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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 Authority Synonyms Record Last Update Mentions Count
FuncAssociate: The Gene Set Functionator
 
Resource Report
Resource Website
10+ mentions
FuncAssociate: The Gene Set Functionator (RRID:SCR_005768) FuncAssociate analysis service resource, data analysis service, production service resource, service resource A web-based tool that accepts as input a list of genes, and returns a list of GO attributes that are over- (or under-) represented among the genes in the input list. Only those over- (or under-) representations that are statistically significant, after correcting for multiple hypotheses testing, are reported. Currently 37 organisms are supported. In addition to the input list of genes, users may specify a) whether this list should be regarded as ordered or unordered; b) the universe of genes to be considered by FuncAssociate; c) whether to report over-, or under-represented attributes, or both; and d) the p-value cutoff. A new version of FuncAssociate supports a wider range of naming schemes for input genes, and uses more frequently updated GO associations. However, some features of the original version, such as sorting by LOD or the option to see the gene-attribute table, are not yet implemented. Platform: Online tool gene, gene ontology, statistical analysis, web service, bio.tools is listed by: Gene Ontology Tools
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
has parent organization: Roth Laboratory
NIH ;
Canadian Institute for Advanced Research ;
NINDS NS054052;
NINDS NS035611;
NHLBI HL081341;
NHGRI HG0017115;
NHGRI HG004233;
NHGRI HG003224
PMID:19717575
PMID:14668247
Free for academic use, Acknowledgement requested biotools:funcassociate, OMICS_02264, nlx_149233 http://llama.mshri.on.ca/cgi/func/funcassociate, https://bio.tools/funcassociate SCR_005768 SciCrunch Registry 2026-11-07 12:02:36 36
STRAP
 
Resource Report
Resource Website
100+ mentions
STRAP (RRID:SCR_005675) STRAP data processing software, software application, software resource Software program that automatically annotates a protein list with information that helps in the meaningful interpretation of data from mass spectrometry and other techniques. It takes protein lists as input, in the form of plain text files, protXML files (usually from the TPP), or Dat files from MASCOT search results. From this, it generates protein annotation tables, and a variety of GO charts to aid individual and differential analysis of proteomics data. It downloads information from mainly the Uniprot and EBI QuickGO databases. STRAP requires Windows XP or higher with at least version 3.5 of the Microsoft .NET Framework installed. Platform: Windows compatible protein, gene, annotation, mass spectrometry, proteomics, visualization, browser, differential analysis, analysis, ontology or annotation browser, ontology or annotation visualization, differential analysis of proteomics data sets, windows, protein annotation, data visualization, c#, pathway, FASEB list is listed by: Gene Ontology Tools
is listed by: OMICtools
is related to: Gene Ontology
is related to: UniProt
is related to: QuickGO
has parent organization: Boston University School of Medicine; Massachusetts; USA
NHLBI contract N01 HV28178;
NCRR P41 RR10888
PMID:19839595 Open unspecified license, Acknowledgement requested OMICS_02277, nlx_149115 SCR_005675 SciCrunch Registry Software Tool for Rapid Annotation of Proteins, STRAP for GO Annotation, STRAP - Software Tool for Rapid Annotation of Proteins 2026-11-07 12:01:15 122
OntoMate
 
Resource Report
Resource Website
1+ mentions
OntoMate (RRID:SCR_018493) service resource, software application, software resource, text-mining software Software text mining tool aiding curation at Rat Genome Database. Ontology driven, concept based literature search engine developed at RGD. Tags abstracts with gene names, gene mutations, organism names and terms from ontologies vocabularies used at RGD. Open and fully customizable. Curation, Rat Genome Database, text mining, ontology, concept based, literature search engine, search engine is related to: Rat Genome Database (RGD) NHLBI HL064541;
NHLBI HL094271
PMID:25619558 Free, Freely available SCR_018493 SciCrunch Registry 2026-11-07 12:01:39 1
Rat Genome Database (RGD)
 
Resource Report
Resource Website
100+ mentions
Rat Genome Database (RGD) (RRID:SCR_006444) RGD data or information resource, data repository, database, service resource, storage service resource Database for genetic, genomic, phenotype, and disease data generated from rat research. Centralized database that collects, manages, and distributes data generated from rat genetic and genomic research and makes these data available to scientific community. Curation of mapped positions for quantitative trait loci, known mutations and other phenotypic data is provided. Facilitates investigators research efforts by providing tools to search, mine, and analyze this data. Strain reports include description of strain origin, disease, phenotype, genetics, immunology, behavior with links to related genes, QTLs, sub-strains, and strain sources. RIN, Resource Information Network, mouse, rat, human, gene, qtl, marker, map, strain, sequence, est, genome, ontology, pathway, comparative genomics, physiology, phenotype, disease, model organism, proteomics, function, genetic, genomic, variation, immunology, behavior, knockout, inbred rat strain, mutant, congenic rat, recombinant inbred rat, data analysis service, organism supplier, genotype, gold standard, FASEB list, RRID Community Authority uses: InterMOD
is used by: ChannelPedia
is used by: Resource Identification Portal
is used by: DisGeNET
is used by: Integrated Animals
is used by: NIH Heal Project
is recommended by: Resource Identification Portal
is listed by: re3data.org
is listed by: InterMOD
is listed by: Resource Information Network
is affiliated with: InterMOD
is related to: Rat Gene Symbol Tracker
is related to: MPO
is related to: NIF Data Federation
is related to: MONARCH Initiative
is related to: Vertebrate Trait Ontology
is related to: Biositemaps
is related to: One Mind Biospecimen Bank Listing
is related to: AmiGO
is related to: OMICtools
is related to: re3data.org
is related to: Integrated Manually Extracted Annotation
is related to: OntoMate
has parent organization: Medical College of Wisconsin; Wisconsin; USA
is parent organization of: Diabetes Disease Portal
is parent organization of: Rat Strain Ontology
is parent organization of: Rat Strain Ontology
is parent organization of: Renal Disease Portal
is organization facet of: Alliance of Genome Resources
NHLBI R01 HL064541 PMID:23434633
PMID:18996890
PMID:17151068
Free, Freely available nif-0000-00134, r3d100010417, OMICS_01660 https://doi.org/10.17616/R3WK60 SCR_006444 SciCrunch Registry , Rat Genome Database, RGD 2026-11-07 11:55:53 280
MAPPFinder
 
Resource Report
Resource Website
10+ mentions
MAPPFinder (RRID:SCR_005791) MAPPFinder data analysis software, data processing software, software application, software resource MAPPFinder is an accessory program for GenMAPP. This program allows users to query any existing GenMAPP Expression Dataset Criterion against GO gene associations and GenMAPP MAPPs (microarray pathway profiles). The resulting analysis provides the user with results that can be viewed directly upon the Gene Ontology hierarchy and within GenMAPP, by selecting terms or MAPPs of interest. Platform: Windows compatible gene, gene ontology, gene association, gene expression, profile, microarray, pathway, statistical analysis is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of California at San Francisco; California; USA
has parent organization: Gene Map Annotator and Pathway Profiler
University of California at San Francisco; California; USA ;
San Francisco General Hospital; California; USA ;
NHLBI ;
NCRR MO1RR00083
PMID:12540299 Free for academic use nlx_149270 SCR_005791 SciCrunch Registry 2026-11-07 11:55:40 26
Mouse Phenome Database (MPD)
 
Resource Report
Resource Website
100+ mentions
Mouse Phenome Database (MPD) (RRID:SCR_003212) MPD data or information resource, data repository, database, experimental protocol, narrative resource, service resource, storage service resource Database enables integration of genomic and phenomic data by providing access to primary experimental data, data collection protocols and analysis tools. Data represent behavioral, morphological and physiological disease-related characteristics in naive mice and those exposed to drugs, environmental agents or other treatments. Collaborative standardized collection of measured data on laboratory mouse strains to characterize them in order to facilitate translational discoveries and to assist in selection of strains for experimental studies. Includes baseline phenotype data sets as well as studies of drug, diet, disease and aging effect., protocols, projects and publications, and SNP, variation and gene expression studies. Provides tools for online analysis. Data sets are voluntarily contributed by researchers from variety of institutions and settings, or retrieved by MPD staff from open public sources. MPD has three major types of strain-centric data sets: phenotype strain surveys, SNP and variation data, and gene expression strain surveys. MPD collects data on classical inbred strains as well as any fixed-genotype strains and derivatives that are openly acquirable by the research community. New panels include Collaborative Cross (CC) lines and Diversity Outbred (DO) populations. Phenotype data include measurements of behavior, hematology, bone mineral density, cholesterol levels, endocrine function, aging processes, addiction, neurosensory functions, and other biomedically relevant areas. Genotype data are primarily in the form of single-nucleotide polymorphisms (SNPs). MPD curates data into a common framework by standardizing mouse strain nomenclature, standardizing units (SI where feasible), evaluating data (completeness, statistical power, quality), categorizing phenotype data and linking to ontologies, conforming to internal style guides for titles, tags, and descriptions, and creating comprehensive protocol documentation including environmental parameters of the test animals. These elements are critical for experimental reproducibility. female, genomic location, genotype, inbred strain, male, mouse strain, phenome, phenotype, qtl, reference data, single-nucleotide polymorphism, strain allele, strain characteristic, strain, trait, gene expression, variation, hypothesis testing, data set, bio.tools, FASEB list is used by: NIF Data Federation
is used by: Integrated Datasets
is used by: NIH Heal Project
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: Special Mouse Strains Resource
is related to: Vertebrate Trait Ontology
is related to: GenomeMUSter
has parent organization: Jackson Laboratory
NHGRI HG003057;
NHLBI HL66611;
NIA AG025707;
NIA AG038070;
NIDA ;
NIDA DA028420;
NIMH MH071984
PMID:24243846
PMID:22102583
PMID:18987003
PMID:17151079
Free, Freely available biotools:mpd, nif-0000-03160, r3d100010101 https://bio.tools/mpd, https://doi.org/10.17616/R3PC7F http://www.jax.org/phenome SCR_003212 SciCrunch Registry Mouse Phenome Database 2026-11-07 11:54:57 230

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