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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 Authority Synonyms Record Last Update Mentions Count
CellFinder
 
Resource Report
Resource Website
10+ mentions
CellFinder (RRID:SCR_006598) CellFinder analysis service resource, data analysis service, data or information resource, database, production service resource, service resource Database of mapped validated gene and protein expression, phenotype and images related to cell types. The data allow characterization and comparison of cell types and can be browsed by using the body browser and by searching for cells or genes. All cells are related to more complex systems such as tissues, organs and organisms and arranged according to their position in development. CellFinder provides long-term data storage for validated and curated primary research data and provides additional expert-validation through relevant information extracted from text. Operated under the Open Source/Access model, community and scientific networking applications will allow users to store and retrieve their data and to explore cells and their interactions on singular and complex resolution levels. The involvement of stem cell registries and banks will allow direct access to selected cells. The set up the stem cell data repository will involve three lines of action: * the acquisition of scientific data and contents * the standardized description of this data, its organization with the help of ontologies and technical implementation * the integration of existing sources/logistics and to ensure sustainable long-term operation cell, gene expression, protein expression, phenotype, image, gene, stem cell, cellome, metadata standard, stem cell therapy, differential expression, protein, cell type, development, adrenal gland, gall bladder, intestine, inferior vena cava, kidney, liver, spleen is related to: Allen Institute for Brain Science
has parent organization: Charite - Universitatsmedizin Berlin; Berlin; Germany
is parent organization of: CELDA Ontology
BMBF ;
DFG
PMID:23599415 nlx_153857 SCR_006598 SciCrunch Registry Cell Finder 2026-11-07 11:56:11 31
DB-PABP: a database of polyanion binding proteins
 
Resource Report
Resource Website
DB-PABP: a database of polyanion binding proteins (RRID:SCR_007603) data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE, documented August 23, 2016. DB-PABP is an attempt to document the publicly available experimentally determined polyanion binding proteins (PABPs). The purpose of the database is to provide life scientists who are interested in PA/PABP interactions with a comprehensive data repository, as well as computer scientists with a publicly available dataset to perform knowledge discovery and datamining studies. The database is manually curated. It uses protein annotations from NCBI protein database and literature information is retrieved from PubMed. Whenever applicable, links to NCBI protein database and PubMed are provided so users may access additional information available in these public databases. pabp, polyanion, polyanion binding protein, polyanion binding protein interaction, polyanion interactions, protein has parent organization: University of Kansas; Kansas; USA THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02724 SCR_007603 SciCrunch Registry DB-PABP 2026-11-07 12:02:53 0
Agile Protein Interactomes DataServer
 
Resource Report
Resource Website
10+ mentions
Agile Protein Interactomes DataServer (RRID:SCR_008871) APID analysis service resource, data access protocol, data analysis service, data or information resource, database, production service resource, service resource, software resource, web service APID Interactomes (Agile Protein Interactomes DataServer) provides information on the protein interactomes of numerous organisms, based on the integration of known experimentally validated protein-protein physical interactions (PPIs). The interactome data includes a report on quality levels and coverage over the proteomes for each organism included. APID integrates PPIs from primary databases of molecular interactions (BIND, BioGRID, DIP, HPRD, IntAct, MINT) and also from experimentally resolved 3D structures (PDB) where more than two distinct proteins have been identified. This collection references protein interactors, through a UniProt identifier. protein, protein interaction, interactions, ppi, interactomes, analysis, gene, ontology, functional, environment, data, network, graphic, visualize is listed by: Gene Ontology Tools
is related to: PSICQUIC Registry
is related to: Gene Ontology
is related to: BIND
is related to: Biological General Repository for Interaction Datasets (BioGRID)
is related to: Database of Interacting Proteins (DIP)
is related to: HPRD - Human Protein Reference Database
is related to: IntAct
is related to: MINT
has parent organization: University of Salamanca; Salamanca; Spain
Junta de Castilla y Leon ;
Spanish Ministerio de Sanidad y Consumo
PMID:27131791
PMID:30715274
Free for academic use r3d100012339, nlx_149321 https://doi.org/10.17616/R3407P, https://doi.org/10.17616/R3407P SCR_008871 SciCrunch Registry Agile Protein Interactomes DataServer, APID, APID Interactomes, Agile Protein Interactomes DataServer (APID), APID (Agile Protein Interactomes DataServer) 2026-11-07 11:56:40 14
UniProt
 
Resource Report
Resource Website
10000+ mentions
UniProt (RRID:SCR_002380) UniProt data or information resource, database Collection of data of protein sequence and functional information. Resource for protein sequence and annotation data. Consortium for preservation of the UniProt databases: UniProt Knowledgebase (UniProtKB), UniProt Reference Clusters (UniRef), and UniProt Archive (UniParc), UniProt Proteomes. Collaboration between European Bioinformatics Institute (EMBL-EBI), SIB Swiss Institute of Bioinformatics and Protein Information Resource. Swiss-Prot is a curated subset of UniProtKB. collection, protein, sequence, annotation, data, functional, information is used by: LIPID MAPS Proteome Database
is used by: ChannelPedia
is used by: Open PHACTS
is used by: DisGeNET
is used by: Smart Dictionary Lookup
is used by: MitoMiner
is used by: Cytokine Registry
is used by: MobiDB
is used by: Pathway Analysis Tool for Integration and Knowledge Acquisition
is used by: Phospho.ELM
is used by: GEROprotectors
is used by: SwissLipids
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: LabWorm
is related to: Clustal W2
is related to: UniProt DAS
is related to: UniParc at the EBI
is related to: ProDom
is related to: LegumeIP
is related to: Pathway Commons
is related to: NIH Data Sharing Repositories
is related to: FlyMine
is related to: IMEx - The International Molecular Exchange Consortium
is related to: 3D-Interologs
is related to: Biomine
is related to: EBIMed
is related to: STOP
is related to: Coremine Medical
is related to: BioExtract
is related to: STRAP
is related to: GOTaxExplorer
is related to: GoAnnotator
is related to: IT-GOM: Integrated Tool for IC-based GO Semantic Similarity Measures
is related to: Whatizit
is related to: MOPED - Model Organism Protein Expression Database
is related to: Polbase
is related to: PredictSNP
is related to: PSICQUIC Registry
is related to: IntAct
is related to: p300db
is related to: UniProt Proteomes
is related to: SARS-CoV-2 mutation effects and 3D structure prediction from sequence covariation
has parent organization: European Bioinformatics Institute
has parent organization: SIB Swiss Institute of Bioinformatics
has parent organization: Protein Information Resource
is parent organization of: UniProtKB
is parent organization of: NEWT
is parent organization of: UniParc
is parent organization of: UniProt Chordata protein annotation program
is parent organization of: UniRef
works with: Genotate
works with: CellPhoneDB
works with: MOLEonline
works with: MiMeDB
ARUK ;
British Heart Foundation ;
EMBL ;
NCI ;
NCRR P20 RR016472;
NEI ;
NHGRI P41 HG02273;
NHGRI U24 HG007722;
NHGRI U41 HG006104;
NHLBI ;
NIAID ;
NIA ;
NIDDK ;
NIGMS 5R01GM080646;
NIGMS R01 GM080646;
NIMH ;
NLM G08 LM010720;
NSF DBI-0850319;
PDUK
PMID:19843607
PMID:18836194
PMID:18045787
PMID:17142230
PMID:16381842
PMID:15608167
PMID:14681372
nif-0000-00377, SCR_018750, r3d100010357 http://www.ebi.uniprot.org, http://www.uniprot.org/uniprot/, http://www.pir.uniprot.org, ftp://ftp.uniprot.org, https://doi.org/10.17616/R3BW2M SCR_002380 SciCrunch Registry , The Universal Protein Resource, Universal Protein Resource, UNIPROT Universal Protein Resource 2026-11-07 12:01:58 19823
Caenorhabditis Genetics Center
 
Resource Report
Resource Website
1000+ mentions
Caenorhabditis Genetics Center (RRID:SCR_007341) CGC biomaterial supply resource, cell repository, material resource, organism supplier Center that acquires, maintains, and distributes genetic stocks and information about stocks of the small free-living nematode Caenorhabditis elegans for use by investigators initiating or continuing research on this genetic model organism. A searchable strain database, general information about C. elegans, and links to key Web sites of use to scientists, including WormBase, WormAtlas, and WormBook are available. non-human animal, caenorhabditis elegans, chromosome, database, model, mutant, nematode, nomenclature, model organism, protein, transgenic, web accessible database, genetic stock, germplasm, genotype, FASEB list is used by: NIF Data Federation
is listed by: One Mind Biospecimen Bank Listing
is related to: C. elegans Gene Knockout Consortium
is related to: Expression Patterns for C. elegans promoter GFP fusions
has parent organization: University of Minnesota Twin Cities; Minnesota; USA
OD P40 OD010440 nif-0000-00240 https://orip.nih.gov/comparative-medicine/programs/invertebrate-models, http://www.cbs.umn.edu/research/resources/cgc http://biosci.umn.edu/CGC/, http://www.cgc.cbs.umn.edu SCR_007341 SciCrunch Registry 2026-11-07 11:56:12 3907
NIH Human Pluripotent Stem Cell Registry
 
Resource Report
Resource Website
1+ mentions
NIH Human Pluripotent Stem Cell Registry (RRID:SCR_003149) NIH Human Embryonic Stem Cell Registry biomaterial supply resource, cell repository, material resource A listing of human embryonic cell lines that are eligible for use in NIH funded research. Those lines that carry disease-specific mutations are noted as such under the line name. Total Eligible Lines = 200. The purpose of the Registry is to provide investigators with: # a unique NIH Code for each cell line that must be used when applying for NIH funding and # contact information to facilitate investigators' acquisition of stem cells. Before submitting a new grant application and supporting materials for consideration of a human embryonic stem cell line, scientists may wish to see what lines are already under consideration: * Human embryonic stem cell lines submitted to NIH that are being reviewed to determine if they may be used in NIH-supported research, http://grants.nih.gov/stem_cells/registry/pending.htm President George W. Bush required that the name of the registry be changed in his Executive Order #13435, issued on June 20, 2007. As a result of this Executive Order, the former National Institutes of Health Human Embryonic Stem Cell Registry will now be called the National Institutes of Health Human Pluripotent Stem Cell Registry. The registry will now include both human embryonic stem cells that were derived consistent with the President's policy of August 9, 2001 and human pluripotent stem cells derived from non-embryonic sources. embryonic, cell, human, registry, stem cell, embryonic stem cell, cell line, human embryonic stem cell line, human pluripotent stem cell, adult, fetal, mutation is listed by: One Mind Biospecimen Bank Listing
is related to: One Mind Biospecimen Bank Listing
is related to: Wisconsin International Stem Cell Bank
is related to: National Stem Cell Bank
is related to: NIF Data Federation
is related to: Integrated Cell Lines
has parent organization: National Institutes of Health
NIH ;
NIH Blueprint for Neuroscience Research
Free, Freely available nif-0000-00565 SCR_003149 SciCrunch Registry NIH Human Embryonic Stem Cell Registry, National Institutes of Health Human Pluripotent Stem Cell Registry 2026-11-07 12:01:25 7
Biobanque de Picardie
 
Resource Report
Resource Website
Biobanque de Picardie (RRID:SCR_004731) biomaterial supply resource, material resource, tissue bank A secure repository of biological samples and data dedicated for medical and research purposes. These biological samples are linked to consenting patient relative data. Biobanque de Picardie provides quality and traceability services for establishment, conservation and use of biological samples collections. It houses collections of human tissue in a variety of areas of disease. Samples are used in basic research and translational studies, physiopathology of diseases and identification of new diagnostic, and as prognostic or therapeutic biomarkers. Biobanque de Picardie also develops healthy or pathological human primary stem cell banks, such as: mesenchymal stem cells in umbilical cord (HUC-MSC), primary hepatocytes (HPH), peripheral blood mononuclear cells (PBMC), and fibroblasts. Biological samples are stored at - 80 degrees C in electric freezers, at - 196 degrees C in liquid nitrogen or -130 degrees C in nitrogen vapor. tissue, stem cell, mesenchymal stem cell, fibroblast, frozen, liquid nitrogen, cryopreserved, fresh, normal control, internal medicine, pediatrics, biobank, human is listed by: One Mind Biospecimen Bank Listing
has parent organization: University of Picardie Jules Verne; Amiens; France
Anti-phospholipid antibody syndrome, Ovarian cancer, Hepathocellular carcinoma, Chlamydia, Acute alcoholic hepatitis, Hepatitis B, Hepatitis C, HT 21, Celiac disease, Crohn's disease, Ulcerative colitis, Giant cell arteritis, Blood disorder, Leukemia, Mastocytosis, Lymphoma, Myeloma, Obesity, Acute Pancreatitis, Rheumatoid arthritis, Kidney transplant, Human immunodeficiency virus French Ministry of Research ;
FEDER
For the scientific community nlx_73857 http://www.biobanque-picardie.com/indexang.htm SCR_004731 SciCrunch Registry 2026-11-07 12:02:26 0
NSR Physiome Project
 
Resource Report
Resource Website
1+ mentions
NSR Physiome Project (RRID:SCR_007379) NSR Physiome Project data or information resource, portal, professional program, simulation software, software application, software resource, topical portal, training resource Database of physiological, pharmacological, and pathological information on humans and other organisms and integration through computational modeling. Models include everything from diagrammatic schema, suggesting relationships among elements composing a system, to fully quantitative, computational models describing the behavior of physiological systems and an organism''s response to environmental change. Each mathematical model is an internally self-consistent summary of available information, and thereby defines a working hypothesis about how a system operates. Predictions from such models are subject to test, with new results leading to new models.BR /> A Tool developed for the NSR Physiome project is JSim, an open source, free software. JSim is a Java-based simulation system for building quantitative numeric models and analyzing them with respect to experimental reference data. JSim''s primary focus is in physiology and biomedicine, however its computational engine is quite general and applicable to a wide range of scientific domains. JSim models may intermix ODEs, PDEs, implicit equations, integrals, summations, discrete events and procedural code as appropriate. JSim''s model compiler can automatically insert conversion factors for compatible physical units as well as detect and reject unit unbalanced equations. JSim also imports the SBML and CellML model archival formats. All JSim models are open source. Goals of the Physiome Project: - To develop and database observations of physiological phenomenon and interpret these in terms of mechanism (a fundamentally reductionist goal). - To integrate experimental information into quantitative descriptions of the functioning of humans and other organisms (modern integrative biology glued together via modeling). - To disseminate experimental data and integrative models for teaching and research. - To foster collaboration amongst investigators worldwide, to speed up the discovery of how biological systems work. - To determine the most effective targets (molecules or systems) for therapy, either pharmaceutic or genomic. - To provide information for the design of tissue-engineered, biocompatible implants. physiome, computational modeling, cell, organ, organism, human, model, physiological, pharmacological, pathological, model repository, sbml, cellml, biophysics, biochemistry, database, proteome, jsim simulation analysis system, data analysis tool, parameter optimization tool, integrating biological system has parent organization: University of Washington; Seattle; USA NSF BE08407;
NHLBI T15 HL88516-01;
NSF BES-0506477;
NHLBI R01HL073598;
NIBIB R01EB001973
nif-0000-00532 SCR_007379 SciCrunch Registry National Simulation Resource Physiome Project 2026-11-07 11:56:13 3
Integrated Manually Extracted Annotation
 
Resource Report
Resource Website
Integrated Manually Extracted Annotation (RRID:SCR_008876) Integrated MEA, Integrated LinkOut, Manually Extracted Annotation, data or information resource, database A virtual database of annotations made by 50 database providers (April 2014) - and growing (see below), that map data to publication information. All NIF Data Federation sources can be part of this virtual database as long as they indicate the publications that correspond to data records. The format that NIF accepts is the PubMed Identifier, category or type of data that is being linked to, and a data record identifier. A subset of this data is passed to NCBI, as LinkOuts (links at the bottom of PubMed abstracts), however due to NCBI policies the full data records are not currently associated with PubMed records. Database providers can use this mechanism to link to other NCBI databases including gene and protein, however these are not included in the current data set at this time. (To view databases available for linking see, http://www.ncbi.nlm.nih.gov/books/NBK3807/#files.Databases_Available_for_Linking ) The categories that NIF uses have been standardized to the following types: * Resource: Registry * Resource: Software * Reagent: Plasmid * Reagent: Antibodies * Data: Clinical Trials * Data: Gene Expression * Data: Drugs * Data: Taxonomy * Data: Images * Data: Animal Model * Data: Microarray * Data: Brain connectivity * Data: Volumetric observation * Data: Value observation * Data: Activation Foci * Data: Neuronal properties * Data: Neuronal reconstruction * Data: Chemosensory receptor * Data: Electrophysiology * Data: Computational model * Data: Brain anatomy * Data: Gene annotation * Data: Disease annotation * Data: Cell Model * Data: Chemical * Data: Pathways For more information refer to Create a LinkOut file, http://neuinfo.org/nif_components/disco/interoperation.shtm Participating resources ( http://disco.neuinfo.org/webportal/discoLinkoutServiceSummary.do?id=4 ): * Addgene http://www.addgene.org/pgvec1 * Animal Imaging Database http://aidb.crbs.ucsd.edu * Antibody Registry http://www.neuinfo.org/products/antibodyregistry/ * Avian Brain Circuitry Database http://www.behav.org/abcd/abcd.php * BAMS Connectivity http://brancusi.usc.edu/ * Beta Cell Biology Consortium http://www.betacell.org/ * bioDBcore http://biodbcore.org/ * BioGRID http://thebiogrid.org/ * BioNumbers http://bionumbers.hms.harvard.edu/ * Brain Architecture Management System http://brancusi.usc.edu/bkms/ * Brede Database http://hendrix.imm.dtu.dk/services/jerne/brede/ * Cell Centered Database http://ccdb.ucsd.edu * CellML Model Repository http://www.cellml.org/models * CHEBI http://www.ebi.ac.uk/chebi/ * Clinical Trials Network (CTN) Data Share http://www.ctndatashare.org/ * Comparative Toxicogenomics Database http://ctdbase.org/ * Coriell Cell Repositories http://ccr.coriell.org/ * CRCNS - Collaborative Research in Computational Neuroscience - Data sharing http://crcns.org * Drug Related Gene Database https://confluence.crbs.ucsd.edu/display/NIF/DRG * DrugBank http://www.drugbank.ca/ * FLYBASE http://flybase.org/ * Gene Expression Omnibus http://www.ncbi.nlm.nih.gov/geo/ * Gene Ontology Tools http://www.geneontology.org/GO.tools.shtml * Gene Weaver http://www.GeneWeaver.org * GeneDB http://www.genedb.org/Homepage * Glomerular Activity Response Archive http://gara.bio.uci.edu * GO http://www.geneontology.org/ * Internet Brain Volume Database http://www.cma.mgh.harvard.edu/ibvd/ * ModelDB http://senselab.med.yale.edu/modeldb/ * Mouse Genome Informatics Transgenes ftp://ftp.informatics.jax.org/pub/reports/MGI_PhenotypicAllele.rpt * NCBI Taxonomy Browser http://www.ncbi.nlm.nih.gov/Taxonomy/taxonomyhome.html * NeuroMorpho.Org http://neuromorpho.org/neuroMorpho * NeuronDB http://senselab.med.yale.edu/neurondb * SciCrunch Registry http://neuinfo.org/nif/nifgwt.html?tab=registry * NIF Registry Automated Crawl Data http://lucene1.neuinfo.org/nif_resource/current/ * NITRC http://www.nitrc.org/ * Nuclear Receptor Signaling Atlas http://www.nursa.org * Olfactory Receptor DataBase http://senselab.med.yale.edu/ordb/ * OMIM http://omim.org * OpenfMRI http://openfmri.org * PeptideAtlas http://www.peptideatlas.org * RGD http://rgd.mcw.edu * SFARI Gene: AutDB https://gene.sfari.org/autdb/Welcome.do * SumsDB http://sumsdb.wustl.edu/sums/ * Temporal-Lobe: Hippocampal - Parahippocampal Neuroanatomy of the Rat http://www.temporal-lobe.com/ * The Cell: An Image Library http://www.cellimagelibrary.org/ * Visiome Platform http://platform.visiome.neuroinf.jp/ * WormBase http://www.wormbase.org * YPED http://medicine.yale.edu/keck/nida/yped.aspx * ZFIN http://zfin.org biomedical, bibliographic, linkout, literature is used by: NIF Data Federation
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Gene Ontology Tools
is related to: BAMS Connectivity
is related to: Biological General Repository for Interaction Datasets (BioGRID)
is related to: BioNumbers
is related to: PubMed
is related to: Brain Architecture Management System
is related to: CellML Model Repository
is related to: CHEBI
is related to: Comparative Toxicogenomics Database (CTD)
is related to: Coriell Cell Repositories
is related to: Drug Related Gene Database
is related to: DrugBank
is related to: Gene Weaver
is related to: Internet Brain Volume Database
is related to: Cell Centered Database
is related to: Brede Database
is related to: ModelDB
is related to: NeuronDB
is related to: NeuroMorpho.Org
is related to: Nuclear Receptor Signaling Atlas
is related to: Cell Image Library (CIL)
is related to: Animal Imaging Database
is related to: Olfactory Receptor DataBase
is related to: Glomerular Activity Response Archive
is related to: CRCNS
is related to: OMIM
is related to: Rat Genome Database (RGD)
is related to: Visiome Platform
is related to: NIDA Data Share
is related to: bioDBcore
is related to: Addgene
is related to: Antibody Registry
is related to: Beta Cell Biology Consortium
is related to: FlyBase
is related to: SumsDB
is related to: SciCrunch Registry
is related to: Mouse Genome Informatics Transgenes
is related to: NCBI Taxonomy
is related to: OpenNeuro
is related to: PeptideAtlas
is related to: Temporal-Lobe: Hippocampal - Parahippocampal Neuroanatomy of the Rat
is related to: NIF Registry Automated Crawl Data
is related to: AutDB
is related to: Gene Expression Omnibus
is related to: Gene Ontology
is related to: Avian Brain Circuitry Database
is related to: Zebrafish Information Network (ZFIN)
is related to: GeneDB
is related to: WormBase
is related to: YPED
has parent organization: Integrated
PMID:20387131
PMID:18975149
Data are licensed by their respective owners. Use and distribution is subject to the Terms of Use by the original resource as well as the, Creative Commons Attribution License nlx_149407 http://neuinfo.org/nif/nifgwt.html?query=nlx_149407, https://neuinfo.org/mynif/search.php?q=*&t=indexable&list=cover&nif=nlx_149407-1 SCR_008876 SciCrunch Registry Integrated Manually Extracted Annotation View, NIF Integrated LinkOut, NIF Integrated Manually Extracted Annotation, NIF LinkOut 2026-11-07 12:03:10 0
Stroke Patient Recovery Research Database (SPReD)
 
Resource Report
Resource Website
Stroke Patient Recovery Research Database (SPReD) (RRID:SCR_005508) SPReD data or information resource, database, image THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 28,2025. The Stroke Patient Recovery Research Database (SPReD) initiative creates the infrastructure needed for the collection of a wide range of data related to stroke risk factors and to stroke recovery. It also promotes the analysis and management of large brain and vessel images. A major goal is to create a comprehensive electronic database Stroke Patient Recovery Research Database or SPReD and populate it with patient data, including demographic, biomarker, genetic and proteomic data and imaging data. SPReD will enable us to combine descriptions of our stroke patients from multiple projects that are geographically distributed. We will do this in a uniform fashion in order to enhance our ability to document rates of recovery; to study the effects of vascular risk factors and inflammatory biomarkers; and to use these data to improve their physical and cognitive recovery through innovative intervention programs. This comprehensive database will provide an integrated repository of data with which our researchers will investigate and test original ideas, ultimately leading to knowledge that can be applied clinically to benefit stroke survivors. stroke, demographic, biomarker, genetic, proteomic, imaging, clinical, brain, vessel, risk factor, recovery THIS RESOURCE IS NO LONGER IN SERVICE nlx_144609 SCR_005508 SciCrunch Registry Stroke Patient Recovery Research Database 2026-11-07 12:02:08 0
The NeuroCommons Project
 
Resource Report
Resource Website
The NeuroCommons Project (RRID:SCR_007171) community building portal, data or information resource, portal, software application, software development tool, software resource, systems interoperability software, topical portal The Neurocommons project is an Open Source knowledge management platform for biological research. It seeks to make all scientific research materials - research articles, annotations, data, physical materials - as available and as usable as they can be. We do this by both fostering practices that render information in a form that promotes uniform access by computational agents - sometimes called interoperability. We want knowledge sources to combine meaningfully, enabling semantically precise queries that span multiple information sources. Our work covers general data and knowledge sources used in computational biology as well as sources specific to neuroscience and neuromedicine. The practices that we develop and promote are designed to play well on the Semantic Web. We view our technical work not as creating a new service or content library, although we do both, but rather as helping to promote the growth of semantically linked scientific information. analytic tools, bundles, common naming), documenting, installer, interoperation, ontologies, protocol, rdf, rdf distribution, semantic web, software repository, sparql - protocol for querying triple stores, text processing - automated text to rdf, triple store, uris (manifesto, user interface, ontology, owl nif-0000-01644 SCR_007171 SciCrunch Registry NeuroCommons 2026-11-07 11:56:10 0
Michigan Molecular Interactions
 
Resource Report
Resource Website
1+ mentions
Michigan Molecular Interactions (RRID:SCR_003521) MiMI analysis service resource, data access protocol, data analysis service, data or information resource, database, production service resource, service resource, software resource, web service MiMi Web gives you an easy to use interface to a rich NCIBI data repository for conducting your systems biology analyses. This repository includes the MiMI database, PubMed resources updated nightly, and text mined from biomedical research literature. The MiMI database comprehensively includes protein interaction information that has been integrated and merged from diverse protein interaction databases and other biological sources. With MiMI, you get one point of entry for querying, exploring, and analyzing all these data. MiMI provides access to the knowledge and data merged and integrated from numerous protein interactions databases and augments this information from many other biological sources. MiMI merges data from these sources with deep integration into its single database with one point of entry for querying, exploring, and analyzing all these data. MiMI allows you to query all data, whether corroborative or contradictory, and specify which sources to utilize. MiMI displays results of your queries in easy-to-browse interfaces and provides you with workspaces to explore and analyze the results. Among these workspaces is an interactive network of protein-protein interactions displayed in Cytoscape and accessed through MiMI via a MiMI Cytoscape plug-in. MiMI gives you access to more information than you can get from any one protein interaction source such as: * Vetted data on genes, attributes, interactions, literature citations, compounds, and annotated text extracts through natural language processing (NLP) * Linkouts to integrated NCIBI tools to: analyze overrepresented MeSH terms for genes of interest, read additional NLP-mined text passages, and explore interactive graphics of networks of interactions * Linkouts to PubMed and NCIBI's MiSearch interface to PubMed for better relevance rankings * Querying by keywords, genes, lists or interactions * Provenance tracking * Quick views of missing information across databases. Data Sources include: BIND, BioGRID, CCSB at Harvard, cPath, DIP, GO (Gene Ontology), HPRD, IntAct, InterPro, IPI, KEGG, Max Delbreuck Center, MiBLAST, NCBI Gene, Organelle DB, OrthoMCL DB, PFam, ProtoNet, PubMed, PubMed NLP Mining, Reactome, MINT, and Finley Lab. The data integration service is supplied under the conditions of the original data sources and the specific terms of use for MiMI. Access to this website is provided free of charge. The MiMI data is queryable through a web services api. The MiMI data is available in PSI-MITAB Format. These files represent a subset of the data available in MiMI. Only UniProt and RefSeq identifiers are included for each interactor, pathways and metabolomics data is not included, and provenance is not included for each interaction. If you need access to the full MiMI dataset please send an email to mimi-help (at) umich.edu. gene, interaction, molecule, protein, protein interaction, protein-protein interaction is related to: MiMI Plugin for Cytoscape
has parent organization: National Center for Integrative Biomedical Informatics
Michigan Center for Biological Information ;
National Center for Integrative Biomedical Informatics ;
Pfizer ;
Medical and Academic Partnerships ;
Howard Hughes Medical Institute ;
Microsoft Corporation ;
NLM R01 LM008106;
NIDA U54 DA021519;
NSF IIS 0219513
PMID:18978014
PMID:17130145
nif-0000-00214 SCR_003521 SciCrunch Registry 2026-11-07 11:55:06 5
Longitudinal Assessment of Bariatric Surgery
 
Resource Report
Resource Website
1+ mentions
Longitudinal Assessment of Bariatric Surgery (RRID:SCR_001536) LABS data or information resource, disease-related portal, narrative resource, portal, research forum portal, resource, topical portal Consortium comprised of six clinical centers and a data coordinating center to facilitate coordinated clinical, epidemiological, and behavioral research in the field of bariatric surgery, through the cooperative development of common clinical protocols and a bariatric surgery database that will collect information from participating clinical centers. LABS will help pool the necessary clinical expertise and administrative resources to facilitate the conduct of multiple clinical studies in a timely, efficient manner. Also, the use of standardized definitions, clinical protocols, and data-collection instruments will enhance the investigator's ability to provide meaningful evidence-based recommendations for patient evaluation, selection, and follow-up care. The consortium was funded in September 2003. The investigators have collaboratively developed a core database and clinical protocols, and subject enrollment began in early 2005. A repository of data and biological specimens for future research also will be collected by the centers participating in LABS. These will provide valuable resources for future study of obesity and its complications. clinical, epidemiology, behavior, longitudinal, risk, benefit, surgical procedure, clinical outcome, database, clinical trial, experimental protocol, biomaterial supply resource is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Research Resources
has parent organization: University of Pittsburgh; Pennsylvania; USA
Bariatric surgery, Obesity NIDDK 5U01DK066557 nlx_152842 SCR_001536 SciCrunch Registry Longitudinal Assessment of Bariatric Surgery Consortium, LABS consortium, Longitudinal Assessment of Bariatric Surgery (LABS) Consortium 2026-11-07 11:54:33 1
Aspergillus Genomes
 
Resource Report
Resource Website
Aspergillus Genomes (RRID:SCR_001880) Aspergillus Genomes analysis service resource, data analysis service, data or information resource, database, production service resource, service resource A resource for viewing annotated genes arising from various Aspergillus sequencing and annotation projects, resulting from the merging of Central Aspergillus Data REpository (CADRE) and The Aspergillus Website, which took place in June 2008. The principal role of CADRE is to aid the Aspergillus research community by managing Aspergillus genome data and by providing visualization tools, ranging from relatively simple annotation displays to more complex data integration displays. In contrast, The Aspergillus Website provides a range of information to the medical community (i.e., clinicians, patients and scientists) regarding the genus Aspergillus and the diseases, such as Aspergillosis, that it can cause. CADRE has been implemented using the Ensembl v22 suite. This suite comprises: * a database schema, which has been devised for storing annotated eukaryotic genomes. The schema is implemented with the MySQL relational database management system. * several specialized programming modules for building interfaces (i.e., BioPerl and Ensembl API modules). * a series of programs (i.e., Perl CGI scripts using the API modules) for viewing genomic data within a web browser., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. genome, eukaryotic genome, gene, gene annotation, aspergillosis, aspergillus, pathway, annotation, sequence, metabolic pathway, genomics, clinical, strain, dna, peptide, blast Fungal Research Trust PMID:19039001 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02577, r3d100011253 https://doi.org/10.17616/R3005P SCR_001880 SciCrunch Registry 2026-11-07 11:54:35 0
Glyco-CD
 
Resource Report
Resource Website
Glyco-CD (RRID:SCR_001574) GlycoCD, data or information resource, data set Manually curated, comprehensive repository of clusters of differentiation (CDs) which are a) defined as distinct oligosaccharide sequences as part of either glycoproteins and/or glycosphingolipids and b) defined as proteins which have carbohydrate recognition sites (CRDs) or as carbohydrate binding lectins. The data base is generated by exhaustive search of literature and other online data banks related to carbohydrates and proteins. This data bank is the beginning of an effort to provide concise, relevant information of carbohydrate-related CDs in a user- friendly manner. For users convenience the data bank under menu browse of GlycoCD is arranged in two section namely carbohydrate recognition CDs (CRD CD) and glycan CD. The carbohydrate recognition CD part is the collection of proteins which recognize glycan structures by means of the CRDs. Glycan CD is the part in which CDs are summarized which characterize specific oligosaccharide structures. The GlycoCD databank has been developed with the aim to assist the immunologist, cell biologist as well as the clinician who wants to keep up with the present knowledge in this field of glycobiology. carbohydrate, glycobiology, glycan, lectin, antigen, interaction, protein, cell surface molecule, microarray, carbohydrate recognition, cluster of differentiation, oligosaccharide sequence, glycoprotein, glycosphingolipid, carbohydrate recognition site, leukocyte, antibody, endothelial cell, epithelial cell has parent organization: glycosciences.de European Union FP7/2007-2013 215536 PMID:22847935 THIS RESOURCE IS NO LONGER IN SERVICE nlx_152887 http://www.glycosciences.de//Glyco-CD/ SCR_001574 SciCrunch Registry GlycoCD database, Glyco-CD databank, Glyco-CD database 2026-11-07 12:04:20 0
RETICULUM - Neuroscience History Resources
 
Resource Report
Resource Website
RETICULUM - Neuroscience History Resources (RRID:SCR_004371) RETICULUM data or information resource, portal, topical portal THIS RESOURCE IS NO LONGER IN SERVICE, documented September 6, 2016. RETICULUM is a gateway to Internet resources for history and historians of basic, clinical, and behavioral neuroscience. Links to existing sites are reviewed for salience and accuracy, organized by topic for convenient access, and regularly tested for availability. Comments, questions, and additional resource suggestions and submissions are welcomed. Major categories include: Calendar/Announcements, Professional societies and associations, Internet forums, Placement opportunities, Funding opportunities, Education opportunities, Repositories and collections, Catalogs and indexes, Texts on the Internet, Images on the Internet, Exhibits on the Internet, Periodicals, Commercial resources, Subject guides, Internet introductions, tutorials and tools, Questions-Comments-Suggestions-Submissions, Credits has parent organization: University of California at Los Angeles; California; USA THIS RESOURCE IS NO LONGER IN SERVICE nlx_38747 SCR_004371 SciCrunch Registry 2026-11-07 11:55:46 0
PhylomeDB
 
Resource Report
Resource Website
50+ mentions
PhylomeDB (RRID:SCR_007850) data or information resource, database Database for phylomes, that is, complete collections of phylogenetic trees for all proteins encoded in a given genome. It aims at providing a repository of high-quality phylogenies and alignments for proteins encoded in model species. To derive a phylome, each protein encoded in a given genome is used as a seed to retrieve its homologs in other complete genomes. These sequences are aligned and processed to derive reliable phylogenies using several phylogenetic methods. Besides providing the evolutionary history of the gene families, phylomeDB includes phylogeny based predictions of orthology and paralogy relationships., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. Genome-wide collections, gene phylogenies, phylogenetic trees collection, proteins encoded, genome, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
PMID:17962297
PMID:21075798
PMID:24275491
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-03281, biotools:PhylomeDb https://bio.tools/PhylomeDB SCR_007850 SciCrunch Registry PhylomeDB 2026-11-07 12:02:57 52
NCBI BioProject
 
Resource Report
Resource Website
10000+ mentions
NCBI BioProject (RRID:SCR_004801) data or information resource, database Database of biological data related to a single initiative, originating from a single organization or from a consortium. A BioProject record provides users a single place to find links to the diverse data types generated for that project. It is a searchable collection of complete and incomplete (in-progress) large-scale sequencing, assembly, annotation, and mapping projects for cellular organisms. Submissions are supported by a web-based Submission Portal. The database facilitates organization and classification of project data submitted to NCBI, EBI and DDBJ databases that captures descriptive information about research projects that result in high volume submissions to archival databases, ties together related data across multiple archives and serves as a central portal by which to inform users of data availability. BioProject records link to corresponding data stored in archival repositories. The BioProject resource is a redesigned, expanded, replacement of the NCBI Genome Project resource. The redesign adds tracking of several data elements including more precise information about a project''''s scope, material, and objectives. Genome Project identifiers are retained in the BioProject as the ID value for a record, and an Accession number has been added. Database content is exchanged with other members of the International Nucleotide Sequence Database Collaboration (INSDC). BioProject is accessible via FTP. genome sequencing, sequencing, genotype, phenotype, sequence variant, epigenetic, data set, genome, assembly, annotation, mapping, cellular organism, gene mapping, gene expression, biological tag, gene rearrangement, genetic algorithm, genetic code, genetic genealogy, gold standard, bio.tools is listed by: 3DVC
is listed by: re3data.org
is listed by: Debian
is listed by: bio.tools
is related to: INSDC
has parent organization: NCBI
NLM PMID:22139929 Free, Freely available r3d100013330, nlx_143909, biotools:bioproject http://www.ncbi.nlm.nih.gov/genomeprj, https://bio.tools/bioproject, https://doi.org/10.17616/R31NJMS2 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=search&DB=genomeprj SCR_004801 SciCrunch Registry NCBI BioProject Database, BioProject 2026-11-07 12:02:05 14025
ButterflyBase
 
Resource Report
Resource Website
1+ mentions
ButterflyBase (RRID:SCR_000727) data or information resource, database An open-access Genomic Database for Lepidoptera. It includes all the Lepidoptera cDNA sequences available in NCBI's dbEST. Support for genomic-DNA sequences such as BACs and the Bombyx mori genome is being generated. Tools available on this website include BLAST search, Annotation search, Primer design, and Microsatellite repeat finders. Users can also download all data and sequences. Within the site, the Expressed Sequence Tag sequences are made with Trace2dbest from raw sequence data if available or downloaded from NCBI. We cluster them using PartiGene into gene-objects to reduce redundancy. Subsequently, we perform hierarchical BLAST searches to provide accurate similarity annotation and a robust protein translation protocol using prot4EST. Putative proteins objects have been further annotated with the Gene Ontology biological vocabulary (GO terms) and InterPro (EBI) domains to facilitate gene-hunters. The repository is open for all Lepidopteran researchers. bombyx mori, butterfly, moth, lepidoptera, lepidoptera cdna, lepidoptera genome is listed by: 3DVC
has parent organization: University of Cambridge; Cambridge; United Kingdom
PMID:17933781 Please cite: Papanicolaou A, Gebauer-Jung S, Blaxter ML, Owen McMillan W, Jiggins CD. ButterflyBase: a platform for lepidopteran genomics. Nucleic Acids Res. 2008 Jan;36(Database issue):D582-7. Epub 2007 Oct 12. nif-0000-02627 SCR_000727 SciCrunch Registry ButterflyBase 2026-11-07 12:01:55 3
BioGrid Australia
 
Resource Report
Resource Website
100+ mentions
BioGrid Australia (RRID:SCR_006334) BioGrid Australia analysis service resource, data analysis service, data or information resource, database, production service resource, service resource A federated data sharing platform and infrastructure that provides access to real-time clinical, imaging and biospecimen data across jurisdictions, institutions and diseases. The web-based platform provides a secure infrastructure that advances health research by linking privacy-protected and ethically approved data among a wide network of health collaborators. Access to de-identified health records data is granted to authorized researchers after an application process so patient privacy and intellectual property are protected. BioGrid Australia''s approved researchers are provided access to multiple institutional databases, via the BioGrid interface, preventing gaps in patient records and research analysis. This legal and ethical arrangement with participating collaborators allows BioGrid to connect data through a common platform where data governance and access is managed by a highly skilled team. Data governance, security and ethics are at the core of BioGrid''s federated data sharing platform that securely links patient level clinical, biospecimen, genetic and imaging data sets across multiple sites and diseases for the purpose of medical research. BioGrid''s infrastructure and data management strategies address the increasing need by authorized researchers to dynamically extract and analyze data from multiple sources whilst protecting patient privacy. BioGrid has the capability to link data with other datasets, produce tailored reports for auditing and reporting and provide statistical analysis tools to conduct more advanced research analysis. In the health sector, BioGrid is a trusted independent virtual real-time data repository. Government investment in BioGrid has facilitated a combination of technology, collaboration and ethics approval processes for data sharing that exist nowhere else in the world. endocrinology, neuroscience, imaging, medicine, oncology, population, cancer, cystic fibrosis, diabetes, pet, mri, clinical, respiratory, health, epilepsy, neuropsychiatry, data sharing, FASEB list Cancer, Diabetes, Epilepsy, Cystic fibrosis, Respiratory disease, Multiple Sclerosis, Stroke, Bone density Closed; Authorized researchers only. nlx_152036, r3d100012476 https://doi.org/10.17616/R3921N http://www.biogrid.org.au/wps/portal SCR_006334 SciCrunch Registry BioGrid Australia Limited 2026-11-07 11:55:52 297

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