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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
Integrated Animals
 
Resource Report
Resource Website
Integrated Animals (RRID:SCR_001421) organism supplier, material resource, biomaterial supply resource 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 2026-02-12 09:43:09 0
Cold Spring Harbor Protocols: Collected Resources - Behavioral Assays
 
Resource Report
Resource Website
100+ mentions
Cold Spring Harbor Protocols: Collected Resources - Behavioral Assays (RRID:SCR_001697) CSH Protocols - Behavioral Assays data or information resource, bibliography A bibliography of published Behavioral Assays by Cold Spring Harbor Protocols. Cold Spring Harbor Protocols is an interdisciplinary journal providing a definitive source of research methods in cell, developmental and molecular biology, genetics, bioinformatics, protein science, computational biology, immunology, neuroscience and imaging. Each monthly issue details multiple essential methods - a mix of cutting-edge and well-established techniques. Newly commissioned protocols and unsolicited submissions are supplemented with articles based on Cold Spring Harbor Laboratorys renowned courses and manuals. All protocols are up-to-date and presented in a consistent, easy-to-follow format. genetics, bioinformatics, cell, computational biology, development, imaging, immunology, journal, molecular, neuroscience, protein, research, behavioral assay, behavior, ant, honeybee, learning, courtship, larvae, adult, stress, olfactory, aggression, sleep, movement, locomotor, circadian, feeding has parent organization: Cold Spring Harbor Laboratory Free, Freely Available nif-0000-10198 SCR_001697 Cold Spring Harbor Protocols - Behavioral Assays 2026-02-12 09:43:13 108
Ensembl Variation
 
Resource Report
Resource Website
1+ mentions
Ensembl Variation (RRID:SCR_001630) Ensembl Variation analysis service resource, service resource, production service resource, database, data analysis service, data or information 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 2026-02-12 09:43:12 4
Ancora
 
Resource Report
Resource Website
10+ mentions
Ancora (RRID:SCR_001623) Ancora analysis service resource, service resource, production service resource, database, data analysis service, data or information 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 2026-02-12 09:43:12 19
Reactome
 
Resource Report
Resource Website
1000+ mentions
Reactome (RRID:SCR_003485) analysis service resource, service resource, production service resource, database, data analysis service, data or information 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
Ontario Research Fund ;
European Molecular Biology Laboratory ;
NHGRI P41 HG003751;
European Union FP6 ENFIN LSHG-CT-2005-518254;
NIGMS GM080223;
NIGMS R01 GM100039
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 2026-02-12 09:43:37 4282
OwlSim
 
Resource Report
Resource Website
1+ mentions
OwlSim (RRID:SCR_006819) OwlSim software application, software resource, data processing software Software package that provides the ability to do a number of standard semantic similarity methods and includes novel methods for combining these with dynamic selection of anonymous grouping classes. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible functional similarity, semantic similarity, ontology, phenotype, annotation, windows, mac os x, linux, unix is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Berkeley Bioinformatics Open-Source Projects
has parent organization: OWLTools
Biomedical Information Science and Technology Initiative ;
National Center for Biomedical Ontology ;
NHGRI U54 HG004028;
NHGRI HG002659
PMID:19956802 Open unspecified license - Free for academic use nlx_149312 SCR_006819 2026-02-12 09:44:25 5
FishFace - An atlas of zebrafish craniofacial development
 
Resource Report
Resource Website
1+ mentions
FishFace - An atlas of zebrafish craniofacial development (RRID:SCR_008894) FishFace data or information resource, atlas, reference atlas ishFace is an atlas of zebrafish craniofacial development. How do the elements of the craniofacial skeleton arise, grow, and reshape? Answers to this question are coming from both molecular-genetic and cell-biological approaches, which rely, first of all, on precise description of the developmental events and processes that comprise skeletogenesis. Zebrafish, with a sophisticated knowledge of its genetics and genomics, with favorable attributes for phenotypic analyses of development, and with patterns of development conserved among all vertebrates, provides a powerful animal model for learning about craniofacial development. In particular, with current transgenic approaches one can examine craniofacial skeletal elements in exquisite cellular detail during an extended period of development within living, intact embryos and larvae an investigative method unsurpassed in accuracy and sensitivity. We constructed this developmental atlas of the craniofacial skeleton, FishFace, to serve as a guide for such study. We hope that the FishFace Atlas will be particularly useful in comparative and mutational analyses where there is interest in understanding the cellular basis of early skeletogenesis. The heart of the FishFace Atlas uses high magnification (generally a 40x objective) confocal image stacks showing transgenically-labelled chondrocytes or osteoblasts, along with mineralized bone matrix, which is visualized by vital staining with Alizarin red. We present these stacks in sequences that follow particular individual cartilages and bones of the first two pharyngeal arches as they develop during embryonic and larval stages. To do so, we build on the foundation set out in the gold standard reference for describing comprehensively skeletal elements in the zebrafish craniofacial complex, Cubbage and Mabee (1996), which used fixed preparations stained for cartilage and bone through adult stages. The FishFace Atlas element development section adds considerable detail to arch one and two early development, particularly at the cellular level, but also in description of element growth and shaping. Other sections of the FishFace Atlas, at lower magnification, provide anatomical context for the element development section, including an interactive tool made by optical projection tomography (OPT) for learning the anatomy of the entire larval skull. Hence, the FishFace Atlas provides the community with an interactive resource with which the user can understand not only the cellular details, but also complex 3D anatomical relationships, of developing elements in the craniofacial skeleton of the zebrafish. craniofacial development has parent organization: FaceBase ARRA ;
NIDCR 5RC1DE020655;
NICHD PO1 HD22486;
NIDCR 1RO1 DE13834;
NIDCR U01DE020057
nlx_151378 SCR_008894 FishFace: An Atlas of zebrafish craniofacial development, FishFace Atlas 2026-02-12 09:44:44 4
BonZeb project
 
Resource Report
Resource Website
BonZeb project (RRID:SCR_021388) data or information resource, portal, project portal Portal provides tools for investigating visuomotor integration specific to high speed kinematic tracking in small model organisms in closed loop experiments. University of Toronto scientists developed suite of Bonsai modules for specifically tracking and analyzing zebrafish movements and integrating these data with closed-loop experiments. BonZeb modules can also be used in an open-loop fashion for collecting, analyzing, and integrating data from multiple sources in real time, or from offline sources for batch processing of pre-recorded data. Tacking and analyzing zebrafish movements, integrating zebrafish movements data with closed loop experiments, zebrafish movements, OpenBehavior is listed by: OpenBehavior
is related to: BonZeb
has parent organization: University of Toronto; Ontario; Canada
Free, Freely available SCR_021388 BonZeb 2026-02-12 09:47:19 0
Stem Cell Commons
 
Resource Report
Resource Website
1+ mentions
Stem Cell Commons (RRID:SCR_004415) Stem Cell Commons analysis service resource, source code, software resource, data repository, service resource, production service resource, storage service resource, database, data or information resource, data set Open source environment for sharing, processing and analyzing stem cell data bringing together stem cell data sets with tools for curation, dissemination and analysis. Standardization of the analytical approaches will enable researchers to directly compare and integrate their results with experiments and disease models in the Commons. Key features of the Stem Cell Commons * Contains stem cell related experiments * Includes microarray and Next-Generation Sequencing (NGS) data from human, mouse, rat and zebrafish * Data from multiple cell types and disease models * Carefully curated experimental metadata using controlled vocabularies * Export in the Investigation-Study-Assay tabular format (ISA-Tab) that is used by over 30 organizations worldwide * A community oriented resource with public data sets and freely available code in public code repositories such as GitHub Currently in development * Development of Refinery, a novel analysis platform that links Commons data to the Galaxy analytical engine * ChIP-seq analysis pipeline (additional pipelines in development) * Integration of experimental metadata and data files with Galaxy to guide users to choose workflows, parameters, and data sources Stem Cell Commons is based on open source software and is available for download and development. therapeutic target, blood, stem cell, self-renewal, embryonic stem cell, hematopoietic stem cell, leukemia stem cell, gene, protein, phenotype, therapeutic, annotate, share, analyze, data sharing, statistics, visualize, analyze, microarray, next-generation sequencing, statistics, transcription profiling, genome, genome browser, disease model is related to: Galaxy
is related to: ISA Infrastructure for Managing Experimental Metadata
has parent organization: Harvard Stem Cell Institute
Normal, Acute Myelogenous Leukemia, Glioblastoma, Primitive Neuroectodermal Tumor, Etc. PMID:24303302 Open unspecified license nlx_42085 http://bloodprogram.hsci.harvard.edu/ SCR_004415 HSCI Blood Genomics, Harvard Stem Cell Institute Blood Genomics, Harvard Stem Cell Institute Blood Program, HSCI Blood Program 2026-02-12 09:43:48 2
SeqAnt
 
Resource Report
Resource Website
1+ mentions
SeqAnt (RRID:SCR_005186) SeqAnt analysis service resource, software resource, service resource, production service resource, data analysis service 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 2026-02-12 09:44:04 2
Gene Weaver
 
Resource Report
Resource Website
10+ mentions
Gene Weaver (RRID:SCR_003009) analysis service resource, data repository, service resource, production service resource, storage service resource, database, data analysis service, data or information resource Freely accessible phenotype-centered database with integrated analysis and visualization tools. It combines diverse data sets from multiple species and experiment types, and allows data sharing across collaborative groups or to public users. It was conceived of as a tool for the integration of biological functions based on the molecular processes that subserved them. From these data, an empirically derived ontology may one day be inferred. Users have found the system valuable for a wide range of applications in the arena of functional genomic data integration. phenotype, microarray, gene, genome, functional genomics, process, pathway, function, gene set, genomic data integration, analysis, visualization is used by: NIF Data Federation
is used by: Integrated Datasets
is listed by: OMICtools
is related to: Integrated Manually Extracted Annotation
has parent organization: Jackson Laboratory
Integrative Neuroscience Initiative on Alcoholism ;
NIAAA U01 AA13499;
NIAAA U24 AA13513;
NIAAA R01 AA18776
PMID:22080549
PMID:19733230
Free, Freely available r3d100012464, OMICS_02232, nif-0000-00517 http://ontologicaldiscovery.org/
https://doi.org/10.17616/R3248T
SCR_003009 GeneWeaver, GeneWeaver - A system for the integration of functional genomics experiments, Ontological Discovery Environment, GeneWeaver.org 2026-02-12 09:43:30 34
RAVEN
 
Resource Report
Resource Website
100+ mentions
RAVEN (RRID:SCR_001937) RAVEN analysis service resource, service resource, production service resource, database, data analysis service, data or information resource Tool to search for putative regulatory genetic variation in your favorite gene. Single nucleotide polymorphisms (SNPs) (from dbSNP and user defined) are analyzed for overlap with potential transcription factor binding sites (TFBS) and phylogenetic footprinting using UCSC phastCons scores from multiple alignments of 8 vertebrate genomes., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. transcription factor binding site, phylogenetic footprint, regulatory sequence variation, genetic variation, in silico, regulatory sequence, FASEB list uses: Embassy-domsearch
is listed by: OMICtools
has parent organization: University of British Columbia; British Columbia; Canada
PMID:18208319 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01932 SCR_001937 Regulatory analysis of Variation in Enhancers, RAVEN - Regulatory analysis of Variation in ENhancers 2026-02-12 09:43:16 127
IDEAL - Intrinsically Disordered proteins with Extensive Annotations and Literature
 
Resource Report
Resource Website
10+ mentions
IDEAL - Intrinsically Disordered proteins with Extensive Annotations and Literature (RRID:SCR_006027) IDEAL analysis service resource, service resource, production service resource, database, data analysis service, data or information resource IDEAL, Intrinsically Disordered proteins with Extensive Annotations and Literature, is a collection of knowledge on experimentally verified intrinsically disordered proteins (IDPs) or intrinsically disordered regions (IDRs). IDEAL contains manually curated annotations on IDPs in locations, structures, and functional sites such as protein binding regions and posttranslational modification sites together with references and structural domain assignments. Protean segment One of the unique phenomena seen in IDPs is so-called the coupled folding and binding, where a short flexible segment can bind to its binding partner with forming a specific structure to act as a molecular recognition element. IDEAL explicitly annotates these regions as protean segment (ProS) when unstructured and structured information are both available in the region. Access to the data All the entries are tabulated in the list and individual entries can be retrieved by using the search tool at the upper-right corner in this page. IDEAL also provides the BLAST search, which can find homologs in IDEAL. All the information in IDEAL can be downloaded in the XML file. intrinsically disordered protein, protein, intrinsically disordered region, region, location, structure, functional site, protein binding region, binding region, posttranslational modification site, reference, structural domain assignment, blast, homolog, simian virus 40, epstein-barr virus, human herpesvirus 1, residue, protean segment, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: Nagoya University; Nagoya; Japan
Japanese Ministry of Education Culture Sports Science and Technology MEXT PMID:22067451 biotools:ideal, nlx_151427 https://bio.tools/ideal SCR_006027 IDEAL - Intrinsically Disordered proteins with Extensive Annotations Literature, Intrinsically Disordered proteins with Extensive Annotations and Literature 2026-02-12 09:44:09 10
Zebrafish Neurophenome Project Database
 
Resource Report
Resource Website
1+ mentions
Zebrafish Neurophenome Project Database (RRID:SCR_004482) ZNP data repository, service resource, storage service resource, data or information resource, data set Database of neurobehavioral and physiological data of adult zebrafish models, complementing the available repositories for zebrafish genetic information, by providing a dynamic, open-access data repository of comprehensive, curated collection of results from zebrafish neurobehavioral experiments. As of May 2012, it contains over 4,500 experimental results, from over 75 unique physiological and behavioral tests and 330 different drug treatments. ZNP incorporates validated and curated data from work published in this field, to improve the accessibility of current knowledge to researchers interested in using adult zebrafish models. Overall, this program will allow investigators to rapidly review data, to direct their research using these models. Data and protocol submissions are now being accepted. zebrafish, behavior, pharmacology, psychopharmacology, drug, adult zebrafish, phenotype, model, neurobehavior, physiology is listed by: 3DVC
has parent organization: Tulane University School of Medicine; Louisiana; USA
has parent organization: Zebrafish Neuroscience Research Consortium
Tulane University; Louisiana; USA ;
NIDA DA030900-02
PMID:22171801 Open-access, Please cite nlx_143762 http://www.tulane.edu/%E2%88%BCznpindex/search SCR_004482 ZNPdb, Zebrafish Neurophenome Project, ZNP Database, Zebrafish Neurophenome Database 2026-02-12 09:43:51 2
Zebrafish International Resource Center
 
Resource Report
Resource Website
100+ mentions
Zebrafish International Resource Center (RRID:SCR_005065) ZIRC organism supplier, material resource, biomaterial supply resource Center that supplies access to wild-type, mutant, and transgenic zebrafish lines, EST's/cDNAs, antibodies and fish health services. ZIRC Health Services include diagnostic pathology testing for zebrafish and other small laboratory fish species. RIN, Resource Information Network, zebrafish line, expressed sequence tag, cdna, fish, antibody, pathology, research, embryo, adult, 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: ZMP
is related to: NIF Data Federation
is related to: Zebrafish Information Network (ZFIN)
is related to: zfishbook
has parent organization: University of Oregon; Oregon; USA
NICHD HD12546;
NCRR RR12546;
W.M. Keck Foundation ;
NIH Office of the Director P40 OD011021
Restricted nif-0000-00242 http://zebrafish.org/home/guide.php SCR_005065 Zebrafish International Resource Center 2026-02-12 09:44:02 445
ZF-screens
 
Resource Report
Resource Website
ZF-screens (RRID:SCR_003910) data or information resource, portal, service resource, organization portal A commercial organization with expertise and multiple departments that focus on both fish physiology and molecular cell biology. ZF-pharma has developed patented technology for the automated in vivo high-throughput screening of pharmaceutical drug candidates against diseases. They seek industrial partners that are interested in obtaining a license for this technology or, alternatively, would prefer to outsource screening of TB drugs to ZF-pharma. NewCatch BV has developed a tool for use in sustainable aquaculture. The tool will first be used for reproduction of the highly valued fish species eel, pikeperch and sole. They seek industrial / aquaculture partners interested in obtaining a license for ZF-implants in other fish species. NewCatch BV carries out fish reproductive research, for instance European eel (Anguilla anguilla), exploring maturation and reproduction. ZF-Genomics offers multiple sequencing services, including mRNAseq and microRNA analysis and de novo and reference genome assemblies. In addition they also offer the bioinformatics services that are needed to make sense of the sequence data. In addition, they perform Next generation sequencing tasks for (inter)national research project partners and for external customers. next generation sequencing, pharmaceutical, in vivo, reproduction, mrnaseq, microrna, maturation, fish physiology, fish molecular cell biology is related to: Predict-TB Commercial nlx_158253 SCR_003910 ZF Screens, ZF-screens BV, ZF-screens B.V. 2026-02-12 09:43:42 0
Spliceman
 
Resource Report
Resource Website
1+ mentions
Spliceman (RRID:SCR_005354) Spliceman service resource, analysis service resource, production service resource, data analysis service An online tool that takes a set of DNA sequences with point mutations and returns a ranked list to predict the effects of point mutations on pre-mRNA splicing. The current implementation includes 11 genomes: human, chimp, rhesus, mouse, rat, dog, cat, chicken, guinea pig, frog and zebrafish. dna sequence, pre-mrna, splicing, pre-mrna splicing, point mutation, mutation, sequence variation, fasta is listed by: OMICtools
has parent organization: Brown University; Rhode Island; USA
PMID:22328782 Free, Non-commercial, Commercial use requires license OMICS_02259 SCR_005354 2026-02-12 09:44:03 5
GOrilla: Gene Ontology Enrichment Analysis and Visualization Tool
 
Resource Report
Resource Website
100+ mentions
GOrilla: Gene Ontology Enrichment Analysis and Visualization Tool (RRID:SCR_006848) GOrilla service resource, analysis service resource, production service resource, data analysis service A tool for identifying and visualizing enriched GO terms in ranked lists of genes. It can be run in one of two modes: * Searching for enriched GO terms that appear densely at the top of a ranked list of genes or * Searching for enriched GO terms in a target list of genes compared to a background list of genes. gene, genetic, ontology, ontology or annotation visualization, statistical analysis, term enrichment, visualization, analysis, protein is listed by: Gene Ontology Tools
is listed by: OMICtools
is related to: Gene Ontology
European Union FP6 ;
Yeshaya Horowitz Association
PMID:19192299 Acknowledgement requested, Free, Public nlx_80425, OMICS_02282 SCR_006848 Gene Ontology enRIchment anaLysis and visuaLizAtion tool, GOrilla: Gene Ontology Enrichment Analysis Visualization Tool 2026-02-12 09:44:28 492
GeneTrail
 
Resource Report
Resource Website
100+ mentions
GeneTrail (RRID:SCR_006250) GeneTrail service resource, analysis service resource, production service resource, data analysis service 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 2026-02-12 09:44:12 106
CRISPRdirect
 
Resource Report
Resource Website
100+ mentions
CRISPRdirect (RRID:SCR_018186) analysis service resource, software resource, data access protocol, service resource, web service, production service resource Software for designing CRISPR/Cas guide RNA with reduced off target sites. Used for rational design of CRISPR/Cas target. Web server for selecting rational CRISPR/Cas targets from input sequence. Server currently incorporates genomic sequences of human, mouse, rat, marmoset, pig, chicken, frog, zebrafish, Ciona, fruit fly, silkworm, Caenorhabditis elegans, Arabidopsis, rice, Sorghum and budding yeast. CRISP/Cas guide RNA, reduced off target site, design of CRISP/Cas target, selecting rational target, sequence, genomic sequence, RNA, bio.tools is listed by: Debian
is listed by: bio.tools
Japan Science and Technology Agency ;
Ministry of Education ;
Culture ;
Sports ;
Science and Technology of Japan
PMID:25414360 Free, Freely available biotools:CRISPRdirect https://bio.tools/CRISPRdirect SCR_018186 2026-02-12 09:47:00 452

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    1. Use quotes around phrases you want to match exactly
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    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 FDI Lab - SciCrunch.org 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.