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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
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PopTools Resource Report Resource Website 10+ mentions |
PopTools (RRID:SCR_022840) | software resource | Software to allow construction, analysis, and simulation of complex models in spreadsheet format. | construction, analysis, simulation, complex models, spreadsheet format | Free, Available for download, Freely available | https://www.maa.org/press/periodicals/loci/resources/poptools | SCR_022840 | 2026-02-14 02:04:48 | 49 | ||||||||||
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National Institutes of Health Research Portfolio Online Reporting Tool Resource Report Resource Website 10+ mentions |
National Institutes of Health Research Portfolio Online Reporting Tool (RRID:SCR_006874) | RePORTER, RePORT | data or information resource, database | A database of federally funded biomedical research projects conducted at universities, hospitals, and other research institutions that provides a central point of access to reports, data, and analyses of NIH research. The RePORTER has replaced the CRISP database. The database, maintained by the Office of Extramural Research at the National Institutes of Health, includes projects funded by the National Institutes of Health (NIH), Substance Abuse and Mental Health Services (SAMHSA), Health Resources and Services Administration (HRSA), Food and Drug Administration (FDA), Centers for Disease Control and Prevention (CDCP), Agency for Health Care Research and Quality (AHRQ), and Office of Assistant Secretary of Health (OASH). | government grant information, government grant, grant data, granting agency, grant, funding, award, biomedical, research, report, analysis, nih research |
is used by: Integrated Grants is used by: NIF Data Federation is used by: Ranking Tables of NIH Funding to US Medical Schools in 2010 has parent organization: Office of Extramural Research NIH |
nif-0000-10319 | SCR_006874 | NIH RePORT, NIH RePORTER | 2026-02-14 02:06:01 | 35 | ||||||||
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National Library of Health: Medical Literature Analysis and Retrieval System Online Fact Sheet Resource Report Resource Website 10+ mentions |
National Library of Health: Medical Literature Analysis and Retrieval System Online Fact Sheet (RRID:SCR_006994) | data or information resource, database | MEDLINE (Medical Literature Analysis and Retrieval System Online) is the U.S. National Library of Medicine''s (NLM) premier bibliographic database that contains over 16 million references to journal articles in life sciences with a concentration on biomedicine. MEDLINE is the primary component of PubMed, part of the Entrez series of databases provided by NLM''s National Center for Biotechnology Information (NCBI). MEDLINE may also be searched via the NLM Gateway. Currently, citations from approximately 5,200 worldwide journals in 37 languages; 60 languages for older journals. Citations for MEDLINE are created by the NLM, international partners, and collaborating organizations. The subject scope of MEDLINE is biomedicine and health, broadly defined to encompass those areas of the life sciences, behavioral sciences, chemical sciences, and bioengineering needed by health professionals and others engaged in basic research and clinical care, public health, health policy development, or related educational activities. MEDLINE also covers life sciences vital to biomedical practitioners, researchers, and educators, including aspects of biology, environmental science, marine biology, plant and animal science as well as biophysics and chemistry. Sponsors: Services/products providing access to MEDLINE data are also developed and made available by organizations that lease the database from NLM. | environmental science, analysis, animal science, behavioral science, bioengineering, biology, biomedical practitioner, biomedicine, biophysics, biotechnology, chemical science, chemistry, health, life science, literature, marine biology, medical, plant science, journal article | nif-0000-10470 | SCR_006994 | NIH NLM: Medline Fact Sheet | 2026-02-14 02:05:57 | 11 | ||||||||||
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Proteomics Research Center for Integrative Biology Resource Report Resource Website |
Proteomics Research Center for Integrative Biology (RRID:SCR_001098) | Proteomics Resource for Integrative Biology | biomedical technology research center, training resource | Biomedical technology research center that develops and integrates new proteomic technologies for collaborative and service studies, disseminating the new technologies and training scientists in their use. | systems biology technology center, proteomics, mass spectrometry, data management, analysis | has parent organization: Pacific Northwest National Laboratory | NIGMS 4P41GM103493-14 | nlx_152684 | SCR_001098 | Proteomics Research Resource for Integrative Biology | 2026-02-14 02:07:17 | 0 | |||||||
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National Resource for the Mass Spectrometric Analysis of Biological Macromolecules Resource Report Resource Website |
National Resource for the Mass Spectrometric Analysis of Biological Macromolecules (RRID:SCR_009007) | National Resource for the Mass Spectrometric Analysis of Biological Macromolecules | biomedical technology research center, training resource | Biomedical technology research center that develops cutting-edge mass spectrometric tools for analyzing peptides and proteins. It makes its software tools developed for data analysis freely available. | systems biology technology center, mass spectrometric, analysis, peptide, protein, software, proteomic, cellular function | has parent organization: Rockefeller University; New York; USA | NIGMS | nlx_152683 | SCR_009007 | 2026-02-14 02:08:00 | 0 | ||||||||
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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 | 2026-02-14 02:06:41 | 0 | |||||||
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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 | 2026-02-14 02:06:12 | 4 | ||||||
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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 | 2026-02-14 02:06:41 | 0 | |||||||||
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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 | NIGMS R01 GM071966; NHGRI R01 HG005998; NHLBI U54 HL117798; NIGMS P20 GM103534; NHGRI T32 HG003284; NCI T32 CA009528; NIGMS P50 GM071508; 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 | 2026-02-14 02:06:53 | 74 | ||||||||
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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 | 2026-02-14 02:06:54 | 0 | |||||||||
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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 | NIGMS GM0077465; NIDDK DK43351; NIDDK DK57521; Australian NHMRC ; Burroughs Wellcome Fund Career Award in the Biomedical Sciences ; Howard Hughes Medical Institute ; Charles E. Culpeper Scholarship in Medical Science |
PMID:26450961 PMID:18614015 |
Free, Freely available | SCR_018165 | MitoCarta2.0 | 2026-02-14 02:06:25 | 183 | ||||||||
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Molecular Signatures Database Resource Report Resource Website 500+ 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 |
uses: GSEA uses: Gene Set Enrichment Analysis has parent organization: Broad Institute |
NCI ; NIH ; NIGMS |
Free, Freely available, Registration required to download GSEA software | SCR_016863 | Molecular Signatures Database, The Molecular Signatures Database, MSigDB, MSigDB database v6.2 | 2026-02-14 02:06:54 | 762 | |||||||
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Evolutionary Lineage Inferred from Structural Analysis Resource Report Resource Website 1+ mentions |
Evolutionary Lineage Inferred from Structural Analysis (RRID:SCR_002343) | data or information resource, database | THIS RESOURCE IS NO LONGER IN SERVICE, documented August 23, 2016. ELISA is an online database that combines functional annotation with structure and sequence homology modeling to place proteins into sequence-structure-function neighborhoods. The atomic unit of the database is a set of sequences and structural templates that those sequences encode. A graph that is built from the structural comparison of these templates is called PDUG (protein domain universe graph). It introduces a method of functional inference through a probabilistic calculation done on an arbitrary set of PDUG nodes. Further, all PDUG structures are mapped onto all fully sequenced proteomes allowing an easy interface for evolutionary analysis and research into comparative proteomics. ELISA is the first database with applicability to evolutionary structural genomics explicitly in mind. | evolutionary, function, functional, analysis, annotation, atomic unit, calculation, comparative, domain, genomic, homology, modeling, place, probabilistic, protein, protein domain and protein classification databases, proteome, proteomic, sequence, structural, structure, template | has parent organization: Boston University; Massachusetts; USA | PMID:12952559 | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-21141 | SCR_002343 | ELISA | 2026-02-14 02:06:09 | 1 | |||||||
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REDCap Resource Report Resource Website 10000+ mentions |
REDCap (RRID:SCR_003445) | REDCap | web application, software resource | Web application that allows users to build and manage online surveys and databases. Using REDCap's stream-lined process for rapidly developing projects, you may create and design projects using 1) the online method from your web browser using the Online Designer; and/or 2) the offline method by constructing a "data dictionary" template file in Microsoft Excel, which can be later uploaded into REDCap. Both surveys and databases (or a mixture of the two) can be built using these methods. REDCap provides audit trails for tracking data manipulation and user activity, as well as automated export procedures for seamless data downloads to Excel, PDF, and common statistical packages (SPSS, SAS, Stata, R). Also included are a built-in project calendar, a scheduling module, ad hoc reporting tools, and advanced features, such as branching logic, file uploading, and calculated fields. REDCap has a quick and easy software installation process, so that you can get REDCap running and fully functional in a matter of minutes. Several language translations have already been compiled for REDCap (e.g. Chinese, French, German, Portuguese), and it is anticipated that other languages will be available in full versions of REDCap soon. The REDCap Shared Library is a repository for REDCap data collection instruments and forms that can be downloaded and used by researchers at REDCap partner institutions. | online survey, survey, database, translational research, informatics, workflow, clinical research, clinical, metadata, biomedical, online form, data capture, management, analysis, data sharing, data collection, data standard, best practice, data collection instrument, electronic data capture |
is listed by: Biositemaps is listed by: SoftCite is related to: Clinical and Translational Science Awards Consortium has parent organization: Vanderbilt University; Tennessee; USA works with: redcap-completion works with: aux-file-upload |
NIH ; UL1 RR029882 ; UL1 TR000062 ; UL1 RR026314 ; UL1 TR000077 ; UL1 RR024975 ; UL1 TR000445 ; G12 RR003051 ; G12 MD007600 ; UL1 RR024150 ; UL1 TR000135 ; R24 HD042849 ; UL1 RR024989 ; UL1 TR000439 |
PMID:23149159 PMID:18929686 |
Software is available at no cost for REDCap Consortium Partners. If not in the consortium, See the Become a Partner page to find more information about joining our group. | nif-0000-33254 | SCR_003445 | RED Cap, Research Electronic Data Capture, The REDCap Consortium | 2026-02-15 09:18:33 | 20615 | |||||
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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 | 2026-02-15 09:18:24 | 609 | ||||||
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Examl Resource Report Resource Website 50+ mentions |
Examl (RRID:SCR_016087) | Examl | software application, source code, software resource | 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 | 2026-02-15 09:21:46 | 60 | ||||
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BioJupies Resource Report Resource Website 50+ mentions |
BioJupies (RRID:SCR_016346) | web application, software resource | Software as an open source web server that automatically generates RNA-seq data analysis of jupyter notebooks. It allows creation and containment of documents that have live code, visualizations and narrative text. | automatically, generate, RNAseq, data, analysis, notebook, create, visualize, report, custom, raw, processed, user, interface | is affiliated with: Icahn School of Medicine at Mount Sinai; New York; USA | Free, Available for download, Freely available | SCR_016346 | 2026-02-15 09:21:51 | 65 | ||||||||||
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MRTool Resource Report Resource Website 1+ mentions |
MRTool (RRID:SCR_015956) | data or information resource, topical portal, portal | Software toolkit for analysis of MR brain imaging data. MRTool runs on Apple computers and PCs and requires SPM12. | brain, imaging, neuroimaging, analysis, magnetic, resonance, mr | requires: SPM | DOI:10.1007/s12021-018-9355-3 | Free, Available for download, Runs on MAC OS, Runs on Windows | SCR_015956 | 2026-02-15 09:21:00 | 8 | |||||||||
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FEI Helios Nanolab 600i DualBeam Resource Report Resource Website |
FEI Helios Nanolab 600i DualBeam (RRID:SCR_027033) | instrument resource | Scanning Electron Microscope advanced DualBeam for ultra-high resolution imaging, analysis and fabrication at the nanoscale. Helios NanoLab 600i builds on the success of FEI’s winning DualBeam series offering advances in ion beam, electron beam, patterning and range of features to make milling, imaging, analysis and sample preparation down to nanoscale. | Scanning Electron Microscope, imaging, analysis, nanoscale, microscope, electron microscope, | Model_Number_Helios_NanoLab_600i | SCR_027033 | FEI Helios NanoLab 600i DuaBeam, , FEI Helios NanoLab 600i DuaBeam Scanning Electron Microscope, Helios NanoLab 600i | 2026-02-14 02:09:48 | 0 | ||||||||||
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Ion Torrent Genexus Integrated Sequencer Resource Report Resource Website 1+ mentions |
Ion Torrent Genexus Integrated Sequencer (RRID:SCR_026449) | instrument resource | Ion Torrent Genexus Integrated Sequencer is part of the Ion Torrent Genexus System. Instrument that can automate library construction, templating, and sequencing in single-instrument run. | sequencer, automate NGS library preparation, sequencing, analysis | Model_Number_Genexus | SCR_026449 | Genexus Integrated Sequencer | 2026-02-14 02:09:35 | 1 |
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