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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
CHASM/SNV-Box
 
Resource Report
Resource Website
1+ mentions
CHASM/SNV-Box (RRID:SCR_006445) CHASM/SNV-Box data or information resource, database, software resource CHASM is a method that predicts the functional significance of somatic missense mutations observed in the genomes of cancer cells, allowing mutations to be prioritized in subsequent functional studies, based on the probability that they give the cells a selective survival advantage. SNV-Box is a database of pre-computed features of all possible amino acid substitutions at every position of the annotated human exome. Users can rapidly retrieve features for a given protein amino acid substitution for use in machine learning. is listed by: OMICtools Cancer NCI CA152432;
NCI CA135866;
NSF DBI0845275
Acknowledgement requested, Free, Non-commercial OMICS_00127 SCR_006445 CHASM / SNV-Box, Cancer-specific High-throughput Annotation of Somatic Mutations 2026-09-19 12:51:11 3
FlyBase
 
Resource Report
Resource Website
1000+ mentions
FlyBase (RRID:SCR_006549) FB data or information resource, data repository, database, organism-related portal, portal, service resource, storage service resource, topical portal Database of Drosophila genetic and genomic information with information about stock collections and fly genetic tools. Gene Ontology (GO) terms are used to describe three attributes of wild-type gene products: their molecular function, the biological processes in which they play a role, and their subcellular location. Additionally, FlyBase accepts data submissions. FlyBase can be searched for genes, alleles, aberrations and other genetic objects, phenotypes, sequences, stocks, images and movies, controlled terms, and Drosophila researchers using the tools available from the "Tools" drop-down menu in the Navigation bar. RIN, Resource Information Network, mutant, gene, genome, blast, genotype, phenotype, allele, sequence, stock, image, movie, controlled term, video resource, image collection, life-cycle, genome, expression, rna-seq, genetics, drosophilidae, bio.tools, FASEB list, RRID Community Authority is used by: NIF Data Federation
is used by: Resource Identification Portal
is used by: PhenoGO
is used by: Integrated Animals
is used by: Drososhare
is recommended by: NIDDK Information Network (dkNET)
is recommended by: National Library of Medicine
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: re3data.org
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: Resource Information Network
is related to: FlyMine
is related to: Virtual Fly Brain
is related to: AmiGO
is related to: Drosophila melanogaster Exon Database
is related to: HomoloGene
is related to: UniParc at the EBI
is related to: UniParc
is related to: Gene Ontology
is related to: NIH Data Sharing Repositories
is related to: GBrowse
is related to: Integrated Manually Extracted Annotation
is related to: PhenoGO
has parent organization: Harvard University; Cambridge; United States
has parent organization: University of Cambridge; Cambridge; United Kingdom
has parent organization: Indiana University; Indiana; USA
has parent organization: University of New Mexico; New Mexico; USA
is parent organization of: Drosophila anatomy and development ontologies
is parent organization of: Fly Taxonomy
is parent organization of: FlyBase Controlled Vocabulary
is parent organization of: Drosophila Development Ontology
is organization facet of: Alliance of Genome Resources
Indiana Genomics Initiative ;
MRC ;
NIH Blueprint for Neuroscience Research ;
NIHGRI P41 HG000739;
NSF
PMID:24234449
PMID:22127867
PMID:18948289
PMID:18641940
PMID:18160408
PMID:17099233
PMID:16381917
PMID:15608223
PMID:12519974
PMID:11752267
PMID:11465064
PMID:9847148
PMID:9399806
PMID:9045212
PMID:8594600
PMID:8578603
PMID:7937045
PMID:7925011
nif-0000-00558, r3d100010591, OMICS_01649, biotools:flybase https://bio.tools/flybase, https://doi.org/10.17616/R3903Q http://flybase.net SCR_006549 flybase A Drosophila Genomic and Genetic Database, FlyBase: A Database of Drosophila Genes and Genomes, FLYBASE, FlyBase: A Database of Drosophila Genes & Genomes, FB 2026-09-19 12:51:13 4234
Decombinator
 
Resource Report
Resource Website
10+ mentions
Decombinator (RRID:SCR_006732) data analysis software, data processing software, software application, software resource, software toolkit Software suite for analysis of T cell receptor repertoire data. Used for fast, efficient analysis of T cell receptor (TcR) repertoire samples, designed to be accessible to those with no previous programming experience. Python, t-cell receptor sequence, t-cell receptor, sequence, deep sequencing, TCR repertoires, repertoire data, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: University College London; London; United Kingdom
PMID:23303508
PMID:32853330
Free, Available for download, Freely available biotools:decombinator, OMICS_00001 https://github.com/innate2adaptive/Decombinator, https://bio.tools/decombinator SCR_006732 Decombinator v2.2, Decombinator v4.0.3 2026-09-19 12:51:17 32
FDM
 
Resource Report
Resource Website
1+ mentions
FDM (RRID:SCR_006733) FDM software resource A graph-based statistical method to detect differential transcription using RNA-seq data. is listed by: OMICtools OMICS_01332 SCR_006733 2026-09-19 12:51:17 1
htSeqTools
 
Resource Report
Resource Website
10+ mentions
htSeqTools (RRID:SCR_006614) htSeqTools software resource Software tools for quality control, visualization and processing for High-Throughput Sequencing data. These include MDS plots (analogues to PCA), detecting inefficient immuno-precipitation or over-amplification artifacts, tools to identify and test for genomic regions with large accumulation of reads, and visualization of coverage profiles. high-throughput sequencing, chip-seq, rnaseq is listed by: OMICtools
has parent organization: Bioconductor
OMICS_01233 SCR_006614 2026-09-19 12:51:14 11
InterPro
 
Resource Report
Resource Website
5000+ mentions
InterPro (RRID:SCR_006695) InterPro analysis service resource, data access protocol, data analysis service, data or information resource, database, production service resource, service resource, software resource, web service Service providing functional analysis of proteins by classifying them into families and predicting domains and important sites. They combine protein signatures from a number of member databases into a single searchable resource, capitalizing on their individual strengths to produce a powerful integrated database and diagnostic tool. This integrated database of predictive protein signatures is used for the classification and automatic annotation of proteins and genomes. InterPro classifies sequences at superfamily, family and subfamily levels, predicting the occurrence of functional domains, repeats and important sites. InterPro adds in-depth annotation, including GO terms, to the protein signatures. You can access the data programmatically, via Web Services. The member databases use a number of approaches: # ProDom: provider of sequence-clusters built from UniProtKB using PSI-BLAST. # PROSITE patterns: provider of simple regular expressions. # PROSITE and HAMAP profiles: provide sequence matrices. # PRINTS provider of fingerprints, which are groups of aligned, un-weighted Position Specific Sequence Matrices (PSSMs). # PANTHER, PIRSF, Pfam, SMART, TIGRFAMs, Gene3D and SUPERFAMILY: are providers of hidden Markov models (HMMs). Your contributions are welcome. You are encouraged to use the ''''Add your annotation'''' button on InterPro entry pages to suggest updated or improved annotation for individual InterPro entries. protein, classify, prediction, protein domain, genome, protein family, functional site, protein sequence, protein function, analysis, nucleic acid, amino acid, amino acid sequence, gold standard is listed by: re3data.org
is listed by: OMICtools
is related to: TIGRFAMS
is related to: TIGRFAMS
is related to: FlyMine
is related to: GeneSpeed- A Database of Unigene Domain Organization
is related to: Biomine
is related to: InterProScan
is related to: GeneTerm Linker
is related to: Gene Ontology
is related to: ProDom
is related to: Algal Functional Annotation Tool
has parent organization: European Bioinformatics Institute
European Union FP7 Scientific Data Repositories 213037;
BBSRC BB/F010508/1;
NIGMS GM081084
PMID:22096229
PMID:21082426
PMID:18940856
PMID:18428686
PMID:18025686
PMID:17202162
PMID:16909843
PMID:15608177
PMID:12520011
PMID:12230031
PMID:11159333
PMID:11119311
PMID:11125043
Acknowledgement requested, Free, Public, The community can contribute to this resource nif-0000-03035, OMICS_01694, r3d100010798 https://doi.org/10.17616/R3FS61 SCR_006695 InterPro: protein sequence analysis & classification, InterPro protein sequence analysis and classification 2026-09-19 12:51:16 7722
SToRM
 
Resource Report
Resource Website
100+ mentions
SToRM (RRID:SCR_006696) SToRM software resource A software tool primarily proposed for mapping SOLiD reads or Illumina reads to a reference genome. It was based on seeding techniques adapted to the statistical characteristics of the reads: the default seeds are for example designed (using the Iedera software) to comply with the properties of the SOLiD color encoding, or Illumina more classical encoding as well as the observed reading error distribution along the read., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. c, linux, macos, solid is listed by: OMICtools
has parent organization: University Lille 1 - Sciences and Technologies; Lille; France
PMID:20936175 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00692 SCR_006696 2026-09-19 12:51:16 205
GARM
 
Resource Report
Resource Website
10+ mentions
GARM (RRID:SCR_006731) GARM software resource A new software pipeline to merge and reconcile assemblies from different algorithms or sequencing technologies. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01420 SCR_006731 Genome Assembler Reconcilation and Merging 2026-09-19 12:51:17 12
DGIdb
 
Resource Report
Resource Website
100+ mentions
DGIdb (RRID:SCR_006608) DGIdb application programming interface, data access protocol, data or information resource, database, software resource A database of drug-gene relationships that provides drug-gene interactions and potential druggability data given list of genes. There are about 15 data sources that are being aggregated by DGIdb, with update date and these data sources are listed on this page: http://dgidb.genome.wustl.edu/sources, THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. drug, gene, interaction, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Washington University in St. Louis; Missouri; USA
Cancer NHGRI U54 HG003079 PMID:24122041 THIS RESOURCE IS NO LONGER IN SERVICE nlx_155686, biotools:DGIdb, OMICS_01579 https://bio.tools/DGIdb SCR_006608 Drug-Gene Interaction database, Drug Gene Interaction Database 2026-09-19 12:51:14 408
PROGENY
 
Resource Report
Resource Website
100+ mentions
PROGENY (RRID:SCR_006647) Progeny commercial organization, data management software, software application, software resource Fully customizable, comprehensive genetic pedigree and clinical data management software including a multi-user relational database with an integrated pedigree drawing component to manage genetic and pedigree data in one database. Manage Pedigrees, Individuals, SNPs, STRs, Samples, Plates, Genotypes and exports to multiple analysis platforms. (entry from Genetic Analysis Software) * LIMS software, providing advanced sample tracking and management (including functionality to generate and record barcodes) and configurable workflows for your specific environment. * Full genotype management gives users the ability to track not only family-based studies, but Whole Genome Association studies containing 1000''s of samples with large arrays. gene, genetic, genomic, c++, active x control, ms-windows, pedigree, clinical, genotype, data management, drawing, family history, questionnaire, sample, lab management, FASEB list is listed by: OMICtools
is listed by: Genetic Analysis Software
nlx_154553, OMICS_00216 SCR_006647 Progeny Software LLC, Progeny Software 2026-09-19 12:51:15 416
FLUX CAPACITOR
 
Resource Report
Resource Website
1+ mentions
FLUX CAPACITOR (RRID:SCR_006651) FLUX CAPACITOR software resource Software to recontruct abundances of known transcript forms from RNAseq data. The algorithm works by distributing the reads mapping to a given exonic region (or splice junction) among the transcripts including the exon (or splice junction). The input is the annotation of a reference transcriptome and reads from RNAseq technologies aligned to the genome. From the reference annotation, splicing graphs are produced and reads are mapped to corresponding edges in these graphs according to the position where they align in the genomic sequence. The resulting graph with edges labelled by the number of reads can be interpreted as a flow network where each transcript representing a transportation path from its start to its end and consequently each edge a possibly shared segment of transportation along which a certain number of reads per nucleotide -- i.e., a flux -- is observed. Given a density function of reads along a transcript, the expected participation of each transcript in an edge under consideration can be estimated. The basic idea is to cast back from these latter participations and the observed number of reads - allowing for a certain amount of noise - to the original transcript abundancies. To do so, a linear constraint is formalized for each edge, and an optimal solution for the complete set of constraints is found by a standard linear program solver. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:20220756 biotools:the_flux_capacitor, OMICS_01293 https://bio.tools/the_flux_capacitor SCR_006651 The FLUX CAPACITOR, FluxCapacitor 2026-09-19 12:51:15 2
TIGAR
 
Resource Report
Resource Website
10+ mentions
TIGAR (RRID:SCR_006650) TIGAR software resource Software to estimate transcript isoform abundances from RNA-Seq data by variational Bayesian inference. The statistical method can handle gapped alignments of reads against reference sequences so that it allows insertion or deletion errors within reads. is listed by: OMICtools PMID:23821651 OMICS_01294 SCR_006650 TIGAR: Transcript isoform abundance estimation method with gapped alignment of RNA-Seq data by variational Bayesian inference 2026-09-19 12:51:15 46
APOLLOH
 
Resource Report
Resource Website
10+ mentions
APOLLOH (RRID:SCR_006648) APOLLOH software resource A hidden Markov model (HMM) for predicting somatic loss of heterozygosity and allelic imbalance in whole tumour genome sequencing data. is listed by: OMICtools
has parent organization: BC Cancer Agency
OMICS_00306 SCR_006648 2026-09-19 12:51:15 21
MaizeGDB
 
Resource Report
Resource Website
1000+ mentions
MaizeGDB (RRID:SCR_006600) MaizeGDB analysis service resource, data analysis service, data or information resource, data repository, database, organism-related portal, portal, production service resource, service resource, storage service resource, topical portal Collection of data related to crop plant and model organism Zea mays. Used to synthesize, display, and provide access to maize genomics and genetics data, prioritizing mutant and phenotype data and tools, structural and genetic map sets, and gene models and to provide support services to the community of maize researchers. Data stored at MaizeGDB was inherited from the MaizeDB and ZmDB projects. Sequence data are from GenBank. Data are searchable by phenotype, traits, Pests, Gel Pattern, and Mutant Images. zea mays, corn, model organism, genome, locus, metabolic pathway, genetics, genomics, sequence, gene product, function, literature reference, phenotype, trait, pest, gel pattern, mutant, blast, gene, image, corn, genotype-environment interaction, gene mapping, plant genome mapping, plant genome, gold standard, bio.tools, FASEB list is listed by: re3data.org
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: GenBank
has parent organization: University of Maryland; Maryland; USA
works with: Maize Database of Images and Genomes
National Corn Growers Association ;
NSF ;
USDA/ARS ;
USDA
PMID:21624896
PMID:18769488
PMID:15888678
PMID:14681441
Free, Freely available, Acknowledgement requested, The community can contribute to this resource OMICS_01655, biotools:MaizeDIG, nif-0000-03096, r3d100010795 https://bio.tools/MaizeDIG, https://doi.org/10.17616/R3V32B SCR_006600 Maize Genetics and Genomics Database, MaizeGDB, MaizeGDB Locus 2026-09-19 12:51:14 1047
Samscope
 
Resource Report
Resource Website
Samscope (RRID:SCR_006715) Samscope software resource A lightweight SAM/BAM file viewer that makes visually exploring next generation sequencing data intuitive and maybe even fun! Quickly and easily generate aggregate statistics from SAM/BAM files like coverage, polarity, and minor allele frequencies, then scroll and explore freely with a simple mouse based interface. Multiple windows can be synchronized for careful comparison across multiple experiments. c++, visualization, opengl, next generation sequencing is listed by: OMICtools
has parent organization: SourceForge
GNU Affero General Public License OMICS_00892 SCR_006715 samscope - A lightweight OpenGL SAM/BAM viewer 2026-09-19 12:51:16 0
DMEAS
 
Resource Report
Resource Website
1+ mentions
DMEAS (RRID:SCR_006679) DMEAS software resource A user-friendly DNA methylation analysis tool for DNA methylation pattern extraction, DNA methylation level estimation, DNA methylation entropy analysis and multi-sample comparison. It was developed in order to assess the DNA methylation variations for a given genomic locus or genome-wide methylation data. c# is listed by: OMICtools
has parent organization: SourceForge
Creative Commons Attribution License OMICS_00598 SCR_006679 DNA Methylation Entropy Analysis Software, DMEAS - DNA Methylation Entropy Analysis Software 2026-09-19 12:51:16 2
DeconRNASeq
 
Resource Report
Resource Website
10+ mentions
DeconRNASeq (RRID:SCR_006713) DeconRNASeq software resource An R package for deconvolution of heterogeneous tissues based on mRNA-Seq data. It modeled expression levels from heterogeneous cell populations in mRNA-Seq as the weighted average of expression from different constituting cell types and predicted cell type proportions of single expression profiles. is listed by: OMICtools
has parent organization: Bioconductor
OMICS_01230 SCR_006713 2026-09-19 12:51:16 44
methVisual
 
Resource Report
Resource Website
1+ mentions
methVisual (RRID:SCR_006705) methVisual software resource Software package that allows the visualization of DNA methylation data after bisulfite sequencing. is listed by: OMICtools
has parent organization: Bioconductor
GNU General Public License, v2 or greater OMICS_00604 SCR_006705 methVisual - Methods for visualization and statistics on DNA methylation data 2026-09-19 12:51:16 1
balony
 
Resource Report
Resource Website
10+ mentions
balony (RRID:SCR_010968) balony software resource Image analysis and data inspection software for agar plates generated in high-throughput yeast genetics and genomics experiments. is listed by: OMICtools
has parent organization: Google Code
PMID:24305553 OMICS_00839 SCR_010968 balony - Software for the analysis of high-throughput solid media-based screens 2026-09-19 12:52:03 11
OligoFaktory
 
Resource Report
Resource Website
1+ mentions
OligoFaktory (RRID:SCR_010962) OligoFaktory software resource A free software for Mac OS X which designs long oligos for DNA microarrays, primers for PCR, siRNAs, and more�� is listed by: OMICtools Free OMICS_00829 SCR_010962 2026-09-19 12:52:03 1

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