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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
Organelle DB
 
Resource Report
Resource Website
1+ mentions
Organelle DB (RRID:SCR_007837) Organelle DB data repository, service resource, d spatial image, storage service resource, database, data or information resource, image collection Database of organelle proteins, and subcellular structures / complexes from compiled protein localization data from organisms spanning the eukaryotic kingdom. All data may be downloaded as a tab-delimited text file and new localization data (and localization images, etc) for any organism relevant to the data sets currently contained in Organelle DB is welcomed. The data sets in Organelle DB encompass 138 organisms with emphasis on the major model systems: S. cerevisiae, A. thaliana, D. melanogaster, C. elegans, M. musculus, and human proteins as well. In particular, Organelle DB is a central repository of yeast protein localization data, incorporating results from both previous and current (ongoing) large-scale studies of protein localization in Saccharomyces cerevisiae. In addition, we have manually curated several recent subcellular proteomic studies for incorporation in Organelle DB. In total, Organelle DB is a singular resource consolidating our knowledge of the protein composition of eukaryotic organelles and subcellular structures. When available, we have included terms from the Gene Ontologies: the cellular component, molecular function, and biological process fields are discussed more fully in GO. Additionally, when available, we have included fluorescent micrographs (principally of yeast cells) visualizing the described protein localization. Organelle View is a visualization tool for yeast protein localization. It is a visually engaging way for high school and undergraduate students to learn about genetics or for visually-inclined researchers to explore Organelle DB. By revealing the data through a colorful, dimensional model, we believe that different kinds of information will come to light. gene, fly, vertebrate, human, mouse, plant, worm, yeast, protein, k-12, organelle, protein localization, function, subcellular structure, protein complex, sequence, annotation, micrograph, visualization, data analysis service is related to: Gene Ontology
has parent organization: University of Michigan; Ann Arbor; USA
American Cancer Society Research Scholar Grant RSG-06-179-01-MBC;
March of Dimes Basil O'Connor Starter Scholar Research award 5-FY05-1224;
NSF DBI-0543017
PMID:17130152
PMID:15608270
Free, Acknowledgement requested nif-0000-03226 SCR_007837 Organelle DB: A Database of Organelles and Protein Complexes 2026-02-12 09:44:36 7
GeneMerge
 
Resource Report
Resource Website
10+ mentions
GeneMerge (RRID:SCR_005744) GeneMerge analysis service resource, software resource, service resource, production service resource, software application, data analysis service THIS RESOURCE IS NO LONGER IN SERVCE, documented September 2, 2016. Web-based and standalone application that returns a wide range of functional genomic data for a given set of study genes and provides rank scores for over-representation of particular functions or categories in the data. It uses the hypergeometric test statistic which returns statistically correct results for samples of all sizes and is the #2 fastest GO tool available (Khatri and Draghici, 2005). GeneMerge can be used with any discrete, locus-based annotation data, including, literature references, genetic interactions, mutant phenotypes as well as traditional Gene Ontology queries. GeneMerge is particularly useful for the analysis of microarray data and other large biological datasets. The big advantage of GeneMerge over other similar programs is that you are not limited to analyzing your data from the perspective of a pre-packaged set of gene-association data. You can download or create gene-association files to analyze your data from an unlimited number of perspectives. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene, genomics, functional genomic data, analysis, post-genomic analysis, data mining, hypothesis testing, statistical analysis, slimmer-type tool, term enrichment, text mining, false discovery rate, bonferroni correction, false discovery rate and bonferroni correction, perl, microarray is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Harvard University; Cambridge; United States
PMID:12724301 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149203 http://genemerge.cbcb.umd.edu/ SCR_005744 2026-02-12 09:44:14 26
GeneCodis
 
Resource Report
Resource Website
100+ mentions
GeneCodis (RRID:SCR_006943) GeneCodis analysis service resource, data access protocol, software resource, service resource, web service, production service resource, data analysis service Web-based tool for the ontological analysis of large lists of genes. It can be used to determine biological annotations or combinations of annotations that are significantly associated to a list of genes under study with respect to a reference list. As well as single annotations, this tool allows users to simultaneously evaluate annotations from different sources, for example Biological Process and Cellular Component categories of Gene Ontology., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. functional analysis, gene, annotation, statistical analysis, functional genomics, 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
is related to: KEGG
has parent organization: Spanish National Research Council; Madrid; Spain
Juan de la Cierva research program ;
Spanish Minister of Science and Innovation BIO2010-17527;
Government of Madrid P2010/BMD-2305
PMID:22573175
PMID:19465387
PMID:17204154
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02221, biotools:genecodis3, nlx_149254 https://bio.tools/genecodis3 SCR_006943 Gene annotations co-ocurrence discovery, GeneCodis - Gene annotations co-ocurrence discovery 2026-02-12 09:44:36 348
HomoloGene
 
Resource Report
Resource Website
100+ mentions
HomoloGene (RRID:SCR_002924) HomoloGene data or information resource, database, service resource Automated system for constructing putative homology groups from complete gene sets of wide range of eukaryotic species. Databse that provides system for automatic detection of homologs, including paralogs and orthologs, among annotated genes of sequenced eukaryotic genomes. HomoloGene processing uses proteins from input organisms to compare and sequence homologs, mapping back to corresponding DNA sequences. Reports include homology and phenotype information drawn from Online Mendelian Inheritance in Man, Mouse Genome Informatics, Zebrafish Information Network, Saccharomyces Genome Database and FlyBase. homolog, paralog, ortholog, genome, gene, protein, protein alignment, phenotype, conserved domain, homology, amino acid sequence, cell, dna, gold standard is used by: NIF Data Federation
is used by: Nowomics
is used by: MitoMiner
is listed by: OMICtools
is listed by: re3data.org
is related to: OMIM
is related to: Mouse Genome Informatics (MGI)
is related to: Zebrafish Information Network (ZFIN)
is related to: SGD
is related to: FlyBase
is related to: ProbeMatchDB 2.0
is related to: Biomine
is related to: Consensus CDS
has parent organization: NCBI
PMID:23193264 Free, Freely availalbe nif-0000-02975, r3d100010781, OMICS_01544 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=homologene
https://doi.org/10.17616/R3889F
SCR_002924 NCBI HomoloGene 2026-02-12 09:43:29 437
Arabidopsis thaliana Genome Database
 
Resource Report
Resource Website
10+ mentions
Arabidopsis thaliana Genome Database (RRID:SCR_001901) AtGDB analysis service resource, service resource, production service resource, database, data analysis service, data or information resource Database providing a sequence-centered genome view for Arabidopsis thaliana, with a narrow focus on gene structure annotation. The current genome assembly displayed at AtGDB is version TAIR9. Annotated gene models are TAIR10. They have mapped the complete set of 176,915 publicly available Arabidopsis EST sequences onto the Arabidopsis genome using GeneSeqer, a spliced alignment program incorporating sequence similarity and splice site scoring. About 96% of the available ESTs could be properly aligned with a genomic locus, with the remaining ESTs deriving from organelle genomes and non-Arabidopsis sources or displaying insufficient sequence quality for alignment. The mapping provides verified sets of EST clusters for evaluation of EST clustering programs. Analysis of the spliced alignments suggests corrections to current gene structure annotation and provides examples of alternative and non-canonical pre-mRNA splicing. expressed sequence tag, est sequence, contig, gene structure, genome, arabidopsis thaliana, cdna, plant database, blast, annotation has parent organization: Iowa State University; Iowa; USA NSF IOS-0606909;
NSF DBI-0110254;
NSF DBI-0321600
PMID:16219921
PMID:14681433
PMID:12805580
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02582 SCR_001901 Arabidopsis thaliana Genome DB 2026-02-12 09:43:15 10
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
Arabidopsis thaliana Protein Interactome Database
 
Resource Report
Resource Website
1+ mentions
Arabidopsis thaliana Protein Interactome Database (RRID:SCR_001896) AtPID data repository, service resource, storage service resource, database, data or information resource Centralized platform to depict and integrate the information pertaining to protein-protein interaction networks, domain architecture, ortholog information and GO annotation in the Arabidopsis thaliana proteome. The Protein-protein interaction pairs are predicted by integrating several methods with the Naive Baysian Classifier. All other related information curated is manually extracted from published literature and other resources from some expert biologists. You are welcomed to upload your PPI or subcellular localization information or report data errors. Arabidopsis proteins is annotated with information (e.g. functional annotation, subcellular localization, tissue-specific expression, phosphorylation information, SNP phenotype and mutant phenotype, etc.) and interaction qualifications (e.g. transcriptional regulation, complex assembly, functional collaboration, etc.) via further literature text mining and integration of other resources. Meanwhile, the related information is vividly displayed to users through a comprehensive and newly developed display and analytical tools. The system allows the construction of tissue-specific interaction networks with display of canonical pathways. gene, gene expression, domain, annotation, ineractome, metabolic pathway, phylogenetic, protein, protein-protein interaction, signaling pathway, proteome, protein subcellular location, ortholog, gene regulation, pathway, phenotype is listed by: OMICtools
is related to: Gene Ontology
has parent organization: Northeast Forest University; Harbin; China
National Basic Research Program of China 2010CB945400;
National Basic Research Program of China 2007CB108800;
National High Technology Research and Development Program of China 2006AA02Z313;
National High Technology Research and Development Program of China 2006AA10Z129;
National Natural Science Foundation of China 30870575;
National Natural Science Foundation of China 30730078;
Science and Technology Commission of Shanghai Municipality 06DZ22923
PMID:21036873
PMID:17962307
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01898, nif-0000-02585 http://atpid.biosino.org/ SCR_001896 AtPID Database 2026-02-12 09:43:15 8
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
PhosPhAt
 
Resource Report
Resource Website
50+ mentions
PhosPhAt (RRID:SCR_003332) PhosPhAt analysis service resource, data repository, service resource, production service resource, storage service resource, database, data analysis service, data or information resource Database containing information on Arabidopsis phosphorylation sites which were identified by mass spectrometry in large scale experiments from different research groups. Specific information on the peptide properties as well as on the experimental and analytical context is given. The PhosPhAt service has a built-in plant specific phosphorylation site predictor trained on the experimental dataset for Serine, threonine and tyrosine phosphorylation (pSer, pThr, pTyr). Protein sequences or Arabidopsis AGI gene identifier can be submitted to the predictor. Users and researchers are encouraged to assist in keeping the database current by submitting either published data or unpublished data (MS/MS data required). phosphorylation, peptide, function, mass spectrometry, kinase, serine, threonine, tyrosine, phosphoprotein, phosphopeptide, tryptic phosphopeptide, serine phosphosite, threonine phosphosite, tyrosine phosphosite, FASEB list has parent organization: University of Hohenheim; Baden-Wurttemberg; Germany PMID:23172287
PMID:19880383
PMID:17984086
Free, Freely available nif-0000-03277 http://phosphat.mpimp-golm.mpg.de/app.html SCR_003332 Arabidopsis Protein Phosphorylation Site Database 2026-02-12 09:43:35 57
PubSearch
 
Resource Report
Resource Website
1+ mentions
PubSearch (RRID:SCR_005830) PubSearch data or information resource, database, service resource, software resource THIS RESOURCE IS NO LONGER IN SERVCE, documented September 2, 2016. PubSearch is a web-based literature curation tool, allowing curators to search and annotate genes to keywords from articles. It has a simple mySQL database backend and uses a set of Java Servlets and JSPs for querying, modifying, and adding gene, gene-annotation, and literature information. PubSearch can be downloaded from GMOD. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene, annotate, editor, literature curation tool, literature, ontology or annotation editor is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: TAIR
has parent organization: Stanford University; Stanford; California
NHGRI R01HG02728 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149338 SCR_005830 2026-02-12 09:44:11 1
mirEX
 
Resource Report
Resource Website
10+ mentions
mirEX (RRID:SCR_006060) mirEX analysis service resource, service resource, production service resource, database, atlas, data analysis service, data or information resource mirEX is a comprehensive platform for comparative analysis of primary microRNA expression data. quantitative real-time PCR-based gene expression profiles are stored in a universal and expandable database scheme and wrapped by an intuitive user-friendly interface. A new way of accessing gene expression data in mirEX includes a simple mouse operated querying system and dynamic graphs for data mining analyses. In contrast to other publicly available databases, the mirEX interface allows a simultaneous comparison of expression levels between various microRNA genes in diverse organs and developmental stages. Currently, mirEX integrates information about the expression profile of 190 Arabidopsis thaliana pri-miRNAs in seven different developmental stages: seeds, seedlings and various organs of mature plants. Additionally, by providing RNA structural models, publicly available deep sequencing results, experimental procedure details and careful selection of auxiliary data in the form of web links, mirEX can function as a one-stop solution for Arabidopsis microRNA information. This database aims to be useful to anyone investigating the role of microRNAs in shaping plant development, organ formation and response to different biotic and abiotic stresses. To start exploring the database just press the "Browse Atlas" button or search for a particular microRNA record by typing at least two numbers from its ID in the window. microrna gene expression, microrna, gene expression, gene, organ, developmental stage, plant, seed, seedling, mature plant, pri-mirna, biotic stress, abiotic stress, organ formation, primer, cdna has parent organization: Adam Mickiewicz University in Poznan; Poznan; Poland Foundation for Polish Science ;
European Union ;
Regional Development Fund MPD 2010/3;
Polish Ministry of Science and Higher Education 3011/B/P01/2009/37
PMID:22013167 nlx_151462 http://bioinfo.amu.edu.pl/mirex SCR_006060 2026-02-12 09:44:16 10
CSHL - Hannon Lab
 
Resource Report
Resource Website
50+ mentions
CSHL - Hannon Lab (RRID:SCR_005982) Hannon Lab data or information resource, portal, laboratory portal, organization portal The Hannon laboratory comprises a broad spectrum of programs in small RNA biology, mammalian genetics and genomics. We study RNAi and related pathways in a wide variety of organisms to extract common themes that define both the mechanisms by which small RNAs act and the biological processes which they impact. Currently, we focus on microRNAs, endogenous siRNAs and piRNAs and their roles in gene regulation, cancer biology, stem cell biology and in defense of the genome against transposons. In collaboration with Steve Elledge (Harvard) and Scott Lowe (CSHL), we develop genome-wide shRNA tools for RNAi-based genetics in mammalian cells, and we are now producing similar collections of artificial microRNAs for Arabidopsis with Detlef Weigel (MPI), Dick McCombie (CSHL) and Rob Martienssen (CSHL) as part of the 2010 project (see 2010.cshl.edu). Our genomic efforts include the application of RNAi-based genetic screens to cancer biology and stem cells. We also make heavy use of next generation sequencing methodologies for probing small RNA populations, in part as a member of the ENCODE consortium (with Tom Gingeras, CSHL). Finally, we develop (with Dick McCombie) and apply focal re-sequencing methods for identifying disease relevant mutations, for probing the epigenetic landscape and for the study of human evolution. rnai, rna, mammal, genetics, genomics, microrna, sirna, pirna, gene regulation, cancer biology, stem cell biology, defense, genome, transposon, cancer, stem cell has parent organization: Cold Spring Harbor Laboratory nlx_151354 SCR_005982 Cold Spring Harbor Laboratory - Hannon Lab 2026-02-12 09:44:09 66
Saskatoon Arabidopsis T-DNA mutant population SK Collection
 
Resource Report
Resource Website
1+ mentions
Saskatoon Arabidopsis T-DNA mutant population SK Collection (RRID:SCR_004939) SK-FST material resource, biomaterial supply resource Population of almost 50,000 activation tagged Arabidopsis thaliana lines that have been archived as individual lines to the T3 generation. The population is an excellent tool for both reverse and forward genetic screens and has been used successfully to identify a number of novel mutants. Flanking sequence tags (FST) have been generated and mapped for 15,507 lines to enable further application of the population, while providing a clear distribution of T-DNA insertions across the genome. The population is being screened for a number of biochemical and developmental phenotypes. The population provides an additional tool for plant researcher's to assist with determining gene function for the many as yet uncharacterized genes annotated within the Arabidopsis genome sequence. The presence of enhancer elements on the inserted T-DNA element (pSKI015) allows both knock-out and dominant activation phenotypes to be identified for traits of interest. arabidopsis thaliana, genetics, mutant, biochemical, developmental, phenotype, gene function, flanking sequence tag, trait, t-dna is related to: TAIR AAFC Canadian Crop Genomics Initiative ;
NSERC
PMID:19646253
PMID:19347643
Free, Public nlx_91019 SCR_004939 SK population 2026-02-12 09:44:02 3
GlimmerHMM
 
Resource Report
Resource Website
500+ mentions
GlimmerHMM (RRID:SCR_002654) GlimmerHMM source code, software resource A gene finder based on a Generalized Hidden Markov Model (GHMM). Although the gene finder conforms to the overall mathematical framework of a GHMM, additionally it incorporates splice site models adapted from the GeneSplicer program and a decision tree adapted from GlimmerM. It also utilizes Interpolated Markov Models for the coding and noncoding models . Currently, GlimmerHMM's GHMM structure includes introns of each phase, intergenic regions, and four types of exons (initial, internal, final, and single). gene, hidden markov model is related to: Glimmer
has parent organization: Johns Hopkins University; Maryland; USA
NIH ;
NLM R01-LM06845;
NLM R01-LM007938
PMID:15145805 Free, Available for download, Freely available nlx_156092 SCR_002654 GlimmerHMM - Eukaryotic Gene-Finding System 2026-02-12 09:43:25 576
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
ADGO
 
Resource Report
Resource Website
1+ mentions
ADGO (RRID:SCR_006343) ADGO service resource, analysis service resource, production service resource, data analysis service A web-based tool that provides composite interpretations for microarray data comparing two sample groups as well as lists of genes from diverse sources of biological information. It provides multiple gene set analysis methods for microarray inputs as well as enrichment analyses for lists of genes. It screens redundant composite annotations when generating and prioritizing them. It also incorporates union and subtracted sets as well as intersection sets. Users can upload their gene sets (e.g. predicted miRNA targets) to generate and analyze new composite sets. microarray, gene, annotation, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:21624890 Acknowledgement requested OMICS_02229, biotools:adgo https://bio.tools/adgo SCR_006343 2026-02-12 09:44:31 3
BaCelLo
 
Resource Report
Resource Website
10+ mentions
BaCelLo (RRID:SCR_011965) BaCelLo service resource, analysis service resource, production service resource, data analysis service A predictor for the subcellular localization of proteins in eukaryotes that is based on a decision tree of several support vector machines (SVMs). It classifies up to four localizations for Fungi and Metazoan proteins and five localizations for Plant ones. BaCelLo's predictions are balanced among different classes and all the localizations are considered as equiprobable. protein, data set, proteome is listed by: OMICtools
is listed by: SoftCite
has parent organization: University of Bologna; Bologna; Italy
PMID:16873501 OMICS_01616 SCR_011965 2026-02-12 09:45:46 45

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