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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
GermOnline
 
Resource Report
Resource Website
10+ mentions
GermOnline (RRID:SCR_002807) GermOnline data or information resource, database Cross-species microarray expression database focusing on high-throughput expression data relevant for germline development, meiosis and gametogenesis as well as the mitotic cell cycle. The database contains a unique combination of information: 1) High-throughput expression data obtained with whole-genome high-density oligonucleotide microarrays (GeneChips). 2) Sample annotation (mouse over the sample name and click on it) using the Multiomics Information Management and Annotation System (MIMAS 3.0). 3) In vivo protein-DNA binding data and protein-protein interaction data (available for selected species). 4) Genome annotation information from Ensembl version 50. 5) Orthologs are identified using data from Ensembl and OMA and linked to each other via a section in the report pages. The portal provides access to the Saccharomyces Genomics Viewer (SGV) which facilitates online interpretation of complex data from experiments with high-density oligonucleotide tiling microarrays that cover the entire yeast genome. The database displays only expression data obtained with high-density oligonucleotide microarrays (GeneChips)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 15,2026. fertility, development, germline, microarray, annotation, in vivo, protein-dna binding, protein-protein interaction, genome, ortholog, high-density oligonucleotide microarray, gene expression, genome annotation, gene orthology, genechip, tiling array, development, meiosis, gametogenesis, mitotic cell cycle, data set, data repository, bio.tools is listed by: 3DVC
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: Ensembl
is related to: OMA Browser
has parent organization: National Institute of Health and Medical Research; Rennes; France
Swiss Institute of Bioinformatics ;
bioinformatics platform of Biogenouest ;
National Institute of Health and Medical Research; Rennes; France ;
University of Rennes 1; Rennes; France
PMID:21149299 THIS RESOURCE IS NO LONGER IN SERVICE biotools:germonline, nif-0000-02906, r3d100010248 https://bio.tools/germonline
https://doi.org/10.17616/R37K5Q
SCR_002807 2026-02-11 10:56:35 17
MapViewer
 
Resource Report
Resource Website
100+ mentions
MapViewer (RRID:SCR_003092) Map Viewer data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 4, 2023. Database that provides special browsing capabilities for a subset of organisms in Entrez Genomes. Map Viewer allows users to view and search an organism's complete genome, display chromosome maps, and zoom into progressively greater levels of detail, down to the sequence data for a region of interest. If multiple maps are available for a chromosome, it displays them aligned to each other based on shared marker and gene names, and, for the sequence maps, based on a common sequence coordinate system. genome, mapping, sequencing, chromosome is listed by: OMICtools
is related to: NCBI Genome
is related to: Consensus CDS
has parent organization: NCBI
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00921, nif-0000-03103 SCR_003092 Entrez Map Viewer, NCBI Map Viewer 2026-02-11 10:56:38 242
HINT
 
Resource Report
Resource Website
100+ mentions
HINT (RRID:SCR_002762) HINT data or information resource, database A database of high-quality protein-protein interactions in different organisms. protein-protein interaction, bio.tools, FASEB list is used by: Mutation Annotation and Genomic Interpretation
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Cornell University; New York; USA
PMID:22846459 Free, Freely available, Available for download OMICS_02898, biotools:hint https://bio.tools/hint SCR_002762 High-quality INTeractomes 2026-02-11 10:56:32 306
SignaLink
 
Resource Report
Resource Website
50+ mentions
SignaLink (RRID:SCR_003569) SignaLink data or information resource, database An integrated resource to analyze signaling pathway cross-talks, transcription factors, miRNAs and regulatory enzymes. The multi-layered database structure is made up of signaling pathways, their pathway regulators (e.g., scaffold and endocytotic proteins) and modifier enzymes (e.g., phosphatases, ubiquitin ligases), as well as transcriptional and post-transcriptional regulators of all of these components. The website allows the interactive exploration of how each signaling protein is regulated. Features * experimental data not only from humans but from two invertebrate model organisms, C. elegans and D. melanogaster; * combines manual curation with large-scale datasets; * provides confidence scores for each interaction; * operates a customizable download page with multiple file formats (e.g., BioPAX, Cytoscape, SBML). analyze, signaling, pathway, cross-talk, transcription factor, mirna, regulatory enzyme, protein, interaction, regulatory network, signaling pathway, scaffold protein, enzyme, signaling, drug discovery, regulatory, network, post-transcriptional regulator, transcriptional regulator, protein-protein interaction, post-translational modification, pathway regulator, FASEB list is related to: ConsensusPathDB
has parent organization: Eotvos Lorand University; Budapest; Hungary
PMID:23331499
PMID:20542890
Acknowledgement requested, Free for non-profit use nlx_157704 SCR_003569 2026-02-11 10:56:45 58
modENCODE
 
Resource Report
Resource Website
100+ mentions
modENCODE (RRID:SCR_006206) modENCODE analysis service resource, service resource, production service resource, data analysis service, data or information resource, data set A comprehensive encyclopedia of genomic functional elements in the model organisms C. elegans and D. melanogaster. modENCODE is run as a Research Network and the consortium is formed by 11 primary projects, divided between worm and fly, spanning the domains of gene structure, mRNA and ncRNA expression profiling, transcription factor binding sites, histone modifications and replacement, chromatin structure, DNA replication initiation and timing, and copy number variation. The raw and interpreted data from this project is vetted by a data coordinating center (DCC) to ensure consistency and completeness. The entire modENCODE data corpus is now available on the Amazon Web Services EC2 cloud. What this means is that virtual machines and virtual compute clusters that you run within the EC2 cloud can mount the modENCODE data set in whole or in part. Your software can run analyses against the data files directly without experiencing the long waits and logistics associated with copying the datasets over to your local hardware. You may also view the data using GBrowse, Dataset Search, or download the data via FTP, as well as download pre-release datasets. epigenomics, epigenetics, genomics, functional element, model organism, genome, copy number variation, gene structure, genome sequence, histone modification, histone replacement, chromatin binding site, expression profiling, replication, transcription factor binding site, transcription factor, binding site, chromatin, rna, expression profiling, regulatory network, mrna, ncrna, dna replication, genotype is related to: ENCODE
is related to: Encode
NHGRI PMID:19536255 Public, With some restrictions on its use for 9 months following publication, Acknowledgement requested nlx_151752 SCR_006206 NHGRI model organism ENCyclopedia Of DNA Elements, National Human Genome Research Institute model organism ENCyclopedia Of DNA Elements, model organism ENCyclopedia Of DNA Elements 2026-02-12 09:44:19 255
Cscan
 
Resource Report
Resource Website
1+ mentions
Cscan (RRID:SCR_006756) Cscan analysis service resource, service resource, production service resource, database, data analysis service, data or information resource Data resource that includes a large collection of genome-wide ChIP-Seq experiments performed on transcription factors (TFs), histone modifications, RNA polymerases and others. Enriched peak regions from the ChIP-Seq experiments are crossed with the genomic coordinates of a set of input genes, to identify which of the experiments present a statistically significant number of peaks within the input genes' loci. The input can be a cluster of co-expressed genes, or any other set of genes sharing a common regulatory profile. Users can thus single out which TFs are likely to be common regulators of the genes, and their respective correlations. Also, by examining results on promoter activation, transcription, histone modifications, polymerase binding and so on, users can investigate the effect of the TFs (activation or repression of transcription) as well as of the cell or tissue specificity of the genes' regulation and expression. regulator, gene, genome-wide chip-seq, chip-seq, gene, genome is listed by: OMICtools PMID:22669907 Free OMICS_00529 SCR_006756 2026-02-12 09:44:24 4
EGAN: Exploratory Gene Association Networks
 
Resource Report
Resource Website
1+ mentions
EGAN: Exploratory Gene Association Networks (RRID:SCR_008856) EGAN software resource, software application, data analysis software, data processing software Exploratory Gene Association Networks (EGAN) is a software tool that allows a bench biologist to visualize and interpret the results of high-throughput exploratory assays in an interactive hypergraph of genes, relationships (protein-protein interactions, literature co-occurrence, etc.) and meta-data (annotation, signaling pathways, etc.). EGAN provides comprehensive, automated calculation of meta-data coincidence (over-representation, enrichment) for user- and assay-defined gene lists, and provides direct links to web resources and literature (NCBI Entrez Gene, PubMed, KEGG, Gene Ontology, iHOP, Google, etc.). EGAN functions as a module for exploratory investigation of analysis results from multiple high-throughput assay technologies, including but not limited to: * Transcriptomics via expression microarrays or RNA-Seq * Genomics via SNP GWAS or array CGH * Proteomics via MS/MS peptide identifications * Epigenomics via DNA methylation, ChIP-on-Chip or ChIP-Seq * In-silico analysis of sequences or literature EGAN has been built using Cytoscape libraries for graph visualization and layout, and is comparable to DAVID, GSEA, Ingenuity IPA and Ariadne Pathway Studio. There are pre-collated EGAN networks available for human (Homo sapiens), mouse (Mus musculus), rat (Rattus norvegicus), chicken (Gallus gallus), zebrafish (Danio rerio), fruit fly (Drosophila melanogaster), nematode (Caenorhabditis elegans), mouse-ear cress (Arabidopsis thaliana), rice (Oryza sativa) and brewer's yeast (Saccharomyces cerevisiae). There is now an EGAN module available for GenePattern (human-only). Platform: Windows compatible, Mac OS X compatible, Linux compatible gene, gene association, network, protein-protein interaction, pathway, interaction, annotation, signaling pathway, enrichment, cytoscape, visualization is listed by: 3DVC
is listed by: Gene Ontology Tools
is related to: Gene Ontology
is related to: Cytoscape
has parent organization: UCSF Helen Diller Family Comprehensive Cancer Center Biostatistics Core
NCI P30 CA92103 PMID:19933825 Free for academic use nlx_149222 SCR_008856 Exploratory Gene Association Networks, Exploratory Gene Association Networks (EGAN) 2026-02-12 09:44:42 8
GeneInfoViz
 
Resource Report
Resource Website
GeneInfoViz (RRID:SCR_005680) GeneInfoViz analysis service resource, service resource, production service resource, database, data analysis service, data or information resource GeneInfoViz is a web based tool for batch retrieval of gene function information, visualization of GO structure and construction of gene relation networks. It takes a input list of genes in the form of LocusLink ID, UniGeneID, gene symbol, or accession number and returns their functional genomic information. Based on the GO annotations of the given genes, GeneInfoViz allows users to visualize these genes in the DAG structure of GO, and construct a gene relation network at a selected level of the DAG. Platform: Online tool gene network, gene ontology, visualization, gene, ontology or annotation browser is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of Tennessee Health Science Center; Tennessee; USA
PMID:15724283 Free for academic use nlx_149121 SCR_005680 GeneInfoViz: Constructing and Visualizing Gene Relation Networks 2026-02-12 09:44:08 0
neuroVIISAS
 
Resource Report
Resource Website
1+ mentions
neuroVIISAS (RRID:SCR_006010) neuroVIISAS software resource, d visualization software, software application, network graph visualization software, data processing software, data analytics software, data visualization software An open framework for integrative data analysis, visualization and population simulations for the exploration of network dynamics on multiple levels. This generic platform allows the integration of neuroontologies, mapping functions for brain atlas development, and connectivity data administration; all of which are required for the analysis of structurally and neurobiologically realistic simulations of networks. What makes neuroVIISAS unique is the ability to integrate neuroontologies, image stacks, mappings, visualizations, analyzes and simulations to use them for modelling and simulations. Based on the analysis of over 2020 tracing studies, atlas terminologies and registered histological stacks of images, neuroVIISAS permits the definition of neurobiologically realistic networks that are transferred to the simulation engine NEST. The analysis on a local and global level, the visualization of connectivity data and the results of simulations offer new possibilities to study structural and functional relationships of neural networks. neuroVIISAS provide answers to questions like: # How can we assemble data of tracing studies? (Metastudy) # Is it possible to integrate tracing and brainmapping data? (Data Integration) # How does the network of analyzed tracing studies looks like? (Visualization) # Which graph theoretical properties posses such a network? (Analysis) # Can we perform population simulations of a tracing study based network? (Simulation and higher level data integration) neuroVIISAS can be used to organize mapping and connectivity data of central nervous systems of any species. The rat brain project of neuroVIISAS contains 450237 ipsi- and 175654 contralateral connections. A list of evaluated tracing studies are available. PyNEST script generation does work using WINDOWS OS, however, the script must be transferred to a UNIX OS with installed NEST. The results file of the NEST simulation can be visualized and analyzed by neuroVIISAS on a WINDOWS OS. platform, simulation, mapping data, connectivity data, central nervous system, tracing, connectivity, java, image modality, pynest, nest, animation, brain, nervous system, brain mapping, neuroimaging, terminology, ontology, connectomics, atlas, population spike analysis, analytics, connectome, 3d visualization, visual analytics, ontology is listed by: 3DVC
has parent organization: University of Rostock; Mecklenburg-Vorpommern; Germany
PMID:22350719 nlx_151398 http://139.30.176.116/index-Dateien/Page455.htm SCR_006010 neuro Visualization Imagemapping Information System for Analysis and Simulation 2026-02-12 09:44:22 8
WormBase
 
Resource Report
Resource Website
1000+ mentions
WormBase (RRID:SCR_003098) WB, WB REF, WP data repository, service resource, storage service resource, database, data or information resource Central data repository for nematode biology including complete genomic sequence, gene predictions and orthology assignments from range of related nematodes.Data concerning genetics, genomics and biology of C. elegans and related nematodes. Derived from initial ACeDB database of C. elegans genetic and sequence information, WormBase includes genomic, anatomical and functional information of C. elegans, other Caenorhabditis species and other nematodes. Maintains public FTP site where researchers can find many commonly requested files and datasets, WormBase software and prepackaged databases. RIN, Resource Information Network, catalog, database, blast, genomic sequence, gene prediction, orthology assignment, gene function, ortholog, roundworm, geneotype, phenotype, gene mapping, genomics, gene expression, transposon family, c elegans, wormmart, FASEB list, RRID Community Authority uses: InterMOD
is used by: NIF Data Federation
is used by: Resource Identification Portal
is used by: PhenoGO
is used by: Integrated Animals
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: OMICtools
is listed by: re3data.org
is listed by: InterMOD
is listed by: Resource Information Network
is affiliated with: InterMOD
is related to: AmiGO
is related to: GBrowse
is related to: Textpresso
is related to: Expression Patterns for C. elegans promoter GFP fusions
is related to: C. elegans Gene Knockout Consortium
is related to: NIH Data Sharing Repositories
is related to: UniParc at the EBI
is related to: UniParc
is related to: Integrated Manually Extracted Annotation
is related to: PhenoGO
has parent organization: Cold Spring Harbor Laboratory
has parent organization: Washington University in St. Louis; Missouri; USA
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
is parent organization of: C. elegans Development Vocabulary
is parent organization of: C. elegans Gross Anatomy Vocabulary
is parent organization of: C. elegans Phenotype Vocabulary
is parent organization of: OpenWorm
works with: A plasmid Editor
NHGRI ;
NIH Blueprint for Neuroscience Research ;
MRC ;
BBSRC ;
NHGRI U41 HG002223;
NIHGRI P41 HG02223
PMID:24194605
PMID:19910365
PMID:17991679
PMID:15608221
nif-0000-00053, OMICS_01664, r3d100010424 http://www.wormbase.org/#01-23-6
https://doi.org/10.17616/R3089Z
SCR_003098 , WB, Worm Base, WB REF, WP 2026-02-12 09:43:31 1825
Unified Human Interactome
 
Resource Report
Resource Website
10+ mentions
Unified Human Interactome (RRID:SCR_005805) UniHI data or information resource, database A database of human molecular interaction networks that integrates human protein-protein and transcriptional regulatory interactions from 15 distinct resources and aims to give direct and easy access to the integrated data set and to enable users to perform network-based investigations. The database includes tools (i) to search for molecular interaction partners of query genes or proteins in the integrated dataset, (ii) to inspect the origin, evidence and functional annotation of retrieved proteins and interactions, (iii) to visualize and adjust the resulting interaction network, (iv) to filter interactions based on method of derivation, evidence and type of experiment as well as based on gene expression data or gene lists and (v) to analyze the functional composition of interaction networks. molecular interaction network, interactome, protein, protein interaction network, protein interaction, pathway, function, visualization, protein-protein interaction, transcriptional regulatory interaction, network is listed by: OMICtools
has parent organization: University of Algarve; Faro; Portugal
PMID:24214987
PMID:22218860
PMID:18984619
PMID:17158159
Public, Non-commercial OMICS_01911, nif-0000-03609 http://www.mdc-berlin.de/unihi SCR_005805 2026-02-11 10:57:14 19
DroID - Drosophila Interactions Database
 
Resource Report
Resource Website
10+ mentions
DroID - Drosophila Interactions Database (RRID:SCR_006634) DroID data or information resource, database A gene and protein interactions database designed specifically for the model organism Drosophila including protein-protein, transcription factor-gene, microRNA-gene, and genetic interactions. For advanced searches and dynamic graphing capabilities the IM Browser and a DroID Cytoscape plugin are available. interaction, gene, protein, protein interaction, annotation, transcription factor, rna, protein-protein interaction, interactome, gene expression, phenotype, interolog, ortholog is listed by: OMICtools
is related to: Cytoscape
has parent organization: Wayne State University School of Medicine; Michigan; USA
PMID:21036869
PMID:18840285
Free, Public, Acknowledgement requested nif-0000-02767, OMICS_01908 SCR_006634 DroID - The Drosophila Interactions Database 2026-02-11 10:57:26 35
ECgene: Gene Modeling with Alternative Splicing
 
Resource Report
Resource Website
10+ mentions
ECgene: Gene Modeling with Alternative Splicing (RRID:SCR_007634) ECgene data or information resource, database Database of functional annotation for alternatively spliced genes. It uses a gene-modeling algorithm that combines the genome-based expressed sequence tag (EST) clustering and graph-theoretic transcript assembly procedures. It contains genome, mRNA, and EST sequence data, as well as a genome browser application. Organisms included in the database are human, dog, chicken, fruit fly, mouse, rhesus, rat, worm, and zebrafish. Annotation is provided for the whole transcriptome, not just the alternatively spliced genes. Several viewers and applications are provided that are useful for the analysis of the transcript structure and gene expression. The summary viewer shows the gene summary and the essence of other annotation programs. The genome browser and the transcript viewer are available for comparing the gene structure of splice variants. Changes in the functional domains by alternative splicing can be seen at a glance in the transcript viewer. Two unique ways of analyzing gene expression is also provided. The SAGE tags deduced from the assembled transcripts are used to delineate quantitative expression patterns from SAGE libraries available publicly. The cDNA libraries of EST sequences in each cluster are used to infer qualitative expression patterns. est cluster, genome, alternative splicing, splice, gene, mrna, est, annotation, gene modeling, structure, function, gene expression, transcript, genome browser, differential expression, snp is listed by: OMICtools
is related to: Gene Ontology
has parent organization: Ewha Womans University; Seoul; South Korea
PMID:17132829
PMID:15805497
PMID:15608289
nif-0000-02780, OMICS_01884 http://genome.ewha.ac.kr/ECgene/ SCR_007634 ECgene - Genome Annotation for Alternative Splicing 2026-02-11 10:57:40 12
Connectome Mapping Toolkit
 
Resource Report
Resource Website
1+ mentions
Connectome Mapping Toolkit (RRID:SCR_001644) Connectome Mapping Toolkit data set, software toolkit, software resource, data management software, software application, data processing software, data or information resource, image processing software, image analysis software A Python-based open source toolkit for magnetic resonance connectome mapping, data management, sharing, visualization and analysis. The toolkit includes the connectome mapper (a full DMRI processing pipeline), a new file format for multi modal data and metadata, and a visualization application. magnetic resonance, connectome, mapping, data management, data sharing, visualization, analysis, connectome mapper, processing pipeline, python, connectomics, multi-modal, network analysis, neuroimaging, neuroinformatics tool, mri, knowledge-base, semantic, technology, mapping, source code is related to: Diffusion MRI of Traumatic Brain Injury
has parent organization: University of Lausanne; Lausanne; Switzerland
has parent organization: Ecole Polytechnique Federale de Lausanne; Lausanne; Switzerland
is parent organization of: Connectome Viewer
Swiss National Science Foundation 33CM30-124089 PMID:21713110 Free, Available for download, Freely available nlx_153920 http://www.cmtk.org/
http://www.connectome.ch/
SCR_001644 2026-02-12 09:43:12 7
PITA
 
Resource Report
Resource Website
1000+ mentions
PITA (RRID:SCR_010853) PITA data or information resource, data set Catalogs of predicted microRNA targets in worm (based on ce6 genome assembly), fly (dm3), mouse (mm9) and human (hg18). We follow standard seed parameter settings and consider seeds of length 6-8 bases, beginning at position 2 of the microRNA. No mismatches or loops are allowed, but a single G:U wobble is allowed in 7- or 8-mers. In genes missing a 3' UTR annotation, 500 bp (fly), 800 bp (human and mouse) or 300 bp (worm) downstream of the annotated end of the coding sequence were used as the predicted UTR. For each organism, a catalog with zero flank and with a flank of 3 and 15 bases upstream and downstream. is listed by: OMICtools OMICS_00412 SCR_010853 2026-02-11 10:58:22 1047
InteroPorc
 
Resource Report
Resource Website
1+ mentions
InteroPorc (RRID:SCR_002067) InteroPorc analysis service resource, source code, software resource, service resource, production service resource, database, software application, data analysis service, data analysis software, data processing software, data or information resource Automatic prediction tool to infer protein-protein interaction networks, it is applicable for lots of species using orthology and known interactions. The interoPORC method is based on the interolog concept and combines source interaction datasets from public databases as well as clusters of orthologous proteins (PORC) available on Integr8. Users can use this page to ask InteroPorc for all species present in Integr8. Some results are already computed and users can run InteroPorc to investigate any other species. Currently, the following databases are processed and merged (with datetime of the last available public release for each database used): IntAct, MINT, DIP, and Integr8. orthology, prediction, protein interaction, tool, sequenced genome, proteinprotein interaction, inferred interaction, molecular interaction, interaction, protein, bio.tools is listed by: bio.tools
is listed by: Debian
is related to: Integr8 : Access to complete genomes and proteomes
is related to: IntAct
is related to: MINT
is related to: Database of Interacting Proteins (DIP)
is related to: PSICQUIC Registry
has parent organization: CEA; Gif sur Yvette; France
European Union FELICS 021902 RII3;
Marie Curie Fellowship ;
French National Agency of Research ANR Biosys06_134823 SULFIRHOM;
French Atomic Energy Commission
PMID:18508856 Open unspecified license, Acknowledgement requested nif-0000-20816, biotools:interoporc https://bio.tools/interoporc SCR_002067 InteroPorc: Automatic molecular interaction predictions, Automatic molecular interaction predictions 2026-02-12 09:43:17 6
Caenorhabditis elegans Natural Diversity Resource (CeNDR)
 
Resource Report
Resource Website
10+ mentions
Caenorhabditis elegans Natural Diversity Resource (CeNDR) (RRID:SCR_014958) CeNDR organism supplier, material resource, biomaterial supply resource Supplier and researcher of wild C. elegans strains. CeNDR supplies organisms, analyzes whole-genome sequences, and facilitates genetic mappings to aid researchers in gene discovery. c. elegans, caenorhabditis elegans, strains, n2, roundworm, nematode, gene analysis, organism supplier, portal has parent organization: Northwestern University; Illinois; USA American Cancer Society Research Scholar Award ;
Amazon Web Services Research Grant ;
Weinberg College of Arts and Sciences starter innovation award ;
Northwestern University Start-up Funds ;
NIGMS R01GM107227;
NSF DGE-1324585
PMID:27701074 Available to the research community SCR_014958 Caenorhabditis elegans Natural Diversity Resource 2026-02-12 09:46:05 22
Information Hyperlinked Over Proteins
 
Resource Report
Resource Website
10+ mentions
Information Hyperlinked Over Proteins (RRID:SCR_004829) iHOP data or information resource, database, service resource Information system that provides a network of concurring genes and proteins extends through the scientific literature touching on phenotypes, pathologies and gene function. It provides this network as a natural way of accessing millions of PubMed abstracts. By using genes and proteins as hyperlinks between sentences and abstracts, the information in PubMed can be converted into one navigable resource, bringing all advantages of the internet to scientific literature research. Moreover, this literature network can be superimposed on experimental interaction data (e.g., yeast-two hybrid data from Drosophila melanogaster and Caenorhabditis elegans) to make possible a simultaneous analysis of new and existing knowledge. The network contains half a million sentences and 30,000 different genes from humans, mice, D. melanogaster, C. elegans, zebrafish, Arabidopsis thaliana, yeast and Escherichia coli. phenotype, gene, protein, interaction, pathology, physiology, gene network, network, literature, gene function, text-mining, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: PubMed
has parent organization: Autonomous University of Madrid; Madrid; Spain
European Union IST-2001- 32688;
European Union QLRT-2001-00015
PMID:15226743 Creative Commons Attribution-NoDerivs License, Works v3 biotools:ihop, nif-0000-00232, OMICS_01185 https://bio.tools/ihop SCR_004829 iHOP - Information Hyperlinked over Proteins 2026-02-12 09:43:55 24
mirWIP
 
Resource Report
Resource Website
1+ mentions
mirWIP (RRID:SCR_005055) mirWIP service resource, analysis service resource, production service resource, data analysis service Tool to search for targets of conserved microRNAs in Caenorhabditis elegans by weighting RISC-immunoprecipitation-enriched parameters. immunoprecipitation-enriched parameter, site, target, mirna, ribonucleoprotein, transcript is listed by: OMICtools
has parent organization: University of Massachusetts Medical School; Massachusetts; USA
PMID:19160516 OMICS_02284 SCR_005055 mirWIP - miRNA Targets by Weighting RISC-IP Enriched Parameters, miRNA targets by weighting immunoprecipitation-enriched parameters 2026-02-12 09:44:02 4
FuncAssociate: The Gene Set Functionator
 
Resource Report
Resource Website
10+ mentions
FuncAssociate: The Gene Set Functionator (RRID:SCR_005768) FuncAssociate service resource, analysis service resource, production service resource, data analysis service A web-based tool that accepts as input a list of genes, and returns a list of GO attributes that are over- (or under-) represented among the genes in the input list. Only those over- (or under-) representations that are statistically significant, after correcting for multiple hypotheses testing, are reported. Currently 37 organisms are supported. In addition to the input list of genes, users may specify a) whether this list should be regarded as ordered or unordered; b) the universe of genes to be considered by FuncAssociate; c) whether to report over-, or under-represented attributes, or both; and d) the p-value cutoff. A new version of FuncAssociate supports a wider range of naming schemes for input genes, and uses more frequently updated GO associations. However, some features of the original version, such as sorting by LOD or the option to see the gene-attribute table, are not yet implemented. Platform: Online tool gene, gene ontology, statistical analysis, web service, bio.tools is listed by: Gene Ontology Tools
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
has parent organization: Roth Laboratory
NIH ;
Canadian Institute for Advanced Research ;
NINDS NS054052;
NINDS NS035611;
NHLBI HL081341;
NHGRI HG0017115;
NHGRI HG004233;
NHGRI HG003224
PMID:19717575
PMID:14668247
Free for academic use, Acknowledgement requested biotools:funcassociate, OMICS_02264, nlx_149233 http://llama.mshri.on.ca/cgi/func/funcassociate
https://bio.tools/funcassociate
SCR_005768 2026-02-12 09:44:16 36

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

  3. Logging in and Registering

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

  4. Searching

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

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

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

  6. Facets

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

  7. Further Questions

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