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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
dbMHC
 
Resource Report
Resource Website
10+ mentions
dbMHC (RRID:SCR_002302) dbMHC data or information resource, data repository, database, service resource, storage service resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 23, 2019 Database was open, publicly accessible platform for DNA and clinical data related to human Major Histocompatibility Complex (MHC). Data from IHWG workshops were provided as well., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. human leukocyte antigen, microsatellite, dna, clinical, major histocompatibility complex, primer, probe, sequence, allele, haplotype, sequence, histocompatibility, leucocyte, alignment is listed by: re3data.org
is related to: NIDDK Information Network (dkNET)
is related to: IMGT/HLA
has parent organization: NCBI
PMID:14705985 Free, Available for download, Freely available nif-0000-02729, r3d100010881 https://doi.org/10.17616/R37W4F http://www.ncbi.nlm.nih.gov/gv/mhc/main.cgi?cmd=init SCR_002302 Major Histocompatibility Complex Database 2026-08-29 11:21:13 22
DNA DataBank of Japan (DDBJ)
 
Resource Report
Resource Website
500+ mentions
DNA DataBank of Japan (DDBJ) (RRID:SCR_002359) DDBJ data or information resource, data repository, database, service resource, storage service resource Maintains and provides archival, retrieval and analytical resources for biological information. Central DDBJ resource consists of public, open-access nucleotide sequence databases including raw sequence reads, assembly information and functional annotation. Database content is exchanged with EBI and NCBI within the framework of the International Nucleotide Sequence Database Collaboration (INSDC). In 2011, DDBJ launched two new resources: DDBJ Omics Archive and BioProject. DOR is archival database of functional genomics data generated by microarray and highly parallel new generation sequencers. Data are exchanged between the ArrayExpress at EBI and DOR in the common MAGE-TAB format. BioProject provides organizational framework to access metadata about research projects and data from projects that are deposited into different databases. nucleotide sequence, genome, dna, dna database, dna research, nucleotide, phylogenetics, protein, sequence, protein binding, gene expression, gene, genetics, nucleoid, genomics, protein binding, gold standard, bio.tools, FASEB list 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: re3data.org
is listed by: Debian
is listed by: bio.tools
is related to: INSDC
is related to: GenBank
is related to: INSDC
is related to: European Nucleotide Archive (ENA)
is related to: GenBank
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: Worldwide Protein Data Bank (wwPDB)
is related to: Biological Magnetic Resonance Data Bank (BMRB)
is related to: PDBe - Protein Data Bank in Europe
is related to: PDBe - Protein Data Bank in Europe
is related to: European Nucleotide Archive (ENA)
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: NCBI Assembly Archive Viewer
has parent organization: National Institute of Genetics; Shizuoka; Japan
is parent organization of: DDBJ Omics Archive
is parent organization of: BodyMap-Xs
is parent organization of: DDBJ Sequence Read Archive
is parent organization of: CIBEX: Center for Information Biology gene EXpression database
is parent organization of: Japanese Genotype-phenotype Archive (JGA)
Japanese Ministry of Education Culture Sports Science and Technology MEXT PMID:26578571
PMID:25477381
Free, Freely available, OMICS_01644, biotools:ddbj, nif-0000-02740, r3d100010218 https://bio.tools/ddbj, https://doi.org/10.17616/R3M01R SCR_002359 DNA DataBank of Japan (DDBJ), DNA DataBank of Japan, DDBJ, DNA Data Bank of Japan, DDBJ - DNA Data Bank of Japan 2026-08-29 11:21:13 709
NCBI Genome
 
Resource Report
Resource Website
500+ mentions
NCBI Genome (RRID:SCR_002474) Genome data or information resource, data repository, database, service resource, storage service resource Database that organizes information on genomes including sequences, maps, chromosomes, assemblies, and annotations in six major organism groups: Archaea, Bacteria, Eukaryotes, Viruses, Viroids, and Plasmids. Genomes of over 1,200 organisms can be found in this database, representing both completely sequenced organisms and those for which sequencing is in progress. Users can browse by organism, and view genome maps and protein clusters. Links to other prokaryotic and archaeal genome projects, as well as BLAST tools and access to the rest of the NCBI online resources are available. chromosome, organelle, plasmid, viroid, virus, genome, sequence, map, assembly, annotation, gene mapping, dna, blast, protein cluster, gold standard is listed by: re3data.org
is related to: MapViewer
is related to: UniProt Proteomes
is related to: CaspBase
has parent organization: NCBI
works with: nTrackAnnotator
Free, Freely avaialble nif-0000-02802, r3d100010785 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=Genome, https://doi.org/10.17616/R3R89S SCR_002474 Entrez Genomes, Entrez Genome, NCBI, Genome, Genome Database, Genome: Information by genome sequence 2026-08-29 11:21:21 618
Rainbow
 
Resource Report
Resource Website
10+ mentions
Rainbow (RRID:SCR_002724) data analysis software, data processing software, sequence analysis software, software application, software resource Software developed to provide an ultra-fast and memory-efficient solution to clustering and assembling short reads produced by RAD-seq. software, tool, clustering, assembling, short, read, restriction, site, DNA, sequence, analysis, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:22942077
DOI:10.1093/bioinformatics/bts482
Free, Freely available, Available for download SCR_015992, OMICS_03722, biotools:rainbow https://bio.tools/rainbow, https://sources.debian.org/src/bio-rainbow/ SCR_002724 RAD-seq: Restriction-site Associated DNA sequencing, Bio-rainbow, RAD-seq 2026-08-29 11:21:11 41
Gabi Primary Database
 
Resource Report
Resource Website
10+ mentions
Gabi Primary Database (RRID:SCR_002755) GABI analysis service resource, data analysis service, data or information resource, data repository, database, production service resource, service resource, storage service resource Database that collects, integrates and links all relevant primary information from the GABI plant genome research projects and makes them accessible via internet. Its purpose is to support plant genome research in Germany, to yield information about commercial important plant genomes, and to establish a scientific network within plant genomic research.
GreenCards is the main interface for text based retrieval of sequence, SNP, mapping data etc. Sharing and interchange of data among collaborating research groups, industry and the patent- and licensing agency are facilitated.
* GreenCards: Text based search for sequence, mapping, SNP data etc. * Maps: Visualization of genetic or physical maps. * BLAST: Secure BLAST search against different public databases or non-public sequence data stored in GabiPD. * Proteomics: View interactive 2D-gels and view or download information for identified protein spots. Registered users can submit data via secure file upload.
molecular plant physiology, plant genome, genome, blast, sequence, snp, mapping, proteomics, image collection has parent organization: Max Planck Institute of Molecular Plant Physiology; Golm; Germany German Resource Center for Genome Research RZPD GmbH ;
Max Planck Society ;
BMBF 0312272;
BMBF 0313112;
BMBF 0315046
PMID:18812395 Free, Freely available nif-0000-02866, r3d100012432 http://gabi.rzpd.de/, https://doi.org/10.17616/R3QB61 SCR_002755 GabiPD 2026-08-29 11:21:12 13
StreamingTrim
 
Resource Report
Resource Website
1+ mentions
StreamingTrim (RRID:SCR_002922) software resource A DNA reads trimming software, written in Java, with which researchers are able to analyse the quality of DNA sequences in fastq files and to search for low-quality zones in a very conservative way. standalone software, java, 16s rrna, sequence is listed by: OMICtools PMID:24128146 Free, Available for download, Freely available OMICS_05196 SCR_002922 2026-08-29 11:21:36 8
Sal-Site
 
Resource Report
Resource Website
50+ mentions
Sal-Site (RRID:SCR_002850) Sal-Site analysis service resource, data analysis service, data or information resource, database, image collection, organism-related portal, portal, production service resource, service resource, topical portal Portal that supports Ambystoma-related research and educational efforts. It is composed of several resources: Salamander Genome Project, Ambystoma EST Database, Ambystoma Gene Collection, Ambystoma Map and Marker Collection, Ambystoma Genetic Stock Center, and Ambystoma Research Coordination Network. gene, genomic, expressed sequence tag, blast, model organism, genome, salamander, animal model, genetic map, genetic marker, gene expression, limb regeneration, microarray, quantitative-pcr, rna-seq, nanostring, husbandry, embryo, limb, mutant, strain, neural, olfaction, phentotype, regeneration, renal, retina, sequence, vision, human, chicken, xenopus tropicalis, FASEB list has parent organization: University of Kentucky; Kentucky; USA NCRR R24 RR016344;
NIH Office of the Director R24 OD010435;
NSF DBI0443496;
NSF OB0242833
PMID:16359543 Free, Freely available nif-0000-25309 https://orip.nih.gov/comparative-medicine/programs/vertebrate-models SCR_002850 Ambystoma Resources for Model Amphibians Database 2026-08-29 11:21:21 92
Computational Biology Center
 
Resource Report
Resource Website
50+ mentions
Computational Biology Center (RRID:SCR_002877) data or information resource, disease-related portal, portal, topical portal, training resource Computational biology research at Memorial Sloan-Kettering Cancer Center (MSKCC) pursues computational biology research projects and the development of bioinformatics resources in the areas of: sequence-structure analysis; gene regulation; molecular pathways and networks, and diagnostic and prognostic indicators. The mission of cBio is to move the theoretical methods and genome-scale data resources of computational biology into everyday laboratory practice and use, and is reflected in the organization of cBio into research and service components ~ the intention being that new computational methods created through the process of scientific inquiry should be generalized and supported as open-source and shared community resources. Faculty from cBio participate in graduate training provided through the following graduate programs: * Gerstner Sloan-Kettering Graduate School of Biomedical Sciences * Graduate Training Program in Computational Biology and Medicine Integral to much of the research and service work performed by cBio is the creation and use of software tools and data resources. The tools that we have created and utilize provide evidence of our involvement in the following areas: * Cancer Genomics * Data Repositories * iPhone & iPod Touch * microRNAs * Pathways * Protein Function * Text Analysis * Transcription Profiling drug, evolution, experiment, gene, algorithm, bioinformatics, biology, cancer, clinical, computational, diagnostic, genome, human, initiation, kinetics, laboratory, leukemia, ligand, metastasis, microrna, mirna, model, molecular, network, pathway, phenotype, prognostic, progression, protein, regulation, research, resistance, rna, sequence, stem cell, structure, t cell, therapy, treatment, tumor is parent organization of: TMBETA-GENOME- Annotation of Beta-Barrel Membrane Proteins in Genomic Sequences Free, Freely available nif-0000-25560 SCR_002877 cBio 2026-08-29 11:21:16 71
Tuschl Laboratory: RNA Molecular Biology
 
Resource Report
Resource Website
1+ mentions
Tuschl Laboratory: RNA Molecular Biology (RRID:SCR_002866) data or information resource, laboratory portal, organization portal, portal RNA is not only a carrier of genetic information, but also a catalyst and a guide for sequence-specific recognition and processing of other RNA molecules. This lab investigates the regulatory mechanisms of RNA interference, RNA-mediated translational control, and nuclear pre-mRNA splicing. Classical and combinatorial biochemical techniques are used to analyze the function of the RNA- and protein-components involved in those processes. genetics, biochemical, biology, catalyst, mechanism, mirna, molecule, process., protein, regulation, rna, sequence, sirna, technique has parent organization: Rockefeller University; New York; USA Free, Freely available nif-0000-25546 http://www.rockefeller.edu/labheads/tuschl/sirna.html SCR_002866 Tuschl Lbaoratory 2026-08-29 11:21:21 5
DnaSP
 
Resource Report
Resource Website
5000+ mentions
DnaSP (RRID:SCR_003067) DnaSP data analysis software, data processing software, software application, software resource A software package for the analysis of nucleotide polymorphism from aligned DNA sequence data. DnaSP can estimate several measures of DNA sequence variation within and between populations (in noncoding, synonymous or nonsynonymous sites, or in various sorts of codon positions), as well as linkage disequilibrium, recombination, gene flow and gene conversion parameters. DnaSP can also carry out several tests of neutrality: Hudson, Kreitman and Aguad (1987), Tajima (1989), McDonald and Kreitman (1991), Fu and Li (1993), and Fu (1997) tests. Additionally, DnaSP can estimate the confidence intervals of some test-statistics by the coalescent. The results of the analyses are displayed on tabular and graphic form. genetics, dna, population genetics, sequence, polymorphism, nucleotide polymorphism, dna sequence, population, noncoding, synonymous, nonsynonymous is listed by: OMICtools
has parent organization: University of Barcelona; Barcelona; Spain
Spanish Direccion General de Investigacion Cientifica y Technica PB91-0245;
Spanish Direccion General de Investigacion Cientifica y Technica PB94-0923;
Spanish Direccion General de Investigacion Cientifica y Technica PB97-0918;
Spanish Direccion General de Investigacion Cientifica y Technica TXT98-1802;
Spanish Direccion General de Investigacion Cientifica y Technica BMC2001-2906;
Spanish Direccion General de Investigacion Cientifica y Technica BFU2004-02253;
Spanish Direccion General de Investigacion Cientifica y Technica BFU2007-6292
PMID:19346325
PMID:19378153
PMID:14668244
PMID:10089204
PMID:9183537
PMID:8808578
Free, Available for download, Freely available OMICS_01820, nif-0000-30461 SCR_003067 DNA Sequence Polymorphism 2026-08-29 11:21:21 6215
GenePaint
 
Resource Report
Resource Website
100+ mentions
GenePaint (RRID:SCR_003015) GenePaint.org atlas, data or information resource, database, expression atlas, reference atlas Digital atlas of gene expression patterns in developing and adult mouse. Several reference atlases are also available through this site. Expression patterns are determined by non-radioactive in situ hybridization on serial tissue sections. Sections are available from several developmental ages: E10.5, E14.5 (whole embryos), E15.5, P7 and P56 (brains only). To retrieve expression patterns, search by gene name, site of expression, GenBank accession number or sequence homology. For viewing expression patterns, GenePaint.org features virtual microscope tool that enables zooming into images down to cellular resolution. gene expression, adult mouse, annotated, c57bl6, mouse, mouse embryo, mrna, non radioactive in situ hybridization, light microscopy, molecular neuroanatomy resource, in situ hybridization, embryonic, postnatal, adult, brain, head, annotation, rna probe, sequence, anatomical structure, FASEB list has parent organization: Max Planck Institute for Biophysical Chemistry; Gottingen; Germany
is parent organization of: GenePaint E15 Atlas
is parent organization of: GenePaint P7 Atlas
is parent organization of: GenePaint P56 Mouse Atlas
is parent organization of: GenePaint Interactive Anatomy Atlas
BMBF ;
Burroughs Wellcome Fund ;
European Union ;
Max Planck Society ;
Merck Genome Research Institute ;
NINDS ;
Romansky Endowment
PMID:14681479
PMID:22936000
nif-0000-00009, SCR_017526 SCR_003015 Atlas of Gene Expression Patterns in Mouse Embryo 2026-08-29 11:21:39 164
Gutentag
 
Resource Report
Resource Website
Gutentag (RRID:SCR_003051) software resource An interactive, user-editable genetic sequence database tool, targeted at molecular biology research groups that can be browsed using tags. The tool is Web 2.0-flavoured, allowing users to do more than just retrieve information. Its focus on user-editability is supported by the use of tags (metadata) associated with genetic sequences. Several methods of retrieving stored data are available including tag-clouds, BLAST and keyword searches. Also, sequence tags related to HGNC gene names, conserved domains (CDD) and GO terms can be automatically generated given sequence data. The tool is constructed using the high-level Python web framework, Django, with a SQLite3 backend. standalone software, python, django, genetics, sequence is listed by: OMICtools
has parent organization: Google Code
PMID:14640709 Free, Available for download, Freely available OMICS_02396 SCR_003051 gutentag - A genetic sequence database for labs that can be browsed using tags 2026-08-29 11:21:21 0
DIALIGN
 
Resource Report
Resource Website
10+ mentions
DIALIGN (RRID:SCR_003041) DIALIGN analysis service resource, data access protocol, data analysis service, production service resource, service resource, software resource, web service Tool for multiple sequence alignment using various sources of external information that is particularly useful to detect local homologies in sequences with low overall similarity. While standard alignment methods rely on comparing single residues and imposing gap penalties, DIALIGN constructs pairwise and multiple alignments by comparing entire segments of the sequences. No gap penalty is used. This approach can be used for both global and local alignment, but it is particularly successful in situations where sequences share only local homologies. Several versions of DIALIGN are available online at GOBICS, http://dialign.gobics.de/ dna, protein, sequence alignment, sequence, alignment, fasta, genome, genomic sequence, homology, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
has parent organization: Bielefeld University; North Rhine-Westphalia; Germany
PMID:15215344
PMID:23620293
DOI:10.1186/1748-7188-3-6
Free, Available for download, Freely available nif-0000-30417, OMICS_24606, OMICS_00973, biotools:dialign-tx http://dialign.gobics.de/, https://bio.tools/dialign-tx https://sources.debian.org/src/dialign-tx/ SCR_003041 DIALIGN at GOBICS 2026-08-29 11:21:40 44
FastUniq
 
Resource Report
Resource Website
1+ mentions
FastUniq (RRID:SCR_000682) software resource A software tool for removal of de novo duplicates in paired short DNA sequences. de novo, dna, sequence, duplicate, is listed by: OMICtools
has parent organization: SourceForge
DOI:10.1371/journal.pone.0052249 Free, Available for download, Freely available OMICS_01044 SCR_000682 2026-08-29 11:20:34 4
HapCompass
 
Resource Report
Resource Website
1+ mentions
HapCompass (RRID:SCR_000942) algorithm Software that utilizes a fast cycle basis algorithm for the accurate haplotype assembly of sequence data. It is able to create pairwise SNP phasings. algorithm, haplotype, sequence, genome, dna, rna, snp is listed by: OMICtools
has parent organization: Brown University; Rhode Island; USA
NSF 1048831;
NSF 1321000
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00197 SCR_000942 2026-08-29 11:20:52 1
R453Plus1Toolbox
 
Resource Report
Resource Website
1+ mentions
R453Plus1Toolbox (RRID:SCR_001105) data analysis software, data processing software, sequence analysis software, software application, software resource, software toolkit R software toolbox of functions for the analysis of data generated by Roche's 454 sequencing platform. Additional functions are included for quality assurance, annotation and visualization of detected variants, complementing the software tools shipped by Roche with their product. A pipeline for the detection of structural variants is provided. genome, sequence, visualization, structural variants, r, sequence analysis software is listed by: OMICtools
is hosted by: Bioconductor
PMID:21349869 Free, Available for download, Freely available OMICS_01354 SCR_001105 2026-08-29 11:20:43 4
BreakFusion
 
Resource Report
Resource Website
1+ mentions
BreakFusion (RRID:SCR_001102) BreakFusion software resource Software package written in Perl and C++ that provides a computational pipeline for identifying gene fusions from RNA-seq data. computational pipeline, gene fusions, rna, sequence, data, perl, c++ is listed by: OMICtools
has parent organization: University of Texas MD Anderson Cancer Center
PMID:22563071
DOI:10.1093/bioinformatics/bts272
Free, Available for download, Freely available OMICS_01342 SCR_001102 2026-08-29 11:20:43 3
Kyoto Encyclopedia of Genes and Genomes Expression Database
 
Resource Report
Resource Website
1000+ mentions
Kyoto Encyclopedia of Genes and Genomes Expression Database (RRID:SCR_001120) KEGG Expression Database data or information resource, data repository, database, service resource, storage service resource Database for mapping gene expression profiles to pathways and genomes. Repository of microarray gene expression profile data for Synechocystis PCC6803 (syn), Bacillus subtilis (bsu), Escherichia coli W3110 (ecj), Anabaena PCC7120 (ana), and other species contributed by the Japanese research community. encyclopedia, endogenous, environment, enzyme, escherichia coli, exogenous, expression, family, functional, gene, genetic, anabaena, bacillus subtilis, biological system, biology, building block, cell, cellular, chemical, community, complex, genome, genomic, hierarchy, interaction, japanese, mapping, metabolic, metabolic pathway databases, microarray, molecular, molecular wiring, nomenclature, order, organism, ortholog, pathway, process, protein, reaction, research, sequence, specie, substance, synechocystis, FASEB list is listed by: LabWorm
is affiliated with: KEGG
has parent organization: Kyoto University; Kyoto; Japan
PMID:9847135
PMID:10592173
Free, Available for download, Freely available r3d100011570, nif-0000-21234 https://doi.org/10.17616/R3792T SCR_001120 Kyoto Encyclopedia of Genes and Genomes Expression Database 2026-08-29 11:20:36 1279
Reaper - Demultiplexing trimming and filtering sequencing data
 
Resource Report
Resource Website
1+ mentions
Reaper - Demultiplexing trimming and filtering sequencing data (RRID:SCR_001144) Reaper software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 23, 2022. Software program for demultiplexing, trimming and filtering short read sequencing data. c, alignment, sequence, demultiplex, trim, filter, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: European Bioinformatics Institute
THIS RESOURCE IS NO LONGER IN SERVICE biotools:reaper, OMICS_02157 https://bio.tools/reaper SCR_001144 2026-08-29 11:20:44 1
Genome Trax
 
Resource Report
Resource Website
1+ mentions
Genome Trax (RRID:SCR_001234) Genome Trax service resource Service that provides a comprehensive compilation of variant knowledge that allows you to identify pathogenic variants in human whole genome or exome sequences. It makes it easy to upload a complete genome?s worth of variations and identify the biologically relevant subset of known mutations, mutations that are novel and appear in a candidate disease genes, or mutations that are predicted to have a deleterious effect. The database includes a comprehensive collection of disease causing mutations from HGMD Professional, regulatory sites from TRANSFAC , and disease genes, drug targets and pathways from PROTEOME, as well as pharmacogenomic variants. It integrates the best public data-sets on somatic mutations, allele frequencies and clinical variants, in their most up-to-date version, for a total of more than 165 million annotations. It is possible to identify known pathogenic variants, remove harmless common variants, and obtain deleterious predictions for novel variants. With family data, it is possible to identify variants that are de novo, compound heterozygous only in the offspring. All of the results can be downloaded to Excel for further review. For core facilities and bioinformaticians, the complete underlying data is made available for download and easy integration into custom analysis pipelines. Genome Trax data is optimized to work with many other software packages, such as ANNOVARTM, CLC bio, Alamut, SimulConsult, and Cartagenia. next-generation sequencing, genome, exome, sequence, variation, mutation, pathogenic, database, bio.tools, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: BIOBASE Corporation
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02109, biotools:genome_trax https://bio.tools/genome_trax SCR_001234 Genome Trax for Next Generation Sequencing 2026-08-29 11:20:38 2

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