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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
MIPS Ustilago maydis Database
 
Resource Report
Resource Website
1+ mentions
MIPS Ustilago maydis Database (RRID:SCR_007563) data or information resource, database The MIPS Ustilago maydis Genome Database aims to present information on the molecular structure and functional network of the entirely sequenced, filamentous fungus Ustilago maydis. The underlying sequence is the initial release of the high quality draft sequence of the Broad Institute. The goal of the MIPS database is to provide a comprehensive genome database in the Genome Research Environment in parallel with other fungal genomes to enable in depth fungal comparative analysis. The specific aims are to: 1. Generate and assemble Whole Genome Shotgun sequence reads yielding 10X coverage of the U. maydis genome 2. Integrate the genomic sequence assembly with physical maps generated by Bayer CropScience 3. Perform automated annotation of the sequence assembly 4. Align the strain 521 assembly with the FB1 assembly provided by Exelixis 5. Release the sequence assembly and results of our annotation and analysis to public Ustilago maydis is a basidiomycete fungal pathogen of maize and teosinte. The genome size is approximately 20 Mb. The fungus induces tumors on host plants and forms masses of diploid teliospores. These spores germinate and form haploid meiotic products that can be propagated in culture as yeast-like cells. Haploid strains of opposite mating type fuse and form a filamentous, dikaryotic cell type that invades plant tissue to reinitiate infection. Ustilago maydis is an important model system for studying pathogen-host interactions and has been studied for more than 100 years by plant pathologists. Molecular genetic research with U. maydis focuses on recombination, the role of mating in pathogenesis, and signaling pathways that influence virulence. Recently, the fungus has emerged as an excellent experimental model for the molecular genetic analysis of phytopathogenesis, particularly in the characterization of infection-specific morphogenesis in response to signals from host plants. Ustilago maydis also serves as an important model for other basidiomycete plant pathogens that are more difficult to work with in the laboratory, such as the rust and bunt fungi. Genomic sequence of U. maydis will also be valuable for comparative analysis of other fungal genomes, especially with respect to understanding the host range of fungal phytopathogens. The analysis of U. maydis would provide a framework for studying the hundreds of other Ustilago species that attack important crops, such as barley, wheat, sorghum, and sugarcane. Comparisons would also be possible with other basidiomycete fungi, such as the important human pathogen C. neoformans. Commercially, U. maydis is an excellent model for the discovery of antifungal drugs. In addition, maize tumors caused by U. maydis are prized in Hispanic cuisine and there is interest in improving commercial production. The complete putative gene set of the Broad Institute''s second release is loaded into the database and in addition all deviating putative genes from a putative gene set produced by MIPS with different gene prediction parameters are also loaded. The complete dataset will then be analysed, gene predictions will be manually corrected due to combined information derived from different gene prediction algorithms and, more important, protein and EST comparisons. Gene prediction will be restricted to ORFs larger than 50 codons; smaller ORFs will be included only if similarities to other proteins or EST matches confirm their existence or if a coding region was postulated by all prediction programs used. The resulting proteins will be annotated. They will be classified according to the MIPS classification catalogue receiving appropriate descriptions. All proteins with a known, characterized homolog will be automatically assigned to functional categories using the MIPS functional catalog. All extracted proteins are in addition automatically analysed and annotated by the PEDANT suite. drug, environment, filamentous, functional, fungal, fungal genome databases, fungus, gene, genetic, basidiomycete, cell, codon, culture, dikaryotic, diploid, genome, genomic, germinate, haploid, host, human, infection, maize, mating, meiotic, model, molecular, morphogenesis, network, orf, pathogen, pathologist, phytopathogen, phytopathogenesis, plant, protein, recombination, sequence, signal, spore, strain, structure, teliospore, teosinte, tissue, tumor, ustilago maydis, virulence, yeast nif-0000-21276 SCR_007563 MUMDB 2026-09-03 05:02:29 9
Topology Data Bank of Transmembrane Proteins
 
Resource Report
Resource Website
1+ mentions
Topology Data Bank of Transmembrane Proteins (RRID:SCR_007964) TOPDB data or information resource, database Collection of transmembrane protein datasets containing experimentally derived topology information from the literature and from public databases. Web interface of TOPDB includes tools for searching, relational querying and data browsing, visualisation tools for topology data. collection, transmembrane, protein, dataset, topology, public, data, sequence, database has parent organization: Hungarian Academy of Sciences; Budapest; Hungary
works with: CCTOP
Bolyai János Scholarship ;
Hungarian research and development funds ;
OTKA ;
Öveges fellowship
PMID:17921502 Free, Available for download, Freely available for non commercial users nif-0000-03568 SCR_007964 Topology Data Bank of Transmembrane Proteins, TOPDB 2026-09-03 05:02:53 6
SIMAP
 
Resource Report
Resource Website
10+ mentions
SIMAP (RRID:SCR_007927) SIMAP data or information resource, database It provides a database based on a pre-computed similarity matrix covering the similarity space formed by >4 million amino acid sequences from public databases and completely sequenced genomes. The database is capable of handling very large datasets and is updated incrementally. For sequence similarity searches and pairwise alignments, we implemented a grid-enabled software system, which is based on FASTA heuristics and the Smith Waterman algorithm. SimpleSIMAP and AdvancedSIMAP retrieve homologs for given protein sequences that need to be contained in the SIMAP database. While SimpleSIMAP provides only selected parameters and preconfigured search spaces, the AdvancedSIMAP allows the user to specify search space, filtering and sorting parameters in a flexible manner. Both types of queries result in lists of homologs that are linked in turn to their homologs. So the web interfaces allow users to explore quickly and interactively the protein world by homology. Sponsors: SIMAP is supported by the Department of Genome Oriented Bioinformatics of the Technische Universitt Mnchen and the Institute for Bioinformatics of the GSF-National Research Center for Environment and Health. genome, alignment, amino acid, homolog, matrix, protein, protein domain and protein classification databases, sequence SCR_007927 The Similarity Matrix of Proteins, Similarity Matrix of Proteins 2026-09-03 05:02:51 14
Rhode Island INBRE Molecular Informatics Core Facility
 
Resource Report
Resource Website
10+ mentions
Rhode Island INBRE Molecular Informatics Core Facility (RRID:SCR_017685) access service resource, core facility, service resource Core provides sequencing and bioinformatics support for INBRE and non-INBRE researchers. Provides data science services adjacent to traditional bioinformatics; access to computational and software resources for INBRE network institutions, particularly primarily undergraduate institutions; training for students and faculty in data science methods. Maintains professional network with other core and user facilities in Rhode Island and beyond to maximize resources available to our users.Utilizes novel technologies such as virtual/augmented reality for use in teaching and research. Analysis, interpretation, nucleotide, amino acid, sequence, protein, domain, structure, service, 3D visualization, modeling, USEDit has parent organization: University of Rhode Island; Rhode Island; USA
has parent organization: USEDit
NIGMS P20 GM103430 Open ABRF_3 SCR_017685 Rhode Island INBRE Molecular Informatics, RI-INBRE Bioinformatics Core; RI Genomics and Sequencing Center 2026-09-03 05:08:25 16
Kansas University at Lawrence Applied Bioinformatics Laboratory Core Facility
 
Resource Report
Resource Website
Kansas University at Lawrence Applied Bioinformatics Laboratory Core Facility (RRID:SCR_017751) ABL access service resource, core facility, service resource Research oriented service laboratory providing informatics support to research community. Services include data analysis and mining in proteomics, genomics and chemistry, systems biology approaches such as pathway, network and interaction analyses, large scale statistical and machine learning studies, protein structure, function and stability prediction, sequence and domain analyses,d esign and implementation of relational databases and software programs, consultation on experimental design involving data acquisition, management and analysis, report, grant, and manuscript preparation. Data, analysis, mining, pathway, network, interaction, prediction, protein, structure, function, stability, sequence, domain, acquisition, management, report, grant, manuscript, service, core Open ABRF_252 SCR_017751 Molecular Graphics and Modeling Laboratory 2026-09-03 05:08:19 0
University of Sheffield Genomic Core Facility
 
Resource Report
Resource Website
University of Sheffield Genomic Core Facility (RRID:SCR_017912) access service resource, core facility, service resource Core provides DNA sequencing services including DNA extraction, cell line identification, microsatellite analysis, and antibody sequencing,DNA Sequencing, Monoclonal Antibody Sequencing,Nucleic Acid Quantification,PCR Machine Hire,Real-Time PCR Robotic Liquid Handling,Taqman SNP Analysis. DNA, sequence, extraction, cell, line, identification, microsatellite, analysis, antibody, monoclonal, quantification, PCR, RTPCR, taqman, SNP, analysis, service, core, ABRF is listed by: ABRF CoreMarketplace Open ABRF_786 SCR_017912 Core Genomic Facility 2026-09-03 05:08:27 0
kraken2
 
Resource Report
Resource Website
1000+ mentions
kraken2 (RRID:SCR_026838) software application, software resource, source code Software tool as second version of Kraken taxonomic sequence classification system. taxonomic sequence classification system, taxonomic, sequence, classification system, NIGMS R01 GM118568;
NIGMS R35 GM130151;
NSF
PMID:31779668 Free, Available for download, Freely available SCR_026838 2026-09-03 05:11:18 1421
HVSeeker
 
Resource Report
Resource Website
1+ mentions
HVSeeker (RRID:SCR_026120) software application, software resource Software tool for distinguishing between bacterial and phage sequences. Consists of two separate models: one analyzing DNA sequences and the other focusing on proteins. genome, bacteria, phage, sequence, distinguishing between bacterial and phage sequences, German Research Foundation INST 37/935-1 FUGG;
King Fahd University of Petroleum and Minerals
Free, Available for download, Freely available, SCR_026120 2026-09-03 05:10:39 1
SCANDAN-DICOM-labelling
 
Resource Report
Resource Website
1+ mentions
SCANDAN-DICOM-labelling (RRID:SCR_028365) software application, software resource, source code, text extraction software, text-mining software Software tool for rules for DICOM tag based labelling. Regular expression used during the SCANDAN project to label MRI scans based on DICOM tag. sequence, MRI, DICOM standard, Text-mining algorithm, Brain DOI:10.1101/2025.10.21.25338469 Free, Available for download, Freely available SCR_028365 2026-09-03 05:12:32 1
Xenbase
 
Resource Report
Resource Website
100+ mentions
Xenbase (RRID:SCR_003280) XenBase data or information resource, data repository, database, image repository, service resource, storage service resource Data collection for Xenopus laevis and Xenopus tropicalis biology and genomics. molecular neuroanatomy resource, dna target, protein target, gene, genome, function, sequence, orthology, publication, gene expression, model organism, genomics, development, annotation, blast, development stage, publication, in situ hybridization, immunohistochemistry, video resource, organism-related portal, experimental protocol, organism supplier, data analysis service, developmental stage, gold standard, bio.tools, FASEB list, RRID Community Authority is listed by: OMICtools
is listed by: One Mind Biospecimen Bank Listing
is listed by: bio.tools
is listed by: Debian
is related to: Bgee: dataBase for Gene Expression Evolution
has parent organization: University of Calgary; Alberta; Canada
is parent organization of: Xenopus Anatomy Ontology
NICHD P41 HD064556;
NICHD R01 HD045776
PMID:23125366
PMID:19884130
PMID:36755307
Free, Available for download, Freely available biotools:xenbase, OMICS_01665, nif-0000-01286, r3d100010279 http://www.xenbase.org/entry/, https://bio.tools/xenbase, https://doi.org/10.17616/R3MP4S SCR_003280 Xenbase: Xenopus laevis and tropicalis biology and genomics resource 2026-09-03 04:46:09 484
ProbeMatchDB 2.0
 
Resource Report
Resource Website
ProbeMatchDB 2.0 (RRID:SCR_003433) ProbeMatchDB analysis service resource, data analysis service, data or information resource, database, production service resource, service resource Matches a list of microarray probes across different microrarray platforms (GeneChip, EST from different vendors, Operon Oligos) and species (human, mouse and rat), based on NCBI UniGene and HomoloGene. The capability to match protein sequence IDs has just been added to facilitate proteomic studies. The ProbeMatchDB is mainly used for the design of verification experiments or comparing the microarray results from different platforms. It can be used for finding equivalent EST clones in the Research Genetics sequence verified clone set based on results from Affymetirx GeneChips. It will also help to identify probes representing orthologous genes across human, mouse and rat on different microarray platforms. experiment, human, microarray, mouse, oligo, operon, platform, probe, protein, proteomic, rate, sequence, study, gene, est, cdna, sts marker, orthologous gene, ortholog, microarray probe, nucleotide sequence is related to: UniGene
is related to: HomoloGene
has parent organization: University of Michigan; Ann Arbor; USA
University of Michigan Microarray Network ;
Nancy Pritzker Depression Research Network ;
Department of Psychiatry pilot study ;
NIMH L99 MH60398;
NIDA R21 DA13754-01
PMID:11934751 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-33156 SCR_003433 2026-09-03 04:46:23 0
RINS
 
Resource Report
Resource Website
10+ mentions
RINS (RRID:SCR_003652) RINS software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 6, 2023. An intersection-based pathogen detection workflow that utilizes a user-provided custom reference genome set for identification of nonhuman sequences in deep sequencing datasets. This is a package recommended for advanced users only. virus, rna-seq, dna-seq, viral integration, clipped-sequence, paired-end, reconstruction, fusion transcript, sequence, perl is listed by: OMICtools
has parent organization: Stanford University School of Medicine; California; USA
PMID:22377895 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00223 SCR_003652 2026-09-03 04:46:24 26
Centre for Modeling Human Disease Gene Trap Resource
 
Resource Report
Resource Website
1+ mentions
Centre for Modeling Human Disease Gene Trap Resource (RRID:SCR_002785) CMHD Gene Trap Resource biomaterial manufacture, material service resource, production service resource, service resource Generate gene trap insertions using mutagenic polyA trap vectors, followed by sequence tagging to develop a library of mutagenized ES cells freely available to the scientific community. This library is searchable by sequence or key word searches including gene name or symbol, chromosome location, or Gene Ontology (GO) terms. In addition,they offer a custom email alert service in which researchers are able to submit search criteria. Researchers will receive automated e-mail notification of matching gene trap clones as they are entered into the library and database. The resource features the use of complementary second and third generation polyA trap vectors developed by the Stanford lab and the laboratory of Professor Yasumasa Ishida of the Nara Institute of Science and Technology (NAIST) in Japan to mutagenize murine embryonic stem (ES) cells. CMHD gene trap clones are distributed by the Canadian Mouse Mutant Repository(CMMR). Information about ordering, services, and pricing can be found on their web site (http://www.cmmr.ca/services/index.html)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 15,2026. embryonic stem cell, polya trap vector, gene trap, insertion, mutagenic polya trap vector, sequence, expression, mutagenesis, gene, mutation, expression profile, phenotype, database, gene expression, vector insertion, expressed sequence tag, blast, clone is related to: Gene Ontology
is related to: CMMR - Canadian Mouse Mutant Repository
is related to: International Gene Trap Consortium
has parent organization: CMHD - Centre for Modeling Human Disease
Canadian Institutes of Health Research ;
Genome Canada ;
Genome Prairie ;
NIH
PMID:14681480 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02891 http://www.cmhd.ca/sub/genetrap.asp SCR_002785 Centre for Modeling Human Disease (CMHD) Gene Trap Resource 2026-09-03 04:45:38 3
Community Cyberinfrastructure for Advanced Marine Microbial Ecology Research and Analysis
 
Resource Report
Resource Website
50+ mentions
Community Cyberinfrastructure for Advanced Marine Microbial Ecology Research and Analysis (RRID:SCR_002676) CAMERA analysis service resource, data analysis service, data or information resource, data repository, organization portal, portal, production service resource, service resource, storage service resource THIS RESOURCE IS NO LONGER IN SERVICE, documented May 26, 2016; however, the URL provides links to associated projects and data. A suite of data query, download, upload, analysis and sharing tools serving the needs of the microbial ecology research community, and other scientists using metagenomics data. ecology, energy, environment, gene, analysis, bioinformatics, biological, biology, community, cyberinfrastructure, data, dna, genome, genomics, health care, map, marine, metadata, metagenomic, microbial, microbiology, molecular biology, organism, research, scientific, sequence, sequencing, software, tool, training, viral is listed by: OMICtools
is related to: VIROME
has parent organization: University of California at San Diego; California; USA
Gordon and Betty Moore Foundation PMID:21045053 THIS RESOURCE IS NO LONGER IN SERVICE SCR_011924, OMICS_01476, nif-0000-23292 SCR_002676 2026-09-03 04:45:40 83
Honey Bee Genome Project
 
Resource Report
Resource Website
1+ mentions
Honey Bee Genome Project (RRID:SCR_002890) data or information resource, portal, topical portal The HGSC has sequenced the honey bee, Apis mellifera. The version 4.0 assembly was released in March 2006 and published in October 2006. The genome sequence is being upgraded with additional sequence coverage. The honey bee is important in the agricultural community as a producer of honey and as a facilitator of pollination. It is a model organism for studying the following human health issues: immunity, allergic reaction, antibiotic resistance, development, mental health, longevity and diseases of the X chromosome. In addition, biologists are interested in the honey bee's social organization and behavioral traits. This project was proposed to the HGSC by a group of dedicated insect biologists, headed by Gene Robinson. Following a workshop at the HGSC and a honey bee white paper, the HGSC began the project in 2002. A 6-fold coverage WGS, BAC sequence from pooled arrays, and an initial genome assembly (Amel_v1.0) were released beginning in 2003. This has been a challenging project with difficulty in recovering AT-rich regions. The WGS data had lower coverage in AT-rich regions and BAC data from clones showed evidence of internal deletions. Additional reads from AT enriched DNA addressed these underrepresented regions. The current assembly Amel_4.0 was produced with Atlas and includes 2.7 million reads (1.8 Gb) or 7.5x coverage of the (clonable) genome. About 97% of STSs, 98% of ESTs, and 96% of cDNAs are represented in the 231 Mb assembly. About 2,500 reads were also produced from a strain of Africanized honey bee and SNPs were extracted. These were released in dbSNP and the NCBI Trace Archive. Analysis of the genome by a consortium of 20 labs has been completed. This produced a gene list derived from five different methods melded through the GLEAN software. Publications include a main paper in Nature and up to forty companion papers in Genome Research and Insect Molecular Biology. Sponsors: Sequencing of the honey bee is jointly funded by National Human Genome Research Institute (NHGRI) and the Department of Agriculture (USDA). Multiple drones from the same queen (strain DH4) were obtained from Danny Weaver of B. Weaver Apiaries. All libraries were made from DNA isolated from these drones. The honey bee BAC library (CHORI-224) was prepared by Pieter de Jong and Katzutoyo Osoegawa at the Children's Hospital Oakland Research Institute. gene, agricultural, allergy, antibiotic, apis mellifera, array, behavioral, biologist, chromosome, development, disease, genome, heath, honey bee, human, immunity, insect, mental heath, organism, pollination, reaction, resistance, sequence, trait has parent organization: Baylor University; Texas; USA THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-25604 http://www.hgsc.bcm.tmc.edu/project-species-i-Apis%20mellifera.hgsc?pageLocation=Apis%20mellifera SCR_002890 Honey Bee 2026-09-03 04:45:43 4
Assembly/Alignment/Annotation of 12 Related Drosophila Species
 
Resource Report
Resource Website
10+ mentions
Assembly/Alignment/Annotation of 12 Related Drosophila Species (RRID:SCR_002921) data or information resource, data set, organism-related portal, portal, topical portal A single source for sequences, assemblies, annotations and analyses of the genomes of members of the fruitfly genus Drosophlia. It is meant as resource for Drosophilists and other researchers interested in comparative analysis of these species and their genomes. There are pages for each species, as well as pages for different types of multi-species resources (e.g. alignments). If you have a public resource that will help this project, please consider making it available through this page by emailing multiple_at_fruitfly.org. sequence, annotation, analysis, genome, fruitfly, drosophila, research, comparative, alignment, assembly has parent organization: Lawrence Berkeley National Laboratory THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-30021 SCR_002921 AAA: 12 Drosophila Genomes 2026-09-03 04:45:54 35
Protein Information Resource
 
Resource Report
Resource Website
50+ mentions
Protein Information Resource (RRID:SCR_002837) PIR data or information resource, portal, topical portal Integrated public bioinformatics resource to support genomic, proteomic and systems biology research and scientific studies. Provides databases and protein sequence analysis tools to scientific community, including Protein Sequence Database which grew out from the Atlas of Protein Sequence and Structure. Conducts research in biomedical text mining and ontology, computational systems biology, and bioinformatics cyberinfrastructure. In 2002 PIR, along with its international partners, EBI (European Bioinformatics Institute) and SIB (Swiss Institute of Bioinformatics), were awarded a grant from NIH to create UniProt, a single worldwide database of protein sequence and function, by unifying the PIR-PSD, Swiss-Prot, and TrEMBL databases. Currently, PIR major activities include: i) UniProt (Universal Protein Resource) development, ii) iProClass protein data integration and ID mapping, iii) PRO protein ontology, and iv) iProLINK protein literature mining and ontology development. The FTP site provides free download for iProClass, PIRSF, and PRO. annotation, genomic, mining, protein, protein bioinformatics, proteomic, research, sequence, structure, systems biology, gold standard, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
is related to: NCBI Protein Database
has parent organization: University of Delaware; Delaware; USA
has parent organization: Georgetown University; Washington D.C.; USA
is parent organization of: PRO
is parent organization of: PIRSF
is parent organization of: PR
is parent organization of: UniProt
NLM P41 LM05798 PMID:12520019 Free, Freely available biotools:pir, nif-0000-21327, nif-0000-00143, SCR_008229 https://bio.tools/pir, http://pir.georgetown.edu/ SCR_002837 PIR - Protein Information Resource 2026-09-03 04:45:40 85
Tribolium castaneum Genome Project
 
Resource Report
Resource Website
10+ mentions
Tribolium castaneum Genome Project (RRID:SCR_002848) data or information resource, database, portal, topical portal This portal provides information about the Tribolium castabeum Genome Project. The Tribolium castaneum genome sequence and its analysis has been published in Nature, two companion journal issues (IBMB and DGE) and numerous other publications listed below. The red flour beetle, Tribolium castaneum, a common pest that is also a genetic model for the Coleoptera. The genome has been sequenced to 7-fold coverage using a whole genome shotgun approach and assembled using the HGSC's assembly engine, Atlas, with methods employed for the Drosophila pseudoobscura genome assembly. Approximately 90% of the genome sequence has been mapped to chromosomes in collaboration with Dick Beeman (USDA ARS) and Sue Brown (Kansas State University). Access to the Data :- Genome Assembly: The long term home of the Tribolium genome is Beetlebase. Tcas 3.0 is now available in GenBank and on our FTP site. Note there are no restrictions of any kind on the Tribolium data as it has been published. Version 2 of the assembly, Tcas_2.0 is available for download using the FTP Data link in the sidebar. The assembly is described in detail in the README in that directory. T.cas_1.0 was a preliminary genome assembly that did not include large insert paired end information and has been moved to a previous assemblies folder. A genboree browser of the Tcas2.0 sequence is available here: There are also links to the genboree browser from the blast results (at the bottom of each reported HSP) if you use the blast server on this page. The original linear scaffold file, Tcas2.0/linearScaffolds/Tcas20050914-genome, posted on the ftp site did not include singleton contigs from the assembly and thus did not fully reflect the tribolium genome sequence, missing ~4.4Mb of sequence in 1860 contigs and reptigs or approximately 2.5% of the assembled sequence. A corrected Tcas20051011-genome file containing these missing sequences is now available on the ftp site. The blast databases have also been updated to reflect this change. All other data is correct, and not affected by this change. :- BLAST Searches: The BLAST link is located in the sidebar. :* Linearized chromosome and unplaced scaffold sequences :* Assembled contigs :* Bin0 unassembled reads and Repeat reads Traces are available from the NCBI Trace Archive by using the link in the sidebar, or by using NCBI MegaBLAST with a same species or cross species query. Sponsors: Funding for this project has been provided by the National Human Genome Research Institute (NHGRI U54 HG003273), which is part of the National Institutes of Health (NIH), and the U.S. Department of Agriculture's Agricultural Research Service (USDA ARS Agreement No. 58-5430-3-338). genetic, chromosome, coleoptera, drosophila, genome, model, pest, red flour beetle, sequence, tribolium castaneum has parent organization: Baylor University; Texas; USA Free, Freely available nif-0000-25607 http://www.hgsc.bcm.tmc.edu/project-species-i-Tribolium%20castaneum.hgsc?pageLocation=Tribolium%20castaneum SCR_002848 Tribolium 2026-09-03 04:45:48 10
International HapMap Project
 
Resource Report
Resource Website
5000+ mentions
International HapMap Project (RRID:SCR_002846) HapMap data or information resource, database, experimental protocol, narrative resource THIS RESOURCE IS NO LONGER IN SERVICE, documented August 22, 2016. A multi-country collaboration among scientists and funding agencies to develop a public resource where genetic similarities and differences in human beings are identified and catalogued. Using this information, researchers will be able to find genes that affect health, disease, and individual responses to medications and environmental factors. All of the information generated by the Project will be released into the public domain. Their goal is to compare the genetic sequences of different individuals to identify chromosomal regions where genetic variants are shared. Public and private organizations in six countries are participating in the International HapMap Project. Data generated by the Project can be downloaded with minimal constraints. HapMap project related data, software, and documentation include: bulk data on genotypes, frequencies, LD data, phasing data, allocated SNPs, recombination rates and hotspots, SNP assays, Perlegen amplicons, raw data, inferred genotypes, and mitochondrial and chrY haplogroups; Generic Genome Browser software; protocols and information on assay design, genotyping and other protocols used in the project; and documentation of samples/individuals and the XML format used in the project. genetic variant, disease, genetic sequence, genetic variation, single nucleotide polymorphism, genetic diversity, dna, sequence, catalog, genome, chromosome, bio.tools is used by: BioSample Database at EBI
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: SNAP - SNP Annotation and Proxy Search
is related to: Haploview
is related to: NHGRI Sample Repository for Human Genetic Research
is related to: DistiLD - Diseases and Traits in LD
is related to: SNP at Ethnos
is related to: GBrowse
is related to: Broad Institute Genomics Platform
has parent organization: NCBI
Chinese Academy of Sciences ;
Chinese Ministry of Science and Technology ;
Delores Dore Eccles Foundation ;
Genome Canada ;
Genome Quebec ;
Hong Kong Innovation and Technology Commission ;
Japanese Ministry of Education Culture Sports Science and Technology MEXT ;
National Natural Science Foundation of China ;
SNP Consortium ;
University Grants Committee of Hong Kong ;
Wellcome Trust ;
W. M. Keck Foundation ;
NIH
PMID:14685227 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02940, biotools:int_hapmap_project, r3d100011835, OMICS_00273 http://www.hapmap.org/, https://bio.tools/int_hapmap_project, https://doi.org/10.17616/R3H06Q http://snp.cshl.org SCR_002846 HapMap Project 2026-09-03 04:45:41 6854
HIV Sequence Database
 
Resource Report
Resource Website
100+ mentions
HIV Sequence Database (RRID:SCR_002906) HIV Sequence Database analysis service resource, data analysis service, data or information resource, database, production service resource, service resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 4, 2023. HIV Sequence Database is a database of annotated HIV sequences, plus a variety of tools and information for researchers studying HIV and SIV. The main aim of this website is to provide easy access to our sequence database, alignments, and the tools and interfaces we have produced. The HIV Sequence Database focuses on five primary goals: * Collecting HIV and SIV sequence data (all sequences since 1987) * Curating and annotating this data, and making it available to the scientific community * Computer analysis of HIV and related sequences * Production of software for the analysis of (sequence) data * The data and analyses on this site and published in a yearly printed publication, the HIV sequence Compendium, which is available free of charge. drug resistance, genetics, mutation, vaccine, human immunodeficiency virus, siv, sequence, alignment, simian immunodeficiency virus, FASEB list has parent organization: HIV Databases Human immunodeficiency virus, Simian immunodeficiency virus NIAID THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02967 SCR_002906 2026-09-03 04:45:53 110

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    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 NIF 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.