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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
Oufti
 
Resource Report
Resource Website
10+ mentions
Oufti (RRID:SCR_016244) image analysis software, software application, data processing software, software resource Software designed for analysis of microscopy data. It performs sub-pixel precision detection, quantification of cells and fluorescence signals, as well as other image analysis functions. microscopy, data, imaging, image, analysis, pixel, fluorescent, bio.tools is listed by: Debian
is listed by: bio.tools
NIGMS R01 GM065835 PMID:26538279 biotools:oufti https://bio.tools/oufti SCR_016244 outfi 2026-08-06 09:28:49 13
PASTEClassifier
 
Resource Report
Resource Website
10+ mentions
PASTEClassifier (RRID:SCR_017645) PASTEC software application, data processing software, software resource Software tool for automatic transposable element classification. Used for searching for structural features and similarity to classify transposable elements. Automatic, transposable, element, classification, bio.tools, bio.tools is listed by: Debian
is listed by: bio.tools
French National Research Agency PMID:24786468 Free, Available for download, Freely available biotools:PAStEClassifier https://urgi.versailles.inra.fr/download/repet/PASTEClassifier-1.0.tar.gz, https://bio.tools/repet, https://bio.tools/PASTEClassifier SCR_017645 Pseudo Agent System for Transposable Elements Classification, PASTEC 2026-08-06 09:29:10 11
Sniffles
 
Resource Report
Resource Website
50+ mentions
Sniffles (RRID:SCR_017619) software application, data processing software, software resource Software tool as structural variation caller using third generation sequencing (PacBio or Oxford Nanopore). It detects all types of SVs (10bp+) using evidence from split-read alignments, high-mismatch regions, and coverage analysis. Used to avoid single molecule long read sequencing high error rates. Structural, variation, caller, third, generation, sequencing, SV, split, read, alignment, mismatch, region, analysis, error, bio.tools is listed by: bio.tools
is listed by: Debian
NHGRI R01 HG006677;
NHGRI UM1 HG008898
PMID:29713083 Free, Available for download, Freely available biotools:sniffles https://bio.tools/sniffles SCR_017619 2026-08-06 09:29:07 59
MEGAHIT
 
Resource Report
Resource Website
1000+ mentions
MEGAHIT (RRID:SCR_018551) software application, data processing software, software resource Software tool as Next Generation Sequencing assembler. Optimized for metagenomes, but also works well on generic single genome assembly (small or mammalian size) and single cell assembly. Can assemble genome sequences from metagenomic datasets of hundreds of Giga base-pairs in time and memory efficient manner on single server. NGS metagenome, Next Generation Sequencing assembler, metagenome, genome assembly, genome sequence, metagenomic dataset, giga base pairs, bio.tools is listed by: bio.tools
is listed by: Debian
is listed by: OMICtools
Hong Kong GRF ;
Innovation and Technology Fund
PMID:25609793
PMID:27012178
Free, Available for download, Freely available OMICS_07234, biotools:megahit https://bio.tools/megahit, https://sources.debian.org/src/megahit/ SCR_018551 MEGAHIT v0.1 2026-08-06 09:29:27 1451
TGS-GapCloser
 
Resource Report
Resource Website
10+ mentions
TGS-GapCloser (RRID:SCR_017633) software application, data processing software, software resource Software tool that uses long reads to enhance genome assembly. Fast and accurate gap closing software tool that uses low coverage of error-prone long reads generated by third generation sequence techniques (Pacbio, Oxford Nanopore, etc.) or preassembled contigs for large genomes. Error, prone, third, generation, sequencing, long, read, gap, closing, genome, assembly, contig, bio.tools is listed by: Debian
is listed by: bio.tools
Free, Available for download, Freely available biotools:tGS-GapCloser https://bio.tools/TGS-GapCloser SCR_017633 2026-08-06 09:29:10 35
parSMURF
 
Resource Report
Resource Website
1+ mentions
parSMURF (RRID:SCR_017560) software application, data processing software, software resource Open source software package as high performance computing imbalance aware machine learning tool for genome wide detection of pathogenic variants. High, performance, computing, imbalance, aware, machine, learning, genome, wide, detection, pathogenic, variant, bio.tools is listed by: bio.tools
is listed by: Debian
Free, Available for download, Freely available biotools:parsmurf https://bio.tools/parsmurf SCR_017560 2026-08-06 09:29:06 1
EHRtemporalVariability
 
Resource Report
Resource Website
1+ mentions
EHRtemporalVariability (RRID:SCR_018663) software application, data processing software, software resource Software R package for delineating temporal dataset shifts in electronic health records. Functions to delineate temporal dataset shifts in electronic health records through projection and visualization of dissimilarities among data temporal batches.Enables exploration and identification of dataset shifts, contributing to broadly examine and repurpose large, longitudinal datasets. Used to help ensure reliable data reuse to biomedical data users. Delineating temporal data set shift, data set shift, electronic health record, temporal variability, delineate temporal data set shift, data dissimilarities, reliable data reuse, examine data set, biomedical data reuse, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: CRAN
is related to: Shiny
DOI:10.1101/2020.04.07.20056564 Free, Available for download, Freely available biotools:ehrtemporalvariability https://cran.r-project.org/web/packages/EHRtemporalVariability/readme/README.html, https://bio.tools/ehrtemporalvariability SCR_018663 Electronic Health Records temporal variability 2026-08-06 09:29:28 3
rna-stability
 
Resource Report
Resource Website
1+ mentions
rna-stability (RRID:SCR_019259) software application, data processing software, software resource Software tool as parallel processing framework for large scale generation of secondary RNA structures and folding statistics for transcriptome of any species. Secondary RNA structures generation, large scale generation, RNA structures, transcriptome folding statistics, , bio.tools is listed by: bio.tools
is listed by: Debian
Free, Freely available biotools:rna-stability https://bio.tools/rna-stability SCR_019259 2026-08-06 09:29:27 1
mosdepth
 
Resource Report
Resource Website
10+ mentions
mosdepth (RRID:SCR_018929) software application, data processing software, software resource Software command line tool for rapidly calculating genome wide sequencing coverage. Measures depth from BAM or CRAM files at either each nucleotide position in genome or for sets of genomic regions. Used for fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing quick coverage calculation for genomes and exomes. Calculating genome, wide sequencing coverage, depth measurement, BAM file, CRAM file, nucleotide position, genome, genomic region set, WGS exom, targeted sequencing, coverage calculation, exom, bio.tools is listed by: Debian
is listed by: bio.tools
is listed by: OMICtools
NHGRI R01 HG006693;
NHGRI R01 HG009141;
NIGMS R01 GM124355;
NCI U24 CA209999
PMID:29096012 Free, Available for download, Freely available OMICS_20873, biotools:mosdepth https://bio.tools/mosdepth, https://sources.debian.org/src/mosdepth/ SCR_018929 2026-08-06 09:29:24 38
RADAR-base
 
Resource Report
Resource Website
1+ mentions
RADAR-base (RRID:SCR_019233) portal, project portal, data or information resource Open source mobile health platform for collecting, monitoring, and analyzing data using sensors, wearables, and mobile devices. Enables study design and set up, active and passive remote data collection, secure data transmission via Wifi and/or Bluetooth and scalable solutions for data storage, management and access. Allows study participants to share their health data with clinicians and researchers in secure way. Data collection, remote data collection, data collection platform, collecting mHealth datasets, mental health, mobile applications, remote sensing technology, telemedicine, bio.tools is listed by: bio.tools
is listed by: Debian
GSTT Charity ;
Maudsley Charity ;
NIHR Biomedical Research Centre at South London ;
Maudsley NHS Foundation Trust ;
King’s College London ;
EU IMI2 ;
UK National Institute for Health Research
Free, Available for download, Freely available biotools:RADAR-base https://radar-base.org/index.php/getting-started-with-radar-base/, https://radar-base.org/index.php/getting-started-with-radar-base/demo-using-prmt-app/, https://bio.tools/RADAR-base SCR_019233 Remote Assessment of Disease And Relapses, Radar-base 2026-08-06 09:29:32 1
Vienna RNA
 
Resource Report
Resource Website
100+ mentions
Vienna RNA (RRID:SCR_008550) database, data or information resource, software resource This server provides programs, web services, and databases, related to our work on RNA secondary structures. For general information and other offerings from our group see the main TBI web server. With the 1st of May 2009 we updated our servers to the Vienna RNA package version 1.8.2! The Vienna RNA Servers: * RNAfold server predicts minimum free energy structures and base pair probabilities from single RNA or DNA sequences. * RNAalifold server predicts consensus secondary structures from an alignment of several related RNA or DNA sequences. You need to upload an alignment. * RNAinverse server allows you to design RNA sequences for any desired target secondary structure. * RNAcofold server allows you to predict the secondary structure of a dimer. * RNAup server allows you to predict the accessibility of a target region. * LocARNA server generates structural alignments from a set of sequences. In collaboration with the Bioinformatics Group Freiburg. * barriers server allows you to get insights into RNA folding kinetics. * RNAz server will assist you in detecting thermodynamically stable and evolutionarily conserved RNA secondary structures in multiple sequence alignments. * Structure conservation analysis server will assist you in detecting evolutionarily conserved RNA secondary structures in multiple sequence alignments. * RNAstrand server allows you to predict the reading direction of evolutionarily conserved RNA secondary structures. * RNAxs server assists you in siRNA design. * Bcheck predicts rnpB genes Downloads Get the Source code for: * the Vienna RNA Package, our basic RNA secondary structure analysis software. * The ALIDOT package for finding conserved structure motifs (add-on) * The barriers program for analysis of RNA folding landscapes. Databases * Atlas of conserved Viral RNA Structures found by ALIDOT bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
is related to: ANNOgesic
has parent organization: University of Vienna; Vienna; Austria
DOI:10.1186/1748-7188-6-26 biotools:vienna_rna_package, nif-0000-31411, OMICS_09351 https://bio.tools/vienna_rna_package, https://sources.debian.org/src/vienna-rna/ SCR_008550 Vienna RNA 2026-08-06 09:27:10 404
Eukaryote Genes
 
Resource Report
Resource Website
10+ mentions
Eukaryote Genes (RRID:SCR_008617) database, data or information resource Provides summary of gene and genomic information from eukaryotic organism databases. This includes gene symbol and full name, chromosome, genetic and molecular map information, Gene Ontology (Function/Location/Process) and gene homology, product information, links to extended gene information. eukaryote, eukaryotic gene ontology, eukaryotic genome, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: Indiana University; Indiana; USA
Indiana University Center for Genomics and Bioinformatics ;
NSF DBI 0090782;
NSF DBI 9982851
Free, Freely available nif-0000-31969, biotools:eugenes, SCR_013197, nif-0000-02818 https://bio.tools/eugenes SCR_008617 euGenes 2026-08-06 09:27:15 17
GMAP
 
Resource Report
Resource Website
500+ mentions
GMAP (RRID:SCR_008992) GMAP source code, software resource, image analysis software, alignment software, data processing software, software application THIS RESOURCE IS NO LONGER IN SERVICE, documented August 29, 2016. A software program for mapping and aligning cDNA sequences to a genome. The program maps and aligns a single sequence with minimal startup time and memory requirements, and provides fast batch processing of large sequence sets. The program generates accurate gene structures, even in the presence of substantial polymorphisms and sequence errors, without using probabilistic splice site models. Methodology underlying the program includes a minimal sampling strategy for genomic mapping, oligomer chaining for approximate alignment, sandwich DP for splice site detection, and microexon identification with statistical significance testing. mrna, est sequence, expressed sequence tag, sequence, cdna sequence, genome, cdna, bio.tools is used by: deFuse
is listed by: Debian
is listed by: bio.tools
has parent organization: Genentech
PMID:15728110 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_15072, biotools:gmap, nlx_152505 https://bio.tools/gmap, https://sources.debian.org/src/gmap/ SCR_008992 2026-08-06 09:27:15 594
NetOGlyc
 
Resource Report
Resource Website
500+ mentions
NetOGlyc (RRID:SCR_009026) NetOGlyc software resource, service resource, production service resource, data analysis service, software application, analysis service resource Server that produces predictions of mucin-type GalNAc O-glycosylation sites in mammalian proteins. neural network, predict, mucin, galnac, o-glycosylation site, protein, o-glycosylation, glycoprotein, o-glycoproteome, glycosite, proteome, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: CBS Prediction Servers
PMID:23584533 Acknowledgement requested nlx_153864, biotools:netoglyc https://bio.tools/netoglyc SCR_009026 NetOGlyc Server 2026-08-06 09:27:19 601
elastix
 
Resource Report
Resource Website
100+ mentions
elastix (RRID:SCR_009619) elastix software resource, image analysis software, registration software, software toolkit, data processing software, software application THIS RESOURCE IS NO LONGER IN SERVICE. Documented on February 23,2023. Software toolbox for rigid and nonrigid registration of images. elastix is open source software, based on the well-known Insight Segmentation and Registration Toolkit (ITK). The software consists of a collection of algorithms that are commonly used to solve (medical) image registration problems. The modular design of elastix allows the user to quickly configure, test, and compare different registration methods for a specific application. A command-line interface enables automated processing of large numbers of data sets, by means of scripting. A paper describing elastix contains more details: S. Klein, M. Staring, K. Murphy, M.A. Viergever, J.P.W. Pluim, elastix: a toolbox for intensity based medical image registration,; IEEE Transactions on Medical Imaging, vol. 29, no. 1, pp. 196 - 205, January 2010., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. reusable library, analyze, c++, console (text based), domain independent, nifti, nrrd, os independent, philips par/rec, registration, resampling, spatial transformation, bio.tools is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Debian
is listed by: bio.tools
is related to: Insight Segmentation and Registration Toolkit
has parent organization: Utrecht University; Utrecht; Netherlands
PMID:19923044 THIS RESOURCE IS NO LONGER IN SERVICE nlx_155845, biotools:elastix http://www.nitrc.org/projects/elastix, https://bio.tools/elastix, https://sources.debian.org/src/elastix/ SCR_009619 2026-08-06 09:27:21 167
IMGT-ONTOLOGY
 
Resource Report
Resource Website
IMGT-ONTOLOGY (RRID:SCR_010342) IMGT-ONTOLOGY controlled vocabulary, ontology, data or information resource Ontology for immunogenetics and immunoinformatics. Provides semantic specification of terms to be used in immunogenetics and immunoinformatics and manages related knowledge, thus allowing standardization for immunogenetics data from genome, proteome, genetics, two-dimensional (2D) and three-dimensional (3D) structures. Manages the knowledge through diverse facets relying on seven axioms, IDENTIFICATION, CLASSIFICATION, DESCRIPTION, NUMEROTATION, LOCALIZATION, ORIENTATION and OBTENTION. These axioms postulate that any object, any process and any relation can be identified, classified, described, numbered, localized and orientated, and the way it is obtained can be characterized. The axioms constitute the Formal IMGT-ONTOLOGY, also designated as IMGT-Kaleidoscope. As the same axioms can be used to generate concepts for multi-scale level approaches, the Formal IMGT-ONTOLOGY represents a paradigm for system biology ontologies, which need to identify, to classify, to describe, to number, to localize and to orientate objects, processes and relations at the molecule, cell, tissue, organ, organism or population levels. IMGT, the international ImMunoGeneTics information system, has been built on IMGT-ONTOLOGY. The version 1.0.2 of IMGT-ONTOLOGY includes the concepts of IDENTIFICATION and the concepts of CLASSIFICATION. owl, ontology, immunogenetics, immunoinformatics, terms semantic specification, bio.tools is listed by: BioPortal
is listed by: Debian
is listed by: bio.tools
has parent organization: IMGT - the international ImMunoGeneTics information system
Free, Freely available nlx_157436, biotools:IMGt-ONtOLOGY http://www.imgt.org/IMGTindex/ontology.php, https://bio.tools/IMGT-ONTOLOGY SCR_010342 2026-08-06 09:27:32 0
Evex
 
Resource Report
Resource Website
10+ mentions
Evex (RRID:SCR_010509) software resource, text-mining software, data or information resource, software application, database EVEX is a text mining resource built on top of PubMed abstracts and PubMed Central full texts. It contains over 40 million bio-molecular events among more than 76 million automatically extracted gene/protein name mentions. The text mining data further has been enriched with gene normalization results, allowing straightforward integration with external resources. Further, gene families from Ensembl and HomoloGene provide homology-based event generalizations. EVEX presents both direct and indirect associations between genes and proteins, enabling explorative browsing of relevant literature. gene, protein, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: Ghent University; Ghent; Belgium
biotools:evex, nlx_158731 https://bio.tools/evex SCR_010509 2026-08-06 09:27:35 18
miRDB
 
Resource Report
Resource Website
1000+ mentions
miRDB (RRID:SCR_010848) miRDB service resource, production service resource, data analysis service, data or information resource, analysis service resource, database An online database for miRNA target prediction and functional annotations. mirna, target, pathway, bio.tools, FASEB list is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:18426918
PMID:18048393
OMICS_00403, biotools:miRDb https://bio.tools/miRDB SCR_010848 2026-08-06 09:27:40 1862
Glimmer
 
Resource Report
Resource Website
500+ mentions
Glimmer (RRID:SCR_011931) Glimmer software resource, service resource, production service resource, data analysis service, analysis service resource A software system for finding genes in microbial DNA, especially the genomes of bacteria, archaea, and viruses. microbial, gene, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
is related to: Glimmer-MG
is related to: GlimmerHMM
has parent organization: Johns Hopkins University; Maryland; USA
DOI:10.1093/nar/26.2.544 Open unspecified license, OSI certified OMICS_01486, biotools:glimmer https://bio.tools/glimmer, https://sources.debian.org/src/tigr-glimmer/ SCR_011931 Glimmer - Microbial Gene-Finding System 2026-08-06 09:27:48 637
MAFFT
 
Resource Report
Resource Website
10000+ mentions
MAFFT (RRID:SCR_011811) MAFFT software resource, alignment software, image analysis software, software toolkit, data processing software, software application Software package as multiple alignment program for amino acid or nucleotide sequences. Can align up to 500 sequences or maximum file size of 1 MB. First version of MAFFT used algorithm based on progressive alignment, in which sequences were clustered with help of Fast Fourier Transform. Subsequent versions have added other algorithms and modes of operation, including options for faster alignment of large numbers of sequences, higher accuracy alignments, alignment of non-coding RNA sequences, and addition of new sequences to existing alignments. alignment, amino acid, nucleotide, sequence, DNA, sequence alignment, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
EMBL ;
Ministry of Education ;
Culture ;
Sports ;
Science and Technology of Japan
PMID:12136088
PMID:17118958
PMID:16362903
PMID:15661851
PMID:18439255
PMID:23023983
DOI:10.1093/bib/bbn013
biotools:MAFFT, OMICS_00979 https://www.ebi.ac.uk/Tools/msa/mafft/, https://www.genome.jp/tools-bin/mafft, https://myhits.isb-sib.ch/cgi-bin/mafft, https://bio.tools/MAFFT, https://sources.debian.org/src/mafft/ SCR_011811 Multiple Alignment using Fast Fourier Transform, MAFFT version 5, MAFFT version 7 2026-08-06 09:27:50 22450

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