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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.

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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
GeneTrail
 
Resource Report
Resource Website
100+ mentions
GeneTrail (RRID:SCR_006250) GeneTrail analysis service resource, data analysis service, production service resource, service resource A web-based application that analyzes gene sets for statistically significant accumulations of genes that belong to some functional category. Considered category types are: KEGG Pathways, TRANSPATH Pathways, TRANSFAC Transcription Factor, GeneOntology Categories, Genomic Localization, Protein-Protein Interactions, Coiled-coil domains, Granzyme-B clevage sites, and ELR/RGD motifs. The web server provides two statistical approaches, "Over-Representation Analysis" (ORA) comparing a reference set of genes to a test set, and "Gene Set Enrichment Analysis" (GSEA) scoring sorted lists of genes., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. pathway, microarray, enrichment, genomic, proteomic, function, transcription factor, genomic localization, protein-protein interaction, coiled-coil domain, granzyme-b clevage site, motif, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: KEGG
is related to: TRANSPATH
is related to: TRANSFAC
is related to: Gene Ontology
has parent organization: Saarland University; Saarbrucken; Germany
PMID:17526521 THIS RESOURCE IS NO LONGER IN SERVICE biotools:genetrail, OMICS_02236 https://bio.tools/genetrail SCR_006250 2026-08-20 09:27:05 114
SeqAnt
 
Resource Report
Resource Website
1+ mentions
SeqAnt (RRID:SCR_005186) SeqAnt analysis service resource, data analysis service, production service resource, service resource, software resource A free web service and open source software package that performs rapid, automated annotation of DNA sequence variants (single base mutations, insertions, deletions) discovered with any sequencing platform. Variant sites are characterized with respect to their functional type (Silent, Replacement, 5' UTR, 3' UTR, Intronic, Intergenic), whether they have been previously submitted to dbSNP, and their evolutionary conservation. Annotated variants can be viewed directly on the web browser, downloaded in a tab delimited text file, or directly uploaded in a Browser Extended Data (BED) format to the UCSC genome browser. SeqAnt further identifies all loci harboring two or more coding sequence variants that help investigators identify potential compound heterozygous loci within exome sequencing experiments. In total, SeqAnt resolves a significant bottleneck by allowing an investigator to rapidly prioritize the functional analysis of those variants of interest. annotation, dna sequence variant, single base mutation, insertion, deletion, sequencing, mutation, variant, sequence variant, perl, sequence, genome is listed by: OMICtools
has parent organization: Emory University; Georgia; USA
has parent organization: SourceForge
PMID:20854673 GNU General Public License, v2 OMICS_00182 SCR_005186 SeqAnt - Sequence Annotator 2026-08-21 12:37:31 2
GeneMANIA
 
Resource Report
Resource Website
1000+ mentions
GeneMANIA (RRID:SCR_005709) GeneMANIA analysis service resource, data analysis service, data or information resource, database, production service resource, service resource, software resource Data analysis service to predict the function of your favorite genes and gene sets. Indexing 1,421 association networks containing 266,984,699 interactions mapped to 155,238 genes from 7 organisms. GeneMANIA interaction networks are available for download in plain text format. GeneMANIA finds other genes that are related to a set of input genes, using a very large set of functional association data. Association data include protein and genetic interactions, pathways, co-expression, co-localization and protein domain similarity. You can use GeneMANIA to find new members of a pathway or complex, find additional genes you may have missed in your screen or find new genes with a specific function, such as protein kinases. Your question is defined by the set of genes you input. If members of your gene list make up a protein complex, GeneMANIA will return more potential members of the protein complex. If you enter a gene list, GeneMANIA will return connections between your genes, within the selected datasets. GeneMANIA suggests annotations for genes based on Gene Ontology term enrichment of highly interacting genes with the gene of interest. GeneMANIA is also a gene recommendation system. GeneMANIA is also accessible via a Cytoscape plugin, designed for power users. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene, association data, protein interaction, genetic interaction, pathway, co-expression, co-localization, protein, software library, statistical analysis, term enrichment, analysis, browser, gene ontology, gene predicting, gene prioritization, database or data warehouse, other analysis, interaction browser, protein-protein interaction, interaction, FASEB list is listed by: Gene Ontology Tools
is related to: Cytoscape
is related to: Gene Ontology
is related to: PSICQUIC Registry
has parent organization: University of Toronto; Ontario; Canada
Genome Canada ;
Ontario Ministry of Research and Innovation 2007-OGI-TD-05
PMID:20576703
PMID:18613948
PMID:20926419
Open unspecified license, Free for academic use nlx_149159, r3d100013978 https://doi.org/10.17616/R31NJNA2 SCR_005709 2026-08-21 12:37:37 4535
GoFish
 
Resource Report
Resource Website
1+ mentions
GoFish (RRID:SCR_005682) GoFish analysis service resource, data analysis service, production service resource, service resource, software resource, source code Software program, available as a Java applet online or to download, allows the user to select a subset of Gene Ontology (GO) attributes, and ranks genes according to the probability of having all those attributes., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, ontology or annotation browser, java, windows, mac os x, linux, unix, bio.tools is listed by: Gene Ontology Tools
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
has parent organization: University of Toronto; Ontario; Canada
has parent organization: Harvard Medical School; Massachusetts; USA
Aventis Pharmaceuticals ;
Howard Hughes Medical Institute ;
NHGRI
PMID:12691998 THIS RESOURCE IS NO LONGER IN SERVICE biotools:gofish, nlx_149126, OMICS_02272 http://llama.mshri.on.ca/Software.html, https://bio.tools/gofish SCR_005682 2026-08-21 12:37:46 1
Integrated Animals
 
Resource Report
Resource Website
Integrated Animals (RRID:SCR_001421) biomaterial supply resource, material resource, organism supplier Integrated Animals is a virtual database currently indexing available animal strains and mutants from: AGSC (Ambystoma), BCBC (mice), BDSC (flies), CWRU Cystic Fibrosis Mouse Models (mice), DGGR (flies), FlyBase (flies), IMSR (mice), MGI (mice), MMRRC (mice), NSRRC (pig), NXR (Xenopus), RGD (rats), Sperm Stem Cell Libraries for Biological Research (rats), Tetrahymena Stock Center (Tetrahymena), WormBase (worms), XGSC (Xiphophorus), ZFIN (zebrafish), and ZIRC (zebrafish). non human animal, mutant, database, integrated, nif, FASEB list uses: Mouse Genome Informatics (MGI)
uses: Beta Cell Biology Consortium
uses: Zebrafish Information Network (ZFIN)
uses: International Mouse Strain Resource
uses: Bloomington Drosophila Stock Center
uses: Rat Genome Database (RGD)
uses: Zebrafish International Resource Center
uses: Ambystoma Genetic Stock Center
uses: Kyoto Stock Center
uses: FlyBase
uses: Mutant Mouse Resource and Research Center
uses: National Swine Resource and Research Center
uses: National Xenopus Resource
uses: CWRU In Vivo Animal Facilities
uses: Sperm Stem Cell Libraries for Biological Research
uses: Tetrahymena Stock Center
uses: WormBase
uses: Xiphophorus Genetic Stock Center
is used by: NIF Data Federation
is used by: NIDDK Information Network (dkNET)
has parent organization: Integrated
Free, Freely Available nif-0000-08137 https://legacy.neuinfo.org/mynif/search.php?q=*&t=indexable&nif=nlx_154697-1 http://neuinfo.org/nif/nifgwt.html?query=nif-0000-08137, https://www.neuinfo.org/mynif/search.php?q=*&t=indexable&nif=nif-0000-08137-1 SCR_001421 NIF Animals, NIF Integrated Animals, Integrated Animal 2026-08-21 12:36:23 0
Drosophila anatomy and development ontologies
 
Resource Report
Resource Website
Drosophila anatomy and development ontologies (RRID:SCR_001607) FBbt controlled vocabulary, data or information resource, ontology A structured controlled vocabulary of the anatomy of Drosophila melanogaster. These ontologies are query-able reference sources for information on Drosophila anatomy and developmental stages. They also provide controlled vocabularies for use in annotation and classification of data related to Drosophila anatomy, such as gene expression, phenotype and images. They were originally developed by FlyBase, who continue to maintain them and have used them for over 200,000 annotations of phenotypes and expression. Extensive use of synonyms means that, given a suitably sophisticated autocomplete, users can find relevant content by searching with almost any anatomical term they find in the literature. These ontologies are developed in the web ontology language OWL2. Their extensive formalization in OWL can be used to drive sophisticated query systems. anatomy, development, developmental stage, gene expression, phenotype, owl is related to: OBO
is related to: Flannotator
is related to: REDfly Regulatory Element Database for Drosophilia
is related to: Bgee: dataBase for Gene Expression Evolution
has parent organization: FlyBase
has parent organization: SourceForge
NHGRI P41 HG000739 Free, Freely available nlx_153871 SCR_001607 Drosophila anatomy & dev ontologies 2026-08-21 12:36:26 0
Ensembl Variation
 
Resource Report
Resource Website
1+ mentions
Ensembl Variation (RRID:SCR_001630) Ensembl Variation analysis service resource, data analysis service, data or information resource, database, production service resource, service resource Public database that stores areas of genome that differ between individual genomes (variants) and, where available, associated disease and phenotype information. Different types of variants for several species: single nucleotide polymorphisms (SNPs), short nucleotide insertions and/or deletions, and longer variants classified as structural variants (including CNVs). Effects of variants on the Ensembl transcripts and regulatory features for each species are predicted. You can run same analysis on your own data using Variant Effect Predictor. These data are integrated with other data sources in Ensembl, and can be accessed using the API or website. For several different species in Ensembl, they import variation data (SNPs, CNVs, allele frequencies, genotypes, etc) from a variety of sources (e.g. dbSNP). Imported variants and alleles are subjected to quality control process to flag suspect data. In human, they calculate linkage disequilibrium for each variant, by population. genome, disease, phenotype, genomic variant, single nucleotide polymorphism nucleotide, insertion, deletion, structural variant, copy number variation, inversion, translocation, somatic variant, allele frequency, genotype, disease phenotype, inherited disease is used by: MONARCH Initiative
is related to: dbSNP
is related to: Database of Genomic Variants Archive (DGVa)
is related to: PubMed
is related to: Animal QTLdb
is related to: OMIA - Online Mendelian Inheritance in Animals
has parent organization: Ensembl
PMID:23203987
PMID:20562413
PMID:20459810
PMID:20459805
Free, Available for download, Freely available nlx_153897 SCR_001630 ensembl variation 2026-08-21 12:36:32 6
Ancora
 
Resource Report
Resource Website
10+ mentions
Ancora (RRID:SCR_001623) Ancora analysis service resource, data analysis service, data or information resource, database, production service resource, service resource Web resource that provides data and tools for exploring genomic organization of highly conserved noncoding elements (HCNEs) for multiple genomes. It includes a genome browser that shows HCNE locations and features novel HCNE density plots as a powerful tool to discover developmental regulatory genes and distinguish their regulatory elements and domains. They identify HCNEs as non-exonic regions of high similarity between genome sequences from distantly related organisms, such as human and fish, and provide tools for studying the distribution of HCNEs along chromosomes. Major peaks of HCNE density along chromosomes most often coincide with developmental regulatory genes. Their aim with this site is to aid discovery of developmental regulatory genes, their regulatory domains and their fundamental regulatory elements. genome, highly conserved noncoding element, noncoding element, regulatory gene, regulatory domain, regulatory element, developmental regulatory gene, evolution, enhancer is related to: MONARCH Initiative
has parent organization: University of Bergen; Bergen; Norway
Research Council of Norway ;
Bergen Research Foundation ;
Sars Centre
PMID:18279518 Free, Freely available nlx_153891 SCR_001623 Atlas of Noncoding Conserved Regions in Animals 2026-08-21 12:36:32 20
FlyMove
 
Resource Report
Resource Website
1+ mentions
FlyMove (RRID:SCR_002257) FlyMove data or information resource, database, image collection, narrative resource, training material, video resource Database combining movies, animated schemata, interactive modules and pictures that will greatly facilitate the understanding of Drosophila development. The resource is aimed at university students and teachers of developmental biology classes. Contribute your own movies, images and illustrations to FlyMove. Illustrating developmental processes using first hand research data will allow students to gain a better understanding of the real organism, and it will allow you to draw their attention to your field of research and to your group. All donors of media integrated in FlyMove will be cited and links to their homepages will be made. fruit fly, development, drosophila, image, movie, process, undergraduate, in vivo, graphic, animation, virtual experiment, life cycle, stage, organogenesis, genetics, method, quiz has parent organization: University of Munster; North Rhine-Westphalia; Germany BMBF PMID:12801722 Free, Available for download, Freely available nif-0000-20976 SCR_002257 Fly Move 2026-08-21 12:36:38 1
NLSdb: a database of nuclear localization signals
 
Resource Report
Resource Website
1+ mentions
NLSdb: a database of nuclear localization signals (RRID:SCR_003273) NLSdb analysis service resource, data analysis service, data or information resource, database, production service resource, service resource A database of nuclear localization signals (NLSs) and of nuclear proteins targeted to the nucleus by NLS motifs. NLSs are short stretches of residues mediating transport of nuclear proteins into the nucleus. The database contains 114 experimentally determined NLSs that were obtained through an extensive literature search. Using "in silico mutagenesis" this set was extended to 308 experimental and potential NLSs. This final set matched over 43% of all known nuclear proteins and matches no currently known non-nuclear protein. NLSdb contains over 6000 predicted nuclear proteins and their targeting signals from the PDB and SWISS-PROT/TrEMBL databases. The database also contains over 12 500 predicted nuclear proteins from six entirely sequenced eukaryotic proteomes (Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorhabditis elegans, Arabidopsis thaliana and Saccharomyces cerevisiae). NLS motifs often co-localize with DNA-binding regions. This observation was used to also annotate over 1500 DNA-binding proteins. From this site you can: * Query NLSdb * Find out how to use NLSdb * Browse the entries in NLSdb * Find out if your protein has an NLS using PredictNLS * Predict subcellular localization of your protein using LOCtree nuclear localization signal, nuclear protein, nucleus, motif, predict, protein has parent organization: Columbia University; New York; USA NIGMS 1-P50-GM62413-01;
NSF DBI-0131168
PMID:12520032 Free for academic use, Acknowledgement requested, All others should inquire about a commercial license nif-0000-03191 http://cubic.bioc.columbia.edu/db/NLSdb/ SCR_003273 NLSdb - a database of nuclear localization signals 2026-08-21 12:37:05 4
Reactome
 
Resource Report
Resource Website
1000+ mentions
Reactome (RRID:SCR_003485) analysis service resource, data analysis service, data or information resource, database, production service resource, service resource Collection of pathways and pathway annotations. The core unit of the Reactome data model is the reaction. Entities (nucleic acids, proteins, complexes and small molecules) participating in reactions form a network of biological interactions and are grouped into pathways (signaling, innate and acquired immune function, transcriptional regulation, translation, apoptosis and classical intermediary metabolism) . Provides website to navigate pathway knowledge and a suite of data analysis tools to support the pathway-based analysis of complex experimental and computational data sets. pathway, interaction, reaction, nucleic acid, protein, complex, small molecule, signaling pathway, immune function, transcriptional regulation, translation, apoptosis, metabolism, ortholog, visualization, protein-protein interaction, web service, book, biomart, gold standard, bio.tools, FASEB list is used by: NIF Data Federation
is used by: DisGeNET
is used by: Pathway Analysis Tool for Integration and Knowledge Acquisition
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: WikiPathways
is related to: Pathway Commons
is related to: ConsensusPathDB
is related to: FlyMine
is related to: AmiGO
is related to: PSICQUIC Registry
is related to: Integrated Molecular Interaction Database
is related to: NCBI BioSystems Database
is related to: MOPED - Model Organism Protein Expression Database
is related to: KOBAS
is related to: PSICQUIC Registry
is related to: Pathway Interaction Database
is related to: hiPathDB - human integrated Pathway DB with facile visualization
is related to: Algal Functional Annotation Tool
has parent organization: Ontario Institute for Cancer Research
has parent organization: Cold Spring Harbor Laboratory
has parent organization: European Bioinformatics Institute
has parent organization: New York University School of Medicine; New York; USA
works with: PathwayMatcher
European Molecular Biology Laboratory ;
European Union FP6 ENFIN LSHG-CT-2005-518254;
NHGRI P41 HG003751;
NIGMS GM080223;
NIGMS R01 GM100039;
Ontario Research Fund
PMID:21082427
PMID:21067998
Open source, Public, Freely available r3d100010285, nif-0000-03390, biotools:reactome https://bio.tools/reactome, https://doi.org/10.17616/R3V59P SCR_003485 Reactome Functional Interaction Network 2026-08-21 12:37:01 4810
GeneSpeed- A Database of Unigene Domain Organization
 
Resource Report
Resource Website
GeneSpeed- A Database of Unigene Domain Organization (RRID:SCR_002779) analysis service resource, data analysis service, data or information resource, database, production service resource, resource, 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 2026-08-21 12:36:52 0
Aging Genes and Interventions Database
 
Resource Report
Resource Website
1+ mentions
Aging Genes and Interventions Database (RRID:SCR_002701) AGEID data or information resource, data repository, database, service resource, storage service resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on February 17,2023. A database of genes and interventions connected with aging phenotypes including those with respect to their effects on life-span or age-related neurological diseases. Information includes: organism, aging phenotype, allele type, strain, gene function, phenotypes, mutant, and homologs. If you know of published data (or your own unpublished data that you'd like to share) not currently in the database, please use the Submit a Gene/Intervention link. allele, strain, gene function, phenotype, mutant, homolog, mutation, degeneration, gene, intervention, life-span is used by: Aging Portal
is used by: NIF Data Federation
has parent organization: University of Washington; Seattle; USA
Aging, Age-related neurological disease, Neurological disease Ellison Medical Foundation PMID:12044961 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-23326 http://sageke.sciencemag.org/highlights/gidb/ SCR_002701 Aging Genes DB, Aging Genes Database, Genes/Interventions Database 2026-08-21 12:36:50 2
I2D
 
Resource Report
Resource Website
10+ mentions
I2D (RRID:SCR_002957) I2D analysis service resource, data analysis service, data or information resource, database, production service resource, service resource Database of known and predicted mammalian and eukaryotic protein-protein interactions, it is designed to be both a resource for the laboratory scientist to explore known and predicted protein-protein interactions, and to facilitate bioinformatics initiatives exploring protein interaction networks. It has been built by mapping high-throughput (HTP) data between species. Thus, until experimentally verified, these interactions should be considered predictions. It remains one of the most comprehensive sources of known and predicted eukaryotic PPI. It contains 490,600 Source Interactions, 370,002 Predicted Interactions, for a total of 846,116 interactions, and continues to expand as new protein-protein interaction data becomes available. interaction, prediction, protein-protein interaction, high-throughput, model organism, mammal, eukaryote, visualization, interolog, protein is related to: Interaction Reference Index
is related to: IMEx - The International Molecular Exchange Consortium
is related to: PSICQUIC Registry
is related to: IntAct
has parent organization: University of Toronto; Ontario; Canada
National Science and Engineering Research Council RGPIN 203833-02;
NIGMS P50-GM62413
PMID:17535438
PMID:15657099
Free, Available for download, Freely available nif-0000-03005, r3d100010675 https://doi.org/10.17616/R3BG8R SCR_002957 Interologous Interaction Database, OPHID, I2D - Interologous Interaction Database 2026-08-21 12:36:51 23
N-Browse
 
Resource Report
Resource Website
N-Browse (RRID:SCR_004253) software resource, web application Interactive graphical browser for biological networks and molecular interaction data. The N-Browse server at NYU currently provides access to a variety of large-scale functional genomic datasets from several species. graphical browser, molecular data interface, functional genomics has parent organization: New York University; New York; USA Department of the Army award W81XWH-04-1-0307;
NYSTAR contract C040066
PMID:18819079 Free, Account required nlx_26609 SCR_004253 N-Browse.PNG, NBrowse 2026-08-21 12:37:24 0
Drososhare
 
Resource Report
Resource Website
1+ mentions
Drososhare (RRID:SCR_014976) biomaterial supply resource, material resource, organism supplier Website resource for researchers to order and send Drosophilia specimens to each other. This community-driven supplier also works with the FlyBase Drosophilia database to search for synonyms for fly species. community driven, organism supplier, community building portal, drosophila, fly, specimen uses: FlyBase Available to the research community SCR_014976 Drososhare GmbH 2026-08-21 12:40:31 1
larvalign
 
Resource Report
Resource Website
1+ mentions
larvalign (RRID:SCR_015815) data analysis software, data or information resource, data processing software, data set, sequence analysis software, software application, software resource, software toolkit Software package including computational methods for aligning gene expression patterns from the larval brain of Drosophila melanogaster. Its method includes evaluation of the registration framework involved in template generation and mapping. drosophila melanogaster, computational method, gene expression, alignment, larval brain, larvae, template generation, mapping, bio.tools is listed by: Debian
is listed by: bio.tools
Free, Available for download biotools:larvalign https://bio.tools/larvalign SCR_015815 2026-08-21 12:40:48 1
The WWW Virtual Library: Model Organisms
 
Resource Report
Resource Website
The WWW Virtual Library: Model Organisms (RRID:SCR_007007) data or information resource, portal, topical portal Catalog of internet resources relating to biological model organisms, and is part of the Biosciences area of the Virtual Library project. The main Model Organisms Library discussed in this website are: * E. coli (bacterium) * Yeasts (Saccharomyces cerevisiae, and other species) * Dictyostelium discoideum (slime mold) * Drosophila melanogaster (fruit fly) * Xenopus laevis (African clawed frog) Many aspects of biology are similar in most or all organisms, but it is frequently much easier to study particular aspects in particular organisms - for instance, genetics is easier in small organisms that breed quickly, and very difficult in humans! The most popular model organisms have strong advantages for experimental research, and become even more useful when other scientists have already worked on them, discovering techniques, genes and other useful information. bacterium, cerevisiae, model organism, saccharomyces, s. cerevisiae, slime mold, xenopus, catalog, link aggregator is listed by: 3DVC nif-0000-20953 SCR_007007 VL 2026-08-21 12:38:17 0
Biological General Repository for Interaction Datasets (BioGRID)
 
Resource Report
Resource Website
1000+ mentions
Biological General Repository for Interaction Datasets (BioGRID) (RRID:SCR_007393) BioGRID data or information resource, database Curated protein-protein and genetic interaction repository of raw protein and genetic interactions from major model organism species, with data compiled through comprehensive curation efforts. budding yeast, fission yeast, protein, gene, protein interaction, genetic interaction, model organism, interaction, dataset, gene annotation, phenotype, orthologous interaction, yeast, cellular interaction network, physical interaction, protein-peptide, protein-rna, protein-protein interaction, genetics, publication, raw protein, genetic interaction, web service, pathway, network, biology, gene mapping, statistics, bio.tools, FASEB list is used by: NIF Data Federation
is recommended by: National Library of Medicine
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: re3data.org
is listed by: OMICtools
is listed by: DataCite
is listed by: NIH Data Sharing Repositories
is listed by: bio.tools
is listed by: Debian
is related to: TissueNet - The Database of Human Tissue Protein-Protein Interactions
is related to: Pathway Commons
is related to: Cytoscape
is related to: Interaction Reference Index
is related to: ConsensusPathDB
is related to: FlyMine
is related to: IMEx - The International Molecular Exchange Consortium
is related to: Integrated Molecular Interaction Database
is related to: PSICQUIC Registry
is related to: PSI-MI
is related to: NIH Data Sharing Repositories
is related to: Agile Protein Interactomes DataServer
is related to: Integrated Manually Extracted Annotation
has parent organization: Princeton University; New Jersey; USA
has parent organization: University of Edinburgh; Scotland; United Kingdom
has parent organization: University of Montreal; Quebec; Canada
works with: IMEx - The International Molecular Exchange Consortium
BBSRC ;
Canadian Institutes of Health Research ;
NCRR R01 RR024031;
NHGRI HG02223;
NIH Office of the Director R24 OD011194
PMID:23203989
PMID:21071413
PMID:16381927
PMID:12620108
Free, Freely available nif-0000-00432, r3d100010350, OMICS_01901, biotools:the_grid https://orip.nih.gov/comparative-medicine/programs/genetic-biological-and-information-resources, https://bio.tools/the_grid, https://doi.org/10.17616/R34C7G SCR_007393 , BioGRID, Biological General Repository for Interaction Datasets 2026-08-21 12:38:08 2824
Bloomington Drosophila Stock Center
 
Resource Report
Resource Website
1000+ mentions
Bloomington Drosophila Stock Center (RRID:SCR_006457) BDSC biomaterial supply resource, material resource, organism supplier Collects, maintains and distributes Drosophila melanogaster strains for research. Emphasis is placed on genetic tools that are useful to a broad range of investigations. These include basic stocks of flies used in genetic analysis such as marker, balancer, mapping, and transposon-tagging strains; mutant alleles of identified genes, including a large set of transposable element insertion alleles; defined sets of deficiencies and a variety of other chromosomal aberrations; engineered lines for somatic and germline clonal analysis; GAL4 and UAS lines for targeted gene expression; enhancer trap and lacZ-reporter strains with defined expression patterns for marking tissues; and a collection of transposon-induced lethal mutations. RIN, Resource Information Network, disease model, deficiency, deletion, transposon insertion, sequenced strain, duplication, protein trap, human disease model, transposon, fly, gene, genetic, genetic analysis, database, deficiency, germline, insertion, invertebrate, scientist, somatic, stock, transposon, mutation, genetic construct, FASEB list, RRID Community Authority is used by: Integrated Animals
is listed by: One Mind Biospecimen Bank Listing
is listed by: Resource Information Network
is related to: One Mind Biospecimen Bank Listing
is related to: NIF Data Federation
has parent organization: Indiana University; Indiana; USA
Human disease model NIH Office of the Director P40 OD018537 nif-0000-00241 https://orip.nih.gov/comparative-medicine/programs/invertebrate-models http://flystocks.bio.indiana.edu/bloomhome.htm SCR_006457 Bloomington Drosophila Stock Center at Indiana University 2026-08-21 12:37:57 3419

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  1. PRECISE-TBI Resources

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