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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
Predictions for Entire Proteomes
 
Resource Report
Resource Website
500+ mentions
Predictions for Entire Proteomes (RRID:SCR_002803) data analysis software, data processing software, software application, sequence analysis software, web application, software resource Web application for sequence analysis and the prediction of protein structure and function. The user interface intakes protein sequences or alignments and returned multiple sequence alignments, motifs, and nuclear localization signals., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 15,2026. sequence analysis database, protein structure prediction, protein structure, protein function, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
has parent organization: Columbia University; New York; USA
BMBF PMID:24799431
DOI:10.1093/nar/gkh377
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-00136, OMICS_07135, biotools:predictprotein https://bio.tools/predictprotein, https://sources.debian.org/src/predictprotein/ http://cubic.bioc.columbia.edu/pep/ SCR_002803 PredictProtein 2026-08-09 09:03:38 643
OpenSim
 
Resource Report
Resource Website
500+ mentions
OpenSim (RRID:SCR_002683) simulation software, software application, software resource OpenSim is an open-source software system that lets users develop models of musculoskeletal structures and create dynamic simulations of movement. The software provides a platform on which the biomechanics community can build a library of simulations that can be exchanged, tested, analyzed, and improved through multi-institutional collaboration. The underlying software is written in ANSI C++, and the graphical user interface (GUI) is written in Java. OpenSim technology makes it possible to develop customized controllers, analyses, contact models, and muscle models among other things. These plugins can be shared without the need to alter or compile source code. Users can analyze existing models and simulations and develop new models and simulations from within the GUI. muscle-driven simulation, musculoskeletal biomechanics, neuromuscular simulation, modeling software, simulation software is related to: Simtk.org
is related to: Neuromuscular Models Library
has parent organization: Stanford University; Stanford; California
Simbios ;
NIGMS U54 GM072970;
DARPA
Public, Free, Acknowledgement requested nif-0000-23308 https://simtk.org/home/opensim, http://opensim.stanford.edu/support/index.html SCR_002683 2026-08-09 09:03:34 612
Human Genetics Laboratory: WFS1 Gene Mutation and Polymorphism Database
 
Resource Report
Resource Website
1+ mentions
Human Genetics Laboratory: WFS1 Gene Mutation and Polymorphism Database (RRID:SCR_001113) database, data or information resource, service resource, storage service resource, data repository This web site lists the disease causing mutations and polymorphisms found in the Wolfram syndrome (WFS1) gene. Sponsors: This resource is supported by the University of Michigan at Ann Arbor. frequency, gene, auditory, disease, hearing, neuropathy, polymorphism, research, wolfram syndrome has parent organization: University of Michigan; Ann Arbor; USA nif-0000-10276 SCR_001113 WFS1 2026-08-09 09:03:07 3
Qvalue
 
Resource Report
Resource Website
10+ mentions
Qvalue (RRID:SCR_001073) data analysis software, software resource, software application, data processing software R package that takes a list of p-values resulting from the simultaneous testing of hypotheses and estimates their q-values. It is designed to measure the proportion of false positives when a test is significant. The software is capable of generating plots for visualization. It can be applied to problems in genomics, brain imaging, astrophysics, and data mining. p value, false positive, null hypothesis, genomics, brain imaging, astrophysics, data mining, r, visualization is listed by: OMICtools
is hosted by: Bioconductor
Free, Available for download, Freely available OMICS_00624 https://github.com/jdstorey/qvalue SCR_001073 2026-08-09 09:03:06 32
ToppCluster
 
Resource Report
Resource Website
100+ mentions
ToppCluster (RRID:SCR_001503) ToppCluster service resource, resource, data analysis service, analysis service resource, production service resource A tool for performing multi-cluster gene functional enrichment analyses on large scale data (microarray experiments with many time-points, cell-types, tissue-types, etc.). It facilitates co-analysis of multiple gene lists and yields as output a rich functional map showing the shared and list-specific functional features. The output can be visualized in tabular, heatmap or network formats using built-in options as well as third-party software. It uses the hypergeometric test to obtain functional enrichment achieved via the gene list enrichment analysis option available in ToppGene. term enrichment, gene, analysis, gene enrichment analysis, connectivity, heatmap, ortholog, microarray, function, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: GenitoUrinary Development Molecular Anatomy Project
is related to: ToppGene Suite
NIDDK 1U01DK70219;
NIDDK P30DK078392;
NCRR U54 RR025216;
NIDCR U01DE020049
PMID:20484371 Free OMICS_02225, nlx_152801, biotools:toppcluster https://bio.tools/toppcluster SCR_001503 ToppCluster: A multiple gene list feature analyzer for the dissection of biological systems 2026-08-09 09:03:11 152
Gene Weaver
 
Resource Report
Resource Website
10+ mentions
Gene Weaver (RRID:SCR_003009) database, data or information resource, service resource, storage service resource, data repository, data analysis service, analysis service resource, production service resource Freely accessible phenotype-centered database with integrated analysis and visualization tools. It combines diverse data sets from multiple species and experiment types, and allows data sharing across collaborative groups or to public users. It was conceived of as a tool for the integration of biological functions based on the molecular processes that subserved them. From these data, an empirically derived ontology may one day be inferred. Users have found the system valuable for a wide range of applications in the arena of functional genomic data integration. phenotype, microarray, gene, genome, functional genomics, process, pathway, function, gene set, genomic data integration, analysis, visualization is used by: NIF Data Federation
is used by: Integrated Datasets
is listed by: OMICtools
is related to: Integrated Manually Extracted Annotation
has parent organization: Jackson Laboratory
Integrative Neuroscience Initiative on Alcoholism ;
NIAAA U01 AA13499;
NIAAA U24 AA13513;
NIAAA R01 AA18776
PMID:22080549
PMID:19733230
Free, Freely available r3d100012464, OMICS_02232, nif-0000-00517 http://ontologicaldiscovery.org/, https://doi.org/10.17616/R3248T SCR_003009 GeneWeaver, GeneWeaver - A system for the integration of functional genomics experiments, Ontological Discovery Environment, GeneWeaver.org 2026-08-09 09:03:38 39
vIST/e
 
Resource Report
Resource Website
1+ mentions
vIST/e (RRID:SCR_001627) vIST/e image processing software, data processing software, software application, image analysis software, software toolkit, software resource Open source, platform-independent application for the visualization and analysis of complex, high-dimensional imaging data such as Diffusion Tensor Imaging (DTI) and High Angular Resolution Diffusion Imaging (HARDI). It has a plugin-based architecture which allows third parties to develop new plugins to extend the tool. Overview of the many features: * vIST/e is programmed in C++. It uses the Visualization Toolkit for visualization and pipelined data processing, as well as the cross-platform toolkit Qt Framework for an easy-to-use Graphical User Interface. * vIST/e introduces a powerful new plugin system, which allows for modular development with increased extensibility and stability. * Powerful GPU-based visualization techniques allow for smooth, real-time visualization of large data sets. Using custom ray tracing algorithms created with OpenGL, vIST/e can render DTI ellipsoids and HARDI spherical harmonics glyphs up to 4th order. The high frame rates offered by modern GPU technology allows for interactive exploration of this complex data. * Diffusion Tensor Imaging data can be visualized and interactively explored in a number of ways, including multiple cross-sections, volume rendering, and tensor glyphs. Derived scalar volumes, including various different anisotropy measures, can be computed and visualized. Data from other modalities, such as structural MRI, can be shown alongside the DTI data. * Various fiber tracking methods allow for fast and accurate reconstruction of fiber pathways. Interactively defined Regions of Interest (ROIs) can be used for seeding and filtering of fibers. Fibers are visualized either as lines, optionally using a powerful, GPU-based lighting engine, or as 3D structures such as tubes. * Scalar volumes, glyphs, and fibers can be colored using a wide array of coloring option. Customizable color loop-up tables allow for highly flexible visualization of scalar data. * Visualization and processing of various different HARDI formats is supported. HARDI data is interactively visualized using highly detailed glyphs rendered on the GPU. HARDI glyphs can be visualized in combination with DTI glyphs, for a better overview of complex diffusion data. * vIST/e includes support for NVIDIA's Compute Unified Device Architecture (CUDA), which enables highly parallel, GPU-based data processing, allowing for significant speed-up of computationally expensive algorithms. diffusion tensor imaging, high angular resolution diffusion imaging, visualization, cross-section, volume rendering, tensor glyph, mri, fiber tracking is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is related to: Diffusion MRI of Traumatic Brain Injury
has parent organization: Eindhoven University of Technology; North Brabant; Netherlands
Free, Available for download, Freely available nlx_153923 http://www.nitrc.org/projects/viste SCR_001627 DTITool 2026-08-09 09:03:13 4
Code Analysis Repository and Modelling for e-Neuroscience
 
Resource Report
Resource Website
10+ mentions
Code Analysis Repository and Modelling for e-Neuroscience (RRID:SCR_002795) CARMEN database, data or information resource, service resource, storage service resource, software repository, data repository, software resource THIS RESOURCE IS NO LONGER IN SERVICE.Documented on January 14, 2023. Infrastructure for sharing data, tools and services, this virtual research environment (VRE) supports e-Neuroscience and is designed to provide services for data and processing of that data. While the system is initially focused on electrophysiology data (neural activity recordings are the primary data types), it is equally applicable to many domains outside neuroscience. The Portal Provides: * User login and customization. * Data upload/download. * Data handling including custom permissions for public, shared or private data. * The ability to invoke custom public, shared or private services that consume and produce data. For example, it would allow spike series to be run through a sorter, producing new data representing the sorted spikes. * The ability to host services written in a number of languages including, but not limited to Matlab, R, Python, Perl, Java. * A system to support metadata for data objects, which provides extensive support for entering metadata at the point of upload, and allows the generation of metadata from services to provide provenance information. * The ability to invoke additional visualization for the data, for example, via the Signal Data Explorer. A core part is the development of: (i) minimum reporting guidelines for annotation of data and other computational resources for the purpose of sharing, and; (ii) intermediate formats and APIs for translation between proprietary and bespoke data types. These recommendations are being implemented and the global community is encouraged both to engage in their specification and make use of them for their own data sharing systems. * MINI: Minimum Information about a Neuroscience Investigation - This framework represents the formalized opinion of the CARMEN consortium and its associates, and identifies the minimum reporting information required to support the use of electrophysiology in a neuroscience study, for submission to the CARMEN system. * NDTF: Neurophysiology Data Translation Format - This framework provides a vendor-independent mechanism for translating between raw and processed neurphysiology data in the form of time and image series. They are implementing NDTF in CARMEN but it may also be useful for third party applications. neural activity recording, signal, image series, neurophysiology, data sharing, metadata standard, collaboration, electrophysiology, FASEB list has parent organization: Newcastle University; Newcastle upon Tyne; United Kingdom
is parent organization of: Retinal wave repository
EPSRC EP/E002331/1 PMID:20679128
PMID:18674883
THIS RESOURCE IS NO LONGER IN SERVICE r3d100012284, nif-0000-00442 https://doi.org/10.17616/R3W94G SCR_002795 Code Analysis Repository & Modelling for E-Neuroscience 2026-08-09 09:03:34 29
Seg3D
 
Resource Report
Resource Website
100+ mentions
Seg3D (RRID:SCR_002552) Seg3D image processing software, data processing software, rendering software, software application, image analysis software, segmentation software, data visualization software, software resource A free volume processing segmenting tool that combines a flexible manual interface with powerful image processing and segmentation algorithms. Users can explore and label image volumes using slice windows and 3D volume rendering. analyze, c++, dicom, image display, linux, macos, microsoft, magnetic resonance, nrrd, posix/unix-like, rendering, segmentation, three dimensional display, visualization, volume rendering, win32 (ms windows), windows is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: University of Utah; Utah; USA
NIGMS 8 P41 GM103545-15 PMID:29083867 Free, Available for download, Freely available nlx_155959 http://www.nitrc.org/projects/seg3d SCR_002552 2026-08-09 09:03:28 106
UK Sheep Genome Mapping Project
 
Resource Report
Resource Website
1+ mentions
UK Sheep Genome Mapping Project (RRID:SCR_002272) database, portal, data or information resource, topical portal THIS RESOURCE IS NO LONGER IN SERVICE, documented August 23, 2016. The project aims to apply genome mapping research to sheep, utilizing previous research in sheep (in other countries) and in other species (in the UK and abroad) to the benefit of the UK sheep industry. The project itself uses existing breeding structures, knowledge of the sheep genome and experimental resources. It has three main aims: i) To use the Suffolk, Texel and Charollais Sire Referencing Schemes to detect and verify quantitative trait loci (QTLs) for growth and carcass composition traits ii) To investigate candidate genes and/or chromosomal regions for associations with production traits. iii) To investigate approaches for optimizing future genotyping strategies within the sire referencing schemes for practical and cost effective application of marker-assisted selection By using commercial breeding populations for the research, immediate application of beneficial results is possible. Potential benefits include increased genetic progress through marker assisted selection which utilizes the genotype information, correction of possible parentage errors (ultimately leading to additional genetic progress) and opportunities for using marker information for product certification. The project will benefit the UK sheep industry by the use of Marker Assisted Selection (MAS) utilizing QTL or gene variants identified in the project. Additional benefits may arise from parentage verification and correction of errors e.g. misallocation of lamb to ewe. In the longer term, opportunities may exist to use markers for quality control, tracing products to their source. The major advantage of the design of this project is that the results are immediately applicable to the breeding schemes within which the QTLs and/or genes are detected. The time lag in the application of the results that is often seen with experimental populations is minimized. The project requires close involvement with the Sire Reference Schemes, in return for their assistance the results have immediate benefit to animals within these groups. gene, animal, breed, breeding, chromosomal, chromosome, genome, genotype, genotyping, lamb, map, mapping, marker, population, production, region, sheep, specie, structure, trait THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-20995 SCR_002272 UKSGMP 2026-08-09 09:03:31 1
Mind Research Network - COINS
 
Resource Report
Resource Website
10+ mentions
Mind Research Network - COINS (RRID:SCR_000805) COINS data or information resource, service resource, storage service resource, data set, data repository A web-based neuroimaging and neuropsychology software suite that offers versatile, automatable data upload/import/entry options, rapid and secure sharing of data among PIs, querying and export all data, real-time reporting, and HIPAA and IRB compliant study-management tools suitable to large institutions as well as smaller scale neuroscience and neuropsychology researchers. COINS manages over over 400 studies, more than 265,000 clinical neuropsychological assessments, and 26,000 MRI, EEG, and MEG scan sessions collected from 18,000 participants at over ten institutions on topics related to the brain and behavior. As neuroimaging research continues to grow, dynamic neuroinformatics systems are necessary to store, retrieve, mine and share the massive amounts of data. The Collaborative Informatics and Neuroimaging Suite (COINS) has been created to facilitate communication and cultivate a data community. This tool suite offers versatile data upload/import/entry options, rapid and secure sharing of data among PIs, querying of data types and assessments, real-time reporting, and study-management tools suitable to large institutions as well as smaller scale researchers. It manages studies and their data at the Mind Research Network, the Nathan Kline Institute, University of Colorado Boulder, the Olin Neuropsychiatry Research Center (at) Hartford Hospital, and others. COINS is dynamic and evolves as the neuroimaging field grows. COINS consists of the following collaboration-centric tools: * Subject and Study Management: MICIS (Medical Imaging Computer Information System) is a centralized PostgreSQL-based web application that implements best practices for participant enrollment and management. Research site administrators can easily create and manage studies, as well as generate reports useful for reporting to funding agencies. * Scan Data Collection: An automated DICOM receiver collects, archives, and imports imaging data into the file system and COINS, requiring no user intervention. The database also offers scan annotation and behavioral data management, radiology review event reports, and scan time billing. * Assessment Data Collection: Clinical data gathered from interviews, questionnaires, and neuropsychological tests are entered into COINS through the web application called Assessment Manager (ASMT). ASMT's intuitive design allows users to start data collection with little or no training. ASMT offers several options for data collection/entry: dual data entry, for paper assessments, the Participant Portal, an online tool that allows subjects to fill out questionnaires, and Tablet entry, an offline data entry tool. * Data Sharing: De-identified neuroimaging datasets with associated clinical-data, cognitive-data, and associated meta-data are available through the COINS Data Exchange tool. The Data Exchange is an interface that allows investigators to request and share data. It also tracks data requests and keeps an inventory of data that has already been shared between users. Once requests for data have been approved, investigators can download the data directly from COINS. mri, fmri, neuropsychological assessment, neuroimaging, diffusion tensor imaging assay, magnetic resonance imaging assay, functional mri assay, diffusion magnetic resonance imaging, magnetoencephalography, electroencephalography, brain, behavior, data sharing, data management, clinical, computed tomography, magnetic resonance, single photon emission computed tomography, positron emission tomography, clinical assessment clinical neuroinformatics, image collection, mri 2d image, database application is used by: Consortium for Reliability and Reproducibility
is used by: DataLad
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is related to: NKI-RS Enhanced Sample
has parent organization: Mind Research Network
is parent organization of: MCIC
Aging NIBIB 1 R01 EB 000840;
NIBIB 1 R01 EB 006841;
NIBIB 1 R01 EB 005846
PMID:22275896 THIS RESOURCE IS NO LONGER IN SERVICE nlx_144067 http://www.nitrc.org/projects/coins SCR_000805 Mind Research Network - Collaborative Informatics and Neuroimaging Suite, Collaborative Informatics Neuroimaging Suite, Collaborative Informatics and Neuroimaging Suite 2026-08-09 09:03:02 20
Neal's DNA Mutation Site
 
Resource Report
Resource Website
1+ mentions
Neal's DNA Mutation Site (RRID:SCR_002947) Neal's DNA Mutation Site data analysis software, database, data or information resource, topical portal, portal, data processing software, software application, software resource This site provides access to mutation databases and software including the human hprt database, Human p53 database, Transgenic lacZ database, and Transgenic lacI database. Other avaialble programs include Mutational spectra comparison and relational database data entry. The most recent hprt database contains information on over 2,300 mutations found in vivo and in vitro in the human hprt gene and runs under Windows. The version for evaluation on this homepage has fewer mutations and is a DOS program. The database contains information on the mutagen, dose, spontaneous and induced mutant fraction, base position, amino acid position, amino acid change, local DNA sequence, cell type, citation, and other items. In addition, information regarding the cause and effect of mutations affecting splicing is given. Routines have been developed for the analysis of single base substitutions. The p53 database contains information on nearly 5,867 mutations found in the human p53 gene. The database itself has been updated in April of 1997. The database contains information on the cancer type, loss of heterozygosity, base position, amino acid position, amino acid change, local DNA sequence,citation, and other items. Routines have been developed for the analysis of single base substitutions. The Transgenic lacZ database contains information on 405 mutations found in vivo in the transgenic lacZ gene. It has last been updated in January of 1998. It provides information on the mutagen, dose, organ, mutant fraction, base position, amino acid position, amino acid change, local DNA sequence, citation, and other items. The Transgenic lacI database contains information on over 1700 mutations found in vivo in the transgenic lacI gene and on nearly 8000 mutations in the lacI gene in native E. coli. The database was updated in January 1998. The database contains information on the mutagen, dose, organ, mutant fraction, base position, amino acid position, amino acid change, local DNA sequence, citation, and other items. Routines have been developed for the analysis of single base substitutions for each of the databases. The software runs only on IBM-compatible PCs. human, mouse has parent organization: University of North Carolina at Chapel Hill; North Carolina; USA Free, Available for download, Freely available nif-0000-02995 SCR_002947 Human p53 Human hprt Rodent lacI and Rodent lacZ Databases and Software, Human p53 Human hprt Rodent lacI and Rodent lacZ Databases, Human p53 Human hprt Rodent lacI Rodent lacZ Databases 2026-08-09 09:03:36 4
Pathway Analysis Tool for Integration and Knowledge Acquisition
 
Resource Report
Resource Website
1+ mentions
Pathway Analysis Tool for Integration and Knowledge Acquisition (RRID:SCR_002100) PATIKA database, data or information resource, pathway analysis software The human pathway database which contains different biological entities and reactions and software tools for analysis. PATIKA Database integrates data from several sources, including Entrez Gene, UniProt, PubChem, GO, IntAct, HPRD, and Reactome. Users can query and access this data using the PATIKAweb query interface. Users can also save their results in XML or export to common picture formats. The BioPAX and SBML exporters can be used as part of this Web service. human, pathway, reaction, database, pathway analysis software, web service, biological entity, biological reaction uses: Entrez Gene
uses: UniProt
uses: PubChem
uses: Gene Ontology
uses: IntAct
uses: HPRD - Human Protein Reference Database
uses: Reactome
PMID:12117798
PMID:14960461
THIS RESOURCE IS NO LONGER IS SERVICE. nif-0000-20882 http://www.cs.bilkent.edu.tr/~patikaweb/ SCR_002100 Pathway Analysis Tool for Integration and Knowledge Acquisition (PATIKA), PATIKA - Pathway Analysis Tools for Integration and Knowledge Acquisition 2026-08-09 09:03:21 2
Monte Carlo Simulation Software: tMCimg
 
Resource Report
Resource Website
1+ mentions
Monte Carlo Simulation Software: tMCimg (RRID:SCR_002588) tMCimg simulation software, software application, software resource Software application that uses a Monte Carlo algorithm to model the transport of photons through 3D volumes with spatially varying optical properties. Both highly-scattering tissues (e.g. white matter) and weakly scattering tissues (e.g. cerebral spinal fluid) are supported. Using the anatomical information provided by MRI, X-ray CT, or ultrasound, accurate solutions to the photon migration forward problems are computed in times ranging from minutes to hours, depending on the optical properties and the computing resources available. c, computed tomography, macos, microsoft, modeling, monte carlo, magnetic resonance, optical imaging, posix/unix-like, windows, mri, x-ray ct, ultrasound, photon is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC) PMID:19424345 Free, Available for download, Freely available nlx_155993 http://www.nitrc.org/projects/tmcimg SCR_002588 Monte Carlo Photon Transport 2026-08-09 09:03:31 1
HCV Databases
 
Resource Report
Resource Website
50+ mentions
HCV Databases (RRID:SCR_002863) HCV Databases portal, data or information resource, disease-related portal, topical portal The Hepatitis C Virus (HCV) Database Project strives to present HCV-associated genetic and immunologic data in a user-friendly way, by providing access to the central database via web-accessible search interfaces and supplying a number of analysis tools. hcv, hepatitis c virus, hepatitis c, database, data analysis service, sequence, immunology, annotation, FASEB list has parent organization: HIV Databases
is parent organization of: HCV Sequence Database
is parent organization of: HCV Immunology Database
Hepatitis C NIAID Free, Freely available nif-0000-02944 SCR_002863 Hepatitis C Virus Database, Hepatitis C Virus Database Project, HCV Database, Hepatitis C Virus Databases, Hepatitis C Virus (HCV) Database Project 2026-08-09 09:03:35 71
Annotation Ontology
 
Resource Report
Resource Website
1+ mentions
Annotation Ontology (RRID:SCR_002862) AO data or information resource, controlled vocabulary, ontology Provides vocabulary for performing several types of annotation - comment, entities annotation (or semantic tags), textual annotation (classic tags), notes, examples, erratum... - on any kind of electronic document (text, images, audio, tables...) and document parts. AO is not providing any domain ontology but it is fostering the reuse of the existing ones for not breaking the principle of scalability of the Semantic Web. annotation, semantic tag, text mining, semantic web, standard is listed by: FORCE11
is related to: Annotea
is related to: W3C Open Annotation Community Group
is related to: DOMEO
has parent organization: Harvard Medical School; Massachusetts; USA
EMD Serono ;
Inc. ;
Eli Lilly and Company
PMID:21624159 Free, Freely available, Available for download nif-0000-02943 https://www.force11.org/node/4718 SCR_002862 AO - Annotation Ontology, annotation-ontology 2026-08-09 09:03:38 1
StatAlign
 
Resource Report
Resource Website
1+ mentions
StatAlign (RRID:SCR_001892) data analysis software, data processing software, software application, sequence analysis software, software resource Software package for Bayesian analysis of protein, DNA and RNA sequences. It utilizes multiple alignments, phylogenetic trees and evolutionary parameters to quantify uncertainty in these analyses. It is written in Java. software package, bayesian, protein, dna, rna, sequencing, java, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
PMID:23335014 Free, Available for download, Freely available biotools:StatAlign, OMICS_03743 https://bio.tools/StatAlign SCR_001892 StatAlign 2.0 2026-08-09 09:03:18 1
YLoc
 
Resource Report
Resource Website
10+ mentions
YLoc (RRID:SCR_002464) YLoc service resource, production service resource, web service, data analysis service, analysis service resource, software resource, data access protocol An interpretable web server for predicting subcellular localization. In addition to the predicted location, YLoc gives a reasoning why this prediction was made and which biological properties of the protein sequence lead to this prediction. Moreover, a confidence estimate helps users to rate predictions as trustworthy. YLoc+ is able to predict the location of multiple-targeted proteins with high accuracy. The YLoc webserver is also accessible via SOAP. subcellular localization, protein is listed by: OMICtools
has parent organization: University of Tubingen; Tubingen; Germany
PMID:20507917
PMID:20299325
Acknowledgement requested OMICS_01638 SCR_002464 Yloc - Interpretable Subcellular Localization Prediction 2026-08-09 09:03:35 36
MashMap
 
Resource Report
Resource Website
10+ mentions
MashMap (RRID:SCR_022194) alignment software, data processing software, software application, image analysis software, software resource Software tool as fast approximate aligner for long DNA sequences. Used for computing local alignment boundaries between long DNA sequences. mapping genome assembly, long DNA sequences, long reads, reference genome, long DNA sequences aligner NSF CCF1816027;
National Human Genome Research Institute ;
NIH
PMID:30423094
DOI:10.1007/978-3-319-56970-3_5
Free, Available for download, Freely available SCR_022194 2026-08-09 09:07:50 31
TORTOISE
 
Resource Report
Resource Website
100+ mentions
TORTOISE (RRID:SCR_001645) TORTOISE image processing software, data processing software, software application, image analysis software, software resource An integrated and flexible software package for processing of DTI data, and in general for the correction of diffusion weighted images to be used for DTI and potentially for high angular resolution diffusion imaging (HARDI) analysis. It can be run on both Linux and Mac platforms. It is composed of two modules named DIFF PREP and DIFF CALC. * DIFF_PREP - software for image resampling, motion, eddy current distortion and susceptibility induced EPI distortion corrections, and for re-orientation of data to a common space * DIFF_CALC - software for tensor fitting, error analysis, color map visualization and ROI analysis In addition, TORTOISE contains additional Utilities, such as a tool for the analysis of multi-center phantom data. diffusion mri, dti, image motion correction, distortion correction, tensor computation, visualization, analysis, tensor fitting, modeling, magnetic resonance, tensor metric is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is related to: Diffusion MRI of Traumatic Brain Injury
has parent organization: National Institute of Child Health and Human Development
NICHD Free, Available for download, Freely available nlx_153921 http://www.nitrc.org/projects/tortoise SCR_001645 Tolerably Obsessive Registration and Tensor Optimization Indolent Software Ensemble 2026-08-09 09:03:14 108

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