Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Preparing word cloud

×

SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Keywords:sequence (facet)

Facets


Recent searches

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

569 Results - per page

Show More Columns | Download 569 Result(s)

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
HIV Brain Sequence Database
 
Resource Report
Resource Website
1+ mentions
HIV Brain Sequence Database (RRID:SCR_008819) HIVBrainSeqDB data or information resource, database The HIV Brain Sequence Database (HIVBrainSeqDB) is a public database of HIV envelope sequences, directly sequenced from brain and other tissues from the same patients. For inclusion in the database, sequences must: (i) be deposited in Genbank; (ii) include some portion of the HIV env region; (iii) be clonal, amplified directly from tissue; and (iv) be sampled from the brain, or sampled from a patient for which the database already contains brain sequence. Sequences are annotated with clinical data including viral load, CD4 count, antiretroviral status, neurocognitive impairment, and neuropathological diagnosis, all curated from the original publication. Tissue source is coded using an anatomical ontology, the Foundational Model of Anatomy, to capture the maximum level of detail available, while maintaining ontological relationships between tissues and their subparts. 44 tissue types are represented within the database, grouped into 4 categories: (i) brain, brainstem, and spinal cord; (ii) meninges, choroid plexus, and CSF; (iii) blood and lymphoid; and (iv) other (bone marrow, colon, lung, liver, etc). Currently, the database contains 2517 envelope sequences from 90 patients, obtained from 22 published studies. 1272 sequences are from brain; the remaining 1245 are from blood, lymph node, spleen, bone marrow, colon, lung and other non-brain tissues. The database interface utilizes a faceted interface, allowing real-time combination of multiple search parameters to assemble a meta-dataset, which can be downloaded for further analysis. This online resource will greatly facilitate analysis of the genetic aspects of HIV macrophage tropism, HIV compartmentalization and evolution within the brain and other tissue reservoirs, and the relationship of these findings to HIV-associated neurological disorders and other clinical consequences of HIV infection. human immunodeficiency virus, hiv, brain, sequence, hiv envelope sequence, brain sequence, clone, tissue, brainstem, spinal cord, meninges, choroid plexus, csf, blood, lymphoid, bone marrow, colon, lung, liver, aids is related to: FMA
has parent organization: Harvard University; Cambridge; United States
Human immunodeficiency virus ARRA ;
NIMH 3ROI MH83588-12S1;
NIMH MH83588
PMID:21156070 nlx_149217 SCR_008819 The HIV Brain Sequence Database 2026-02-14 02:06:10 1
Webproanalyst
 
Resource Report
Resource Website
Webproanalyst (RRID:SCR_008348) data analysis service, production service resource, service resource, analysis service resource WebProAnalyst provides web-accessible analysis for scanning the quantitative structure-activity relationships in protein families. It searches for a sequence region, whose substitutions are correlated with variations in the activities of a homologous protein set, the so-called activity modulating sites. WebProAnalyst allows users to search for the key physicochemical characteristics of the sites that affect the changes in protein activities. It enables the building of multiple linear regression and neural networks models that relate these characteristics to protein activities. WebProAnalyst implements multiple linear regression analysis, back propagation neural networks and the Structure-Activity Correlation/Determination Coefficient (SACC/SADC). A back propagation neural network is implemented as a two-layered network, one layer as input, the other as output (Rumelhart et al, 1986). WebProAnalyst uses alignment of amino acid sequences and data on protein activity (pK, Km, ED50, among others). The input data are the numerical values for the physicochemical characteristics of a site in the multiple alignment given by a slide window. The output data are the predicted activity values. The current version of WebProAnalyst handles a single activity for a single protein. The SACC/SADC may be defined as an estimate of the strongest multiple correlation between the physicochemical characteristics of a site in a multiple alignment and protein activities. The SACC/SADC coefficient makes possible the calculation of the possible highest correlation achievable for the quantitative relationship between the physicochemical properties of sites and protein activities. The SACC/SADC is a convenient means for an arrangement of positions by their functional significance. WebProAnalyst outputs a list of multiple alignment positions, the respective correlation values, also regression analysis parameters for the relationships between the amino acid physicochemical characteristics at these positions and the protein activity values. family, functional, activity, alignment, amino acid, homologous, modulating site, neural, physicochemical, propagation, protein, quantitative, region, relationship, scan, sequence, structure, substitution, variation, bio.tools is listed by: bio.tools
is listed by: Debian
nif-0000-25212, biotools:webproanalyst https://bio.tools/webproanalyst SCR_008348 Webproanalyst 2026-02-14 02:06:13 0
PhyloPythiaS
 
Resource Report
Resource Website
10+ mentions
PhyloPythiaS (RRID:SCR_011923) PPS data analysis service, production service resource, service resource, analysis service resource Web Server for Taxonomic Assignment of Metagenome Sequences that is a fast and accurate sequence composition-based classifier that utilizes the hierarchical relationships between clades. Taxonomic assignments with the web server can be made with a generic model, or with sample-specific models that users can specify and create. Several interactive visualization modes and multiple download formats allow quick and convenient analysis and downstream processing of taxonomic assignments. metagenome, sequence, taxonomy, classification is listed by: OMICtools PMID:22745671
PMID:21358620
OMICS_01460 http://phylopythias.cs.uni-duesseldorf.de/index.php?phase=wait SCR_011923 2026-02-14 02:06:14 12
Sequence Search and Alignment by Hashing Algorithm
 
Resource Report
Resource Website
1+ mentions
Sequence Search and Alignment by Hashing Algorithm (RRID:SCR_000544) SSAHA2 software resource, source code A program designed for the efficient mapping of sequence reads onto genomic references. The software is capable of reading most sequencing platforms and giving a range of outputs are supported. sequence, genomic, analysis, search, alignment, algorithm, mapping, bio.tools is listed by: OMICtools
is listed by: bio.tools
is related to: SMALT
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
PMID:11591649 THIS RESOURCE IS NO LONGER IN SERVICE biotools:ssaha2, OMICS_00690, nlx_93831 https://bio.tools/ssaha2 SCR_000544 ssaha2, ssaha, Sequence Search and Alignment by Hashing Algorithm 2026-02-14 02:07:17 6
4Peaks
 
Resource Report
Resource Website
10+ mentions
4Peaks (RRID:SCR_000015) 4Peaks software resource, software application Software application for viewing and editing sequence trace files. mac os x, sequence, trace file is listed by: OMICtools Free OMICS_01015 SCR_000015 2026-02-14 02:06:28 15
Toolbox at the European Bioinformatics Institute
 
Resource Report
Resource Website
50+ mentions
Toolbox at the European Bioinformatics Institute (RRID:SCR_002872) software resource, software toolkit The European Bioinformatics Institute (EBI) toolbox area provides a comprehensive range of tools for the field of bioinformatics. These are subdivided into categories in the left menu for convenience. EBI has developed a large number of very useful bioinformatics tools. A few examples include: - Similarity & Homology - the BLAST or FASTA programs can be used to look for sequence similarity and infer homology. - Protein Functional Analysis - InterProScan can be used to search for motifs in your protein sequence. - Proteomic Services NEW - UniProt DAS server allows researchers to show their research results in the context of UniProtKB/Swiss-Prot annotation. - Sequence Analysis - ClustalW2 a sequence alignment tool. - Structural Analysis - MSDfold can be used to query your protein structure and compare it to those in the Protein Data Bank (PDB). - Web Services - provide programmatic access to the various databases and retrieval/analysis services EBI provides. - Tools Miscellaneous - Expression Profiler a set of tools for clustering, analysis and visualization of gene expression and other genomic data. Sponsors: This resource is sponsored by EBI. expression, functional, gene, bioinformatics, database, genomic, homology, protein, proteomic, sequence, structural, toolbox has parent organization: European Bioinformatics Institute Free nif-0000-25553 SCR_002872 EBI Bioinformatics Tools 2026-02-14 02:06:56 85
Rhode Island INBRE Molecular Informatics Core Facility
 
Resource Report
Resource Website
10+ mentions
Rhode Island INBRE Molecular Informatics Core Facility (RRID:SCR_017685) core facility, access service resource, 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 2026-02-14 02:08:31 12
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 core facility, access service resource, 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 2026-02-14 02:08:10 0
University of Sheffield Genomic Core Facility
 
Resource Report
Resource Website
University of Sheffield Genomic Core Facility (RRID:SCR_017912) core facility, access service resource, 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 2026-02-14 02:08:07 0
SignalP
 
Resource Report
Resource Website
5000+ mentions
SignalP (RRID:SCR_015644) software resource, web application Web application for prediction of the presence and location of signal peptide cleavage sites in amino acid sequences from different organisms. The method incorporates a prediction of cleavage sites and a signal peptide/non-signal peptide prediction based on a combination of several artificial neural networks. prediction, signal peptide, cleavage site, amino acid, sequence, artificial neural network is listed by: SoftCite
has parent organization: DTU Center for Biological Sequence Analysis
PMID:28451972 Freely available, Acknowledgment requested, Free, Available for download, Runs on Windows, Runs on Mac OS SCR_015644 2026-02-14 02:04:43 9406
DynaMine
 
Resource Report
Resource Website
10+ mentions
DynaMine (RRID:SCR_014559) software resource, web application An NMR based method for protein folding prediction. Users can enter a UniProt identifier, FASTA sequences, or upload a file containing FASTA sequences and results are returned., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. nmr, protein folding, prediction, fasta, sequence, dynamics PMID:24225580 THIS RESOURCE IS NO LONGER IN SERVICE http://dynamine.ibsquare.be SCR_014559 2026-02-14 02:04:50 39
Kazusa Arabidopsis data opening site
 
Resource Report
Resource Website
1+ mentions
Kazusa Arabidopsis data opening site (RRID:SCR_013511) data or information resource, database This site has been developed by Kazusa DNA Research Institute for the purpose of offering the science community the analyzed sequence data produced by a multi-national Arabidopsis genome sequencing project coordinated by the Arabidopsis Genome Initiatives (AGI). The aim of this service is to enable users to browse the annotated sequence data produced by all the sequencing teams of AGI through an user-friendly graphic display system and search engines. Gene structures proposed on the annotated sequences as well as those predicted by computer programs are presented and each graphic item has a hyperlink to detailed information of the corresponding area. The nucleotide sequence data deposited in GenBank by AGI was downloaded, re-computer-analyzed at Kazusa and parsed results are displayed graphically. annoated, arabidopsis, dna, genome, sequence nif-0000-20958 SCR_013511 KAOS 2026-02-14 02:06:43 6
NBRP Medaka CRISPR target site
 
Resource Report
Resource Website
1+ mentions
NBRP Medaka CRISPR target site (RRID:SCR_018159) production service resource, service resource, analysis service resource Web tool to show micro homology sequences striding over double strand break point created by CRISPR/Cas9 system. Used to search for CRISPR target site with micro-homology sequences. Used to predict deletion pattern. Micro homology sequence, double strand break point, CRISPR/Cas9 system, predict deletion pattern, sequence, mutation, target gene Free, Freely available SCR_018159 2026-02-14 02:06:55 2
CIS-BP
 
Resource Report
Resource Website
100+ mentions
CIS-BP (RRID:SCR_017236) web service, data or information resource, data access protocol, software resource, database Software tool as catalog of inferred sequence binding preferences. Online library of transcription factors and their DNA binding motifs. catalog, inferred, sequence, binding, preference, transcription, factor, DNA, motif, FASEB list Canadian Institutes of Health Research ;
Canadian Institute for Advanced Research Junior Fellows Genetic Networks Program ;
NICHD P01 HD39691;
NIGMS GM082971;
EU Marie Curie International Outgoing Fellowship ;
NSF MCB-1024999;
Howard Hughes Medical Institute ;
Gordon and Betty Moore Foundation ;
Millennium Nucleus for Fungal Integrative and Synthetic Biology ;
Fondo Nacional de Desarrollo Científico y Tecnológico
PMID:25215497 Free, Freely available r3d100013971 https://doi.org/10.17616/R31NJN9V SCR_017236 Catalog of Inferred Sequence Binding Preferences 2026-02-14 02:06:31 104
miRWalk
 
Resource Report
Resource Website
1000+ mentions
miRWalk (RRID:SCR_016509) data or information resource, database Software tool to store the predicted and the experimentally validated microRNA (miRNA)-target interaction pairs. Predictions within the complete sequence of genes of human, mouse, and rat genomes. Integrates a comparative platform of miRNA-binding sites resulting from ten different prediction datasets. microRNA, target, interaction, pair, binding, site, sequence, gene, data, FASEB list is listed by: OMICtools PMID:26226356 Free, Available for download, Freely available SCR_016509 2026-02-14 02:06:47 1180
Xenopus Gene Collection
 
Resource Report
Resource Website
1+ mentions
Xenopus Gene Collection (RRID:SCR_007023) XGC biomaterial supply resource, material resource NIH initiative to support production of cDNA libraries, clones and 5'/3' sequences and to provide set of full-length (open reading frame) sequences and cDNA clones of expressed genes for Xenopus laevis and Xenopus tropicalis. Clones distribution is outsourced to for profit companies. Project concluded in September 2008. Resources generated by XGC are publicly accessible to biomedical research community. All sequences are deposited into GenBank.Corresponding clones are available through IMAGE clone distribution network. With conclusion of XGC project, GenBank records of XGC sequences will be frozen, without further updates. Since knowledge of what constitutes full-length coding region for some of genes and transcripts for which we have XGC clones will likely change in future, users planning to order XGC clones will need to monitor for these changes. Users can make use of genome browsers and gene-specific databases, such as UCSC Genome browser, NCBI's Map Viewer, and Entrez Gene, to view relevant regions of genome (browsers) or gene-related information (Entrez Gene). est sequencing, expressed gene, frog, gene, adult, cdna, genomic, open reading frame, sequencing, stage, tag, xenopus laevis, xenopus tropicalis, sequence, expressed sequence tag, cdna, vector, cdna library, clone, 5'/3' sequence, frozen is listed by: One Mind Biospecimen Bank Listing
is related to: One Mind Biospecimen Bank Listing
is related to: ATCC
is related to: GenBank
is related to: Invitrogen Clones
has parent organization: National Cancer Institute
NIH Blueprint for Neuroscience Research ;
NIH
Free, Freely available nif-0000-00224 https://genecollections.nci.nih.gov/XGC/ SCR_007023 Xenopus Gene Collection 2026-02-14 02:06:40 4
Zebrafish Gene Collection
 
Resource Report
Resource Website
1+ mentions
Zebrafish Gene Collection (RRID:SCR_007054) ZGC biomaterial supply resource, material resource Part of zebrafish genome project. ZGC project to produce cDNA libraries, clones and sequences to provide complete set of full-length (open reading frame) sequences and cDNA clones of expressed genes for zebrafish. All ZGC sequences are deposited in GenBank and clones can be purchased from distributors of IMAGE consortium. With conclusion of ZGC project in September 2008, GenBank records of ZGC sequences will be frozen, without further updates. Since definition of what constitutes full-length coding region for some of genes and transcripts for which we have ZGC clones will likely change in future, users planning to order ZGC clones will need to monitor for these changes. Users can make use of genome browsers and gene-specific databases, such as UCSC Genome browser, NCBI's Map Viewer, and Entrez Gene, to view relevant regions of genome (browsers) or gene-related information (Entrez Gene). cdna library, clone, sequence, full-length open reading frame, cdna clone, frozen, fish, gene, genetic, genome, genomic is listed by: One Mind Biospecimen Bank Listing
is related to: One Mind Biospecimen Bank Listing
is related to: NIDDK Information Network (dkNET)
is related to: Mammalian Gene Collection
is related to: GenBank
is related to: ATCC
has parent organization: National Cancer Institute
NIH Blueprint for Neuroscience Research Free, Freely available nif-0000-00567 https://genecollections.nci.nih.gov/ZGC/ SCR_007054 Zebrafish Gene Collection 2026-02-14 02:07:03 1
EBI Genomes
 
Resource Report
Resource Website
10+ mentions
EBI Genomes (RRID:SCR_002426) data or information resource, data set The EBI genomes pages give access to a large number of complete genomes including bacteria, archaea, viruses, phages, plasmids, viroids and eukaryotes. Methods using whole genome shotgun data are used to gain a large amount of genome coverage for an organism. WGS data for a growing number of organisms are being submitted to DDBJ/EMBL/GenBank. Genome entries have been listed in their appropriate category which may be browsed using the website navigation tool bar on the left. While organelles are all listed in a separate category, any from Eukaryota with chromosome entries are also listed in the Eukaryota page. Within each page, entries are grouped and sorted at the species level with links to the taxonomy page for that species separating each group. Within each species, entries whose source organism has been categorized further are grouped and numbered accordingly. Links are made to: * taxonomy * complete EMBL flatfile * CON files * lists of CON segments * Project * Proteomes pages * FASTA file of Proteins * list of Proteins eukaryote genome, gene, gene browser, genome, archaea genome, bacteria genome, phage genome, plasmid genome, viroid genome, viruse genome, sequence, protein, nucleotide, complete genome, gold standard has parent organization: European Bioinformatics Institute nif-0000-02778 SCR_002426 Genomes Pages - At the EBI, ENA Genomes Server 2026-02-14 02:07:47 26
Fungal Genome Initiative
 
Resource Report
Resource Website
10+ mentions
Fungal Genome Initiative (RRID:SCR_003169) FGI data or information resource, data set Produces and analyzes sequence data from fungal organisms that are important to medicine, agriculture and industry. The FGI is a partnership between the Broad Institute and the wider fungal research community, with the selection of target genomes governed by a steering committee of fungal scientists. Organisms are selected for sequencing as part of a cohesive strategy that considers the value of data from each organism, given their role in basic research, health, agriculture and industry, as well as their value in comparative genomics. sequence, fungi, gene annotation, genome is listed by: 3DVC
has parent organization: Broad Institute
NHGRI ;
NSF ;
NIAID ;
USDA
Free, Freely available nif-0000-30591 SCR_003169 2026-02-14 02:07:29 18
University of Delaware Skate Genome Project
 
Resource Report
Resource Website
1+ mentions
University of Delaware Skate Genome Project (RRID:SCR_005300) Skate Genome Project core facility, access service resource, service resource Core facility provides a model for collaborative approaches to use specialized resources and expertise in an integrated process. Core builds on the expertise and resources provided by the Bioinformatics Cores of the five northeastern states that form NECC. The Skate Genome Annotation Workshops and Jamborees offer training and opportunities for faculty and students to work with and annotate genome sequences. Workshops include lectures, tutorials and exercises annotating the genome of the little skate, Leucoraja erinacea. skate, genome, genomics, bioinformatics, sequencing, annotate, sequence, workshop has parent organization: North East Cyberinfrastructure Consortium
has parent organization: University of Delaware; Delaware; USA
is parent organization of: SkateBase
Available to external user nlx_144349 SCR_005300 , University of Delaware, Genome Project, Skate 2026-02-14 02:07:30 1

Can't find your Tool?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.

Can't find the RRID you're searching for? X
X
  1. RRID Portal Resources

    Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.

  2. Navigation

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