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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

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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
CoMUT
 
Resource Report
Resource Website
1+ mentions
CoMUT (RRID:SCR_027745) software library, software resource, software toolkit, source code Software Python library for creating comutation plots to visualize genomic and phenotypic information. Used for visualizing genomic and phenotypic information via comutation plots. genomic DNA, phenotype, visualizing genomic and phenotypic information, comutation plots, NCI R01 CA227388;
NCI R37 CA222574;
NCI U01 CA233100;
NIGMS T32 GM008313;
NSF
PMID:32502231 Free, Available for download, Freely available SCR_027745 2026-09-05 06:35:57 4
Conditional AutoRegressive Deconvolution
 
Resource Report
Resource Website
1+ mentions
Conditional AutoRegressive Deconvolution (RRID:SCR_026310) CARD software resource, software toolkit, source code Software R package for spatial transcriptomics. Deconvolution method that combines cell-type-specific expression information from single-cell RNA sequencing (scRNA-seq) with correlation in cell-type composition across tissue locations. Deconvolution method, spatial transcriptomics, cell-type-specific expression, single-cell RNA sequencing, cell-type composition across tissue locations, NHGRI R01HG011883;
NIGMS R01GM126553;
NIGMS R01GM144960
PMID:35501392 Free, Available for download, Freely available SCR_026310 , CARD: Conditional AutoRegressive Deconvolution, Conditional autoregressive-based deconvolution 2026-09-05 06:35:18 3
AutoDockTools
 
Resource Report
Resource Website
1000+ mentions
AutoDockTools (RRID:SCR_026401) ADT software application, software resource Software graphical user interface to help to set up which bonds will treated as rotatable in the ligand and to analyze dockings. Used for automated docking with selective receptor flexibility. Designed to predict how small molecules, such as substrates or drug candidates, bind to receptor of known 3D structure. automated docking, selective receptor flexibility, predict binding, bind to receptor of known 3D structure, ligand, analyze dockings NIGMS RO1 GM069832 PMID:19399780 Free, Available for download, Freely available https://autodock.scripps.edu/ SCR_026401 AutoDockTools: the Graphical User Interface for AutoDock 2026-09-05 06:35:21 2063
NucleAIzer
 
Resource Report
Resource Website
1+ mentions
NucleAIzer (RRID:SCR_026500) software resource, source code Software tool as parameter-free deep learning framework for nucleus segmentation using image style transfer. Cell segmentation tool. nucleus segmentation, image style transfer, Academy of Finland ;
European Regional Development Funds ;
NIGMS R35 GM122547;
Swedish Research Council
DOI:10.1016/j.cels.2020.04.003 Free, Available for download, Freely available SCR_026500 2026-09-05 06:35:23 4
Mitochondrial Function and In Vivo Imaging Core
 
Resource Report
Resource Website
Mitochondrial Function and In Vivo Imaging Core (RRID:SCR_028891) MF-II Core access service resource, core facility, service resource The Mitochondrial Function and In Vivo Imaging (MF-II) Core provides specialized expertise, advanced instrumentation, and comprehensive services for assessing mitochondrial function, metabolism, cardiopulmonary physiology, and in vivo structure and function. The Core supports cardiovascular, pulmonary, and vascular research through high-resolution metabolic and mitochondrial analyses, noninvasive imaging, hemodynamic assessment, and established preclinical disease models. The MF-II Core works collaboratively with investigators to provide experimental design consultation, technical expertise, data acquisition, and analysis to generate high-quality, reproducible data. Mitochondrial Function, Mitochondrial Bioenergetics, Cellular Metabolism, Oxygen Consumption, Glycolysis, High-Resolution Respirometry, Seahorse XFe96, Oroboros, Echocardiography, Cardiac Function, Hemodynamics, In Vivo Imaging, Micro-CT, PET Imaging, Laser Doppler, Cardiopulmonary Physiology, Preclinical Imaging, Animal Models, Pulmonary Hypertension, Cardiovascular Biology NIGMS P30GM149398 SCR_028891 2026-09-05 06:36:21 0
Structure-function linkage database
 
Resource Report
Resource Website
10+ mentions
Structure-function linkage database (RRID:SCR_001375) SFLD data or information resource, database A database of hierarchical classification of enzymes that relates specific sequence-structure features to specific chemical capabilities. The SFLD classifies evolutionarily related enzymes according to shared chemical functions and maps these shared functions to conserved active site features. The classification is hierarchical, where broader levels encompass more distantly related proteins with fewer shared features. It thus serves as the analysis and archive site for superfamilies targeted by the Enzyme Function Initiative, and is developed by the Babbitt Laboratory in collaboration with the UCSF Resource for Biocomputing, Visualization, and Informatics. The resource also provides a collection of tools and data for investigating sequence-structure-function relationships and hypothesizing function. software, enzyme, structure-function relationship, blast, reaction, superfamily, hidden markov model, sequence alignment, protein similarity network, sequence, structure, function uses: UCSF Chimera
has parent organization: Resource for Biocomputing Visualization and Informatics
NIGMS R01GM60595;
NIGMS P01GM071790;
NIGMS U54GM093342
PMID:18428763
PMID:16489747
Free, Freely available, nlx_152532 SCR_001375 2026-09-05 06:24:34 18
Sherlock
 
Resource Report
Resource Website
50+ mentions
Sherlock (RRID:SCR_001628) Sherlock data or information resource, service resource Service to discover disease genes in GWAS using eQTL signature matching by simply submitting your list of GWAS associations (SNPs and p-values). It is important to upload all SNPs in your association study, not just the top hits. Sherlock may be able to group multiple lower-confidence SNPs to discover functionally-important genes. genome-wide association study, expression quantitative trait locus, disease gene, snp, gene expression, gene, disease, association, p-value, cis, trans, genetic variation, mapping, phenotype, FASEB list has parent organization: University of California at San Francisco; California; USA NIGMS R01GM070808;
NIGMS U19GM61390;
NIGMS P50 GM081879
PMID:23643380 Free, Freely available nlx_153895 SCR_001628 2026-09-05 06:24:36 90
ALFRED
 
Resource Report
Resource Website
50+ mentions
ALFRED (RRID:SCR_001730) ALFRED data or information resource, data repository, database, service resource, storage service resource A public curated compilation of allele frequency data on anthropologically defined human population samples linked to the molecular genetics-human genome databases. Only data on well defined population samples that are large enough to yield reasonably accurate frequencies and for polymorphisms sufficiently defined to be replicable can be included in ALFRED. Researchers wishing to have their data entered into ALFRED should contact them. Initially, ALFRED contained primarily data generated in the laboratories of K.K. and J.R. Kidd in the Department of Genetics at Yale, including extensive unpublished data. Data from the published literature are being entered into ALFRED in a systematic way, with a focus on polymorphisms studied in many different populations. ALFRED is distinct from such databases as dbSNP, which catalogs sequence variation. ALFRED's focus is on allele frequencies in diverse anthropologically defined populations. It is not a compendium of human DNA polymorphisms but of frequencies of selected polymorphisms with an emphasis on those that have been studied in multiple populations. All of the data in ALFRED are considered to be in the public domain and available for use in research and teaching. ALFRED provides easy searching options including versatile "Keyword search" and also has numerous summary tables providing quick overviews of contents by chromosome, population, average heterozygosity, Fst and others, all available under various tabs from the ALFRED homepage. allele frequency, dna polymorphism, haplotype, high throughput, genome, population, sample, education, polymorphism, allele, chromosome, heterozygosity, fst, loci, pathway, genetics, FASEB list has parent organization: Yale School of Medicine; Connecticut; USA NIGMS P01GM 57672 PMID:19325849
PMID:11125124
PMID:12209575
Free, Freely Available nif-0000-02541, r3d100012700 https://doi.org/10.17616/R3GZ2J SCR_001730 The ALlele FREquency Database, ALlele FREquency Database 2026-09-05 06:24:38 74
ASAP
 
Resource Report
Resource Website
50+ mentions
ASAP (RRID:SCR_001849) ASAP data or information resource, data repository, database, service resource, storage service resource Database and web interface developed to store, update and distribute genome sequence data and gene expression data. ASAP was designed to facilitate ongoing community annotation of genomes and to grow with genome projects as they move from the preliminary data stage through post-sequencing functional analysis. The ASAP database includes multiple genome sequences at various stages of analysis, and gene expression data from preliminary experiments. Use of some of this preliminary data is conditional, and it is the users responsibility to read the data release policy and to verify that any use of specific data obtained through ASAP is consistent with this policy. There are four main routes to viewing the information in ASAP: # a summary page, # a form to query the genome annotations, # a form to query strain collections, and # a form to query the experimental data. Navigational buttons appear on every page allowing users to jump to any of these four points., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene expression, genome, genome sequence, multiple genome sequence, post sequencing functional analysis, preliminary experiment, blast, annotation, data analysis service is used by: NIF Data Federation
is listed by: SoftCite
is related to: AmiGO
has parent organization: University of Wisconsin-Madison; Wisconsin; USA
USDA 2001-52100-11316;
NIGMS GM62994-02;
NIGMS GM35682-15A1
PMID:12519969 Free, Freely available nif-0000-02571, r3d100010666 https://omictools.com/asap-3-tool SCR_001849 A Systematic Annotation Package for Community Analysis of Genome, ASAP: a systematic annotation package for community analysis of genomes, A systematic annotation package for community analysis of genomes 2026-09-05 06:24:40 53
PhosphoSitePlus: Protein Modification Site
 
Resource Report
Resource Website
1000+ mentions
PhosphoSitePlus: Protein Modification Site (RRID:SCR_001837) PSP data or information resource, knowledge environment resource, portal A freely accessible on-line systems biology resource devoted to all aspects of protein modification, as well as other post-translational modifications. It provides valuable and unique tools for both cell biologists and mass spectroscopists. PhosphoSite is a human- and mouse-centric database. It includes features such as: viewing the locations of modified residues on molecular models; browsing and searching MS2 records by disease, tissue, and cell line; submitting lists of peptides to identify previously reported genes; searching by sub-cellular localization, treatment, tissues, cell types, cell lines and diseases, and protein types and protein domains; searching for experimentally-verified kinase substrates and viewing preferred substrate motifs; and viewing MS2 spectra for peptides and sites not previously published. portal, mass spectroscopist, molecular model, mouse, post translational, subcellular localization, protein modification, post-translational modification, protein phosphorylation, protein structure, protein function, ubiquitinylation, acetylation, cellular component, cell type, visualization, data repository, bio.tools, FASEB list is listed by: bio.tools
is listed by: Debian
is related to: Cytoscape
is related to: ConsensusPathDB
has parent organization: Cell Signaling Technology
NCI ;
NIAAA R44 AA014848;
NIGMS R43 GM65768
PMID:22135298 Free, Freely available biotools:phosphositeplus, nif-0000-10399 https://bio.tools/phosphositeplus SCR_001837 PhosphoSitePlus, PhosphoSite 2026-09-05 06:24:40 1003
SPP
 
Resource Report
Resource Website
1+ mentions
SPP (RRID:SCR_001790) data analysis software, data processing software, software application, software resource R analysis and processing package for Illumina platform Chip-Seq data. chip seq data, illummina, r package, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
NHGRI U01HG004258;
NIGMS R01GM082798;
NCRR UL1RR024920
DOI:10.1038/nbt.1508 Free, Available for download, Freely available OMICS_00425, biotools:spp https://bio.tools/spp https://sites.google.com/a/brown.edu/bioinformatics-in-biomed/spp-r-from-chip-seq SCR_001790 SPP Package 2026-09-05 06:24:39 9
BioCyc
 
Resource Report
Resource Website
1000+ mentions
BioCyc (RRID:SCR_002298) data or information resource, database A collection of Pathway/Genome Databases which describes the genome and metabolic pathways of a single organism. The BioCyc collection of Pathway/Genome Databases (PGDBs) provides an electronic reference source on the genomes and metabolic pathways of sequenced organisms. BioCyc PGDBs are generated by software that predicts the metabolic pathway complements of completely sequenced organisms from their genome sequences. They also include the results of a number of other computational inference procedures applied to these genomes, including predictions of which genes code for missing enzymes in metabolic pathways, and predicted operons. The BioCyc Web site provides a suite of software tools for database searching and visualization, for omics data analysis, and for comparative genomics and comparative pathway questions. The databases within the BioCyc collection are organized into tiers according to the amount of manual review and updating they have received. Tier 1 PGDBs have been created through intensive manual efforts, and receive continuous updating. Tier 2 PGDBs were computationally generated by the PathoLogic program, and have undergone moderate amounts of review and updating. Tier 3 PGDBs were computationally generated by the PathoLogic program, and have undergone no review and updating. There are 967 DBs in Tier 3. The downloadable version of BioCyc that includes the Pathway Tools software provides more speed and power than the BioCyc Web site. database, pathway/genome databases, PGDB, genome, metabolic pathway, microbiome, FASEB list uses: Pathway Tools
is used by: PathCase Pathways Database System
lists: Pathway Tools
lists: EcoCyc
lists: MetaCyc
lists: HumanCyc: Encyclopedia of Homo sapiens Genes and Metabolism
is listed by: LabWorm
is listed by: Human Microbiome Project
is related to: Pathway Tools
is related to: PathCase Pathways Database System
is related to: EcoCyc
is related to: MetaCyc
is related to: HumanCyc: Encyclopedia of Homo sapiens Genes and Metabolism
is related to: EcoCyc
is related to: Gramene
is related to: NCBI BioSystems Database
is related to: KOBAS
is related to: Tuberculosis Database
is related to: Pathway Tools
has parent organization: Stanford Research Institute International
NIGMS GM080746 PMID:16246909 Restricted nif-0000-00369, r3d100011259 https://doi.org/10.17616/R36G8H SCR_002298 BioCyc Database Collection 2026-09-05 06:24:46 1063
Community Structure-Activity Resource
 
Resource Report
Resource Website
10+ mentions
Community Structure-Activity Resource (RRID:SCR_002206) CSAR data or information resource, data repository, data set, service resource, storage service resource Experimental datasets of crystal structures and binding affinities for diverse protein-ligand complexes. Some datasets are generated in house while others are collected from the literature or deposited by academic labs, national centers, and the pharmaceutical industry. For the community to improve their approaches, they need exceptional datasets to train scoring functions and develop new docking algorithms. They aim to provide the highest quality data for a diverse collection of proteins and small molecule ligands. They need input from the community in developing target priorities. Ideal targets will have many high-quality crystal structures (apo and 10-20 bound to diverse ligands) and affinity data for 25 compounds that range in size, scaffold, and logP. It is best if the ligand set has several congeneric series that span a broad range of affinity, with low nanomolar to mid-micromolar being most desirable. They prefer Kd data over Ki data over IC50 data (no % activity data). They will determine solubility, pKa, logP/logD data for the ligands whenever possible. They have augmented some donated IC50 data by determining Kon/Koff and ITC data. crystal structure, binding affinity, protein-ligand complex, protein, small molecule, ligand, compound is used by: NIF Data Federation
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
has parent organization: University of Michigan; Ann Arbor; USA
NIGMS THIS RESOURCE IS NO LONGER IN SERVICE nlx_154720 SCR_002206 2026-09-05 06:24:45 16
Simtk.org
 
Resource Report
Resource Website
10+ mentions
Simtk.org (RRID:SCR_002680) SimTK simulation software, software application, software repository, software resource A National NIH Center for Biomedical Computing that focuses on physics-based simulation of biological structures and provides open access to high quality simulation tools, accurate models and the people behind them. It serves as a repository for models that are published (as well as the associated code) to create a living archive of simulation scholarship. Simtk.org is organized into projects. A project represents a research endeavor, a software package or a collection of documents and publications. Includes sharing of image files, media, references to publications and manuscripts, as well as executables and applications for download and source code. Simulation tools are free to download and space is available for developers to manage, share and disseminate code. model, modeling, rna folding, protein folding, myosin dynamics, neuromuscular biomechanics, cardiovascular dynamics, biomolecular simulation, biomedical computing, repository, cardiovascular, neuromuscular, myosin, rna, simulation, biocomputation is used by: NIF Data Federation
lists: Adaptively Sampled Particle Fluids
lists: OpenMM
lists: CPODES numerical integrator
is listed by: Biositemaps
is listed by: Integrated Models
is listed by: DataCite
is listed by: re3data.org
is related to: OpenSim
is related to: Simbody(tm): SimTK Multibody Dynamics Toolset
is related to: SimVascular
is related to: SAFA Footprinting Software
is related to: Ion Simulator Interface
is related to: LAPACK linear algebra library
is related to: Neuromuscular Models Library
has parent organization: Simbios
is parent organization of: FEATURE
is parent organization of: Cardiovascular Model Repository
is parent organization of: ConTrack
is parent organization of: Allopathfinder
is parent organization of: Molecular Simulation Trajectories Archive of a Villin Variant
is parent organization of: LAPACK linear algebra library
is parent organization of: SimTKCore
NIH ;
NIGMS U54 GM072970
Free, Available for download, Freely available nif-0000-23302, DOI:10.17616/R3QJ4B, DOI:10.18735 https://doi.org/10.17616/R3QJ4B, https://doi.org/10.17616/r3qj4b, https://doi.org/10.18735/, https://dx.doi.org/10.18735/ SCR_002680 Simulation Toolkit, SimTK - the Simulation Toolkit 2026-09-05 06:24:51 20
BioPortal
 
Resource Report
Resource Website
100+ mentions
BioPortal (RRID:SCR_002713) BioPortal controlled vocabulary, data or information resource, data repository, ontology, repository, service resource, storage service resource Open repository of biomedical ontologies that provides access via Web browsers and Web services to ontologies. It supports ontologies in OBO format, OWL, RDF, Rich Release Format (RRF), Protege frames, and LexGrid XML. Functionality includes the ability to browse, search and visualize ontologies as well as to comment on, and create mappings for ontologies. Any registered user can submit an ontology. The NCBO Annotator and NCBO Resource Index can also be accessed via BioPortal. Additional features: * Add Reviews: rate the ontology according to several criteria and describe your experience using the ontology. * Add Mappings: submit point-to-point mappings or upload bulk mappings created with external tools. Notification of new Mappings is RSS-enabled and Mappings can be browsed via BioPortal and accessed via Web services. * NCBO Annotator: Tool that tags free text with ontology terms. NCBO uses the Annotator to generate ontology annotations, creating an ontology index of these resources accessible via the NCBO Resource Index. The Annotator can be accessed through BioPortal or directly as a Web service. The annotation workflow is based on syntactic concept recognition (using the preferred name and synonyms for terms) and on a set of semantic expansion algorithms that leverage the ontology structure (e.g., is_a relations). * NCBO Resource Index: The NCBO Resource Index is a system for ontology based annotation and indexing of biomedical data; the key functionality of this system is to enable users to locate biomedical data linked via ontology terms. A set of annotations is generated automatically, using the NCBO Annotator, and presented in BioPortal. This service uses a concept recognizer (developed by the National Center for Integrative Biomedical Informatics, University of Michigan) to produce a set of annotations and expand them using ontology is_a relations. * Web services: Documentation on all Web services and example code is available at: BioPortal Web services. biomedical, thesaurus, ontology mapping, annotation, metadata standard, ontology repository, portal, web service, obo, owl, rdf, rrf protege frame, lexgrid xml lists: MeGO
lists: Porifera Ontology
lists: EnvO
lists: Research Network and Patient Registry Inventory Ontology
lists: Semantic DICOM Ontology
lists: Time Event Ontology
lists: Variation Ontology
lists: Vertebrate Skeletal Anatomy Ontology
lists: Epoch Clinical Trial Ontology
lists: Gazetteer
lists: Human Disease Ontology
lists: Information Artifact Ontology
lists: NCBITaxon
lists: Amphibian Taxonomy Ontology
lists: Anatomic Pathology Lexicon
lists: HIV ontology
lists: International Classification of Primary Care - 2 PLUS
lists: Mathematical Modelling Ontology
lists: Nursing Interventions Classification
lists: Phylogenetic Ontology
lists: Bleeding History Phenotype Ontology
lists: Body System Terms from ICD11
lists: Synthetic Biology Open Language Visual Ontology
lists: Teleost Anatomy Ontology
lists: Teleost Taxonomy Ontology
lists: ECO
lists: Bioassay Ontology
lists: RightField
lists: Gene Ontology
lists: HGNC
lists: Interaction Ontology
lists: International Classification for Nursing Practice
lists: Spider Ontology
lists: Vertebrate Trait Ontology
lists: Mental Functioning Ontology
lists: Ascomycete Phenotype Ontology
lists: Beta Cell Genomics Ontology
lists: Biological Collections Ontology
lists: Chemical Methods Ontology
lists: Chemical Information Ontology
lists: Common Anatomy Reference Ontology
lists: Experimental Conditions Ontology
lists: Dictyostelium Discoideum Anatomy Ontology
lists: Fission Yeast Phenotype Ontology
lists: Fly Taxonomy
lists: FlyBase Controlled Vocabulary
lists: Hymenoptera Anatomy Ontology
lists: Influenza Ontology
lists: Lipid Ontology
lists: Kinetic Simulation Algorithm Ontology
lists: Malaria Ontology
lists: FMA
lists: Minimal Anatomical Terminology
lists: NEMO Ontology
lists: Ontology for Genetic Interval
lists: Ontology for Parasite LifeCycle
lists: Ontology of Adverse Events
lists: Ontology of Medically Related Social Entities
lists: Ontology of Vaccine Adverse Events
lists: Rat Strain Ontology
lists: Plant Environmental Conditions
lists: Plant Trait Ontology
lists: Population and Community Ontology
lists: RNA Ontology
lists: Rat Strain Ontology
lists: Subcellular Anatomy Ontology
lists: Software Ontology
lists: Suggested Ontology for Pharmacogenomics
lists: Vertebrate Taxonomy Ontology
lists: PharmGKB Ontology
lists: Physico-Chemical Process
lists: International Classification for Patient Safety
lists: Adverse Event Reporting Ontology
lists: Experimental Factor Ontology
lists: Mass Spectrometry Ontology
lists: Master Drug Data Base Clinical Drugs
lists: Medaka Fish Anatomy and Development Ontology
lists: Medical Diagnostic Categories - Diagnosis Related Groups
lists: Medical Dictionary for Regulatory Activities
lists: Minimal Standard Terminology of Digestive Endoscopy
lists: Minimal Standard Terminology of Digestive Endoscopy - French
lists: Ontology of Physical Exercises
lists: Mosquito Gross Anatomy Ontology
lists: Systematized Nomenclature of Medicine - International Version
lists: Mosquito Insecticide Resistance Ontology
lists: Mouse Experimental Design Ontology
lists: Mouse Gross Anatomy and Development Ontology
lists: Systematized Nomenclature of Medicine - Clinical Terms
lists: Systems Chemical Biology and Chemogenomics Ontology
lists: Mouse Pathology Ontology
lists: NIF Cell Ontology
lists: NHS Quality Indicators
lists: Neural-Immune Gene Ontology
lists: Ontology of Physics for Biology
lists: Cell Type Ontology
lists: Xenopus Anatomy Ontology
lists: SO
lists: Ontology of Pneumology
lists: Open Biological and Biomedical Ontologies Relationship Types
lists: Biomedical Resource Ontology
lists: MGED Ontology
lists: Pharmacovigilance Ontology
lists: PhenX Phenotypic Terms
lists: Bioinformatics Web Service Ontology
lists: SysMO JERM Ontology of Systems Biology for Micro-Organisms
lists: MeSH
lists: PATO
lists: BFO
lists: MPO
lists: PR
lists: Cereal Plant Development Ontology
lists: PhenomeBLAST Ontology
lists: VIVO
lists: Computer Assisted Brain Injury Rehabilitation Ontology
lists: Computer Retrieval of Information on Scientific Projects Thesaurus
lists: NIFSTD
lists: Cell Line Ontology
lists: Student Health Record Ontology
lists: Zebrafish Anatomical Ontology
lists: Physical Medicine and Rehabilitation
lists: Randomized Controlled Trials Ontology
lists: Human Phenotype Ontology
lists: Read Codes Clinical Terms Version 3
lists: Reference Sequence Annotation
lists: Regulation of Gene Expression Ontolology
lists: Neurobehavior Ontology
lists: Regulation of Transcription Ontology
lists: Reproductive Trait and Phenotype Ontology
lists: Skin Physiology Ontology
lists: Vaccine Ontology
lists: OMIM
lists: MedlinePlus
lists: Adult Mouse Anatomy Ontology
lists: Bone Dysplasia Ontology
lists: Bone and Cartilage Tissue Engineering Ontology
lists: Botryllus schlosseri anatomy and development ontology
lists: EDAM Ontology
lists: LexGrid
lists: RxNorm
lists: Breast Cancer Grading Ontology
lists: Breast Tissue Cell Lines Ontology
lists: SBO
lists: Resource of Asian Primary Immunodeficiency Diseases Phenotype Ontology
lists: Brucellosis Ontology
lists: Sleep Domain Ontology
lists: C. elegans Development Vocabulary
lists: Physician Data Query
lists: C. elegans Gross Anatomy Vocabulary
lists: Plant Ontology
lists: C. elegans Phenotype Vocabulary
lists: CPTAC Proteomics Pipeline Infrastructure Ontology
lists: Cancer Research and Management ACGT Master Ontology
lists: Cancer Chemoprevention Ontology
lists: Cell Behavior Ontology
lists: Cereal Plant Gross Anatomy Ontology
lists: Cardiac Electrophysiology Ontology
lists: Cerebrotendinous Xanthomatosis Ontology
lists: Cell Cycle Ontology
lists: Cell Culture Ontology
lists: Cerrado concepts and plant community dynamics
lists: Clinical Signs and Symptoms Ontology
lists: Clusters of Orthologous Groups Analysis Ontology
lists: Computational Neuroscience Ontology
lists: BIRNLex
lists: Computer-Based Patient Record Ontology
lists: Congenital Heart Defects Ontology
lists: Drug Interaction Knowledge Base Ontology
lists: Healthcare Common Procedure Coding System
lists: Host Pathogen Interactions Ontology
lists: Human Dermatological Disease Ontology
lists: Solanaceae Phenotype Ontology
lists: Soy Ontology
lists: Spatial Ontology
lists: Surgical Secondary Events
lists: eagle-i research resource ontology
lists: Biological Pathways Exchange
lists: Autism Spectrum Disorder Phenotype Ontology
lists: BRENDA Tissue and Enzyme Source Ontology
lists: BioTop Ontology
lists: Family Health History Ontology
lists: International Classification of Diseases Version 9 - Clinical Modification
lists: BioModels Ontology
lists: Bilingual Ontology of Alzheimer
lists: BioPortal Metadata Ontology
lists: Biochemical Substructure Ontology
lists: Biodiversity Ontology
lists: Biological Imaging Methods Ontology
lists: International Classification of Functioning Disability and Health
lists: Biologie Hors Nomenclature
lists: International Classification of Primary Care
lists: Biomedical Research Integrated Domain Group Model
lists: KB Bio 101
lists: Bionutrition Ontology
lists: Artificial Intelligence Rheumatology Consultant System Ontology
lists: Leukocyte Surface Marker Ontology
lists: Cell Line Ontology by Mahadevan
lists: Cellular microscopy phenotype ontology
lists: ABA Adult Mouse Brain Ontology
lists: AEO
lists: African Traditional Medicine Ontology
lists: Alzheimer's disease ontology
lists: Amino Acid Ontology
lists: Amphibian Gross Anatomy Ontology
lists: Animal Natural History and Life History Ontology
lists: Coding Symbols for a Thesaurus of Adverse Reaction Terms
lists: Cognitive Atlas Ontology
lists: Common Terminology Criteria for Adverse Events
lists: Comparative Data Analysis Ontology
lists: Content Archive Resource Exchange Lexicon
lists: Crop Ontology
lists: Current Procedural Terminalogy Hierarchy
lists: Current Procedural Terminology
lists: DICOM Controlled Terminology
lists: Dataset processing
lists: Dengue Fever Ontology
lists: Dermatology Lexicon
lists: Diagnosis Ontology of Clinical Care Classification
lists: Diagnostic Ontology
lists: Disease core ontology applied to Rare Diseases
lists: Dispedia Core Ontology
lists: Drosophila Development Ontology
lists: Drosophila Gross Anatomy Ontology
lists: EDDA Study Design Terminology
lists: Electrocardiography Ontology
lists: Eligibility Feature Hierarchy
lists: Enzyme Mechanism Ontology
lists: Enzyme Reaction Ontology for partial chemical perspectives
lists: Epilepsy Ontology
lists: Loggerhead Nesting Ontology
lists: Fanconi Anemia Ontology
lists: Fire Ontology
lists: Flora Phenotype Ontology
lists: Fungal Gross Anatomy Ontology
lists: Human Developmental Anatomy Ontology abstract version 1
lists: G Protein-Coupled Receptor BioAssays Ontology
lists: Galen Ontology
lists: Gene Expression Ontology
lists: Gene Ontology Extension
lists: General Formal Ontology
lists: General Formal Ontology for Biology
lists: Genome Component Ontology
lists: Genomic Clinical Decision Support Ontology
lists: GeoSpecies Ontology
lists: Glycomics Ontology
lists: Habronattus Courtship Ontology
lists: Health Indicator Ontology
lists: Health Level Seven Reference Implementation Model Version 3
lists: Human Developmental Anatomy Ontology abstract version 2
lists: Human Developmental Anatomy Ontology timed version
lists: Human Interaction Network Ontology
lists: Human Physiology Simulation Ontology
lists: Logical Observation Identifier Names and Codes
lists: IMGT-ONTOLOGY
lists: Image and Data Quality Assessment Ontology
lists: Immune Disorder Ontology
lists: Infectious Disease Ontology
lists: InterNano Nanomanufacturing Taxonomy
lists: Interaction Network Ontology
lists: International Classification of External Causes of Injuries
lists: International Classification of Diseases Version 10
lists: International Classification of Diseases Version 10 - Clinical Modification
lists: International Classification of Diseases Version 10 - Procedure Coding System
lists: MR dataset acquisition
lists: Maize Gross Anatomy Ontology
lists: Major Histocompatibility Complex Ontology
lists: Medical image simulation
lists: Menelas Project Top-Level Ontology
lists: Mental State Assessment
lists: Metagenome Sample Vocabulary
lists: Metagenome and Microbes Environmental Ontology
lists: MicroRNA Ontology
lists: Microbial Culture Collection Vocabulary
lists: Microbial Typing Ontology
lists: Minimal Information about any Sequence Controlled Vocabularies
lists: Minimal Information about any Sequence Ontology
lists: NIF Dysfunction Ontlogy
lists: NIF Subcellular Ontology
lists: NMR-Instrument Component of Metabolomics Investigations Ontology
lists: Name Reaction Ontology
lists: NanoParticle Ontology
lists: National Cancer Institute Thesaurus
lists: National Drug Data File
lists: National Drug File - Reference Terminology
lists: Natural Products Ontology
lists: Neglected Tropical Disease Ontology
lists: Neomark Oral Cancer Ontology version 3
lists: Neomark Oral Cancer Ontology version 4
lists: Neural Motor Recovery Ontology
lists: NeuroMorpho.Org species ontology
lists: NeuroMorpho.Org species ontology old
lists: Non-Randomized Controlled Trials Ontology
lists: Nursing Care Coordination Ontology
lists: Ontological Knowledge Base Model for Cystic Fibrosis
lists: Ontology for Drug Discovery Investigations
lists: Ontology for General Medical Science
lists: Ontology for Genetic Disease Investigations
lists: Ontology for Genetic Susceptibility Factor
lists: Ontology for MicroRNA Target Prediction
lists: Symptom Ontology
lists: Ontology for Newborn Screening Follow-up and Translational Research
lists: Ontology of Alternative Medicine French
lists: Ontology of Biological and Clinical Statistics
lists: Ontology of Clinical Research
lists: Ontology of Core Data Mining Entities
lists: Ontology of Data Mining Investigations
lists: Pediatric Terminology
lists: Ontology of Experimental Variables and Values
lists: Ontology of General Purpose Datatypes
lists: Ontology of Geographical Region
lists: Ontology of Glucose Metabolism Disorder
lists: Ontology of Homology and Related Concepts in Biology
lists: Ontology of Language Disorder in Autism
lists: Orphanet Rare Disease Ontology
lists: Parasite Experiment Ontology
lists: Pathogen Transmission Ontology
lists: Pathogenic Disease Ontology
lists: Pharmacogenomic Relationships Ontology
lists: Physico-Chemical Methods and Properties
lists: Plant Anatomy
lists: Syndromic Surveillance Ontology
lists: Plant Structure Development Stage
lists: Portfolio Management Application
lists: Protein Modification Ontology
lists: Protein-Protein Interaction Ontology
lists: Proteomics Data and Process Provenance Ontology
lists: Provenance Ontology
lists: QUDT
lists: Quantitative Imaging Biomarker Ontology
lists: Radiology Lexicon
lists: Robert Hoehndorf Version of MeSH
lists: Role Ontology
lists: STATistics Ontology
lists: Sage Bionetworks Synapse Ontology
lists: Sample Processing and Separation Techniques Ontology
lists: Santa Barbara Coastal Observation Ontology
lists: Semantic Types Ontology
lists: Semantic Web for Earth and Environment Technology Ontology
lists: Semanticscience Integrated Ontology
lists: Single-Nucleotide Polymorphism Ontology
lists: Situation-Based Access Control Ontology
lists: Taxonomic Rank Vocabulary
lists: Taxonomy for Rehabilitation of Knee Conditions
lists: Terminological and Ontological Knowledge Resources Ontology
lists: Tick Gross Anatomy Ontology
lists: Tissue Microarray Ontology
lists: Traditional Medicine Constitution Value Set
lists: Traditional Medicine Meridian Value Sets
lists: Traditional Medicine Other Factors Value Set
lists: Traditional Medicine Signs and Symptoms Value Set
lists: Translational Medicine Ontology
lists: Tribolium Ontology
lists: Units Ontology
lists: Units of Measurement Ontology
lists: Upper-Level Cancer Ontology
lists: Vertebrate Homologous Organ Group Ontology
lists: Veterans Health Administration National Drug File
lists: Vital Sign Ontology
lists: WHO Adverse Reaction Terminology
lists: Web-Service Interaction Ontology
lists: Wheat Trait Ontology
lists: XEML Environment Ontology
lists: suicideo
lists: suicideonto
lists: Pseudogene
lists: Terminology for the Description of Dynamics
lists: Gene Regulation Ontology
lists: UBERON
lists: CHEBI
lists: Cognitive Paradigm Ontology
lists: Emotion Ontology
lists: Clinical Measurement Ontology
lists: Measurement Method Ontology
lists: NCI Thesaurus
lists: Ontology for Biomedical Investigations
lists: Biological Pathways Exchange
is listed by: Biositemaps
is listed by: FORCE11
is related to: Provisional Cell Ontology
has parent organization: National Center for Biomedical Ontology
has parent organization: Stanford University; Stanford; California
has parent organization: Stanford Center for Biomedical Informatics Research
is parent organization of: NCBO Annotator
NIGMS U24 GM143402 PMID:19483092
PMID:21672956
PMID:18999306
Free, Available for download, Freely available nif-0000-23346, r3d100012344 https://www.force11.org/node/4646, https://doi.org/10.17616/R3J362 SCR_002713 BioPortal Knowledgebase 2026-09-05 06:24:52 363
Molecular Simulation Trajectories Archive of a Villin Variant
 
Resource Report
Resource Website
Molecular Simulation Trajectories Archive of a Villin Variant (RRID:SCR_002704) Molecular Simulation Trajectories Archive of a Villin Variant d spatial image, data or information resource, data set An archive of hundreds of all-atom, explicit solvent molecular dynamics simulations that were performed on a set of nine unfolded conformations of a variant of the villin headpiece subdomain (HP-35 NleNle). It includes scripts for accessing the archive of villin trajectories as well as a VMD plug-in for viewing the trajectories. In addition, all starting structures used in the trajectories are also provided. The simulations were generated using a distributed computing method utilizing the symmetric multiprocessing paradigm for individual nodes of the Folding_at_home distributed computing network. The villin trajectories in the archive are divided into two projects: PROJ3036 and PROJ3037. PROJ3036 contains trajectories starting from nine non-folded configurations. PROJ3037 contains trajectories starting from the native (folded) state. Runs 0 through 8 (in PROJ3036) correspond to starting configurations 0 through 8 discussed in the paper in J. Mol. Biol. (2007) 374(3):806-816 (see the publications tab for a full reference), whereas RUN9 uses the same starting configuration as RUN8. Each run contains 100 trajectories (named clone 0-99), each with the same starting configuration but different random velocities. Trajectories vary in their length of time and are subdivided into frames, also known as a generation. Each frame contains around 400 configurational snapshots, or timepoints, of the trajectory, with the last configurational snapshot of frame i corresponding to the first configurational snapshot of generation i+1. The goal is to allow researchers to analyze and benefit from the many trajectories produced through the simulations. dynamic, atom, headpiece, molecular, simulation, solvent, protein folding, villin, molecule, trajectory, simulation, molecular dynamics trajectory is listed by: Biositemaps
has parent organization: Simtk.org
Stanford University; California; USA ;
Graduate Fellowship ;
NIH ;
NIGMS R01-GM062868;
NSF MCB-0317072
PMID:17950314 Acknowledgement requested, Available in Gromacs and PDB formats. nif-0000-23331 SCR_002704 2026-09-05 06:24:52 0
UCSF Chimera
 
Resource Report
Resource Website
1000+ mentions
UCSF Chimera (RRID:SCR_004097) Chimera d visualization software, data processing software, software application, software resource Software tool for interactive visualization and analysis of molecular structures and related data, including density maps, supramolecular assemblies, sequence alignments, docking results, trajectories, and conformational ensembles. High-quality images and animations can be generated. Chimera includes complete documentation and several tutorials. molecular modeling, electron microscopy, interactive visualization and analysis, molecular structures is used by: Structure-function linkage database
is listed by: 3DVC
is listed by: SoftCite
is related to: Integrative Modeling Platform
is related to: UCSF ChimeraX
is related to: UCSF ChimeraX
has parent organization: Resource for Biocomputing Visualization and Informatics
NCRR P41 RR001081;
NIGMS P41 GM103311
PMID:15264254 Restricted nlx_143560 http://plato.cgl.ucsf.edu/chimera/ SCR_004097 Chimera - an Extensible Molecular Modeling System, UCSF Chimera - an Extensible Molecular Modeling System 2026-09-05 06:25:14 2257
MEGA
 
Resource Report
Resource Website
1000+ mentions
MEGA (RRID:SCR_000667) MEGA, MEGA6, MEGA4, MEGA 4, MEGA 11 data analysis software, data processing software, sequence analysis software, software application, software resource, software toolkit Software integrated tool for conducting automatic and manual sequence alignment, inferring phylogenetic trees, mining web based databases, estimating rates of molecular evolution, and testing evolutionary hypotheses. Used for comparative analysis of DNA and protein sequences to infer molecular evolutionary patterns of genes, genomes, and species over time. MEGA version 4 expands on existing facilities for editing DNA sequence data from autosequencers, mining Web-databases, performing automatic and manual sequence alignment, analyzing sequence alignments to estimate evolutionary distances, inferring phylogenetic trees, and testing evolutionary hypotheses. MEGA version 6 enables inference of timetrees, as it implements RelTime method for estimating divergence times for all branching points in phylogeny. comparative, analysis, DNA, protein, sequence, molecular, evolution, pattern, gene, genome, evolution, FASEB list has parent organization: Pennsylvania State University Burroughs-Wellcome Fund ;
Japan Society for the Promotion of Science ;
NHGRI HG002096;
NHGRI HG006039;
NIGMS R01GM126567;
NIGMS R35GM139504;
NSF ABI 1661218
DOI:10.1093/molbev/msab120
PMID:24132122
PMID:31904846
PMID:22923298
PMID:21546353
PMID:17488738
PMID:15260895
PMID:11751241
PMID:8019868
Free, Available for download, Freely available SCR_023017, nlx_156838 https://www.megasoftware.net/mega4/ SCR_000667 MEGA11, Molecular Evolutionary Genetics Analysis, Molecular Evolutionary Genetics Analysis 6, Molecular Evolutionary Genetics Analysis 4 2026-09-05 06:24:23 2774
Transporter Classification Database
 
Resource Report
Resource Website
100+ mentions
Transporter Classification Database (RRID:SCR_004490) TCDB, TC analysis service resource, data analysis service, data analysis software, data or information resource, data processing software, data repository, database, production service resource, service resource, software application, software resource, source code, storage service resource Curated, relational database containing sequence, classification, structural, functional and evolutionary information about transport systems from variety of living organisms based on IUBMB-approved transporter classification (TC) system. Descriptions, TC numbers, and examples of over 600 families of transport proteins are provided. TC system is analogous to Enzyme Commission (EC) system for classification of enzymes, except that it incorporates both functional and phylogenetic information. TCDB users may submit their own sequenced proteins and descriptions for inclusion into database. The software tools used are all freely available for download. These programs are used for analysis of Protein and DNA sequences. Programs require UNIX server to run. membrane transport, protein sequence, transporter, bio.tools, FASEB list is recommended by: National Library of Medicine
is listed by: bio.tools
is listed by: Debian
has parent organization: University of California at San Diego; California; USA
NIGMS GM1077402 PMID:19022853
PMID:16381841
Free, Freely available nlx_47724, biotools:tcdb https://bio.tools/tcdb SCR_004490 Transporter Classification Database 2026-09-05 06:25:20 343
U-Compare
 
Resource Report
Resource Website
1+ mentions
U-Compare (RRID:SCR_004911) U-Compare data processing software, service resource, software application, software resource, text-mining software, workflow software An integrated text mining / natural language processing system based on the Unstructured Information Management Architecture (UIMA) Framework. It allows interoperability of text mining tools and allows the creation of text mining workflows, comparison and visualization of tools. U-Compare can be launched straight from the web or downloaded. As the name implies comparison of components and workflows is a central feature of the system. U-Compare allows sets of components to be run in parallel on the same inputs and then automatically generates statistics for all possible combinations of these components. Once a workflow has been created in U-Compare it can be exported and shared with other users or used with other UIMA compatible tools and so in addition to comparison, U-Compare also functions as a general purpose workflow creation tool. It contains a repository of 50+ biomedical text mining components. These components are included in the U-Compare single-click-to-launch package, ready to use by just drag-and-drop. You can also use this repository independent from the U-Compare system. Link with Taverna It has a link with Taverna for scientific workflows, http://bioinformatics.oxfordjournals.org/content/26/19/2486.abstract, where you can use U-Compare and its workflow from within the Taverna workflow. There are two ways, the U-Compare Taverna plugin and the U-Compare command line mode as a Taverna activity. We have recently integrated it with Peter Murray-Rust''''s OSCAR for Chemistry (see http://www.nactem.ac.uk/cheta/) Web Demo: http://www.nactem.ac.uk/software/cheta/ statistics, text mining, natural language processing, interoperability, comparison, workflow, computational linguistics is listed by: FORCE11
is related to: Taverna
is related to: Chemistry Using Text Annotations
is related to: Oscar3
has parent organization: University of Tokyo; Tokyo; Japan
has parent organization: National Centre for Text Mining
has parent organization: University of Colorado Denver; Colorado; USA
NIGMS R01 GM083649-04;
NLM R01 LM008111-07;
NIGMS R01GM083649;
NLM R01LM008111;
NLM R01LM009254
PMID:19414535 nlx_87780 SCR_004911 2026-09-05 06:25:26 5

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