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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
NHGRI Dog Genome Project
 
Resource Report
Resource Website
1+ mentions
NHGRI Dog Genome Project (RRID:SCR_002256) NHGRI Dog Genome Project data or information resource, database The Dog Genome Project at the National Human Genome Research Institute is working to develop resources necessary to map and clone canine genes in an effort to utilize dogs as a model system for genetics and cancer research. The US National Human Genome Research Institute (NHGRI) agreed to fund a project to sequence the entire genome of a boxer dog named Tasha, because it recognized the value of the dog as an unrivaled model for the study of human disease. The National Human Genome Research Institute (NHGRI) led the National Institutes of Health's (NIH) contribution to the International Human Genome Project, which had as its primary goal the sequencing of the human genome. This project was successfully completed in April 2003. Now, the NHGRI's mission has expanded to encompass a broad range of studies aimed at understanding the structure and function of the human genome and its role in health and disease. To that end NHGRI supports the development of resources and technology that will accelerate genome research and its application to human health. A critical part of the NHGRI mission continues to be the study of the ethical, legal and social implications (ELSI) of genome research. NHGRI also supports the training of investigators and the dissemination of genome information to the public and to health professionals. gene, genetic, cancer, canine, clone, disease, dog, genome, health, human, map, model, system PMID:16102268 nif-0000-20975 SCR_002256 National Human Genome Research Institute Dog Genome Project 2026-02-14 02:05:38 1
GeneCards
 
Resource Report
Resource Website
5000+ mentions
GeneCards (RRID:SCR_002773) GeneCards data or information resource, database Database of human genes that provides concise genomic, proteomic, transcriptomic, genetic and functional information on all known and predicted human genes. Information featured in GeneCards includes orthologies, disease relationships, mutations and SNPs, gene expression, gene function, pathways, protein-protein interactions, related drugs and compounds and direct links to cutting edge research reagents and tools such as antibodies, recombinant proteins, clones, expression assays and RNAi reagents. genome, human gene, genome, gene, genomic, proteomic, transcriptomic, genetic, function, ortholog, disease, mutation, single nucleotide polymorphism, gene expression, gene function, pathway, protein-protein interaction, drug, compound, reagent, antibody, recombinant protein, clone, expression assay, rnai reagent, FASEB list is listed by: OMICtools
is related to: MOPED - Model Organism Protein Expression Database
PMID:20689021 Free, Freely available nif-0000-02879, OMICS_01652, r3d100012015 http://bioinfo.weizmann.ac.il/genecards/
https://doi.org/10.17616/R3D643
SCR_002773 GeneCards - The Human Gene Compendium 2026-02-14 02:05:41 6546
HIV Molecular Immunology Database
 
Resource Report
Resource Website
1+ mentions
HIV Molecular Immunology Database (RRID:SCR_002893) HIV Molecular Immunology Database data or information resource, database An annotated, searchable collection of HIV-1 cytotoxic and helper T-cell epitopes and antibody binding sites, plus related tools and information. The goal of this database is to provide a comprehensive listing of defined HIV epitopes. These data are also printed in the HIV Molecular Immunology compendium, which is updated yearly and provided free of charge to scientific researchers, both by online download and as a printed copy. The data included in this database are extracted from the HIV immunology literature. HIV-specific B-cell and T-cell responses are summarized and annotated. Immunological responses are divided into three sections, CTL (CD8+), T helper (CD4+), and antibody. Within these sections, defined epitopes are organized by protein and binding sites within each protein, moving from left to right through the coding regions spanning the HIV genome. We include human responses to natural HIV infections, as well as vaccine studies in a range of animal models and human trials. Responses that are not specifically defined, such as responses to whole proteins or monoclonal antibody responses to discontinuous epitopes, are summarized at the end of each protein sub-section. Studies describing general HIV responses to the virus, but not to any specific protein, are included at the end of each section. The annotation includes information such as cross-reactivity, escape mutations, antibody sequence, TCR usage, functional domains that overlap with an epitope, immune response associations with rates of progression and therapy, and how specific epitopes were experimentally defined. Basic information such as HLA specificities for T-cell epitopes, isotypes of monoclonal antibodies, and epitope sequences are included whenever possible. All studies that we can find that incorporate the use of a specific monoclonal antibody are included in the entry for that antibody. A single T-cell epitope can have multiple entries, generally one entry per study. Finally, tables and maps of all defined linear epitopes relative to the HXB2 reference proteins are provided. Alignments of CTL, helper T-cell, and antibody epitopes are available through the search interfaces. Only responses to HIV-1 and HIV-2 are included in the database. cytotoxic t cell, cytotoxic t lymphocyte, helper t-cell, antibody, binding site, epitope, t cell epitope, human immunodeficiency virus, immunology, molecule, genome, protein, alignment, b-cell, t-cell, annotation, ctl, t helper, coding region, cross-reactivity, escape mutation, antibody sequence, tcr usage, functional domain, immune response, progression, therapy has parent organization: HIV Databases Human immunodeficiency virus NIAID nif-0000-02965 http://hiv-web.lanl.gov/immunology/ SCR_002893 Human Immunodeficiency Virus Molecular Immunology Database 2026-02-14 02:05:41 2
GermOnline
 
Resource Report
Resource Website
10+ mentions
GermOnline (RRID:SCR_002807) GermOnline data or information resource, database Cross-species microarray expression database focusing on high-throughput expression data relevant for germline development, meiosis and gametogenesis as well as the mitotic cell cycle. The database contains a unique combination of information: 1) High-throughput expression data obtained with whole-genome high-density oligonucleotide microarrays (GeneChips). 2) Sample annotation (mouse over the sample name and click on it) using the Multiomics Information Management and Annotation System (MIMAS 3.0). 3) In vivo protein-DNA binding data and protein-protein interaction data (available for selected species). 4) Genome annotation information from Ensembl version 50. 5) Orthologs are identified using data from Ensembl and OMA and linked to each other via a section in the report pages. The portal provides access to the Saccharomyces Genomics Viewer (SGV) which facilitates online interpretation of complex data from experiments with high-density oligonucleotide tiling microarrays that cover the entire yeast genome. The database displays only expression data obtained with high-density oligonucleotide microarrays (GeneChips)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 15,2026. fertility, development, germline, microarray, annotation, in vivo, protein-dna binding, protein-protein interaction, genome, ortholog, high-density oligonucleotide microarray, gene expression, genome annotation, gene orthology, genechip, tiling array, development, meiosis, gametogenesis, mitotic cell cycle, data set, data repository, bio.tools is listed by: 3DVC
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: Ensembl
is related to: OMA Browser
has parent organization: National Institute of Health and Medical Research; Rennes; France
Swiss Institute of Bioinformatics ;
bioinformatics platform of Biogenouest ;
National Institute of Health and Medical Research; Rennes; France ;
University of Rennes 1; Rennes; France
PMID:21149299 THIS RESOURCE IS NO LONGER IN SERVICE biotools:germonline, nif-0000-02906, r3d100010248 https://bio.tools/germonline
https://doi.org/10.17616/R37K5Q
SCR_002807 2026-02-14 02:05:41 17
Zebrafish Information Network (ZFIN)
 
Resource Report
Resource Website
500+ mentions
Zebrafish Information Network (ZFIN) (RRID:SCR_002560) ZFIN data or information resource, database Model organism database that serves as central repository and web-based resource for zebrafish genetic, genomic, phenotypic and developmental data. Data represented are derived from three primary sources: curation of zebrafish publications, individual research laboratories and collaborations with bioinformatics organizations. Data formats include text, images and graphical representations.Serves as primary community database resource for laboratory use of zebrafish. Developed and supports integrated zebrafish genetic, genomic, developmental and physiological information and link this information extensively to corresponding data in other model organism and human databases. expression, gene, anatomy, development, disease, genomic, model, molecular, mutant, neuronal, organism, phenotype, physiological, synteny, zebrafish, gene expression, genome sequence, molecular neuroanatomy resource, genotype, anatomical structure, publication, genome, image collection, gold standard, bio.tools, FASEB list, RRID Community Authority uses: InterMOD
is used by: NIF Data Federation
is used by: Resource Identification Portal
is used by: Morpholino Database
is used by: Integrated Animals
is used by: NIH Heal Project
is recommended by: Resource Identification Portal
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: OMICtools
is listed by: InterMOD
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: AmiGO
is related to: Phenoscape Knowledgebase
is related to: MONARCH Initiative
is related to: Bgee: dataBase for Gene Expression Evolution
is related to: NIH Data Sharing Repositories
is related to: HomoloGene
is related to: Zebrafish International Resource Center
is related to: Integrated Manually Extracted Annotation
is related to: Zebrafish Genome Project
has parent organization: University of Oregon; Oregon; USA
is parent organization of: ZFIN Antibody Database
is parent organization of: Zebrafish Anatomical Ontology
is parent organization of: ZFIN Protocol Wiki
is parent organization of: ZFIN Antibody Wiki
NHGRI P41 HG002659;
NHGRI R01 HG004834
PMID:23074187
PMID:21036866
PMID:16381936
Free, Available for download, Freely available OMICS_01666, nif-0000-21427, biotools:zfin, r3d100010421, SCR_017504 http://zfin.org/ZFIN/misc_html/tips.html#newrecord
https://wiki.zfin.org/display/general/ZFIN+Data+Submissions
https://bio.tools/zfin
https://doi.org/10.17616/R3CK5Z
SCR_002560 Zebrafish Database, The Zebrafish Model Organism Database, Zebra Model Organism Database, ZebraFish Information Network, ZFIN 2026-02-14 02:05:47 898
object-oriented Transcription Factors Database
 
Resource Report
Resource Website
1+ mentions
object-oriented Transcription Factors Database (RRID:SCR_002435) data or information resource, database ooTFD (object-oriented Transcription Factors Database) is a successor to TFD, the original Transcription Factors Database. This database is aimed at capturing information regarding the polypeptide interactions which comprise and define the properties of transcription factors. ooTFD contains information about transcription factor binding sites, as well as composite relationships within transcription factors, which frequently occur as multisubunit proteins that form a complex interface to cellular processes outside the transcription machinery through protein-protein interactions. ooTFD contains information represented in TFD but also allows the representation of containment, composite, and interaction relationships between transcription factor polypeptides. It is designed to represent information about all transcription factors, both eukaryotic and prokaryotic, basal as well as regulatory factors, and multiprotein complexes as well as monomers. eukaryotic, expression, factor, gene, basal, binding site, biochemical, biology, cellular, complex, genome, genomic, information, interaction, molecule, monomer, multisubunit, nucleotide sequences, transcriptional regulator sites, transcription factors, object, polypeptide, process, prokaryotic, property, protein, protein-protein interaction, regulatory, sequence, transcription has parent organization: IFTI-Mirage PMID:10592257
PMID:9847215
PMID:9399874
Free, Freely available nif-0000-21303 SCR_002435 ooTFD 2026-02-14 02:06:07 2
ABS: A Database of Annotated Regulatory Binding Sites From Orthologous Promoters
 
Resource Report
Resource Website
1+ mentions
ABS: A Database of Annotated Regulatory Binding Sites From Orthologous Promoters (RRID:SCR_002276) ABS data or information resource, database Public database of known binding sites identified in promoters of orthologous vertebrate genes that have been manually curated from bibliography. We have annotated 650 experimental binding sites from 68 transcription factors and 100 orthologous target genes in human, mouse, rat or chicken genome sequences. Computational predictions and promoter alignment information are also provided for each entry. For each gene, TFBSs conserved in orthologous sequences from at least two different species must be available. Promoter sequences as well as the original GenBank or RefSeq entries are additionally supplied in case of future identification conflicts. The final TSS annotation has been refined using the database dbTSS. Up to this release, 500 bps upstream the annotated transcription start site (TSS) according to REFSEQ annotations have been always extracted to form the collection of promoter sequences from human, mouse, rat and chicken. For each regulatory site, the position, the motif and the sequence in which the site is present are available in a simple format. Cross-references to EntrezGene, PubMed and RefSeq are also provided for each annotation. Apart from the experimental promoter annotations, predictions by popular collections of weight matrices are also provided for each promoter sequence. In addition, global and local alignments and graphical dotplots are also available. gene, alignment, annotation, binding, computational, genome, nucleotide, ortholog, prediction, promoter, sequence, target, transcription, transcriptional factor, binding site, promoter sequence, protein motif, benchmark, transcription factor binding site, bio.tools is listed by: bio.tools
is listed by: Debian
is related to: IntegromeDB
has parent organization: Center for Genomic Regulation; Barcelona; Spain
European Union FP6 contract LSHG-CT-2003-503265 PMID:16381947 Acknowledgement requested, GNU General Public License, v2 biotools:alggen, nif-0000-21006 https://bio.tools/alggen SCR_002276 A database of Annotated regulatory Binding Sites from orthologous promoters 2026-02-14 02:06:09 1
EcoCyc
 
Resource Report
Resource Website
100+ mentions
EcoCyc (RRID:SCR_002433) EcoCyc, EcoCyc REF data or information resource, database Database for the bacterium Escherichia coli K-12 MG1655, the EcoCyc project performs literature-based curation of the entire genome, and of transcriptional regulation, transporters, and metabolic pathways. The long-term goal of the project is to describe the molecular catalog of the E. coli cell, as well as the functions of each of its molecular parts, to facilitate a system-level understanding of E. coli. EcoCyc is an electronic reference source for E. coli biologists, and for biologists who work with related microorganisms. genome, metabolic pathway, transcription, transporters, escherichia coli, transcriptional regulation, metabolism, pathway, FASEB list uses: Pathway Tools
is used by: NIF Data Federation
is listed by: OMICtools
is listed by: BioCyc
is related to: MultiFun
is related to: BioCyc
is related to: BioCyc
is related to: AmiGO
is related to: NCBI BioSystems Database
is related to: Pathway Tools
has parent organization: Stanford Research Institute International
NCRR ;
NIGMS GM077678;
NIGMS GM71962
PMID:23143106
PMID:21097882
Free, Freely available OMICS_01645, nif-0000-02783, r3d100011277 https://doi.org/10.17616/R34K99 SCR_002433 EcoCyc REF 2026-02-14 02:05:40 482
CampyDB: Campylobacter Database
 
Resource Report
Resource Website
1+ mentions
CampyDB: Campylobacter Database (RRID:SCR_002299) data or information resource, database CampyDB is a database for comparative genome analysis of For Campylobacter, Helicobacter and Wolinella. The database contains information on: -Campylobacter coli RM2228 -Campylobacter concisus 13826 -Campylobacter curvus 525.92 -Campylobacter fetus subsp. fetus 82-40 -Campylobacter hominis ATCC BAA-381 -Campylobacter jejuni RM1221 -Campylobacter jejuni subsp. doylei 269.97 -Campylobacter jejuni subsp. jejuni 260.94 -Campylobacter jejuni subsp. jejuni 81-176 -Campylobacter jejuni subsp. jejuni 81-176 -Campylobacter jejuni subsp. jejuni 84-25 -Campylobacter jejuni subsp. jejuni CF93-6 -Campylobacter jejuni subsp. jejuni CG8486 -Campylobacter jejuni subsp. jejuni HB93-13 -Campylobacter jejuni subsp. jejuni NCTC 11168 -Campylobacter lari RM2100 -Campylobacter upsaliensis RM3195 -Helicobacter acinonychis str. Sheeba -Helicobacter hepaticus ATCC 51449 -Helicobacter pylori 26695 -Helicobacter pylori HPAG1 -Helicobacter pylori J99 -Thiomicrospira denitrificans ATCC 33889 -Wolinella succinogenes DSM 1740 Sponsors: The project was originally conceived in 2002 by Roy Chaudhuri and Mark Pallen at the University of Birmingham, as part of a BBSRC funded Exploiting Genomics (ExGen) consortium. CampyDB is developed and maintained by Nick Loman and Lori Snyder working in the Pallen Research Group at University of Birmingham and is supported by a 5 year BBSRC grant until Feburary 2012. campylobacter, comparative, genome, helicobacter, prokaryote databases, wolinella nif-0000-21075 SCR_002299 CampyDB 2026-02-14 02:05:39 4
Entrez Gene
 
Resource Report
Resource Website
1000+ mentions
Entrez Gene (RRID:SCR_002473) NCBI_Gene, NCBI Genen NCBI Entrez data or information resource, database Database for genomes that have been completely sequenced, have active research community to contribute gene-specific information, or that are scheduled for intense sequence analysis. Includes nomenclature, map location, gene products and their attributes, markers, phenotypes, and links to citations, sequences, variation details, maps, expression, homologs, protein domains and external databases. All entries follow NCBI's format for data collections. Content of Entrez Gene represents result of curation and automated integration of data from NCBI's Reference Sequence project (RefSeq), from collaborating model organism databases, and from many other databases available from NCBI. Records are assigned unique, stable and tracked integers as identifiers. Content is updated as new information becomes available. gene, gene expression, gene location, gene map, gene prediction, genome, genome sequence analysis, phenotype, nomenclature, gene mapping, protein, genetic code, function, annotation, gold standard, bio.tools is used by: Animal QTLdb
is used by: NIF Data Federation
is used by: LIPID MAPS Proteome Database
is used by: DisGeNET
is used by: Nowomics
is used by: Cytokine Registry
is used by: Pathway Analysis Tool for Integration and Knowledge Acquisition
is used by: Vesiclepedia
is listed by: OMICtools
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: Rat Gene Symbol Tracker
is related to: Gene Reference into Function
is related to: Integrated Molecular Interaction Database
is related to: Biomine
is related to: SEGS
is related to: STOP
is related to: Coremine Medical
is related to: Consensus CDS
is related to: WebGestalt: WEB-based GEne SeT AnaLysis Toolkit
is related to: Array Information Library Universal Navigator
is related to: biomaRt
has parent organization: NCBI
works with: Open Regulatory Annotation Database
PMID:17148475
PMID:21115458
Free, Freely available nif-0000-02801, biotools:entrez_gene, OMICS_01651, r3d100010650 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene
https://bio.tools/entrez_gene
https://doi.org/10.17616/R3603S
SCR_002473 NCBI Gene, Gene - Gene mapped phenotypes, Gene - Gene and mapped phenotypes, Gene Database, GeneID 2026-02-14 02:06:07 2830
Fungal Databases
 
Resource Report
Resource Website
100+ mentions
Fungal Databases (RRID:SCR_002350) data or information resource, database This website contains a list of five fungal genome databases from The J. Craig Venter Institute. Aspergillus genomes: -Aspergillus fumigatus (strain-Af 293) -Aspergillus clavatus -Neosartorya fischeri Other Fungal Genomes: -Cryptococcus neoformans (strain-JEC21) -Coccidioides posadasii fumigatus, fungal, fungal genome databases, aspergillus, clavatus, coccidioides posadasii, cryptococcus neoformans, genome, neosartorya fischeri, FASEB list has parent organization: J. Craig Venter Institute nif-0000-21158 SCR_002350 Fungal Databases 2026-02-14 02:06:09 281
DBTSS: Database of Transcriptional Start Sites
 
Resource Report
Resource Website
100+ mentions
DBTSS: Database of Transcriptional Start Sites (RRID:SCR_002354) DBTSS data or information resource, database Database of transcriptional start sites (TSSs) representing exact positions in the genome based on a unique experimentally validated TSS sequencing method, TSS Seq. A major part of human adult and embryonic tissues are covered. DBTSS contains 491 million TSS tag sequences collected from a total of 20 tissues and 7 cell cultures. Also integrated is generated RNA-seq data of subcellular- fractionated RNAs and ChIP Seq data of histone modifications, RNA polymerase II and several transcriptional regulatory factors in cultured cell lines. Also included is external epigenomic data, such as chromatin map of the ENCODE project. They associated those TSS information with public and original SNV data, in order to identify single nucleotide variations (SNVs) in the regulatory regions. cdna, cdna library, transcriptional start site, transcriptome, transcriptome analysis, tss-seq, genome, adult human, embryonic, cell, rna-seq, subcellular, rna, chip seq data, histone modification, rna polymerase ii, transcriptional regulatory factor, cell line, single nucleotide variation, regulatory region, genetic valuation, transcriptional regulation, bio.tools, FASEB list is used by: Transcriptional Regulatory Element Database
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Tokyo; Tokyo; Japan
Japan Society for the Promotion of Science ;
Japanese Ministry of Education Culture Sports Science and Technology MEXT
PMID:22086958
PMID:19910371
PMID:17942421
PMID:16381981
PMID:14681363
PMID:11752328
nif-0000-02738, biotools:dbtss, OMICS_01860 https://bio.tools/dbtss SCR_002354 DBTSS: Database of Transcriptional Start Sites, DataBase of Transcriptional Start Sites 2026-02-14 02:05:39 124
GeneSeer
 
Resource Report
Resource Website
GeneSeer (RRID:SCR_002626) GeneSeer data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 14,2026. Database to access gene information through common names and allows identification of homologs and paralogs for a given gene. This publicly available tool leverages public sequence data, gene metadata information, and other publicly available data to calculate and display orthologous and paralogous gene relationships for all genes from several species, including yeasts, insects, worms, vertebrates, mammals, and primates such as humans. gene, homolog, paralog, genome, search engine, ortholog PMID:16176584 THIS RESOURCE IS NO LONGER IN SERVICE nlx_156048 http://katahdin.mssm.edu/geneseer/scripts/main.pl http://geneseer.cshl.org/ SCR_002626 2026-02-14 02:05:40 0
MachiBase
 
Resource Report
Resource Website
1+ mentions
MachiBase (RRID:SCR_003078) MachiBase data or information resource, database Database for Drosophila melanogaster transcription profiling that allows users to search the Drosophilia genome, see sequence overviews, and look at various transcripts. The data were generated in conjunction with the recently developed high-throughput genome sequencer Illumina / Solexa using a newly developed 5'-end mRNA collection method. Approximately 25 million 25-27 nucleotide (nt) 5'-end mRNA tags from the embryos, larvae, young males, young females, old males, old females, and S2 (culture cell line) of D. melanogaster were collected. By arranging this vast amount of expression tag with other annotated data, they have built a one-stop service for Drosophila melanogaster transcription profiling. transcription profiling, genome, sequence, transcript, mrna, promoter, gene expression, development, embryo, larvae, young, male, female, old, s2, culture, cell line, expressed sequence tag, solexa is listed by: OMICtools
has parent organization: University of Tokyo; Tokyo; Japan
PMID:18842623 Free, Available for download, Freely available OMICS_01878, nif-0000-03092 SCR_003078 2026-02-14 02:06:10 1
Protein Clusters
 
Resource Report
Resource Website
1+ mentions
Protein Clusters (RRID:SCR_003459) ProtClustDB data or information resource, database Database of related protein sequences (clusters) consisting of proteins derived from the annotations of whole genomes, organelles and plasmids. It currently limited to Archaea, Bacteria, Plants, Fungi, Protozoans, and Viruses. It contains annotation information, publications, domains, structures, and external links and analysis tools including multiple alignments, phylogenetic trees, and genomic neighborhoods (ProtMap). Data is available for download via Protein Clusters FTP bacteriophage, mitochondrial organelle, chloroplast organelle, plasmid, phylogeny, nucleotide sequence, chloroplast, dna, virus, genome, organelle, gold standard is listed by: re3data.org
has parent organization: NCBI
NIH ;
Intramural Research Program ;
NLM
PMID:18940865 Free, Available for download, Freely available nif-0000-03354, r3d100010861 https://doi.org/10.17616/R3TS52 SCR_003459 Protein Clusters Database, NCBI Protein Clusters, Entrez Protein Clusters 2026-02-14 02:05:44 4
MapViewer
 
Resource Report
Resource Website
100+ mentions
MapViewer (RRID:SCR_003092) Map Viewer data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 4, 2023. Database that provides special browsing capabilities for a subset of organisms in Entrez Genomes. Map Viewer allows users to view and search an organism's complete genome, display chromosome maps, and zoom into progressively greater levels of detail, down to the sequence data for a region of interest. If multiple maps are available for a chromosome, it displays them aligned to each other based on shared marker and gene names, and, for the sequence maps, based on a common sequence coordinate system. genome, mapping, sequencing, chromosome is listed by: OMICtools
is related to: NCBI Genome
is related to: Consensus CDS
has parent organization: NCBI
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00921, nif-0000-03103 SCR_003092 Entrez Map Viewer, NCBI Map Viewer 2026-02-14 02:05:49 242
Mammalian Mitochondrial Genomics Database
 
Resource Report
Resource Website
Mammalian Mitochondrial Genomics Database (RRID:SCR_003084) MamMiBase data or information resource, database Database developed to assist the phylogeneticist user in retrieving individual gene sequence alignments for genes in complete mammalian mitochondrial genomes. Data retrieval in MamMiBase requires three stages. At the first stage, the user must select the mammalian species or group that (s)he wishes to study. In the second stage, the user will select the outgroup from a list that included all species selected in the first stage plus Xenopus laevis and Gallus gallus. Finally, at the third stage, the user will select individual mitochondrial gene alignments or a phylogenetic tree that (s)he wishes to download. phylogeny, mitochondrial, genome, gene, sequence has parent organization: National Laboratory for Scientific Computing; Rio de Janeiro; Brazil Brazilian Ministry of Science Technology and Innovation ;
National Research Council ;
Rio de Janeiro Science Foundation ;
FAPERJ
PMID:15713730 Free, Freely available nif-0000-03099 SCR_003084 2026-02-14 02:06:13 0
Influenza Virus Resource
 
Resource Report
Resource Website
50+ mentions
Influenza Virus Resource (RRID:SCR_002984) Influenza Virus Resource data or information resource, database Database of data obtained from the NIAID Influenza Genome Sequencing Project as well as from GenBank, combined with tools for flu sequence analysis and annotation. In addition, it provides links to other resources that contain flu sequences, publications and general information about flu viruses. Users can search the Flu database, build queries, retrieve sequences, and apply analysis tools. This includes selecting influenza sequences by virus, subtype, host, and other criteria, finding complete genome sets, aligning sequence and others in the database (up to 1000 sequences), viewing clustering and phylogenetic trees, BLAST searching a flu sequence against the database, and more. genomics, genome, flu, variation, annotation, blast, cluster, phylogenetic tree, align, data analysis service is listed by: re3data.org
is related to: GenBank
is related to: Virus Variation
has parent organization: NCBI
Influenza virus PMID:17942553 Free, Available for download, Freely available nif-0000-03023, r3d100011004 https://doi.org/10.17616/R3S61C SCR_002984 NCBI Influenza Virus Resource 2026-02-14 02:05:48 83
Factorbook
 
Resource Report
Resource Website
10+ mentions
Factorbook (RRID:SCR_004086) Factorbook data or information resource, database A Wiki-based database for transcription factor-binding data generated by the ENCODE consortium. transcription factor, genome, transcription factor binding region, chip-seq is listed by: OMICtools
is related to: ENCODE
PMID:22955990 OMICS_00533 SCR_004086 2026-02-14 02:05:45 18
My Cancer Genome
 
Resource Report
Resource Website
50+ mentions
My Cancer Genome (RRID:SCR_004140) MCG data or information resource, database A freely available online personalized cancer medicine knowledge resource for physicians, patients, caregivers and researchers that gives up-to-date information on what mutations make cancers grow and related therapeutic implications, including available clinical trials. It is a one-stop tool that matches tumor mutations to therapies, making information accessible and convenient for busy clinicians. genome, disease, genome, medicine, clinical trial, mutation, therapy, FASEB list is listed by: OMICtools
has parent organization: Vanderbilt University; Tennessee; USA
Cancer, Tumor PMID:32483629 OMICS_01552 SCR_004140 MyCancerGenome.org 2026-02-14 02:06:16 97

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    You are currently on the Community Resources tab looking through categories and sources that NIF 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 NIF then you can log in from here to get additional features in NIF 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 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.