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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 Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
Stanford TMA Software
 
Resource Report
Resource Website
1+ mentions
Stanford TMA Software (RRID:SCR_005598) Stanford TMA software resource Software Tools for High-Throughput Analysis and Archiving of Immunohistochemistry Staining Data Obtained with Tissue Microarrays. tissue microarray is listed by: OMICtools
is related to: TMA-Combiner
has parent organization: Stanford University; Stanford; California
PMID:12414504 OMICS_00819 SCR_005598 Stanford TMA Software website, Stanford Tissue Microarray Software 2026-02-14 02:00:58 1
OXBench
 
Resource Report
Resource Website
1+ mentions
OXBench (RRID:SCR_005591) OXBench software resource A suite of programs aimed at developers of alignment methods rather than end-users to assess the accuracy of multiple sequence alignment methods. It includes a reference database of protein multiple sequence alignments that were generated by consideration of protein three-dimensional structure. alignment, linux, protein, sequence alignment is listed by: OMICtools
has parent organization: University of Dundee; Scotland; United Kingdom
PMID:14552658 Acknowledgement requested OMICS_00983 http://www.compbio.dundee.ac.uk/Software/Oxbench/oxbench.html Alt. URL: http://www.compbio.dundee.ac.uk/software.html SCR_005591 2026-02-14 02:00:57 2
Staden Package
 
Resource Report
Resource Website
50+ mentions
Staden Package (RRID:SCR_005629) software resource A fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin) for Unix, Linux, MacOSX and MS Windows. c, unix/linux, sequence assembly, dna/protein analysis, spin, sequence alignment, genome, genome viewer, c++, fortran, tcl, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:20513662
DOI:10.1093/bioinformatics/btq268
BSD License OMICS_00894, biotools:staden https://bio.tools/staden
https://sources.debian.org/src/staden/
SCR_005629 Staden Package 2026-02-14 02:01:09 79
Chromaseq
 
Resource Report
Resource Website
1+ mentions
Chromaseq (RRID:SCR_005587) Chromaseq software resource A software package in Mesquite that processes chromatograms, makes contigs, base calls, etc., using in part the programs Phred and Phrap. chromatogram, sequence, mesquite is listed by: OMICtools
has parent organization: Oregon State University; Oregon; USA
NSF EF-0531754 Acknowledgement required OMICS_01017 SCR_005587 Chromaseq: a package for processing chromatograms and sequence data in Mesquite 2026-02-14 02:01:09 7
Burroughs Wellcome Fund
 
Resource Report
Resource Website
100+ mentions
Burroughs Wellcome Fund (RRID:SCR_005772) BWF institution The Burroughs Wellcome Fund is an independent private foundation dedicated to advancing the biomedical sciences by supporting research and other scientific and educational activities. Within this broad mission, BWF has two primary goals: * To help scientists early in their careers develop as independent investigators * To advance fields in the basic biomedical sciences that are undervalued or in need of particular encouragement BWF''s financial support is channeled primarily through competitive peer-reviewed award programs. * BWF''s endowment: $586.8 million at the end of FY 2009 * BWF approved $26.4 million in grants during FY 2009 BWF makes grants primarily to degree-granting institutions on behalf of individual researchers, who must be nominated by their institutions. To complement these competitive award programs, BWF also makes grants to nonprofit organizations conducting activities intended to improve the general environment for science. A Board of Directors comprising distinguished scientists and business leaders governs BWF. BWF was founded in 1955 as the corporate foundation of the pharmaceutical firm Burroughs Wellcome Co. In 1993, a generous gift from the Wellcome Trust in the United Kingdom, enabled BWF to become fully independent from the company, which was acquired by Glaxo in 1995. BWF has no affiliation with any corporation. biomedical sciences, research, science, education Wellcome Trust nlx_149371, grid.427464.7, Wikidata: Q5000488, ISNI: 0000 0000 8727 8697, Crossref funder ID: 100000861 https://ror.org/01d35cw23 SCR_005772 2026-02-14 02:01:11 103
Finnish Cancer Registry
 
Resource Report
Resource Website
1+ mentions
Finnish Cancer Registry (RRID:SCR_005881) Finnish Cancer Registry institution The Finnish Cancer Registry maintains a nation-wide database on all cancer cases in Finland going back to 1953. It is also an internationally active institute for statistical and epidemiological cancer research. The Mass Screening Registry is a department of the Finnish Cancer Registry, and is responsible of planning and evaluating national cancer screening programs in Finland. The site contains information on cancer research and up to date statistics on the prevalence of different types of cancer in Finland, the Nordic countries and on a global level. The web pages include information for participants in cancer screening and for professionals involved in organizing such screening. Cancer Cancer Society of Finland grid.424339.b, nlx_149446, ISNI: 0000 0000 8634 0612 https://ror.org/00j15sg62 SCR_005881 2026-02-14 02:01:01 8
MAGMA
 
Resource Report
Resource Website
100+ mentions
MAGMA (RRID:SCR_005757) MAGMA software resource Software that utilizes a multiobjective evolutionary algorithm for genetic mapping. It is based on a the ECJ evolutionary software package written by Sean Luke and includes the Strength Pareto Evoluationary Algorithm Version 2 changes for multiobjective analysis. The code runs on any platform with Java Version 2. A genetic mapping project, typically implemented during a search for genes responsible for a disease, requires the acquisition of a set of data from each of a large number of individuals. This data set includes the values of multiple genetic markers. These genetic markers occur at discrete positions along the genome, which is a collection of one or more linear chromosomes. Typing the value of a marker in an individual carries a cost; one seeks to minimize the number of markers typed without excessively jeopardizing the probability of detecting an association between a marker and a disease phenotype. MAGMA is a project which employ''s a multiobjective evolutionary algorithm to solve this problem. gene, genetic mapping, algorithm, genomics, single nucleotide polymorphism, population study, haplotype-block elucidation, java has parent organization: SourceForge Juvenile Diabetes Research Foundation PMID:12875658 Open unspecified license nlx_149220 SCR_005757 Multiobjective Analyzer for Genetic Marker Acquisition, MAGMA: Multiobjective Analyzer for Genetic Marker Acquisition 2026-02-14 02:01:00 456
Icahn School of Medicine at Mount Sinai; New York; USA
 
Resource Report
Resource Website
1+ mentions
Icahn School of Medicine at Mount Sinai; New York; USA (RRID:SCR_005793) ISMMS, MSSM university Icahn School of Medicine at Mount Sinai, formerly Mount Sinai School of Medicine, is graduate medical school in Manhattan, New York City. Leader in medical and scientific training and education, biomedical research and patient care. medicine, medical, school, university, doctorate, phd uses: Scizzle
is affiliated with: BioJupies
is related to: Alzheimers Disease Genetics Consortium
is related to: Beta Cell Biology Consortium
is related to: Clinical and Translational Science Awards Consortium
is related to: proMODMatcher
is parent organization of: Enrichr
is parent organization of: Neuropathology of CTE and Delayed Effects of TBI: Toward In-Vivo Diagnostics
is parent organization of: NeuronStudio
is parent organization of: Rayburst Open-Source Code
is parent organization of: Volume Integration and Alignment System
is parent organization of: Volume Integration and Alignment System Source Code
is parent organization of: NeuroGL
is parent organization of: TIFF Stack Sub-Sampler
is parent organization of: Cre-X-Mice: A Database of Cre Transgenic Lines
is parent organization of: Mount Sinai School of Medicine: In-Vivo Molecular Imaging Laboratory
is parent organization of: Mount Sinai Biobank
is parent organization of: ChEA
is parent organization of: Kismeth
is parent organization of: Lists2Networks
is parent organization of: Mount Sianai Department of Neuroscience
is parent organization of: NetworKIN
is parent organization of: Mount Sinai Alzheimer's Disease Research Center
is parent organization of: Manhattan HIV Brain Bank
is parent organization of: Computational Neurobiology and Imaging Center
is parent organization of: L1000 Characteristic Direction Signature Search Engine
is parent organization of: L1000 Fireworks Display
is parent organization of: Drug Gene Budger
is parent organization of: COVID-19 Crowd Generated Gene and Drug Set Library
is parent organization of: GeneOverlap
is parent organization of: Datanator
is parent organization of: BioSimulations
is parent organization of: DE-Sim
is parent organization of: Appyters
is parent organization of: ezTrack project
is parent organization of: Minian
is parent organization of: TargetRanger
is parent organization of: GeneRanger
is parent organization of: Kinase Enrichment Analysis 3
is parent organization of: X2K Web
is parent organization of: Diabetes Data and Hypothesis Hub
is parent organization of: Icahn School of Medicine at Mount Sinai Microscopy and Advanced Bioimaging Core Facility
is parent organization of: Icahn School of Medicine at Mount Sinai Transgenic and Genome Editing Core Facility
is parent organization of: Icahn School of Medicine at Mount Sinai Stem Cell Engineering Core Facility
is parent organization of: Icahn School of Medicine at Mount Sinai Metabolomics Core Facility
is parent organization of: Icahn School of Medicine at Mount Sinai Neuropathology Brain Bank and Research CoRE Facility
is parent organization of: Icahn School of Medicine at Mount Sinai RNA Nanocore Core Facility
is parent organization of: Icahn School of Medicine at Mount Sinai Human Immune Monitoring Center Core Facility
is parent organization of: Icahn School of Medicine at Mount Sinai Center for Advanced Genomics Technology Core Facility
is parent organization of: Icahn School of Medicine at Mount Sinai Biorepository and Pathology Core Facility
is parent organization of: Icahn School of Medicine at Mount Sinai Mount Sinai Cryo-EM CoRE Core Facility
nlx_55912, grid.59734.3c, Crossref funder ID:100007277, ISNI:0000 0001 0670 2351, Wikidata:Q1950740 https://ror.org/04a9tmd77 SCR_005793 Mount Sinai School of Medicine, Icahn School of Medicine, Icahn School of Medicine at Mount Sinai 2026-02-14 02:00:58 6
SPLINTER
 
Resource Report
Resource Website
10+ mentions
SPLINTER (RRID:SCR_005826) SPLINTER software resource Software that detects and quantifies short IN/DELs as well as single nucleotide substitutions in pooled-DNA samples. is listed by: OMICtools
has parent organization: Washington University in St. Louis; Missouri; USA
Cancer Free for academic / non-profit use, Commercial use requires license OMICS_00100 SCR_005826 Short IN/DEL Prediction by Large deviation Inference and Non-linear True frequency Estimation by Recursion 2026-02-14 02:01:01 13
GOEx - Gene Ontology Explorer
 
Resource Report
Resource Website
10+ mentions
GOEx - Gene Ontology Explorer (RRID:SCR_005779) GOEx software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented July 5, 2018. Gene Ontology Explorer (GOEx) combines data from protein fold changes with GO over-representation statistics to help draw conclusions in proteomic experiments. It is tightly integrated within the PatternLab for Proteomics project and, thus, lies within a complete computational environment that provides parsers and pattern recognition tools designed for spectral counting. GOEx offers three independent methods to query data: an interactive directed acyclic graph, a specialist mode where key words can be searched, and an automatic search. A recent hack included in GOEx is to load the sparse matrix index file directly into GOEx, instead of going through the report generation using the AC/T-fold methods. This makes it easy for GOEx to analyze any list of proteins as long as the list follows the index file format (described in manuscript) . Please note that if using this alternative strategy, there will be no protein fold information. Platform: Windows compatible proteomics, visualization, statistical analysis, gene ontology, parse, pattern recognition, spectral counting, analysis, protein fold is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Scripps Research Institute
CNPq ;
CAPES ;
FAPERJ BBP grant ;
PAPES ;
PDTIS ;
Ary Frauzino Foundation ;
NIAID ;
NIH ;
genesis molecular biology laboratory ;
Fiocruz-INCA collaboration ;
NIAID UCSD/MCB0237059;
NCRR P41RR011823;
NIMH 5R01 MH067880
PMID:19239707 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149249 http://pcarvalho.com/patternlab/goex.shtml SCR_005779 Gene Ontology Explorer, GO Explorer 2026-02-14 02:01:00 26
AppliChem
 
Resource Report
Resource Website
1000+ mentions
AppliChem (RRID:SCR_005814) commercial organization An Antibody supplier nlx_152277 SCR_005814 PanReac AppliChem, AppliChem GmbH 2026-02-14 02:00:59 4849
OWLTools
 
Resource Report
Resource Website
10+ mentions
OWLTools (RRID:SCR_005732) OWLTools software resource OWLTools (aka OWL2LS - OWL2 Life Sciences) is a java API for accessing ontologies in either OBO or OWL. OWLTools provides a bio-ontologies friendly wrapper on top of the Manchester OWL API. It provides many features, including: * convenience methods for OBO-like properties such as synonyms, textual definitions, obsoletion, replaced_by * simple graph-like operations over ontologies * visualization using the QuickGO graphs libraries Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible software library, ontology is listed by: Gene Ontology Tools
is related to: OBO
has parent organization: Gene Ontology
has parent organization: Google Project Hosting
is parent organization of: OwlSim
Open unspecified license - Free for academic use nlx_149192 SCR_005732 OWL2LS - OWL2 Life Sciences, OWL Tools 2026-02-14 02:01:10 18
Blip: Biomedical Logic Programming
 
Resource Report
Resource Website
1+ mentions
Blip: Biomedical Logic Programming (RRID:SCR_005733) Blip, blipkit software resource Biomedical Logical Programming (Blip) is a research-oriented deductive database and prolog application library for handling biological and biomedical data. It includes packages for advanced querying of ontologies and annotations. Blip underpins the Obol tool. Here are some distinguishing characteristics of Blip * Lightweight. Bloat-free: Blip only has as many modules as it needs to do its job. * Fast. * Declarative. Say what you want to do, not how you want to do it * Blip can be Query-oriented: specify your data sources and ask your query * Blip can be Application-oriented: it is designed to be used as an application library used by other bioinformatics tools * Mature and fully functional ontology module for handling both OBO-style ontologies and OWL ontologies. * Modules for handling biological sequences and sequence features. (currently limited functionality, added as needed) * A systems biology module for querying pathway and interaction data. (currently limited functionality, added as needed) * Relational database integration. SQL can be viewed as a highly restricted dialect of Prolog. Although the SWI-Prolog in-memory database is fast and scalable, sometimes it is nice to be able to fetch data from an external database. Blip contains a generic SQL utility module and predicate mappings for the GO database, Ensembl and Chado * Integration with a variety of bioinformatics file formats. SWI-Prolog has a variety of fast libraries for dealing with XML, RDF and tabular data files. Blip provides bridges from bio file formats encoded using these syntaxes into its native models. For other syntaxes, Blip seamlessly integrates other packages such as BioPerl and go-perl. Although these dependencies require extra installation, there is no point reinventing the wheel * Rapid development of web applications. Blip extends SWI-Prolog''''s excellent http support with a simple and powerful logical-functional-programming style application server, serval. This has been used to prototype a fully-featured next-generation replacement for the GO project amigo browser. * Scalable. Blip is not intended to be a toy system on toy data (although it is happy to be used as a toy if you like!). It is intended to be used as an application component and a tool operating on real-world biological and biomedical data Blip is written in SWI-Prolog, a fast, robust and scalable implementation of ISO Prolog. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible biology, biomedical, ontology, annotation, software library, bioinformatics, module is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Berkeley Bioinformatics Open-Source Projects
GNU Lesser General Public License nlx_149193 SCR_005733 Blip - Biomedical Logic Programming, Biomedical Logical Programming (Blip), Biomedical Logic Programming 2026-02-14 02:00:58 2
American Cancer Society
 
Resource Report
Resource Website
100+ mentions
American Cancer Society (RRID:SCR_005756) ACS non profit organization The American Cancer Society is the nationwide, community-based, voluntary health organization dedicated to eliminating cancer as a major health problem by preventing cancer, saving lives, and diminishing suffering from cancer, through research, education, advocacy, and service. Together with our millions of supporters, the American Cancer Society (ACS) saves lives and creates a world with less cancer and more birthdays by helping people stay well, helping people get well, by finding cures, and by fighting back. Headquartered in Atlanta, Georgia, the ACS has 12 chartered Divisions, more than 900 local offices nationwide, and a presence in more than 5,100 communities. cancer, breast cancer, colon, lung, prostate, skin, breast Cancer grid.422418.9, Wikidata: Q463665, nlx_149219, ISNI: 0000 0004 0371 6485, Crossref funder ID: 100000048 https://ror.org/02e463172 SCR_005756 American Cancer Society - The Official Sponsor of Birthdays 2026-02-14 02:01:09 476
Antigenix America
 
Resource Report
Resource Website
1+ mentions
Antigenix America (RRID:SCR_005871) commercial organization An Antibody supplier nlx_152276 SCR_005871 Antigenix America Inc. 2026-02-14 02:01:12 1
ClueGO
 
Resource Report
Resource Website
1000+ mentions
ClueGO (RRID:SCR_005748) ClueGO software resource A Cytoscape plug-in that visualizes the non-redundant biological terms for large clusters of genes in a functionally grouped network. It can be used in combination with GOlorize. The identifiers can be uploaded from a text file or interactively from a network of Cytoscape. The type of identifiers supported can be easily extended by the user. ClueGO performs single cluster analysis and comparison of clusters. From the ontology sources used, the terms are selected by different filter criteria. The related terms which share similar associated genes can be combined to reduce redundancy. The ClueGO network is created with kappa statistics and reflects the relationships between the terms based on the similarity of their associated genes. On the network, the node colour can be switched between functional groups and clusters distribution. ClueGO charts are underlying the specificity and the common aspects of the biological role. The significance of the terms and groups is automatically calculated. ClueGO is easy updatable with the newest files from Gene Ontology and KEGG. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible, THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. statistical analysis, function, gene ontology, pathway, annotation, network, plugin, gene is listed by: Gene Ontology Tools
is listed by: SoftCite
is related to: Gene Ontology
is related to: Cytoscape
is related to: KEGG
is related to: BioCarta Pathways
has parent organization: National Institute of Health and Medical Research; Rennes; France
National Institute of Health and Medical Research; Rennes; France ;
Ville de Paris ;
INCa ;
Austrian Ministry for Science and Research ;
BINII ;
European Union 7FP 202230
PMID:19237447 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149209 SCR_005748 2026-02-14 02:00:58 2943
University of Louisville; Kentucky; USA
 
Resource Report
Resource Website
1+ mentions
University of Louisville; Kentucky; USA (RRID:SCR_005749) UL university Public research university in Louisville, Kentucky. It is part of the Kentucky state university system. is parent organization of: University of Louisville Labs and Facilities
is parent organization of: University of Louisville Micro/Nano Technology Center
is parent organization of: University of Louisville Micro/Nano Technology Center Core Facility
is parent organization of: University of Louisville School of Medicine Molecular Modeling Core Facility
is parent organization of: University of Louisville Biophysical Core Facility
is parent organization of: University of Louisville Medicinal Chemistry Core Facility
is parent organization of: University of Louisville Protein Expression and Purification Core Facility
is parent organization of: University of Louisville Nuclear Magnetic Resonance Spectroscopy Core Facility
is parent organization of: University of Louisville Sequencing Technology Center Genomics Services Core Facility
is parent organization of: University of Louisville Proteomics Technology Center PTC Core Facility
Wikidata:Q1317143, grid.266623.5, Crossref funder ID:100007924, nlx_26318, ISNI:0000 0001 2113 1622 https://ror.org/01ckdn478 SCR_005749 UofL, U of L, University of Louisville 2026-02-14 02:01:09 1
Andrew W. Mellon Foundation
 
Resource Report
Resource Website
10+ mentions
Andrew W. Mellon Foundation (RRID:SCR_005864) Andrew W. Mellon Foundation funding resource The Andrew W. Mellon Foundation currently makes grants in five core program areas: * Higher Education and Scholarship * Scholarly Communications and Information Technology * Art History, Conservation, and Museums * Performing Arts * Conservation and the Environment Within each of its core programs, the Foundation concentrates most of its grantmaking in a few areas. Institutions and programs receiving support are often leaders in fields of Foundation activity, but they may also be promising newcomers, or in a position to demonstrate new ways of overcoming obstacles to achieve program goals. Our grantmaking philosophy is to build, strengthen and sustain institutions and their core capacities, rather than be a source for narrowly defined projects. As such, we develop thoughtful, long-term collaborations with grant recipients and invest sufficient funds for an extended period to accomplish the purpose at hand and achieve meaningful results. grant, higher education, scholarship, scholarly communication, information technology, art history, conservation, museum, performing arts, environment nlx_149404 SCR_005864 2026-02-14 02:01:01 13
American Urological Association
 
Resource Report
Resource Website
100+ mentions
American Urological Association (RRID:SCR_005859) AUA institution The American Urological Association (AUA), founded in 1902, is the premier professional association for the advancement of urologic patient care, and works to ensure that its more than 18,000 members are current on the latest research and practices in urology. The AUA also pursues its mission of fostering the highest standards of urologic care by providing a wide range of servicesincluding publications, research, the Annual Meeting, continuing medical education (CME) and the formulation of health policy. urology, research is listed by: Collaborating for the Advancement of Interdisciplinary Research in Benign Urology
is parent organization of: AmerUrological's channel - YouTube
Urologic disease grid.422576.0, ISNI: 0000 0001 2222 2235, Wikidata: Q4745327, Crossref funder ID: 100006280, nlx_149398 https://ror.org/00sbaqa70 SCR_005859 American Urological Association (AUA) 2026-02-14 02:01:01 252
EDASeq
 
Resource Report
Resource Website
100+ mentions
EDASeq (RRID:SCR_006751) EDASeq software resource Software for numerical and graphical summaries of RNA-Seq read data. Within-lane normalization procedures to adjust for GC-content effect (or other gene-level effects) on read counts: loess robust local regression, global-scaling, and full-quantile normalization (Risso et al., 2011). Between-lane normalization procedures to adjust for distributional differences between lanes (e.g., sequencing depth): global-scaling and full-quantile normalization (Bullard et al., 2010)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. data analysis, normalization, rna-seq is listed by: OMICtools
has parent organization: Bioconductor
has parent organization: National Cancer Institute
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01231 SCR_006751 EDASeq: Exploratory Data Analysis and Normalization for RNA-Seq data 2026-02-14 02:01:23 254

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