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
Sherman
 
Resource Report
Resource Website
100+ mentions
Sherman (RRID:SCR_001294) Sherman software resource Software tool to simulate FastQ files for high-throughput sequencing experiments. It allows the user to introduce various "contaminants" into the sequences, such as basecall errors, SNPs, adapter fragments etc., in order to evaluate the influence of common problems observed in many Next-Gen Sequencing experiments. perl, bisulfite sequencing, high-throughput sequencing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Babraham Institute
Free, Available for download, Freely available biotools:sherman, OMICS_02041 http://www.bioinformatics.babraham.ac.uk/projects/sherman/ SCR_001294 Sherman - bisulfite-treated Read FastQ Simulator 2026-08-01 12:01:37 122
GenomicTools
 
Resource Report
Resource Website
GenomicTools (RRID:SCR_001205) GenomicTools software resource A flexible computational platform, comprising both a command-line set of tools and a C++ API, for the analysis and manipulation of high-throughput sequencing data such as DNA-seq, RNA-seq, ChIP-seq and MethylC-seq. It implements a variety of mathematical operations between sets of genomic regions thereby enabling the prototyping of computational pipelines that can address tasks from preprocessing and quality control to meta-analyses. The user can create average read profiles across transcriptional start sites or enhancer sites, quickly prototype customized peak discovery methods for ChIP-seq experiments, perform genome-wide statistical tests such as enrichment analyses, design controls via appropriate randomization schemes, among other applications. In addition to enabling rapid prototyping, the platform is designed to analyze large-datasets in a single-pass fashion in order to minimize memory and intermediate file requirements. The platform supports the widely used BED format to facilitate visualization as well as integration with existing platforms and pipelines such as Galaxy or BioConductor. high-throughput sequencing, rna-seq, chip-seq, genomics, sequencing, hi-c, epigenetics, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Google Code
PMID:22113082 Free, Available for download, Freely available biotools:genomictools, OMICS_02144 https://bio.tools/genomictools SCR_001205 GenomicTools: a computational platform for developing high-throughput analytics in genomics. 2026-08-01 12:01:34 0
PARalyzer
 
Resource Report
Resource Website
1+ mentions
PARalyzer (RRID:SCR_001208) PARalyzer software resource Software tool to generate a high resolution map of interaction sites between RNA-binding proteins and their targets. The algorithm utilizes the deep sequencing reads generated by the newly developed PAR-CLIP (Photoactivatable-Ribonucleoside-Enhanced Crosslinking and Immunoprecipitation) protocol. The use of photoactivatable nucleotides in the PAR-CLIP protocol results in a more efficient crosslinking between the RNA-binding protein and its target relative to other CLIP methods; in addition a nucleotide substitution occurs at the site of crosslinking during Illumina library preparation. PARalyzer utilizes this nucleotide substition in a kernel density estimate classifier to generate the high resolution set of Protein-RNA interaction sites. interaction, rna-binding protein, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Duke University; North Carolina; USA
PMID:21851591 THIS RESOURCE IS NO LONGER IN SERVICE biotools:paralyzer, OMICS_02137 https://bio.tools/paralyzer SCR_001208 PAR-CLIP data analyzer, PARalyzer (PAR-CLIP data analyzer) 2026-08-01 12:01:42 6
ProbRNA
 
Resource Report
Resource Website
1+ mentions
ProbRNA (RRID:SCR_001288) ProbRNA software resource Software for computational identification of protein binding sites on RNAs using high-throughput RNA structure-probing data. high-throughput sequencing, probe, rna structure, rna, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Chinese University of Hong Kong; Hong Kong; China
PMID:24376038 THIS RESOURCE IS NO LONGER IN SERVICE biotools:probrna, OMICS_02195 https://bio.tools/probrna SCR_001288 2026-08-01 12:01:37 1
Sequedex
 
Resource Report
Resource Website
1+ mentions
Sequedex (RRID:SCR_001233) Sequedex software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 18,2025.Software to classify the function and phylogeny of reads as short as 30 bp. It is flexible, which can utilize multiple data modules and downstream analysis scripts. It is fast, reading in signature lists of 5-500 million peptide signatures in 1-15 minutes, and subsequently processes genomic fragments at the rate of 6 Gbp/hr. It parallelizes without significant increase in memory requirements until I/O bound on multiple input files; parallelization works well on 64 processors. phylogenetic, function, profile, metagenomics, synthetic, dna sequence, classification, java, linux, mac os, genomic analysis, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Los Alamos National Laboratory
PMID:22925230 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02110, biotools:sequedex https://bio.tools/sequedex SCR_001233 2026-08-01 12:01:25 1
PeakAnalyzer
 
Resource Report
Resource Website
1+ mentions
PeakAnalyzer (RRID:SCR_001194) PeakAnalyzer software resource A set of standalone software programs for the automated processing of any genomic loci, with an emphasis on datasets consisting of ChIP-derived signal peaks. The software is able to identify individual binding / modification sites from enrichment loci, retrieve peak region sequences for motif discovery, and integrate experimental data with different classes of annotated elements throughout the genome. PeakAnalyzer requires a peak file and a feature annotation file in BED or GTF format. Complete annotation files for the current builds of the human (HG19) and mouse (MM9) genomes are provided with the software distribution. genome, chip, signal peak, binding site, modification site, enrichment loci, peak region, sequence, motif, chip-seq, chip-chip, c++, java, linux, mac os x, windows, bed, gtf, annotation, r, high-throughput sequencing, chromatin binding, modification loci, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: European Bioinformatics Institute
PMID:20691053 Free, Available for download, Freely available biotools:peakanalyzer, OMICS_02156 https://bio.tools/peakanalyzer SCR_001194 2026-08-01 12:01:34 3
BreakSeq
 
Resource Report
Resource Website
1+ mentions
BreakSeq (RRID:SCR_001186) BreakSeq software resource Software for scanning reads from short-read sequenced genomes against a human breakpoint library to accurately identify structural variants (SVs). The library of breakpoints at nucleotide resolution were assembled from collating and standardizing ~2,000 published structural variants (SVs). For each breakpoint, its ancestral state (through comparison to primate genomes) was inferred and its mechanism of formation (e.g., nonallelic homologous recombination, NAHR). structural variant, breakpoint, nucleotide, fasta, gff, bowtie, genomic variation, junction mapping, insertion sequence, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Yale University; Connecticut; USA
PMID:20037582 THIS RESOURCE IS NO LONGER IN SERVICE biotools:breakseq, OMICS_02168 https://bio.tools/breakseq SCR_001186 Breakpoint Library and BreakSeq 2026-08-01 12:01:24 1
SLOPE
 
Resource Report
Resource Website
SLOPE (RRID:SCR_001185) SLOPE software resource Software that consists of two command-line utilities, slope_align (which finds the best split-read alignments to the reference genome) and slope_cluster (which clusters and outputs the alignments)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. c++, alignment, cluster, command-line, reference genome, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Utah; Utah; USA
PMID:20876606 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02169, biotools:slope https://bio.tools/slope SCR_001185 2026-08-01 12:01:34 0
Genometa
 
Resource Report
Resource Website
Genometa (RRID:SCR_001181) Genometa software resource A Java based bioinformatics program which allows rapid analysis of metagenomic short read datasets. Millions of short reads can be accurately analysed within minutes and visualised in the browser component. A large database of diverse bacteria and archaea has been constructed as a reference sequence. The approach is based upon the established open source visualisation tool IGB and supported by the rapid alignment program bowtie. The Picard toolset for SAM files is also made use of. metagenomic, classify, windows, linux, java, bio.tools, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Hannover Medical School; Lower Saxony; Germany
PMID:22927906 Free, Available for download, Freely available biotools:genometa, OMICS_02175 https://bio.tools/genometa SCR_001181 Genometa - Rapid analysis of metagenomic short reads 2026-08-01 12:01:34 0
piCALL
 
Resource Report
Resource Website
1+ mentions
piCALL (RRID:SCR_001242) piCALL software resource Software to detect short insertion / deletion variants (and SNPs) from population sequence data, i.e. sequence reads generated from a population of individuals. It uses a probabilistic model to utilize sequence reads from a population of individuals to automatically account for context-specific sequencing errors associated with indels. piCALL is implemented in C for use on Linux platforms and can be applied to sequence data from different sequencing platforms. However, the method requires each individual in a dataset to be sequenced using the same platform. The reads for each individual should be aligned to the same reference genome sequence. Note that the program will not be able to call indels from individual sequence datasets or data from a small number of individuals. c, genotyping, indel, population, high-throughput sequencing, insertion, deletion, variant, single nucleotide polymorphism, linux, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Scripps Research Institute
PMID:21653520 OMICS_02098, biotools:picall https://bio.tools/picall http://polymorphism.scripps.edu/~vbansal/software/piCALL/ SCR_001242 2026-08-01 12:01:44 1
mapDamage
 
Resource Report
Resource Website
100+ mentions
mapDamage (RRID:SCR_001240) mapDamage software resource Software for tracking and quantifying DNA damage patterns among ancient DNA sequencing reads generated by Next-Generation Sequencing platforms. python, r, illumina, windows, perl, dna damage, dna sequencing, next-generation sequencing, dna, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Copenhagen; Copenhagen; Denmark
PMID:23613487
PMID:21659319
DOI:10.1093/bioinformatics/btt193
Free, Available for download, Freely available OMICS_02099, biotools:mapdamage https://bio.tools/mapdamage, https://sources.debian.org/src/mapdamage/ SCR_001240 mapDamage 2.0, mapDamage: tracking and quantifying damage patterns in ancient DNA sequences, mapDamage2.0 2026-08-01 12:01:35 363
DSK
 
Resource Report
Resource Website
1+ mentions
DSK (RRID:SCR_001246) DSK software resource A k-mer counting software that can count k-mers of large Illumina datasets on laptops and desktop computers. illumina, k-mer, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:23325618 Free, Freely available biotools:dsk, OMICS_02094 https://bio.tools/dsk SCR_001246 disk streaming of k-mers, DSK: disk streaming of k-mers 2026-08-01 12:01:44 1
wateRmelon
 
Resource Report
Resource Website
100+ mentions
wateRmelon (RRID:SCR_001296) wateRmelon software resource Software package for Illumina 450 methylation array normalization and metrics including 15 flavors of betas and three performance metrics, with methods for objects produced by methylumi, minfi and IMA packages. dna methylation, microarray, preprocessing, quality control, two channel, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Bioconductor
PMID:23631413 Free, Available for download, Freely available OMICS_02039, biotools:watermelon https://bio.tools/watermelon SCR_001296 2026-08-01 12:01:46 296
NGSrich
 
Resource Report
Resource Website
10+ mentions
NGSrich (RRID:SCR_001333) software resource Software for target enrichment performance for next-generation sequencing. standalone software, java, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:22290614 Free, Available for download, Freely available OMICS_03603, biotools:ngsrich https://bio.tools/ngsrich SCR_001333 2026-08-01 12:01:39 10
oneChannelGUI
 
Resource Report
Resource Website
10+ mentions
oneChannelGUI (RRID:SCR_001325) oneChannelGUI software resource Software library that provides a graphical interface for microarray gene and exon level analysis as well as miRNA/mRNA-seq data analysis. The package was developed to simplify the use of Bioconductor tools for beginners having limited or no experience in writing R code. differential expression, gui, microarray, multiple comparison, preprocessing, quality control, rna-seq, exon, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Bioconductor
PMID:17875544 Free, Available for download, Freely available biotools:onechannelgu, OMICS_02004 http://www.bioconductor.org/packages/release/bioc/html/oneChannelGUI.html SCR_001325 2026-08-01 12:01:27 13
CYCLE
 
Resource Report
Resource Website
10+ mentions
CYCLE (RRID:SCR_001328) CYCLE software resource Software package for the identification of periodically expressed genes using Fourier analysis and the statistical assessment of significance using different background models. r, microarray, time course, periodic expression pattern, time-series, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Humboldt University of Berlin; Berlin; Germany
has parent organization: Bioconductor
PMID:18310054 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02010, biotools:cycle http://www.bioconductor.org/packages/release/bioc/html/cycle.html, https://bio.tools/cycle SCR_001328 2026-08-01 12:01:28 31
affylmGUI
 
Resource Report
Resource Website
10+ mentions
affylmGUI (RRID:SCR_001320) affylmGUI software resource R software package providing a Graphical User Interface for analysis of Affymetrix microarray data, using the limma package (Linear Models for MicroArray data). While not as powerful as limma to the expert user, it offers a simple point-and-click interface to many of the commonly-used limma and affy functions. You need to have R 1.9.0 or later, Tcl/Tk 8.3 or later (ActiveTcl for Windows, Tcl/Tk Source for Linux/Unix, or X11 Tcl/Tk for MacOSX) and the limma, affylmGUI, and tkrplot R packages. It has been succesfully tested on Windows 2000, Windows XP, RedHat/Fedora Linux, and on Mac OSX with X11. affymetrix, differential expression, r, data import, differential expression, gui, microarray, multiple comparison, one channel, preprocessing, quality control, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Walter and Eliza Hall Institute of Medical Research; Victoria; Australia
has parent organization: Bioconductor
PMID:16455752 Free, Available for download, Freely available biotools:affylmgui, OMICS_02016 http://www.bioconductor.org/packages/release/bioc/html/affylmGUI.html, https://bio.tools/affylmgui SCR_001320 Affymetrix linear modeling Graphical User Interface 2026-08-01 12:01:47 31
plgem
 
Resource Report
Resource Website
10+ mentions
plgem (RRID:SCR_001355) plgem software resource Software to detect differential expression in microarray and proteomics datasets. Its use has been shown to improve the detection of differentially expressed genes or proteins in these datasets. differential expression, microarray, proteomics, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
Free, Available for download, Freely available OMICS_01984, biotools:plgem https://bio.tools/plgem SCR_001355 Power Law Global Error Model 2026-08-01 12:01:49 16
fRMA
 
Resource Report
Resource Website
50+ mentions
fRMA (RRID:SCR_001345) fRMA software resource Preprocessing and analysis software for single microarrays and microarray batches. microarray, preprocessing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Bioconductor
PMID:23044545 Free, Available for download, Freely available biotools:frma, OMICS_01994 https://bio.tools/frma SCR_001345 fRMA - Frozen RMA and Barcode 2026-08-01 12:01:28 74
dyebias
 
Resource Report
Resource Website
dyebias (RRID:SCR_001308) dyebias software resource Software package using the GASSCO method for correcting for slide-dependent gene-specific dye bias. microarray, preprocessing, quality control, two channel, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
PMID:17623705 GNU General Public License, v3 biotools:dyebias, OMICS_02025 https://bio.tools/dyebias SCR_001308 dyebias - The GASSCO method for correcting for slide-dependent gene-specific dye bias 2026-08-01 12:01:27 0

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.