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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
MIRIAM Resources
 
Resource Report
Resource Website
1+ mentions
MIRIAM Resources (RRID:SCR_006697) web service, catalog, data or information resource, data access protocol, software resource, narrative resource, database, standard specification A set of online services created in support of MIRIAM, a set of guidelines for the annotation and curation of computational models. The core of MIRIAM Resources is a catalogue of data types (namespaces corresponding to controlled vocabularies or databases), their URIs and the corresponding physical URLs or resources. Access to this data is made available via exports (XML) and Web Services (SOAP). MIRIAM Resources are developed and maintained under the BioModels.net initiative, and are free for use by all. MIRIAM Resources are composed of four components: a database, some Web Services, a Java library and this web application. * Database: The core of the system is a MySQL database. It allows us to store the data types (which can be controlled vocabularies or databases), their URIs and the corresponding physical URLs, and other details such as documentation and resource identifier patterns. Each entry contains a diverse set of details about the data type: official name and synonyms, root URI, pattern of identifiers, documentation, etc. Moreover, each data type can be associated with several resources (or physical locations). * Web Services: Programmatic access to the data is available via Web Services (based on Apache Axis and SOAP messages). In addition, REST-based services are currently being developed. This API allows one to not only resolve model annotations, but also to generate appropriate URIs, based upon the provision of a resource name and accession number. A list of available web services, and a WSDL are provided. A browser-based online demonstration of the Web Services is also available to try. * Java Library: A Java library is provided to access the Web Services. The documentation explains where to download it, its dependencies, and how to use it. * Web Application: A Web application, using an Apache Tomcat server, offers access to the whole data set via a Web browser. It is possible to browse by data type names as well as browse by tags. A search engine is also provided. life science, bio.tools is used by: Identifiers.org
is listed by: bio.tools
is listed by: Debian
has parent organization: European Bioinformatics Institute
PMID:22140103
PMID:18078503
Free nlx_69582, biotools:miriam https://bio.tools/miriam SCR_006697 MIRIAM Registry 2026-02-14 02:01:21 1
Immune Epitope Database and Analysis Resource (IEDB)
 
Resource Report
Resource Website
100+ mentions
Immune Epitope Database and Analysis Resource (IEDB) (RRID:SCR_006604) IEDB data repository, storage service resource, data analysis service, analysis service resource, production service resource, service resource Repository contains antibody/B cell and T cell epitope information and epitope prediction and analysis tools. Immune epitopes are defined as molecular structures recognized by specific antigen receptors of the immune system, namely antibodies, B cell receptors, and T cell receptors. Immune epitopes from infectious diseases, excluding HIV, and immune-mediated diseases and the accompanying biological information are included. human, non-human primate, rodent, pig, cat, non-human animal, t cell, b cell, epitope, infectious disease, major histocompatibility complex, bio.tools, FASEB list is listed by: NIH Data Sharing Repositories
is listed by: Debian
is listed by: bio.tools
has parent organization: University of California at San Diego; California; USA
is organization facet of: La Jolla Institute for Immunology Bioinformatics Core Facility
National Institute of Allergy and Infectious Diseases PMID:19906713 Restricted nif-0000-03017, biotools:iedb, r3d100012702 http://www.iedb.org/
https://bio.tools/iedb
https://doi.org/10.17616/R3X217
SCR_006604 Immune Epitope Database and Analysis Resource, , IEDB 2026-02-14 02:01:20 383
SpliceTrap
 
Resource Report
Resource Website
10+ mentions
SpliceTrap (RRID:SCR_006728) SpliceTrap software resource A statistic tool for quantifying exon inclusion ratios in paired-end RNA-seq data, with broad applications for the study of alternative splicing. SpliceTrap approaches to exon inclusion level estimation as a Bayesian inference problem. For every exon it quantifies the extent to which it is included, skipped or subjected to size variations due to alternative 3?/5? splice sites or Intron Retention. In addition, SpliceTrap can quantify alternative splicing within a single cellular condition, with no need of a background set of reads. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Galaxy
has parent organization: Cold Spring Harbor Laboratory
PMID:21896509 biotools:splicetrap, OMICS_01292 https://bio.tools/splicetrap SCR_006728 2026-02-14 02:01:14 16
BEDTools
 
Resource Report
Resource Website
10000+ mentions
BEDTools (RRID:SCR_006646) BEDTools software resource A powerful toolset for genome arithmetic allowing one to address common genomics tasks such as finding feature overlaps and computing coverage. Bedtools allows one to intersect, merge, count, complement, and shuffle genomic intervals from multiple files in widely-used genomic file formats such as BAM, BED, GFF/GTF, VCF. While each individual tool is designed to do a relatively simple task (e.g., intersect two interval files), quite sophisticated analyses can be conducted by combining multiple bedtools operations on the UNIX command line. genomics, bed, sam, bam, overlap, sequencing, intersect, coverage, gff, vcf, bedgraph, interval, genome arithmetic, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
is related to: Hydra
is related to: pybedtools
is required by: SL-quant
PMID:20110278
DOI:10.1093/bioinformatics/btq033
GNU General Public License, v2, Acknowledgement requested OMICS_01159, biotools:bedtools https://code.google.com/p/bedtools/
https://bio.tools/bedtools
https://sources.debian.org/src/bedtools/
SCR_006646 bedtools - a swiss army knife for genome arithmetic, bedtools: a flexible suite of utilities for comparing genomic features 2026-02-14 02:01:21 10394
Dictyostelium discoideum genome database
 
Resource Report
Resource Website
100+ mentions
Dictyostelium discoideum genome database (RRID:SCR_006643) dictyBase, dictyBase gene name, dictyBase REF, DictyBase biomaterial supply resource, organism supplier, material resource Model organism database for the social amoeba Dictyostelium discoideum that provides the biomedical research community with integrated, high quality data and tools for Dictyostelium discoideum and related species. dictyBase houses the complete genome sequence, ESTs, and the entire body of literature relevant to Dictyostelium. This information is curated to provide accurate gene models and functional annotations, with the goal of fully annotating the genome to provide a ''''reference genome'''' in the Amoebozoa clade. They highlight several new features in the present update: (i) new annotations; (ii) improved interface with web 2.0 functionality; (iii) the initial steps towards a genome portal for the Amoebozoa; (iv) ortholog display; and (v) the complete integration of the Dicty Stock Center with dictyBase. The Dicty Stock Center currently holds over 1500 strains targeting over 930 different genes. There are over 100 different distinct amoebozoan species. In addition, the collection contains nearly 600 plasmids and other materials such as antibodies and cDNA libraries. The strain collection includes: * strain catalog * natural isolates * MNNG chemical mutants * tester strains for parasexual genetics * auxotroph strains * null mutants * GFP-labeled strains for cell biology * plasmid catalog The Dicty Stock Center can accept Dictyostelium strains, plasmids, and other materials relevant for research using Dictyostelium such as antibodies and cDNA or genomic libraries. genome, sequence, est, literature, gene model, functional annotation, reference genome, gene, antibody, cdna, bacteria, dictyostelium discoideum, dictyostelium purpureum, dictyostelium fasciculatum, polysphondylium pallidium, bio.tools is used by: NIF Data Federation
is listed by: One Mind Biospecimen Bank Listing
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: AmiGO
is related to: Textpresso
has parent organization: Northwestern University; Illinois; USA
has parent organization: Baylor University; Texas; USA
has parent organization: University of Cologne; Cologne; Germany
is parent organization of: Dictyostelium Discoideum Anatomy Ontology
is parent organization of: Dictyostelium Anatomy Ontology
is parent organization of: dictyBase - Teaching Tools Using Dictyostelium discoideum
NIGMS GM64426;
NIGMS GM087371;
NHGRI HG0022;
European Union
PMID:23172289
PMID:21087999
PMID:18974179
PMID:14681427
PMID:16381903
nif-0000-20974, biotools:dictybase, SCR_008149, nif-0000-02751, OMICS_03158 https://bio.tools/dictybase http://genome.imb-jena.de/dictyostelium/ SCR_006643 dictyBase gene name, dictyBase REF, Dicty, dictyBase, Dictyostelium discoideum 2026-02-14 02:01:10 306
Descriptions of Plant Viruses
 
Resource Report
Resource Website
10+ mentions
Descriptions of Plant Viruses (RRID:SCR_006656) data or information resource, portal, database, topical portal DPVweb provides a central source of information about viruses, viroids and satellites of plants, fungi and protozoa. Comprehensive taxonomic information, including brief descriptions of each family and genus, and classified lists of virus sequences are provided. The database also holds detailed, curated, information for all sequences of viruses, viroids and satellites of plants, fungi and protozoa that are complete or that contain at least one complete gene. For comparative purposes, it also contains a single representative sequence of all other fully sequenced virus species with an RNA or single-stranded DNA genome. The start and end positions of each feature (gene, non-translated region and the like) have been recorded and checked for accuracy. As far as possible, nomenclature for genes and proteins are standardized within genera and families. Sequences of features (either as DNA or amino acid sequences) can be directly downloaded from the website in FASTA format. The sequence information can also be accessed via client software for PC computers (freely downloadable from the website) that enable users to make an easy selection of sequences and features of a chosen virus for further analyses. The public sequence databases contain vast amounts of data on virus genomes but accessing and comparing the data, except for relatively small sets of related viruses can be very time consuming. The procedure is made difficult because some of the sequences on these databases are incorrectly named, poorly annotated or redundant. The NCBI Reference Sequence project (1) provides a comprehensive, integrated, non-redundant set of sequences, including genomic DNA, transcript (RNA) and protein products, for major research organisms. This now includes curated information for a single sequence of each fully sequenced virus species. While this is a welcome development, it can only deal with complete sequences. An important feature of DPV is the opportunity to access genes (and other features) of multiple sequences quickly and accurately. Thus, for example, it is easy to obtain the nucleotide or amino acid sequences of all the available accessions of the coat protein gene of a given virus species or for a group of viruses. To increase its usefulness further, DPVweb also contains a single representative sequence of all other fully sequenced virus species with an RNA or single-stranded DNA (ssDNA) genome. Sponsors: This site is supported by the Association of Applied Biologists and the Zhejiang Academy of Agricultural Sciences, Hangzhou, People''s Republic of China. family, fungi, gene, amino acid, comparative, development, dna, genome, genomic, genus, nomenclature, non-translated, nucleotide, organism, plant, product, protein, protozoa, region, rna, satellite, sequence, single, specie, taxonomic, transcript, viral databases, viroid, virus, bio.tools is listed by: bio.tools
is listed by: Debian
nif-0000-21127, biotools:dpvweb https://bio.tools/dpvweb SCR_006656 DPV 2026-02-14 02:01:20 11
PySurfer
 
Resource Report
Resource Website
10+ mentions
PySurfer (RRID:SCR_002524) PySurfer data visualization software, data processing software, software library, software toolkit, software application, software resource Software Python tool for visualization and interaction with cortical surface representations of neuroimaging data from Freesurfer. It extends Mayavi powerful visualization engine with interface for working with MRI and MEG data. PySurfer offers command-line interface designed to broadly replicate Freesurfer program as well as Python library for writing scripts to explore complex datasets., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. eeg, meg, electrocorticography, magnetic resonance, mri, python, neuroimaging is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Debian
is related to: FreeSurfer
Free, Available for download, Freely available nlx_155930 http://www.nitrc.org/projects/pysurfer
https://sources.debian.org/src/python3-surfer/
SCR_002524 2026-02-14 02:00:25 29
ShotGun
 
Resource Report
Resource Website
10+ mentions
ShotGun (RRID:SCR_002529) sequence analysis software, data processing software, data analysis software, software application, software resource, simulation software Software for short read simulating in order to facilitate sequencing-based study designs. sequence based study design, short read stimulation, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of North Carolina at Chapel Hill; North Carolina; USA
PMID:23357921 Free, Available for download, Freely available biotools:abcd, OMICS_00255 https://bio.tools/abcd SCR_002529 ShotGun: a Flexible Short Read Simulator to Facilitate Sequencing-based Study Designs 2026-02-14 02:00:26 32
Gibbs Motif Sampler
 
Resource Report
Resource Website
1+ mentions
Gibbs Motif Sampler (RRID:SCR_002550) Gibbs Motif Sampler data analysis service, analysis service resource, production service resource, service resource, software resource Software to identify motifs, conserved regions, in DNA or protein sequences. dna, protein, motif, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
Free, Available for download, Freely available biotools:gibbs_motif_sampler, OMICS_00496 https://bio.tools/gibbs_motif_sampler SCR_002550 The Gibbs Motif Sampler 2026-02-14 02:00:17 2
pymzML
 
Resource Report
Resource Website
10+ mentions
pymzML (RRID:SCR_002500) software resource Python module to parse mzML data in Python based on cElementTree. It is an extension to Python that offers (i) an easy access to mass spectrometry (MS) data that allows the rapid development of tools, (ii) a very fast parser for mzML data and (iii) a set of functions to compare or handle spectra., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. standalone software, python, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: mzML
has parent organization: University of Munster; North Rhine-Westphalia; Germany
PMID:22302572 Free, Available for download, Freely available biotools:pymzml, OMICS_03355 https://bio.tools/pymzml SCR_002500 2026-02-14 02:00:17 18
discoSnp
 
Resource Report
Resource Website
1+ mentions
discoSnp (RRID:SCR_002612) sequence analysis software, data processing software, data analysis software, software application, software resource Software designed for discovering Single Nucleotide Polymorphism (SNP) from raw sets of reads obtained with Next Generation Sequencers (NGS). single nucleotide polymorphism, snp discovery, discover snp, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
SOFIPROTEOL under the FASO project PEAPOL ;
INRIA ANR-12-BS02-0008
PMID:25404127 Free, Freely available biotools:discosnp, OMICS_00267 https://bio.tools/discosnp
https://sources.debian.org/src/discosnp/
SCR_002612 DiscoSnp++, discovering Single Nucleotide Polymorphism, discovering Single Nucleotide Polymorphism (discoSNP) 2026-02-14 02:00:25 9
IMEx - The International Molecular Exchange Consortium
 
Resource Report
Resource Website
100+ mentions
IMEx - The International Molecular Exchange Consortium (RRID:SCR_002805) IMEx data repository, storage service resource, community building portal, portal, consortium, data or information resource, organization portal, service resource, database Interaction database from international collaboration between major public interaction data providers who share curation effort and develop set of curation rules when capturing data from both directly deposited interaction data or from publications in peer reviewed journals. Performs complete curation of all protein-protein interactions experimentally demonstrated within publication and makes them available in single search interface on common website. Provides data in standards compliant download formats. IMEx partners produce their own separate resources, which range from all encompassing molecular interaction databases, such as are maintained by IntAct, MINT and DIP, organism-centric resources such as BioGrid or MPIDB or biological domain centric, such as MatrixDB. They have committed to making records available, via PSICQUIC webservice, which have been curated to IMEx rules and are available to users as single, non-redundant set of curated publications which can be searched at the IMEx website. Data is made available in standards-compliant tab-deliminated and XML formats, enabling to visualize data using wide range of tools. Consortium is open to participation of additional partners and encourages deposition of data, prior to publication, and will supply unique accession numbers which may be referenced within final article. Submitters may send their data directly to any of member databases using variety of formats, but should conform to guidelines as to minimum information required to describe data. protein-protein interaction, nonredundant, protein interaction, interaction, proteomics, metadata standard, short course, molecular interaction, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is affiliated with: MINT
is related to: MatrixDB
is related to: MPIDB
is related to: Database of Interacting Proteins (DIP)
is related to: Database of Interacting Proteins (DIP)
is related to: InnateDB
is related to: IntAct
is related to: Interaction Reference Index
is related to: MPIDB
is related to: UniProt
is related to: InnateDB
is related to: MatrixDB
is related to: Biological General Repository for Interaction Datasets (BioGRID)
is related to: I2D
is related to: Molecular Connections NetPro
is related to: SIB Swiss Institute of Bioinformatics
is related to: IntAct
is related to: PSI-MI
is related to: PSICQUIC Registry
is related to: mentha
is related to: Bioconductor
has parent organization: European Bioinformatics Institute
works with: CellPhoneDB
works with: Cytoscape
works with: IntAct
works with: MINT
works with: MPact: Representation of Interaction Data at MIPS
works with: Molecular Connections NetPro
works with: Biological General Repository for Interaction Datasets (BioGRID)
works with: InnateDB
works with: BIND
European Union PMID:22453911
PMID:17893861
Free, Freely available, Available for download nif-0000-00447, OMICS_01545, r3d100010669, biotools:imex http://imex.sourceforge.net/
https://bio.tools/imex
https://doi.org/10.17616/R3090W
SCR_002805 The International Molecular Exchange Consortium, International Molecular Exchange Consortium 2026-02-14 02:00:27 144
sapFinder
 
Resource Report
Resource Website
sapFinder (RRID:SCR_002685) software resource An R software package, for detection of the variant peptides based on tandem mass spectrometry (MS/MS)-based proteomics data. It automates (1) variation-associated database construction, (2) database searching, (3) post-processing, (4) HTML-based report generation in shotgun proteomics. standalone software, r, mass spectrometry, proteomics, rna-seq, report writing, snp, visualization, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Bioconductor
PMID:25053745 Free, Available for download, Freely available biotools:sapfinder, OMICS_05285 https://bio.tools/sapfinder SCR_002685 sapFinder - A package for variant peptides detection and visualization in shotgun proteomics. 2026-02-14 02:00:26 0
leeHom
 
Resource Report
Resource Website
50+ mentions
leeHom (RRID:SCR_002710) software resource Software program for the Bayesian reconstruction of ancient DNA fragments. The algorithm removes the adaptors and reconstructs the original DNA sequences using a Bayesian maximum a posteriori probability approach. standalone software, illumina, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:25100869 Free, Available for download, Freely available biotools:leehom, OMICS_05254 https://bio.tools/leehom SCR_002710 2026-02-14 02:00:26 53
ANDES
 
Resource Report
Resource Website
10+ mentions
ANDES (RRID:SCR_002791) data processing software, data analysis software, software toolkit, software application, software resource Software library and a suite of applications, written in Perl and R, for deep sequencing statistical analyses. deep sequencing, biomarker detection, statistical analysis, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:20633290 Free, Freely available, Available for download biotools:andes, OMICS_01119 https://bio.tools/andes SCR_002791 Statistical tools for the Analyses of Deep Sequencing (ANDES), Statistical tools for the Analyses of Deep Sequencing, Statistical tools for the ANalyses of Deep Sequencing 2026-02-14 02:00:32 25
NCBI database of Genotypes and Phenotypes (dbGap)
 
Resource Report
Resource Website
500+ mentions
NCBI database of Genotypes and Phenotypes (dbGap) (RRID:SCR_002709) dbGaP data repository, storage service resource, data or information resource, service resource, database Database developed to archive and distribute clinical data and results from studies that have investigated interaction of genotype and phenotype in humans. Database to archive and distribute results of studies including genome-wide association studies, medical sequencing, molecular diagnostic assays, and association between genotype and non-clinical traits. clinical, trial, genotype, interaction, homology, cell, morphology, interaction, phenotype, molecular diagnosis, genetic recombination, gold standard, bio.tools is used by: International Genomics of Alzheimers Project
is used by: NIDDK Inflammatory Bowel Disease Genetics Consortium
is used by: NIH Heal Project
is used by: Genomic Data Commons Data Portal (GDC Data Portal)
is recommended by: National Library of Medicine
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: OMICtools
is listed by: re3data.org
is listed by: NIDDK Information Network (dkNET)
is listed by: bio.tools
is listed by: Debian
is related to: NIDDK Central Repository
is related to: eMERGE Network: electronic Medical Records and Genomics
is related to: Framingham Heart Study
is related to: PhenoExplorer
is related to: Chronic Renal Insufficiency Cohort Study
is related to: DbGaP Cleaner
is related to: Psychiatric Genomics Consortium
is related to: ISCA Consortium
is related to: Allen Institute for Brain Science
has parent organization: NCBI
is parent organization of: Resource for Genetic Epidemiology Research on Adult Health and Aging
NLM PMID:24297256
PMID:17898773
Restricted nif-0000-23342, OMICS_00263, biotools:dbgap, r3d100010788 http://www.ncbi.nlm.nih.gov/sites/entrez?db=gap
https://bio.tools/dbgap
https://doi.org/10.17616/R3GS4K
SCR_002709 database of Genotypes and Phenotypes (dbGaP), dbGaP, NCBI, Database of Genotypes and Phenotypes 2026-02-14 02:00:30 683
Pathview
 
Resource Report
Resource Website
500+ mentions
Pathview (RRID:SCR_002732) software resource A tool set for pathway-based data integration and visualization. It maps and renders a wide variety of biological data on relevant pathway graphs. All users need is to supply their data and specify the target pathway. Pathview automatically downloads the pathway graph data, parses the data file, maps user data to the pathway, and render pathway graph with the mapped data. In addition, Pathview also seamlessly integrates with pathway and gene set (enrichment) analysis tools for large-scale and fully automated analysis. software package, r, differential expression, gene expression, gene set enrichment, genetics, graph, network, metabolomics, microarray, pathway, proteomics, rna-seq, sequencing, systems biology, visualization, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Bioconductor
PMID:23740750 Free, Freely available, Available for download biotools:pathview, OMICS_05212 http://pathview.r-forge.r-project.org/
https://bio.tools/pathview
SCR_002732 path view 2026-02-14 02:00:30 520
SuperPred: Drug classification and target prediction
 
Resource Report
Resource Website
SuperPred: Drug classification and target prediction (RRID:SCR_002691) SuperPred web service, data or information resource, data access protocol, software resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on November 24,2025. Publicly available web-server to predict medical indication areas based on properties and similarity of chemical compounds. The web-server translates a user-defined molecule into a structural fingerprint that is compared to about 6300 drugs, which are enriched by 7300 links to molecular targets of the drugs, derived through text mining followed by manual curation. Links to the affected pathways are provided. The similarity to the medical compounds is expressed by the Tanimoto coefficient that gives the structural similarity of two compounds. A similarity score higher than 0.85 results in correct ATC prediction for 81% of all cases. As the biological effect is well predictable, if the structural similarity is sufficient, the web-server allows prognoses about the medical indication area of novel compounds and to find new leads for known targets. The combination of physicochemical property and similarity searching provides the possibility to detect new biologically active compounds and novel targets for drug-like compounds. SuperPred can be applied for drug repositioning purposes, too. A further intention of SuperPred is to find side effects elicited by drugs caused through off-target hits. drug, drug class, drug target, addiction, anatomical therapeutic chemical, application area, biological activity, chemical, chemical classification, chemical property, classification, compound, molecular target, molecule, nervous system, pathway, pharmacological property, physicochemical property, prediction, activity spectra, substance, structural similarity, structure, tanimoto coefficient, tanimoto score, target prediction, target-prediction server, therapeutic approach, therapeutic property, drug classification, target prediction, similarity score, target, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: Charite - Universitatsmedizin Berlin; Berlin; Germany
SFB 449 ;
IRTG Berlin-Boston-Kyoto and Deutsche Krebshilfe. ;
DFG
PMID:18499712
PMID:24878925
THIS RESOURCE IS NO LONGER IN SERVICE biotools:superpred, nif-0000-00415 https://bio.tools/superpred SCR_002691 2026-02-14 02:00:29 0
Rainbow
 
Resource Report
Resource Website
10+ mentions
Rainbow (RRID:SCR_002724) sequence analysis software, data processing software, data analysis software, software application, software resource Software developed to provide an ultra-fast and memory-efficient solution to clustering and assembling short reads produced by RAD-seq. software, tool, clustering, assembling, short, read, restriction, site, DNA, sequence, analysis, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:22942077
DOI:10.1093/bioinformatics/bts482
Free, Freely available, Available for download SCR_015992, OMICS_03722, biotools:rainbow https://bio.tools/rainbow
https://sources.debian.org/src/bio-rainbow/
SCR_002724 RAD-seq: Restriction-site Associated DNA sequencing, Bio-rainbow, RAD-seq 2026-02-14 02:00:30 41
Coding Potential Calculator
 
Resource Report
Resource Website
100+ mentions
Coding Potential Calculator (RRID:SCR_002764) CPC data analysis service, analysis service resource, production service resource, service resource, software resource A Support Vector Machine-based classifier to assesses the protein-coding potential of a transcript based on six biologically meaningful sequence features. CPC can discriminate coding from noncoding transcripts with high accuracy and speed. In addition to predicting the coding potential of the input transcripts, the CPC web server also graphically displays detailed sequence features and additional annotations of the transcript that may facilitate users' further investigation. The coding potential calculator tool reads FASTA data format as input. fasta, transcript, protein coding, coding potential, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: Peking University; Beijing; China
PMID:17631615 Free, Freely available biotools:cpc, rid_000106 https://bio.tools/cpc SCR_002764 2026-02-14 02:00:31 198

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    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.