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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
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University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis Immunology Core Resource Report Resource Website |
University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis Immunology Core (RRID:SCR_015409) | resource, access service resource, core facility, service resource | Core facility which provides a variety of assay services to evaluate cell-mediated and humoral responses to in animal models of gene therapies. | cell assay, assay service, gene therapy, animal model |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Pennsylvania Perelman School of Medicine; Pennsylvania; USA has parent organization: University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis is organization facet of: University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis |
Cystic Fibrosis | NIDDK P30DK047757 | Available to the research community | SCR_015409 | 2026-08-04 09:43:40 | 0 | ||||||||
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MMPC-University of Michigan Medical School Microvascular Complications Core Resource Report Resource Website |
MMPC-University of Michigan Medical School Microvascular Complications Core (RRID:SCR_015376) | resource, access service resource, core facility, service resource | Core which provides a complete range of microvascular phenotyping of murine models of diabetes, obesity and metabolic disease, including validated, reproducible and standardized phenotyping of the three major microvascular complications: diabetic polyneuropathy, nephropathy and retinopathy. | microvascular complications, dpn, dr, dn |
is listed by: NIDDK Information Network (dkNET) has parent organization: National Mouse Metabolic Phenotyping Centers has parent organization: University of Michigan; Ann Arbor; USA has parent organization: MMPC-University of Michigan Medical School is organization facet of: MMPC-University of Michigan Medical School |
NIDDK U2C-DK110768 | Available to the research community | SCR_015376 | 2026-08-04 09:43:39 | 0 | |||||||||
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MMPC-Vanderbilt University School of Medicine Metabolic Regulation Core Resource Report Resource Website |
MMPC-Vanderbilt University School of Medicine Metabolic Regulation Core (RRID:SCR_015377) | resource, access service resource, core facility, service resource | Core whose services include determining the components of energy balance with high precision and time resolution, providing robust imaging technology to monitor the dynamics of cellular process, and providing innovative mouse bariatric surgery models with application to basic and translational research. | pathophysiology, in vivo, metabolic core, metabolic imaging |
is listed by: NIDDK Information Network (dkNET) has parent organization: National Mouse Metabolic Phenotyping Centers has parent organization: MMPC-Vanderbilt University School of Medicine is organization facet of: MMPC-Vanderbilt University School of Medicine |
NIDDK U24 DK059637 | Available to the research community | SCR_015377 | 2026-08-04 09:43:38 | 0 | |||||||||
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MMPC-University of Massachusetts Medical School Humanized Mouse Cell Transplantation and Assessment Core Resource Report Resource Website |
MMPC-University of Massachusetts Medical School Humanized Mouse Cell Transplantation and Assessment Core (RRID:SCR_015372) | resource, access service resource, core facility, service resource | Core which provides humanized mice that enable clinically relevant in vivo studies of human cells, tissues, and immune system without putting patients at risk and expert in vivo functional analysis of transplanted human islets and stem cell-derived b-cells in immunodeficient mice that are highly valuable to the mouse research community. | mouse cell transportation, humanized mouse, cell assessment |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Massachusetts Medical School; Massachusetts; USA has parent organization: National Mouse Metabolic Phenotyping Centers has parent organization: University of Massachusetts Medical School Metabolic Disease Research Center Core Facility is organization facet of: University of Massachusetts Medical School Metabolic Disease Research Center Core Facility |
NIDDK UC2-DK093000 | Available to the research community | SCR_015372 | 2026-08-04 09:43:39 | 0 | |||||||||
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MMPC-University of Massachusetts Medical School Islet Core Resource Report Resource Website |
MMPC-University of Massachusetts Medical School Islet Core (RRID:SCR_015370) | resource, access service resource, core facility, service resource | Core which provides comprehensive in vivo, ex vivo, and in vitro analysis of pancreatic function and islet structure. Its services include mouse pancreas preparation for histological experiments, surgical isolation of mouse islets, and islet structural analysis. | islet, insulin, pancreatic function, islet structure |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Massachusetts Medical School; Massachusetts; USA has parent organization: National Mouse Metabolic Phenotyping Centers has parent organization: University of Massachusetts Medical School Metabolic Disease Research Center Core Facility is organization facet of: University of Massachusetts Medical School Metabolic Disease Research Center Core Facility |
NIDDK UC2-DK093000 | Available to the research community | SCR_015370 | 2026-08-04 09:43:38 | 0 | |||||||||
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UCSF Liver Center Immunology Core Resource Report Resource Website |
UCSF Liver Center Immunology Core (RRID:SCR_015596) | access service resource, core facility, service resource | Core that takes advantage of local expertise and resources to enable Center members to analyze cell populations in mouse or human livers. It performs complex analyses on small numbers of human cells, such as those obtained from liver biopsies. | immunology, single cell analysis, flow cytometry, QPCR |
is listed by: NIDDK Information Network (dkNET) has parent organization: UCSF Liver Center is organization facet of: UCSF Liver Center |
liver disease | NIDDK P30 DK026743 | Available to the research community | SCR_015596 | 2026-08-04 09:43:42 | 0 | ||||||||
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University of Chicago Digestive Diseases Research Core Center Host-Microbe Core Resource Report Resource Website 1+ mentions |
University of Chicago Digestive Diseases Research Core Center Host-Microbe Core (RRID:SCR_015603) | access service resource, core facility, service resource | Core that consists of two components: The Enteric Microbiology and The Gnotobiotic Mouse components. The Enteric Microbiology component offers novel screening and advanced technologies for compositional and functional profiling of the resident microbial communities in the gastrointestinal tract. The Gnotobiotic Mouse component enables investigators to study the effects and causal role of specific microorganisms or profiles in vivo. | host microbe, Enteric Microbiology, Gnotobiotic Mouse, inflammatory bowel diseases |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Chicago Digestive Diseases Research Core Center is organization facet of: University of Chicago Digestive Diseases Research Core Center |
digestive disease | NIDDK P30 DK042086 | Available to affiliated researchers, Available to DDRCC researchers | SCR_015603 | 2026-08-04 09:43:41 | 1 | ||||||||
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ANNOVAR Resource Report Resource Website 5000+ mentions |
ANNOVAR (RRID:SCR_012821) | ANNOVAR | software application, software resource | An efficient software tool to utilize update-to-date information to functionally annotate genetic variants detected from diverse genomes (including human genome hg18, hg19, as well as mouse, worm, fly, yeast and many others). Given a list of variants with chromosome, start position, end position, reference nucleotide and observed nucleotides, ANNOVAR can perform: 1. gene-based annotation. 2. region-based annotation. 3. filter-based annotation. 4. other functionalities. (entry from Genetic Analysis Software) | genomic analysis, imaging genomics, next generation sequencing, snp, gene, bio.tools |
is listed by: OMICtools is listed by: Genetic Analysis Software is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC) is listed by: Debian is listed by: bio.tools is listed by: SoftCite is related to: wANNOVAR has parent organization: OpenBioinformatics.org |
PMID:20601685 | Free | nlx_154225, biotools:annovar, OMICS_00165 | https://bio.tools/annovar, https://bio.tools/annovar | SCR_012821 | functional ANNOtation of genetic VARiants, ANNOVAR: Functional annotation of genetic variants | 2026-08-04 09:43:05 | 5946 | |||||
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Kravitz Dataset 2 Resource Report Resource Website 1+ mentions |
Kravitz Dataset 2 (RRID:SCR_000296) | data set, data or information resource | Dataset of the spike and laser timestamps from Kravitz, Owen and Kretizer's 2012 paper "Optogenetic identification of striatal projection neuron subtypes during in vivo recordings." The code will analyze spike trains around laser pulses to determine if a cell is significantly activated by the laser, and therefore expresses an excitatory opsin, such as channelrhodopsin-2. It returns an excel sheet that simply identifies the activated cells. | data set, neuron, spike train, optogenetic, in vivo, laser, channelrhodopsin, matlab | has parent organization: University of California at San Francisco; California; USA | Addiction, Parkinson's disease, Tourette's syndrome | PMID:23178332 | nlx_151410 | SCR_000296 | 2026-08-04 09:40:06 | 1 | ||||||||
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Mammalian Brain Methylomes Resource Report Resource Website |
Mammalian Brain Methylomes (RRID:SCR_001648) | Mammalian Brain Methylomes | data set, data or information resource | THIS RESOURCE IS NO LONGER IN SERVICE. Datasets described in the manuscript: "Global Epigenomic Reconfiguration During Mammalian Brain Development" (Science, 2013 - DOI: 10.1126/science.1237905. This study provides genome-wide composition, patterning, cell specificity, and dynamics of DNA methylation at single-base resolution in human and mouse frontal cortex throughout their lifespan. Widespread methylome reconfiguration occurs during fetal to young adult development, coincident with synaptogenesis. | epigenetics, methylation, frontal cortex, development, neuron, methylome, maturation, learning, young adult, fetus | has parent organization: Salk Institute for Biological Studies | PMID:23828890 | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_153926 | SCR_001648 | Mammalian Brain Methylomes | 2026-08-04 09:40:26 | 0 | ||||||
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Connectomic reconstruction of the inner plexiform layer in the mouse retina Resource Report Resource Website 1+ mentions |
Connectomic reconstruction of the inner plexiform layer in the mouse retina (RRID:SCR_002246) | MPIN Connectomics | data set, data or information resource | Data set of the dense reconstruction of 950 neurons and their mutual contacts for the mouse inner plexiform layer--the main computational neuropil region in the mammalian retina. This was achieved by applying a combination of crowd-sourced manual annotation and machine-learning-based volume segmentation to serial block-face electron microscopy data. They characterize a new type of retinal bipolar interneuron and show that they can subdivide a known type based on connectivity. Circuit motifs that emerge from their data indicate a functional mechanism for a known cellular response in a ganglion cell that detects localized motion, and predict that another ganglion cell is motion sensitive. A Data browser is also available for download | connectome, retina, retina inner plexiform layer | has parent organization: Max Planck Institute for Biological Intelligence | Max-Planck-Gesellschaft ; DFG ; Gatsby Charitable Foundation |
PMID:23925239 | Free, Freely available | nlx_155563 | SCR_002246 | 2026-08-04 09:40:36 | 1 | ||||||
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Center for In Vivo Microscopy Resource Report Resource Website 10+ mentions |
Center for In Vivo Microscopy (RRID:SCR_001426) | CIVM | biomedical technology research center, training resource | Biomedical technology research center dedicated to the development of novel imaging methods for the basic scientist and the application of the methods to important biomedical questions. The CIVM has played a major role in the development of magnetic resonance microscopy with specialized MR imaging systems capable of imaging at more than 500,000x higher resolution than is common in the clinical domain. The CIVM was the first to demonstrate MR images using hyperpolarized 3He which has been moved from mouse to man with recent clinical trials performed at Duke in collaboration with GE. More recently the CIVM has developed the molecular imaging workbench---a system dedicated to multimodality cardiopulmonary imaging in the rodent. Their collaborators are employing these unique imaging systems in an extraordinary range of mouse and rat models of neurologic disease, cardiopulmonary disease and cancer to illuminate the underlying biology and explore new therapies. | imaging, magnetic resonance microscopy, magnetic resonance imaging, clinical, mri, ct, x-ray, ultrasound, confocal, optical, spect | has parent organization: Duke University; North Carolina; USA | Cardiopulmonary disease, Cancer, Neurological disease | NIBIB 4P41EB015897-27 | Free, Freely Available | nlx_152650 | SCR_001426 | Duke Center for In Vivo Microscopy | 2026-08-04 09:40:23 | 10 | |||||
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EID: Exon-Intron Database Resource Report Resource Website 10+ mentions |
EID: Exon-Intron Database (RRID:SCR_002469) | EID | data set, data or information resource | Data sets of protein-coding intron-containing genes that contain gene information from humans, mice, rats, and other eukaryotes, as well as genes from species whose genomes have not been completely sequenced. This is a comprehensive and convenient dataset of sequences for computational biologists who study exon-intron gene structures and pre-mRNA splicing. The database is derived from GenBank release 112, and it contains protein-coding genes that harbor introns, along with extensive descriptions of each gene and its DNA and protein sequences, as well as splice motif information. They have created subdatabases of genes whose intron positions have been experimentally determined. The collection also contains data on untranslated regions of gene sequences and intron-less genes. For species with entirely sequenced genomes, species-specific databases have been generated. A novel Mammalian Orthologous Intron Database (MOID) has been introduced which includes the full set of introns that come from orthologous genes that have the same positions relative to the reading frames. | eukaryote genome, exon, exon-intro, gene structure, genome splicing, intron, ortholog, fasta, gene, protein-coding gene, splice, motif, gene prediction, structure, coding region |
is listed by: OMICtools has parent organization: University of Toledo; Ohio; USA |
PMID:16772261 PMID:10592221 |
Free, Available for download, Freely available | OMICS_01886, nif-0000-02793 | http://www.utoledo.edu/med/depts/bioinfo/database.html | http://www.meduohio.edu/bioinfo/eid/, http://mcb.harvard.edu/gilbert/EID | SCR_002469 | The Exon-Intron Database, Exon-Intron Database | 2026-08-04 09:40:40 | 11 | ||||
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Mouse Genome Informatics Transgenes Resource Report Resource Website 1+ mentions |
Mouse Genome Informatics Transgenes (RRID:SCR_003468) | MGI Transgene | data set, data or information resource |
Data set of collected and annotated expression and activity data for recombinase-containing transgenes and knock-in alleles. As the authoritative source of official names for mouse genes, alleles, and strains, MGI makes this list of transgenes available as a service and includes all known transgenes and synonyms. NIF provides a database interface so that researchers may have a better idea whether the trangene or transgenic animal that they are searching for is available. Nomenclature follows the rules and guidelines established by the International Committee on Standardized Genetic Nomenclature for Mice. |
transgene, allele, phenotype |
is used by: NIF Data Federation is related to: Integrated Manually Extracted Annotation has parent organization: Mouse Genome Informatics (MGI) |
Acknowledgement requested, Non-commercial, Commercial with permission, Copyrighted | nif-0000-34000 | SCR_003468 | 2026-08-04 09:40:55 | 3 | ||||||||
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Ancillary Domains Associated With Human and Mouse Proteases Resource Report Resource Website 1+ mentions |
Ancillary Domains Associated With Human and Mouse Proteases (RRID:SCR_008363) | Ancillary domains associated with human and mouse proteases | data set, data or information resource | Domains found in human and mouse proteases colour-coded according to the catalytic class in which they appear. Some of them appear in more than one catalytic group, and two-colours are used. Yellow, aspartyl proteases; blue, cysteine proteases; green, metalloproteases; and red, serine proteases. | protease, ancillary domain, catalytic domain, aspartyl protease, cysteine protease, metalloprotease, serine protease |
is related to: Mammalian Degradome Database has parent organization: University of Oviedo; Oviedo; Spain |
nif-0000-25547 | SCR_008363 | Ancillary Domains | 2026-08-04 09:42:08 | 2 | ||||||||
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National Institutes of Health Stem Cell Tables Resource Report Resource Website |
National Institutes of Health Stem Cell Tables (RRID:SCR_008359) | NIH Stem Cells | data set, data or information resource | Data tables providing an overview of information about stem cells that have been derived from mice and humans. The tables summarize published research that characterizes cells that are capable of developing into cells of multiple germ layers (i.e., multipotent or pluripotent) or that can generate the differentiated cell types of another tissue (i.e., plasticity) such as a bone marrow cell becoming a neuronal cell. The tables do not include information about cells considered progenitor or precursor cells or those that can proliferate without the demonstrated ability to generate cell types of other tissues. The tables list the tissue from which the cells were derived, the types of cells that developed, the conditions under which differentiation occurred, the methods by which the cells were characterized, and the primary references for the information. | ectoderm, endoderm, adipocyte, astrocyte, bone marrow, brain, cardiac, chondrocyte, differentiation, germ layer, hematopoietic stem cell, human, liver, mesenchymal stem cell, mesoderm, mouse, muscle, neuron, neuronal, osteoblast, pancreas, plasticity, platelet, red blood cell, skeletal, skin, spinal cord, neural stem cell, tenocyte, tissue, white blood cell, stem cell, multipotent stem cell, pluripotent stem cell, embryonic stem cell, embryonic primordial germ cell, primordial germ cell, neural progenitor cell, mesenchymal progenitor cell | has parent organization: National Institutes of Health | NIH | nif-0000-25459 | http://stemcells.nih.gov/info/scireport/appendixD.asp | SCR_008359 | 2026-08-04 09:42:07 | 0 | |||||||
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Virtual NeuroMorphology Electronic Database Resource Report Resource Website 1+ mentions |
Virtual NeuroMorphology Electronic Database (RRID:SCR_007118) | data set, data or information resource | A database of virtually generated anatomically plausible neurons for several morphological classes, including cerebellar Purkinje cells, hippocampal pyramidal and granule cells, and spinal cord motoneurons. It presently contains 542 cells. In the trade neurons collection the database contains an amaral cell archive, neuron morpho reconstructions, and mouse alpha motoneurons. Their collection of generated neurons include motoneurons, Purkinje cells, and hippocampal pyramidal cells. | neuron, morphology, computational neuroanatomy, neuroanatomy, neuronal reconstruction, neuron model, purkinje cell, motor neuron, ca1, ca3, hippocampal pyramidal cell, axon, hippocampus, triceps surae | has parent organization: George Mason University; Virginia; USA | Human Brain Project ; NINDS R01-NS39600-01 |
Acknowledgement requested | nif-0000-10546 | http://krasnow.gmu.edu/cn3/L-Neuron/database/ http://krasnow1.gmu.edu/L-Neuron/L-Neuron/database/ | SCR_007118 | LN Database, L-Neuron Database | 2026-08-04 09:41:45 | 1 | ||||||
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Integrated Technology Resource for Biomedical Glycomics Resource Report Resource Website 1+ mentions |
Integrated Technology Resource for Biomedical Glycomics (RRID:SCR_009003) | Integrated Technology Resource for Biomedical Glycomics | biomedical technology research center, training resource | Biomedical technology research center that develops and implements new technologies to investigate the glycome of cells, including glycoproteomics and glycoconjugate analysis, transcript analysis and bioinformatics. It develops the tools and technology to analyze in detail the glycoprotein and glycolipid expression of mouse embryonic stem cells and the cells into which they differentiate. The technology developed in the Center will allow an understanding of how glycosylation is controlled during differentiation and will allow the development of tools to promote the use of stem cells to treat human disease. In addition, the technology developed will be applicable to the study of other cell types, including cancer cells that are progressing to a more invasive phenotype. The technology developed will also allow others in the scientific community to participate in glycomics research through dissemination of the new methods developed and through the analytical services provided by the resource to other scientists requesting assistance in glycomic analyses. | systems biology technology center, glycome, cell, glycoproteomics, glycoconjugate analysis, transcript analysis, bioinformatics, glycoprotein, glycolipid, embryonic stem cell, glycosylation, stem cell, glycomics | has parent organization: University of Georgia; Georgia; USA | NCRR ; NIGMS |
nlx_152678 | SCR_009003 | NCRR Integrated Technology Resource for Biomedical Glycomics | 2026-08-04 09:42:17 | 1 | |||||||
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CellMarker Resource Report Resource Website 100+ mentions |
CellMarker (RRID:SCR_018503) | database, data or information resource, service resource | Database provides cell markers for various cell types in tissues of human and mouse. Manually curated resource of cell markers in human and mouse. Provides user-friendly interface for browsing, searching and downloading markers of diverse cell types of different tissues. Summarized marker prevalence in each cell type is graphically presented., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | Cell marker, cell type, tissue, graphical presentation, searching data, downloading data, marker, FASEB list | has parent organization: Harbin Medical University; Heilongjiang; China | National High Technology Research and Development Program of China ; National Natural Science Foundation of China ; China Postdoctoral Science Foundation |
PMID:30289549 | THIS RESOURCE IS NO LONGER IN SERVICE | SCR_018503 | 2026-08-04 09:44:21 | 485 | ||||||||
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tfcheckpoint Resource Report Resource Website 1+ mentions |
tfcheckpoint (RRID:SCR_023880) | database, data or information resource | Collection of transcription factors annotated according to experimental and other evidence on their function as true DbTFs. Provides reference for both small scale experiments and genome scale studies. Curated compendium of specific DNA-binding RNA polymerase II transcription factors. | transcription factor, DNA-binding RNA polymerase II transcription factors, DNA-binding, RNA polymerase II transcription factors, | Norwegian Cancer Society ; Liaison Committee between the Central Norway Regional Health Authority ; Norwegian University of Science and Technology |
PMID:23933972 | Free, Freely available | SCR_023880 | 2026-08-04 09:45:22 | 3 |
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