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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
Blood Group Antigen Gene Mutation Database
 
Resource Report
Resource Website
Blood Group Antigen Gene Mutation Database (RRID:SCR_002297) BGMUT data or information resource, data repository, database, service resource, storage service resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 23, 2019.BGMUT was database that provided publicly accessible platform for DNA sequences and curated set of blood mutation information. Data Archive are available at ftp://ftp.ncbi.nlm.nih.gov/pub/mhc/rbc/Final Archive. blood, gene, genetic, allele, allelic, alteration, antigen, blood group, human, mutation, genetic variation, non-human animal, orthologous gene, orthologue, phenotype, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: NCBI dbRBC
has parent organization: Albert Einstein College of Medicine; New York; USA
has parent organization: Roswell Park Comprehensive Cancer Center
has parent organization: Medical University of Graz; Graz; Austria
has parent organization: Human Genome Variation Society
Albert Einstein College of Medicine; New York; USA ;
David Opochinsky/Blumenfeld Family Fund ;
NIH
PMID:22084196 THIS RESOURCE IS NO LONGER IN SERVICE. nif-0000-21064, biotools:bgmut https://bio.tools/bgmut http://www.bioc.aecom.yu.edu/bgmut/index.htm, http://www.ncbi.nlm.nih.gov/projects/gv/rbc/xslcgi.fcgi?cmd=bgmut SCR_002297 Blood Group Antigen Gene Mutation Database (BGMUT), BGMUT - Blood Group Antigen Gene Mutation Database 2026-09-12 12:55:39 0
MashMap
 
Resource Report
Resource Website
10+ mentions
MashMap (RRID:SCR_022194) alignment software, data processing software, image analysis software, software application, software resource Software tool as fast approximate aligner for long DNA sequences. Used for computing local alignment boundaries between long DNA sequences. mapping genome assembly, long DNA sequences, long reads, reference genome, long DNA sequences aligner National Human Genome Research Institute ;
NIH ;
NSF CCF1816027
PMID:30423094
DOI:10.1007/978-3-319-56970-3_5
Free, Available for download, Freely available SCR_022194 2026-09-12 01:00:06 31
Thermo Fisher: Orbitrap Eclipse nanoLC/MS system
 
Resource Report
Resource Website
10+ mentions
Thermo Fisher: Orbitrap Eclipse nanoLC/MS system (RRID:SCR_022212) instrument resource System includes Thermo Orbitrap Eclipse Tribid mass spectrometer and Waters M-Class Acquity nanoUPLC. This platform features sequential acquisition capabilities and multiple fragmentation types, enabling complex, in depth proteomic experiments. Thermo Orbitrap Eclipse Tribrid mass spectrometer, Waters M-Class Acquity nanoUPLC, instrument, equipment, USEDit is used by: Stanford University Vincent Coates Foundation Mass Spectrometry Laboratory Core Facility NIH S10 OD030473 https://raw.githubusercontent.com/SciCrunch/RRID-Instruments/refs/heads/main/PDF/SCR_022212.pdf SCR_022212 Thermo Orbitrap Eclipse nanoLC/MS, Orbitrap Eclipse nanoLC/MS 2026-09-12 01:00:06 16
Biomedical Resource Ontology
 
Resource Report
Resource Website
1+ mentions
Biomedical Resource Ontology (RRID:SCR_004443) BRO controlled vocabulary, data or information resource, ontology THIS RESOURCE IS NO LONGER IN SERVICE. Documented on April 27,2023. A controlled terminology of resources, which is used to improve the sensitivity and specificity of web searches. It includes ''resource_type'', ''area of research'', and ''activity''. It is under development by a number of NIH-funded researchers who have a combined interest in classification of biomedical resources. The biositemaps site is no longer available but the biomedical resource ontology is still available via bioportal Biomedical Resource Ontology (BRO). sitemap, resource type, owl, resource is listed by: BioPortal
is listed by: Biositemaps
is related to: Biositemaps
is related to: iBIOFind
is related to: bioDBcore
has parent organization: National Centers for Biomedical Computing
NIH THIS RESOURCE IS NO LONGER IN SERVICE nlx_143813 http://bioportal.bioontology.org/ontologies/1104, https://bioportal.bioontology.org/ontologies/BRO SCR_004443 2026-09-12 01:00:10 4
Pathbase
 
Resource Report
Resource Website
10+ mentions
Pathbase (RRID:SCR_006141) Pathbase controlled vocabulary, data access protocol, data or information resource, data repository, database, image collection, image repository, ontology, service resource, software resource, storage service resource, web service Database of histopathology photomicrographs and macroscopic images derived from mutant or genetically manipulated mice. The database currently holds more than 1000 images of lesions from mutant mice and their inbred backgrounds and further images are being added continuously. Images can be retrieved by searching for specific lesions or class of lesion, by genetic locus, or by a wide set of parameters shown on the Advanced Search Interface. Its two key aims are: * To provide a searchable database of histopathology images derived from experimental manipulation of the mouse genome or experiments conducted on genetically manipulated mice. * A reference / didactic resource covering all aspects of mouse pathology Lesions are described according to the Pathbase pathology ontology developed by the Pathbase European Consortium, and are available at the site or on the Gene Ontology Consortium site - OBO. As this is a community resource, they encourage everyone to upload their own images, contribute comments to images and send them their feedback. Please feel free to use any of the SOAP/WSDL web services. (under development) histopathology, photomicrograph, macroscopic, mutant, genetically manipulated, pathology, transgenic, rodent, mpath ontology, mouse pathology ontology, skinbase, genotype, skin, gene, tissue, hair, mutant mouse strain, bio.tools is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
has parent organization: University of Cambridge; Cambridge; United Kingdom
is parent organization of: Mouse Pathology Ontology
Lesion, Mutant mouse strain, Inbred mouse strain North American Hair Research Society ;
Ellison Medical Foundation ;
European Union QLRI-1999-00320;
European Union LSHG-CT-2006-037188;
NCI CA089713;
NCRR RR17436;
NIH AR49288
PMID:20587689
PMID:15623888
PMID:14681470
Except where otherwise noted, Creative Commons Attribution-NonCommercial-ShareAlike License, v3 Unported, Images on the database remain the property of the persons generously allowing their images to be used and are acknowledged within each record. Images should not be modified, Reproduced or disseminated without the express permission of the submitter. biotools:pathbase, nlx_151637 https://bio.tools/pathbase SCR_006141 Pathbase - European mutant mouse pathology database 2026-09-12 01:00:11 11
PhysioNet
 
Resource Report
Resource Website
500+ mentions
PhysioNet (RRID:SCR_007345) PhysioNet analysis service resource, data analysis service, data or information resource, data repository, database, production service resource, service resource, storage service resource Collection of dissemination and exchange recorded biomedical signals and open-source software for analyzing them. Provides facilities for cooperative analysis of data and evaluation of proposed new algorithm. Providies free electronic access to PhysioBank data and PhysioToolkit software. Offers service and training via on-line tutorials to assist users at entry and more advanced levels. In cooperation with annual Computing in Cardiology conference, PhysioNet hosts series of challenges, in which researchers and students address unsolved problems of clinical or basic scientific interest using data and software provided by PhysioNet. All data included in PhysioBank, and all software included in PhysioToolkit, are carefully reviewed. Researchers are further invited to contribute data and software for review and possible inclusion in PhysioBank and PhysioToolkit. Please review guidelines before submitting material. physiologic, physiology, signal, software, research, biomedical, cardiopulmonary, neural, healthy, patient, cardiac, death, congestive heart failure, epilepsy, gait, disorder, sleep apnea, cardioogy, computation, physiologic signal, workspace, time series, FASEB list, DRKB is recommended by: National Library of Medicine
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: DataCite
is listed by: re3data.org
is listed by: FAIRsharing
has parent organization: Massachusetts Institute of Technology; Massachusetts; USA;
is parent organization of: CHB-MIT Scalp EEG Database
is parent organization of: EEG Motor Movement/Imagery Dataset
is parent organization of: Sleep-EDF Database
Aging NIBIB ;
NIGMS ;
NIH EB037545
PMID:22256277
PMID:14716615
PMID:14632011
PMID:11446213
PMID:10851218
Free, Freely available r3d100011561, DOI:10.17616/R3D06S, nif-0000-00250, DOI:10.25504/FAIRsharing.bemzxg, DOI:10.13026 https://doi.org/10.17616/R3D06S, https://doi.org/10.17616/r3d06s, https://doi.org/10.13026/, https://dx.doi.org/10.13026/, https://fairsharing.org/10.25504/FAIRsharing.bemzxg, https://doi.org/10.17616/R3D06S SCR_007345 Physionet: The Research Resource for Complex Physiologic Signals, PhysioNet, PhysioNet: The Research Resource for Complex Physiologic Signals 2026-09-12 01:00:13 841
Human Reference Protein Interactome Project
 
Resource Report
Resource Website
10+ mentions
Human Reference Protein Interactome Project (RRID:SCR_015670) HuRI data or information resource, database, portal, project portal, software resource, web application Project portal for the Human Reference Protein Interactome Project, which aims generate a first reference map of the human protein-protein interactome network by identifying binary protein-protein interactions (PPIs). It achieves this by systematically interrogating all pairwise combinations of predicted human protein-coding genes using proteome-scale technologies. protein interactome, protein-protein interaction, ppi, pairwise combination, proteome, human reference NHGRI R01/U01HG001715;
NHGRI P50HG004233;
NHLBI U01HL098166;
NHLBI U01HL108630;
NCI U54CA112962;
NCI R33CA132073;
NIH RC4HG006066;
NICHD ARRA R01HD065288;
NICHD ARRA R21MH104766;
NICHD ARRA R01MH105524;
NIMH R01MH091350;
NSF CCF-1219007;
NSERC RGPIN-2014-03892
PMID:25416956 Freely Available, Free, Available for download SCR_015670 HuRI: The Human Reference Protein Interactome Mapping Project 2026-09-12 01:00:17 20
Kids First Data Resource Portal
 
Resource Report
Resource Website
1+ mentions
Kids First Data Resource Portal (RRID:SCR_016493) DRP data or information resource, data repository, database, disease-related portal, organization portal, portal, service resource, storage service resource, topical portal Portal for analysis and interpretation of pediatric genomic and clinical data to advance personalized medicine for detection, therapy, and management of childhood cancer and structural birth defects. For patients, researchers, and clinicians to create centralized database of well curated clinical and genetic sequence data from patients with childhood cancer or structural birth defects. pediatric, genomic, clinical, disease, data, children, cancer, birth, defect, analysis is recommended by: National Library of Medicine pediatric cancer, birth defect NIH ;
the Common Fund’s Gabriella Miller Kids First Pediatric Research Program
Restricted SCR_016553 https://commonfund.nih.gov/kidsfirst, https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001168.v1.p1, https://commonfund.nih.gov/kidsfirst SCR_016493 Data Resource Portal 2026-09-12 01:00:19 6
BeWith
 
Resource Report
Resource Website
BeWith (RRID:SCR_016573) BeWith data analysis software, data processing software, software application, software resource Software tool for discovering relationships between cancer modules via integrated analysis of mutual exclusivity, co-occurrence and functional interactions. clustering, framework, identify, module, mutation, interaction, pattern, gene, cancer Naomi Kadar award ;
NIH
DOI:10.1371/journal.pcbi.1005695 Free, Available for download, Freely available SCR_016573 BEtweenWITHin, Between-Within, BeWith 2026-09-12 01:00:19 0
Musculoskeletal Knowledge Portal
 
Resource Report
Resource Website
10+ mentions
Musculoskeletal Knowledge Portal (RRID:SCR_023171) MSK-KP data or information resource, disease-related portal, portal, topical portal Portal enables browsing, searching, and analysis of human genetic and genomic information linked to musculoskeletal traits and diseases, while protecting the integrity and confidentiality of underlying data. genomic data mining, human genetic data, genomic information, musculoskeletal traits and diseases data, DRKB musculoskeletal disease NIH AR085003 PMID:34686856 Free, Freely available https://msk.hugeamp.org/ SCR_023171 2026-09-12 01:00:36 26
Exemplar Microscopy Images of Tissues
 
Resource Report
Resource Website
1+ mentions
Exemplar Microscopy Images of Tissues (RRID:SCR_021052) EMIT 2d spatial image, data or information resource, data repository, data set, experimental protocol, image, image collection, image repository, immuno detection protocol, immunofluorescence, narrative resource, service resource, storage service resource Reference dataset of multiplexed immunofluorescence microscopy images collected at HMS Laboratory of Systems Pharmacology. Includes set of images of different types for development and benchmarking of computational methods for image processing. As of 4/2/2021, EMIT comprises tissue microarray containing cores from 34 cancer, non-neoplastic diseases, and normal tissue collected from clinical discards under IRB supervised protocol. TMA was imaged using cyclic immunofluorescence method. Additional extensions of EMIT are currently in the planning stages. Long term goal is to compose ImageNet like resource for highly multiplexed images of tissues and tumors by consolidating high quality curated datasets. Reference dataset, multiplexed immunofluorescence microscopy images, tissue microarray, cyclic immunofluorescence, tissues images, tumors images is related to: Synapse
is related to: Harvard Medical School; Massachusetts; USA
glioblastoma, lung adenocarcinoma, prostate adenocarcinoma, seminoma, meningioma, mesothelioma, GI stromal tumor, liver cirrhosis, leiomyosarcoma, high-grade serous ovarian cancer, diverticulitis, acute appendicitis, metastatic melanoma, dedifferentiated liposarcoma Ludwig Center at Harvard Medical School and the Ludwig Cancer Research Foundation ;
NCI U2C CA233262;
NCI U2C CA233280;
NIH U54 CA225088
DOI:10.1101/2021.03.15.435473 Restricted SCR_021052 Exemplar Microscopy Images of Tissues ( and Tumors) 2026-09-12 12:59:50 3
Neurodata Extensions Catalog
 
Resource Report
Resource Website
1+ mentions
Neurodata Extensions Catalog (RRID:SCR_021340) NDX Catalog catalog, data or information resource, database, software application, software resource Community led catalog of extensions to Neurodata Without Borders data standard. Extensions catalog, NWB, Neurodata Without Borders, data standard, Neurodata Without Borders data standard, software tools catalog is related to: Neurodata Without Borders
is related to: PyNWB
is related to: Hierarchical Data Modeling Framework
NIH Free, Available for download, Freely Available https://github.com/nwb-extensions SCR_021340 2026-09-12 12:59:54 1
BiGG Database
 
Resource Report
Resource Website
100+ mentions
BiGG Database (RRID:SCR_005809) BiGG data or information resource, database A knowledgebase of Biochemically, Genetically and Genomically structured genome-scale metabolic network reconstructions. BiGG integrates several published genome-scale metabolic networks into one resource with standard nomenclature which allows components to be compared across different organisms. BiGG can be used to browse model content, visualize metabolic pathway maps, and export SBML files of the models for further analysis by external software packages. Users may follow links from BiGG to several external databases to obtain additional information on genes, proteins, reactions, metabolites and citations of interest. biochemical, genetics, genomics, genome, metabolic network, reconstruction, model, metabolic pathway, gene, protein, reaction, metabolite, metabolic reconstruction, compound, pathway, FASEB list uses: SBML
is used by: BiGGR
is listed by: 3DVC
has parent organization: University of California at San Diego; California; USA
NIH ;
Ruth L. Kirschstein National Research Service Award - NIH Bioinformatics Training ;
University of California at San Diego; California; USA ;
Calit2 summer research scholarship ;
NIGMS GM00806-06
PMID:20426874 nlx_149299, r3d100011567 https://doi.org/10.17616/R3MG9M SCR_005809 BiGG: a Biochemical Genetic and Genomic knowledgebase of large scale metabolic reconstructions, BiGG - a Biochemical Genetic and Genomic knowledgebase 2026-09-12 01:01:39 145
GO-Module
 
Resource Report
Resource Website
1+ mentions
GO-Module (RRID:SCR_005813) GO-Module analysis service resource, data analysis service, production service resource, service resource GO-Module provides an interface to reduce the dimensionality of GO enrichment results and produce interpretable biomodules of significant GO terms organized by hierarchical knowledge that contain only true positive results. Users can download a text file of GO terms annotated with their significance and identified biomodules, a network visualization of resultant GO IDs or terms in PDF format, and view results in an online table. Platform: Online tool functional similarity, visualization, other analysis, reduce the dimensionality of go enrichment results, produce interpretable biomodules of significant go terms, gene ontology, ontology or annotation visualization, annotation is listed by: Gene Ontology Tools
is related to: Gene Ontology
is related to: AmiGO
has parent organization: University of Illinois at Chicago; Illinois; USA
NIH ;
Cancer Research Foundation ;
NLM K22 LM008308;
NCI 1U54CA121852;
NCRR UL1 RR024999
PMID:21421553 Free for academic use nlx_149322 SCR_005813 Hierarchical optimization of enriched GO terms 2026-09-12 01:01:39 3
Worldwide Protein Data Bank (wwPDB)
 
Resource Report
Resource Website
1000+ mentions
Worldwide Protein Data Bank (wwPDB) (RRID:SCR_006555) wwPDB data or information resource, database Public global Protein Data Bank archive of macromolecular structural data overseen by organizations that act as deposition, data processing and distribution centers for PDB data. Members are: RCSB PDB (USA), PDBe (Europe) and PDBj (Japan), and BMRB (USA). This site provides information about services provided by individual member organizations and about projects undertaken by wwPDB. Data available via websites of its member organizations. 3-dimentional, bioinformatics, protein, research, structure, macromolecule, structural data, 3d spatial image, gold standard is used by: Ligand Expo
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is related to: Biological Magnetic Resonance Data Bank (BMRB)
is related to: Proteopedia - Life in 3D
is related to: NRG-CING
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: DNA DataBank of Japan (DDBJ)
is related to: PDBe - Protein Data Bank in Europe
is related to: PDBe - Protein Data Bank in Europe
is related to: PDBj - Protein Data Bank Japan
is related to: Biological Magnetic Resonance Data Bank (BMRB)
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: PDB Validation Server
is related to: Structural Antibody Database
is parent organization of: PDB-Dev
works with: PDB-REDO
BBSRC ;
DOE ;
European Molecular Biology Laboratory ;
European Union ;
Heidelberg; Germany ;
Japan Science and Technology Agency ;
NBDC - National Bioscience Database Center ;
NCI ;
NIDDK ;
NIGMS ;
NIH ;
NINDS ;
NLM ;
NSF ;
Wellcome Trust
PMID:14634627 Free, Freely available nif-0000-23903, r3d100011104 https://doi.org/10.17616/R3462V SCR_006555 World Wide Protein DataBank, wwPDB, Worldwide Protein Data Bank (wwPDB), World Wide Protein Data Bank, Worldwide Protein DataBank 2026-09-12 01:01:43 1340
Gait in Parkinson's Disease
 
Resource Report
Resource Website
1+ mentions
Gait in Parkinson's Disease (RRID:SCR_006891) data or information resource, database Database that contains measures of gait from 93 patients with idiopathic PD (mean age: 66.3 years; 63% men), and 73 healthy controls (mean age: 66.3 years; 55% men). The database includes the vertical ground reaction force records of subjects as they walked at their usual, self-selected pace for approximately 2 minutes on level ground. Underneath each foot were 8 sensors (Ultraflex Computer Dyno Graphy, Infotronic Inc.) that measure force (in Newtons) as a function of time. The output of each of these 16 sensors has been digitized and recorded at 100 samples per second, and the records also include two signals that reflect the sum of the 8 sensor outputs for each foot. This database also includes demographic information, measures of disease severity (i.e., using the Hoehn & Yahr staging and/or the Unified Parkinson's Disease Rating Scale) and other related measures (available in HTML or xls spreadsheet format). A subset of the database includes measures recorded as subjects performed a second task (serial 7 subtractions) while walking, which shows excerpts of swing time series from a patient with PD and a control subject, under usual walking conditions and when performing serial 7 subtractions. Under usual walking conditions, variability is larger in the patient with PD (Coefficient of Variation = 2.7%), compared to the control subject (CV = 1.3%). Variability increases during dual tasking in the subject with PD (CV = 6.5%), but not in the control subject (CV = 1.2%). gait, speed, treadmill, stride variability is used by: NIF Data Federation
is used by: Aging Portal
has parent organization: Physiobank
Parkinson's disease NIH ;
National Parkinson's Foundation ;
Parkinson's Disease Foundation
PMID:16053531 Acknowledgement requested nif-0000-00248 SCR_006891 2026-09-12 01:01:44 1
Mutation Annotation and Genomic Interpretation
 
Resource Report
Resource Website
Mutation Annotation and Genomic Interpretation (RRID:SCR_002800) MAGI analysis service resource, data analysis service, production service resource, service resource A tool for annotating, exploring, and analyzing gene sets that may be associated with cancer. mutation, interaction, transcript, copy number aberration, network uses: The Cancer Genome Atlas
uses: HINT
uses: HPRD - Human Protein Reference Database
uses: Pfam
uses: SMART
uses: Conserved Domain Database
is listed by: OMICtools
has parent organization: Brown University; Rhode Island; USA
Cancer NSF ;
NIH ;
Brown University; Rhode Island; USA
Free, Freely available, Available for download OMICS_06145 SCR_002800 MAGI - A tool for Mutation Annotation and Genomic Interpretation 2026-09-12 01:01:26 0
UNC Infant 0-1-2 Atlases
 
Resource Report
Resource Website
1+ mentions
UNC Infant 0-1-2 Atlases (RRID:SCR_002569) UNC Infant 0-1-2 Atlases atlas, data or information resource 3 atlases dedicated for neonates, 1-year-olds, and 2-year-olds. Each atlas comprises a set of 3D images made up of the intensity model, tissue probability maps, and anatomical parcellation map. These atlases are constructed with the help of state-of-the-art infant MR segmentation and groupwise registration methods, on a set of longitudinal images acquired from 95 normal infants (56 males and 39 females) at neonate, 1-year-old, and 2-year-old. analyze, atlas application, linux, macos, microsoft, magnetic resonance, posix/unix-like, infant, pediatric, template, longitudinal, neonate, male, female, mri is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: University of North Carolina at Chapel Hill School of Medicine; North Carolina; USA
Normal NIH ;
NIBIB EB006733;
NIBIB EB008760;
NIBIB EB008374;
NIBIB EB009634;
NIMH MH088520;
NIMH MH070890;
NIMH MH064065;
NINDS NS055754;
NICHD HD053000
PMID:21533194 Free, Available for download, Freely available nlx_155971 http://www.nitrc.org/projects/pediatricatlas SCR_002569 UNC 0-1-2 Infant Atlases 2026-09-12 01:01:26 2
Nucleic Acid Database
 
Resource Report
Resource Website
10+ mentions
Nucleic Acid Database (RRID:SCR_003255) NDB data or information resource, database A database of three-dimensional structural information about nucleic acids and their complexes. In addition to primary data, it contains derived geometric data, classifications of structures and motifs, standards for describing nucleic acid features, as well as tools and software for the analysis of nucleic acids. A variety of search capabilities are available, as are many different types of reports. NDB maintains the macromolecular Crystallographic Information File (mmCIF). nucleic acid, dna, nucleopeptide, nucleoprotein, nucleotide, rna, transfection, sequence, structure, function, bio.tools, FASEB list is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: MINAS - Metal Ions in Nucleic AcidS
is related to: Biological Magnetic Resonance Data Bank (BMRB)
is related to: Jenalib: Jena Library of Biological Macromolecules
has parent organization: Rutgers University; New Jersey; USA
NSF ;
DOE ;
NIH
PMID:24185695
PMID:1384741
Free, Available for download, Freely available nif-0000-03184, biotools:ndb, r3d100010415 https://bio.tools/ndb, https://doi.org/10.17616/R3531R SCR_003255 2026-09-12 01:01:28 37
MITOMAP - A human mitochondrial genome database
 
Resource Report
Resource Website
100+ mentions
MITOMAP - A human mitochondrial genome database (RRID:SCR_002996) MITOMAP data or information resource, database Database of polymorphisms and mutations of the human mitochondrial DNA. It reports published and unpublished data on human mitochondrial DNA variation. All data is curated by hand. If you would like to submit published articles to be included in mitomap, please send them the citation and a pdf. gene, genome, diabetes, disease, disease-association, high resolution screening, human, inversion, metabolism, mitochondrial dna, mutation, phenotype, polymorphism, polypeptide assignment, pseudogene, restriction site, rna, sequence, trna, unpublished, variation, mitochondria, dna, insertion, deletion, FASEB list is used by: HmtVar
is listed by: OMICtools
is related to: Hereditary Hearing Loss Homepage
has parent organization: Childrens Hospital of Philadelphia - Research Institute; Pennsylvania; USA
has parent organization: Emory University School of Medicine; Atlanta; Georgia; USA
NIH ;
Muscular Dystrophy Foundation ;
Ellison Foundation ;
Diputacion General de Aragon Grupos consolidados B33 ;
NIGMS GM46915;
NINDS NS21328;
NHLBI HL30164;
NIA AG10130;
NIA AG13154;
NINDS NS213L8;
NHLBI HL64017;
NIH Biomedical Informatics Training Grant T15 LM007443;
NSF EIA-0321390;
Spanish Fondo de Investigacion Sanitaria PI050647;
Ciber Enfermedades raras CB06/07/0043
PMID:17178747
PMID:15608272
PMID:9399813
PMID:9016535
PMID:8594574
Except where otherwise noted, Creative Commons Attribution License, The community can contribute to this resource nif-0000-00511, OMICS_01641 SCR_002996 2026-09-12 01:01:27 405

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