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

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:bio.tools (facet)

Facets


Recent searches

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

1,647 Results - per page

Show More Columns | Download Top 1000 Results

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
QmRLFS-finder
 
Resource Report
Resource Website
10+ mentions
QmRLFS-finder (RRID:SCR_014584) software application, data analytics software, software resource A software which predicts R-loop Forming Sequences (RLFSs) in nucleic acid sequences based on the experimentally supported structural models of RLFSs. The tool identifies and visualizes RLFS coordinates from natural or artificial DNA or RNA input sequences and creates standard-compliant output files for later annotation and analysis. r-loop, r loop, rlf, rlfs, dna, rna, input sequences, output files, annotation, analysis, bio.tools uses: UCSC Genome Browser
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
Singapore Agency for Science Technology and Research PMID:26400173
PMID:25883153
Open Source biotools:qmrlfs-finder https://omictools.com/qmrlfs-finder-tool, https://bio.tools/qmrlfs-finder SCR_014584 QmRLFS finder 2026-08-06 09:28:23 13
FunRich: Functional Enrichment analysis tool
 
Resource Report
Resource Website
100+ mentions
FunRich: Functional Enrichment analysis tool (RRID:SCR_014467) standalone software, software application, data analytics software, software resource A software tool used for functional enrichment and interaction network analysis of genes and proteins. Users can search against a default background database or load customized database. The results can be depicted as venn, bar, column, pie and doughnut charts. network analysis, background database, charts, data analytics software, standalone software, bio.tools, FASEB list is listed by: bio.tools
is listed by: Debian
PMID:25921073
PMID:26149235
Public, Open Source biotools:funrich https://bio.tools/funrich SCR_014467 2026-08-06 09:28:21 338
CIBERSORT
 
Resource Report
Resource Website
1000+ mentions
CIBERSORT (RRID:SCR_016955) software application, data analytics software, software resource Software tool to provide an estimation of the abundances of member cell types in a mixed cell population, using gene expression data. Used for characterizing cell composition of complex tissues from their gene expression profiles, large scale analysis of RNA mixtures for cellular biomarkers and therapeutic targets. estimation, abundance, cell, type, mixed, population, gene, expression, data, tissue, complex, analysis, RNA, biomarker, therapeutic, target, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: Stanford University; Stanford; California
Doris Duke Charitable Foundation ;
Damon Runyon Cancer Research Foundation ;
B&J Cardan Oncology Research Fund ;
Ludwig Institute for Cancer Research ;
NCI U01 CA154969;
NIAID U19 AI090019;
NCI T32 CA09302;
US Department of Defense ;
Siebel Stem Cell Institute ;
Thomas and Stacey Siebel Foundation
PMID:25822800 Not freely available for download or distribution, Available for non commercial users, Registration required biotools:CIbERSORt https://bio.tools/CIBERSORT SCR_016955 2026-08-06 09:28:59 1239
Myriads
 
Resource Report
Resource Website
1+ mentions
Myriads (RRID:SCR_017447) software application, data analytics software, software resource Software package for p value based multiple testing that also implements dependence test and p-value simulation. P value, multiple, testing, simulation, BRAIN Initiative, bio.tools is recommended by: BRAIN Initiative
is listed by: bio.tools
is listed by: Debian
NIMH MH111416 PMID:29186285 biotools:myriads https://bio.tools/myriads SCR_017447 SGoF+ 2026-08-06 09:29:04 1
PyRosetta
 
Resource Report
Resource Website
10+ mentions
PyRosetta (RRID:SCR_018541) standalone software, software application, software resource Interactive Python based interface to Rosetta molecular modeling suite. Stand alone Python based implementation of Rosetta molecular modeling package that allows users to write custom structure prediction and design algorithms using major Rosetta sampling and scoring functions. Molecular modeling, custom structure prediction, design algorithm, energy function, scoring function, bio.tools uses: Python Programming Language
is listed by: bio.tools
is listed by: Debian
is related to: Rosetta
has parent organization: Johns Hopkins University; Maryland; USA
NIGMS R01 GM73151;
NIGMS R01 GM078221;
NSF 0846324
PMID:20061306 Free, Freely available biotools:pyrosetta https://bio.tools/pyrosetta SCR_018541 Python Rosetta 2026-08-06 09:29:20 20
Segway - a way to segment the genome
 
Resource Report
Resource Website
1+ mentions
Segway - a way to segment the genome (RRID:SCR_004206) source code, software resource The free Segway software package contains a novel method for analyzing multiple tracks of functional genomics data. The method uses a dynamic Bayesian network (DBN) model, which enables it to analyze the entire genome at 1-bp resolution even in the face of heterogeneous patterns of missing data. This method is the first application of DBN techniques to genome-scale data and the first genomic segmentation method designed for use with the maximum resolution data available from ChIP-seq experiments without downsampling. Segway uses the Graphical Models Toolkit (GMTK) for efficient DBN inference. The software has extensive documentation and was designed from the outset with external users in mind. genome annotation, source code, bayesian network model, bayesian, chip seq, dbn, bio.tools is used by: ENCODE
is listed by: Debian
is listed by: bio.tools
has parent organization: University of Washington; Seattle; USA
has parent organization: University of Toronto; Ontario; Canada
PMID:22426492 Free nlx_22911, biotools:segway https://www.pmgenomics.ca/hoffmanlab/proj/segway/, https://bitbucket.org/hoffmanlab/segway/, https://bio.tools/segway http://noble.gs.washington.edu/proj/segway/ SCR_004206 Segway 2026-08-06 09:26:03 8
Biopieces
 
Resource Report
Resource Website
10+ mentions
Biopieces (RRID:SCR_005783) Biopieces source code, software toolkit, software resource A collection of bioinformatics tools that can be pieced together in a very easy and flexible manner to perform both simple and complex tasks. The Biopieces work on a data stream in such a way that the data stream can be passed through several different Biopieces, each performing one specific task: modifying or adding records to the data stream, creating plots, or uploading data to databases and web services. The Biopieces are executed in a command line environment where the data stream is initialized by specific Biopieces which read data from files, databases, or web services, and output records to the data stream that is passed to downstream Biopieces until the data stream is terminated at the end of the analysis. The advantage of the Biopieces is that a user can easily solve simple and complex tasks without having any programming experience. Moreover, since the data format used to pass data between Biopieces is text based, different developers can quickly create new Biopieces in their favorite programming language - and all the Biopieces will maintain compatibility. Finally, templates exist for creating new Biopieces in Perl and Ruby. There are currently ~190 Biopieces (March 2014). bioinformatics, tool, framework, biopieces, language independent, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Google Project Hosting
Danish Agency for Science Technology and Innovation 272-06-0325 GNU General Public License, v2 nlx_149253, biotools:biopieces, OMICS_01036 http://code.google.com/p/biopieces/, https://bio.tools/biopieces SCR_005783 www.biopieces.org, biopieces - Biopieces is a bioinformatic framework of tools easily used and easily created 2026-08-06 09:26:24 40
VIDA
 
Resource Report
Resource Website
100+ mentions
VIDA (RRID:SCR_007111) VIDA data set, data or information resource VIDA contains a collection of homologous protein families derived from open reading frames from complete and partial virus genomes. For each family, users can get an alignment of the conserved regions, functional and taxonomy information, and links to DNA sequences and structures. * Search homologous protein families from particular virus families * Links to complete genome sequence: Arteriviridae, Coronaviridae, Herpesviridae, Poxviridae The Virus Database at University College London has been developed as a system to organize animal virus open reading frame sequences. All known and predicted protein sequences from complete and partial genomes of particular virus families are extracted from GenBank and filtered to remove 100% redundancy. On the basis of sequence similarity the sequences are then clustered into homologous protein families (HPFs). The families are enriched with annotations including function and functional classification, related protein structures, taxonomy, length of the proteins, boundaries of the conserved region/s, virus-specific gene name and links to EMBL entries and SWISSPROT., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. genomics, non-vertebrate, viral genome, homologous protein, hpf, viral genome, virus, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
has parent organization: University College London; London; United Kingdom
BBSRC ;
MRC
PMID:11125070 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-03628, biotools:vida https://bio.tools/vida http://www.biochem.ucl.ac.uk/bsm/virus_database/VIDA.html SCR_007111 Virus Database at University College London, Virus Database, VIDA Virus Database 2026-08-06 09:26:45 193
FusionHunter
 
Resource Report
Resource Website
1+ mentions
FusionHunter (RRID:SCR_011895) FusionHunter source code, software resource Software for identifying fusion transcripts using paired-end RNA-seq. perl, annotation, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
OMICS_01350, biotools:fusionhunter https://bio.tools/fusionhunter SCR_011895 FusionHunter: identifying fusion transcripts using paired-end RNA-seq 2026-08-06 09:27:51 8
CUDASW++
 
Resource Report
Resource Website
1+ mentions
CUDASW++ (RRID:SCR_008862) CUDASW++ source code, software resource CUDASW++ is a bioinformatics software for Smith-Waterman protein database searches that takes advantage of the massively parallel CUDA architecture of NVIDIA Tesla GPUs to perform sequence searches 10x-50x faster than NCBI BLAST. In this algorithm, we deeply explore the SIMT (Single Instruction, Multiple Thread) and virtualized SIMD (Single Instruction, Multiple Data) abstractions to achieve fast speed. This algorithm has been fully tested on Tesla C1060, Tesla C2050, GeForce GTX 280 and GTX 295 graphics cards, and has been incorporated to NVIDIA Tesla Bio Workbench. * Operating System: Linux * Programming language: CUDA and C * Other requirements: CUDA SDK and Toolkits 2.0 or higher smith-waterman, bioinformatics, protein, protein database, sequence, simt, simd, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
has parent organization: Nanyang Technological University; Singapore; Singapore
PMID:19416548
PMID:20370891
Open-source nlx_149212, biotools:cudasw https://bio.tools/cudasw SCR_008862 CUDASW++ (Smith Waterman) 2026-08-06 09:27:17 5
ReactomePA
 
Resource Report
Resource Website
50+ mentions
ReactomePA (RRID:SCR_019316) software resource, data analysis software, data processing software, data visualization software, software application Software R package provides functions for pathway analysis based on REACTOME pathway database. It implements enrichment analysis, gene set enrichment analysis and several functions for visualization. pathway analysis, REACTOME pathway, REACTOME database, enrichment analysis, gene set enrichment analysis, bio.tools is listed by: Bioconductor
is listed by: bio.tools
is listed by: Debian
PMID:26661513 Free, Available for download, Freely available biotools:reactomepa https://bio.tools/reactomepa SCR_019316 Reactome Pathway Analysis 2026-08-06 09:29:31 76
ImJoy
 
Resource Report
Resource Website
1+ mentions
ImJoy (RRID:SCR_020935) data analysis software, software application, software resource, data processing software Software tool as plugin powered hybrid computing platform for deploying deep learning applications such as advanced image analysis tools. Runs on mobile and desktop environment cross different operating systems, can run in the browser, localhost, remote and cloud servers. Deep learning, flexible plugin system, deploying deep learning applications, advanced image analysis, bio.tools is listed by: bio.tools
is listed by: Debian
Free, Available for download,Freely available biotools:ImJoy https://github.com/imjoy-team/ImJoy, https://bio.tools/ImJoy SCR_020935 2026-08-06 09:29:33 3
UEA sRNA Workbench
 
Resource Report
Resource Website
1+ mentions
UEA sRNA Workbench (RRID:SCR_020947) data analysis software, software application, software resource, data processing software Software package for analysing small RNA data. Software suite of tools for analyzing miRNAs and sRNAs. Performs analysis of single or multiple sample small RNA datasets from both plants and animals. Analysing small RNA data, analyzing miRNAs, profiling small RNA expression patterns, genetic data, bio.tools, bio.tools, bio.tools lists: VisSR
is listed by: bio.tools
is listed by: Debian
has parent organization: University of East Anglia; Norwich; United Kingdom
BBSRC BB/L021269/1 PMID:29722807 Free, Available for download, Freely available biotools:siloco, biotools:mircat https://github.com/sRNAworkbenchuea/UEA_sRNA_Workbench, https://bio.tools/mircat, https://bio.tools/siloco, SCR_020947 UEA small RNA Workbench 2026-08-06 09:29:33 7
PhenStat
 
Resource Report
Resource Website
1+ mentions
PhenStat (RRID:SCR_021317) software resource, data analysis software, software toolkit, data processing software, software application Software R package for statistical analysis of phenotypic data.Tool kit for standardized analysis of high throughput phenotypic data. Statistical analysis, phenotypic data, standardized analysis, bio.tools, Bioconductor is listed by: Bioconductor
is listed by: bio.tools
Wellcome Trust ;
NHGRI U54 HG006370
PMID:26147094 Free, Available for download, Freely available biotools:phenstat https://bio.tools/phenstat SCR_021317 2026-08-06 09:29:38 8
vcflib
 
Resource Report
Resource Website
100+ mentions
vcflib (RRID:SCR_001231) vcflib software library, software toolkit, software resource A C++ library for parsing and manipulating Variant Call Format (VCF) files, and many command-line utilities. The API provides a quick and extremely permissive method to read and write VCF files. Extensions and applications of the library provided in the included utilities (*.cpp) comprise the vast bulk of the library's utility for most users. c++, sequence variation, genomic variation, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
Free, Available for download, Freely available biotools:vcflib, OMICS_02112 https://bio.tools/vcflib, https://sources.debian.org/src/libvcflib-dev/ https://sources.debian.org/src/libvcflib-dev/ SCR_001231 2026-08-06 09:25:21 119
CSDeconv
 
Resource Report
Resource Website
CSDeconv (RRID:SCR_000016) CSDeconv data analysis software, software application, software resource, data processing software THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. Software application that maps transcription factor binding sites from ChIP-seq data to high resolution using a blind deconvolution approach. sequence analysis software, transcription factor binding site, chip-seq, blind deconvolution, transcription binding, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Rutgers University; New Jersey; USA
has parent organization: University of South Australia; Adelaide; Australia
PMID:20028542 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00436, biotools:csdeconv https://bio.tools/csdeconv SCR_000016 2026-08-06 09:25:06 0
fastqz
 
Resource Report
Resource Website
fastqz (RRID:SCR_001006) data management software, source code, software application, software resource Source code used to compress FASTQ files. FASTQ is DNA sequencing machine output. compress, source code, fastq output, fastq dna, fastq sequencing, fastq compress, fastq compressor, fastq files, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:23533605 Free, Available for download, Freely available OMICS_00956, biotools:fastqz https://bio.tools/fastqz SCR_001006 2026-08-06 09:25:19 0
Rsubread
 
Resource Report
Resource Website
100+ mentions
Rsubread (RRID:SCR_016945) software resource, image analysis software, alignment software, data analysis software, data processing software, software application Software R package for sequence alignment and counting for R. Used for analyses of second and third generation sequencing data, for read mapping, read counting, SNP calling, short and long read alignment, quantification and mutation discovery. Includes assessment of sequence reads, read alignment, read summarization, exon-exon junction detection, fusion detection, detection of short and long indels, absolute expression calling and SNP calling. Can be used with reads generated from any of the major sequencing platforms including Illumina GA/HiSeq/MiSeq, Roche GS-FLX, ABI SOLiD and LifeTech Ion PGM/Proton sequencers. sequence, alignment, counting, multi, seed, strategy, mapping, read, reference, genome, analysis, data, SNP, calling, mutation, discovery, bio.tools is listed by: Bioconductor
is listed by: Debian
is listed by: bio.tools
is related to: R Project for Statistical Computing
is related to: Subread
Australian National Health and Medical Research Council ;
Victorian State Government Operational Infrastructure Support ;
Australian Government
PMID:23558742 Free, Available for download, Freely available biotools:rsubread https://bio.tools/rsubread SCR_016945 2026-08-06 09:28:59 188
scran
 
Resource Report
Resource Website
50+ mentions
scran (RRID:SCR_016944) SCRAN data analysis software, software application, software resource, data processing software Software package for low-level analyses of single-cell RNA-seq data. Used for quality control, data exploration and normalization, cell cycle phase assignment, identification of highly variable and correlated genes, clustering into subpopulations and marker gene detection. low, level, analysis, scRNA-seq, data, normalization, cell, cycle, phase, gene, variable, correlation, cluster, subpopulation, marker, bio.tools is listed by: Bioconductor
is listed by: Debian
is listed by: bio.tools
is related to: R Project for Statistical Computing
Cancer Research UK ;
National Health and Medical Research Council of Australia ;
EMBL
PMID:27909575 Free, Available for download, Freely available biotools:scran https://bio.tools/scran SCR_016944 Single-Cell Rna-seq data ANalysis, SCRAN 2026-08-06 09:28:56 92
ConsensusClusterPlus
 
Resource Report
Resource Website
100+ mentions
ConsensusClusterPlus (RRID:SCR_016954) data analysis software, software application, software resource, data processing software Software written in R for determining cluster count and membership by stability evidence in unsupervised analysis. Provides quantitative and visual stability evidence for estimating the number of unsupervised classes in a dataset with item tracking, item consensus and cluster consensus plots. cluster, count, stability, evidence, unsupervised, analysis, , bio.tools is listed by: Bioconductor
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
NCI F32CA142039;
Thomas G. Labrecque Foundation ;
NCI U24 CA126554
PMID:20427518 Free, Available for download, Freely available biotools:consensusclusterplus https://bio.tools/consensusclusterplus SCR_016954 2026-08-06 09:28:56 160

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.