Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Preparing word cloud

×

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.

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

26,925 Results - per page

Show More Columns | Download Top 1000 Results

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
University of Texas Health Science Center at San Antonio Department of Pharmacology
 
Resource Report
Resource Website
University of Texas Health Science Center at San Antonio Department of Pharmacology (RRID:SCR_007078) data or information resource, department portal, organization portal, portal The Department of Pharmacology at the Health Science Center at San Antonio is uniquely positioned to carry out research into the most relevant areas in pharmacology as well as to deliver superior training in pharmacology. Our faculty use approaches that range from the molecular and cellular through electrophysiology and systems to behavior. The Department of Pharmacology at the University of Texas Health Science Center at San Antonio (UTHSCSA) has 18 tenure-track or tenured faculty, 11 research-track faculty, 15 graduate students, and 15 postdoctoral fellows. We are very excited about recent developments in pharmacology that allow new and challenging means of exploring the biological effects of drugs. Graduate studies leading to a Doctor of Philosophy degree in the basic biomedical sciences at UTHSCSA are offered in the Integrated Multidisciplinary Graduate Program (IMGP). The Department of Pharmacology administers two tracks within the IMGP: the pharmacology track and the neuroscience track. The Department of Pharmacology has a ten-week summer research program that offers participants a variety of experiences that will help prepare them for success in research-intensive doctoral programs. Participants will have research responsibilities, attend seminars, actively participate in a student journal club and take part in formal course work. Prior research experience is not necessary, and students of all undergraduate levels are encouraged to apply. has parent organization: University of Texas Health Science Center at San Antonio; Texas; USA nif-0000-02269 SCR_007078 UTHSCSA Department of Pharmacology 2026-08-21 12:38:09 0
Broad Institute
 
Resource Report
Resource Website
1000+ mentions
Broad Institute (RRID:SCR_007073) Broad institution Biomedical and genomic research center located in Cambridge, Massachusetts, United States. Nonprofit research organization under the name Broad Institute Inc., and is partners with Massachusetts Institute of Technology, Harvard University, and the five Harvard teaching hospitals. Dedicated to advance understanding of biology and treatment of human disease to improve human health. biomedical, genomic, research, center, nonprofit, organization, human, biology, disease is affiliated with: Massachusetts Institute of Technology; Massachusetts; USA;
is affiliated with: Harvard University; Cambridge; United States
is affiliated with: Integrative Human Microbiome Project
is affiliated with: MIT; Cambridge; Massachusetts; United States
is related to: LINCS Information Framework
is related to: HMS LINCS Database
is related to: Cancer Cell Line Encyclopedia
is related to: GO2MSIG
is parent organization of: ARACHNE
is parent organization of: MuTect
is parent organization of: SiPhy
is parent organization of: ContEst
is parent organization of: Broad Minded
is parent organization of: JBrowse
is parent organization of: Birdseed
is parent organization of: VAAL
is parent organization of: SomaticCall
is parent organization of: BIRDSUITE
is parent organization of: GATK
is parent organization of: SNAP - SNP Annotation and Proxy Search
is parent organization of: SYZYGY
is parent organization of: Genetic Maps of the Rat Genome
is parent organization of: LINCS Connectivity Map
is parent organization of: Classification of Human Lung Carcinomas by mRNA Expression Profiling Reveals Distinct Adenocarcinoma Sub-classes
is parent organization of: Haploview
is parent organization of: Magnaporthe comparative Database
is parent organization of: GeneCruiser
is parent organization of: Fungal Genome Initiative
is parent organization of: Gene Set Enrichment Analysis
is parent organization of: GenePattern
is parent organization of: MAGENTA
is parent organization of: Multiple Myeloma Genomics Portal
is parent organization of: ExAc
is parent organization of: Ricopili
is parent organization of: UnifiedGenotyper
is parent organization of: SomaticIndelDetector
is parent organization of: RNA-SeQC
is parent organization of: Oncotator
is parent organization of: ABSOLUTE
is parent organization of: PathSeq
is parent organization of: V-Phaser 2
is parent organization of: Indelocator
is parent organization of: Scripture
is parent organization of: VICUNA
is parent organization of: Tuberculosis Database
is parent organization of: HaploReg
is parent organization of: CellProfiler Image Analysis Software
is parent organization of: National Institute of Mental Health (NIMH) Human Genetics Initiative
is parent organization of: ChemBank
is parent organization of: GeneCluster 2: An Advanced Toolset for Bioarray Analysis
is parent organization of: Ultrasome
is parent organization of: Diabetes Genetics Initiative
is parent organization of: Dog Genome Project
is parent organization of: Gene Relationships Across Implicated Loci
is parent organization of: InVEx
is parent organization of: Broad Genetic Analysis Platform
is parent organization of: CellProfiler Analyst
is parent organization of: ALLPATHS-LG
is parent organization of: MutSig
is parent organization of: SegSeq
is parent organization of: Argo Genome Browser
is parent organization of: Integrative Genomics Viewer
is parent organization of: MEDEA
is parent organization of: Pathline
is parent organization of: ASPGD
is parent organization of: DGAP
is parent organization of: BARD
is parent organization of: 1000 Genomes: A Deep Catalog of Human Genetic Variation
is parent organization of: Trinity
is parent organization of: Genome Aggregation Database
is parent organization of: GenomeSpace
is parent organization of: Picard
is parent organization of: Connectivity Map 02
is parent organization of: CMap
is parent organization of: IndelGenotyper
is parent organization of: Discovar assembler
is parent organization of: Molecular Signatures Database
is parent organization of: GSEA
is parent organization of: Eagle
is parent organization of: Morpheus by Broad Institute
is parent organization of: Cancer Dependency Map Portal
is parent organization of: LIGER
is parent organization of: Drop-seq tools
is parent organization of: scATAC Pipeline
is parent organization of: Guide Design Resources
is parent organization of: Smart-seq2 Single Sample Pipeline
is parent organization of: Smart-seq2 Single Nucleus Multi Sample Pipeline
is parent organization of: Broad Terra cloud commons for pathogen surveillance
is parent organization of: Single Cell Portal
is parent organization of: CEMBA MethylC Seq Pipeline
is parent organization of: Pegasus
is parent organization of: Cumulus
is parent organization of: Cirrocumulus
is parent organization of: BICCN Anatomy and Morphology Project
is parent organization of: Terra
is parent organization of: JUMP Cell Painting Consortium
is parent organization of: Spectrum Mill
is parent organization of: Polysolver
is parent organization of: Brain Cell Data Viewer
is parent organization of: Eagle
is parent organization of: Broad Institute Imaging Platform Core Facility
is parent organization of: ATAC Pipeline
is parent organization of: ichorCNA
is parent organization of: CRISPick
is parent organization of: FireBrowse
is parent organization of: Cellarium
is parent organization of: multiVIB
is parent organization of: SlideTags.wdl
is parent organization of: Slide-seq Pipeline
is parent organization of: BuildIndices
is parent organization of: Broad Institute Genomics Platform
has organization facet: GATK HaplotypeCaller
has organization facet: GATK VariantFiltration
Eli and Edythe Broad ;
individual donors
nif-0000-31438, grid.66859.34, Wikidata: Q4971893 https://ror.org/05a0ya142 SCR_007073 Broad Institute of MIT and Harvard, Broad Institute Inc. 2026-08-21 12:38:00 1931
American Journal of Psychiatry Podcasts
 
Resource Report
Resource Website
1+ mentions
American Journal of Psychiatry Podcasts (RRID:SCR_007070) AJP Podcasts data or information resource, narrative resource, podcast An audio summary of highlights and key articles from each issue of The American Journal of Psychiatry. Users may subscribe to the podcast to get automatic updates with each issue or download each issue''s audio file individually. audio, psychiatry is used by: NIF Data Federation
is related to: Integrated Podcasts
nlx_39039 http://ajp.psychiatryonline.org/misc/audio.dtl SCR_007070 AJP Audio podcast, The American Journal of Psychiatry Podcast, AJP Podcast, AJP Audio, American Journal of Psychiatry Podcast, American Journal of Psychiatry Audio Downloads 2026-08-21 12:38:00 1
REGARDS - REasons for Geographic and Racial Differences in Stroke
 
Resource Report
Resource Website
100+ mentions
REGARDS - REasons for Geographic and Racial Differences in Stroke (RRID:SCR_007228) data or information resource, portal, topical portal The REasons for Geographic and Racial Differences in Stroke (REGARDS) project, sponsored by the National Institutes of Health (NIH), is a national study focusing on learning more about the factors that increase a person''s risk of having a stroke. REGARDS is an observational study of risk factors for stroke in adults 45 years or older. 30,239 participants were recruited between January 2003 and October 2007. They completed a telephone interview followed by an in-home physical exam. Measurements included traditional risk factors such as blood pressure and cholesterol levels, and an echocardiogram of the heart. At six month intervals, participants are contacted by phone to ask about stroke symptoms, hospitalizations and general health status. The study is ongoing and will follow participants for many years. The purpose of the REGARDS project is to understand why people in some parts of the country develop more strokes than people in other parts of the country, and why blacks develop more strokes than whites. We hope to learn how to reduce the number of people having strokes. has parent organization: National Institutes of Health Department of Health and Human Services ;
NINDS U01 NS041588
nif-0000-01878 SCR_007228 REGARDS, REasons for Geographic and Racial Differences in Stroke 2026-08-21 12:38:20 123
RTPrimerDB- The Real-Time PCR and Probe Database
 
Resource Report
Resource Website
10+ mentions
RTPrimerDB- The Real-Time PCR and Probe Database (RRID:SCR_007106) RTPrimerDB data or information resource, data repository, database, service resource, storage service resource Database for primer and probe sequences used in real-time PCR assays employing popular chemistries (SYBR Green I, Taqman, Hybridization Probes, Molecular Beacon) to prevent time-consuming primer design and experimental optimization, and to introduce a certain level of uniformity and standardization among different laboratories. Researchers are encouraged to submit their validated primer and probe sequence, so that other users can benefit from their expertise. The database can be queried using the official gene name or symbol, Entrez or Ensembl Gene identifier, SNP identifier, or oligonucleotide sequence. Different options make it possible to restrict a query to a particular application (Gene Expression Quantification/Detection, DNA Copy Number Quantification/Detection, SNP Detection, Mutation Analysis, Fusion Gene Quantification/Detection, Chromatin immunoprecipitation (ChIP)), organism (Human, Mouse, Rat, and others) or detection chemistry. primer, probe, sequence, real-time pcr, gene, assay, real-time pcr assay, FASEB list is listed by: OMICtools
has parent organization: Ghent University; Ghent; Belgium
PMID:18948285
PMID:16381959
PMID:12519963
Public, The community can contribute to this resource nif-0000-03431, OMICS_02322 SCR_007106 2026-08-21 12:38:01 49
Cambridge Brain Activation
 
Resource Report
Resource Website
10+ mentions
Cambridge Brain Activation (RRID:SCR_007109) CamBA data processing software, image analysis software, software application, software resource, software toolkit, workflow software Suite of programs developed for fMRI analysis in a Virtual Pipeline Laboratory facilitates combining program modules from different software packages into processing pipelines to create analysis solutions which are not possible with a single software package alone. Current pipelines include fMRI analysis, statistical testing based on randomization methods and fractal spectral analysis. Pipelines are continually being added. The software is mostly written in C. This fMRI analysis package supports batch processing and comprises the following general functions at the first level of individual image analysis: movement correction (interpolation and regression), time series modeling, data resampling in the wavelet domain, hypothesis testing at voxel and cluster levels. Additionally, there is code for second level analysis - group and factorial or ANOVA mapping - after co-registration of voxel statistic maps from individual images in a standard space. The main point of difference from other fMRI analysis packages is the emphasis throughout on the use of data resampling (permutation or randomization) as a basis for inference on individual, group and factorial test statistics at voxel and cluster levels of resolution. analysis, brain, anova, resampling, statistical, wavelet, fmri, pipeline, affine warp, algorithm or reusable library, application, c, image-to-template, java, linux, macos, magnetic resonance, nifti-1, posix/unix-like, registration, regression, spatial transformation, spectral analysis, statistical operation, temporal transformation, time domain analysis, unix shell, warping, wavelet transformation, web environment is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Biositemaps
has parent organization: University of Cambridge; Cambridge; United Kingdom
GlaxoSmithKline ;
Human Brain Project ;
NIMH ;
NIBIB
GNU General Public License nif-0000-00267 http://www-bmu.psychiatry.cam.ac.uk/software/ SCR_007109 2026-08-21 12:38:09 11
CD-HIT
 
Resource Report
Resource Website
1000+ mentions
CD-HIT (RRID:SCR_007105) CD-HIT data processing software, software application, software resource, source code THIS RESOURCE IS NO LONGER IN SERVICE. Documented on February 28,2023. Software program for clustering biological sequences with many applications in various fields such as making non-redundant databases, finding duplicates, identifying protein families, filtering sequence errors and improving sequence assembly etc. It is very fast and can handle extremely large databases. CD-HIT helps to significantly reduce the computational and manual efforts in many sequence analysis tasks and aids in understanding the data structure and correct the bias within a dataset. The CD-HIT package has CD-HIT, CD-HIT-2D, CD-HIT-EST, CD-HIT-EST-2D, CD-HIT-454, CD-HIT-PARA, PSI-CD-HIT, CD-HIT-OTU and over a dozen scripts. * CD-HIT (CD-HIT-EST) clusters similar proteins (DNAs) into clusters that meet a user-defined similarity threshold. * CD-HIT-2D (CD-HIT-EST-2D) compares 2 datasets and identifies the sequences in db2 that are similar to db1 above a threshold. * CD-HIT-454 identifies natural and artificial duplicates from pyrosequencing reads. * CD-HIT-OTU cluster rRNA tags into OTUs The usage of other programs and scripts can be found in CD-HIT user''s guide. CD-HIT was originally developed by Dr. Weizhong Li at Dr. Adam Godzik''s Lab at the Burnham Institute (now Sanford-Burnham Medical Research Institute)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. cluster, protein, sequence, classification, domain, analysis, nucleotide sequence, dna, protein sequence, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
is listed by: OMICtools
has parent organization: University of California at San Diego; California; USA
has parent organization: Google Code
is parent organization of: CD-HIT-OTU
NCRR 1R01RR025030 PMID:20053844
PMID:16731699
DOI:10.1093/bioinformatics/btl158
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_05157, biotools:cd-hit, nif-0000-30240 http://cd-hit.org, https://code.google.com/p/cdhit/, https://bio.tools/cd-hit, https://sources.debian.org/src/cd-hit/ http://bioinformatics.ljcrf.edu/cd-hi/
SCR_007105 CD-HIT Program 2026-08-21 12:38:09 3223
Combine RTS2000
 
Resource Report
Resource Website
1+ mentions
Combine RTS2000 (RRID:SCR_007104) data processing software, image processing software, software application, software resource Software program that performs the auto-alignment and the composition of images to create the mosaic. program, auto, alignment, composition, image, create, mosaic has parent organization: National Center for Microscopy and Imaging Research NCRR P41 RR04050 Free, no longer available nif-0000-10511 SCR_007104 2026-08-21 12:38:18 1
Expression Database in 4D
 
Resource Report
Resource Website
1+ mentions
Expression Database in 4D (RRID:SCR_007066) 4DXpress data or information resource, data repository, database, service resource, storage service resource This database provides a platform to query and compare gene expression data during the development of the major model animals (zebrafish, drosophila, medaka, mouse). The name 4DXpress stands for expression database in 4D. The 4D (four dimensions) of 4DXpress can be interpreted either as: 3 spatial dimensions plus time, or as 1. species 2. gene 3. developmental stage 4. anatomical structure. The major focus of this database lies in cross species comparison. The high resolution expression data was acquired through whole mount in situ hybridsation-, antibody- or transgenic experiments. Data was integrated from several species specific expression pattern databases, such as ZFIN, BDGP, GXD, MEPD as well as directly submitted by researchers of the participating groups at EMBL. The 4DXpress database is a project within the Centre for Computational Biology at EMBL. It is developed by Yannick Haudry, Thorsten Henrich and Ivica Letunic and coordinated by Thorsten Henrich. Hugo Berube is developing the 4D ArrayExpress Data Warehouse at EBI for integrating in situ data with microarray data. genes, anatomical structures, developmental stage, microarray data, species, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: European Molecular Biology Laboratory
European Molecular Biology Laboratory; Heidelberg; Germany PMID:17916571 nif-0000-02524, biotools:4dxpress https://bio.tools/4dxpress SCR_007066 4DXpress Database 2026-08-21 12:38:08 1
Cardiac Electrophysiology Ontology
 
Resource Report
Resource Website
Cardiac Electrophysiology Ontology (RRID:SCR_007065) EP controlled vocabulary, data or information resource, ontology Ontology that contains terms describing single-channel electrophysiological experiments and data obtained using voltage-clamp, current clamp and fluorescence imaging techniques applied at the cell level and multi-channel fluorescence imaging techniques applied at the cell, tissue and whole heart levels. owl is listed by: BioPortal
has parent organization: CardioVascular Research Grid (CVRG)
nlx_157352 SCR_007065 2026-08-21 12:38:17 0
Bone Marrow Donors Worldwide
 
Resource Report
Resource Website
1+ mentions
Bone Marrow Donors Worldwide (RRID:SCR_007186) data or information resource, portal, topical portal Bone Marrow Donors Worldwide (BMDW) is the continuing effort to collect the HLA phenotypes of volunteer stem cell donors and cord blood units, and is responsible for the co-ordination of their worldwide distribution. Participants are 63 stem cell donor registries from 44 countries, and 43 cord blood banks from 25 countries. The current number of donors and cord blood units in the BMDW database is: 14,605,618 (14,178,976 donors and 426,642 CBU''s The original goal to collect the HLA phenotypes of volunteer stem cell donors and cord blood units, and to co-ordinate their world-wide distribution remain their primary goals. But new initiatives have been added: - To maximise the chance of finding a stem cell donor or cord blood unit by providing access to all stem cell donors and cord blood units available in the world. - To minimise the effort required for stem cell donor or cord blood unit searches: only registries with potential stem cell donors or cord blood units need to be contacted. - To provide an estimate of the chance of finding a stem cell donor or cord blood unit for a given patient. - To provide advanced search programs to identify partially matched stem cell donors or cord blood units. - To facilitate search advice requests via the Internet. - To facilitate improvements in family search strategies. - To provide relevant general information for the benefit of the patient. - To provide statistics on the increase of different registries, the number of DNA typed donors, etc. Sponsors: Bone Marrow Donors Worldwide is an initiative of the Immunobiology Working Party of the European Group of Blood and Marrow Transplantation (EBMT) in 1988. Keyworss: Bone marrow, Donor, Cell, Phenotype, Stem cell, Cord blood unit, nif-0000-30155 SCR_007186 BMDW 2026-08-21 12:38:19 8
Brown University Alpert Medical School Department of Molecular Pharmacology Physiology and Biotechnology
 
Resource Report
Resource Website
Brown University Alpert Medical School Department of Molecular Pharmacology Physiology and Biotechnology (RRID:SCR_007222) data or information resource, degree granting program, department portal, graduate program resource, medical school program resource, organization portal, portal, postdoctoral program resource, training resource, undergraduate program resource THIS RESOURCE IS NO LONGER IN SERVICE, documented on August 20, 2021. Department of Molecular Pharmacology, Physiology, and Biotechnology has closed, effective June 30, 2021. Department of Molecular Pharmacology, Physiology and Biotechnology is basic science department within Brown Medical School, and is full participant in undergraduate based Program in Biology within Division of Biology and Medicine at Brown University. has parent organization: Brown University; Rhode Island; USA THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-01905 http://bms.brown.edu/mppb/index.html SCR_007222 BU MPPB, Brown MPPB, Brown University; MPPB 2026-08-21 12:38:19 0
California Institute of Technology; Division of Biology
 
Resource Report
Resource Website
California Institute of Technology; Division of Biology (RRID:SCR_007221) data or information resource, degree granting program, graduate program resource, organization portal, portal, postdoctoral program resource, training resource, undergraduate program resource For more than 75 years, the division of biology has provided many of the major research advances that have made biology the premier science of the 21st century, and has trained many of the world''s most eminent biologists. The division at present has 38 professors of various ranks, who in their classes and laboratories have approximately 100 undergraduates, 100 graduate students, and 160 postdoctoral scholars, as well as more than 250 staff members. We occupy parts or all of seven buildings on the Caltech campus; we also operate a marine laboratory 50 miles from campus. Each building is devoted to state-of-the-art educational facilities and cutting-edge laboratories. We have three major research emphases: Structural, Molecular and Cell Biology; Developmental and Regulatory Biology; and Molecular, Cellular and Integrative Neuroscience. In each area we are trying to solve one of the great problems of modern biology: How do the proteins and other components of cells interact to provide a marvelous nanomachine of more than 100,000 integrated parts, a machine that has numerous extraordinary functions and can reproduce itself? How does a single cell become, by division and formation of new cell types, an entire multicellular organism, which in the case of humans has thousands of different cell types and more than 1 trillion different cells in specific places, communicating to form complex organs? How does the brain, the most complex organ of all, work to allow calculations beyond those of any computer, as well as to demonstrate amazing sensory capabilities, emotions, and consciousness? is related to: The Pancreatic Beta-Cell Consortium nif-0000-01909 SCR_007221 Caltech Biology, Biology at Caltech, Caltech; Division of Biology; Division of Biology at Caltech 2026-08-21 12:38:04 0
Cereal Plant Gross Anatomy Ontology
 
Resource Report
Resource Website
Cereal Plant Gross Anatomy Ontology (RRID:SCR_007061) GRO-CPGA controlled vocabulary, data or information resource, ontology A structured controlled vocabulary for the anatomy of Gramineae. Please note that this ontology has now been superseded by the Plant Ontology, http://bioportal.bioontology.org/ontologies/1587. obo is listed by: BioPortal
is related to: Plant Ontology
has parent organization: Gramene
nlx_157359 http://www.gramene.org/plant_ontology/ SCR_007061 2026-08-21 12:38:00 0
Bayesian Analysis of Common NMR Problems
 
Resource Report
Resource Website
1+ mentions
Bayesian Analysis of Common NMR Problems (RRID:SCR_007182) data analysis software, data processing software, software application, software resource Welcome to the Bayesian Analysis of Common NMR Problems software home page. This Bayesian analysis software is a series of programs with a Java interface that use Bayesian probability theory to solve common data analysis problems that occur in the sciences and in NMR in particular. Click here for a complete list of the applications addressed. The programs that run the various Bayesian analysis, the server software, were developed at Washington University by Dr. G. Larry Bretthorst and the Java language client interface was developed by Dr. Karen Marutyan. The combination of the server and client software is called the Bayesian Analysis of Common NMR Problems software. However, this name is slightly misleading because this software can analyze data from many different sources, not just NMR data. Additionally, unlike the previous interface to this software, this new interface does not require the user to have access to any specialized NMR software, i.e., this interface is completely independent of Varian''s VnmrJ, although the interface can load and process data from a Varian spectrometer. Sponsors: This resource is supported by the Washington University in St. Louis. Keywords: Analysis, Software, Java, Theory, Science, NMR, Server, Data, Spectrometer, has parent organization: Washington University in St. Louis; Missouri; USA nif-0000-30164 SCR_007182 Bayesian Analysis 2026-08-21 12:38:03 5
Osprey: Network Visualization System
 
Resource Report
Resource Website
10+ mentions
Osprey: Network Visualization System (RRID:SCR_007138) data processing software, data visualization software, simulation software, software application, software resource Osprey is a software platform for visualization of complex interaction networks. Osprey builds data-rich graphical representations from Geno Ontology (GO) annotated interaction data maintained by The Grid. The following list describes some of the important characteristics of the Osprey Network Visualization System: * Portability ( cross platform availability ) o Osprey is available on almost all Platforms that support the latest Java Plugin * Tools for Biological Analysis o Osprey provides many features such as network filters, connectivity filters, advanced layouts, and dataset superimposing which are extremely useful to biologists who are interested in analyzing their data * Powerful Support Database o Integrated with Osprey is a powerful database of interactions and annotation, see section 8. The GRID ( The General Repository of Interaction Datasets ). * Ease of use o Osprey provides an extremely user friendly interface for working with interaction data * Online Database Add-on Ability o Osprey can be incorporated as a standard visualization tool with online databases such as The GRID * Support for figures o Osprey networks can be saved in SVG, PNG and JPG format so they can be used with image programs Sponsors: Development of Osprey was funded by a grant from the Canadian Institutes of Health Research. filter, biological analysis, biologist, interaction, software, visualization nif-0000-10394 SCR_007138 Osprey 2026-08-21 12:38:18 27
BioRAT
 
Resource Report
Resource Website
1+ mentions
BioRAT (RRID:SCR_007099) BioRAT software application, software resource, text extraction software, text-mining software THIS RESOURCE IS NO LONGER IN SERVICE. Documented on June 1,2023. An information extraction (IE) tool specifically designed to perform biomedical IE and which is able to locate and analyze both abstracts and full-length papers. BioRAT is a Biological Research Assistant for Text mining, and incorporates a document search ability with domain-specific IE. information extraction, search engine, biomedical, abstract, full-length paper is listed by: OMICtools
is related to: Comparative Toxicogenomics Database (CTD)
has parent organization: University College London; London; United Kingdom
PMID:15231534 THIS RESOURCE IS NO LONGER IN SERVICE SCR_013452, nif-0000-21061, OMICS_01175 SCR_007099 Biological Research Assistant for Text mining 2026-08-21 12:38:18 1
Magnetics Information Consortium
 
Resource Report
Resource Website
10+ mentions
Magnetics Information Consortium (RRID:SCR_007098) MagIC data or information resource, data repository, database, service resource, software resource, storage service resource Databases that accept and provide access to paleomagnetic and rock magnetic data. The paleomagnetic data range from individual measurements to specimen, sample or site level results, including a wide variety of derived parameters or associated rock magnetic measurements. The rock magnetic database includes data collected during rock magnetic experiments on remanence, anisotropy, hysteresis and susceptibility. The MagIC Console Software provides an effective environment in Microsoft Excel where users can collate and prepare their paleomagentic and rock magnetic data for uploading in the Online MagIC Database. paleomagnetism, rock, magnetic, paleomagnetic, geomagnetic, rock magnetic is listed by: CINERGI
has parent organization: San Diego Supercomputer Center
NSF EAR 0202996;
NSF EAR-IF 0318672-0744107-0744108
Non-commercial, For scientific or educational purposes, Acknowledgement required, Copyrighted, The community can contribute to this resource nlx_154712, SciRes_000151, r3d100011910 https://doi.org/10.17616/R3NM0W SCR_007098 Magnetics Information Consortium (MagIC), MagIC Portal, MagIC database 2026-08-21 12:38:01 34
Chromosome 7 Annotation Project
 
Resource Report
Resource Website
10+ mentions
Chromosome 7 Annotation Project (RRID:SCR_007134) Chromosome 7 Annotation Project data or information resource, data repository, database, service resource, storage service resource Database containing the DNA sequence and annotation of the entire human chromosome 7, encompassing nearly 158 million nucleotides of DNA and 1917 gene structures, are presented; the most up to date collation of sequence, gene, and other annotations from all databases (eg. Celera published, NCBI, Ensembl, RIKEN, UCSC) as well as unpublished data. To generate a higher order description, additional structural features such as imprinted genes, fragile sites, and segmental duplications were integrated at the level of the DNA sequence with medical genetic data, including 440 chromosome rearrangement breakpoints associated with disease. The objective of this project is to generate a comprehensive description of human chromosome 7 to facilitate biological discovery, disease gene research and medical genetic applications. There are over 360 disease-associated genes or loci on chromosome 7. A major challenge ahead will be to represent chromosome alterations, variants, and polymorphisms and their related phenotypes (or lack thereof), in an accessible way. In addition to being a primary data source, this site serves as a weighing station for testing community ideas and information to produce highly curated data to be submitted to other databases such as NCBI, Ensembl, and UCSC. Therefore, any useful data submitted will be curated and shown in this database. All Chromosome 7 genomic clones (cosmids, BACs, YACs) listed in GBrowser and in other data tables are freely distributed. duplication, gene expression, family, fish, gene, gene annotation, genome, breakpoint, chromosome, chromosome 7, clinical, deletion, disease, dna sequence, human, insertion, inversion, polymorphism, rearrangement, segmental duplication, snp, translocation, annotation, data analysis service, blat, cosmid, bac, yac, biomaterial supply resource, malignant, non malignant, bio.tools is listed by: One Mind Biospecimen Bank Listing
is listed by: Debian
is listed by: bio.tools
PMID:12690205 Free, (Genomic clones) nif-0000-03550, biotools:chr7, r3d100012136 https://bio.tools/chr7, https://doi.org/10.17616/R3VP9V SCR_007134 The Chromosome 7 Annotation Project, Chromosome 7 Annotation Project 2026-08-21 12:38:10 13
Cell Culture Ontology
 
Resource Report
Resource Website
1+ mentions
Cell Culture Ontology (RRID:SCR_007096) CCONT controlled vocabulary, data or information resource, ontology ontology for the formal representation of cell lines and their correspnding culture conditions. owl is listed by: BioPortal nlx_157354 SCR_007096 2026-08-21 12:38:18 1

Can't find your Tool?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.

Can't find the RRID you're searching for? X
X
  1. NIDDK Information Network Resources

    Welcome to the dkNET Resources search. From here you can search through a compilation of resources used by dkNET and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that dkNET has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on dkNET then you can log in from here to get additional features in dkNET such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into dkNET you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.