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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
LONI ShapeTools
 
Resource Report
Resource Website
1+ mentions
LONI ShapeTools (RRID:SCR_002697) ShapeTools software application, software development tool, software library, software resource, software toolkit Software library that is a collection of Java classes that enable Java programmers to model, manipulate and visualize geometric shapes and associated data values. It simplifies the creation of application programs by providing a ready-made set of support routines. * File format readers that implement ShapeIO interface (modeled after Java ImageIO) are automatically used when appropriate. * Storage of additional metadata of arbitrary type (other than shape vertices and interconnections) is enabled by the use of data attributes. * Shapes may contain a set of child shapes allowing for the construction and manipulation of complex hierarchies of shapes. * The various components of a shape are specified as interfaces with specific implementations, making it easy to create specialized implementations of a shape component when different performance characteristics are required. data visualization, java, shape analysis software, computed tomography, magnetic resonance, pet, spect is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Biositemaps
is related to: LONI ShapeViewer
has parent organization: Laboratory of Neuro Imaging
NIBIB 9P41EB015922-15;
NCRR 2-P41-RR-013642-15;
NCRR U54 RR021813
Free, Freely available nif-0000-23323 SCR_002697 2026-09-03 04:57:56 1
Resource Discovery System
 
Resource Report
Resource Website
Resource Discovery System (RRID:SCR_005554) RDS data or information resource, database Resource Discovery System is a web-accessible and searchable inventory of biomedical research resources. Powered by the Resource Discovery System (RDS) that includes a standards-based informatics infrastructure * Biositemaps Information Model * Biomedical Resource Ontology Extensions * Web Services distributed web-accessible inventory framework * Biositemap Resource Editor * Resource Discovery System Source code and project documentation to be made available on an open-source basis. Contributing institutions: University of Pittsburgh, University of Michigan, Stanford University, Oregon Health & Science University, University of Texas Houston. Duke University, Emory University, University of California Davis, University of California San Diego, National Institutes of Health, Inventory Resources Working Group Members registry, web service, source code, biomedical, software resource, material resource, funding resource, service resource, training resource, people resource has parent organization: Biositemaps Clinical and Translational Science Awards Consortium ;
National Centers for Biomedical Computing ;
NCRR 3UL1RR024153-03S1;
NCRR 5UL1RR024128-03S1;
NCRR 1UL1RR025008-01;
NCRR 1UL1RR024146-01;
NCRR 1UL1RR024986-01;
NCRR 1UL1RR024153-01;
NIDA 3U54DA021519-04S1;
NHGRI 3U54HG004028-04S
nlx_144645 SCR_005554 2026-09-03 05:02:05 0
Recombinase (cre) Activity
 
Resource Report
Resource Website
10+ mentions
Recombinase (cre) Activity (RRID:SCR_006585) Recombinase Activity data or information resource, database Curated data about all recombinase-containing transgenes and knock-ins developed in mice providing a comprehensive resource delineating known activity patterns and allows users to find relevant mouse resources for their studies. cre, recombinase, transgene, knock-in, allele, expression, activity pattern, mutagenesis, promoter, driver, image, tissue, specificity assay is related to: International Mouse Strain Resource
is related to: CREATE
is related to: JAX Cre Repository
is related to: Allen Institute for Brain Science
is related to: CRE Driver Network
is related to: Pleiades Promoter Project: Genomic Resources Advancing Therapies for Brain Disorders
is related to: EUCOMMTOOLS
has parent organization: Mouse Genome Informatics (MGI)
European Union HEALTH-F4-2009-223487;
NCRR RR03 2656;
NICHD HD062499
SCR_017520, nlx_152803 http://www.creportal.org/ SCR_006585 Cre Portal 2026-09-03 05:02:20 22
SHRINE
 
Resource Report
Resource Website
1+ mentions
SHRINE (RRID:SCR_006293) SHRINE software application, software resource, source code Software providing a scalable query and aggregation mechanism that enables federated queries across many independently operated patient databases. This platform enables clinical researchers to solve the problem of identifying sufficient numbers of patients to include in their studies by querying across distributed hospital electronic medical record systems. Through the use of a federated network protocol, SHRINE allows investigators to see limited data about patients meeting their study criteria without compromising patient privacy. This software should greatly enable population-based research, assessment of potential clinical trials cohorts, and hypothesis formation for followup study by combining the EHR assets across the hospital system. In order to obtain the maximum number of cases representing the study population, it is useful to aggregate patient facts across as many sites as possible. Cutting across institutional boundaries necessitates that each hospital IRB remain in control, and that their local authority is recognized for each and every request for patient data. The independence, ownership, and legal responsibilities of hospitals predetermines a decentralized technical approach, such as a federated query over locally controlled databases. The application comes with the SHRINE Core Ontology but it can be used with any ontology, even one that is disease specific. The Core Ontology is designed to enable the widest range of studies possible using facts gathered in the EMR during routine patient care. SHRINE allows multiple ontologies to be used for different research purposes on the same installed systems. software network, clinical database, data sharing, clinical, medical record, federated, platform, network is related to: i2b2 Cross-Institutional Clinical Translational Research project
is related to: i2b2 Research Data Warehouse
has parent organization: Harvard Medical School; Massachusetts; USA
Informatics for Integrating Biology and the Bedside ;
NLM 5 U54 LM008748;
NCRR 1 UL1 RR025758-01
PMID:19567788 Available under a BSD3 Open unspecified license Software license. nlx_151949 SCR_006293 Shared Health Research Informatics NEtwork 2026-09-03 05:02:10 8
Wake Forest Cynomolgus Breeding Colony
 
Resource Report
Resource Website
Wake Forest Cynomolgus Breeding Colony (RRID:SCR_006605) CBC, WFU CBC biomaterial supply resource, material resource, tissue bank The Wake Forest Cynomolgus Breeding Colony (CBC) is a colony of cynomolgus macaques (crab-eating macaques, Macaca fascicularis). The cynomolgus colony is designed to produce specific pathogen free (SPF) cynomolgus monkeys for use in biomedical research. The colony, supported by a grant from the NCRR, addresses the growing need for investigators to use in their protocols animals defined for the absence of specific diseases including CHV-1 (Herpes B), simian immunodeficiency virus, and simian retroviruses. An additional important characteristic of this colony is that, unlike many breeding colonies, the NHPs will be fed two defined diets. The first diet is a soy-free diet, not commercial monkey chow. The second diet has the same macronutrients but the protein source is from soy; similar in isoflavone content. A drawback of chow diets is that the exact nutritional product composition is unknown from lot to lot. However, they are always rich in soy bean meal, isoflavones and other constituents of soy bean meal that are known confounders of several types of research projects. All research using the cynomolgus colony must be reviewed and approved by the colony''s scientific board and the Wake Forest Animal Care and Use Committee (ACUC) before any work can be initiated. The scientific board meets regularly to assess the scientific value of each request and to determine whether or not animals/samples/data can be made available. This includes all requests for: # The purchase of animals for use outside the colony # The use of animals within the colony for the collection of blood/tissue samples, behavioral observations or other kinds of testing # The use of the CBC sample/tissue repository # The use of the CBC data repository long-tailed macaque, non-human primate, blood, tissue, macaca fascicularis, animal model is listed by: One Mind Biospecimen Bank Listing
has parent organization: Wake Forest Primate Center
Macaca fascicularis NCRR Public nlx_146209 SCR_006605 WFU Cynomolgus Breeding Colony, Cynomolgus Breeding Colony 2026-09-03 05:02:15 0
lapdftext
 
Resource Report
Resource Website
lapdftext (RRID:SCR_006167) lapdftext, LA-PDFText, software application, software resource, text extraction software Software that facilitates accurate extraction of text from PDF files of research articles for use in text mining applications. It is intended for both scientists and natural language processing (NLP) engineers interested in getting access to text within specific sections of research articles. The system extracts text blocks from PDF-formatted full-text research articles and classifies them into logical units based on rules that characterize specific sections. The LA-PDFText system focuses only on the textual content of the research articles. The current version of LA-PDFText is a baseline system that extracts text using a three-stage process: * identification of blocks of contiguous text * classification of these blocks into rhetorical categories * extraction of the text from blocks grouped section-wise. text mining, pdf, text extraction, natural language processing is listed by: FORCE11
has parent organization: University of Southern California; Los Angeles; USA
NSF 0849977;
NIGMS RO1-GM083871;
NIMH 1R01MH079068-01A2;
NCRR U24 RR025736-01
PMID:22640904 Acknowledgement requested, GNU General Public License, v3 nlx_151668 SCR_006167 Layout-Aware PDF Text Extraction, Layout-Aware Text Extraction from Full-text PDF of Scientific Articles, lapdftext: Layout-Aware Text Extraction from Full-text PDF of Scientific Articles 2026-09-03 05:01:51 0
Bioscholar
 
Resource Report
Resource Website
1+ mentions
Bioscholar (RRID:SCR_001380) BioScholar software application, software resource, source code Knowledge management and engineering system software for experimental biomedical scientists permitting a single scientific worker (at the level of a graduate student or postdoctoral worker) to design, construct and manage a shared knowledge repository for a research group derived on a local store of PDF files. Usability is especially emphasized within a laboratory so that this software could provide support to experimental scientists attempting to construct a personalized representation of their own knowledge on a medium scale. The BioScholar system uses a graphical interface to create experimental designs based on the experimental variables in the system. The design is then analyzed to construct a tabular input form based on the data flow. They call this methodology "Knowledge Engineering from Experimental Design" or "KEfED". The approach is domain-independent but domain-specific modules reasoning can be constructed to generate interpretations from the observational data represented in the KEfED model. The application is available for download as platform-specific installers including Linux, Unix, Mac OS, and Windows. The installer will install an application that will run the BioScholar server. This server uses Jetty as its integrated web server. knowledge engineering from experimental design, protocol, lab data management, knowledge engineering, kefed, experimental design, curate, model, scientific experiment, data repository, experimental variable, biomedical, bioinformatics is related to: Knowledge Engineering from Experimental Design
has parent organization: University of Southern California; Los Angeles; USA
NCRR 1 U24 RR025736;
NIGMS R01-GM083871
PMID:21859449 THIS RESOURCE IS NO LONGER IN SERVICE nlx_152541 SCR_001380 2026-09-03 05:01:39 1
EcoCyc
 
Resource Report
Resource Website
500+ mentions
EcoCyc (RRID:SCR_002433) EcoCyc, EcoCyc REF data or information resource, database Database for the bacterium Escherichia coli K-12 MG1655, the EcoCyc project performs literature-based curation of the entire genome, and of transcriptional regulation, transporters, and metabolic pathways. The long-term goal of the project is to describe the molecular catalog of the E. coli cell, as well as the functions of each of its molecular parts, to facilitate a system-level understanding of E. coli. EcoCyc is an electronic reference source for E. coli biologists, and for biologists who work with related microorganisms. genome, metabolic pathway, transcription, transporters, escherichia coli, transcriptional regulation, metabolism, pathway, FASEB list uses: Pathway Tools
is used by: NIF Data Federation
is listed by: OMICtools
is listed by: BioCyc
is related to: MultiFun
is related to: BioCyc
is related to: BioCyc
is related to: AmiGO
is related to: NCBI BioSystems Database
is related to: Pathway Tools
has parent organization: Stanford Research Institute International
NCRR ;
NIGMS GM077678;
NIGMS GM71962
PMID:23143106
PMID:21097882
Free, Freely available OMICS_01645, nif-0000-02783, r3d100011277 https://doi.org/10.17616/R34K99 SCR_002433 EcoCyc REF 2026-09-03 05:00:57 511
MS-GF+
 
Resource Report
Resource Website
100+ mentions
MS-GF+ (RRID:SCR_015646) software resource Software that performs peptide identification by scoring MS/MS spectra against peptides derived from a protein sequence database. protein idenitification, peptide sequence, ms, ms spectrum, proteomic, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
has parent organization: Pacific Northwest National Laboratory
NCRR RR018522;
NCRR 1-P41-RR024851;
NIAID ;
W.R. Wiley Environmental Molecular Science Laboratory
PMID:25358478 Free, Available for download, Acknowledgment requested biotools:ms-gf https://github.com/sangtaekim/msgfplus, https://bio.tools/ms-gf SCR_015646 MSGF+, MSGFPlus 2026-09-03 04:53:16 159
ImageVis3D
 
Resource Report
Resource Website
10+ mentions
ImageVis3D (RRID:SCR_009566) ImageVis3D data processing software, software application, software resource A new volume rendering program developed by the NIH/NCRR Center for Integrative Biomedical Computing (CIBC). The main design goals of ImageVis3D are: simplicity, scalability, and interactivity. Simplicity is achieved with a new user interface that gives an unprecedented level of flexibility (as shown in the images). Scalability and interactivity for ImageVis3D mean that both on a notebook computer as well as on a high end graphics workstation, the user can interactively explore terabyte sized data sets. Finally, the open source nature as well as the strict component-by-component design allow developers not only to extend ImageVis3D itself but also reuse parts of it, such as the rendering core. This rendering core, for instance, is planned to replace the volume rendering subsystems in many applications at the SCI Institute and with their collaborators. magnetic resonance, rendering is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Debian
has parent organization: University of Utah; Utah; USA
NCRR P41-RR12553-15;
DOE DEFC0206ER25781
Free, Available for download, Freely available nlx_155776 http://www.nitrc.org/projects/imagevis3d, https://sources.debian.org/src/imagevis3d/ SCR_009566 2026-09-03 05:00:48 10
Age Related Atrophy Dataset
 
Resource Report
Resource Website
Age Related Atrophy Dataset (RRID:SCR_009528) Age Related Atrophy Dataset data or information resource, data set, software resource, source code Dataset of structural MR images of 70 subjects collected during 2008-2010 across a wide range of ages. The dataset also contains resting state fMRI for most subjects. The structural images are T1 weighted, T2 weighted-FLAIR, 25 direction DTI, and the T1 mapping DESPOT [1] sequence. Reconstructed T1 maps for each subject are also available. The aquisition protocol was designed to study structural differences between young and older adults including both shape and intensity changes. Anonymized DICOM image sessions and processed images for each subject are available. The data is licensed under the Creative Commons Attribution License. It may be used freely for commercial, academic, or other use, as long as the original source is properly cited. http://www.bsl.ece.vt.edu/index.php?page=ara-dataset magnetic resonance, image collection, mri is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: Virginia Polytechnic Institute and State University; Virginia; USA
Aging NIH Roadmap for Medical Research ;
NCRR U54 RR021813
Creative Commons Attribution License nlx_155692 http://www.nitrc.org/projects/aradata SCR_009528 2026-09-03 05:00:18 0
cBioPortal
 
Resource Report
Resource Website
10000+ mentions
cBioPortal (RRID:SCR_014555) data or information resource, database, portal A portal that provides visualization, analysis and download of large-scale cancer genomics data sets. cancer, genomics, database, portal, data sets, FASEB list is used by: NaviCom NCI U24CA143840;
NCRR RR031228-02
PMID:23550210
PMID:22588877
Please cite, Software is available via GitHub, Open source https://github.com/cBioPortal/cbioportal/ https://github.com/cBioPortal/cbioportal/blob/master/docs/README.md SCR_014555 cBioPortal for Cancer Genomics 2026-09-03 05:00:09 10348
ProteomeTools
 
Resource Report
Resource Website
10+ mentions
ProteomeTools (RRID:SCR_018535) data or information resource, portal, project portal Project for building molecular and digital tools from human proteome to facilitate biomedical research, drug discovery, personalized medicine and life science research. Molecular tool, human proteome, proteome, human, peptide, data is related to: ProteomicsDB
is related to: ProteomeXchange
Alexander von Humboldt Foundation ;
American Recovery and Reinvestment Act ;
European Research Council ;
German Federal Ministry of Education and Research ;
NCRR S10 RR027584;
NHGRI RC2 HG005805;
NIGMS P50 GM076547;
NIGMS R01 GM087221;
Swiss National Science Foundation
PMID:28135259 Free, Freely available http://www.proteometools.org SCR_018535 2026-09-03 05:00:23 23
Berkeley Advanced Reconstruction Toolbox
 
Resource Report
Resource Website
10+ mentions
Berkeley Advanced Reconstruction Toolbox (RRID:SCR_016168) BART data processing software, image analysis software, image reconstruction software, software application, software resource Image reconstruction software for MRI. Its library provides common operations on multi-dimensional arrays, Fourier and wavelet transforms, as well as generic implementations of iterative optimization algorithms. mri, reconstruction, magnetic, resonance, neuroimaging, array, transform, algorithm is listed by: Debian American Heart Association 12BGIA9660006;
GE Healthcare ;
NCRR R41 RR09784;
NIBIB R01 EB009690;
Sloan Research Fellowship ;
UC Discovery 193037
Open source, Free https://mrirecon.github.io/bart/, https://sources.debian.org/src/bart/ SCR_016168 2026-09-03 04:58:27 11
Fitness Browser
 
Resource Report
Resource Website
1+ mentions
Fitness Browser (RRID:SCR_018981) data access protocol, data or information resource, software resource, web service Web tool for browsing genome wide fitness experiments for diverse bacteria from Deutschbauer lab, the Arkin lab, and collaborators. Collection of mutant phenotypes for bacterial genes of unknown function. Genome browser, bacteria, mutant phenotype, bacterial genes, unknown function, data has parent organization: University of California at Berkeley; Berkeley; USA NCRR S10 RR027303;
NCRR S10 RR029668;
NIH Office of the Director OD018174;
Office of Science of the US Department of Energy
PMID:29769716 Free, Freely available SCR_018981 2026-09-03 04:58:36 9
Alternative Splicing Annotation Project II Database
 
Resource Report
Resource Website
1+ mentions
Alternative Splicing Annotation Project II Database (RRID:SCR_000322) ASAP II data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE, documented on 8/12/13. An expanded version of the Alternative Splicing Annotation Project (ASAP) database with a new interface and integration of comparative features using UCSC BLASTZ multiple alignments. It supports 9 vertebrate species, 4 insects, and nematodes, and provides with extensive alternative splicing analysis and their splicing variants. As for human alternative splicing data, newly added EST libraries were classified and included into previous tissue and cancer classification, and lists of tissue and cancer (normal) specific alternatively spliced genes are re-calculated and updated. They have created a novel orthologous exon and intron databases and their splice variants based on multiple alignment among several species. These orthologous exon and intron database can give more comprehensive homologous gene information than protein similarity based method. Furthermore, splice junction and exon identity among species can be valuable resources to elucidate species-specific genes. ASAP II database can be easily integrated with pygr (unpublished, the Python Graph Database Framework for Bioinformatics) and its powerful features such as graph query, multi-genome alignment query and etc. ASAP II can be searched by several different criteria such as gene symbol, gene name and ID (UniGene, GenBank etc.). The web interface provides 7 different kinds of views: (I) user query, UniGene annotation, orthologous genes and genome browsers; (II) genome alignment; (III) exons and orthologous exons; (IV) introns and orthologous introns; (V) alternative splicing; (IV) isoform and protein sequences; (VII) tissue and cancer vs. normal specificity. ASAP II shows genome alignments of isoforms, exons, and introns in UCSC-like genome browser. All alternative splicing relationships with supporting evidence information, types of alternative splicing patterns, and inclusion rate for skipped exons are listed in separate tables. Users can also search human data for tissue- and cancer-specific splice forms at the bottom of the gene summary page. The p-values for tissue-specificity as log-odds (LOD) scores, and highlight the results for LOD >= 3 and at least 3 EST sequences are all also reported. exon, gene structure, genome, alternative splicing, cancer genome alignment, intron, isoform, orthologous exon, orthologous gene, orthologous intron, protein sequence, splice site, tissue, genome alignment, cancer is related to: ASAP: the Alternative Splicing Annotation Project
has parent organization: University of California at Los Angeles; California; USA
NCRR U54 RR021813;
NIDCR DE-FC02-02ER63421
PMID:17108355 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02572 SCR_000322 ASAP II Database, Alternative Splicing Annotation Project II 2026-09-03 05:00:42 2
WTCHG Genome Scan Viewer
 
Resource Report
Resource Website
1+ mentions
WTCHG Genome Scan Viewer (RRID:SCR_001635) GSCANDB data or information resource, database, service resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 23,2022. Database / display tool of genome scans, with a web interface that lets the user view the data. It does not perform any analyses - these must be done by other software, and the results uploaded into it. The basic features of GSCANDB are: * Parallel viewing of scans for multiple phenotypes. * Parallel analyses of the same scan data. * Genome-wide views of genome scans * Chromosomal region views, with zooming * Gene and SNP Annotation is shown at high zoom levels * Haplotype block structure viewing * The positions of known Trait Loci can be overlayed and queried. * Links to Ensembl, MGI, NCBI, UCSC and other genome data browsers. In GSCANDB, a genome scan has a wide definition, including not only the usual statistical genetic measures of association between genetic variation at a series of loci and variation in a phenotype, but any quantitative measure that varies along the genome. This includes for example competitive genome hybridization data and some kinds of gene expression measurements. genome, gene, snp, trait, genotype, phenotype, visualization, region, chromosome, quantitative trait locus, hybridization, gene expression has parent organization: University of Oxford; Oxford; United Kingdom NIAAA U01AA014425;
NCRR R24RR015116;
NIGMS R01GM072863;
NINDS R01NS049445;
NIMH P20-MH 62009;
NIAAA U24AA13513
THIS RESOURCE IS NO LONGER IN SERVICE nlx_153902 SCR_001635 Wellcome Trust Centre for Human Genetics Genome Scan Viewer, Genome Scan Viewer, Genome Scan Database 2026-09-03 05:01:16 3
Wisconsin National Primate Research Center
 
Resource Report
Resource Website
1+ mentions
Wisconsin National Primate Research Center (RRID:SCR_012987) WNPRC data or information resource, portal, service resource, topical portal Research center aimed towards increasing understanding of basic primate biology and improving human health and quality of life. Its goals include helping discover treatments, preventative measures and cures for human disease; gathering knowledge of primate biology and ecosystems; providing resources to scientists world wide; and collecting and disseminating research to the larger scientific community and public. NPRC, NPRC Consortium, ORIP, ecosystem, embryonic, fertility, fetal, gene, animal, ctl, development, differentiation, disease, hiv, immunodeficiency, immunogenetic, medicine, metabolic, molecular, neuroendocrinology, obesity, ocular, ovarian, parkinson's disease, polycystic, presbyopia, primate, reproduction, restriction, stem cell, t-cell, vaccine, virology, virus, caloric restriction, obesity, diabetes mellitus, osteoporosis, ocular aging, glaucoma, neurodegeneration, gene expression profiling, simian immunodeficiency virus, cytotoxic t cell, embryonic stem cell, fertility regulation, embryonic differentiation, maternal-fetal health, reproductive neuroendocrinology, polycystic ovarian syndrome, endometriosis, reproductive tract, gene therapy is listed by: Biositemaps
is listed by: National Primate Research Center Consortium
is related to: NIA Nonhuman Primate Tissue Bank
has parent organization: University of Wisconsin-Madison; Wisconsin; USA
is parent organization of: Primate Info Net
is parent organization of: Wisconsin National Primate Research Center Pathology Services Core Facility
Aging NCRR RR000167;
NIH Office of the Director P51 OD011106
Available to the research community nif-0000-24362 https://orip.nih.gov/comparative-medicine/programs/vertebrate-models SCR_012987 2026-09-03 04:52:25 3
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 2026-09-03 04:46:54 2257
Velvet-SC
 
Resource Report
Resource Website
1+ mentions
Velvet-SC (RRID:SCR_004377) Velvet SC data analysis software, data processing software, sequence analysis software, software application, software resource Software package for short read data from single cells that improves assembly through use of progressively increasing coverage cutoff. Used for single cell Illumina sequences, allows variable coverage datasets to be utilized with assembly of E. coli and S. aureus single cell reads. Assembles single cell genome of uncultivated SAR324 clade of Deltaproteobacteria. genome, single, cell, short, read, assembly is listed by: OMICtools
is related to: Velvet
has parent organization: University of California at San Diego; California; USA
NCRR P41 RR024851;
NHGRI R01 HG003647;
Sloan Foundation
PMID:21926975 Free, Available for download, Freely available OMICS_01504 SCR_004377 Velvet Single Cell 2026-09-03 04:47:22 5

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