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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.

(last updated: Oct 12, 2019)

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Resource NameResource TypeDescriptionKeywordsResource IDProper CitationParent OrganizationRelated ConditionFunding AgencyRelationReferenceWebsite StatusAlternate IDsAlternate URLsOld URLs
RettBASE: IRSF MECP2 Variation DatabaseResource, data or information resource, databaseDatabase constructed by merging mutation and polymorphism data from the published literature pertaining to Rett syndrome and related clinical disorders, and by incorporating unpublished mutation and polymorphism data that have been submitted directly. RettBase is updated on a very frequent basis manually by curators to ensure the validity of the data submitted.genetics; metadata, polymorphismSCR_001066(RettBASE: IRSF MECP2 Variation Database, RRID:SCR_001066)Rett Syndromelisted by: 3DVCLast checked upnif-0000-00156
EyeBrowseResource, data set, data or information resourceEyeBrowse displays expressed sequence tag (EST) cDNA clones from eye tissues (derived from NEIBank and other sources) aligned with current versions of the human, rhesus, mouse, rat, dog, cow, chicken, or zebrafish genomes, including reference sequences for known genes. This gives a simplified view of gene expression activity from different parts of the eye across the genome. The data can be interrogated in several ways. Specific gene names can be entered into the search window. Alternatively, regions of the genome can be displayed. For example, entering two STS markers separated by a semicolon (e.g. RH18061;RH80175) allows the display of the entire chromosomal region associated with the mapping of a specific disease locus. ESTs for each tissue can then be displayed to help in the selection of candidate genes. In addition, sequences can be entered into a BLAT search and rapidly aligned on the genome, again showing eye derived ESTs for the same region. EyeBrowse includes a custom track display SAGE data for human eye tissues derived from the EyeSAGE project. The track shows the normalized sum of SAGE tag counts from all published eye-related SAGE datasets centered on the position of each identifiable Unigene cluster. This indicates relative activity of each gene locus in eye. Clicking on the vertical count bar for a particular location will bring up a display listing gene details and linking to specific SAGE counts for each eye SAGE library and comparisons with normalized sums for neural and non-neural tissues. To view or alter settings for the EyeSAGE track on EyeBrowse, click on the vertical gray bar at the left of the display. Other custom tracks display known eye disease genes and mapped intervals for candidate loci for retinal disease, cataract, myopia and cornea disease. These link back to further information at NEIBank. For mouse, there is custom track data for ChIP-on-Chip of RNA-Polymerase-II during photoreceptor maturation.est, expressed sequence tag, eye, gene, genome, cataract, cdna, chicken, clone, cluster, cornea, cornea disease, cow, data, disease, dog, human, locus, maturation, mouse, myopia, photoreceptor, rat, retina, rhesus, rna polymerase-ii, tag, zebrafish, data analysis software, eye tracking deviceSCR_008000(EyeBrowse, RRID:SCR_008000)University of California at Santa Cruz; California; USA Retinal disease, Cataract, Myopia, Cornea diseaseNEIBanklisted by: 3DVCLast checked upnif-0000-07733
Albinism databaseResource, data set, service resource, data repository, storage service resource, data or information resourceDatabase of mutations associated with all major known forms of oculocutaneous and ocular albinism. The Albinism Database is part of the Locus Specific Mutation Databases of the Human Genome Variation Society and accepts the submission of new mutations. A link is provided for submission of new mutations. Columns in the database include: type of albinism, human locus, omim link, link to table of mutations and polymorphisms, and map of mutation locations.oculocutaneous albinism, deletion, mutation, polymorphism, pigment, data setSCR_000632(Albinism database, RRID:SCR_000632)HGVS Locus Specific Mutation Databases , University of Minnesota Twin Cities; Minnesota; USA Oculocutaneous albinism, Ocular albinism, Albinismlisted by: 3DVCLast checked upnif-0000-06691http://albinismdb.med.umn.edu/
CTDatabaseResource, data or information resource, databaseA database of information about each Cancer-Testis (CT) gene, its gene products and the immune response induced in cancer patients by these proteins. CT antigens are proteins normally expressed only in the human germ line but that are also present in a significant subset of malignant tumors. The practical importance of these proteins is that due to their restricted expression pattern they are frequently recognized by the immune system of cancer patients. Moreover, this antigenicity has raised the possibility of their being used as vaccines to actively stimulate immune responses in order to combat tumor growth. As a result worldwide research into many aspects of CT antigens is rapidly growing prompting the construction of this database as a resource for investigators involved in this area.data setSCR_007614(CTDatabase, RRID:SCR_007614)Cancerlisted by: 3DVCLast checked upnif-0000-02704
Interagency Modeling and Analysis GroupResource, groupThe purpose of IMAG is to bring together program officers who have a shared interest in applying modeling and analysis methods to biomedical systems. The meetings are formatted to facilitate an open discussion of what is currently being supported, and for planning future directions in these areas. At each meeting, time is allotted to hear focused presentations from one or two participants to discuss issues relating to modeling and analysis across the government agencies. Discussions also occur online, and participants are informed of talks, conferences and other activities of interest to the group. The NIH BISTIC, (Biomedical Information Science and Technology Consortium), is very supportive of IMAG and serves as the larger body at NIH for disseminating IMAG activities. Associated agencies: NIH: Center for Scientific Review, National Cancer Institute, National Center for Research Resources, National Heart, Lung and Blood Institute, National Human Genome Research Institute, National Institute on Aging, National Institute of Allergy and Infectious Diseases, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institute of Biomedical Imaging and Bioengineering, National Institute of Child Health and Human Development, National Institute on Deafness and Other Communication Disorders, National Institute on Drug Abuse, National Institute of Environmental Health Sciences, National Institute of General Medical Sciences, National Institute of Mental Health, National Institute of Neurological Disorders and Stroke, National Library of Medicine NSF (National Science Foundation): Directorate for Biological Sciences, Directorate for Computer and Information Science and Engineering, Directorate for Engineering, Directorate for Mathematical and Physical Sciences NASA (National Aeronautics and Space Administration): Human Research Program DOE (Department of Energy), Office of Advanced Scientific Computing Research, Office of Biological and Environmental Research DOD (Department of Defense): Air Force Office of Scientific Research (AFOSR), Army, Defense Advanced Research Projects Agency, Office of Naval Research, Telemedicine and Advanced Technology Research Center, USDA (United States Department of Agriculture), USDVA (Unites States Department of Veteran Affairs) Soliciting programs: Predictive Multiscale Models of the Physiome in Health and Disease (MSM Physiome) Initiative; and Multi-Scale Modeling (MSM) InitiativeKey words: MRI, Imaging, human.national institutes of health, modeling, fundingSCR_007432(Interagency Modeling and Analysis Group, RRID:SCR_007432)National Institute of Biomedical Imaging and Bioengineering Aginglisted by: 3DVCLast checked upnif-0000-00562
Olfactory Receptor DataBaseResource, data analysis service, production service resource, analysis service resource, database, service resource, storage service resource, data repository, data or information resourceDatabase of vertebrate olfactory receptors genes and proteins. It supports sequencing and analysis of these receptors by providing a comprehensive archive with search tools for this expanding family. The database also incorporates a broad range of chemosensory genes and proteins, including the taste papilla receptors (TPRs), vomeronasal organ receptors (VNRs), insect olfaction receptors (IORs), Caenorhabditis elegans chemosensory receptors (CeCRs), and fungal pheromone receptors (FPRs). ORDB currently houses chemosensory receptors for more than 50 organisms. ORDB contains public and private sections which provide tools for investigators to analyze the functions of these very large gene families of G protein-coupled receptors. It also provides links to a local cluster of databases of related information in SenseLab, and to other relevant databases worldwide. The database aims to house all of the known olfactory receptor and chemoreceptor sequences in both nucleotide and amino acid form and serves four main purposes: * It is a repository of olfactory receptor sequences. * It provides tools for sequence analysis. * It supports similarity searches (screens) which reduces duplicate work. * It provides links to other types of receptor information, e.g. 3D models. The database is accessible to two classes of users: * General public www users have full access to all the public sequences, models and resources in the database. * Source laboratories are the laboratories that clone olfactory receptors and submit sequences in the private or public database. They can search any sequence they deposited to the database against any private or public sequence in the database. This user level is suited for laboratories that are actively cloning olfactory receptors.fungal, pheromone receptor, gene, chemosensory, chemosensory receptor, g protein-coupled receptor, olfaction receptor, protein, receptor, taste papilla receptor, vomeronasal organ receptor, olfactory receptor, nucleotide, amino acid, chemoreceptor sequence, olfactory receptor sequence, chemoreceptor, sequenceSCR_007830(Olfactory Receptor DataBase, RRID:SCR_007830)Yale School of Medicine; Connecticut; USA AgingHuman Brain Project, Multidisciplinary University Research Initiative, National Aeronautics and Space Administration, NIA, NICD, NIDCD, NIMH, NINDS, NLMrelated to: Odor Molecules DataBase, Monarch Initiative, Integrated Manually Extracted Annotation, used by: NIF Data Federation, listed by: 3DVCReferences (3)Last checked upnif-0000-03213
BTKbaseResource, data or information resource, databaseA mutation registry for X-linked agammaglobulinemia (XLA). BTKbase lists mutation entries of 1,111 patients from 973 unrelated families showing 602 unique molecular events. Agammaglobulinemia is characterized by failure to produce mature B lymphocyte cells and is associated with a failure of Ig heavy chain rearrangement. Two thirds of cases are familial, and one third of cases are believed to arise from new mutations. Mutations of the BTK gene are found in approximately 80% of patients with agammaglobulinemia. The localization of the mutations on the gene and protein for BTK can be analyzed by clicking sequences on the web pages. It includes a mutation browser, which gives users access to mutations in Bruton tyrosine kinase (BTK) protein sequences, and XLA fact file, and forms for users to submit mutation to the dataset.bruton tyrosine kinase, xla, x-linked agammaglobulinemiaSCR_013101(BTKbase, RRID:SCR_013101)University of Tampere; Tampere; Finland Agammaglobulinemialisted by: 3DVCLast checked downnif-0000-02625
CellMLResource, narrative resource, interchange format, markup language, standard specification, data or information resourceThe CellML language is an open standard based on the XML markup language. The purpose of CellML is to store and exchange computer-based mathematical models. CellML allows scientists to share models even if they are using different model-building software. It also enables them to reuse components from one model in another, thus accelerating model building. Although CellML was originally intended for the description of biological models; CellML includes information about model structure (how the parts of a model are organizationally related to one another), mathematics (equations describing the underlying processes) and metadata (additional information about the model that allows scientists to search for specific models or model components in a database or other repository). The CellML team is committed to providing freely available tools for creating, editing, and using CellML models. We provide information regarding tools we are developing internally and links to external projects developing tools which utilize the CellML format. Please let us know if you have an open source CellML tool looking for a home on the internet, as we are able to offer limited hosting services on cellml.org.biological model, cell, mathematical model, mathematics, metadata, model structure, model, xml, annotation, mark up languageSCR_008061(CellML, RRID:SCR_008061)University of Auckland; Auckland; New Zealand aneurIST, Foundation for Research Science and Technology, International Union of Physiological Sciences: Physiome Project, Maurice Wilkins Centre for Molecular Biodiscovery, NZIMA, VPH NoE, Wellcome Trustrelated to: PathGuide: the pathway resource list, listed by: 3DVCReferences (7)Last checked upnif-0000-10448
ButterflyBaseResource, data or information resource, databaseAn 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 genomeSCR_000727(ButterflyBase, RRID:SCR_000727)University of Cambridge; Cambridge; United Kingdom listed by: 3DVCPMID:17933781Last checked downnif-0000-02627
GEN2PHEN Knowledge CentreResource, organization portal, data or information resource, portal, consortium, databasePortal that unifies human and model organism genetic variation databases towards increasingly holistic views into Genotype-To-Phenotype (G2P) data, and links this system into other biomedical knowledge sources via genome browser functionality. The project has the following specific objectives: *To analyze the G2P field and thus determine emerging needs and practices *To develop key standards for the G2P database field *To create generic database components, services and integration infrastructures for the G2P database domain *To create search modalities and data presentation solutions for G2P knowledge *To facilitate the process of populating G2P databases *To build a major G2P internet portal *To deploy GEN2PHEN solutions to the community *To address system durability and long-term financing *To undertake a whole-system utility and validation pilot study The GEN2PHEN Consortium members have been selected from a talented pool of European research groups and companies that are interested in the G2P database challenge. Additionally, a few non-EU participants have been included to bring extra capabilities to the initiative. The final constellation is characterized by broad and proven competence, a network of established working relationships, and high-level roles/connections within other significant projects in this domain. There is a listing of Locus-specific databases (LSDBs) where you may search by gene symbol or database name. The wiki contains documents and discussions about Gen2Phen's efforts to produce exchange formats and consistent interfaces for LSDBs. Standardizing access to LSDB data is one of the core aims of Gen2Phen. Improved abilities to query, visualize and federate data can be achieved by having well-defined interfaces and consistent exchange formats. See the Use Cases wiki page for our consideration of what makes these issues important.genotype-phenotype, data federationSCR_000790(GEN2PHEN Knowledge Centre, RRID:SCR_000790)Seventh Framework Programmerelated to: BioResource Impact Factor, listed by: 3DVCLast checked downnif-0000-30605
Bio-Job.orgResource, job resourceBio-Job.org is a sister site to PROTOCOL-ONLINE.ORG and offers free job posting to not-for-profit employers such as universities, governments, research institutions/organizations. Currently industrial job listing is also free. * Employer's Services: Post a Job, Manage Jobs Posts, View Resumes * Jobseeker: Announce your availability and submit your resume to hundreds of Employers that visit this site. Employers can contact you directly as soon as a suitable position becomes available. Why is this site created: It's never been an easy job to recruit qualified people for employer or PI who runs a lab--Not only have you to pay a fee for job listing that could be as high as hundreds of dollars, you have to go through all the hassle of setting up an account, dealing with your account manager and making the payment. In an era when science is free, genome data is free, publications are free, and why is job posting not free? With this belief in mind, we created this site to allow free job posting for academia. What types of jobs can be posted here: Jobs in any scientific discipline and biotech jobs can be posted.data setSCR_000933(Bio-Job.org, RRID:SCR_000933)listed by: 3DVCLast checked upnlx_81563
Resource for Biocomputing Visualization and InformaticsResource, biomedical technology resource center, training resourceBiomedical technology resource center that develops software and web-based resources for the visualization and analysis of molecular structure, and related data, at scales ranging from the atomic to the supramolecular. They create tools for handling and integrating diverse types of biomolecular data, including atomic-resolution coordinates, density maps, sequences, annotations, and networks. Their primary efforts are in the visualization and analysis of structures of molecules and molecular assemblies, enzyme sequence-structure-function relationships, and network representations of protein similarity, binding interactions, and biological pathways. They provide technologies to enable identifying the molecular bases of disease and phenotypic variation, annotating proteins of unknown function, identifying targets for drug development, designing drugs, and engineering proteins with new functions. RBVI distributes software tools, including the popular UCSF Chimera visualization and analysis package, develops and hosts the Structure-Function Linkage Database, and provides access to state-of-the-art computational resources in support of research projects in these areas.training resource, molecular modeling, software, molecular graphics, visualization, modeling, molecular structure, analysis, computation, computing and informatics technology centerSCR_001374(Resource for Biocomputing Visualization and Informatics, RRID:SCR_001374)University of California at San Francisco; California; USA NIGMSlisted by: 3DVCLast checked upnlx_152531
National Center for Integrative Biomedical InformaticsResource, narrative resource, software resource, data or information resource, training material, databaseThe Center develops conceptual models, computational infrastructure, an integrated knowledge repository, and query and analysis tools that enable scientists to effectively access and integrate the wealth of biological data. The National Center for Integrative Biomedical Informatics (NCIBI) was founded in October 2005 and is one of seven National Centers for Biomedical Computing (NCBC) in the NIH Roadmap. NCIBI is based at the University of Michigan as a part of the Center for Computational Medicine and Biology (CCMB). NCIBI is composed of biomedical researchers, computational biologists, computer scientists, developers and human-computer interaction specialists organized into seven major core functions. They work in interdisciplinary teams to collectively develop tools that are not only computationally powerful but also biologically relevant and meaningful. The four initial Driving Biological Projects (prostate cancer progression, Type 1 and type 2 diabetes and bipolar disorder) provide the nucleation point from which tool development is informed, launched, and tested. In addition to testing tools for function, a separate team is dedicated to testing usability and user interaction that is a unique feature of this Center. Once tools are developed and validated the goal of the Center is to share and disseminate data and software throughout the research community both internally and externally. This is achieved through various mechanisms such as training videos, tutorials, and demonstrations and presentations at national and international scientific conferences. NCIBI is supported by NIH Grant # U54-DA021519.analysis tools, bipolar disorder, code, computational infrastructure, conceptual models, data, diabetes, knowledge repository, presentations, prostate cancer, query tools, seminar material, tool development, tutorials, videos, modelSCR_001538(National Center for Integrative Biomedical Informatics, RRID:SCR_001538)University of Michigan; Michigan; USA related to: Biological Concept Diagram Editor, Gene Interaction Extraction from the Literature, National Centers for Biomedical Computing, listed by: 3DVCLast checked upnif-0000-09660
Genome Network PlatformResource, data or information resource, databaseIntegrated database of experiment data generated by participating research institutes and public databases relating to: 1) transcription starting position of human genes in the human genome, 2) conjunction to control region on transcriptional factors and the human genome 3) protein-protein interaction with a central focus on transcription factors organized for use in genome level research. Gene Search is the function to search the integrated database by using keywords and public IDs. The search results can be visualized by: * Genome Explorer : provides annotation of landmarks (genes, transcription start sites, etc.) aligned in accordance with their genome locations. * PPI Network : provides a graphical view of protein-protein interaction (PPI) network from the experimental data generated under the project and the public datasets. * Expression Profile : clusters genes by expression pattern and display the result with heatmap. The function provides genes which have relation of coregulation and anti-coregulation. * Comparison Viewer : This function gives the view to compare the genomic regions between human and mouse homologous genes. The viewer shows the distribution of transcription start sites (TSS) as the way of separable by tissues or time points with other landmarks on genome region. * Gene Stock : This is the function to save the gene list that you are interested until the session is closed.gene, genome, chip, human, interaction, micro array, protein, protein-protein interaction, qrt-pcr, rat, rna, sequence, short rna, tiling array, transcription, transcription control, transcription factor, transcription starting position, yeast two hybrid, data set, cage, data analysis serviceSCR_001737(Genome Network Platform, RRID:SCR_001737)National Institute of Genetics; Shizuoka; Japan listed by: 3DVCLast checked upnif-0000-10237
NeuroExplorerResource, software resource, software application, data analysis software, data processing software, commercial organizationData analysis software for neurophysiology with a multitude of features, including: * Import of native data files created by many popular data acquisition systems * All standard histogram and raster analyses * Shift predictors in crosscorrelograms and color markers in perievent rasters * Joint PSTH, burst analysis and many more analyses of timestamped data * Spectral analysis of spike and continuous data * 3D data view and animation * Fully customizable WYSIWYG graphics * Custom analysis and batch mode processing with internal scripting language * Direct data link to Matlab and Excel * Statistical tests via direct link to R-projectneurophysiology, spike train, spike, statistical test, analysis, windows, mac, 3d data, animation, burst analysis, channel, cross correlogram, electrophysiology, matlab, raster analysis, scriptingSCR_001818(NeuroExplorer, RRID:SCR_001818)listed by: 3DVCLast checked upnif-0000-10382, nif-0000-10382, nlx_158483http://www.plexon.com/products/neuroexplorer
BarleyBaseResource, data or information resource, databaseA MIAME/Plant-compliant and plant ontology enhanced expression database for Barley microarray data. It contains data from two Affymetrix genome arrays, Barley1 and Arabidopsis ATH1. Users can search based on experiment type, experimental factors, array design, or experimenter. They can also choose to browse lists of available data.arabidopsis ath1, barley, barley1, microarray, plant, plant pathogenSCR_001946(BarleyBase, RRID:SCR_001946)Iowa State University; Iowa; USA related to: MIAME, listed by: 3DVCLast checked upnif-0000-02596
Dataverse Network ProjectResource, database, catalog, service resource, portal, storage service resource, project portal, data repository, data or information resourceProject portal for publishing, citing, sharing and discovering research data. Software, protocols, and community connections for creating research data repositories that automate professional archival practices, guarantee long term preservation, and enable researchers to share, retain control of, and receive web visibility and formal academic citations for their data contributions. Researchers, data authors, publishers, data distributors, and affiliated institutions all receive appropriate credit. Hosts multiple dataverses. Each dataverse contains studies or collections of studies, and each study contains cataloging information that describes the data plus the actual data files and complementary files. Data related to social sciences, health, medicine, humanities or other sciences with an emphasis in human behavior are uploaded to the IQSS Dataverse Network (Harvard). You can create your own dataverse for free and start adding studies for your data files and complementary material (documents, software, etc). You may install your own Dataverse Network for your University or organization.data, repository, collection, publishing, citing, sharing, discovering, research, community, connectionSCR_001997(Dataverse Network Project, RRID:SCR_001997)Harvard University; Cambridge; United States Alfred P. Sloan Foundation, Microsoft Research, NSFused by: UCSF DataShare, Agri-environmental Research Data Repository, listed by: 3DVCLast checked upnif-0000-00316https://dataverse.org/
Arabidopsis ReactomeResource, data or information resource, databaseCurated database of core pathways and reactions in plant biology that covers biological pathways ranging from the basic processes of metabolism to high-level processes such as cell cycle regulation. While it is targeted at Arabidopsis pathways, it also includes many biological events from other plant species. This makes the database relevant to the large number of researchers who work on other plants. Arabidopsis Reactome currently contains both in-house curated pathways as well as imported pathways from AraCyc and KEGG databases. All the curated information is backed up by its provenance: either a literature citation or an electronic inference based on sequence similarity. Their ontology ensures that the various events are linked in an appropriate spatial and temporal context.pathway, reaction, biological processSCR_002063(Arabidopsis Reactome, RRID:SCR_002063)John Innes Centre; Norwich; United Kingdom European Unionuses: AraCyc, KEGG, listed by: 3DVCLast checked downnif-0000-20812
MEDLINEResource, data or information resource, bibliography, databaseA premier bibliographic database that contains over 18 million references to journal articles in life sciences with a concentration on biomedicine. A distinctive feature is that the records are indexed with NLM Medical Subject Headings (MeSH). PubMed provides free access to MEDLINE and links to full text articles when possible. The great majority of journals are selected for MEDLINE based on the recommendation of the Literature Selection Technical Review Committee (LSTRC), an NIH-chartered advisory committee of external experts analogous to the committees that review NIH grant applications. Some additional journals and newsletters are selected based on NLM-initiated reviews, e.g., history of medicine, health services research, AIDS, toxicology and environmental health, molecular biology, and complementary medicine, that are special priorities for NLM or other NIH components. These reviews generally also involve consultation with an array of NIH and outside experts or, in some cases, external organizations with which NLM has special collaborative arrangements. MEDLINE is the primary component of PubMed, part of the Entrez series of databases provided by the NLM National Center for Biotechnology Information (NCBI). MEDLINE may also be searched via the NLM Gateway. Time coverage: generally 1946 to the present, with some older material. Source: Currently, citations from approximately 5,516 worldwide journals in 39 languages; 60 languages for older journals. Citations for MEDLINE are created by the NLM, international partners, and collaborating organizations.software, biomedicine, gold standardSCR_002185(MEDLINE, RRID:SCR_002185)National Library of Medicine related to: KLEIO, FACTA+., MeSH, XplorMed, MeSH, MuGeX, EBIMed, MEDIE, GREC Corpus, GENIA Project: Mining literature for knowledge in molecular biology, PubMed, Automated recognition of brain region mentions in neuroscience literature., PubMed, PIE the search, Coremine Medical, Whatizit, Cochrane Central Register of Controlled Trials, used by: CoPub, DisGeNET, Molecular Imaging and Contrast Agent Database, listed by: 3DVCLast checked upnlx_53277
GlycoMapsDBResource, data analysis service, database, analysis service resource, production service resource, service resource, storage service resource, data repository, data or information resourceA data base system for the management of conformational maps and profiles, the system allows conformational maps to be archived in a standard format, and it provides search and comparison facilities. An interface to structures from Sweet-DB is implemented. GlycoMapsDB also offers scientists the possibility of adding their own publicized structures to the database via a web interface. GlycoMapsDB provides maps of 3D and 2D mono- and disaccharides. It provides users conformational information on carbohydrates and glycoproteins.disaccharide, monosaccharide, protein conformation, modeling, conformational map, structure, fragment, conformation, carbohydrateSCR_002810(GlycoMapsDB, RRID:SCR_002810)glycosciences.de DFGrelated to: Distance Mapping, CARP, listed by: 3DVCPMID:17202175Last checked upnif-0000-02913
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