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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | ||||||||||||||
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SMD Resource Report Resource Website 10+ mentions |
SMD (RRID:SCR_004987) | SMD | analysis service resource, data analysis service, data or information resource, data repository, database, production service resource, service resource, storage service resource | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on December 17, 2021. Database to store, annotate, view, analyze and share microarray data. It provides registered users access to their own data, provides users access to public data, and tools with which to analyze those data, to any public user anywhere in the world. The GenePattern software package has been incorporated directly into SMD, providing access to many new analysis tools, as well as a plug-in architecture that allows users to directly integrate and share additional tools through SMD. This extension is available with the SMD source code that is fully and freely available to others under an Open Source license, enabling other groups to create a local installation of SMD with an enriched data analysis capability. SMD search options allow the user to Search By Experiments, Search By Datasets, or Search By Gene Names. Web services are provided using common standards, such as Simple Object Access Protocol (SOAP). This enables both local and remote researchers to connect to an installation of the database and retrieve data using pre-defined methods, without needing to resort to use of a web browser. | data set, microarray, gene, image, gene expression, adenovirus disease, apoptosis, leukemia, source code, web service |
is listed by: 3DVC is listed by: re3data.org is listed by: OMICtools is related to: Longhorn Array Database is related to: Tuberculosis Database has parent organization: Princeton University; New Jersey; USA is parent organization of: SOURCE |
NCI ; Howard Hughes Medical Institute ; Stanford University School of Medicine; California; USA ; NHGRI R01 HG003469 |
PMID:18953035 PMID:17182626 PMID:15608265 PMID:12519956 PMID:11125075 |
Public, Open-source license, The community can contribute to this resource, Acknowledgement requested, THIS RESOURCE IS NO LONGER IN SERVICE | nlx_94141, OMICS_00870, r3d100010555 | https://doi.org/10.17616/R3DW40 | http://genome-www.stanford.edu/microarray/, http://smd.stanford.edu/ | SCR_004987 | SciCrunch Registry | Stanford Microarray Database | 2026-11-07 11:55:42 | 12 | |||
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OpenTopography Resource Report Resource Website 10+ mentions |
OpenTopography (RRID:SCR_002204) | OpenTopo | data or information resource, data repository, service resource, storage service resource | Accepts and provides access to high-resolution (meter to sub-meter scale) Earth science-oriented topography data (e.g. LiDAR) and bathymetric data, and related tools and resources. The OpenTopography Tool Registry provides a community populated clearinghouse of software, utilities, and tools oriented towards high-resolution topography data (e.g. collected with LiDAR technology) handling, processing, and analysis. Tools registered range from source code to full-featured software applications. Contributions to the registry via the Contribute a Tool page are welcome. OpenTopography also hosts a dataset catalog to which users can register datasets hosted elsewhere; these entries are discoverable by users alongside OpenTopography hosted datasets. Lidar point cloud data are available in LAS, LAZ and ASCII formats. Raster datasets and derived products can be downloaded in Arc ASCII, IMG, and GeoTIFF formats. Derived products and visualizations are available in Google Earth KML format. The OpenTopography user community and advisory committee provides feedback to define the scope of collaborations on data hosting and cyberinfrastructure development | topography, topographical surveying, cloud, earth sciences, aerial photography, topographic map, geography, bathymetric map, geological mapping, geographic information system, bathymetry |
is listed by: CINERGI is listed by: re3data.org is listed by: DataCite has parent organization: San Diego Supercomputer Center has parent organization: University of California; California; USA |
NSF 1948857; NSF 1948994; NSF 1948997 |
Free, Available for download, Freely available | nlx_154717, r3d100010655 | https://api.datacite.org/dois?prefix=10.5069, https://doi.org/10.17616/R3J616 | SCR_002204 | SciCrunch Registry | , OpenTopography Facility, Open Topography, NSF OpenTopography Facility | 2026-11-07 11:54:34 | 22 | |||||
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DOQCS - Database of Quantitative Cellular Signaling Resource Report Resource Website 10+ mentions |
DOQCS - Database of Quantitative Cellular Signaling (RRID:SCR_007284) | DOQCS | data or information resource, database | A repository of models of signaling pathways that includes reaction schemes, concentrations, rate constants, as well as annotations on the models. The database provides a range of search, navigation, and comparison functions. | cellular, molecular, model, simulation, cell signaling, signaling pathway | has parent organization: Tata Institute of Fundamental Research; Mumbai; India | nif-0000-00047 | SCR_007284 | SciCrunch Registry | 2026-11-07 12:02:49 | 10 | |||||||||
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PharmGKB Resource Report Resource Website 1000+ mentions |
PharmGKB (RRID:SCR_002689) | PharmGKB | data access protocol, data or information resource, data repository, data set, database, service resource, software resource, storage service resource, web service | Database and central repository for genetic, genomic, molecular and cellular phenotype data and clinical information about people who have participated in pharmacogenomics research studies. The data includes, but is not limited to, clinical and basic pharmacokinetic and pharmacogenomic research in the cardiovascular, pulmonary, cancer, pathways, metabolic and transporter domains. PharmGKB welcomes submissions of primary data from all research into genes and genetic variation and their effects on drug and disease phenotypes. PharmGKB collects, encodes, and disseminates knowledge about the impact of human genetic variations on drug response. They curate primary genotype and phenotype data, annotate gene variants and gene-drug-disease relationships via literature review, and summarize important PGx genes and drug pathways. PharmGKB is part of the NIH Pharmacogenomics Research Network (PGRN), a nationwide collaborative research consortium. Its aim is to aid researchers in understanding how genetic variation among individuals contributes to differences in reactions to drugs. A selected subset of data from PharmGKB is accessible via a SOAP interface. Downloaded data is available for individual research purposes only. Drugs with pharmacogenomic information in the context of FDA-approved drug labels are cataloged and drugs with mounting pharmacogenomic evidence are listed. | pharmacogenomics, microarray, pathway, phenotype, snp array, genotype, clinical, genetic variation, drug, gene, genetic variation, disease, cardiovascular, pulmonary, cancer, metabolic, transporter, drug response, small molecule, research, drug response, FASEB list |
is used by: NIF Data Federation is listed by: OMICtools is related to: WikiPathways is related to: ConsensusPathDB is related to: Integrated Molecular Interaction Database is related to: MalaCards is related to: phenomeNET has parent organization: Stanford University; Stanford; California is parent organization of: PharmGKB Ontology |
NIGMS R24 GM61374 | PMID:11908751 | Free, Freely available | nif-0000-00414, OMICS_01586, r3d100012325 | https://doi.org/10.17616/R31H1N | SCR_002689 | SciCrunch Registry | Pharmacogenomics Knowledge Base | 2026-11-07 11:54:44 | 1276 | ||||
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Database of Genomic Variants Archive (DGVa) Resource Report Resource Website 100+ mentions |
Database of Genomic Variants Archive (DGVa) (RRID:SCR_004896) | DGVa | data or information resource, data repository, database, service resource, storage service resource | Public repository that accepts direct submissions and provides archiving, accessioning and distribution of publicly available genomic structural variants, in all species. Variants are accessioned at the study and sample level, granting stable identifiers that can be used in publications. DGVa data is integrated with other EBI resources, including comprehensive EBI search and Ensembl genome browser. Exchanges data with companion database, dbVar, at National Center for Biotechnology Information.NOTE: since 2019 DGVa doesn't accept submissions. Please send the data for submission to European Variation Archive (EVA). | genome, dna, gene, expression, genetics, mapping, structural, variant, gold standard |
is recommended by: NIDDK Information Network (dkNET) is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases is listed by: re3data.org is related to: dbVar is related to: ISCA Consortium is related to: Database of Genomic Variants is related to: Ensembl Variation has parent organization: European Bioinformatics Institute |
PMID:23193291 PMID:24174537 |
Free, Freely available | nlx_86626, r3d100010814 | https://doi.org/10.17616/R3HK7Z | http://www.ebi.ac.uk/dgva/page.php, http://www.ebi.ac.uk/dgva/ | SCR_004896 | SciCrunch Registry | , DGVarchive, DGVa, Database of Genomic Variants Archive | 2026-11-07 11:55:40 | 211 | ||||
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Thieme Chemistry Resource Report Resource Website |
Thieme Chemistry (RRID:SCR_014699) | bibliography, data or information resource, journal article resource | Publishing company which provides access to its four journals SYNTHESIS, SYNLETT, SynOpen, and SYNFACTS; their reference works Science of Synthesis and Pharmaceutical Substances; and the paired encyclopedia ROEMPP. | publish, publishing company, article repository, journal article resource, chemistry, synthetic organic chemistry | Available in an electronic format | SCR_014699 | SciCrunch Registry | 2026-11-07 12:00:38 | 0 | |||||||||||
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Federation of International Mouse Resources Resource Report Resource Website 1+ mentions |
Federation of International Mouse Resources (RRID:SCR_006137) | FIMRe | community building portal, data or information resource, portal, topical portal | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 7, 2022. Federation of International Mouse Resources (FIMRe) is a collaborating group of Mouse Repository and Resource Centers worldwide whose collective goal is to archive and provide strains of mice as cryopreserved embryos and gametes, ES cell lines, and live breeding stock to the research community. Goals of the Federation of International Mouse Resources: * Coordinate repositories and resource centers to: ** archive valuable genetically defined mice and ES cell lines being created worldwide ** meet research demand for these genetically defined mice and ES cell lines * Establish consistent, highest quality animal health standards in all resource centers * Provide genetic verification and quality control for genetic background and mutations * Provide resource training to enhance user ability to utilize cryopreserved resources | embryo, gamete, embryonic stem cell, embryonic stem cell line, live breeding stock, live mouse, resource center, international network, mouse model, human disease, gene, genome, biomaterial supply resource, cell repository, organism supplier, biospecimen repository, mutation, cryopreserved |
is related to: Jackson Laboratory is related to: Mutant Mouse Resource and Research Center is related to: European Mouse Mutant Archive is related to: RIKEN BioResource Center has parent organization: Mouse Genome Informatics (MGI) |
PMID:16688526 | THIS RESOURCE IS NO LONGER IN SERVICE. | nlx_151627 | SCR_006137 | SciCrunch Registry | Federation of International Mouse Resources (FIMRe) | 2026-11-07 11:55:49 | 4 | ||||||
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dbMHC Resource Report Resource Website 10+ mentions |
dbMHC (RRID:SCR_002302) | dbMHC | data or information resource, data repository, database, service resource, storage service resource | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 23, 2019 Database was open, publicly accessible platform for DNA and clinical data related to human Major Histocompatibility Complex (MHC). Data from IHWG workshops were provided as well., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | human leukocyte antigen, microsatellite, dna, clinical, major histocompatibility complex, primer, probe, sequence, allele, haplotype, sequence, histocompatibility, leucocyte, alignment |
is listed by: re3data.org is related to: NIDDK Information Network (dkNET) is related to: IMGT/HLA has parent organization: NCBI |
PMID:14705985 | Free, Available for download, Freely available | nif-0000-02729, r3d100010881 | https://doi.org/10.17616/R37W4F | http://www.ncbi.nlm.nih.gov/gv/mhc/main.cgi?cmd=init | SCR_002302 | SciCrunch Registry | Major Histocompatibility Complex Database | 2026-11-07 11:54:39 | 22 | ||||
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Natural Products Magnetic Resonance Database Resource Report Resource Website 10+ mentions |
Natural Products Magnetic Resonance Database (RRID:SCR_026534) | NP-MRD | data or information resource, data repository, database, service resource, storage service resource | Database and respository for NMR data associated with natural products and specialized metabolites. | Free, Freely available | SCR_026534 | SciCrunch Registry | 2026-11-07 12:06:32 | 18 | |||||||||||
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GeneTalk Resource Report Resource Website 10+ mentions |
GeneTalk (RRID:SCR_005231) | GeneTalk | blog, community building portal, data or information resource, data repository, database, narrative resource, portal, service resource, storage service resource | A web-based tool, knowledgebase and community for analysis and interpretation of human variant files. VCFs (Variant Call Formats) are preprocessed and annotated, you can filter them, access all databases and provide your expertise to the community by creating annotations. | sequence variant, annotation, exome sequencing, genetic variant, gene, data sharing, bio.tools |
is listed by: OMICtools is listed by: Debian is listed by: bio.tools |
PMID:22826540 | The community can contribute to this resource, Free, (during beta period) | OMICS_00270, biotools:genetalk | https://bio.tools/genetalk | SCR_005231 | SciCrunch Registry | GeneTalk - The Professional Network and Online Tool for Geneticists | 2026-11-07 12:00:46 | 31 | |||||
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Brain Score Resource Report Resource Website 1+ mentions |
Brain Score (RRID:SCR_027769) | data or information resource, data repository, service resource, storage service resource | Platform provides accurate, machine-executable computational models of how the brain gives rise to the mind. Enables researchers to quickly get a sense of the alignment of their model(s) to neural and behavioral measurements, and provides these models to experimentalists to prototype new experiments and make sense of biological data. All code is open-source and community members may choose to make their data or model weights fully public. | Benchmark, benchmarking, modeling, experimental data, computational models, neural and behavioral measurements, | Free, Freely available | https://github.com/brain-score | SCR_027769 | SciCrunch Registry | 2026-11-07 12:07:44 | 4 | ||||||||||
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T1DBase Resource Report Resource Website 100+ mentions |
T1DBase (RRID:SCR_007959) | data or information resource, data repository, database, resource, service resource, storage service resource | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 26,2019. In October 2016, T1DBase has merged with its sister site ImmunoBase (https://immunobase.org). Documented on March 2020, ImmunoBase ownership has been transferred to Open Targets (https://www.opentargets.org). Results for all studies can be explored using Open Targets Genetics (https://genetics.opentargets.org). Database focused on genetics and genomics of type 1 diabetes susceptibility providing a curated and integrated set of datasets and tools, across multiple species, to support and promote research in this area. The current data scope includes annotated genomic sequences for suspected T1D susceptibility regions; genetic data; microarray data; and global datasets, generally from the literature, that are useful for genetics and systems biology studies. The site also includes software tools for analyzing the data. | genetics, beta cell, gene, variant, region, genomics, gene expression, genome-wide association study, data analysis service, bio.tools |
is used by: NIF Data Federation is used by: NIDDK Information Network (dkNET) is listed by: NIDDK Information Network (dkNET) is listed by: Debian is listed by: bio.tools is related to: dkCOIN has parent organization: University of Cambridge; Cambridge; United Kingdom |
Type 1 diabetes. Diabetes | Wellcome Trust ; NIDDK ; Juvenile Diabetes Research Foundation |
PMID:20937630 | THIS RESOURCE IS NO LONGER IN SERVICE. | nif-0000-03531, biotools:t1dbase | https://bio.tools/t1dbase | SCR_007959 | SciCrunch Registry | T1DBase - Type 1 Diabetes Database | 2026-11-07 11:56:27 | 147 | ||||
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Allelic Variations of The XP Genes Resource Report Resource Website 1+ mentions |
Allelic Variations of The XP Genes (RRID:SCR_003376) | Allelic Variations of the XP Genes | data or information resource, data repository, database, service resource, storage service resource | Interactive repository of mutations and other allelic variations of the genes involved in the DNA repair disorders, Xeroderma Pigmentosum (XP), Cockayne Syndrome (CS), Trichothiodystrophy (TTD), and other UV-sensitivity disorders. Any omitted data or new data may be submitted by using the on-line data submission form. There is a message board system to support discussions amongst those interested in XP and DNA Repair. RESOURCES * Educational module of the molecular biology of Nucleotide Excision Repair * Introduction to the DNA Repair disorders (XP, CS, TTD, UVs) * Background on each of the XP genes * A searchable database of mutations and sequence variations for the XP genes * Contact point for the submission of new mutation data * Discussion Forums and a Guest Book * Web Links to Additional Resources | nucleotide excision repair, dna, excision, function, gene, allele, cell, sensitivity, trichothiodystrophy, ultra violet, variation, xeroderma pigmentosum, pigment, mutation, allelic variation, dna repair | has parent organization: University of California at San Francisco; California; USA | DNA repair disorder, Xeroderma Pigmentosum, Cockayne Syndrome, Trichothiodystrophy, UV-sensitivity disorder | Xeroderma Pigmentosum Society | PMID:10447254 | Free, Freely available | nif-0000-32042 | SCR_003376 | SciCrunch Registry | xpmutations.org | 2026-11-07 11:55:02 | 2 | ||||
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Protein-RNA Interaction Database Resource Report Resource Website 1+ mentions |
Protein-RNA Interaction Database (RRID:SCR_000398) | PRID | data or information resource, database | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 2,2022. It is a repository of interactions found by Entangle and compiled into various tables for use by the RNA community. This data does not have a user interface, but data can be accessed in tables. It contains raw Excel/Access Databases and data processed into useful Figures for people who don't want to wade through the primary data. At present it contains informations from 42 PDBs. | protein-protein interaction, rna | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-20906 | SCR_000398 | SciCrunch Registry | Protein-RNA Interaction Database | 2026-11-07 12:01:53 | 2 | ||||||||
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SCAR Antarctic Biodiversity Portal Resource Report Resource Website 1+ mentions |
SCAR Antarctic Biodiversity Portal (RRID:SCR_023136) | data repository, service resource, storage service resource | International effort that seeks to increase our knowledge and understanding of Antarctic and Southern Ocean biodiversity.It is a community of researchers, data custodians and developers from around the world that supports the mobilisation publication, retrieval and analysis of Antarctic and Southern Ocean biodiversity data in a free and open manner in line with the Antarctic treaty and the FAIR data Principles (Finable, Accessible, Interoperable, Reusable). The SCAR Antarctic biodiversity Portal has a number of portals dedicated to specific types of data and information on Antarctic and Southern Ocean Biodiversity.We aim to create an information ecosystem of various data bases, data systems, web services tools etc that can be used by anyone with an interest in Antarctic and Southern Ocean biodiversity.Biodiversity.aq is an international initiative of the Scientific Committee on Antarctic Research (SCAR). It finds it roots in the Census of Antarctic Marine Life and started in 2005. The central facilities are hosted by the Royal Belgian Institute for Natural sciences (RBINS, www.naturalsciences.be) and the Belgian Biodiversity Platform (BBPf, www.biodiversity.be).The SCAR Antarctic Biodiversity Portal is the regional thematic node of the Ocean Biodiversity Information System (OBIS, www.obis.org), the Global Biodiversity Information Facility (GBIF, www.gbif.org) and works closely together with the Southern Ocean Observation System (SOOS, www.soos.aq). | is listed by: DataCite | Free, Freely available | DOI:10.48361 | https://doi.org/10.48361, https://dx.doi.org/10.48361 | SCR_023136 | SciCrunch Registry | SCAR Antarctic Biodiversity Portal | 2026-11-07 12:01:03 | 9 | ||||||||
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Parkinsons Disease Map Resource Report Resource Website 1+ mentions |
Parkinsons Disease Map (RRID:SCR_016156) | data or information resource, database, disease-related portal, portal, topical portal | Knowledge repository established to describe molecular mechanisms of Parkinson's Disease. It compiles literature-based information on PD into an easy to explore and freely accessible molecular interaction map and offers research-facilitating functionalities such as the overlay of experimental data and the identification of drug targets on the map | parkinson, disease, pd, molecular biology, interaction, drug, target | Parkinsons disease | Publicly available | SCR_016156 | SciCrunch Registry | Parkinsons Map Viewer, Parkinsons Map | 2026-11-07 11:58:12 | 1 | |||||||||
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Benchmarking Graph Pipelines Resource Report Resource Website 1+ mentions |
Benchmarking Graph Pipelines (RRID:SCR_026567) | software resource, software toolkit, source code | Software pipelines for benchmarking workflow for evaluating graph-based pangenome construction tools. The repository contains scripts to compare the performance of Minigraph-Cactus, PGGB, Minigraph pipelines using both simulated and real-world datasets. It includes data processing steps, evaluation metrics, and reproducible scripts for analyzing structural variants in pangenomes. | benchmarking workflow, evaluating graph-based pangenome construction tools, | Free, Available for download, Freely available | SCR_026567 | SciCrunch Registry | , Benchmarking Pangenome Graph Pipelines, Benchmarking Pangenome Graph pipelines | 2026-11-07 12:07:00 | 1 | ||||||||||
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ORModelDB Resource Report Resource Website |
ORModelDB (RRID:SCR_014578) | data or information resource, database | A repository of the results of the efforts of the scientific community in computationally elucidating the structure of the olfactory receptor with a view to establishing a mechanistic basis for OR-odorant binding. | database, olfactory, model, olfactory receptor, computational methodology | works with: Odor Molecules DataBase | Public | SCR_014578 | SciCrunch Registry | Olfactory Receptors Model Database | 2026-11-07 12:03:18 | 0 | |||||||||
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da Vinci European Biobank Resource Report Resource Website |
da Vinci European Biobank (RRID:SCR_004908) | daVEB | biomaterial supply resource, material resource | BioBank that collects, stores, processes and distributes biospecimens and the associated data. The biospecimens are human and non-human genetic materials, proteins, cells, tissues and biofluids. The data are the biological information associated to the samples and, in the case of human samples, the clinical information pertaining to the donor. The da Vinci European BioBank (daVEB) is a multicenter biobank with a centralized IT infrastructure and a main repository located at the Polo Scientifico (Scientific Campus of the University of Florence) in Sesto Fiorentino (Florence, Italy). Hosted by the Magnetic Resonance Center (CERM), an expert center on protein structure and metabolomics, daVEB's aim is to host as rich as possible biological human sample collections, stored accordingly to EU guidelines, in order to offer a powerful tool in the study of complex diseases. At the end of July 2011, the da Vinci European BioBank of the Pharmacogenomics FiorGen Onlus Foundation has been audited and got the quality certification according to UNI EN ISO 9001:2008 for Collection, storage and distribution of biological samples and the associated data for scientific research. Besides the samples stored at da Vinci European BioBank in Sesto Fiorentino (Florence), the daVEB is also the administrative biobank for research sample collections that are stored in the delocalized repositories. All the sample collections must be registered in the biobank: * sample collections taken within the regular health care * samples taken from healthy individuals or other persons out of the regular health care * samples that have been taken in hospitals within research protocols on specific pathologies all transferred to daVEB endowed with a transfer agreement signed by the donor. The Research Units actually afferent to daVEB are delocalized in the Florence, Prato, Pisa and Siena provinces. Delocalized repositories are under construction in Tuscany. | clinical data, metabolomics via 1h-nmr, complex disease |
is listed by: One Mind Biospecimen Bank Listing has parent organization: University of Florence; Florence; Italy |
Normal, Disease, Healthy | nlx_87590 | SCR_004908 | SciCrunch Registry | 2026-11-07 12:03:11 | 0 | ||||||||
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CBFBIRN Resource Report Resource Website 1+ mentions |
CBFBIRN (RRID:SCR_009543) | CBFBIRN | data or information resource, data repository, data set, service resource, storage service resource |
THIS RESOURCE IS NO LONGER IN SERVICE. Documented August 23, 2017. A web based central repository for individual and group analysis of Arterial Spin Labeling (ASL) data sets and ASL pulse sequences developed at CMFRI UCSD for MRI researchers. This resource currently hosts more 1300 ASL data sets from 22 projects and consists of mainly two main tools 1) The Cerebral Blood Flow Database and Analysis Pipeline (CBFDAP) is a web enabled data and workflow management system extended from the HID codebase on NITRC specialized for Arterial Spin Labeling data management and analysis (including group analysis) in a centralized manner. 2) Pulse Sequence Distribution System (PSDS) for managing dissamination of ASL pulse sequences developed at the UCSD CFMRI. This resource also includes web and video tutorials for end users. |
java, javascript, matlab, magnetic resonance, os independent, web environment, arterial spin labeling, mri |
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC) is related to: Cerebral Blood Flow Database and Analysis Pipeline has parent organization: University of California at San Diego; California; USA |
NIH | PMID:24151465 | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_155722 | http://www.nitrc.org/projects/cbfbirn | SCR_009543 | SciCrunch Registry | Cerebral Blood Flow Biomedical Informatics Research Network | 2026-11-07 11:56:52 | 3 |
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