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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 Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
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 2026-02-14 02:01:23 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 2026-02-14 02:01:13 10
Ensembl Genomes
 
Resource Report
Resource Website
100+ mentions
Ensembl Genomes (RRID:SCR_006773) web service, data or information resource, data access protocol, software resource, database 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, nlx_65207, biotools:ensembl_genomes https://bio.tools/ensembl_genomes
https://doi.org/10.17616/R3MW6M
SCR_006773 Ensembl Genomes: Extending Ensembl across the taxonomic space, EnsemblGenomes, Ensembl Genome 2026-02-14 02:01:23 276
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 2026-02-14 02:01:22 0
JointSNVMix
 
Resource Report
Resource Website
10+ mentions
JointSNVMix (RRID:SCR_006804) JointSNVMix data analysis software, software resource, data processing software, software application 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 2026-02-14 02:01:13 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 2026-02-14 02:01:22 0
REDfly Regulatory Element Database for Drosophilia
 
Resource Report
Resource Website
10+ mentions
REDfly Regulatory Element Database for Drosophilia (RRID:SCR_006790) REDfly data repository, storage service resource, data or information resource, service resource, database 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
NSF EF0843229;
NIGMS U24 GM144232
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 2026-02-14 02:01:16 14
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 2026-02-14 02:01:23 19
Psort
 
Resource Report
Resource Website
100+ mentions
Psort (RRID:SCR_007038) PSORT data processing software, data analysis service, portal, analysis service resource, data set, data or information resource, production service resource, data analysis software, 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 2026-02-14 02:01:17 209
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 2026-02-14 02:01:25 10
ProDom
 
Resource Report
Resource Website
100+ mentions
ProDom (RRID:SCR_006969) ProDom data analysis service, analysis service resource, data or information resource, production service resource, service resource, database 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
‘Programme de Bio-Informatique InterOrganismes ;
Re´seau des Ge´nopoles ;
European Union
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 2026-02-14 02:01:19 352
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 2026-02-14 02:01:15 11
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 2026-02-14 02:01:24 13
ArtificialFastqGenerator
 
Resource Report
Resource Website
10+ mentions
ArtificialFastqGenerator (RRID:SCR_006880) ArtificialFastqGenerator software resource Software to evaluate and improve the accuracy of sequencing error under different experimental conditions. It can identify which components of a system may be suboptimal and which regions of the genome may be problematic. matlab, java, Next Generation Sequencing, aligns reads, reference genome is listed by: OMICtools
is listed by: Debian
PMID:23152858 GNU GPL v3 OMICS_00248, SCR_015979 https://sources.debian.org/src/artfastqgenerator/ SCR_006880 Artfastqgenerator - Ouputs artificial FASTQ files derived from a reference genome 2026-02-14 02:01:24 10
BarraCUDA
 
Resource Report
Resource Website
1+ mentions
BarraCUDA (RRID:SCR_006881) BarraCUDA software resource A sequence mapping software that utilizes the massive parallelism of graphics processing units to accelerate the inexact alignment of short sequence reads to a particular location on a reference genome. It can align a paired-end library containing 14 million pairs of 76bp reads to the Human genome in about 27 minutes (from fastq files to SAM alignment) using a ��380 NVIDIA Geforce GTX 680*. The alignment throughput can be boosted further by using multiple GPUs (up to 8) at the same time. Being based on BWA (http://bio-bwa.sf.net) from the Sanger Institute, BarraCUDA delivers a high level of alignment fidelity and is comparable to other mainstream alignment programs. It can perform gapped alignment with gap extensions, in order to minimise the number of false variant calls in re-sequencing studies. gpu/cuda, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Cambridge; Cambridge; United Kingdom
has parent organization: SourceForge
PMID:22244497
PMID:19451168
Acknowledgement requested OMICS_00650, biotools:barracuda https://bio.tools/barracuda SCR_006881 2026-02-14 02:01:17 4
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 2026-02-14 02:01:25 204
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 2026-02-14 02:01:26 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 2026-02-14 02:01:18 2
SimSeq
 
Resource Report
Resource Website
10+ mentions
SimSeq (RRID:SCR_006947) SimSeq software resource, simulation software, software application 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 2026-02-14 02:01:26 29
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 repository, storage service resource, data or information resource, service resource, database 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 2026-02-14 02:01:28 48

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