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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
Ancient conserved untranslated sequences
 
Resource Report
Resource Website
Ancient conserved untranslated sequences (RRID:SCR_008130) ACUTS data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE, Documented on August 12, 2014. Database that identifies new regulatory elements in untranslated regions of protein-coding genes (5 prime flanks, 5 prime UTRs, introns, 3 prime UTRs and 3 prime flanks). The analyses is focused on genes from metazoan species (essentially vertebrates, insects and nematodes). Information on highly conserved regions (sequences, alignments, annotations, bibliographic references) are compiled. Currently 176 out of 326 detected highly conserved regions (HCRs) have been analyzed and incorporated in the database. You can also access the list of annotated conserved elements and the list of conserved elements that remain to be processed. Their approach is based on comparative sequence analysis, for the identification of phylogenetic footprints. echinoderm, footprint, fragment, functional, gene, alignment, analysis, annotation, chordate, cis-element, coding, degradation, divergence, dna, dnase, highly conserved region, homologous, intron, metazoan, mrna, non-coding, nucleotide, phylogenetic, post-transcriptional, promoter, protein, region, regulatory, segment, sequence, structural, transcriptional repressor, translation, untranslated region has parent organization: Claude Bernard University Lyon 1; Lyon; France PMID:9204283 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-20934 SCR_008130 2026-09-12 01:01:57 0
Integrated Tumor Transcriptome Array and Clinical data Analysis
 
Resource Report
Resource Website
1+ mentions
Integrated Tumor Transcriptome Array and Clinical data Analysis (RRID:SCR_008182) ITTACA data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE, documented on 6/12/25. ITTACA is a database created for Integrated Tumor Transcriptome Array and Clinical data Analysis. ITTACA centralizes public datasets containing both gene expression and clinical data and currently focuses on the types of cancer that are of particular interest to the Institut Curie: breast carcinoma, bladder carcinoma, and uveal melanoma. ITTACA is developed by the Institut Curie Bioinformatics group and the Molecular Oncology group of UMR144 CNRS/Institut Curie. A web interface allows users to carry out different class comparison analyses, including comparison of expression distribution profiles, tests for differential expression, patient survival analyses, and users can define their own patient groups according to clinical data or gene expression levels. The different functionalities implemented in ITTACA are: - To test if one or more gene, of your choice, is differentially expressed between two groups of samples exhibiting distinct phenotypes (Student and Wilcoxon tests). - The detection of genes differentially expressed (Significance Analysis of Microarrays) between two groups of samples. - The creation of histograms which represent the expression level according to a clinical parameter for each sample. - The computation of Kaplan Meier survival curves for each group. ITTACA has been developed to be a useful tool for comparing personal results to the existing results in the field of transcriptome studies with microarrays. expression, gene, analysis, array, bioinformatics, bladder, breast, cancer, carcinoma, clinical, integrated, melanoma, microarray, molecular, oncology, patient, phenotype, survival, transcriptome, tumor, uveal has parent organization: Curie Institute; Paris; France PMID:16381943 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-21227 SCR_008182 ITTACA 2026-09-12 01:01:58 4
International Database of Tetrahydrobiopterin Deficiencies
 
Resource Report
Resource Website
International Database of Tetrahydrobiopterin Deficiencies (RRID:SCR_008171) data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE, documented on August 26, 2016. The BIODEF database have tabulated the most common clinical and laboratory data related to hyperphenylalaninaemia and tetrahydrobiopterin deficiencies. Additionally, there are data regarding treatment, outcome, and DNA analysis. Approximately 2% of newborns with hyperphenylalaninaemia are deficient in tetrahydrobiopterin. Selective screening must be performed in all instances where hyperphenylalaninaemia is detected by neonatal screening. In the last 20 years, 308 patients with tetrahydrobiopterin deficiencies have been recognized as a result of screening carried out, worldwide, in Departments of Paediatrics. Of these 308 patients, 181 suffered from 6-pyruvoyltetrahydropterin synthase deficiency, 92 from dihydropteridine reductase deficiency, 13 from pterin-4a-carbinolamine dehydratase deficiency, 12 from GTP cyclohydrolase I deficiency, and 10 are still unclassified. The BIODEF database have tabulated the most common clinical and laboratory data related to hyperphenylalaninaemia and tetrahydrobiopterin deficiencies. Additionally, there are data regarding treatment, outcome, and DNA analysis. Preliminary evaluation reveals that the degree of hyperphenylalaninaemia can vary from normal to 2500 mumol/L. Analyses of pterins in urine and measurement of dihydropteridine reductase activity from Guthrie cards are absolutely essential tests for accurate diagnosis. There is a regional (demographic) variation in the frequency of tetrahydrobiopterin deficiencies indicating the highest incidence in Saudi Arabia, probably a consequence of the high consanguinity rate. ethnic, frequency, 6-pyruvoyltetrahydropterin synthase deficiency, analysis, bh4, clinical, deficiency, demographic, diagnosis, dihydropteridine reductase deficiency, dna, gtp cyclohydrolase i deficiency, hyperphenylalaninaemia, measurement, neonatal, origin, outcome, pterin, pterin-4a-carbinolamine dehydratase deficiency, sex, tetrahydrobiopterin, treatment, urine THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-21052 SCR_008171 BIODEF 2026-09-12 01:01:58 0
Cerebellar Platform
 
Resource Report
Resource Website
1+ mentions
Cerebellar Platform (RRID:SCR_001700) Cerebellar Platform software repository, software resource THIS RESOURCE IS NO LONGER IN SERVICE, documented January 13, 2022. Digital research archive for cerebellar research including mini-reviews of contemporary cerebellar research, list of papers and mathematical models for cerebellar operation. electrophysiology, function, analysis, cerebellar, data, imaging, mathematical, model, molecular biology, paper, plasticity, program, review, script, structure, theory, book, cerebellum is used by: NIF Data Federation
is related to: Integrated Software
has parent organization: RIKEN Brain Science Institute
Japan Society for the Promotion of Science THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-10193 SCR_001700 2026-09-12 01:02:26 1
The Cancer Genome Atlas
 
Resource Report
Resource Website
5000+ mentions
The Cancer Genome Atlas (RRID:SCR_003193) TCGA biomaterial supply resource, material resource Project exploring the spectrum of genomic changes involved in more than 20 types of human cancer that provides a platform for researchers to search, download, and analyze data sets generated. As a pilot project it confirmed that an atlas of changes could be created for specific cancer types. It also showed that a national network of research and technology teams working on distinct but related projects could pool the results of their efforts, create an economy of scale and develop an infrastructure for making the data publicly accessible. Its success committed resources to collect and characterize more than 20 additional tumor types. Components of the TCGA Research Network: * Biospecimen Core Resource (BCR); Tissue samples are carefully cataloged, processed, checked for quality and stored, complete with important medical information about the patient. * Genome Characterization Centers (GCCs); Several technologies will be used to analyze genomic changes involved in cancer. The genomic changes that are identified will be further studied by the Genome Sequencing Centers. * Genome Sequencing Centers (GSCs); High-throughput Genome Sequencing Centers will identify the changes in DNA sequences that are associated with specific types of cancer. * Proteome Characterization Centers (PCCs); The centers, a component of NCI's Clinical Proteomic Tumor Analysis Consortium, will ascertain and analyze the total proteomic content of a subset of TCGA samples. * Data Coordinating Center (DCC); The information that is generated by TCGA will be centrally managed at the DCC and entered into the TCGA Data Portal and Cancer Genomics Hub as it becomes available. Centralization of data facilitates data transfer between the network and the research community, and makes data analysis more efficient. The DCC manages the TCGA Data Portal. * Cancer Genomics Hub (CGHub); Lower level sequence data will be deposited into a secure repository. This database stores cancer genome sequences and alignments. * Genome Data Analysis Centers (GDACs) - Immense amounts of data from array and second-generation sequencing technologies must be integrated across thousands of samples. These centers will provide novel informatics tools to the entire research community to facilitate broader use of TCGA data. TCGA is actively developing a network of collaborators who are able to provide samples that are collected retrospectively (tissues that had already been collected and stored) or prospectively (tissues that will be collected in the future). genome, genome sequencing, breast, central nervous system, endocrine, gastrointestinal, gynecologic, head, neck, hematologic, skin, soft tissue, thoracic, urologic, clinical, genomic characterization, analysis, tumor genome, demographic, gene expression, copy number alteration, epigenetic, dna sequence, exome, snp, methylation, mrna, mirna, FASEB list is used by: Mutation Annotation and Genomic Interpretation
is used by: BioXpress
is used by: cancerRxTissue
is listed by: One Mind Biospecimen Bank Listing
is related to: Cancer3D
is related to: Cancer Research Data Commons
is related to: CancerMIRNome
is related to: Broad Institute Genomics Platform
has parent organization: National Cancer Institute
works with: FireBrowse
Cancer, Tumor, Normal, Breast cancer, Central Nervous System cancer, Endocrine cancer, Gastrointestinal cancer, Gynecologic cancer, Head cancer, Neck cancer, Hematologic cancer, Skin cancer, Soft tissue cancer, Thoracic cancer, Urologic cancer NCI 261200800001E-12-0-1 nlx_156913 SCR_003193 Cancer Genome Atlas 2026-09-12 01:02:29 7443
IgBLAST
 
Resource Report
Resource Website
500+ mentions
IgBLAST (RRID:SCR_002873) software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE.Documented on January 4,2023. IgBLAST was developed at NCBI to facilitate analysis of immunoglobulin V region sequences in GenBank. In addition to performing a regular BLAST search, IgBLAST has several additional functions: - Reports the germline V, D and J gene matches to the query sequence. - Annotates the immunoglobulin domains (FWR1 through FWR3). - Matches the returned hits (for databases other than germline genes) to the closest germline V genes, making it easier to identify related sequences. - Reveals the V(D)J junction details such as nucleotide homology between the ends of V(D)J segments and N nucleotide insertions. D and J gene reporting is only for nucleotide sequence search and requires a stretch of five or more nucleotide identity between the query and D or J genes. Sponsors: This resource is supported by the National Center for Biotechnology Information, a division of the U.S. National Library of Medicine. gene, analysis, domain, homology, immunoglobulin v, nucleotide, sequence, bio.tools is listed by: Debian
is listed by: bio.tools
is listed by: OMICtools
has parent organization: NCBI
PMID:23671333 Free, Freely available nif-0000-25554, biotools:igblast, OMICS_06083 https://bio.tools/igblast, https://sources.debian.org/src/ncbi-igblast/ SCR_002873 IgBLAST 2026-09-12 01:02:29 625
Atlases of amygdala and hippocampus for pediatric populations
 
Resource Report
Resource Website
Atlases of amygdala and hippocampus for pediatric populations (RRID:SCR_014085) atlas, data or information resource Anatomical atlases constructed by Computational Anatomy of Johns Hopkins University for analysis of shape vectors. The atlases were generated from segmented hippocampal and amygdala structures in acquired populations of children, adolescents and young adults in neuroimaging studies of major depression disorder (MDD) at Washington University at St Louis. atlas, amygdala, hippocampus, children, adolescent, young adult, human brain, depression, shape vector, analysis is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: Johns Hopkins University; Maryland; USA
SCR_014085 2026-09-12 01:02:13 0
HumanBase
 
Resource Report
Resource Website
50+ mentions
HumanBase (RRID:SCR_016145) data or information resource, database Formerly known as GIANT (Genome-scale Integrated Analysis of gene Networks in Tissues), HumanBase applies machine learning algorithms to learn biological associations from massive genomic data collections. These integrative analyses reach beyond existing "biological knowledge" represented in the literature to identify novel, data-driven associations. genome, analysis, tissue, network, gene, machine, learning, biology NCI T32 CA009528;
NHGRI R01 HG005998;
NHGRI T32 HG003284;
NHLBI U54 HL117798;
NIGMS P20 GM103534;
NIGMS P50 GM071508;
NIGMS R01 GM071966;
US Department Of Health And Human Services HHSN272201000054C
PMID:25915600 Free, Public SCR_016145 GIANT (Genome-scale Integrated Analysis of gene Networks in Tissues), GIANT 2026-09-12 01:02:16 95
Examl
 
Resource Report
Resource Website
50+ mentions
Examl (RRID:SCR_016087) Examl software application, software resource, source code Source code for large-scale phylogenetic analyses on whole-transcriptome and whole-genome alignments using supercomputers. phylogenetic, analysis, database, large scale, whole genome, whole transcriptome, alignment, efficiency, bio.tools, FASEB list is listed by: bio.tools
is listed by: Debian
is listed by: OMICtools
Heidelberg Institute for Theoretical Studies PMID:25819675 Free, Available for download OMICS_08024, biotools:ExaML https://bio.tools/ExaML, https://sources.debian.org/src/examl/ SCR_016087 Examl:Exascale Maximum Likelihood 2026-09-12 01:02:16 62
Intra- and inter-scanner reliability of RS-fMRI BOLD and ASL with eyes closed vs. eyes open
 
Resource Report
Resource Website
Intra- and inter-scanner reliability of RS-fMRI BOLD and ASL with eyes closed vs. eyes open (RRID:SCR_016935) data or information resource, database Data collected from subjects scanned 3 times (V1, V2, V3), with V1 and V2 on a scanner, V3 on another scanner in another site. Resting state blood oxygenation level dependent functional MRI (BOLD fMRI), pseudo continuous arterial spin labeling (pCASL), and high resolution 3D T1 imaging were performed under eyes open (EO) and eyes closed (EC) conditions. neuroimaging, dataset, resting, state, functional, magnetic, resonance, imaging, investigate, intra, inter, scanner, reliability, scaled, subprofile, model, principal, component, analysis, blood, oxygenation, level, dependent, image, arterial, spin, labeling is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: Hangzhou Normal University; Hangzhou; China
Natural Science Foundation of China ;
Qian Jiang Distinguished Professor program
PMID:29887795 SCR_016935 2026-09-12 01:02:17 0
MitoCarta
 
Resource Report
Resource Website
100+ mentions
MitoCarta (RRID:SCR_018165) data or information resource, database Collection of genes encoding proteins with strong support of mitochondrial localization. Inventory of genes encoding mitochondrial-localized proteins and their expression across 14 mouse tissues. Database is based on human and mouse RefSeq proteins that are mapped to NCBI Gene loci. MitoCarta 2.0 inventory provides molecular framework for system-level analysis of mammalian mitochondria. Gene, protein, mitochondrial protein, protein expression, data, human, mouse, RefSeq protein, analysis, mammalian mitochondra, FASEB list Australian NHMRC ;
Burroughs Wellcome Fund Career Award in the Biomedical Sciences ;
Charles E. Culpeper Scholarship in Medical Science ;
Howard Hughes Medical Institute ;
NIDDK DK43351;
NIDDK DK57521;
NIGMS GM0077465
PMID:26450961
PMID:18614015
Free, Freely available SCR_018165 MitoCarta2.0 2026-09-12 01:02:18 208
Molecular Signatures Database
 
Resource Report
Resource Website
1000+ mentions
Molecular Signatures Database (RRID:SCR_016863) MSigDB data or information resource, database Collection of annotated gene sets for use with Gene Set Enrichment Analysis (GSEA) software. collection, annotated, gene, set, GSEA, enrichment, analysis, genome, RNA, expression, data, FASEB list, DRKB uses: GSEA
uses: Gene Set Enrichment Analysis
has parent organization: Broad Institute
NCI CA295532;
NIGMS ;
NIH
Free, Freely available, Registration required to download GSEA software https://www.gsea-msigdb.org/gsea/msigdb/ SCR_016863 Molecular Signatures Database, The Molecular Signatures Database, MSigDB, MSigDB database v6.2 2026-09-12 01:02:17 1702
mzMatch
 
Resource Report
Resource Website
1+ mentions
mzMatch (RRID:SCR_000543) software resource, software toolkit A software to provide small tools for common processing tasks for LC/MS data. It is an extension to the metabolomics analysis pipeline mzMatch.R. The software is modular, open source, platform independent and written in Java. metabolomics, analysis, java, tool, peak extraction, filtering, normalization, derivative detection, identification, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:23162054 Free, Available for download, Freely available, biotools:mzmatch, OMICS_02642 https://bio.tools/mzmatch SCR_000543 2026-09-12 01:02:23 5
Onto-Design
 
Resource Report
Resource Website
Onto-Design (RRID:SCR_000601) Onto-Design data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 6,2023. Many Laboratories chose to design and print their own microarrays. At present, the choice of the genes to include on a certain microarray is a very laborious process requiring a high level of expertise. Onto-Design database is able to assist the designers of custom microarrays by providing the means to select genes based on their experiment. Design custom microarrays based on GO terms of interest. User account required. Platform: Online tool microarray, gene, biological process, molecular function, cellular component, data-mining, browser, visualization, analysis, design, search engine, ontology or annotation browser, ontology or annotation search engine, ontology or annotation visualization, database or data warehouse, other analysis, design custom microarrays based on go terms of interest is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Wayne State University; Michigan; USA
PMID:15215428 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149109 SCR_000601 2026-09-12 01:02:23 0
Shiny
 
Resource Report
Resource Website
500+ mentions
Shiny (RRID:SCR_001626) software resource, software toolkit Open source R package that provides web framework for building web applications using R. Used to create interactive web apps in native R, without needing to use HTML, CSS, or JavaScript. R, analysis, interactive, web, application uses: shinythemes
is used by: ClustVis
is used by: shinyGEO
is used by: PlotsOfData
is used by: shinyCircoss
is used by: AlloMate
is used by: VenomView
is used by: bulkAnalyseR
is related to: rSPRITE
is related to: EHRtemporalVariability
is related to: robvis
is related to: Omics Data Paper Generator
is related to: Mitochondrial Neuron Ubiquitin
is related to: chevreul
is related to: Click-qPCR
is related to: EMImR
is related to: Mona
has parent organization: RStudio
works with: BoxPlotR
works with: shinyhelper
works with: ShinyCell
works with: Breedverse
works with: GenoBrew
PMID:34642739
PMID:26225240
Free, Available for download, Freely available nlx_153894 SCR_001626 2026-09-12 01:02:26 590
Open Babel
 
Resource Report
Resource Website
100+ mentions
Open Babel (RRID:SCR_014920) data analytics software, data processing software, software application, software resource Software toolbox that is used to convert, analyze, or store data from molecular modeling, chemistry, biochemistry and other related areas. This software is used to read, write, and convert into over 110 chemical file formats. toolbox, conversion, analysis, molecular model, chemistry, biochemistry, chemical file, bio.tools is listed by: bio.tools
is listed by: Debian
Open source biotools:open_babel https://bio.tools/open_babel SCR_014920 2026-09-12 01:01:03 100
BZ-H3A analyzer software
 
Resource Report
Resource Website
10+ mentions
BZ-H3A analyzer software (RRID:SCR_017375) data processing software, image analysis software, software application, software resource Software tool as analysis application BZ-H3A by Keyence, Osaka, Japan for fluorescence microscope BZ-X series. Analysis, Keyence, Japan, fluorescence, microscope, BZ-X SCR_017375 2026-09-12 01:01:05 13
Center for Computational Biology at JHU
 
Resource Report
Resource Website
1+ mentions
Center for Computational Biology at JHU (RRID:SCR_016680) CCB at JHU data or information resource, organization portal, portal Center for Computational Biology as a joint research center in the McKusick-Nathans Institute of Genetic Medicine, spanning the School of Medicine, the Whiting School of Engineering, the Bloomberg School of Public Health, and the Krieger School of Arts & Sciences. Multidisciplinary center dedicated to research on genomics, genetics, DNA sequencing technology, and computational methods for DNA and RNA sequence analysis. center, computational, biology, genomics, genetics, DNA, RNA, sequence, technology, analysis has parent organization: Johns Hopkins University; Maryland; USA
is parent organization of: Centrifuge Classifier
SCR_016680 CCB at Johns Hopkins University, CCB at JHU, Center for Computational Biology at JHU, Center for Computational Biology at Johns Hopkins University 2026-09-12 01:01:04 1
ReproNim: A Center for Reproducible Neuroimaging Computation
 
Resource Report
Resource Website
10+ mentions
ReproNim: A Center for Reproducible Neuroimaging Computation (RRID:SCR_016001) ReproNim data or information resource, organization portal, portal Center to help neuroimaging researchers to find and share data in FAIR fashion, to describe their data and analysis workflows in replicable fashion, to manage their computational resource options so that outcomes of neuroimaging research are more reproducible. Neuroimaging, share, data, FAIR, analysis, manage, reproducible is related to: ABCD-ReproNim Course
is related to: SVNTest
is parent organization of: ReproIn: The ReproNim image input management system (featuring DataLad)
NIBIB P41 EB019936 Restricted SCR_016005 http://repronim.org SCR_016001 2026-09-12 01:01:04 16
Oufti
 
Resource Report
Resource Website
10+ mentions
Oufti (RRID:SCR_016244) data processing software, image analysis software, software application, software resource Software designed for analysis of microscopy data. It performs sub-pixel precision detection, quantification of cells and fluorescence signals, as well as other image analysis functions. microscopy, data, imaging, image, analysis, pixel, fluorescent, bio.tools is listed by: Debian
is listed by: bio.tools
NIGMS R01 GM065835 PMID:26538279 biotools:oufti https://bio.tools/oufti SCR_016244 outfi 2026-09-12 01:01:04 15

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