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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 Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
TASSEL
 
Resource Report
Resource Website
1000+ mentions
TASSEL (RRID:SCR_012837) TASSEL software application, software resource Software package which performs a variety of genetic analyses including association mapping, diversity estimation and calculating linkage disequilibrium. The association analysis between genotypes and phenotypes can be performed by either a general linear model or a mixed linear model. The general linear model now allows users to analyze complex field designs, environmental interactions, and epistatic interactions. The mixed model is specially designed to handle polygenic effects at multiple levels of relatedness including pedigree information. These new analyses should permit association analysis in a wide range plant and animal species. (entry from Genetic Analysis Software) gene, genetic, genomic, java, web-based, bio.tools is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
nlx_154674, biotools:tassel http://sourceforge.net/projects/tassel/, https://bio.tools/tassel SCR_012837 and Linkage, Trait Analysis by aSSociation, Evolution 2026-09-12 01:02:48 2476
MCLEEPS
 
Resource Report
Resource Website
MCLEEPS (RRID:SCR_013062) software application, software resource Software application (entry from Genetic Analysis Software) gene, genetic, genomic, c++, unix, macos is listed by: Genetic Analysis Software nlx_154469 SCR_013062 Monte Carlo Likelihood Estimation of Effective Population Size PANGAEA 2026-09-12 01:02:48 0
UTIL
 
Resource Report
Resource Website
1+ mentions
UTIL (RRID:SCR_009424) UTIL software application, software resource Software application (entry from Genetic Analysis Software) gene, genetic, genomic, pascal, ms-windows, linux is listed by: Genetic Analysis Software PMID:23546798 nlx_154685 SCR_009424 statistical genetics UTILity programs 2026-09-12 01:02:46 2
TREESELECT
 
Resource Report
Resource Website
1+ mentions
TREESELECT (RRID:SCR_009422) software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 6th,2023. Software package for inferring natural selection from unusual population differentiation between closely related populations. (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154682 SCR_009422 2026-09-12 01:02:46 4
DETONATE
 
Resource Report
Resource Website
1+ mentions
DETONATE (RRID:SCR_017035) DETONATE data analysis software, data processing software, sequence analysis software, software application, software resource Software tool to evaluate de novo transcriptome assemblies from RNA-Seq data. Consists of RSEM-EVAL and REF-EVAL packages. RSEM-EVAL is reference-free evaluation method. REF-EVAL is reference based and can be used to compare sets of any kinds of genomic sequences. evaluate, de novo, transcriptome, assembly, RNAseq, data, RSEM-EVAL, REF-EVAL, dataset, genomic, sequence, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: University of Wisconsin-Madison; Wisconsin; USA
NHGRI R01 HG005232;
NLM T15 LM007359
PMID:25608678 Free, Available for download, Freely available biotools:detonate https://bio.tools/detonate SCR_017035 DE novo TranscriptOme rNa-seq Assembly with or without the Truth Evaluation, DETONATE 2026-09-12 01:00:19 2
Illumina: HiSeq 1500 System
 
Resource Report
Resource Website
1+ mentions
Illumina: HiSeq 1500 System (RRID:SCR_018006) instrument resource High-throughput sequencing system. Support of instrument and supply reagents will be provided through February 28th, 2023. Other instruments that support same applications as HiSeq 1500 System are available. Use Sequencing Platform Comparison Tool to find the best instrument for your needs. Illumina, genomic, hardware, instrument, equipment, sequencer, sequencing Restricted https://raw.githubusercontent.com/SciCrunch/RRID-Instruments/main/PDF/SCR_018006.pdf https://support.illumina.com/content/dam/illumina-support/documents/documentation/system_documentation/hiseq1500/hiseq-1500-system-guide-15035788-03.pdf SCR_018006 HiSeq 1500 System 2026-09-12 12:58:56 1
CoronaVIR
 
Resource Report
Resource Website
1+ mentions
CoronaVIR (RRID:SCR_018338) data or information resource, disease-related portal, portal, topical portal Web based platform on COVID-19 to maintain predicted diagnostic, drug and vaccine candidates and computational resources on novel coronavirus SARS-CoV-2 and its resulting disease COVID-19. Provides collected and organized information from literature and other resources from internet, links to appropriate literature . Integrated multi-omics repository dedicated to current genomic, proteomic, diagnostic and therapeutic knowledge about coronaviruses. COVID-19, SARS-CoV-2, diagnostic, drug, candidate, computational resource. coronavirus, disease, literature, genomic, proteomic, data COVID-19 DOI:10.31219/osf.io/xegzu Free, Freely available SCR_018351 SCR_018338 2026-09-12 12:59:00 4
Blixem
 
Resource Report
Resource Website
1+ mentions
Blixem (RRID:SCR_015994) alignment software, data processing software, image analysis software, software application, software resource Software for sequence alignments that displays multiple match sequences aligned against a single genomic reference sequence. It can be used for manipulation, display and annotation of genomic data, to check the quality of an alignment, to find missing/misaligned sequence, and to identify splice sites and polyA sites. software, sequence, alignment, annotation, genomic, reference, data, display, manipulation, DNA is related to: SEQtools
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
NHGRI U54 HG00455;
Wellcome Trust Grant 098051
PMID:26801397 Free, Available for download SCR_015994 SEQtools Blixem 2026-09-12 12:58:34 2
Allen Brain Atlas
 
Resource Report
Resource Website
100+ mentions
Allen Brain Atlas (RRID:SCR_017001) atlas, data or information resource, portal, project portal Portal provides access to data and web based applications created for benefit of global research community by Allen Institute for Brain Science. Projects to ombine genomics with neuroanatomy by creating gene expression maps for mouse and human brain. Mouse Brain Atlas, Human Brain Atlas, Developing Mouse Brain Atlas, Developing Human Brain Atlas, Mouse Connectivity Atlas, Non-Human Primate Atlas, and Mouse Spinal Cord Atlas and three related projects Glioblastoma, Mouse Diversity, and Sleep data banks, are used to advance various fields of science especially in neurobiological diseases. genomic, data, neuroanatomy, gene, expression, map, mouse, human, brain, atlas, neurobiology is related to: Allen Software Development Kit
is related to: Common Cell Type Nomenclature
has parent organization: Allen Institute
has parent organization: Allen Institute for Brain Science
is parent organization of: Allen Mouse Brain Reference Atlas
is parent organization of: Allen Human Brain Atlas
is parent organization of: Allen Developing Mouse Brain Atlas
is parent organization of: Allen Mouse Brain Connectivity Atlas
is parent organization of: Allen Mouse Spinal Cord Atlas
is parent organization of: CellTax vignette
is parent organization of: Allen Brain Atlas expression map of Cre and other drivers
provides: ABA Mouse Brain: Atlas
works with: Transcriptomics Explorer
works with: Kinase Associated Neural Phospho Signaling
Free, Freely available SCR_017530 SCR_017001 Allen Brain Atlas, Brain Atlases, Allen Mouse Brain Atlas, The Allen Brain Atlas, Allen Human Brain Atlas 2026-09-12 12:58:47 237
OmicsSIMLA
 
Resource Report
Resource Website
1+ mentions
OmicsSIMLA (RRID:SCR_017011) simulation software, software application, software resource, software toolkit Software tool for generating multi omics data with disease status. Simulates genomics (SNPs and copy number variations), epigenomics ( whole genome bisulphite sequencing), transcriptomics ( RNA seq), and proteomics (normalized reverse phase protein array) data at the whole genome level. Available as desktop and web application version. multi, omics, data, simulator, disease, genomic, epigenomic, transcriptomic, proteomic, genome, sequencing, protein, RNA is listed by: OMICtools Ministry of Science and Technology in Taiwan DOI:10.1101/426510 Freely available, Available to download, Free OMICS_31363 SCR_017011 2026-09-12 12:58:47 1
Italian Institute for Genomic Medicine; Turin; Italy
 
Resource Report
Resource Website
Italian Institute for Genomic Medicine; Turin; Italy (RRID:SCR_017062) IIGM, HuGeF data or information resource, portal, topical portal Private research institute in Turin, Italy. Research programs in immunogenetics, functional genomics, genomic epidemiology, tumour diagnostic and prognostic biomarker research, epigenetic modifications in disease, quantitative biology and computational neuroscience. institute, private, research, human, genetic, genomic, epigenomic, immunogenetic, quantitative, biology, computational, neuroscience is parent organization of: HaTSPiL SCR_017062 2026-09-12 12:58:48 0
Genomic Ranges
 
Resource Report
Resource Website
1+ mentions
Genomic Ranges (RRID:SCR_017051) data analysis software, data processing software, software application, software resource, software toolkit Software R package for computing and annotating genomic ranges. Used for storing and manipulating genomic intervals and variables defined along genome. computing, annotating, genomic, range, storing, manipulating, interval, variable, bio.tools is listed by: Bioconductor
is listed by: Debian
is listed by: bio.tools
is related to: R Project for Statistical Computing
NHGRI P41 HG004059;
NHGRI U41 HG004059;
NHLBI R01 HL086601;
NHLBI R01 HL093076;
NHLBI R01 HL094635
PMID:23950696 Free, Available for download, Freely available biotools:genomicranges https://bio.tools/genomicranges SCR_017051 2026-09-12 12:58:47 2
Nuclear Hormone Receptor Scan
 
Resource Report
Resource Website
1+ mentions
Nuclear Hormone Receptor Scan (RRID:SCR_016975) NHR-scan analysis service resource, data access protocol, production service resource, service resource, software resource, web service Web interface for computational prediction of nuclear hormone receptor binding sites in genomic sequences. Flexible Hidden Markov Model framework to allow for variable spacing and orientation of half sites. Allows for parameter modifications. prediction, nuclear, hormone, receptor, binding, site, genomic, sequence, parameter, modification, analysis is listed by: OMICtools Canadian Institutes of Health Research ;
Pharmacia Corporation to the Center for Genomics and Bioinformatics
PMID:15563547 Free, Available, Acknowledgement requested OMICS_14042 SCR_016975 NHR-scan, NHR Scan, NHRScan, Nuclear Hormoe Receptor Scan 2026-09-12 12:58:46 5
Genome Institute of Singapore Scientific and Research Computing Core Facility
 
Resource Report
Resource Website
Genome Institute of Singapore Scientific and Research Computing Core Facility (RRID:SCR_017193) GIS Scientific and Research Computing access service resource, analysis service resource, core facility, data analysis service, production service resource, service resource, software resource Core provides research computing resources including bioinformatics, application development, data management and IT infrastructure to support next generation sequencing technologies, human genotyping, high throughput screening and computational biology researchers. bioinformatics, genomic, data, management, next, generation, sequencing, genotyping, analysis Open SCR_017193 Core Facility, GIS, Scientific & Research Computing, Scientific and Research Computing, Genome Institute of Singapore 2026-09-12 12:58:49 0
Montreal Clinical Research Bioinformatics Core Facility
 
Resource Report
Resource Website
Montreal Clinical Research Bioinformatics Core Facility (RRID:SCR_017176) IRCM BIF, BIF access service resource, analysis service resource, core facility, data analysis service, data or information resource, production service resource, service resource, training service resource Core to support scientists within and outside IRCM in analysis of biological and clinical data, in particular high throughput genomic data. Operating on collaborative basis and paid services. Provides assistance with Data analysis for RNA-Seq, ChIP-Seq, RIP-Seq, DNA methylation, DNA-Seq, targeted sequencing of rRNAs, microarrays, customized training courses. bioinformatics, genomic, omics, data, analysis, RNA-Seq, CHIP-Seq, RIP-Seq, DNA, methylation, DNA-Seq, rRNA, microarray Restricted SCR_017176 , Institute of Clinical Research of Montreal, IRCM, Bioinformatics Core Facility, BIF 2026-09-12 12:58:49 0
RepeatFiller
 
Resource Report
Resource Website
10+ mentions
RepeatFiller (RRID:SCR_017414) alignment software, data processing software, image analysis software, software application, software resource Software tool to incorporate newly detected repeat overlapping alignments into pairwise alignment chains. It only aligns local genomic regions that are bounded by colinear aligning blocks, as provided in chains, which makes it feasible to consider all seeds including those that overlap repetitive regions. Used to improve genome alignments by incorporating previously undetected local alignments between repetitive sequences. Repeat, overlapping, alignment, pairwise, chain, local, genomic, region, colinear, block, sequence, undetected, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: Max Planck Institute of Molecular Cell Biology and Genetics; Dresden; Germany
DOI:10.1101/696922 Free, Freely available biotools:RepeatFiller, BioTools:RepeatFiller https://bio.tools/RepeatFiller, https://bio.tools/RepeatFiller, https://bio.tools/RepeatFiller SCR_017414 2026-09-12 12:58:52 16
GCE
 
Resource Report
Resource Website
10+ mentions
GCE (RRID:SCR_017332) data analysis software, data processing software, software application, software resource Software tool for estimation of genomic characteristics by analyzing k-mer frequency in de novo genome projects. Used as general and assembly independent method for estimating genomic characteristics. estimation, genomic, characteristic, analysis, k-mer, frequencey, de novo ftp://ftp.genomics.org.cn/pub/gce SCR_017332 Genomic Characteristics Estimation 2026-09-12 12:58:51 15
4D Genome
 
Resource Report
Resource Website
10+ mentions
4D Genome (RRID:SCR_017489) data or information resource, data repository, database, service resource, storage service resource Repository for chromatin interaction data. Records can be queried by genomic regions, gene names, organism, and detection technology. Database is continuously updated by curators. Contributions from scientific community. Repository, chromatic, interaction, data, genomic, region, gene, name, detection, technology, curated has parent organization: University of Pennsylvania; Philadelphia; USA Free, Available for download, Freely available r3d100012282 https://doi.org/10.17616/R3SH37 SCR_017489 2026-09-12 12:58:53 11
AmoebaDB
 
Resource Report
Resource Website
1+ mentions
AmoebaDB (RRID:SCR_017592) analysis service resource, data or information resource, database, production service resource, service resource Integrated genomic and functional genomic database for Entamoeba and Acanthamoeba parasites. Contains genomes of three Entamoeba species and microarray expression data for E. histolytica. Integrates whole genome sequence and annotation and includes experimental data and environmental isolate sequences provided by community researchers. Genomic, functional, database, Entamoeba, Acanthamoeba, parasite, microarray, expression, data, experimental, isolate, sequence, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: Eukaryotic Pathogen Database Resources
Department of Health and Human Services ;
NIDA ;
NIH
PMID:20974635 Free, Freely available biotools:amoebadb, r3d100012457 https://bio.tools/amoebadb, https://doi.org/10.17616/R3PX9Q SCR_017592 2026-09-12 12:58:54 8
Starbase V2.0
 
Resource Report
Resource Website
1000+ mentions
Starbase V2.0 (RRID:SCR_016303) software resource, web application Web based tool to visualize, analyze, discover and download of large-scale functional genomics data. Used for analysis of the CLIP-Seq and Degradome-Seq data sets, exploration of miRNA–target interactions and decoding RNA interaction networks from CLIP-Seq (HITS-CLIP, PAR-CLIP, iCLIP, CLASH) data. To show RNA-RNA and protein-RNA interaction networks in developmental, physiological and pathological processes. visualize, analyze, discover, download, large, genomic, data, set, miRNA, RNA-RNA, protein-RNA, interaction, network, decoding, CLIP-Seq, Degradome-Seq Ministry of Science and Technology of China ;
National Basic Research Program No. 2011CB811300
PMID:24297251 Free, Freely available, Available for download SCR_016303 2026-09-12 12:58:37 1004

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