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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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Brain and Behavior Research Foundation Resource Report Resource Website 10+ mentions |
Brain and Behavior Research Foundation (RRID:SCR_001992) | portal, topical portal, funding resource, data or information resource |
The Brain and Behavior Research Foundation (formerly NARSAD, the National Alliance for Research on Schizophrenia and Depression) is committed to alleviating the suffering of mental illness by awarding grants that will lead to advances and breakthroughs in scientific research. Additionally, learn about brain and behavior disorders and upcoming events. 100% of all donor contributions for research are invested in NARSAD Grants leading to discoveries in understanding causes and improving treatments of disorders in children and adults, such as depression, bipolar disorder, schizophrenia, autism, attention deficit hyperactivity disorder, and anxiety disorders like obsessive-compulsive and post-traumatic stress disorders. Over a quarter of a century, we have awarded nearly $300 million worldwide to more than 3,000 scientists carefully selected by our prestigious Scientific Council. We receive no government funding. All of our work relies on contributions from families, foundations and other caring donors. |
adult, child, attention deficit-hyperactivity disorder, autism, behavior disorder, bipolar disorder, brain, depressive disorder, human, mental health, research, mental disease, neuropsychiatric illness, proceedings, grant, schizophrenia, post-traumatic stress disorder, anxiety disorder, autism, obsessive-compulsive disorder | nif-0000-12459 | http://www.narsad.org/ | SCR_001992 | National Alliance on Research in Schizophrenia and Depression, NARSAD: The Worlds Leading Charity Dedicated to Mental Health Research, NARSAD: The Brain and Behavior Research Fund, Brain & Behavior Research Foundation, Brain Behavior Research Foundation, National Alliance for Research on Schizophrenia Depression | 2026-08-11 09:40:30 | 30 | |||||||||
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Dendritica: Software Tools for Studying Dendritic Signaling Resource Report Resource Website 1+ mentions |
Dendritica: Software Tools for Studying Dendritic Signaling (RRID:SCR_001865) | software application, simulation software, software resource | Dendritica is a program package for relating dendritic geometry and signal propagation. The programs are based on those used for the simulations described in the following paper: Vetter, P., Roth, A. & Husser, M. (2001). Action potential propagation in dendrites depends on dendritic morphology. Journal of Neurophysiology, 85: 926-937. Dendritica can functionally be divided into three main parts: - Interactive morphological analysis and electrophysiological simulation of single cells - Automated batch simulations across a set of morphologies using the same simulation parameters - Automated analysis of batch simulation runs Dendritica requires NEURON 4.1.1 with some modifications described in Appendix 1. It was tested for NEURON 4.1.1 on Linux and SGI IRIX. Some modifications to the Dendritica code may be necessary in order to run it on older or newer versions of NEURON. Sponsors: This work was supported by the Wellcome Trust, the European Community, the Max-Planck-Gesellschaft, the Wellcome Trust 4-year PhD Programme in Neuroscience. | electrophysiological simulation, dendritic geometry, interactive, morphological, morphology, neuron, sigle cell, signal propagation | Free | http://www.dendrite.org/software.html | SCR_001865 | Dendritica | 2026-08-11 09:40:28 | 1 | |||||||||
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www.brainmapping.org Resource Report Resource Website 1+ mentions |
www.brainmapping.org (RRID:SCR_001987) | portal, data or information resource, knowledge environment, training resource, software resource, community building portal, people resource | This is a topical portal dedicated to the communication of news, science, and information of interest to the brain mapping community, and to sharing and promoting the science of brain mapping. The purpose and goal of brain mapping is to advance the understanding of the relationship between structure and function in the human brain. Scientists in this field seek to gain knowledge of the physical processes that underly human sensation, attention, awareness and cognition. These results are immediately applicable to surgical intervention, to the design of medical interventions and to the treatment of psychological and psychiatric disorders. | function, attention, awareness, brain, brain mapping, cognition, cognitive neuroscience, human, journals, manufacturers, mri, mri safety, scientific societies, sensation, structure, subjects, neuroimaging, video | has parent organization: University of California at Los Angeles; California; USA | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-10669 | SCR_001987 | brainmapping.org | 2026-08-11 09:40:30 | 1 | ||||||||
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SPRUSTON / KATH LAB: Neuraling Modeling Database NEURAL MODELING DATABASE Resource Report Resource Website 1+ mentions |
SPRUSTON / KATH LAB: Neuraling Modeling Database NEURAL MODELING DATABASE (RRID:SCR_001869) | software application, data or information resource, database, software resource, simulation software | This database contains morphologies of hippocampal pyramidal cells and interneurons (in Neurolucida, NEURON, and pdf formats) as well as data recorded from those cells. Sponsors:This work was supported by grants from the NIH (T32-GM-08061 to T.J.M., F32-NS-10532 to N.L.G., and R01-NS35180 and R01-NS 46064 to N.S. and W.L.K.) and NSF (IGERT fellowship to Y.K.). NS46064 is part of the NSF/NIH Collaborative Research in Computational Neuroscience Program | cell, hippocampal, interneuron, morphology, neurolucida, neuron, pyramidal cell | Free, Freely available | nif-0000-10434 | http://www.northwestern.edu/neurobiology/faculty/spruston/sk_models/ | SCR_001869 | SPRUSTON / KATH LAB | 2026-08-11 09:40:28 | 5 | ||||||||
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Spike Train Analysis Software by Attila Szucs: Orbital Spike 4 Resource Report Resource Website 1+ mentions |
Spike Train Analysis Software by Attila Szucs: Orbital Spike 4 (RRID:SCR_001868) | data analysis software, data processing software, software resource, software application | Orbital Spike is a tool for time series analysis. It contains a wide range of methods to analyze data from point processes such as spike arrival times, heart beats or other behavioral episodes. It is optimized this program for spike trains but it works with other types of data, too. The program can analyze up to 8 channels recorded simultaneously each containing a maximum of 132,000 events (spikes). Assuming an average firing rate of 10 Hz for a neuron, you can then analyze a time series of approximately 3 and half hours long. There are up to 8 panels shown in the Orbital Spike desktop. The panels will contain the kind of data of interest. The graphs are associated with a bunch of parameters like window width, bin size, resolution, delay etc. All these parameters are listed in the parameter box, which appears on the right side of the desktop. It is pretty easy to change the parameters and what is nice, the corresponding graph(s) will be recalculated immediately. You can also use a dialog box to change parameters. There are a lot of functions, statistics, graphs and diagrams available. A few of them are: * Interspike interval sequences * ISI Poincar * maps or return maps Instantaneous firing rate * ISI histograms and probability densities * Joint ISI and MSI probability densitograms * Autocorrelation, crosscorrelation * Spike density functions using kernel estimators * Fourier-amplitude spectrum and spectogram * Symbolic maps, recurrence plots * Phase plots of spike density functions Sponsors: Support for this work came from the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Engineering and Geosciences, under Grants DE-FG03-90ER14138 and DE-FG03-96ER14592; from the Office of Naval Research under Grant N00014-00-1-0181; from the National Science Foundation under Grant PHY0097134; from the National Institutes of Health under Grants R01 NS-40110-01A2 and 1RO1 NS-40110; and from the Army Research Office under Contract DAAD19-01-1-0026. R. D. Pinto was supported by the State of Sao Paulo Research Foundation (FAPESP). | firing rate, fourier-amplitude spectrum, analyze, behavioral episode, density, interspike interval sequence, neuron, spectogram, spike | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-10433 | SCR_001868 | Orbital Spike 4 | 2026-08-11 09:40:26 | 1 | |||||||||
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World Parkinson Congress Resource Report Resource Website 1+ mentions |
World Parkinson Congress (RRID:SCR_002034) | data or information resource, topical portal, portal, disease-related portal | A nonprofit organization dedicated to providing an international forum for the latest scientific discoveries, medical practices and caregiver initiatives related to Parkinson's disease. It hosts the annual World Parkinson Congress, an event which focuses on bringing physicians, scientists, allied health professionals, caregivers and people diagnosed with Parkinson's disease together, in order to create a global dialogue that will help expedite treatment practices and the discovery of a cure . | parkinson's disease, pd, international forum, disease related portal | Parkinson's disease | Free | nif-0000-11855 | SCR_002034 | World Parkinson's Disease Congress | 2026-08-11 09:40:28 | 1 | ||||||||
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World Parkinson Disease Association Resource Report Resource Website 1+ mentions |
World Parkinson Disease Association (RRID:SCR_002035) | data or information resource, topical portal, portal, disease-related portal | THIS RESOURCE IS NO LONGER IN SERVICE, documented August 23, 2016. The World Parkinson's Disease Association is an alliance of members from all over the world who have come together to share information about Parkinson's disease. In order to further Parkinson's research and better the condition of those diagnosed with the disease, the Association: establishes computerized connections; takes part in and/or finances research activities; urges pharmaceutical companies and government institutions of the various countries to support the guidelines recommended by the associations of Parkinson's patients; and coordinates and promotes interchange of information among its members with the aim of solving problems of mutual interest. | parkinson's disease, research, therapy, pd, topical portal, disease related portal | Parkinson's disease | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-11857 | SCR_002035 | WPDA | 2026-08-11 09:40:31 | 1 | ||||||||
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High Throughput Genomic Sequences Division Resource Report Resource Website 1+ mentions |
High Throughput Genomic Sequences Division (RRID:SCR_002150) | HTG Sequences, HTG Division | service resource, data or information resource, storage service resource, database, data repository | Database of high-throughput genome sequences from large-scale genome sequencing centers, including unfinished and finished sequences. It was created to accommodate a growing need to make unfinished genomic sequence data rapidly available to the scientific community in a coordinated effort among the International Nucleotide Sequence databases, DDBJ, EMBL, and GenBank. Sequences are prepared for submission by using NCBI's software tools Sequin or tbl2asn. Each center has an FTP directory into which new or updated sequence files are placed. Sequence data in this division are available for BLAST homology searches against either the htgs database or the month database, which includes all new submissions for the prior month. Unfinished HTG sequences containing contigs greater than 2 kb are assigned an accession number and deposited in the HTG division. A typical HTG record might consist of all the first-pass sequence data generated from a single cosmid, BAC, YAC, or P1 clone, which together make up more than 2 kb and contain one or more gaps. A single accession number is assigned to this collection of sequences, and each record includes a clear indication of the status (phase 1 or 2) plus a prominent warning that the sequence data are unfinished and may contain errors. The accession number does not change as sequence records are updated; only the most recent version of a HTG record remains in GenBank. | gap, gene, accession, arabidopsis, bac, biological, c. elegans, clone, contig, cosmid, dna, genomic, high-throughput, homology, homo sapiens, invertebrate, nematode, nucleotide, p1, plant, primate, sequence, structure, taxonomy, yac, genome, sequence, nucleotide sequence, dna sequence, nucleotide, dna, gold standard |
is related to: GenBank has parent organization: NCBI |
PMID:9331365 | Free, Freely available | nif-0000-20943 | SCR_002150 | HTG GenBank Division, HTG database, NCBI High-Throughput Genomic Sequences, HTG Sequence, High-Throughput Genomic Sequences | 2026-08-11 09:40:29 | 5 | ||||||
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SeattleSNPs - Variation Discovery Resource Resource Report Resource Website 50+ mentions |
SeattleSNPs - Variation Discovery Resource (RRID:SCR_001859) | portal, topical portal, data or information resource, narrative resource, training material, software resource | The SeattleSNPs PGA is focused on identifying, genotyping, and modeling the associations between single nucleotide polymorphisms (SNPs) in candidate genes and pathways that underlie inflammatory responses in humans. SeattleSNPs is focused on variation analysis in genes related to the inflammatory response. These gene targets are found in specific pathways and from interacting molecules contributing to this response. Available Resources: - Baseline assembled and complete genomic sequence and chromosomal location for candidate gene targets - Mapping of exon and repeat structure for candidate genes - Amplification primers and conditions - SNPs mapped by location in gene structure - SNPs with immediate surrounding sequence for genotype assay design - Genotypes and relative allele frequencies of the SNPs - Special features of SNPs - location (5', coding, etc.), amino acid substitutions, recurrent variation - Manuals on all protocols, data analysis procedures, and use of software tools - Workshop on genetic variation analysis and a gene submission program for variation analysis Sponsors: SeattleSNPs is funded as part of the National Heart Lung and Blood Institute's (NHLBI) Programs for Genomic Applications (PGA). | exon, gene, gene target, allele, amino acid, amplification, assay, chromosomal, genomic sequence, genotyping, humans, inflammatory response, molecule, pathway, primer, recurrent varation, repeat structure, singe nucleotide polymorphism (snp), substitution, variation analysis | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-10423 | http://pga.mbt.washington.edu/ | SCR_001859 | SeattleSNPs | 2026-08-11 09:40:28 | 62 | ||||||||
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Pathway Commons Resource Report Resource Website 10+ mentions |
Pathway Commons (RRID:SCR_002103) | PC | data or information resource, database, web service, software resource, data access protocol | Database of publicly available pathways from multiple organisms and multiple sources represented in a common language. Pathways include biochemical reactions, complex assembly, transport and catalysis events, and physical interactions involving proteins, DNA, RNA, small molecules and complexes. Pathways were downloaded directly from source databases. Each source pathway database has been created differently, some by manual extraction of pathway information from the literature and some by computational prediction. Pathway Commons provides a filtering mechanism to allow the user to view only chosen subsets of information, such as only the manually curated subset. The quality of Pathway Commons pathways is dependent on the quality of the pathways from source databases. Pathway Commons aims to collect and integrate all public pathway data available in standard formats. It currently contains data from nine databases with over 1,668 pathways, 442,182 interactions,414 organisms and will be continually expanded and updated. (April 2013) | biological pathway, pathway, molecule, biopax, standard exchange format, bio.tools |
is listed by: bio.tools is listed by: Debian is listed by: SoftCite is related to: cPath is related to: Biological General Repository for Interaction Datasets (BioGRID) is related to: IntAct is related to: Reactome is related to: MINT is related to: HumanCyc: Encyclopedia of Homo sapiens Genes and Metabolism is related to: Cancer Cell Map is related to: HPRD - Human Protein Reference Database is related to: Integrated Molecular Interaction Database is related to: Pathway Interaction Database is related to: CHEBI is related to: UniProt is related to: PANTHER is related to: WebGestalt: WEB-based GEne SeT AnaLysis Toolkit has parent organization: University of Toronto; Ontario; Canada |
NHGRI P41HG004118; NIGMS 2R01GM070743-06; NIGMS 1T32 GM083937; Cancer Biomedical Informatics Grid |
PMID:21071392 | Free, Freely available | nif-0000-20884, r3d100012731, biotools:PathwayCommons_web_service_API | https://bio.tools/PathwayCommons_web_service_API | SCR_002103 | 2026-08-11 09:40:32 | 14 | |||||
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Shiley-Marcos Alzheimer's Disease Research Center Resource Report Resource Website 1+ mentions |
Shiley-Marcos Alzheimer's Disease Research Center (RRID:SCR_001928) | UCSD ADRC | portal, topical portal, data or information resource, disease-related portal, organization portal | The UCSD ADRC conducts a wide variety of research studies dedicated to understanding the causes, clinical features, and treatments for Alzheimer's disease and related memory disorders. The goal of the center is to discover ways to prevent and eradicate the disease. The Center aims to maintain research subjects, clinical resources, and clinical data to support ongoing and proposed research and to assist in the development of new clinical and interdisciplinary research. An Alzheimer's brain bank with well characterized cases, including Mild Cognitive Impairment and Lewy Body disease, is maintained at the Center. | alzheimer's disease, brain, cognitive, dementia, disease, disorder, impairment, lewy body disease, memory, neurological, neuropathologist, neuropsychological | has parent organization: University of California at San Diego; California; USA | Alzheimer's disease, Lewy Body disease, Memory disorder | Public | nif-0000-10501 | SCR_001928 | University of California at San Diego Shiley-Marcos Alzheimer's Disease Research Center | 2026-08-11 09:40:29 | 1 | ||||||
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University of California at Los Angeles - Department of Energy Institute for Genomics and Proteomics Resource Report Resource Website 1+ mentions |
University of California at Los Angeles - Department of Energy Institute for Genomics and Proteomics (RRID:SCR_001921) | portal, data computation service, data or information resource, database, organization portal | The UCLA-DOE Institute for Genomics and Proteomics carries out research in bioenergy, structural biology, genomics and proteomics, consistent with the research mission of the United States Department of Energy. Major interests of the 12 Principal Investigators and 9 Associate Members include systems approaches to organisms, structural biology, bioinformatics, and bioenergetic systems. The Institute sponsors 5 Core Technology Centers, for X-ray and NMR structural determination, bioinformatics and computation, protein expression and purification, and biochemical instrumentation. Services offered by this Institute: - Databases: * DIP (The Database of Interacting Proteins): The DIPTM database catalogs experimentally determined interactions between proteins. It combines information from a variety of sources to create a single, consistent set of protein-protein interactions. * ProLinks Database of Functional Linkages: The Prolinks database is a collection of inference methods used to predict functional linkages between proteins. These methods include the Phylogenetic Profile method which uses the presence and absence of proteins across multiple genomes to detect functional linkages; the Gene Cluster method, which uses genome proximity to predict functional linkage; Rosetta Stone, which uses a gene fusion event in a second organism to infer functional relatedness; and the Gene Neighbor method, which uses both gene proximity and phylogenetic distribution to infer linkage. - Data-to-Structure Servers: * SAVEs Structure Verification Server * Merohedral Twinning Test Server * SER Surface Entropy Reduction Server * VERIFY3D Structure Verification Server * ERRAT Structure Verification Server - Structure-to-Function Servers: * ProKnow Protein Functionator * Hot Patch Functional Site Locator | expression, functional linkage, gene, biochemical instrumentation, bioenergetic system, bioenergy, bioinformatic, computation, genome, genomic, nmr, organism, protein, protein-protein interaction, proteomic, purification, structural biology, x-ray | nif-0000-10491 | SCR_001921 | UCLA-DOE | 2026-08-11 09:40:29 | 6 | ||||||||||
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Medical Image Processing and Visualization Resource Report Resource Website 1+ mentions |
Medical Image Processing and Visualization (RRID:SCR_002055) | MeVisLab | software application, software toolkit, image analysis software, image processing software, software resource, data processing software | Modular framework for the development of image processing algorithms and visualization and interaction methods, with a special focus on medical imaging. It includes advanced medical imaging modules for segmentation, registration, volumetry, and quantitative morphological and functional analysis. The platform allows fast integration and testing of new algorithms and the development of application prototypes that can be used in clinical environments. In MeVisLab, individual image processing, visualization and interaction modules can be combined to complex image processing networks using a graphical programming approach. The algorithms can easily be integrated using a modular, platform-independent C++ class library. An abstract, hierarchical definition language allows the design of efficient graphical user interfaces, hiding the complexity of the underlying module network to the end user. JavaScript components can be added to implement dynamic functionality on both the network and the user interface level. MeVisLab is based on the Qt application framework, the OpenInventor 3D visualization toolkit and OpenGL. Several clinical prototypes have been realized on the basis of MeVisLab, including software assistants for neuro-imaging, dynamic image analysis, surgery planning, and vessel analysis. Feature Overview: :- Basic image processing algorithms and advanced medical imaging modules :- Full featured, flexible 2D/3D visualization and interaction tools :- High performance for large datasets :- Modular, expandable C++ image processing library :- Graphical programming of complex, hierarchical module networks :- Object-oriented GUI definition and scripting :- Full scripting functionality using Python and JavaScript :- DICOM support and PACS integration :- Intuitive user interface :- Integrated movie and screenshot generation for demonstration purposes :- Generic integration of the Insight Toolkit (ITK) and the Visualization Toolkit (VTK) :- Cross-platform support for Windows, Linux, and MacOS X :- Available for 64-bit operating systems | algorithm, image processing, visualization, image, segmentation, morphological, functional, analysis, neuroimaging, surgery, python, volume rendering, prototype | is listed by: Biositemaps | PMID:17356215 | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-00326 | SCR_002055 | MeVisLab: Medical Image Processing and Visualization | 2026-08-11 09:40:28 | 3 | ||||||
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Stanford Genomics Service Center Core Facility Resource Report Resource Website 10+ mentions |
Stanford Genomics Service Center Core Facility (RRID:SCR_002050) | SFGF, | service resource, core facility, access service resource | Stanford Genomics formerly Stanford Functional Genomics Facility provides services for high throughput sequencing, single cell assays, gene expression and genotyping studies utilizing microarray and real time PCR, and related services. High throughput sequencing (Illumina HiSeq 4000, NextSeq 500, MiSeq and MiniSeq), microarray gene expression and genotyping services (Affymetrix, Agilent and Illumina). Provides 24/7 access to instruments, equipment and software utilized within genomics field. | ABRF, Stanford Genomics, genomics, high throughput sequencing, single cell assays, gene expression, genotyping, microarray, real time PCR, |
is listed by: ABRF CoreMarketplace has parent organization: Stanford University; Stanford; California |
NIAID ; Comprehensive Cancer Center |
Open | SCR_008627, ABRF_200, nif-0000-31997, nif-0000-12246 | https://coremarketplace.org/?FacilityID=200&citation=1 | http://www.microarray.org/sfgf/ | SCR_002050 | Stanford Medicine Stanford Functional Genomics Facility, Stanford University Functional Genomics Core Facility, Stanford Functional Genomics Facility, Stanford Genomics, Stanford Genomics Service Center, Stanford School of Medicine Stanford Functional Genomics Facility | 2026-08-11 09:40:31 | 11 | ||||
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Dataverse Network Project Resource Report Resource Website 10+ mentions |
Dataverse Network Project (RRID:SCR_001997) | Dataverse | service resource, project portal, portal, data or information resource, storage service resource, database, catalog, data repository | Project 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, connection |
is used by: UCSF DataShare is used by: Agri-environmental Research Data Repository is used by: NIH Heal Project is recommended by: NIDDK Information Network (dkNET) is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases is listed by: 3DVC is listed by: re3data.org is related to: PROMIS 2 MY Health has parent organization: Harvard University; Cambridge; United States is parent organization of: Universal Numerical Fingerprint is parent organization of: Agri-environmental Research Data Repository |
Alfred P. Sloan Foundation ; NSF ; Microsoft Research |
Free, Available for download, Freely available | r3d100010051, nif-0000-00316 | https://doi.org/10.17616/R3C880 | http://thedata.org/ | SCR_001997 | Harvard Dataverse, The Dataverse Project, Dataverse, Dataverse Network, Dataverse Network Project, Dataverse Project | 2026-08-11 09:40:30 | 18 | ||||
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NormaCurve Resource Report Resource Website 1+ mentions |
NormaCurve (RRID:SCR_001995) | data analysis software, data processing software, software resource, software application | Analysis methodology that allows simultaneous quantification and normalization of reverse phase protein array (RPPA) data. | analysis, software, code, protein array, RPPA, reverse phase protein array, supplementary material |
is listed by: OMICtools has parent organization: Curie Institute; Paris; France |
PMID:22761696 | Free, Available for download, Freely available | OMICS_00814 | SCR_001995 | 2026-08-11 09:40:30 | 9 | ||||||||
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Glomerular Activity Response Archive Resource Report Resource Website 10+ mentions |
Glomerular Activity Response Archive (RRID:SCR_002089) | GARA | service resource, image collection, analysis service resource, data or information resource, database, data analysis service, production service resource | THIS RESOURCE IS NO LONGER IN SERVICE, documented on April 24, 2017. Database of images depicting the spatial distribution of 2-deoxyglucose uptake evoked in the glomerular layer of the rat olfactory bulb in response to a wide range of defined odorant stimuli. A number of different display and comparison tools are provided allowing patterns to be viewed from different perspectives, and descriptions of the methods and interpretations of these data are provided. Some of the more advanced tools require you to download software. | rat, olfactory bulb, odorant stimuli, odorant, odor, glomerular |
is used by: NIF Data Federation is related to: Integrated Manually Extracted Annotation has parent organization: University of California at Irvine; California; USA |
Human Brain Project ; NIMH ; NIDCD |
THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-00339 | SCR_002089 | Glomerular Response Archive | 2026-08-11 09:40:28 | 10 | ||||||
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National Center for Marine Algae and Microbiota Resource Report Resource Website 50+ mentions |
National Center for Marine Algae and Microbiota (RRID:SCR_002120) | NCMA | biomaterial supply resource, organism supplier, material resource | National marine phytoplankton collection, maintaining over 2700 strains from around the world, most are marine phytoplankton but they also have benthic, macrophytic, freshwater and heterotrophic organisms - now incorporating bacteria and viruses. Strain records have (when available): * collection and isolation information * culturing medium recipes and growth conditions * photographs * GenBank accession link * collection site map * link to the taxonomic database Micro*scope The deposition of new strains are welcome if the strains are a valuable addition to the collection. Examples include strains that are referred to in publications, contain interesting molecular, biochemical or physiological properties, are the basis for taxonomic descriptions, are important for aquaculture, or are from an unusual geographical location or ecological habitat. The NCMA offers a course in phytoplankton culturing techniques and facilities for visiting scientists are available at the new laboratories in East Boothbay, Maine. Services include: Mass Culturing DNA and RNA, Purification, Private Holdings, Culture Techniques Course, Visiting Scientists, Single Cell Genomics, Flow Cytometry, Corporate Alliances and Technology Transfer. | marine phytoplankton, marine, phytoplankton, virus, benthic, macrophytic, freshwater, heterotrophic, microbiota, seawater, FASEB list |
is listed by: One Mind Biospecimen Bank Listing is listed by: CINERGI |
NSF | Restricted | nlx_154729 | SCR_002120 | Provasoli-Guillard National Center for Culture of Marine Phytoplankton, Provasoli-Guillard National Center for Marine Algae and Microbiota, CCMP | 2026-08-11 09:40:32 | 59 | ||||||
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Protein Lounge Resource Report Resource Website 10+ mentions |
Protein Lounge (RRID:SCR_002117) | ProteinLounge | service resource, analysis service resource, data or information resource, database, narrative resource, training material, data analysis service, production service resource | Complete siRNA target database, complete Peptide-Antigen target database and a Kinase-Phosphatase database. They have also developed the largest database of illustrated signal transduction pathways, which are interconnected to their extensive protein database and online gene / protein analysis tools. The interactive web-based databases and software help life-scientists understand the complexity of systems biology. Systems biology efforts focus on understanding cellular networks, protein interactions involved in cell signaling, mechanisms of cell survival and apoptosis leading to development or identification of drug candidates against a variety of diseases. In the post-genomic era, one of the major concerns for life-science researchers is the organization of gene / protein data. Protein Lounge has met this concern by organizing all necessary data about genes / proteins into one portal. | gene, antigen, bioinformatics, kinase, life science, peptide, phosphatase, signal transduction pathway, sirna, systems biology, protein, biology, cellular network, protein interaction, cell signaling, cell survival, apoptosis, peptide-antigen, kinase-phosphatase, image, pathway | Restricted | nif-0000-20903 | SCR_002117 | Protein Lounge - Redefining Biology | 2026-08-11 09:40:28 | 31 | ||||||||
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SAMTOOLS Resource Report Resource Website 10000+ mentions |
SAMTOOLS (RRID:SCR_002105) | SAMtools | data analysis software, software application, software toolkit, software resource, data processing software, sequence analysis software | Original SAMTOOLS package has been split into three separate repositories including Samtools, BCFtools and HTSlib. Samtools for manipulating next generation sequencing data used for reading, writing, editing, indexing,viewing nucleotide alignments in SAM,BAM,CRAM format. BCFtools used for reading, writing BCF2,VCF, gVCF files and calling, filtering, summarising SNP and short indel sequence variants. HTSlib used for reading, writing high throughput sequencing data. | Samtools, BCFtools, HTSlib, next generation sequencing, nucleotide alignments, sequence variant, genomic, c, perl, read, alignment, nucleotide, sequence, data, process, sam, bam, cram, vcf, bcf, bio.tools |
is used by: deFuse is used by: Short Read Sequence Typing for Bacterial Pathogens is used by: ROSE is used by: Fcirc is listed by: OMICtools is listed by: Genetic Analysis Software is listed by: SNVer is listed by: Debian is listed by: bio.tools is listed by: SoftCite is related to: Platypus is related to: shovill is related to: pysam has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom is parent organization of: SAMtools/BCFtools is required by: RelocaTE is required by: Wessim is required by: SL-quant is required by: smMIPfil |
Wellcome Trust ; NHGRI U54 HG002750 |
PMID:19505943 PMID:21903627 DOI:10.1093/bioinformatics/btp352 |
Free, Available for download, Freely available | SCR_018682, biotools:samtools, OMICS_01074, nlx_154607, OMICS_00090 | https://github.com/samtools/samtools, https://github.com/samtools/htslib, https://bio.tools/samtools, https://sources.debian.org/src/samtools/ | http://samtools.sourceforge.net/ | SCR_002105 | samtools, Samtools, Sequence Alignment Map TOOLS, SAMtools, SAM tools | 2026-08-11 09:40:28 | 33299 |
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If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.
Here are the facets that you can filter the data by.
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