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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
MiTCR
 
Resource Report
Resource Website
10+ mentions
MiTCR (RRID:SCR_004989) MiTCR software resource An open source software package aimed at extraction of information on repertoire of T-cell clones from Next Generation Sequencing (NGS) data. It is designed with the knowledge of the critical challenges arising in everyday processing of immunological data. next generation sequencing is listed by: OMICtools PMID:23892897 Apache License OMICS_00003 SCR_004989 MiTCR - T-cell receptor repertoire analysis software 2026-08-15 11:23:04 37
MIP Scaffolder
 
Resource Report
Resource Website
1+ mentions
MIP Scaffolder (RRID:SCR_005072) MIP Scaffolder software resource A software program for scaffolding contigs produced by fragment assemblers using mate pair data such as those generated by ABI SOLiD or Illumina Genome Analyzer. scaffolding, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Helsinki; Helsinki; Finland
OMICS_00044, biotools:mip_scaffolder https://bio.tools/mip_scaffolder SCR_005072 2026-08-15 11:22:58 1
Scarpa
 
Resource Report
Resource Website
10+ mentions
Scarpa (RRID:SCR_005073) Scarpa software resource A stand-alone scaffolding tool for NGS data. It can be used together with virtually any genome assembler and any NGS read mapper that supports SAM format. Other features include support for multiple libraries and an option to estimate insert size distributions from data. scaffolding is listed by: OMICtools
has parent organization: University of Toronto; Ontario; Canada
PMID:23274213 GNU General Public License OMICS_00047 SCR_005073 SCARPA: scaffolding reads with practical algorithms, Scaffolding Reads with Practical Algorithms 2026-08-15 11:23:06 13
NIH Neuroscience Microarray Consortium
 
Resource Report
Resource Website
1+ mentions
NIH Neuroscience Microarray Consortium (RRID:SCR_004930) database, production service resource, data repository, storage service resource, data analysis service, data or information resource, service resource, analysis service resource THIS RESOURCE IS NO LONGER IN SERVICE, documented on April 24, 2012. (no longer being funded) The NIH Microarray Consortium provides for-fee services to a community of NIH grantees, together with a more limited set of services to the public. The primary goal of this consortium is to move basic and translational research forward through acquisition and dissemination of high quality genomic data. This site includes a repository of microarray data sets and offers one-click links to public projects. These datasets were generated by various researchers on these platforms: Affymetrix, Agilent, Ambion, cDNA, Illumina, and Operon. The species currently covered are: Arabidopsis, Bovine, chicken, C. Elegans, Drosophila, Human, Macaca mulatta (Rhesus macaque), Mouse, Rat, Songbird, Xenopus, Yeast, and zebra finch. Basic search functions allows users to choose multiple options for finding the projects that interest them, and raw data files can also be downloaded after user registration. Web-based data analysis tools are also available. Scientists can analyze microarray data from the consortium repository or investigators can upload outside data for analysis. arabidopsis, bos taurus, chicken, caenorhabditis elegans, drosophila, human, rhesus monkey, mouse, rat, songbird, xenopus, yeast, zebra finch is used by: NIF Data Federation
is related to: Songbird Brain Transcriptome Database
has parent organization: National Institutes of Health
NIH Blueprint for Neuroscience Research THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-00074 http://arrayconsortium.tgen.org, http://np2.ctrl.ucla.edu/np2/home.do SCR_004930 NIH Neuroscience Microarray Consortium 2026-08-15 11:22:55 4
German Federal Ministry of Education and Research
 
Resource Report
Resource Website
100+ mentions
German Federal Ministry of Education and Research (RRID:SCR_005066) BMBF government granting agency SCR_005066 Bundesministerium für Bildung und Forschung, Federal Ministry of Education and Research, Federal Ministry of Education and Research (Germany) 2026-08-15 11:23:06 137
Alzheimer's and Dementia Resource Center
 
Resource Report
Resource Website
100+ mentions
Alzheimer's and Dementia Resource Center (RRID:SCR_004924) ADRC biomaterial supply resource, tissue bank, material resource, brain bank The Alzheimer's and Dementia Resource Center (ADRC) facilitates tissue donations for the Brain Bank Research Program in order to help find better treatments, more diagnostic tools and a cure for Alzheimer's disease and dementia. The Brain Bank Program is administered by Mount Sinai Medical Center in Miami Beach and under contract with the Florida Department of Elder Affairs. ADRC also provides caregivers with the educational resources, spiritual comfort and emotional support. The ADRC facilitates training for professional caregivers that meets requirements for the Florida Department of Elder Affairs. alzheimer's disease, dementia, brain, tissue, brain bank, caregiver, educational resource, patient support is listed by: One Mind Biospecimen Bank Listing Alzheimer's disease, Dementia Public, Registration and pre-registration required to access the brain bank nlx_143948 SCR_004924 alzheimer's disease, tissue, brain, patient support, educational resource, caregiver, dementia, brain bank 2026-08-15 11:23:07 421
PhenomeBLAST Ontology
 
Resource Report
Resource Website
1+ mentions
PhenomeBLAST Ontology (RRID:SCR_005139) PHENOMEBLAST ontology, data or information resource, controlled vocabulary A cross-species phenotype and anatomy ontology resulting from combining available anatomy and phenotype ontologies and their definitions. The ontology includes phenotype definitions for yeast, mouse, fish, worm, fly and human phenotypes and diseases. owl is listed by: BioPortal nlx_157549 SCR_005139 2026-08-15 11:23:08 1
T-lex
 
Resource Report
Resource Website
1+ mentions
T-lex (RRID:SCR_005134) T-lex software resource Software package for fast and accurate discovery, annotation, re-annotation and population analysis of Transposable Elements using Next-Generation Sequencing data. transposable element, next-generation sequencing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Stanford University; Stanford; California
has parent organization: SourceForge
GNU General Public License biotools:t-lex2, OMICS_00121 https://bio.tools/t-lex2 SCR_005134 T-lex package 2026-08-15 11:23:08 4
PoPoolation TE
 
Resource Report
Resource Website
1+ mentions
PoPoolation TE (RRID:SCR_005131) PoPoolation TE software resource A quick and simple pipeline for the analysis of transposable element (TE) insertions in (natural) populations using next generation sequencing. It calculates TE insertion frequencies for TEs that are present in the reference genome as well as for novel TE insertions. PoPoolation TE requires paired-end reads from a pooled population, a reference sequence and transposable element sequences (fasta-file). next generation sequencing, transposable element, insertion frequency, genomics, population genetics, illumina is listed by: OMICtools
has parent organization: Google Code
PMID:22291611 Acknowledgement requested, New BSD License OMICS_00119 SCR_005131 2026-08-15 11:23:08 1
Alfred P. Sloan Foundation
 
Resource Report
Resource Website
50+ mentions
Alfred P. Sloan Foundation (RRID:SCR_005099) Sloan Foundation institution The Alfred P. Sloan Foundation is a philanthropic, not-for-profit grantmaking institution based in New York City. Established in 1934 by Alfred Pritchard Sloan Jr., then-President and Chief Executive Officer of the General Motors Corporation, the Foundation makes grants in support of original research and education in science, technology, engineering, mathematics and economic performance. * Promotes research in science, technology, engineering, mathematics, and economic performance * Offers two-year long research fellowships for early career researchers grant, fellowship is related to: MIT Center for Biomedical Innovation
is parent organization of: Datahub
grid.453006.4, Crossref funder ID: 100000879, ISNI: 0000 0004 0508 3060, nlx_144112 https://ror.org/052csg198 SCR_005099 2026-08-15 11:22:59 56
Eurexpress
 
Resource Report
Resource Website
1+ mentions
Eurexpress (RRID:SCR_005093) Eurexpress database, expression atlas, data or information resource, image collection, atlas Genome transcriptome atlas by RNA in situ hybridization on sagittal sections of developing mouse at embryonic day 14.5. Consists of searchable database of annotated images that can be interactively viewed. Anatomy based expression profiles for coding genes and microRNAs, tissue specific genes. Expression data generated by using human and murine tissue arrays. Genome, transcriptome, atlas, RNA, in situ, hybrydization, sagittal, section, developing, mouse, embryo, expression, gene is listed by: GUDMAP Ontology
is listed by: NIDDK Information Network (dkNET)
is related to: EMAGE Gene Expression Database
is related to: aGEM
has parent organization: Telethon Institute of Genetics and Medicine; Naples; Italy
European Union ;
VI Framework ;
Telethon Foundation ;
Swiss National Science Foundation ;
Max Planck Society ;
MRC ;
Association pour la Recherche sur le Cancer ;
Ingenio 2010 MEuropean Union
PMID:21267068 nif-0000-00243 http://www.eurexpress.org/ee/databases/anatomy/treeFrames.jsp, http://www.eurexpress.org/ee/ SCR_005093 Eurexpress atlas, Transcriptome Atlas Database for Mouse Embryo 2026-08-15 11:23:12 3
BEERS
 
Resource Report
Resource Website
10+ mentions
BEERS (RRID:SCR_005090) BEERS software resource A simulation engine for generating RNA-Seq data that was designed to benchmark RNA-Seq alignment algorithms and also algorithms that aim to reconstruct different isoforms and alternate splicing from RNA-Seq data. By default BEERS simulates either mouse or human paired-end RNA-Seq data modeled on the illumina platform. It starts with a large number of gene models (approx 500K) taken from about ten different published annotation efforts, and then chooses a fixed number of these genes at random (30,000 by default). This avoids biasing for or against any particular set of annotations. BEERS then introduces substitutions, indels, alternate spice forms, sequencing errors, and intron signal. BEERS can also simulate strand specific reads. BEERS does not simulate quality scores. There are four configuration files required, these are available for human and mouse. BEERS can also be configured to use any set of gene models. Pre-built indexes for human refseq are given. Using these indexes will generate a much tamer set of transcripts. BEERS is written in perl. perl, rna-seq is listed by: OMICtools
has parent organization: University of Pennsylvania Perelman School of Medicine; Pennsylvania; USA
PMID:21775302 OMICS_01364 SCR_005090 Benchmarker for Evaluating the Effectiveness of RNA-Seq Software (BEERS), Benchmarker for Evaluating the Effectiveness of RNA-Seq Software 2026-08-15 11:22:58 22
University of Kiel; Schleswig-Holstein; Germany
 
Resource Report
Resource Website
1+ mentions
University of Kiel; Schleswig-Holstein; Germany (RRID:SCR_005127) CAU university A university in Germany. is related to: READNA
is parent organization of: Transgenic Hydra Facility
nlx_59306, Crossref funder ID:501100002869, ISNI:0000 0001 2153 9986, Wikidata:Q156737, grid.9764.c https://ror.org/04v76ef78 SCR_005127 Christian-Albrechts-Universitat zu Kiel, Christian Albrechts University, University of Kiel, Christian-Albrechts-Universit�t zu Kiel, Kiel University 2026-08-15 11:23:12 1
Scientific American
 
Resource Report
Resource Website
1+ mentions
Scientific American (RRID:SCR_005243) SA organization portal, data or information resource, portal, narrative resource Scientific American, the oldest continuously published magazine in the U.S., has been bringing its readers unique insights about developments in science and technology for more than 160 years. It is the leading source and authority for science, technology information and policy for a general audience. In an era of rapid innovation, Scientific American founded the first branch of the U.S. Patent Agency, in 1850, to provide technical help and legal advice to inventors. A Washington, D.C., branch was added in 1859. By 1900 more than 100,000 inventions had been patented thanks to Scientific American. * Read in print by 3.5 million worldwide consumers * On average, 2.7 million unique users visit ScientificAmerican.com every month * 14 local language editions worldwide, including the U.S. edition of Scientific American, read in more than 30 countries, with a worldwide audience of more than 5 million people * A third of Scientific American readers hold postgraduate degrees * 144 Nobel Prize Scientists have contributed 234 articles to Scientific American * Part of Macmillan Publishers, owned by Holtzbrinck Group of companies; acquired by Holtzbrinck in 1986 * Three Scientific American features in the Federal Record * Scientific American won the 2011 National Magazine Award for General Excellence. science, technology, information, policy, magazine uses: InnoCentive
is parent organization of: Scientific American Cross-Check
is parent organization of: Scientific American Guest Blog
is parent organization of: Scientific American Observations
is parent organization of: Scientific American Bering in Mind
nlx_144246 SCR_005243 2026-08-15 11:23:01 7
ERANGE
 
Resource Report
Resource Website
10+ mentions
ERANGE (RRID:SCR_005240) ERANGE software resource Software for Mapping and Quantifying Mammalian Transcriptomes by RNA-Seq. Its functions are to (i) assign reads that map uniquely in the genome to their site of origin and, for reads that match equally well to several sites (''multireads''), assign them to their most likely site(s) of origin; (ii) detect splice-crossing reads and assign them to their gene of origin; (iii) organize reads that cluster together, but do not map to an already known exon, into candidate exons or parts of exons; and (iv) calculate the prevalence of transcripts from each known or newly proposed RNA, based on normalized counts of unique reads, spliced reads and multireads. The new candidate RNA regions produced can be thought of as ESTs, and, like ESTs, some are provisionally appended to existing gene models if they meet several additional criteria. Remaining unassigned candidate transcribed regions (labeled RNAFAR features) can then be used in conjunction with other confirming data to develop new or revised gene models. transcriptome, rna-seq, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:18516045 OMICS_01274, biotools:erange https://bio.tools/erange SCR_005240 Enhanced Read Analysis of Gene Expression 2026-08-15 11:23:01 30
RNA-SeQC
 
Resource Report
Resource Website
100+ mentions
RNA-SeQC (RRID:SCR_005120) RNA-SeQC software resource Java software which computes a series of quality control metrics for RNA-seq data and can compare sequencing quality across different samples or experiments to evaluate different experimental parameters. The input can be one or more BAM files, and the output consists of HTML reports and tab delimited files of metrics data. java, bam file, html, sequence comparison, rnaseq, rna sequence, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Broad Institute
PMID:22539670 Acknowledgement requested, Public biotools:rna-seqc, OMICS_01234 https://bio.tools/rna-seqc SCR_005120 2026-08-15 11:23:12 214
Flux Simulator
 
Resource Report
Resource Website
1+ mentions
Flux Simulator (RRID:SCR_005088) Flux Simulator software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 5, 2023. Software that aims at modeling RNA-Seq experiments in silico: sequencing reads are produced from a reference genome according annotated transcripts. The simulation pipeline models different steps as modules, each with a minimal set of parameters that can be estimated by experimental parameters. The first step is-in fact-a transcriptome simulator. Subsequently, common sources of systematic bias in the abundance and distribution of produced reads are simulated by in silico library preparation and sequencing. is listed by: OMICtools THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01365 SCR_005088 2026-08-15 11:23:07 2
jobs.ac.uk
 
Resource Report
Resource Website
1+ mentions
jobs.ac.uk (RRID:SCR_005154) jobs.ac.uk job resource International job board for careers in academic, research, science and related professions in the UK, Europe, Australasia, Africa, America and Asia & Middle East. Launched by the University of Warwick, they have grown to become the top recruitment site in their sector, attracting the most qualified and talented people from the UK, Europe and across the world. Users may subscribe to Jobs by Email for vacancies in universities, colleges, research institutions, commercial and public sector, schools and charities. You may upload your CV to give yourself an advantage by making your CV visible to top employers now! job seeker, employer, career, curriculum vitae, recruit, employment, database, data storage repository is used by: NIF Data Federation
is listed by: OMICtools
is related to: Integrated Jobs
has parent organization: University of Warwick; Coventry; United Kingdom
The community can contribute to this resource OMICS_01829, nlx_144167 SCR_005154 2026-08-15 11:23:09 3
PANTHER Evolutionary analysis of coding SNPs
 
Resource Report
Resource Website
100+ mentions
PANTHER Evolutionary analysis of coding SNPs (RRID:SCR_005145) cSNP Scoring production service resource, data processing software, data analysis service, software application, data analysis software, software resource, service resource, analysis service resource Data analysis service that estimates the likelihood of a particular nonsynonymous (amino-acid changing) coding SNP to cause a functional impact on the protein. To analyze many SNPs, download the PANTHER Coding Snp Analysis tool from the downloads page. is listed by: OMICtools
has parent organization: PANTHER
PMID:23193289 OMICS_00135 SCR_005145 Evolutionary analysis of coding SNPs, PANTHER Coding SNP Analysis Tool 2026-08-15 11:23:12 104
Project HOPE
 
Resource Report
Resource Website
10+ mentions
Project HOPE (RRID:SCR_005141) HOPE production service resource, data analysis service, software resource, source code, service resource, analysis service resource An easy-to-use webserver that analyses the structural effects of your mutation of interest. The server allows you to submit a protein sequence and the mutation. Project HOPE will then collect and combine available information from a series of webservers and databases and will produce a mutation report complete with results, figures and animations. Where available Project HOPE will use the 3D structure of the protein but the server can also build a homology model if necessary. Other information sources include the Uniprot database and a series of DAS prediction servers., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. protein structure, mutation is listed by: OMICtools
has parent organization: Radboud University; Nijmegen; The Netherlands
Inheritable disease PMID:21059217 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00130 SCR_005141 Have yOur Protein Explained, GSITIC 2026-08-15 11:23:12 29

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