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

  • Related Resources:omictools (facet)

Facets


Recent searches

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

2,818 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
mubiomics
 
Resource Report
Resource Website
1+ mentions
mubiomics (RRID:SCR_006785) mubiomics software resource A set of scripts (mostly python) for processing reads generated by the Roche 454 or Illumina next-gen sequencing platforms. Included are quality control, read demultiplexing and microbiome characterisation scripts for use with usearch, pplacer and RDP classifier. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01059 SCR_006785 mubiomics - Scripts for processing next-gen sequencing data 2026-09-19 12:51:18 4
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. 2026-09-19 12:51:19 235
mutationSeq
 
Resource Report
Resource Website
10+ mentions
mutationSeq (RRID:SCR_006815) mutationSeq software resource A software suite using feature-based classifiers for somatic mutation prediction from paired tumour/normal next-generation sequencing data. mutationSeq has the advantages of integrating different features (e.g., base qualities, mapping qualities, strand bias, and tailed distance features), and validated somatic mutations to make predictions. Given paired normal/tumour bam files, mutationSeq will output the probability of each candidate site being somatic. next-generation sequencing, somatic mutation, tumor, normal is listed by: OMICtools
is related to: JointSNVMix
has parent organization: BC Cancer Agency
Tumor, Normal PMID:22084253 OMICS_00086 SCR_006815 2026-09-19 12:51:19 24
RIPSeeker
 
Resource Report
Resource Website
10+ mentions
RIPSeeker (RRID:SCR_006810) RIPSeeker software resource A statistical software package for identifying protein-associated transcripts from RIP-seq experiments. Infer and discriminate RIP peaks from RIP-seq alignments using two-state HMM with negative binomial emission probability. While RIPSeeker is specifically tailored for RIP-seq data analysis, it also provides a suite of bioinformatics tools integrated within this self-contained software package comprehensively addressing issues ranging from post-alignments processing to visualization and annotation. rip-seq is listed by: OMICtools
has parent organization: Bioconductor
GNU General Public License, v2 OMICS_00569 SCR_006810 RIPSeeker: a statistical package for identifying protein-associated transcripts from RIP-seq experiments 2026-09-19 12:51:19 12
Ensembl Genomes
 
Resource Report
Resource Website
100+ mentions
Ensembl Genomes (RRID:SCR_006773) data access protocol, data or information resource, database, software resource, web service Database portal offering integrated access to genome-scale data from non-vertebrate species of scientific interest, developed using the Ensembl genome annotation and visualization platform. Ensembl Genomes consists of five sub-portals (for bacteria, protists, fungi, plants and invertebrate metazoa) designed to complement the availability of vertebrate genomes in Ensembl. Many of the databases supporting the portal have been built in close collaboration with the scientific community - essential for maintaining the accuracy and usefulness of the resource. A common set of user interfaces (which include a graphical genome browser, FTP, BLAST search, a query optimized data warehouse, programmatic access, and a Perl API) is provided for all domains. Data types incorporated include annotation of (protein and non-protein coding) genes, cross references to external resources, and high throughput experimental data (e.g. data from large scale studies of gene expression and polymorphism visualized in their genomic context). Additionally, extensive comparative analysis has been performed, both within defined clades and across the wider taxonomy, and sequence alignments and gene trees resulting from this can be accessed through the site. genome, gold standard, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Ensembl
is related to: Ensembl
is related to: g:Profiler
has parent organization: European Bioinformatics Institute
European Molecular Biology Laboratory ;
European Union FELICS 021902 (RII3);
BBSRC BB/F019793/1
PMID:24163254
PMID:19884133
r3d100011197, OMICS_01648, biotools:ensembl_genomes, nlx_65207 https://bio.tools/ensembl_genomes, https://doi.org/10.17616/R3MW6M SCR_006773 Ensembl Genomes: Extending Ensembl across the taxonomic space, EnsemblGenomes, Ensembl Genome 2026-09-19 12:51:18 320
Qudaich
 
Resource Report
Resource Website
Qudaich (RRID:SCR_006775) Qudaich software resource A software package for local sequence alignment for next-generation sequencing (NGS) data. It generates the pairwise local alignments between a query dataset against a database. The main design purpose of qudaich is to focus on datasets from next generation sequencing. These the datasets generally have hundreds of thousand sequences or more, and so, the input database should contain large number of sequences. Qudaich is flexible and its algorithmic structure imposes no restriction on the absolute limit of the acceptable read length, but the current version of qudaich allow read length <2000 bp. Qudaich can be used to align DNA, translated DNA and protein sequences. next-generation sequencing, alignment is listed by: OMICtools
has parent organization: SourceForge
OMICS_00678 SCR_006775 Queries and unique database alignment inferred by clustering homologs 2026-09-19 12:51:18 0
JointSNVMix
 
Resource Report
Resource Website
10+ mentions
JointSNVMix (RRID:SCR_006804) JointSNVMix data analysis software, data processing software, software application, software resource Software that implements a probabilistic graphical model to analyze sequence data from tumor / normal pairs. The model draws statistical strength by analysing both genome jointly to more accurately classify germline and somatic mutations. It effectively reduces false positive somatic mutation predictions in tumour-normal pair sequencing data. It is highly recommended to post-process results with mutationSeq in order to filter technical artifacts. tumor, cancer, normal, somatic mutation, mutation is listed by: OMICtools
is related to: mutationSeq
has parent organization: BC Cancer Agency
PMID:22285562 GNU General Public License, v3, Registration required OMICS_00085 SCR_006804 2026-09-19 12:51:18 10
GBS barcode splitter
 
Resource Report
Resource Website
GBS barcode splitter (RRID:SCR_006799) GBS barcode splitter software resource PERL script used to split barcode of Illumina sequencing data created by GBS protocol (www.maizegenetics.net). The barcode has variable size. Paired-end reads are supported. illumina is listed by: OMICtools
has parent organization: SourceForge
Free OMICS_01050 SCR_006799 GBS barcode splitter - PERL script for split GBS reads by barcode 2026-09-19 12:51:18 0
REDfly Regulatory Element Database for Drosophilia
 
Resource Report
Resource Website
10+ mentions
REDfly Regulatory Element Database for Drosophilia (RRID:SCR_006790) REDfly data or information resource, data repository, database, service resource, storage service resource Curated collection of known Drosophila transcriptional cis-regulatory modules (CRMs) and transcription factor binding sites (TFBSs). Includes experimentally verified fly regulatory elements along with their DNA sequence, associated genes, and expression patterns they direct. Submission of experimentally verified cis-regulatory elements that are not included in REDfly database are welcome. transcriptional cis-regulatory module, transcription factor binding site, dna sequence, gene, expression pattern, genome, gene expression, transcription factor, cis-regulatory module, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Drosophila anatomy and development ontologies
is related to: FlyMine
has parent organization: University at Buffalo; New York; USA
NIGMS U24 GM144232;
NSF EF0843229
PMID:20965965
PMID:18039705
PMID:16303794
Acknowledgement requested OMICS_01870, biotools:redfly, nif-0000-03393 https://bio.tools/redfly SCR_006790 Regulatory Element Database for Drosophilia, Regulatory Element Database 2026-09-19 12:51:18 15
EBCall
 
Resource Report
Resource Website
10+ mentions
EBCall (RRID:SCR_006791) EBCall software resource A software package for somatic mutation detection (including InDels). EBCall uses not only paired tumor/normal sequence data of a target sample, but also multiple non-paired normal reference samples for evaluating distribution of sequencing errors, which leads to an accurate mutaiton detection even in case of low sequencing depths and low allele frequencies. mutation, cancer, genome, sequencing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Tokyo; Tokyo; Japan
PMID:23471004 Copyright conditions, Acknowledgement required biotools:ebcall, OMICS_00084 https://bio.tools/ebcall SCR_006791 EBCall (Empirical Baysian mutation Calling), Empirical Baysian mutation Calling 2026-09-19 12:51:18 20
Psort
 
Resource Report
Resource Website
100+ mentions
Psort (RRID:SCR_007038) PSORT analysis service resource, data analysis service, data analysis software, data or information resource, data processing software, data set, portal, production service resource, service resource, software application, software resource, topical portal Portal to the PSORT family of computer programs for the prediction of protein localization sites in cells, as well as other datasets and resources relevant to localization prediction. The standalone versions are available for download for larger analyses. subcellular, localization, prediction, gram, gram-positive, gram-negative, sequence, fasta, protein, protein localization, cell, motif, profile, amino acid, subcellular localization is listed by: OMICtools
is related to: PSORT II
has parent organization: Simon Fraser University; British Columbia; Canada
OMICS_01634, nif-0000-31883 http://psort.hgc.jp/ SCR_007038 Psort.org, PSORT: Prediction of Protein Sorting Signals and Localization Sites in Amino Acid Sequences 2026-09-19 12:51:23 222
BAMStats
 
Resource Report
Resource Website
10+ mentions
BAMStats (RRID:SCR_006973) BAMStats software resource A GUI desktop tool for calculating and displaying metrics to assess the success of Next Generation Sequencing mapping tools. BAMstats is written in Java and based around the Picard API. matlab, next generation sequencing, java is listed by: OMICtools
has parent organization: SourceForge
GNU General Public License OMICS_01034 SCR_006973 2026-09-19 12:51:22 10
ProDom
 
Resource Report
Resource Website
100+ mentions
ProDom (RRID:SCR_006969) ProDom analysis service resource, data analysis service, data or information resource, database, production service resource, service resource Comprehensive set of protein domain families automatically generated from UniProt Knowledge Database. Automated clustering of homologous domains generated from global comparison of all available protein sequences., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. set, protein, domain, family, automatically, generated, UniProt, database, homologous, sequence, compare, FASEB list is listed by: OMICtools
is related to: UniProt
is related to: InterPro
has parent organization: PRABI
European Union ;
Re´seau des Ge´nopoles ;
‘Programme de Bio-Informatique InterOrganismes
PMID:15608179
PMID:12230033
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01698, nif-0000-03342 http://prodom.prabi.fr/prodom/current/html/home.php SCR_006969 2026-09-19 12:51:22 354
RamiGO
 
Resource Report
Resource Website
10+ mentions
RamiGO (RRID:SCR_006922) RamiGO software resource Software package with an R interface sending requests to AmiGO visualize, retrieving DAG GO trees, parsing GraphViz DOT format files and exporting GML files for Cytoscape. Also uses RCytoscape to interactively display AmiGO trees in Cytoscape. visualization, analysis, ontology or annotation search engine, ontology or annotation visualization, other analysis, classification, go, graph, network, third party client, windows, mac os x, linux, unix, bio.tools is listed by: Gene Ontology Tools
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
is related to: Cytoscape
is related to: AmiGO
has parent organization: Dana-Farber Cancer Institute
has parent organization: Bioconductor
PMID:23297033 Artistic License, v2 biotools:ramigo, OMICS_02267, nlx_149331 http://bioconductor.org/packages/release/bioc/html/RamiGO.html, https://bio.tools/ramigo SCR_006922 ramigo, RamiGO - AmiGO visualize R interface 2026-09-19 12:51:21 12
RazerS
 
Resource Report
Resource Website
10+ mentions
RazerS (RRID:SCR_006889) RazerS software resource A read mapping software program with adjustable sensitivity based on counting q-grams. RazerS 3 supports shared-memory parallelism, an additional seed-based filter with adjustable sensitivity, a much faster, banded version of the Myers? bit-vector algorithm for verification, memory saving measures and support for the SAM output format. This leads to a much improved performance for mapping reads, in particular long reads with many errors. next-generation sequencing, c++, openmp, linux, mac os x, windows is listed by: OMICtools
has parent organization: Free University of Berlin; Berlin; Germany
PMID:22923295
PMID:19592482
GNU General Public License OMICS_00679 SCR_006889 2026-09-19 12:51:21 13
CROP
 
Resource Report
Resource Website
100+ mentions
CROP (RRID:SCR_006916) CROP software resource A clustering tool designed mainly for Metagenomics studies, which clusters 16S rRNA sequences into Operational Taxonomic Units (OTU). By using a Gaussian Mixture model, CROP can automatically determine the best clustering result for 16S rRNA sequences at different phylogenetic levels without setting a hard cutoff threshold as hierarchical clustering does. Yet, at the same time, it is able to manage large datasets and to overcome sequencing errors. cluster, 16s rrna, otu, gaussian mixture, bayesian, mcmc, metagenomics is listed by: OMICtools
has parent organization: Google Code
has parent organization: University of Southern California; Los Angeles; USA
PMID:21233169 OMICS_01442 SCR_006916 CROP: Clustering 16S rRNA For OTU Prediction 2026-09-19 12:51:21 209
MetMap
 
Resource Report
Resource Website
1+ mentions
MetMap (RRID:SCR_006954) MetMap software resource A computational pipeline for the analysis of MethylSeq experiments., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. is listed by: OMICtools
has parent organization: University of California at Berkeley; Berkeley; USA
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00618 SCR_006954 2026-09-19 12:51:21 9
Myrna
 
Resource Report
Resource Website
1+ mentions
Myrna (RRID:SCR_006951) Myrna software resource A cloud computing tool for calculating differential gene expression in large RNA-seq datasets. It uses Bowtie for short read alignment and R/Bioconductor for interval calculations, normalization, and statistical testing. These tools are combined in an automatic, parallel pipeline that runs in the cloud (Elastic MapReduce in this case) on a local Hadoop cluster, or on a single computer, exploiting multiple computers and CPUs wherever possible. mapreduce, hadoop, cloud computing, differential expression, gene expression, rna-seq, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: ReCount - A multi-experiment resource of analysis-ready RNA-seq gene count datasets
has parent organization: Johns Hopkins University; Maryland; USA
PMID:20701754 Artistic License OMICS_01310, biotools:myrna https://github.com/BenLangmead/myrna, https://bio.tools/myrna SCR_006951 Myrna: Cloud-scale differential gene expression for RNA-seq 2026-09-19 12:51:21 2
SimSeq
 
Resource Report
Resource Website
10+ mentions
SimSeq (RRID:SCR_006947) SimSeq simulation software, software application, software resource An illumina paired-end and mate-pair short read simulator. This project attempts to model as many of the quirks that exist in Illumina data as possible. Some of these quirks include the potential for chimeric reads, and non-biotinylated fragment pull down in mate-pair libraries . bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
Free biotools:simseq, OMICS_00258 https://bio.tools/simseq SCR_006947 2026-09-19 12:51:21 30
RTPrimerDB- The Real-Time PCR and Probe Database
 
Resource Report
Resource Website
10+ mentions
RTPrimerDB- The Real-Time PCR and Probe Database (RRID:SCR_007106) RTPrimerDB data or information resource, data repository, database, service resource, storage service resource Database for primer and probe sequences used in real-time PCR assays employing popular chemistries (SYBR Green I, Taqman, Hybridization Probes, Molecular Beacon) to prevent time-consuming primer design and experimental optimization, and to introduce a certain level of uniformity and standardization among different laboratories. Researchers are encouraged to submit their validated primer and probe sequence, so that other users can benefit from their expertise. The database can be queried using the official gene name or symbol, Entrez or Ensembl Gene identifier, SNP identifier, or oligonucleotide sequence. Different options make it possible to restrict a query to a particular application (Gene Expression Quantification/Detection, DNA Copy Number Quantification/Detection, SNP Detection, Mutation Analysis, Fusion Gene Quantification/Detection, Chromatin immunoprecipitation (ChIP)), organism (Human, Mouse, Rat, and others) or detection chemistry. primer, probe, sequence, real-time pcr, gene, assay, real-time pcr assay, FASEB list is listed by: OMICtools
has parent organization: Ghent University; Ghent; Belgium
PMID:18948285
PMID:16381959
PMID:12519963
Public, The community can contribute to this resource nif-0000-03431, OMICS_02322 SCR_007106 2026-09-19 12:51:24 49

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.