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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
ShortRead
 
Resource Report
Resource Website
100+ mentions
ShortRead (RRID:SCR_006813) ShortRead software resource Software package for input, quality assessment and exploration of high-throughput sequence data. Used for input, quality assurance, and basic manipulation of `short read'' DNA sequences such as those produced by Solexa, 454, and related technologies, including exible import of common short read data formats. high throughput sequence data, short read, DNA sequences, short read data is listed by: OMICtools
is listed by: Debian
is listed by: SoftCite
has parent organization: Bioconductor
PMID:19654119 Free, Available for download, Freely available OMICS_01076 https://sources.debian.org/src/r-bioc-shortread/ SCR_006813 ShortRead - Classes and methods for high-throughput short-read sequencing data. 2026-08-01 12:03:13 225
beadarray
 
Resource Report
Resource Website
100+ mentions
beadarray (RRID:SCR_001314) beadarray software resource Software package to read bead-level data (raw TIFFs and text files) output by BeadScan as well as bead-summary data from BeadStudio. Methods for quality assessment and low-level analysis are provided. microarray, quality control, one channel, preprocessing, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
has parent organization: Bioconductor
PMID:17586828 GNU General Public License, v2 OMICS_02021, biotools:beadarray https://bio.tools/beadarray SCR_001314 beadarray - Quality assessment and low-level analysis for Illumina BeadArray data 2026-08-01 12:01:38 119
ProteinProphet
 
Resource Report
Resource Website
10+ mentions
ProteinProphet (RRID:SCR_000286) software resource Software that automatically validates protein identifications made on the basis of peptides assigned to MS/MS spectra by database search programs such as SEQUEST. standalone software, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
has parent organization: SourceForge
PMID:14632076 OMICS_02521, biotools:proteinprophet https://bio.tools/proteinprophet SCR_000286 2026-08-01 12:01:10 10
GraphPad
 
Resource Report
Resource Website
1000+ mentions
GraphPad (RRID:SCR_000306) commercial organization A commercial graphing software company that offers scientific software for statistical analyses, curve fitting and data analysis. It offers four programs: Prism, InStat, StatMate and QuickCalcs. company, data, graph, scientific, statistical, analysis, curve, fitting is listed by: SoftCite
is parent organization of: GraphPad Prism
Restricted nlx_156835 SCR_000306 2026-08-01 12:01:14 1284
RStudio
 
Resource Report
Resource Website
1000+ mentions
RStudio (RRID:SCR_000432) RStudio software resource Open source and enterprise ready professional software for R statistical computing environment. Integrated development environment for R. Includes console, syntax highlighting editor that supports direct code execution, as well as tools for plotting, history, debugging and workspace management. Available in open source and commercial editions and runs on desktop Windows, Mac, and Linux or in browser connected to RStudio Server or RStudio Server Pro (Debian/Ubuntu, RedHat/CentOS, and SUSE Linux). R, statistical, computing, environment is used by: PlotsOfData
is listed by: Debian
is listed by: SoftCite
is related to: rSPRITE
is related to: shinyCircoss
is parent organization of: Shiny
is required by: circlncRNAnet
Restricted SciRes_000113 https://sources.debian.org/src/rstudio/, https://posit.co/download/rstudio-desktop/ http://www.rstudio.com/ SCR_000432 2026-08-01 12:01:13 1034
FACS
 
Resource Report
Resource Website
1+ mentions
FACS (RRID:SCR_000055) FACS software resource Software for classification of Sequences using Bloom filters that can accurately and rapidly align sequences to a reference sequence. unix/linux, sequence, bio.tools is listed by: OMICtools
is listed by: GitHub
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
has parent organization: SciLifeLab
PMID:20472541 Free, Available for download, Freely available OMICS_02147, biotools:facs https://bio.tools/facs SCR_000055 Fast and Accurate Classification of Sequences 2026-08-01 12:01:08 5
GOLD
 
Resource Report
Resource Website
10+ mentions
GOLD (RRID:SCR_000188) GOLD software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. A software for virtual screening and identifying the binding mode of active molecules. It is comprehensively validated, widely used, and allows for high database enrichments. The software utilizes a novel methodology which avoids computationally expensive sequential docking of ligands into multiple protein structures. virtual screening, binding, active molecules, ligand-protein bonding, computation, protein structures, lead optimization is listed by: OMICtools
is listed by: SoftCite
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01602 SCR_000188 2026-08-01 12:01:12 18
ClueGO
 
Resource Report
Resource Website
1000+ mentions
ClueGO (RRID:SCR_005748) ClueGO software resource A Cytoscape plug-in that visualizes the non-redundant biological terms for large clusters of genes in a functionally grouped network. It can be used in combination with GOlorize. The identifiers can be uploaded from a text file or interactively from a network of Cytoscape. The type of identifiers supported can be easily extended by the user. ClueGO performs single cluster analysis and comparison of clusters. From the ontology sources used, the terms are selected by different filter criteria. The related terms which share similar associated genes can be combined to reduce redundancy. The ClueGO network is created with kappa statistics and reflects the relationships between the terms based on the similarity of their associated genes. On the network, the node colour can be switched between functional groups and clusters distribution. ClueGO charts are underlying the specificity and the common aspects of the biological role. The significance of the terms and groups is automatically calculated. ClueGO is easy updatable with the newest files from Gene Ontology and KEGG. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible, THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. statistical analysis, function, gene ontology, pathway, annotation, network, plugin, gene is listed by: Gene Ontology Tools
is listed by: SoftCite
is related to: Gene Ontology
is related to: Cytoscape
is related to: KEGG
is related to: BioCarta Pathways
has parent organization: National Institute of Health and Medical Research; Rennes; France
National Institute of Health and Medical Research; Rennes; France ;
Ville de Paris ;
INCa ;
Austrian Ministry for Science and Research ;
BINII ;
European Union 7FP 202230
PMID:19237447 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149209 SCR_005748 2026-08-01 12:02:58 2943
Jalview
 
Resource Report
Resource Website
1000+ mentions
Jalview (RRID:SCR_006459) Jalview software resource A free program for multiple sequence alignment editing, visualisation and analysis that is available in two forms: a lightweight Java applet for use in web applications, and a powerful desktop application that employs web services for sequence alignment, secondary structure prediction and the retrieval of alignments, sequences, annotation and structures from public databases and any DAS 1.53 compliant sequence or annotation server. Use it to view and edit sequence alignments, analyse them with phylogenetic trees and principal components analysis (PCA) plots and explore molecular structures and annotation. Jalview has built in DNA, RNA and protein sequence and structure visualisation and analysis capabilities. It uses Jmol to view 3D structures, and VARNA to display RNA secondary structure. edit, analysis, annotation, multiple sequence alignment, wysiwyg, bio.tools, FASEB list is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
has parent organization: University of Dundee; Scotland; United Kingdom
BBSRC BBSB16542 PMID:19151095
DOI:10.1093/bioinformatics/btp033
GNU General Public License, v3, Acknowledgement requested OMICS_00885, biotools:Jalview https://bio.tools/Jalview, https://sources.debian.org/src/jalview/ SCR_006459 2026-08-01 12:03:10 3769
BEDTools
 
Resource Report
Resource Website
10000+ mentions
BEDTools (RRID:SCR_006646) BEDTools software resource A powerful toolset for genome arithmetic allowing one to address common genomics tasks such as finding feature overlaps and computing coverage. Bedtools allows one to intersect, merge, count, complement, and shuffle genomic intervals from multiple files in widely-used genomic file formats such as BAM, BED, GFF/GTF, VCF. While each individual tool is designed to do a relatively simple task (e.g., intersect two interval files), quite sophisticated analyses can be conducted by combining multiple bedtools operations on the UNIX command line. genomics, bed, sam, bam, overlap, sequencing, intersect, coverage, gff, vcf, bedgraph, interval, genome arithmetic, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
is related to: Hydra
is related to: pybedtools
is required by: SL-quant
PMID:20110278
DOI:10.1093/bioinformatics/btq033
GNU General Public License, v2, Acknowledgement requested OMICS_01159, biotools:bedtools https://code.google.com/p/bedtools/, https://bio.tools/bedtools, https://sources.debian.org/src/bedtools/ SCR_006646 bedtools - a swiss army knife for genome arithmetic, bedtools: a flexible suite of utilities for comparing genomic features 2026-08-01 12:03:11 10394
ANALYZE
 
Resource Report
Resource Website
1000+ mentions
ANALYZE (RRID:SCR_009120) ANALYZE software resource, software application A set of useful accessory programs to the LINKAGE package. It simplifies the performance of a large array of parametric and nonparametric tests for linkage and association on data entered in LINKAGE format pedigree and parameter files. (entry from Genetic Analysis Software) gene, genetic, genomic, pascal, unix, sunos, solaris, osf1 is listed by: Genetic Analysis Software
is listed by: SoftCite
nlx_154223 SCR_009120 2026-08-01 12:10:54 1102
QUANTO
 
Resource Report
Resource Website
500+ mentions
QUANTO (RRID:SCR_009084) QUANTO software resource, software application Software program that computes sample size or power for association studies of genes, environmental factors, gene-environment interaction, or gene-gene interaction. Available study designs for a disease (binary) outcome include the unmatched case-control, matched case-control, case-sibling, case-parent, and case-only designs. Study designs for a quantitative tra it include independent individuals and case parent designs. Quanto is a 32-bit Windows application requiring Windows 95, 98, NT, 2000, ME or XP to run. The graphical user interface allows th e user to easily change the model and view the results without having to edit an input file and rerun the program for every model. The results of a session are stored to a log file. This log can be printed or saved to a file for reviewing at a later date. An option is included to create a text file of the log that can be imported into other documents. (entry from Genetic Analysis Software) gene, genetic, genomic, c++, ms-windows, (98/nt/2000/..) is listed by: Genetic Analysis Software
is listed by: SoftCite
nlx_154095 SCR_009084 2026-08-01 12:10:43 915
IMPUTE
 
Resource Report
Resource Website
500+ mentions
IMPUTE (RRID:SCR_009245) IMPUTE software resource, software application Software application for estimating (imputing) unobserved genotypes in SNP association studies. The program is designed to work seamlessly with the output of the genotype calling program CHIAMO and the population genetic simulator HAPGEN, and it produces output that can be analyzed using the program SNPTEST. (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software
is listed by: SoftCite
nlx_154411 SCR_009245 2026-08-01 12:10:58 628
SAGE
 
Resource Report
Resource Website
1000+ mentions
SAGE (RRID:SCR_009302) SAGE software resource, software application Software application that provides researchers with the tools necessary for various types of statistical genetic analysis of human family data. (entry from Genetic Analysis Software) gene, genetic, genomic, c, version 4.0 will be in c++, unix, (dec unix/solaris), ms-windows, (95/nt), linux is listed by: Genetic Analysis Software
is listed by: SoftCite
nlx_154606 SCR_009302 Statistical Analysis for Genetic Epidemiology 2026-08-01 12:10:57 1029
E-Prime
 
Resource Report
Resource Website
100+ mentions
E-Prime (RRID:SCR_009567) E-Prime software resource, software application A suite of applications to fulfill all of your computerized experiment needs. Used by more than 15,000 professionals in the research community, E-Prime provides a truly easy-to-use environment for computerized experiment design, data collection, and analysis. E-Prime provides millisecond precision timing to ensure the accuracy of your data. E-Prime's flexibility to create simple to complex experiments is ideal for both novice and advanced users. The E-Prime suite of applications includes: * E-Studio ? Drag and drop graphical interface for experiment design * E-Basic ? Underlying scripting language of E-Prime * E-Run ? Once the experiment is generated with a single click, E-Run affords you the millisecond precision of stimulus presentation, synchronizations, and data collection. * E-Merge ? Merges your single session data files for group analysis * E-DataAid ? Data management utility * E-Recovery ? Recovers data files experimental control, microsoft, magnetic resonance, visual basic, win32 (ms windows), windows, windows vista, windows xp is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: SoftCite
nlx_155747 http://www.nitrc.org/projects/eprime SCR_009567 E-Prime 2.0 2026-08-01 12:11:01 162
TAGGER
 
Resource Report
Resource Website
50+ mentions
TAGGER (RRID:SCR_009419) software resource, software application Software application (entry from Genetic Analysis Software) gene, genetic, genomic, web-based is listed by: Genetic Analysis Software
is listed by: SoftCite
nlx_154669 SCR_009419 2026-08-01 12:10:59 91
ANNOVAR
 
Resource Report
Resource Website
5000+ mentions
ANNOVAR (RRID:SCR_012821) ANNOVAR software resource, software application An efficient software tool to utilize update-to-date information to functionally annotate genetic variants detected from diverse genomes (including human genome hg18, hg19, as well as mouse, worm, fly, yeast and many others). Given a list of variants with chromosome, start position, end position, reference nucleotide and observed nucleotides, ANNOVAR can perform: 1. gene-based annotation. 2. region-based annotation. 3. filter-based annotation. 4. other functionalities. (entry from Genetic Analysis Software) genomic analysis, imaging genomics, next generation sequencing, snp, gene, bio.tools is listed by: OMICtools
is listed by: Genetic Analysis Software
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
is related to: wANNOVAR
has parent organization: OpenBioinformatics.org
PMID:20601685 Free nlx_154225, biotools:annovar, OMICS_00165 https://bio.tools/annovar, https://bio.tools/annovar SCR_012821 functional ANNOtation of genetic VARiants, ANNOVAR: Functional annotation of genetic variants 2026-08-01 12:11:02 5946
LigandScout
 
Resource Report
Resource Website
100+ mentions
LigandScout (RRID:SCR_014889) software resource, software application Software that takes a macromolecular structure containing a bound ligand and identifies the key features on the ligand which are interacting with points on a protein. Its features include: automatic interpretation of PDB ligands using geometry, dictionaries and rule; advanced handling of co-factors, ions, water molecules and covalently bound ligands; pharmacophore export to Catalyst(tm), MOE(tm) and PHASE(tm) for virtual screening; and the ability to treat co-factors and water molecules as part of the ligand or part of the macromolecule. pharmacophore, macromolecular structure, bound ligand, pdb ligand, virtual screening, ligad based pharmacore design is listed by: SoftCite Available for purchase https://www.chemistryworld.com/ligandscout/1012019.article SCR_014889 2026-08-01 12:10:57 395
SPARTAN
 
Resource Report
Resource Website
500+ mentions
SPARTAN (RRID:SCR_014901) software resource, software application Software program for determining molecular structure and calculating chemical properties. It has a graphical interface and accurate computational models that are compatible with the iPad, iPhone and iPod Touch. When combined with the Spartan'16 Parallel Suite, this enables the first fully-functional open-ended molecular modeling environment on popular mobile technology. molecular structure, chemical properties, modeling, mobile technology, integration is listed by: SoftCite Commercial SCR_014901 2026-08-01 12:11:06 534
SQLite
 
Resource Report
Resource Website
50+ mentions
SQLite (RRID:SCR_017672) software resource, software application Relational database management system contained in C library. SQLite is not client server database engine but it is embedded into the end program. Database, management, system, C library, engine, embedded, the end program is listed by: SoftCite Free, Freely available SCR_017672 2026-08-01 12:11:08 65

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