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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.

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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
PSMC
 
Resource Report
Resource Website
10+ mentions
PSMC (RRID:SCR_017229) data analysis software, data processing software, software application, software resource Software package for implementation of Pairwise Sequentially Markovian Coalescent model. Infers population size history from diploid sequence. pairwise, sequentially, Markovian, coalescent, model, infer, population, size, history, diploid, sequence Free, Available for download, Freely available SCR_017229 Pairwise Sequentially Markovian Coalescent 2026-09-03 04:54:23 17
prank
 
Resource Report
Resource Website
100+ mentions
prank (RRID:SCR_017228) alignment software, data processing software, image analysis software, software application, software resource, software toolkit Software application as probabilistic multiple alignment program for DNA, codon and amino-acid sequences. Allows for defining potential structure for sequences to be aligned and then, simultaneously with the alignment, predicts the locations of structural units in the sequences. multiple, nucleotide, sequence, alignment, DNA, codon, amino acid, phylogenetic, gap, predict, location, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: University of Helsinki; Helsinki; Finland
PMID:24170401
PMID:21110866
Free, Available for download, Freely available biotools:prank, SCR_024174, OMICS_12425 https://www.ebi.ac.uk/goldman-srv/webprank/, https://ariloytynoja.github.io/prank-msa/, https://bio.tools/prank https://omictools.com/prank-tool SCR_017228 PRANK 2026-09-03 04:54:19 281
matemaker
 
Resource Report
Resource Website
1+ mentions
matemaker (RRID:SCR_017199) data analysis software, data processing software, sequence analysis software, software application, software resource, standalone software Software tool to make artificial mate pairs from long sequences for scaffolding. artificial, mate, pair, long, sequence, scaffolding, genomics, genome, assembly Free, Available for download, Freely available SCR_017199 matemaker v1.0.0 2026-09-03 04:54:21 4
Open Ephys: Pulse Pal
 
Resource Report
Resource Website
1+ mentions
Open Ephys: Pulse Pal (RRID:SCR_017203) instrument resource Open source pulse train generator that allows users to create and trigger software defined trains of voltage pulses with high temporal precision. Generates precisely timed pulse sequences for use in research involving electrophysiology or psychophysics. instrument, generator, stimulation, voltage, puls, sequence, electrophysiology, psychophysics McKnight Foundation ;
NIMH R01 MH097061;
NINDS R01 NS07553
DOI:10.3389/fneng.2014.00043 Available for purchase https://sanworks.io/shop/viewproduct?productID=1102, https://github.com/sanworks/PulsePal, https://sites.google.com/site/pulsepalwiki/specifications?authuser=0 SCR_017203 Pulse Pal v2 2026-09-03 04:54:21 2
GraphClust2
 
Resource Report
Resource Website
1+ mentions
GraphClust2 (RRID:SCR_017286) data analysis software, data processing software, software application, software resource, web application Software tool for scalable clustering of RNAs based on sequence and secondary structures similarities. Implemented within Galaxy framework. Used for studying RNA function. scalable, clustering, RNA, sequence, secondary, structure, function, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: University of Freiburg; Baden-Wurttemberg; Germany
German Federal Ministry of Education and Research ;
German Research Foundation Collaborative Research Centre 992 Medical Epigenetics
PMID:31808801
PMID:22689765
Free, Available for download, Freely available biotools:GraphClust2 https://bio.tools/GraphClust2 SCR_017286 GraphClust, GraphClust-2 2026-09-03 04:54:27 4
PILER
 
Resource Report
Resource Website
10+ mentions
PILER (RRID:SCR_017333) data analysis software, data processing software, software application, software resource Software tool for analyzing repetitive DNA found in genome sequences. Software package for identification and classification of genomic repeats. Used for identifying patterns of local alignments induced by certain classes of repeats. analysis, repetitive, DNA, genome, sequence, classification, alignment is listed by: OMICtools PMID:15961452 Free, Available for download, Freely available https://omictools.com/piler-tool SCR_017333 2026-09-03 04:54:32 15
Webcutter
 
Resource Report
Resource Website
10+ mentions
Webcutter (RRID:SCR_017638) analysis service resource, data access protocol, data analysis service, data analysis software, data processing software, production service resource, sequence analysis software, service resource, software application, software resource, web service Software tool to find restriction endonucleases. Helps restriction map nucleotide sequences. Tool with customizable interface, platform independent accessibility, interfaces to NCBI's GenBank, DNA sequence database, and NEB's REBase, and restriction enzyme database. In addition to restriction site mapping, Webcutter 2 also performs degenerate digests, including option of finding restriction sites that can be introduced into sequence by silent mutagenesis. Find, restriction, site, endonuclease, map, nucleotide, DNA, sequence, degenarte, digest, silent, mutagenesis has parent organization: Yale University; Connecticut; USA
works with: GenBank
works with: REBASE
Free, Freely available SCR_017638 Webcutter 2.0, Webcutter 2 2026-09-03 04:54:36 15
refgenie
 
Resource Report
Resource Website
1+ mentions
refgenie (RRID:SCR_017574) data management software, service resource, software application, software resource Software tool to organize, retrieve, and share genome analysis resources. Reference genome assembly asset manager. In addition to genome indexes, can manage any files related to reference genomes, including sequences and annotation files. Includes command line interface and server application that provides RESTful API, so it is useful for both tool development and analysis. Organize, retrive, share, genome, analysis, reference, assembly, asset, manager, sequence, annotation, file, command, line, interface, bio.tools is listed by: Debian
is listed by: bio.tools
DOI:10.1101/698704 Free, Available for download, Freely available biotools:Refgenie https://bio.tools/Refgenie SCR_017574 reference genome manager 2026-09-03 04:54:38 7
SignalP
 
Resource Report
Resource Website
10000+ 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 2026-09-03 04:58:49 10033
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 2026-09-03 04:59:03 44
SPM
 
Resource Report
Resource Website
5000+ mentions
Issue
SPM (RRID:SCR_007037) SPM data analysis software, data processing software, image analysis software, software application, software resource Software package for analysis of brain imaging data sequences. Sequences can be a series of images from different cohorts, or time-series from same subject. Current release is designed for analysis of fMRI, PET, SPECT, EEG and MEG. analysis, brain, imaging, data, sequence, fMRI, PET, SPECT, EEG, MEG, bio.tools uses: Neuroimaging Data Model
uses: imcalc: SPM batch image calculator
is used by: rsfMRI_fconn calculation
is used by: Automatic Analysis
is used by: auto_acpc_reorient
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: 3DVC
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
is affiliated with: Clinical Toolbox for SPM
is affiliated with: Statistical non-Parametric Mapping
is related to: WFU Biological Parametric Mapping Toolbox
is related to: vis: SPM Visualized Statistics toolbox
is related to: LEAD-DBS
is related to: CCHMC Pediatric Brain Templates
is related to: IBMA toolbox
is related to: ArtRepair for robust fMRI
is related to: ASL data processing tool box
is related to: BrainVISA / Anatomist
is related to: MRIcro Software
is related to: xjView: A Viewing Program For SPM
is related to: BrainMagix SPM Viewer
is related to: MarsBaR region of interest toolbox for SPM
is related to: NIRS-SPM
is related to: SPM SS - fMRI functional localizers
is related to: Wisconsin White Matter Hyperintensities Segmentation Toolbox
is related to: Dementia-specific FDG PET Template for SPM analyses
is related to: SPM Anatomy Toolbox
is related to: MIPAV: Medical Image Processing and Visualization
is related to: MATLAB
is related to: hMRI-toolbox
is related to: Sandwich Estimator Toolbox
has parent organization: University College London; London; United Kingdom
is required by: MRTool
provides: TSDiffAna
has plug in: ICN_Atlas
works with: UManitoba - JHU Functionally Defined Human White Matter Atlas
works with: NIAG Addiction Data
works with: ICN_Atlas
works with: spm_auto_reorient_coregister
works with: Computational Anatomy Toolbox for SPM
works with: FieldTrip
works with: POAS4SPM
Free, Available for download, Freely available biotools:SPM https://github.com/spm/spm12, https://bio.tools/SPM https://www.fil.ion.ucl.ac.uk/spm/ SCR_007037 Statistical Parametric Mapping, SPM5, SPM2, SPM12, Statistical Parametric Mapping Software, SPM99, SPM8, SPM, SPM96 2026-09-03 04:58:06 8748
Marvel
 
Resource Report
Resource Website
1+ mentions
Marvel (RRID:SCR_017621) alignment software, data processing software, image analysis software, software application, software resource, software toolkit Software set of tools that facilitate overlapping, patching, correction and assembly of noisy long reads. Overlapping, patching, correction, assembly, noisy, long, read, sequence, align Free, Available for download, Freely available SCR_017621 2026-09-03 04:58:28 2
OrthoFinder
 
Resource Report
Resource Website
1000+ mentions
OrthoFinder (RRID:SCR_017118) data analysis software, data processing software, software application, software resource Software Python application for comparative genomics analysis. Finds orthogroups and orthologs, infers rooted gene trees for all orthogroups and identifies all of gene duplcation events in those gene trees, infers rooted species tree for species being analysed and maps gene duplication events from gene trees to branches in species tree, improves orthogroup inference accuracy. Runs set of protein sequence files, one per species, in FASTA format. comparative, genomic, analysis, find, orthogroup, ortholog, infer, gene, tree, duplicate, accuracy, protein, sequence, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
Bill and Melinda Gates Foundation ;
UKAID
PMID:26243257
DOI:10.1101/466201
Free, Available for download, Freely available biotools:OrthoFinder, OMICS_09733, BioTools:OrthoFinder https://bio.tools/OrthoFinder, https://bio.tools/OrthoFinder, https://bio.tools/OrthoFinder SCR_017118 OrthoFinder2, OrthoFinder 2026-09-03 04:58:26 3413
PASC
 
Resource Report
Resource Website
1+ mentions
PASC (RRID:SCR_016642) PASC analysis service resource, data access protocol, data or information resource, database, production service resource, service resource, software resource, web service Web tool for analysis of pairwise identity distribution within viral families. Used for virus sequence-based classification. Data in the system are updated every day to reflect changes in virus taxonomy and additions of new virus sequences to the public database. analysis, pairwise, identity, distribution, viral, family, sequence, classification, data, taxonomy has parent organization: NCBI National Library of Medicine PMID:25119676 Free, Public SCR_016642 PAirwise Sequence Comparison 2026-09-03 04:58:27 6
IMGT HighV-QUEST
 
Resource Report
Resource Website
10+ mentions
IMGT HighV-QUEST (RRID:SCR_018196) alignment software, analysis service resource, data or information resource, data processing software, image analysis software, portal, production service resource, service resource, software application, software resource Next generation B and T cell sequence alignment and characterization online surface by IMGT. Web portal for immunoglobulin (IG) or antibody and T cell receptor (TR) analysis from NGS high throughput and deep sequencing. Next generation sequencing, B cell, T cell, sequence alignment, immunoglobulin, antibody, T cell receptor, analysis, sequence, bio.tools is listed by: bio.tools
is listed by: Debian
CNRS ;
GENCI ;
MESR ;
NHMRC ;
Université Montpellier 2 ;
France
PMID:22647994
PMID:23995877
PMID:22665256
Restricted biotools:IMGt_HighV-QUESt https://bio.tools/IMGT_HighV-QUEST SCR_018196 IMGT/HighV QUEST, IMGT/HighV-QUEST, IMGT web portal 2026-09-03 04:58:34 15
Residual Variation Intolerance Score (RVIS)
 
Resource Report
Resource Website
1+ mentions
Residual Variation Intolerance Score (RVIS) (RRID:SCR_013850) RVIS data or information resource, narrative resource, standard specification A gene-based score intended to help in the interpretation of human sequence data. The score is designed to rank genes in terms of whether they have more or less common functional genetic variation relative to the genome wide expectation given the amount of apparently neutral variation the gene has. A gene with a positive score has more common functional variation, and a gene with a negative score has less and is referred to as intolerant. gene, score, sequence, interpretation, rank, functional genetic variation is listed by: Columbia University; New York; USA NIH Epi4K Sequencing ;
Bioinformatics and Biostatistics Core U01NS077303
DOI:10.1371/journal.pgen.1003709 SCR_013850 Residual Variation Intolerance Score 2026-09-03 04:52:50 8
University of Delaware Skate Genome Project
 
Resource Report
Resource Website
1+ mentions
University of Delaware Skate Genome Project (RRID:SCR_005300) Skate Genome Project access service resource, core facility, 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 2026-09-03 05:05:55 1
SpliceDB
 
Resource Report
Resource Website
1+ mentions
SpliceDB (RRID:SCR_006262) SpliceDB data or information resource, data set Database of canonical and non-canonical mammalian splice sites. The information about verified splice site sequences for canonical and non-canonical sites is presented with the supporting evidence. Weight matrices were built for the major splice groups, which can be incorporated into gene prediction programs. gene, expressed sequence tag, splice, canonical, non-canonical, splice site, sequence, data set, splice site sequence is listed by: OMICtools
is listed by: 3DVC
is related to: GenBank
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
PMID:11125105
PMID:11058137
nlx_151853, OMICS_01892 http://linux1.softberry.com/berry.phtml?topic=splicedb http://genomic.sanger.ac.uk/spldb/SpliceDB.htm SCR_006262 SpliceDB: canonical and non-canonical splice site sequences in mammalian genes 2026-09-03 05:06:08 2
Fungi Sequencing Projects
 
Resource Report
Resource Website
1+ mentions
Fungi Sequencing Projects (RRID:SCR_008524) data or information resource, data set Fungal genomes available from the Sanger Institute. Data are accessible in a number of ways; for each organism there is a BLAST server, allowing search of the sequences. Sequences can also be down-loaded directly by FTP. In addition, for those organisms being sequenced using a cosmid approach, finished and annotated cosmids are submitted to EMBL and other public databases. genome, genomics, sequence, fungus, blast, data analysis service has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom nif-0000-30593 SCR_008524 Fungi Sequencing 2026-09-03 05:06:23 6
Yeast Resource Center
 
Resource Report
Resource Website
1+ mentions
Yeast Resource Center (RRID:SCR_007942) YRC biomedical technology research center, training resource Biomedical technology research center that (1) exploits the budding yeast Saccharomyces cerevisiae to develop novel technologies for investigating and characterizing protein function and protein structure (2) facilitates research and extension of new technologies through collaboration, and (3) actively disseminates data and technology to the research community. Through collaboration, the YRC freely provides resources and expertise in six core technology areas: Protein Tandem Mass Spectrometry, Protein Sequence-Function Relationships, Quantitative Phenotyping, Protein Structure Prediction and Design, Fluorescence Microscopy, Computational Biology. systems biology technology center, protein function, protein structure, mass spectrometry, protein, structure prediction, fluorescence microscopy, computational biology, sequence, function, phenotyping has parent organization: University of Washington; Seattle; USA NCRR ;
NIGMS P41 GM103533
nif-0000-03650 SCR_007942 YRC 2026-09-03 05:06:31 6

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