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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
BinPacker
 
Resource Report
Resource Website
10+ mentions
BinPacker (RRID:SCR_017038) software application, software resource, data analysis software, data processing software Software tool as de novo trascriptome assembler for RNA-Seq data. Used to assemble full length transcripts by remodeling problem as tracking set of trajectories of items over splicing graph. Input RNA-Seq reads in fasta or fastq format, and ouput all assembled candidate transcripts in fasta format. Operating system Unix/Linux. de novo, transcriptome, assembler, RNAseq, data, full, length, transcript, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
National Natural Science Foundation of China ;
NSF 1553680;
NCRR P20 RR01 6460;
NIGMS P20 GM103429
PMID:26894997 Free, Available for download, Freely available OMICS_11199, biotools:binpacker http://sourceforge.net/projects/transcriptomeassembly/files/BinPacker_1.0.tar.gz/download, http://sourceforge.net/projects/transcriptomeassembly/files/BinPacker_binary.tar.gz/download, https://bio.tools/binpacker SCR_017038 2026-07-28 09:44:30 10
MITE-Tracker
 
Resource Report
Resource Website
1+ mentions
MITE-Tracker (RRID:SCR_017030) MITE Tracker software application, data analysis software, sequence analysis software, software resource, data processing software Open source software tool for identifying miniature inverted repeat transposable elements in large genomes. Used to process large scale genomes, to find and classify MITEs using an efficient alignment strategy to retrieve nearby inverted repeat sequences. genomic, sequence, discover, miniature, inverted, repeat, transposable, element, clustering, cdhit uses: NCBI BLAST
is listed by: OMICtools
is related to: Python Programming Language
National Institute of Agricultural Technology ;
National Council for Science and Technology ;
Argentina
DOI:10.1186/s12859-018-2376-y Free, Available for download, Freely available OMICS_32242 SCR_017030 MITE Tracker, Miniature Inverted repeats Transposable Elements Tracker 2026-07-28 09:44:28 3
SwiftOrtho
 
Resource Report
Resource Website
1+ mentions
SwiftOrtho (RRID:SCR_017122) software application, software resource, data analysis software, data processing software Software tool for orthology analysis to identify orthologs, paralogs and co orthologs for genomes. Used to perform homology classification across genomes of different species in large genomic datasets. orthology, analysis, identify, ortholog, paralog, co ortholog, genome, homology, different, species, large, dataset, bio.tools uses: Python Programming Language
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
DOI:10.1101/543223 Free, Available for download, Freely available OMICS_30890, biotools:SwiftOrtho https://bio.tools/SwiftOrtho SCR_017122 2026-07-28 09:44:31 4
ClustVis
 
Resource Report
Resource Website
500+ mentions
Issue
ClustVis (RRID:SCR_017133) service resource, data analysis service, data access protocol, software resource, production service resource, web service, analysis service resource Web user interface for visualizing clustering of multivariate data. Web server allows users to upload their own data and create Principal Component Analysis plots and heatmaps. visualizing, clustering, multivariate, data, principal, component, analysis, plot, heatmap, bio.tools uses: Shiny
uses: ggplot2
uses: pheatmap
uses: RColorBrewer
uses: FactoMineR
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: R Project for Statistical Computing
has parent organization: University of Tartu; Tartu; Estonia
Innovative Medicines Initiative Joint Undertaking ;
European Union Seventh Framework Programme ;
European Federation of Pharmaceutical Industries and Associations ;
European Regional Development Fund ;
Estonian Research Council ;
European Commission ;
EFPIA
PMID:25969447 biotools:clustvis, OMICS_08539 https://github.com/taunometsalu/ClustVis, https://bio.tools/clustvis SCR_017133 2026-07-28 09:44:31 798
PRSice
 
Resource Report
Resource Website
50+ mentions
PRSice (RRID:SCR_017057) software application, software resource, data analysis software, data processing software Software R package for calculating, applying, evaluating and plotting results of polygenic risk scores analysis. Performs simulation study to estimate P value significance threshold for high resolution PRS studies and produces plots for inspection of results. Operating Unix/Linux. polygenic, risk, score, calculating, applying, plotting, result, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: R Project for Statistical Computing
EU ;
NIHR Biomedical Research Centre
PMID:25550326 Free, Available for download, Freely available OMICS_23656, biotools:prsice https://choishingwan.github.io/PRSice/, https://bio.tools/prsice SCR_017057 prsice, PRSice-2, Polygenic Risk Score software, PRSice1, PRSice2 2026-07-28 09:44:26 97
CentroidFold
 
Resource Report
Resource Website
10+ mentions
CentroidFold (RRID:SCR_017253) software application, data access protocol, software resource, web service, simulation software Web server for RNA secondary structure prediction. Predicts RNA secondary structure from RNA sequence. Based on generalized centroid estimator. RNA, secondary, structure, prediction, centroid, estimator, sequecne, data, alignment, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
New Energy and Industrial Technology Development Organization of Japan ;
Ministry of Education ;
Culture ;
Sports ;
Science and Technology of Japan ;
Internal fund of Computational Biology Research Center
PMID:19435882 Free, Freely available biotools:centroidfold, OMICS_03449 https://bio.tools/centroidfold SCR_017253 2026-07-28 09:44:28 15
WTDBG
 
Resource Report
Resource Website
50+ mentions
WTDBG (RRID:SCR_017225) software application, data analysis software, sequence analysis software, software resource, data processing software, alignment software, image analysis software Software tool as de novo sequence assembler for long noisy reads produced by PacBio or Oxford Nanopore Technologies. It assembles raw reads without error correction and then builds consensus from intermediate assembly output. Desiged to assemble huge genomes in very limited time. sequence, assembler, de novo, long, noisy, read, likelihood, estimator, genome is listed by: OMICtools
is listed by: Debian
NSFC ;
NHGRI R01 HG010040
PMID:31819265 Free, Available for download, Freely available OMICS_24025 https://github.com/ruanjue/wtdbg, https://sources.debian.org/src/wtdbg2/ SCR_017225 Wtdbg2, wtdgb, Wtdgb, wtdgb2 2026-07-28 09:44:32 57
prank
 
Resource Report
Resource Website
100+ mentions
prank (RRID:SCR_017228) software application, software toolkit, software resource, data processing software, alignment software, image analysis software Software application as probabilistic multiple alignment program for DNA, codon and amino-acid sequences. Allows for defining potential structure for sequences to be aligned and then, simultaneously with the alignment, predicts the locations of structural units in the sequences. multiple, nucleotide, sequence, alignment, DNA, codon, amino acid, phylogenetic, gap, predict, location, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: University of Helsinki; Helsinki; Finland
PMID:24170401
PMID:21110866
Free, Available for download, Freely available biotools:prank, SCR_024174, OMICS_12425 https://www.ebi.ac.uk/goldman-srv/webprank/, https://ariloytynoja.github.io/prank-msa/, https://bio.tools/prank https://omictools.com/prank-tool SCR_017228 PRANK 2026-07-28 09:44:32 253
Computational Suite for Bioinformaticians and Biologists
 
Resource Report
Resource Website
1+ mentions
Computational Suite for Bioinformaticians and Biologists (RRID:SCR_017234) CSBB software application, software resource, data analysis software, data processing software Software package for analysis of sequencing data. Command line based bioinformatics suite to analyze biological data acquired through biological experiments. analysis, sequencing, data, command, line, expression, normalization, convert is listed by: OMICtools Free, Available for download, Freely available OMICS_17554 https://github.com/csbbcompbio SCR_017234 CSBB-v3.0, CSBB-v1.0, CSBB-v2.0, Computational Suite for Bioinformaticians and Biologists 2026-07-28 09:44:32 6
PILER
 
Resource Report
Resource Website
10+ mentions
PILER (RRID:SCR_017333) software application, software resource, data analysis software, data processing software Software tool for analyzing repetitive DNA found in genome sequences. Software package for identification and classification of genomic repeats. Used for identifying patterns of local alignments induced by certain classes of repeats. analysis, repetitive, DNA, genome, sequence, classification, alignment is listed by: OMICtools PMID:15961452 Free, Available for download, Freely available https://omictools.com/piler-tool SCR_017333 2026-07-28 09:44:33 15
Phangorn
 
Resource Report
Resource Website
10+ mentions
Phangorn (RRID:SCR_017302) software application, data analysis software, software resource, data processing software, data visualization software, software toolkit Software R package for phylogenetic reconstruction and analysis. Used for estimation of phylogenetic trees and networks using Maximum Likelihood, Maximum Parsimony, distance methods and Hadamard conjugation. Allows to compare trees, models selection and offers visualizations for trees and split networks. phylogenetic, tree, network, reconstruction, analysis, estimation, Maximum, Likelihood, Parsimony, distance, method, Hadamard conjugation is listed by: Debian
is listed by: OMICtools
is related to: CRAN
Muséum National D Histoire Naturelle DOI:10.1093/bioinformatics/btq706 Free, Available for download, Freely available OMICS_12497 https://github.com/KlausVigo/phangorn, https://sources.debian.org/src/r-cran-phangorn/ SCR_017302 Phangorn R package 2026-07-28 09:44:33 24
BioAssay Express
 
Resource Report
Resource Website
BioAssay Express (RRID:SCR_017594) service resource, software resource, data access protocol, web service Web based tool for annotating bioassay protocols using semantic web terms. Enables searching, sorting, clustering and analyzing of assays without needing to read through original text. Exploits Common Assay Template based on underlying vocabularies and semantic standards from BioAssay Ontology, Drug Target Ontology, Cell Line Ontology and others. Users can identify similar assays and examine similarity of assays between and within organizations. Annotating, bioassay, protocol, semantic, web, term, ontology is listed by: OMICtools NCATS R44 TR000185 DOI:10.7717/peerj-cs.61 Free, Freely available https://github.com/cdd/bioassay-template SCR_017594 2026-07-28 09:44:35 0
GADMA
 
Resource Report
Resource Website
1+ mentions
GADMA (RRID:SCR_017680) GADMA software application, software resource, data analysis software, data processing software Software tool to implement methods for automatic inferring joint demographic history of multiple populations from genetic data. Genetic algorithm for inferring demographic history of multiple populations from allele frequency spectrum data. Inferring, demographic, history, population, genetic, data, allele, frequency, spectrum, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
DOI:10.1101/407734 Free, Available for download, Freely available biotools:GADMA https://bio.tools/GADMA SCR_017680 Genetic Algorithm for Demographic Model Analysis 2026-07-28 09:44:32 3
GeneATLAS
 
Resource Report
Resource Website
100+ mentions
GeneATLAS (RRID:SCR_017577) service resource, data or information resource, data analysis service, database, atlas, production service resource, analysis service resource Database of associations between traits and variants using UK Biobank cohort. Searchable atlas of genetic associations. Assists researchers to query UK Biobank. Provides unbiased view of phenotype and genotype associations across of traits. Association, trait, variant, UK Biobank, cohort, atlas, genetic, phenotype, genotype, FASEB list is listed by: OMICtools
has parent organization: University of Edinburgh; Scotland; United Kingdom
Free, Available for download, Freely available SCR_017577 Gene ATLAS, Gene Atlas 2026-07-28 09:44:38 132
immuneXpresso
 
Resource Report
Resource Website
immuneXpresso (RRID:SCR_017578) software application, service resource, data or information resource, software resource, text-mining software Software tool as text-mining engine that structures and standardizes knowledge of immune intercellular communication. Knowledgebase contains interactions and separate mentions of cells or cytokines in context of thousands of diseases. Intercellular interactions were text-mined from all available PubMed abstracts across disease conditions. Structure, standardize, immune, cellular, interaction, cytokine, disease, cell, PubMed, abstract is listed by: NIDDK Information Network (dkNET)
is listed by: OMICtools
NIH ;
NIAID ;
Rappaport Family Institute for Research in the Medical Sciences
PMID:29912209 Free, Freely available SCR_017578 2026-07-28 09:44:35 0
American College of Medical Genetics and Genomics
 
Resource Report
Resource Website
50+ mentions
American College of Medical Genetics and Genomics (RRID:SCR_005769) ACMG data or information resource, organization portal, portal An organization composed of biochemical, clinical, cytogenetic, medical and molecular geneticists, genetic counselors and other health care professionals committed to the practice of medical genetics to Improve Health Through Medical Genetics. The American College of Medical Genetics and Genomics will: * Define and promote excellence in the practice of medical genetics and genomics in the integration of translational research into practice; * Promote and provide medical genetics and genomics education; * Increase access to medical genetics and genomics services and integrate them into patient care; * Advocate for and represent providers of medical genetics and genomics services and their patients; and * Maintain structure and integrity of ACMG and its value to members and the public. genetics, genomics, medical, biochemical, clinical, cytogenetic, molecular, geneticist, genetic counselor, health care professional, medical genetics is listed by: OMICtools PMID:21311339 OMICS_01775, nlx_149234 http://www.acmg.net SCR_005769 American College of Medical Genetics, ACMG - Translating Genes Into Health, American College of Medical Genetics Genomics 2026-07-28 09:41:30 50
Pedigree-Draw
 
Resource Report
Resource Website
1+ mentions
Pedigree-Draw (RRID:SCR_008302) software application, commercial organization, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on April 12,2024. Software application for pedigree drawing (entry from Genetic Analysis Software) gene, genetic, genomic, macos, bio.tools is listed by: Genetic Analysis Software
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: OMICtools
THIS RESOURCE IS NO LONGER IN SERVICE nlx_154520, OMICS_00213, SCR_010795 SCR_008302 PEDIGREE/DRAW 2026-07-28 09:42:04 1
Orphanet
 
Resource Report
Resource Website
100+ mentions
Orphanet (RRID:SCR_006628) Orphanet data or information resource, portal European website providing information about orphan drugs and rare diseases. It contains content both for physicians and for patients. Reference portal for rare diseases and orphan drugs to help improve diagnosis, care and treatment of patients with rare diseases. drug, clinical, diagnostic, test, rare, disease, molecule, gene, orphan, drug is used by: NIF Data Federation
is used by: HmtPhenome
is listed by: OMICtools
is related to: Disease core ontology applied to Rare Diseases
is related to: phenomeNET
has parent organization: National Institute of Health and Medical Research; Rennes; France
is parent organization of: Orphanet Rare Disease Ontology
National Institute of Health and Medical Research ;
Rennes ;
France ;
French Directorate General for Health ;
European Union
Free, Freely available nif-0000-21306, grid.458406.b, Wikidata: Q1515833 https://ror.org/03d3kf570 SCR_006628 2026-07-28 09:41:36 404
TransDecoder
 
Resource Report
Resource Website
1000+ mentions
TransDecoder (RRID:SCR_017647) software application, standalone software, software resource, data processing software Software tool to identify candidate coding regions within transcript sequences, such as those generated by de novo RNA-Seq transcript assembly using Trinity, or constructed based on RNA-Seq alignments to genome using Tophat and Cufflinks.Starts from FASTA or GFF file. Can scan and retain open reading frames (ORFs) for homology to known proteins by using BlastP or Pfam search and incorporate results into obtained selection. Predictions can then be visualized by using genome browser such as IGV. Identify, candidate, coding, region, transcript, sequence, de novo, RNAseq, assembly, alignment, genome, open, reading, frame, homology, protein, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
Free, Available for download, Freely available biotools:transDecoder, OMICS_10852 https://bio.tools/TransDecoder, https://sources.debian.org/src/transdecoder/, https://github.com/TransDecoder/TransDecoder/wiki SCR_017647 , Find Coding Regions Within Transcripts 2026-07-28 09:44:35 1309
NHGRI: Establishing a Central Resource of Data from Genome Sequencing Projects
 
Resource Report
Resource Website
NHGRI: Establishing a Central Resource of Data from Genome Sequencing Projects (RRID:SCR_003205) NHGRI: Establishing a Central Resource of Data from Genome Sequencing Projects project portal, data or information resource, portal THIS RESOURCE IS NO LONGER IN SERVICE. Documented on October 30,2025. 2012 workshop to establish a Central Resource of Data from Genome Sequencing Projects. The workshop addressed the challenges to aggregating and analyzing data sets from genome sequencing studies, such as: * Data sets being generally hard to access. * Data residing in various databases. * Variant and exposure/phenotype data not being comparable across studies. Participants in the workshop discussed options for dealing with these challenges, along with their costs and tradeoffs. Videos and accompanying slides from the workshop are available. Also available as a video playlist on GenomeTV genome, sequencing is listed by: OMICtools
has parent organization: National Human Genome Research Institute
THIS RESOURCE IS NO LONGER IN SERVICE SCR_003205 2026-07-28 09:40:38 0

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