SYSTEM UPDATE: We will be performing system maintenace Saturday September 26 at 9pm to midnight Pacific Time

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


Current Facets and Filters

  • Keywords:bio.tools (facet)


Recent searches

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

1,645 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 Authority Synonyms Record Last Update Mentions Count
UMD-BRCA1/ BRCA2 databases
 
Resource Report
Resource Website
10+ mentions
UMD-BRCA1/ BRCA2 databases (RRID:SCR_006128) UMD-BRCA1/ BRCA2 databases data or information resource, data repository, database, service resource, storage service resource The UMD-BRCA1/BRCA2 databases have been set up in a joined national effort through the network of 16 diagnostic laboratories to provide up-to-date information about mutations of the BRCA1 and BRCA2 genes identified in patients with breast and/or ovarian cancer. These databases currently contain published and unpublished information about the BRCA1/BRCA2 mutations reported in French diagnostic laboratories. This database includes 28 references and 5530 mutations (1440 different mutations and 786 protein variants) The databases of BRCA1 and BRCA2 mutations were built using the Universal Mutation Database tool. For each mutation, information is provided at several levels: * at the gene level: exon and codon number, wild type and mutant codon, mutation event, mutation name and, * at the protein level: wild type and mutant amino acid, binding domain, affected domain. If you want to submit a mutation, please contact R. Lidereau., S. Caputo. or E. Rouleau. cancer, gene, mutation, exon, codon, wild type, mutant, mutation, protein, amino acid, binding domain, affected domain, brca1, brca2, variant, polymorphism, unclassified variant, unknown variant, female, woman, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: National Institute of Health and Medical Research; Rennes; France
Breast cancer, Ovarian cancer French National Cancer Institute ;
European Union FP7/2007-2013;
Association dAide a la Recherche Cancerologique de Saint Cloud
PMID:22144684 The UMD- BRCA1 Locus Specific Databases constitute the intellectual property of the curators of the database. Any unauthorized copying, Storage or distribution of this material without written permission from the curators would lead to copyright infringement with possible ensuing litigation. biotools:brca_share, nlx_151608 https://bio.tools/brca_share SCR_006128 SciCrunch Registry UMD-BRCA1 mutations database, UMD-BRCA1 / BRCA2 databases, UMD-BRCA1/BRCA2 databases 2026-09-19 12:51:05 26
PRED-GPCR
 
Resource Report
Resource Website
1+ mentions
PRED-GPCR (RRID:SCR_006196) PRED-GPCR analysis service resource, data analysis service, data or information resource, data set, production service resource, service resource A prediction tool for GPCR Family Classification from sequence alone based on a probabilistic method that uses family-specific profile Hidden Markov Models. The PRED-GPCR system is based on a probabilistic method that uses family specific profile HMMs in order to determine to which GPCR family a query sequence belongs or resembles. The approach proposed in this method exploits the descriptive power of profile HMMs along with an exhaustive discrimination assessment method to select only highly selective and sensitive profiles, for each family. The collection of these profiles constitutes a signature library, which is scanned, for significant matches with a given query sequence. The output report for a query sequence consists of two sections: * A ranked list of the profile HMM matches, below the selected individual motif E-value cutoff, along with their corresponding family. * A ranked list of the Combined P-values, E-values as well as the number of profiles matched for each family. To cross-evaluate your results you can browse through Swiss-Prot, Trembl, Pfam and Prosite family related entries. g-protein coupled receptor, classification, hidden markov model, sequence, fasta, family classification, motif, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: University of Athens Biophysics and Bioinformatics Laboratory
PMID:15215415 nlx_151741, biotools:pred-gpcr https://bio.tools/pred-gpcr SCR_006196 SciCrunch Registry PRED-GPCR: GPCRs Family classification from sequence alone 2026-09-19 12:51:06 2
MouseBook
 
Resource Report
Resource Website
10+ mentions
MouseBook (RRID:SCR_006358) MouseBook biomaterial supply resource, material resource, organism supplier Databases and portal to data and ordering mouse strains from MRC Harwell including mouse stocks in FESA (Frozen Embryo and Sperm Archive), mutants from the mutagenesis screen, the ENU DNA archive, standardized phenotyping procedures, imprinting genes and chromosome anomalies. The portal integrates curated information from the MRC Harwell stock resource, and other Harwell databases, with information from external data resources to provide added value information above and beyond what is available through other routes such as IMSR (International Mouse Stain Resource). MouseBook can be searched either using an intuitive Google-style free text search or using the Mammalian Phenotype Ontology (MP) tree structure. Text searches can be on gene, allele, strain identifier (e.g. MGI ID) or phenotype term and are assisted by automatic recognition of term types and autocompletion of gene and allele names covered by the database. Results are returned in a tabbed format providing categorized results identified from each of the catalogs in MouseBook. Individual results lines from each catalog include information on gene, allele, chromosomal location and phenotype and provide a simple click-through link to further information as well as ordering the strain. The infrastructure underlying MouseBook has been designed to be extensible, allowing additional data sources to be added enabling other sites to make their data directly available through MouseBook. mutant mouse strain, gene, allele, phenotype, embryonic mouse, embryo, sperm, live, chromosomal location, mutant mouse line, imprint, standard operating procedure, bio.tools is listed by: One Mind Biospecimen Bank Listing
is listed by: Debian
is listed by: bio.tools
is related to: MPO
Motor neuron disease, Chromosomal anomaly MRC PMID:19854936 Public nlx_152127, biotools:mousebook https://bio.tools/mousebook SCR_006358 SciCrunch Registry Mouse Book 2026-09-19 12:51:09 18
IRanges
 
Resource Report
Resource Website
50+ mentions
IRanges (RRID:SCR_006420) IRanges software resource Software tool for computing and annotating genomic ranges.Provides efficient low-level and highly reusable S4 classes for storing ranges of integers, RLE vectors (Run-Length Encoding), and, more generally, data that can be organized sequentially (formally defined as Vector objects), as well as views on these Vector objects. Efficient list-like classes are also provided for storing big collections of instances of the basic classes. All classes in the package use consistent naming and share the same rich and consistent Vector API as much as possible. Annotating genomic ranges, computing genomic ranges, genomic ranges, storing ranges of integers, bio.tools is used by: riboWaltz
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
PMID:23950696 Free, Available for download, Freely available OMICS_01163, biotools:iranges https://bio.tools/iranges SCR_006420 SciCrunch Registry Infrastructure for manipulating intervals on sequences 2026-09-19 12:51:10 88
VICUNA
 
Resource Report
Resource Website
10+ mentions
VICUNA (RRID:SCR_006302) VICUNA software resource A de novo assembly program targeting populations with high mutation rates. c++, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Broad Institute
PMID:22974120 biotools:vicuna, OMICS_02162 https://bio.tools/vicuna SCR_006302 SciCrunch Registry 2026-09-19 12:51:08 26
MSIsensor
 
Resource Report
Resource Website
100+ mentions
MSIsensor (RRID:SCR_006418) MSIsensor software resource A C++ software program for automatically detecting somatic and germline variants at microsatellite regions. It computes length distributions of microsatellites per site in paired tumor and normal sequence data, subsequently using these to statistically compare observed distributions in both samples. c++, somatic variant, germline variant, microsatellite, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
Tumor, Normal PMID:24371154 Copyrighted, See LICENSE biotools:msisensor, OMICS_02192 https://bio.tools/msisensor SCR_006418 SciCrunch Registry 2026-09-19 12:51:10 168
TSSer
 
Resource Report
Resource Website
TSSer (RRID:SCR_006419) TSSer software resource A computational pipeline to analyze differential RNA sequencing (dRNA-seq) data to determine transcription start sites genome-wide. differential rna sequencing, transcription start site, rna-seq, genome, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: University of Basel; Basel; Switzerland
PMID:24371151 GNU General Public License biotools:tsser, OMICS_02191 https://bio.tools/tsser SCR_006419 SciCrunch Registry TSSer: a computational pipeline to identify transcription start sites in bacterial genomes 2026-09-19 12:51:10 0
Flycircuit
 
Resource Report
Resource Website
50+ mentions
Flycircuit (RRID:SCR_006375) atlas, data or information resource, database, service resource, storage service resource FlyCircuit is a public database for online archiving, cell type inventory, browsing, searching, analysis and 3D visualization of individual neurons in the Drosophila brain. drosophila, fly brain, neuron reconstruction, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
is related to: Virtual Fly Brain
has parent organization: National Tsing Hua University; Hsinchu; Taiwan
PMID:21129968 r3d100012173, nif-0000-07738, biotools:FlyCircuit https://bio.tools/FlyCircuit, https://doi.org/10.17616/R3293N SCR_006375 SciCrunch Registry Fly Circuit - A Database of Drosophila Brain Neurons, Fly Circuit, Flycircuit database, Fly Circuit Database, FlyCircuit - A Database of Drosophila Brain Neurons 2026-09-19 12:51:09 50
HUDSEN
 
Resource Report
Resource Website
1+ mentions
HUDSEN (RRID:SCR_006324) HUDSEN community building portal, data or information resource, portal Forum for researchers in human developmental biology and related fields to meet and establish links. development, genetics, embryology, embryonic, bio.tools is listed by: bio.tools
is listed by: Debian
is related to: eMouseAtlas
is related to: aGEM
has parent organization: Newcastle University; Newcastle upon Tyne; United Kingdom
is parent organization of: HUDSEN Electronic Atlas of the Developing Human Brain
is parent organization of: HUDSEN Human Gene Expression Spatial Database
nlx_152025, biotools:hudsen https://bio.tools/hudsen SCR_006324 SciCrunch Registry Human Developmental Studies Network 2026-09-19 12:51:08 5
PomBase
 
Resource Report
Resource Website
100+ mentions
PomBase (RRID:SCR_006586) PomBase data or information resource, database, service resource Model organism database that provides organization of and access to scientific data for the fission yeast Schizosaccharomyces pombe. PomBase supports genomic sequence and features, genome-wide datasets and manual literature curation. PomBase also provides a community hub for researchers, providing genome statistics, a community curation interface, news, events, documentation, mailing lists, and welcomes data submissions. fission yeast, gene ontology, genome sequence, schizosaccharomyces pombe (4896), schizosaccharomyces pombe, dna, protein, cosmic assembly, intron, go, chromosome, telomere, centromere, mating region, data mapping, model organism, genome, bio.tools, FASEB list is used by: NIF Data Federation
is listed by: 3DVC
is listed by: Debian
is listed by: bio.tools
is related to: AmiGO
is related to: GeneDB Spombe
has parent organization: University of Cambridge; Cambridge; United Kingdom
has parent organization: University College London; London; United Kingdom
is parent organization of: Fission Yeast Phenotype Ontology
is parent organization of: Pompep
Wellcome Trust WT090548MA PMID:22039153 Public, Acknowledgement requested biotools:pombase, nlx_144356, r3d100011478 https://bio.tools/pombase, https://doi.org/10.17616/R3NS78 http://www.sanger.ac.uk/Projects/S_pombe/ SCR_006586 SciCrunch Registry Schizosaccharomyces pombeGenome Sequencing Project 2026-09-19 12:51:14 396
COLT-Cancer
 
Resource Report
Resource Website
10+ mentions
COLT-Cancer (RRID:SCR_006485) COLT-Cancer analysis service resource, data analysis service, data or information resource, database, production service resource, service resource The COLT-Cancer database is a collection of shRNA dropout signatures profiles, covering ~16000 human genes, and derived from more than 70 Pancreatic, Ovarian and Breast human cancer cell-lines using the microarray detection platform developed in the COLT (CCBR-OICR Lentiviral Technology) facility at the Moffat Lab. All shRNA dropout profiles are freely available through download or queries via this website. gene, shrna profile, shrna, functional genetics, cancer, cell line, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: University of Toronto; Ontario; Canada
Pancreatic cancer, Ovarian cancer, Breast cancer Ontario Institute for Cancer Research ;
Terry Fox Research Institute ;
Canadian Institutes of Health Research ;
Canada Foundation for Innovation ;
Ontario Research Fund
PMID:22102578 Free biotools:colt-cancer, nlx_149426 https://bio.tools/colt-cancer SCR_006485 SciCrunch Registry CCBR-OICR Lentiviral Technology Cancer, COLT-Cancer database 2026-09-19 12:51:12 11
COHCAP
 
Resource Report
Resource Website
10+ mentions
COHCAP (RRID:SCR_006499) COHCAP software resource An algorithm to analyze single-nucleotide resolution methylation data (Illumina 450k methylation array, targeted BS-Seq, etc.). It provides QC metrics, differential methylation for CpG Sites, differential methylation for CpG Islands, integration with gene expression data, and visualization of methylation values. java, perl, s/r, java swing, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:23598999 Acknowledgement requested, Attribution Assurance License biotools:cohcap, OMICS_00595 https://bio.tools/cohcap SCR_006499 SciCrunch Registry City of Hope CpG Island Analysis Pipeline, COHCAP - City of Hope CpG Island Analysis Pipeline 2026-09-19 12:51:12 19
Phenotypes and eXposures Toolkit
 
Resource Report
Resource Website
50+ mentions
Phenotypes and eXposures Toolkit (RRID:SCR_006532) PhenX Toolkit catalog, data or information resource, data set, database, narrative resource, service resource, standard specification Set of measures intended for use in large-scale genomic studies. Facilitate replication and validation across studies. Includes links to standards and resources in effort to facilitate data harmonization to legacy data. Measurement protocols that address wide range of research domains. Information about each protocol to ensure consistent data collection.Collections of protocols that add depth to Toolkit in specific areas.Tools to help investigators implement measurement protocols. PhenX project, genome, phenotype, genome-wide association study, genetic variation, genomic study, substance abuse, addiction, substance use, environmental exposure, disease susceptibility, outcome, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: RTI International
has parent organization: Consensus Measures for Phenotype and Exposure
has parent organization: Trans-Omics for Precision Medicine (TOPMed) Program
has organization facet: PhenX Phenotypic Terms
is organization facet of: Consensus Measures for Phenotype and Exposure
NCI ;
NHGRI U01 HG004597;
NHGRI U24 HG012556;
NHGRI U41HG007050;
NHLBI ;
NIDA ;
NIMHD ;
NIMH ;
NINDS ;
OBSSR ;
ODP ;
TRSP
PMID:21749974 Restricted SCR_017475, biotools:PhenX_toolkit, nlx_144102 https://bio.tools/PhenX_Toolkit SCR_006532 SciCrunch Registry Phenotypes and eXposures Toolkit 2026-09-19 12:51:13 73
FlyBase
 
Resource Report
Resource Website
1000+ mentions
FlyBase (RRID:SCR_006549) FB data or information resource, data repository, database, organism-related portal, portal, service resource, storage service resource, topical portal Database of Drosophila genetic and genomic information with information about stock collections and fly genetic tools. Gene Ontology (GO) terms are used to describe three attributes of wild-type gene products: their molecular function, the biological processes in which they play a role, and their subcellular location. Additionally, FlyBase accepts data submissions. FlyBase can be searched for genes, alleles, aberrations and other genetic objects, phenotypes, sequences, stocks, images and movies, controlled terms, and Drosophila researchers using the tools available from the "Tools" drop-down menu in the Navigation bar. RIN, Resource Information Network, mutant, gene, genome, blast, genotype, phenotype, allele, sequence, stock, image, movie, controlled term, video resource, image collection, life-cycle, genome, expression, rna-seq, genetics, drosophilidae, bio.tools, FASEB list, RRID Community Authority is used by: NIF Data Federation
is used by: Resource Identification Portal
is used by: PhenoGO
is used by: Integrated Animals
is used by: Drososhare
is recommended by: NIDDK Information Network (dkNET)
is recommended by: National Library of Medicine
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: re3data.org
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: Resource Information Network
is related to: FlyMine
is related to: Virtual Fly Brain
is related to: AmiGO
is related to: Drosophila melanogaster Exon Database
is related to: HomoloGene
is related to: UniParc at the EBI
is related to: UniParc
is related to: Gene Ontology
is related to: NIH Data Sharing Repositories
is related to: GBrowse
is related to: Integrated Manually Extracted Annotation
is related to: PhenoGO
has parent organization: Harvard University; Cambridge; United States
has parent organization: University of Cambridge; Cambridge; United Kingdom
has parent organization: Indiana University; Indiana; USA
has parent organization: University of New Mexico; New Mexico; USA
is parent organization of: Drosophila anatomy and development ontologies
is parent organization of: Fly Taxonomy
is parent organization of: FlyBase Controlled Vocabulary
is parent organization of: Drosophila Development Ontology
is organization facet of: Alliance of Genome Resources
Indiana Genomics Initiative ;
MRC ;
NIH Blueprint for Neuroscience Research ;
NIHGRI P41 HG000739;
NSF
PMID:24234449
PMID:22127867
PMID:18948289
PMID:18641940
PMID:18160408
PMID:17099233
PMID:16381917
PMID:15608223
PMID:12519974
PMID:11752267
PMID:11465064
PMID:9847148
PMID:9399806
PMID:9045212
PMID:8594600
PMID:8578603
PMID:7937045
PMID:7925011
nif-0000-00558, r3d100010591, OMICS_01649, biotools:flybase https://bio.tools/flybase, https://doi.org/10.17616/R3903Q http://flybase.net SCR_006549 SciCrunch Registry flybase A Drosophila Genomic and Genetic Database, FlyBase: A Database of Drosophila Genes and Genomes, FLYBASE, FlyBase: A Database of Drosophila Genes & Genomes, FB 2026-09-19 12:51:13 4234
Decombinator
 
Resource Report
Resource Website
10+ mentions
Decombinator (RRID:SCR_006732) data analysis software, data processing software, software application, software resource, software toolkit Software suite for analysis of T cell receptor repertoire data. Used for fast, efficient analysis of T cell receptor (TcR) repertoire samples, designed to be accessible to those with no previous programming experience. Python, t-cell receptor sequence, t-cell receptor, sequence, deep sequencing, TCR repertoires, repertoire data, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: University College London; London; United Kingdom
PMID:23303508
PMID:32853330
Free, Available for download, Freely available biotools:decombinator, OMICS_00001 https://github.com/innate2adaptive/Decombinator, https://bio.tools/decombinator SCR_006732 SciCrunch Registry Decombinator v2.2, Decombinator v4.0.3 2026-09-19 12:51:17 32
DGIdb
 
Resource Report
Resource Website
100+ mentions
DGIdb (RRID:SCR_006608) DGIdb application programming interface, data access protocol, data or information resource, database, software resource A database of drug-gene relationships that provides drug-gene interactions and potential druggability data given list of genes. There are about 15 data sources that are being aggregated by DGIdb, with update date and these data sources are listed on this page: http://dgidb.genome.wustl.edu/sources, THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. drug, gene, interaction, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Washington University in St. Louis; Missouri; USA
Cancer NHGRI U54 HG003079 PMID:24122041 THIS RESOURCE IS NO LONGER IN SERVICE nlx_155686, biotools:DGIdb, OMICS_01579 https://bio.tools/DGIdb SCR_006608 SciCrunch Registry Drug-Gene Interaction database, Drug Gene Interaction Database 2026-09-19 12:51:14 408
Pseudomonas Genome Database
 
Resource Report
Resource Website
500+ mentions
Pseudomonas Genome Database (RRID:SCR_006590) PseudoCAP analysis service resource, data analysis service, data or information resource, database, production service resource, service resource Database of peer-reviewed, continually updated annotation for the Pseudomonas aeruginosa PAO1 reference strain genome expanded to include all Pseudomonas species to facilitate cross-strain and cross-species genome comparisons with high quality comparative genomics. The database contains robust assessment of orthologs, a novel ortholog clustering method, and incorporates five views of the data at the sequence and annotation levels (Gbrowse, Mauve and custom views) to facilitate genome comparisons. Other features include more accurate protein subcellular localization predictions and a user-friendly, Boolean searchable log file of updates for the reference strain PAO1. The current annotation is updated using recent research literature and peer-reviewed submissions by a worldwide community of PseudoCAP (Pseudomonas aeruginosa Community Annotation Project) participating researchers. If you are interested in participating, you are invited to get involved. Many annotations, DNA sequences, Orthologs, Intergenic DNA, and Protein sequences are available for download. gene, genome, annotation, localization, prokaryote, pseudomonas aeruginosa, sequence, subcellular, cystic fibrosis, ortholog, annotation, dna sequence, intergenic dna, protein sequence, bio.tools, FASEB list is used by: NIF Data Federation
is listed by: Debian
is listed by: bio.tools
is related to: AmiGO
has parent organization: Simon Fraser University; British Columbia; Canada
has parent organization: University of British Columbia; British Columbia; Canada
Cystic Fibrosis Foundation Therapeutics Inc PMID:18978025 nif-0000-03369, r3d100012086, biotools:pseudomonas_genome_database https://bio.tools/pseudomonas_genome_database, https://doi.org/10.17616/R3935H SCR_006590 SciCrunch Registry Pseudomonas Genome Database - Improving Disease Treatment Through Genome Research 2026-09-19 12:51:14 543
FLUX CAPACITOR
 
Resource Report
Resource Website
1+ mentions
FLUX CAPACITOR (RRID:SCR_006651) FLUX CAPACITOR software resource Software to recontruct abundances of known transcript forms from RNAseq data. The algorithm works by distributing the reads mapping to a given exonic region (or splice junction) among the transcripts including the exon (or splice junction). The input is the annotation of a reference transcriptome and reads from RNAseq technologies aligned to the genome. From the reference annotation, splicing graphs are produced and reads are mapped to corresponding edges in these graphs according to the position where they align in the genomic sequence. The resulting graph with edges labelled by the number of reads can be interpreted as a flow network where each transcript representing a transportation path from its start to its end and consequently each edge a possibly shared segment of transportation along which a certain number of reads per nucleotide -- i.e., a flux -- is observed. Given a density function of reads along a transcript, the expected participation of each transcript in an edge under consideration can be estimated. The basic idea is to cast back from these latter participations and the observed number of reads - allowing for a certain amount of noise - to the original transcript abundancies. To do so, a linear constraint is formalized for each edge, and an optimal solution for the complete set of constraints is found by a standard linear program solver. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:20220756 biotools:the_flux_capacitor, OMICS_01293 https://bio.tools/the_flux_capacitor SCR_006651 SciCrunch Registry The FLUX CAPACITOR, FluxCapacitor 2026-09-19 12:51:15 2
MaizeGDB
 
Resource Report
Resource Website
1000+ mentions
MaizeGDB (RRID:SCR_006600) MaizeGDB analysis service resource, data analysis service, data or information resource, data repository, database, organism-related portal, portal, production service resource, service resource, storage service resource, topical portal Collection of data related to crop plant and model organism Zea mays. Used to synthesize, display, and provide access to maize genomics and genetics data, prioritizing mutant and phenotype data and tools, structural and genetic map sets, and gene models and to provide support services to the community of maize researchers. Data stored at MaizeGDB was inherited from the MaizeDB and ZmDB projects. Sequence data are from GenBank. Data are searchable by phenotype, traits, Pests, Gel Pattern, and Mutant Images. zea mays, corn, model organism, genome, locus, metabolic pathway, genetics, genomics, sequence, gene product, function, literature reference, phenotype, trait, pest, gel pattern, mutant, blast, gene, image, corn, genotype-environment interaction, gene mapping, plant genome mapping, plant genome, gold standard, bio.tools, FASEB list is listed by: re3data.org
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: GenBank
has parent organization: University of Maryland; Maryland; USA
works with: Maize Database of Images and Genomes
National Corn Growers Association ;
NSF ;
USDA/ARS ;
USDA
PMID:21624896
PMID:18769488
PMID:15888678
PMID:14681441
Free, Freely available, Acknowledgement requested, The community can contribute to this resource OMICS_01655, biotools:MaizeDIG, nif-0000-03096, r3d100010795 https://bio.tools/MaizeDIG, https://doi.org/10.17616/R3V32B SCR_006600 SciCrunch Registry Maize Genetics and Genomics Database, MaizeGDB, MaizeGDB Locus 2026-09-19 12:51:14 1047
The Human Protein Atlas
 
Resource Report
Resource Website
5000+ mentions
The Human Protein Atlas (RRID:SCR_006710) HPA data or information resource, knowledge base Open access resource for human proteins. Used to search for specific genes or proteins or explore different resources, each focusing on particular aspect of the genome-wide analysis of the human proteins: Tissue, Brain, Single Cell, Subcellular, Cancer, Blood, Cell line, Structure and Interaction. Swedish-based program to map all human proteins in cells, tissues, and organs using integration of various omics technologies, including antibody-based imaging, mass spectrometry-based proteomics, transcriptomics, and systems biology. All the data in the knowledge resource is open access to allow scientists both in academia and industry to freely access the data for exploration of the human proteome. human proteins, human proteome exploration, genome-wide analysis of human proteins, Tissue, Brain, Single Cell, Subcellular, Cancer, Blood, Cell line, Structure and Interaction, bio.tools, FASEB list is used by: MitoMiner
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: aGEM
has parent organization: HUPO Antibody Initiative
Cancer, Tumor, Breast cancer, Colorectal cancer, Lung cancer, Prostate cancer, Normal Knut and Alice Wallenberg Foundation PMID:21139605
PMID:16127175
PMID:18669619
PMID:18853439
Public, Free, For informational purposes, Non-commercial, Acknowledgement required nif-0000-00204, biotools:proteinatlas https://bio.tools/proteinatlas SCR_006710 SciCrunch Registry HPA antibody, Human Protein Atlas 2026-09-19 12:51:16 9312

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.