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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
BSMac
 
Resource Report
Resource Website
BSMac (RRID:SCR_009531) BSMac data processing software, software application, software toolkit, image analysis software, software resource A statistical and graphical visualization MATLAB toolbox for the analysis of fMRI data, called the Bayesian Spatial Model for activation and connectivity (BSMac). BSMac simultaneously performs whole-brain activation analyses at the voxel and region of interest levels as well as task-related functional connectivity (FC) analyses using a flexible Bayesian modeling framework (Bowman et al., 2008). BSMac allows for inputting data in either Analyze or Nifti file formats. The user provides information pertaining to subgroup memberships, scanning sessions, and experimental tasks (stimuli), from which the design matrix is constructed. BSMac then performs parameter estimation based on MCMC methods and generates plots for activation and FC, such as interactive 2D maps of voxel and region-level task-related changes in neural activity and animated 3D graphics of the FC results. computational neuroscience, magnetic resonance, brain activation, connectivity, matlab, statistics, visualization is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: Emory University; Georgia; USA
PMID:22101143
PMID:17936016
Acknowledgement requested, BSD License, GNU Lesser General Public License, GNU General Public License nlx_155706 http://www.nitrc.org/projects/bsmac SCR_009531 BSMAC Software, Bayesian Spatial Model for Brain Activation and Connectivity, BSMac: Bayesian Spatial Model for Brain Activation and Connectivity 2026-08-13 09:28:05 0
Neural Decoding Toolbox
 
Resource Report
Resource Website
10+ mentions
Neural Decoding Toolbox (RRID:SCR_009012) NDT data analysis software, data processing software, software application, software toolkit, software resource Matlab toolbox that makes it easy to apply decoding analyses to neural data. The design of the toolbox revolves around four abstract object classes which enables users to interchange particular modules in order to try different analyses while keeping the rest of the processing stream intact. The toolbox is capable of analyzing data from many different types of recording modalities, and examples are given on how it can be used to decode basic visual information from neural spiking activity and how it can be used to examine how invariant the activity of a neural population is to stimulus transformations. population decoding, neuron, analysis, matlab, data analysis, machine learning, multivariate pattern analysis, neural decoding has parent organization: Massachusetts Institute of Technology; Massachusetts; USA; DARPA ;
IPTO ;
DSO ;
AFSOR-THRL ;
Adobe Systems ;
Honda Research Institute USA ;
King Abdullah University of Science and Technology ;
NEU ;
Sony ;
Eugene McDermott Foundation ;
NSF 0640097;
NSF 0827427;
NSF FA8650-05-C-7262
PMID:23734125 Acknowledgement requested, Account required nlx_152729 SCR_009012 2026-08-13 09:28:02 19
R/QTLBIM
 
Resource Report
Resource Website
1+ mentions
R/QTLBIM (RRID:SCR_009375) software toolkit, software resource, software library, software application Software library for QTL Bayesian Interval Mapping that provides a Bayesian model selection approach to map multiple interacting QTL. It works on experimentally inbred lines and performs a genome-wide search to locate multiple potential QTL. The package can handle continuous, binary and ordinal traits. (entry from Genetic Analysis Software) gene, genetic, genomic, r, bio.tools is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
nlx_154597, biotools:qtlbim http://www.ssg.uab.edu/qtlbim/index.jsp, https://cran.r-project.org/src/contrib/Archive/qtlbim/, https://bio.tools/qtlbim http://www.qtlbim.org/ SCR_009375 2026-08-13 09:28:03 2
Clinical Outcomes Research Initiative
 
Resource Report
Resource Website
1+ mentions
Clinical Outcomes Research Initiative (RRID:SCR_009010) CORI data or information resource, resource, database, service resource, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on December 5, 2022. Endoscopic Reporting Software, aggregated and individual research data and tailor-made services aimed to advance the overall practice of endoscopy. It was developed to study outcomes of gastrointestinal (GI) endoscopic procedures in real life settings, using data obtained from the CORI Endoscopic Reporting Software or from other endoscopic reporting software. Practice sites include hospitals, ambulatory care centers, private practices, universities, and Veteran''''s hospitals (VA''''s). The CORI v4 Endoscopic Reporting Software is a specialty Electronic Health Record used to document endoscopic procedures and provide reporting services to your practice. Data from participating providers is also sent to a central data repository to become part of the National Endoscopic Database (NED), which now contains data from over 2.7 million GI procedures. The CORI v4 Endoscopic Reporting Software offers significant benefits for participating practices, providers and patients, as well as for everyone who benefits from CORI''''s research efforts. You may actively participate in research with CORI. If you have ideas for research using the NED, their research team can help you evaluate those ideas, collect and analyze the data. In addition, you may choose to participate in one of the prospective research projects conducted by CORI research staff. clinical, endoscopy, gastroenterology, gastrointestinal, endoscopic, endoscopy reporting software, outcome, report, electronic health record, aggregator is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Research Resources
has parent organization: Oregon Health and Science University; Oregon; USA
NIDDK THIS RESOURCE IS NO LONGER IN SERVICE nlx_152692 SCR_009010 2026-08-13 09:27:58 6
IDeA Lab brain image processing suite
 
Resource Report
Resource Website
1+ mentions
IDeA Lab brain image processing suite (RRID:SCR_009495) IDeA Lab brain image processing suite data processing software, software application, software toolkit, image analysis software, software resource Suite of tools for brain image analysis. Image manipulation, 2D visualization, linear alignment, BBSI, template-based bias correction, skullstrip. GUI Image analysis tools. Now modified to read/write single file nifti (.nii) format. Other packages to be added. analyze, c++, console (text based), csh/tcsh, image display, image-to-image, image-to-template, intermodal, intersubject, linux, magnetic resonance, nifti, nonlinear warp, posix/unix-like, quantification, registration, resampling, spatial transformation, spline interpolation, tri-linear, two dimensional display, unix shell, visualization, volume measurement, volumetric analysis, warping is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC) nlx_155644 SCR_009495 2026-08-13 09:28:04 1
Groupwise Image Registration Toolbox
 
Resource Report
Resource Website
Groupwise Image Registration Toolbox (RRID:SCR_009492) Groupwise Image Registration data processing software, software application, image analysis software, software resource, registration software A method for group-wise image registration by pairwisely registering similar images identified using graph theoretic techniques. Particularly, they use sparse coding to estimate image similarity measures among images to be registered, yielding asymmetric, group-wise image similarity measures for each image to others in the group. domain independent is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: Chinese Academy of Sciences; Beijing; China
PAMI License, Http://www.nitrc.org/include/glossary.php#690, Non-commercial nlx_155640 SCR_009492 2026-08-13 09:28:04 0
HD Neuro-Informatics
 
Resource Report
Resource Website
1+ mentions
HD Neuro-Informatics (RRID:SCR_009493) HDNI topical portal, data or information resource, portal An international effort to establish resources necessary to study the application of neuroimaging measures as (surrogate) biomarkers in Huntington''s Disease (HD). The primary aims are to develop and apply software tools, imaging protocols, quality control procedures, data archiving, data distribution, and participation guidelines that will accelerate existing and prospective imaging studies. magnetic resonance is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC) Huntington''s disease BSD License nlx_155641 SCR_009493 Huntington Disease Nueroimaging Initiative 2026-08-13 09:27:59 2
BRAINSMush
 
Resource Report
Resource Website
BRAINSMush (RRID:SCR_009485) BRAINSMush segmentation software, data processing software, software application, image analysis software, software resource Tool to generate brain volume mask from input of T1 and T2-weighted images alongside a region of interest brain mask. This volume mask omits dura, skull, eyes, etc. The program is built upon ITK and uses the Slicer3 execution model framework to define the command line arguments and can be fully integrated with Slicer3 using the module discovery capabilities of Slicer3. analyze, application, bsd license, bsd/mit-style open source license, c++, console (text based), dicom, magnetic resonance, nifti, nrrd, segmentation is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC) BSD License nlx_155702 http://www.nitrc.org/projects/brainsmush SCR_009485 2026-08-13 09:28:04 0
GOMO - Gene Ontology for Motifs
 
Resource Report
Resource Website
1+ mentions
GOMO - Gene Ontology for Motifs (RRID:SCR_008864) GOMO data processing software, software application, analysis service resource, production service resource, service resource, data analysis service, software resource Gene Ontology for Motifs (GOMO) is an alignment- and threshold-free comparative genomics approach for assigning functional roles to DNA regulatory motifs from DNA sequence. The algorithm detects associations between a user-specified DNA regulatory motif (expressed as a position weight matrix; PWM) and Gene Ontology terms. The original method for predicting the roles of transcription factors (TFs starts with a PWM motif describing the DNA-binding affinity of the TF. GOMO uses the PWM to score the promoter region of each gene in the genome for its likelihood to be bound by the TF. The resulting ''''affinity'''' scores are then used to test each term in the Gene Ontology for association with high-scoring genes. The algorithm was subsequently extended to leverage conserved signals using multiple, related species in a comparative approach, which greatly improves the resulting annotations. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene, motif, genomics, gene ontology, function, compare, ontology or annotation editor, statistical analysis, dna binding motif, dna binding, dna, transcription factor, sequence is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of Queensland; Brisbane; Australia
has parent organization: MEME Suite - Motif-based sequence analysis tools
Australian Research Council ;
University of Queensland; Brisbane; Australia ;
International Research Tuition Award ;
NCRR R01 RR021692
PMID:20147307
PMID:18544606
Free for academic use nlx_149250 SCR_008864 Gene Ontology for Motifs 2026-08-13 09:28:01 3
Renal Disease Portal
 
Resource Report
Resource Website
Renal Disease Portal (RRID:SCR_009030) Renal Disease Portal topical portal, data or information resource, disease-related portal, data set, portal An integrated resource for information on genes, QTLs and strains associated with a variety of kidney and renal system conditions such as Renal Hypertension, Polycystic Kidney Disease and Renal Insufficiency, as well as Kidney Neoplasms. gene, quantitative trait locus, strain, renal hypertension, kidney neoplasm, phenotype, pathway, biological process, disease, kidney, genome, gviewer, chromosome, molecular function, cellular component, visualization, synteny is related to: NIDDK Information Network (dkNET)
is related to: Gene Ontology
has parent organization: Rat Genome Database (RGD)
Renal disease, Renal hypertension, Polycystic kidney disease, Renal insufficiency, Kidney neoplasm, Diabetes Insipidus, Hyperoxaluria, Renal hypertension, Nephritis, Nephrocalcinosis, Nephrolithiasis, Nephrosis, Renal Fibrosis, Inborn Error of Renal Tubular Transport, Uremia nlx_153941 SCR_009030 RGD Renal Disease Portal 2026-08-13 09:28:03 0
National Geophysical Data Center
 
Resource Report
Resource Website
10+ mentions
National Geophysical Data Center (RRID:SCR_009429) NGDC data or information resource, organization portal, service resource, portal National Data Center that provides scientific stewardship, products, and services for geophysical data from sea floor and solid earth environments, including Earth observations from space. Please note that routine underway geophyiscal shipboard data collected with standard equipment aboard the UNOLS fleet (e.g. bathymetry, subbottom, magnetics, gravity) are routinely transmitted to NGDC via Rolling Deck to Repository (R2R). geophysics, sea floor, solid earth, bathymetry, subbottom, magnetics, gravity is listed by: CINERGI
has parent organization: National Oceanic and Atmospheric Administration
nlx_154716 SCR_009429 2026-08-13 09:28:03 46
National Climatic Data Center
 
Resource Report
Resource Website
100+ mentions
National Climatic Data Center (RRID:SCR_009427) NCDC data or information resource, database, service resource, data repository, storage service resource National Data Center that accepts and makes available weather, climate, paleoclimate, meteorological data. weather, climate, paleoclimate, meteorology, FASEB list is listed by: CINERGI
has parent organization: National Oceanic and Atmospheric Administration
is parent organization of: World Data Center for Paleoclimatology
nlx_154702 SCR_009427 2026-08-13 09:27:58 135
CoCoMac-Paxinos3D viewer
 
Resource Report
Resource Website
CoCoMac-Paxinos3D viewer (RRID:SCR_009548) CoCoMac-Paxinos3D viewer data processing software, software resource, data visualization software, software application An interactive interface of macaque stereotaxic atlas with a connectivity database, allowing integrated data analysis and mapping between 3D structures with database vocabularies. These Java-based tools are capable of reading stacks of polygons described in svg vector format and arrange them in 3D space so that the corresponding structures can be viewed and manipulated individually. An additional excel (currently v. 1997-2003) file maintains the structure abbreviations and their mapping to the terminology of databases that provide supplementary information. Here in particular we have manually drawn the cortical, striatal, thalamic and amygdaloid structures of the 151 frontal sections from the Rhesus Monkey Brain in Stereotactic Coordinates authored by Paxinos and colleagues in 1999. After loading the excel file and a set of the svg files, the view can be rotated, zoomed and individual brain structures be selected for identification and simple geometric measures. A stereotaxic grid is a display option. The abbreviations of the brain structures are mapped to entities recorded in the CoCoMac database of primate brain connectivity. Thereby one can retrieve mapping and connectivity information for the selected structure as text or connecting arrows. magnetic resonance, java, mapping, connectivity is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: CoCoMac
PMID:19145492 GNU General Public License nlx_155728 http://www.nitrc.org/projects/cp3d SCR_009548 2026-08-13 09:28:05 0
GRDR
 
Resource Report
Resource Website
1+ mentions
GRDR (RRID:SCR_008978) GRDR, RaDaR data or information resource, people resource, database, service resource, data repository, storage service resource, patient registry Data repository of de-identified patient data, aggregated in a standardized manner, to enable analyses across many rare diseases and to facilitate various research projects, clinical studies, and clinical trials. The aim is to facilitate drug and therapeutics development, and to improve the quality of life for the many millions of people who are suffering from rare diseases. The goal of GRDR is to enable analyses of data across many rare diseases and to facilitate clinical trials and other studies. During the two-year pilot program, a web-based template will be developed to allow any patient organization to establish a rare disease patient registry. At the conclusion of the program, guidance will be available to patient groups to establish a registry and to contribute de-identified patient data to the GRDR repository. A Request for Information (RFI) was released on February 10, 2012 requesting information from patient groups about their interest in participating in a GRDR pilot project. ORDR selected 30 patient organizations to participate in this pilot program to test the different functionalities of the GRDR. Fifteen (15) organizations with established registries and 15 organizations that do not have patient registry. The 15 patient groups, each without a registry, were selected to assist in testing the implementation of the ORDR Common Data Elements (CDEs) in the newly developed registry infrastructure. These organizations will participate in the development and promotion of a new patient registry for their rare disease. The GRDR program will fund the development and hosting of the registry during the pilot program. Thereafter, the patient registry is expected to be self-sustaining.The 15 established patient registries were selected to integrate their de-identified data into the GRDR to evaluate the data mapping and data import/export processes. The GRDR team will assist these organizations in mapping their existing registry data to the CDEs. Participating registries must have a means to export their de-identified registry data into a specified data format that will facilitate loading the data into the GRDR repository on a regular basis. The GRDR will also develop the capability to link patients'''' data and medical information to donated biospecimens by using a Voluntary Global Unique Patient Identifier (GUID). The identifier will enable the creation of an interface between the patient registries that are linked to biorepositories and the Rare Disease Human Biospecimens/Biorepositories (RD-HUB) http://biospecimens.ordr.info.nih.gov/. clinical, common data element, global unique patient identifier, clinical trial, drug development, therapy is related to: Biospecimens/Biorepositories: Rare Disease-HUB (RD-HUB)
is related to: NIH Data Sharing Repositories
has parent organization: Office of Rare Diseases Research
Rare disease NIH Public, The community can contribute to this resource nlx_152145 http://www.grdr.info/ SCR_008978 Rare Diseases Registry Program (RaDaR), Global Rare Diseases Patient Registry and Data Repository 2026-08-13 09:28:02 1
Onto-Express To Go (OE2GO)
 
Resource Report
Resource Website
Onto-Express To Go (OE2GO) (RRID:SCR_008854) OE2GO text-mining software, software application, analysis service resource, production service resource, service resource, data analysis service, software resource Onto-Express is a web-based tool in the Onto-Tools suite that performs automated function profiling for a list of differentially expressed genes. However, Onto-Express does not support functional profiling for the organisms that do not have annotations in public domain, or use of custom (i.e. user-defined) ontologies. This limitation is also true for most of the other existing tools for functional profiling, which means that researchers working with uncommon organisms and/or new annotations or ontologies may be forced to construct such profiles manually. Onto-Express To Go (OE2GO) is a new tool added to the Onto-Tools ensemble to address these issues. OE2GO is built on top of OE to leverage its existing functionality. In OE2GO, the users now have an option to use either the Onto-Tools database as a source of functional annotations or provide their own annotations in a separate file. Currently, OE2GO supports annotation file in the Gene Ontology format. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene, gene expression, annotation, data mining, ontology browser, annotation browser, ontology search engine, annotation search engine, ontology visualization, annotation visualization, statistical analysis, term enrichment, browser, visualization, search engine is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Wayne State University; Michigan; USA
PMID:17584796 Free for academic use nlx_149112 SCR_008854 Onto-Express-to-go, Onto-Express To Go 2026-08-13 09:28:00 0
Tissue Access for Patient Benefit
 
Resource Report
Resource Website
Tissue Access for Patient Benefit (RRID:SCR_008853) TAPb, TAPB topical portal, data or information resource, portal We aim to facilitate the pathway for access, storage, use and transfer of human organs, cells and tissue between clinical centers within UCL Partners, academic groups in UCL, other universities, hospitals, medical researcher and biotechnology companies, to enhance the ability for researchers to access the materials they need. Alongside this, researchers will be able to exchange information and access guides on regulatory, ethics and practical issues concerning access, transfer and use of this type of material. These guides will be video and documents format, based on talks at organized events given by experts in the relevant fields. All of this information will be accessible on a website that seeks to link groups within UCL and attract attention from the wider world through social media and expansion of existing contacts. Our vision is to develop a centralized human tissue provision and utilization service for academic and commercial researchers UCL has the highest concentration of biomedical researchers in Europe. As part of this, UCL has numerous licensed biobanks and is associated with many research intensive hospitals in North London. The role of a biobank is to prepare and hold human tissue samples in for use by medical researchers to help delivery new treatments. Hospitals can also provide human tissue for research by utilizing waste human tissue taken as part of surgery or diagnostic procedures, but is normally incinerated. The researchers using the human tissue could be working within academic laboratories in UK universities and institutions or as part of commercial companies. Researchers currently cannot easily access human tissue to meet the demands of their research, often due to the long ethical, regulatory and contractual processes. However, with the enormous UCL biobanking and research Hospital resources, UCL could be a leading academic institution in providing human tissue for medical research within the UK and internationally. Our vision is to develop a centralized human tissue provision and utilization service for academic and commercial researchers. This relies on creating an overarching infrastructure, to consolidate information on disparate human tissue resources around UCL, and (where possible) gain centralized ethical and regulatory and contractual approval for use of the tissue. Funding the infrastructure will rely on a cost recovery model for a per sample basis. As a result the time needed to obtain tissue for research will be dramatically reduced, whilst providing a simple costing model for obtaining human tissue. This will make human tissue procurement much more efficient for end users. has parent organization: University College London; London; United Kingdom nlx_149096 SCR_008853 UCL - Tissue Access for Patient Benefit 2026-08-13 09:28:00 0
Mind Lab
 
Resource Report
Resource Website
Mind Lab (RRID:SCR_009025) Mind Lab data or information resource, image collection, video resource Interactive laboratory of the mind composed of 4 themed sessions housing four short introductory movies and sixteen trials with those you can experience visual phenomena and illusions used for study in psychological experiments. visual illusion, sensory perception, visual phenomena, psychological experiment, vision has parent organization: Japan Science and Technology Agency nlx_153853 http://jvsc.jst.go.jp/find/mindlab/english/ SCR_009025 JST Virtual Science Center Mind Lab 2026-08-13 09:28:02 0
Digital Ageing Atlas
 
Resource Report
Resource Website
10+ mentions
Digital Ageing Atlas (RRID:SCR_009020) DAA data or information resource, database, service resource, data repository, storage service resource Database of age-related changes covering different biological levels, including molecular, physiological, psychological and pathological age-related data, to create an interactive portal that serves as a centralized collection of human aging changes and pathologies. To facilitate integrative, system-level studies of aging, the DAA provides a centralized source for aging-related data as well as basic tools to query and visualize the data, including anatomical models. Data in the DAA is manually curated from the literature and retrieved from public databases. For more detailed analyses users are able to download the entire database. More information on how to use the DAA is available on the help page. The DAA primarily focuses on human aging, but also includes supplementary mouse data, in particular gene expression data, to enhance and expand the information on human aging. If you would like to contribute to the database yourself, for instance if you have new data on aging, please use the contribute page to submit your data. late adult human, anatomy, gene, molecular, pathological, physiological, psychological, tissue, reference, cellualar, gene expression has parent organization: University of Liverpool; Liverpool; United Kingdom Aging The community can contribute to this resource, Creative Commons Attribution License, v3 Unported nlx_153874 SCR_009020 Digital Aging Atlas 2026-08-13 09:28:03 15
OME - Open Microscopy Environment
 
Resource Report
Resource Website
1+ mentions
OME - Open Microscopy Environment (RRID:SCR_008849) OME data or information resource, narrative resource, standard specification, source code, software resource Open tools to support data management for biological light microscopy produced by a multi-site collaborative effort among academic laboratories and a number of commercial entities. Designed to interact with existing commercial software, all OME formats and software are free, and all OME source code is available under the GNU General public license or through commercial license from Glencoe Software. OME is developed as a joint project between research-active laboratories at the Dundee, NIA Baltimore, and Harvard Medical School and LOCI. In addition, OME has active collaborations with many imaging and informatics groups. While many other applications could use OME''s architecture and design, their specific implementation is focused on biological and biomedical imaging. Those interested in applying OME''s technology to other applications should contact the developers. OME work is divided into several different standards and software projects: * Bio-Formats: A Java-based library for reading and writing over 90 microscopy file formats. * OMERO Software: The Java-based OMERO software project, which currently includes tools for storing, visualizing, managing, and annotating microscopic images and metadata. * OME-XML & OME-TIFF: The OME-XML and OME-TIFF file format specifications, which are open file formats for sharing microscope image data. * OME Server: This was the original OME server project which has now ended and is a legacy product. It implements image-based analysis of cellular dynamics and image-based screening of cellular localization or phenotypes, and included a fully developed version of the 2003 version of OME-XML Schema language. light microscopy, imaging, biomedical imaging, image, microscope, biomedical has parent organization: University of Dundee; Scotland; United Kingdom
is parent organization of: Bio-Formats
is parent organization of: OMERO
is parent organization of: OME-TIFF Format
Aging PMID:15892875
PMID:20513764
GNU General Public License, Commercial license, (Glencoe Software) nlx_146268 SCR_008849 Open Microscopy Environment 2026-08-13 09:27:56 8
Penn Alzheimer's Disease Center
 
Resource Report
Resource Website
Penn Alzheimer's Disease Center (RRID:SCR_004444) topical portal, data or information resource, disease-related portal, portal A national Alzhiemer's disease research center funded by the National Institute on Aging, and the research arm of the Penn Memory Center. alzheimer's disease, memory, dementia, late adult human, disease related portal has parent organization: University of Pennsylvania Center for Neurodegenerative Disease Research
is parent organization of: University of Pennslyvania Brain Bank
Alzheimer's disease, Dementia, Aging National Institute on Aging nlx_144494 http://www.med.upenn.edu/cndr/pennsalzheimers.shtml SCR_004444 Penn Alzheimer's Disease Center, Penn ADC, University of Pennsylvania Alzheimer's Disease Center 2026-08-13 09:27:07 0

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