854 Onto-Express-to-go, Onto-Express To Go 2026-07-28 09:42:17 0
Renal Disease Portal
 
Resource Report
Resource Website
Renal Disease Portal (RRID:SCR_009030) Renal Disease Portal data set, disease-related portal, data or information resource, topical portal, portal An integrated resource for information on genes, QTLs and strains associated with a variety of kidney and renal system conditions such as Renal Hypertension, Polycystic Kidney Disease and Renal Insufficiency, as well as Kidney Neoplasms. gene, quantitative trait locus, strain, renal hypertension, kidney neoplasm, phenotype, pathway, biological process, disease, kidney, genome, gviewer, chromosome, molecular function, cellular component, visualization, synteny is related to: NIDDK Information Network (dkNET)
is related to: Gene Ontology
has parent organization: Rat Genome Database (RGD)
Renal disease, Renal hypertension, Polycystic kidney disease, Renal insufficiency, Kidney neoplasm, Diabetes Insipidus, Hyperoxaluria, Renal hypertension, Nephritis, Nephrocalcinosis, Nephrolithiasis, Nephrosis, Renal Fibrosis, Inborn Error of Renal Tubular Transport, Uremia nlx_153941 SCR_009030 RGD Renal Disease Portal 2026-07-28 09:42:17 0
Pathway Analysis Tool for Integration and Knowledge Acquisition
 
Resource Report
Resource Website
1+ mentions
Pathway Analysis Tool for Integration and Knowledge Acquisition (RRID:SCR_002100) PATIKA data or information resource, database, pathway analysis software The human pathway database which contains different biological entities and reactions and software tools for analysis. PATIKA Database integrates data from several sources, including Entrez Gene, UniProt, PubChem, GO, IntAct, HPRD, and Reactome. Users can query and access this data using the PATIKAweb query interface. Users can also save their results in XML or export to common picture formats. The BioPAX and SBML exporters can be used as part of this Web service. human, pathway, reaction, database, pathway analysis software, web service, biological entity, biological reaction uses: Entrez Gene
uses: UniProt
uses: PubChem
uses: Gene Ontology
uses: IntAct
uses: HPRD - Human Protein Reference Database
uses: Reactome
PMID:12117798
PMID:14960461
THIS RESOURCE IS NO LONGER IS SERVICE. nif-0000-20882 http://www.cs.bilkent.edu.tr/~patikaweb/ SCR_002100 Pathway Analysis Tool for Integration and Knowledge Acquisition (PATIKA), PATIKA - Pathway Analysis Tools for Integration and Knowledge Acquisition 2026-07-28 09:40:20 2
SynGO
 
Resource Report
Resource Website
100+ mentions
SynGO (RRID:SCR_017330) service resource, data or information resource, data analysis service, production service resource, ontology, 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 2026-07-28 09:44:33 134
GOnet
 
Resource Report
Resource Website
1+ mentions
GOnet (RRID:SCR_018977) service resource, software resource, data access protocol, web service 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 2026-07-28 09:45:02 3
GeneSpeed- A Database of Unigene Domain Organization
 
Resource Report
Resource Website
GeneSpeed- A Database of Unigene Domain Organization (RRID:SCR_002779) service resource, resource, data or information resource, data analysis service, database, production service resource, analysis service resource THIS RESOURCE IS NO LONGER IN SERVICE, documented on July 16, 2013. Database and customized tools to study the PFAM protein domain content of the transcriptome for all expressed genes of Homo sapiens, Mus musculus, Drosophila melanogaster, and Caenorhabditis elegans tethered to both a genomics array repository database and a range of external information resources. GeneSpeed has merged information from several existing data sets including the Gene Ontology Consortium, InterPro, Pfam, Unigene, as well as micro-array datasets. GeneSpeed is a database of PFAM domain homology contained within Unigene. Because Unigene is a non-redundant dbEST database, this provides a wide encompassing overview of the domain content of the expressed transcriptome. We have structured the GeneSpeed Database to include a rich toolset allowing the investigator to study all domain homology, no matter how remote. As a result, homology cutoff score decisions are determined by the scientist, not by a computer algorithm. This quality is one of the novel defining features of the GeneSpeed database giving the user complete control of database content. In addition to a domain content toolset, GeneSpeed provides an assortment of links to external databases, a unique and manually curated Transcription Factor Classification list, as well as links to our newly evolving GeneSpeed BetaCell Database. GeneSpeed BetaCell is a micro-array depository combined with custom array analysis tools created with an emphasis around the meta analysis of developmental time series micro-array datasets and their significance in pancreatic beta cells. molecular neuroanatomy resource, drosophila melanogaster, genome, caenorhabditis elegans, c. elegans, genomics, homo sapiens, mus musculus, protein domain, transcriptome is related to: Gene Ontology
is related to: InterPro
is related to: Pfam
is related to: UniGene
has parent organization: University of Colorado Denver; Colorado; USA
NIDDK P30DK57516;
NIDDK DK61248
PMID:17132830 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02887 http://genespeed.uchsc.edu/, http://genespeed.ccf.org SCR_002779 GeneSpeed Database 2026-07-28 09:40:31 0
GreenPhylDB
 
Resource Report
Resource Website
10+ mentions
GreenPhylDB (RRID:SCR_002834) GreenPhylDB service resource, data or information resource, data analysis service, database, production service resource, analysis 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 2026-07-28 09:40:41 19
FunSimMat
 
Resource Report
Resource Website
1+ mentions
FunSimMat (RRID:SCR_002729) FunSimMat service resource, data or information resource, data analysis service, database, data access protocol, software resource, production service resource, web service, analysis service resource FunSimMat is a comprehensive resource of semantic and functional similarity values. It allows ranking disease candidate proteins for OMIM diseases and searching for functional similarity values for proteins (extracted from UniProt), and protein families (Pfam, SMART). FunSimMat provides several different semantic and functional similarity measures for each protein pair using the Gene Ontology annotation from UniProtKB and the Gene Ontology Annotation project at EBI (GOA). There are several search options available: Disease candidate prioritization: * Rank candidate proteins using any OMIM disease entry * Compare a list of proteins to any OMIM disease entry * Compare all human proteins to any OMIM disease entry Functional similarity: * Compare one protein / protein family to a list of proteins / protein families * Compare a list of GO terms to a list of proteins / protein families Semantic similarity: * For a list of GO terms, FunSimMat performs an all-against-all comparison and displays the semantic similarity values. FunSimMat provides an XML-RPC interface for performing automatic queries and processing of the results as well as a RestLike Interface. Platform: Online tool functional similarity value, protein family, protein similarity, semantic similarity value, similarity value, functional similarity, disease gene candidate prioritization, disease, protein, protein family, disease candidate prioritization, semantic similarity, gene ontology, visualization, annotation, database or data warehouse is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Max-Planck-Institute for Informatics; Saarbrucken; Germany
German National Genome Research Network 01GR0453;
Klinische Forschergruppe KFO 129/1-1;
Klinische Forschergruppe KFO 129/1-2;
European Union LSHG-CT-2003-503265
PMID:19923227
PMID:17932054
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02860 SCR_002729 FunSimMat - Functional Similarity Matrix 2026-07-28 09:40:40 1
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, source code, software resource, image collection 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 2026-07-28 09:40:33 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 service resource, data analysis service, source code, software resource, production service resource, analysis service resource 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 2026-07-28 09:40:39 3
MouseNET
 
Resource Report
Resource Website
1+ mentions
MouseNET (RRID:SCR_003357) mouseNet service resource, data or information resource, data analysis service, database, production service resource, analysis 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 2026-07-28 09:40:46 3
MEME Suite - Motif-based sequence analysis tools
 
Resource Report
Resource Website
1000+ mentions
MEME Suite - Motif-based sequence analysis tools (RRID:SCR_001783) MEME Suite software application, service resource, data analysis software, data or information resource, data analysis service, database, data processing software, software resource, source code, production service resource, analysis service resource Suite of motif-based sequence analysis tools to discover motifs using MEME, DREME (DNA only) or GLAM2 on groups of related DNA or protein sequences; search sequence databases with motifs using MAST, FIMO, MCAST or GLAM2SCAN; compare a motif to all motifs in a database of motifs; associate motifs with Gene Ontology terms via their putative target genes, and analyze motif enrichment using SpaMo or CentriMo. Source code, binaries and a web server are freely available for noncommercial use. gene ontology, motif, comparative genomics, dna regulatory motif, dna sequence, dna, gene, transcription factor, genome, protein, analysis, function analysis, comparison, cluster, enrichment analysis, sequence analysis, bio.tools, FASEB list lists: DREME
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
is related to: Glam2
is related to: ANNOgesic
is related to: memesuite-lite
has parent organization: National Biomedical Computation Resource
is parent organization of: GOMO - Gene Ontology for Motifs
NCRR R01 RR021692 PMID:19458158
DOI:10.1093/nar/gkl198
Free, Freely available nif-0000-10298, biotools:meme_suite, OMICS_08103 https://bio.tools/meme_suite http://meme.sdsc.edu/meme4_6_1/intro.html, http://meme.nbcr.net/meme/, https://sources.debian.org/src/meme/ SCR_001783 The MEME Suite 2026-07-28 09:40:24 2091
AmiGO
 
Resource Report
Resource Website
1000+ mentions
AmiGO (RRID:SCR_002143) AmiGO service resource, data or information resource, data analysis service, database, production service resource, analysis service resource Web tool to search, sort, analyze, visualize and download data of interest. Along with providing details of the ontologies, gene products and annotations, features a BLAST search, Term Enrichment and GO Slimmer tools, the GO Online SQL Environment and a user help guide.Used at the Gene Ontology (GO) website to access the data provided by the GO Consortium. Developed and maintained by the GO Consortium. search, sort, analyze, visualize, data, ontology, gene, annotation, FASEB list uses: GOlr
is used by: NIF Data Federation
is listed by: OMICtools
is listed by: Gene Ontology Tools
is related to: ASAP
is related to: Candida Genome Database
is related to: Berkeley Bioinformatics Open-Source Projects
is related to: ECO
is related to: Zebrafish Information Network (ZFIN)
is related to: Gramene
is related to: WormBase
is related to: NCBI Protein Database
is related to: UniProtKB
is related to: GeneDB Lmajor
is related to: TAIR
is related to: SGD
is related to: GeneDB Tbrucei
is related to: VMD
is related to: JCVI CMR
is related to: go-db-perl
is related to: Mouse Genome Informatics (MGI)
is related to: NCBI
is related to: FlyBase
is related to: GeneDB Pfalciparum
is related to: PomBase
is related to: Pseudomonas Genome Database
is related to: Dictyostelium discoideum genome database
is related to: Plant Ontology
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: MeGO
is related to: ASPGD
is related to: EcoCyc
is related to: Reactome
is related to: SGN
is related to: GO-Module
is related to: Songbird Brain Transcriptome Database
is related to: Rat Genome Database (RGD)
is related to: RamiGO
has parent organization: Gene Ontology
NHGRI P41 HG002273 PMID:19033274 Free, Available for download, Freely available nif-0000-20935, OMICS_02266 http://sourceforge.net/projects/geneontology/ SCR_002143 GO Consortium, AmiGO, AmiGO 2, AmiGene Ontology, Gene Ontology Database, Gene Ontology Consortium, GO Database, The Gene Ontology Consortium 2026-07-28 09:40:21 1242
FlyMine
 
Resource Report
Resource Website
100+ mentions
FlyMine (RRID:SCR_002694) FlyMine data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 14,2026. Integrated database of genomic, expression and protein data for Drosophila, Anopheles, C. elegans and other organisms. You can run flexible queries, export results and analyze lists of data. FlyMine presents data in categories, with each providing information on a particular type of data (for example Gene Expression or Protein Interactions). Template queries, as well as the QueryBuilder itself, allow you to perform searches that span data from more than one category. Advanced users can use a flexible query interface to construct their own data mining queries across the multiple integrated data sources, to modify existing template queries or to create your own template queries. Access our FlyMine data via our Application Programming Interface (API). We provide client libraries in the following languages: Perl, Python, Ruby and & Java API anopheles, genome, c. elegans, drosophila, gene, chromosomal location, genomics, proteomics, gene expression, interaction, homology, function, regulation, protein, phenotype, pathway, disease, publication, FASEB list is related to: FlyBase
is related to: UniProt
is related to: Ensembl
is related to: InterPro
is related to: Biological General Repository for Interaction Datasets (BioGRID)
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: Tree families database
is related to: IntAct
is related to: Gene Ontology
is related to: GOA
is related to: ArrayExpress
is related to: REDfly Regulatory Element Database for Drosophilia
is related to: KEGG
is related to: Reactome
has parent organization: University of Cambridge; Cambridge; United Kingdom
Wellcome Trust 067205;
NHGRI
PMID:17615057 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02845 SCR_002694 2026-07-28 09:40:29 104
GONUTS
 
Resource Report
Resource Website
1+ mentions
GONUTS (RRID:SCR_000653) GONUTS database, data or information resource, wiki, narrative resource A wiki where users of the Gene Ontology can contribute and view notes about how specific GO terms are used. GONUTS can also be used as a GO term browser, or to search for GO annotations of specific genes from included organisms. The rationale for this wiki is based on helping new users of the gene ontology understand and use it. The GONUTS wiki is not an official product of the the Gene Ontology consortium. The GO consortium has a public wiki at their website, http://wiki.geneontology.org/. Maintaining the ontology involves many decisions to carefully choose terms and relationships. These decisions are currently made at GO meetings and via online discussion using the GO mailing lists and the Sourceforge curator request tracker. However, it is difficult for someone starting to use GO to understand these decisions. Some insight can be obtained by mining the tracker, the listservs and the minutes of GO meetings, but this is difficult, as these discussions are often dispersed and sometimes don't contain the GO accessions in the relevant messages. Wikis provide a way to create collaboratively written documentation for each GO term to explain how it should be used, how to satisfy the true path requirement, and whether an annotation should be placed at a different level. In addition, the wiki pages provide a discussion space, where users can post questions and discuss possible changes to the ontology. GONUTS is currently set up so anyone can view or search, but only registered users can edit or add pages. Currently registered users can create new users, and we are working to add at least one registered user for each participating database (So far we have registered users at EcoliHub, EcoCyc, GOA, BeeBase, SGD, dictyBase, FlyBase, WormBase, TAIR, Rat Genome Database, ZFIN, MGI, UCL and AgBase... ontology or annotation browser, ontology or annotation search engine, ontology or annotation editor, protein is listed by: Gene Ontology Tools
is listed by: OMICtools
is related to: Gene Ontology
has parent organization: EcoliHub
NIGMS 1U24 GM077905-01;
NIGMS U24 GM088849
PMID:22110029 Free for academic use, The community can contribute to this resource OMICS_02268, nlx_30164 SCR_000653 Gene Ontology Normal Usage Tracking System, GONUTS wiki 2026-07-28 09:40:04 1
Aging Portal
 
Resource Report
Resource Website
Aging Portal (RRID:SCR_000496) Aging data or information resource, catalog, database, topical portal, portal Portal devoted to aging relevant scientific data and resources. late adult human, senescence uses: Aging Genes and Interventions Database
uses: anage
uses: Human Life-Table Database
uses: Gene Ontology
uses: Grants.gov
uses: Integrated Blogs
uses: Integrated Clinical Trials
uses: Integrated Videos
uses: Integrated Grants
uses: Lifespan Observations Database
uses: One Mind Biospecimen Bank Listing
uses: Gait in Parkinson's Disease
uses: SciCrunch Registry
has parent organization: SciCrunch
Aging NIA 1R03AG043018-01 Restricted nlx_158366 SCR_000496 2026-07-28 09:40:00 0
Semantic Measures Library
 
Resource Report
Resource Website
Semantic Measures Library (RRID:SCR_001383) SML software library, software toolkit, software resource Open source Java library dedicated to semantic measures computation and analysis. Tools based on the SML are also provided through the SML-Toolkit, a command line software giving access to some of the functionalities of the library. The SML and the toolkit can be used to compute semantic similarity and semantic relatedness between semantic elements (e.g. concepts, terms) or entities semantically characterized (e.g. entities defined in a semantic graph, documents annotated by concepts defined in an ontology). semantic measure, semantic similarity, semantic relatedness, functional similarity, gene ontology, annotation, parse, gene, disease ontology, mesh, rdf, owl, umls, snomed-ct, java, semantic, command line is listed by: FORCE11
is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Ecole des Mines d'Ales; Ales; France
Ecole des Mines d'Ales; Ales; France ;
LGI2P Research Center
PMID:24108186 Free, Available for download, Freely available nlx_152555 http://www.semantic-measures-library.org SCR_001383 SML-Toolkit, Semantic Measures Library and ToolKit, Semantic Measures Library & ToolKit 2026-07-28 09:40:14 0
InnateDB
 
Resource Report
Resource Website
100+ mentions
InnateDB (RRID:SCR_006714) InnateDB data or information resource, database Publicly available database of the genes, proteins, experimentally-verified interactions and signaling pathways involved in the innate immune response of humans, mice and bovines to microbial infection. The database captures coverage of the innate immunity interactome by integrating known interactions and pathways from major public databases together with manually-curated data into a centralized resource. The database can be mined as a knowledgebase or used with the integrated bioinformatics and visualization tools for the systems level analysis of the innate immune response. Although InnateDB curation focuses on innate immunity-relevant interactions and pathways, it also incorporates detailed annotation on the entire human, mouse and bovine interactomes by integrating data (178,000+ interactions & 3,900+ pathways) from several of the major public interaction and pathway databases. InnateDB also has integrated human, mouse and bovine orthology predictions generated using Ortholgue software. Ortholgue uses a phylogenetic distance-based method to identify possible paralogs in high-throughput orthology predictions. Integrated human and mouse conserved gene order and synteny information has also been determined to provide further support for orthology predictions. InnateDB Capabilities: * View statistics for manually-curated innate immunity relevant molecular interactions. New manually curated interactions are submitted weekly. * Search for genes and proteins of interest. * Search for experimentally-verified molecular interactions by gene/protein name, interaction type, cell type, etc. * Search genes/interactions belonging to 3,900 pathways. * Visualize interactions using an intuitive subcellular localization-based layout in Cerebral. * Upload your own list of genes along with associated gene expression data (from up to 10 experimental conditions) to interactively analyze this data in a molecular interaction network context. Once you have uploaded your data, you will be able to interactively visualize interaction networks with expression data overlaid; carry out Pathway, Gene Ontology and Transcription Factor Binding Site over-representation analyses; construct orthologous interaction networks in other species; and much more. * Access curated interaction data via a dedicated PSICQUIC webservice. gene, immune response, pathway, protein, signaling pathway, interaction, immune, signaling response, gene, orthology prediction, orthology, ortholg, annotation, interactome, gene expression, molecule, protein-protein interaction, molecular interaction, visualization, nucleic acid-protein, nucleic acid, network, web service, transcription factor binding site, software resource, FASEB list is listed by: re3data.org
is related to: IMEx - The International Molecular Exchange Consortium
is related to: Interaction Reference Index
is related to: ConsensusPathDB
is related to: IMEx - The International Molecular Exchange Consortium
is related to: PSICQUIC Registry
is related to: PSICQUIC Registry
is related to: Gene Ontology
is related to: IntAct
has parent organization: Simon Fraser University; British Columbia; Canada
has parent organization: University of British Columbia; British Columbia; Canada
works with: IMEx - The International Molecular Exchange Consortium
Microbial infection, Allergy, Asthma Michael Smith Foundation for Health Research ;
AllerGen 12ASI1;
AllerGen 12B&B2;
Teagasc RMIS6018;
European Union PSIMEx project contract FP7-HEALTH-2007-223411
PMID:23180781
PMID:18766178
Free, Freely available nif-0000-20808, r3d100010676 https://doi.org/10.17616/R36S43 SCR_006714 A Knowledge Resource for Innate Immunity Interactions and Pathways, InnateDB: Systems Biology of the Innate Immune Response, InnateDB - A Knowledge Resource for Innate Immunity Interactions and Pathways 2026-07-28 09:41:38 496

Can't find your Tool?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.

Can't find the RRID you're searching for? X
X
  1. NIDM Terminology Resources

    Welcome to the nidm-terms Resources search. From here you can search through a compilation of resources used by nidm-terms and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that nidm-terms has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on nidm-terms then you can log in from here to get additional features in nidm-terms such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into nidm-terms you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.