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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
T-profiler
 
Resource Report
Resource Website
10+ mentions
T-profiler (RRID:SCR_003452) T-profiler analysis service resource, data analysis service, production service resource, service resource One of the key challenges in the analysis of gene expression data is how to relate the expression level of individual genes to the underlying transcriptional programs and cellular state. The T-profiler tool hosted on this website uses the t-test to score changes in the average activity of pre-defined groups of genes. The gene groups are defined based on Gene Ontology categorization, ChIP-chip experiments, upstream matches to a consensus transcription factor binding motif, and location on the same chromosome, respectively. If desired, an iterative procedure can be used to select a single, optimal representative from sets of overlapping gene groups. A jack-knife procedure is used to make calculations more robust against outliers. T-profiler makes it possible to interpret microarray data in a way that is both intuitive and statistically rigorous, without the need to combine experiments or choose parameters. Currently, gene expression data from Saccharomyces cerevisiae and Candida albicans are supported. Users can submit their microarray data for analysis by clicking on one of the two organism-specific tabs above. Platform: Online tool expression, gene, binding, cellular, transcriptional, gene expression, microarray, gene ontology, transcription factor, binding motif, chip-chip, chip, motif, t-test, statistical analysis, transcriptome, bio.tools is listed by: Biositemaps
is listed by: Gene Ontology Tools
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
has parent organization: Columbia University; New York; USA
has parent organization: University of Amsterdam; Amsterdam; Netherlands
Netherlands Foundation for Technical Research APB.5504;
NHGRI R01HG003008
PMID:15980543 Free for academic use nif-0000-33354, biotools:t-profiler https://bio.tools/t-profiler SCR_003452 T-profiler: Scoring the Activity of Pre-defined Groups of Genes Using Gene Expression Data 2026-09-03 05:01:15 11
Distant Regulatory Elements
 
Resource Report
Resource Website
10+ mentions
Distant Regulatory Elements (RRID:SCR_003058) DiRE analysis service resource, data analysis service, production service resource, service resource Web server based on the Enhancer Identification (EI) method, to determine the chromosomal location and functional characteristics of distant regulatory elements (REs) in higher eukaryotic genomes. The server uses gene co-expression data, comparative genomics, and combinatorics of transcription factor binding sites (TFBSs) to find TFBS-association signatures that can be used for discriminating specific regulatory functions. DiRE's unique feature is the detection of REs outside of proximal promoter regions, as it takes advantage of the full gene locus to conduct the search. DiRE can predict common REs for any set of input genes for which the user has prior knowledge of co-expression, co-function, or other biologically meaningful grouping. The server predicts function-specific REs consisting of clusters of specifically-associated TFBSs, and it also scores the association of individual TFs with the biological function shared by the group of input genes. Its integration with the Array2BIO server allows users to start their analysis with raw microarray expression data. regulatory element, enhancer identification, genome, prediction, transcription factor binding site, gene, co-expression, co-function, function, transcription factor, comparative genomics, regulatory function, gene locus, chromosome, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: NCBI
NLM ;
Intramural Research Program
PMID:18487623 Free, Freely available nif-0000-30448, biotools:dire https://bio.tools/dire SCR_003058 Distant Regulatory Elements of co-regulated genes 2026-09-03 05:01:08 25
MiST - Microbial Signal Transduction database
 
Resource Report
Resource Website
10+ mentions
MiST - Microbial Signal Transduction database (RRID:SCR_003166) MiST data or information resource, database Database which contains the signal transduction proteins for complete and draft bacterial and archaeal genomes. The MiST2 database identifies and catalogs the repertoire of signal transduction proteins in microbial genomes. signal transduction proteins, bacterial genome, archaeal genome, microbial genome, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: University of Tennessee Knoxville; Tennessee; USA
South Carolina Research Association ;
DOE Office of Science ;
NIH ;
NIGMS GM083177
PMID:19900966 Free, Freely available biotools:mist, nif-0000-03140 https://bio.tools/mist SCR_003166 MiST 2.2, Microbial Signal Transduction Database, Microbial Signal Transduction database (MiST), MiST2 2026-09-03 05:01:29 35
SIDER
 
Resource Report
Resource Website
100+ mentions
SIDER (RRID:SCR_004321) SIDER data or information resource, database Database containing information on marketed medicines and their recorded adverse drug reactions. The information is extracted from public documents and package inserts. The available information include side effect frequency, drug and side effect classifications as well as links to further information, for example drug-target relations. The SIDER Side Effect Resource represents an effort to aggregate dispersed public information on side effects. To our knowledge, no such resource exist in machine-readable form despite the importance of research on drugs and their effects. The creation of this resource was motivated by the many requests for data that we received related to our paper (Campillos, Kuhn et al., Science, 2008, 321(5886):263-6.) on the utilization of side effects for drug target prediction. Inclusion of side effects as readouts for drug treatment should have many applications and we hope to be able to enhance the respective research with this resource. You may browse the drugs by name, browse the side effects by name, download the current version of SIDER, or use the search interface. medicine, drug, side effect, adverse drug reaction, drug-target, phenotype, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Allen Institute Neurowiki
has parent organization: European Molecular Biology Laboratory
PMID:20087340 Except as otherwise noted, Creative Commons Attribution-NonCommercial-ShareAlike License, v3, Commercial use requires permission r3d100012791, nlx_33359, OMICS_01588, biotools:sider https://bio.tools/sider, https://doi.org/10.17616/R3J226 SCR_004321 Side Effect Resource, SIDER: Side Effect Resource 2026-09-03 05:01:36 410
Identifiers.org
 
Resource Report
Resource Website
50+ mentions
Identifiers.org (RRID:SCR_003735) Identifiers.org identifier resolution, production service resource, service resource A system providing resolvable persistent Uniform Resource Identifiers (URIs) used to identify data for the scientific community, with a current focus on the Life Sciences domain. The provision of resolvable identifiers (URLs) fits well with the Semantic Web vision, and the Linked Data initiative. It provides direct access to the identified data using one chosen physical location (or resource). If more than one physical locations providing the data are recorded in the Registry, then you can access them via the top banner or by using a profile. identifier, life sciences, bio.tools uses: MIRIAM Resources
is listed by: bio.tools
is listed by: Debian
has parent organization: European Bioinformatics Institute
Free nlx_157931, biotools:identifiers.org https://bio.tools/identifiers.org SCR_003735 2026-09-03 05:01:52 59
INMEX
 
Resource Report
Resource Website
10+ mentions
INMEX (RRID:SCR_004173) INMEX analysis service resource, data analysis service, production service resource, service resource A web-based tool to support meta-analysis of multiple gene-expression data sets, as well as to enable integration of data sets from gene expression and metabolomics experiments. INMEX contains three functional modules. The data preparation module supports flexible data processing, annotation and visualization of individual data sets. The statistical analysis module allows researchers to combine multiple data sets based on P-values, effect sizes, rank orders and other features. The significant genes can be examined in functional analysis module for enriched Gene Ontology terms or Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, or expression profile visualization. INMEX has built-in support for common gene/metabolite identifiers (IDs), as well as 45 popular microarray platforms for human, mouse and rat. Complex operations are performed through a user-friendly web interface in a step-by-step manner. gene expression, meta-analysis, metabolomics, pathway, gene, metabolite, visualization, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
is related to: KEGG
is related to: Human Metabolome Database
has parent organization: University of British Columbia; British Columbia; Canada
Killam Trust ;
Canadian Institutes of Health Research
PMID:23766290 Acknowledgement requested biotools:inmex, OMICS_01546 https://bio.tools/inmex SCR_004173 INtegrative Meta-analysis of EXpression data, INMEX - INtegrative Meta-analysis of EXpression data 2026-09-03 05:01:38 19
SGD
 
Resource Report
Resource Website
1000+ mentions
SGD (RRID:SCR_004694) SGD, SGD LOCUS, SGD REF data or information resource, database A curated database that provides comprehensive integrated biological information for Saccharomyces cerevisiae along with search and analysis tools to explore these data. SGD allows researchers to discover functional relationships between sequence and gene products in fungi and higher organisms. The SGD also maintains the S. cerevisiae Gene Name Registry, a complete list of all gene names used in S. cerevisiae which includes a set of general guidelines to gene naming. Protein Page provides basic protein information calculated from the predicted sequence and contains links to a variety of secondary structure and tertiary structure resources. Yeast Biochemical Pathways allows users to view and search for biochemical reactions and pathways that occur in S. cerevisiae as well as map expression data onto the biochemical pathways. Literature citations are provided where available. database, yeast, pathway, analysis, gene, nomenclature, predicted sequence, fungi, functional relationship, protein structure, bio.tools, FASEB list uses: InterMOD
is used by: NIF Data Federation
is used by: PhenoGO
is listed by: re3data.org
is listed by: OMICtools
is listed by: InterMOD
is listed by: bio.tools
is listed by: Debian
is affiliated with: InterMOD
is related to: AmiGO
is related to: Yeast Search for Transcriptional Regulators And Consensus Tracking
is related to: HomoloGene
is related to: TXTGate
is related to: PhenoGO
has parent organization: Stanford University School of Medicine; California; USA
has parent organization: Stanford University; Stanford; California
is parent organization of: Ascomycete Phenotype Ontology
is parent organization of: SGD Gene Ontology Slim Mapper
is organization facet of: Alliance of Genome Resources
NHGRI 5P41HG001315-11;
NHGRI 5P41HG002273-05;
NHGRI 5U41HG001315-18;
NHGRI 2U41HG002273-13;
NHGRI 5R01HG004834-04
PMID:24265222
PMID:12519985
PMID:9399804
Free for academic use, The community can contribute to this resource, Non-commercial nif-0000-03456, biotools:sgd, r3d100010419, OMICS_01661 https://bio.tools/sgd, https://doi.org/10.17616/R3N313 http://genome-www.stanford.edu/Saccharomyces/ SCR_004694 SGD LOCUS, Saccharomyces Genome Database, SGD REF 2026-09-03 05:01:40 1950
Pfam
 
Resource Report
Resource Website
10000+ mentions
Pfam (RRID:SCR_004726) data or information resource, database A database of protein families, each represented by multiple sequence alignments and hidden Markov models (HMMs). Users can analyze protein sequences for Pfam matches, view Pfam family annotation and alignments, see groups of related families, look at the domain organization of a protein sequence, find the domains on a PDB structure, and query Pfam by keywords. There are two components to Pfam: Pfam-A and Pfam-B. Pfam-A entries are high quality, manually curated families that may automatically generate a supplement using the ADDA database. These automatically generated entries are called Pfam-B. Although of lower quality, Pfam-B families can be useful for identifying functionally conserved regions when no Pfam-A entries are found. Pfam also generates higher-level groupings of related families, known as clans (collections of Pfam-A entries which are related by similarity of sequence, structure or profile-HMM). database, clan, structure, sequence, protein family, domain, bio.tools, FASEB list is used by: Mutation Annotation and Genomic Interpretation
is used by: MobiDB
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Conserved Domain Database
is related to: SUPFAM
is related to: DBD: Transcription factor prediction database
is related to: DOMINE: Database of Protein Interactions
is related to: GeneSpeed- A Database of Unigene Domain Organization
is related to: Eukaryotic Linear Motif
is related to: TopoSNP
is related to: GOTaxExplorer
is related to: TrED
is related to: ProOpDB
is related to: Algal Functional Annotation Tool
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
EMBL core funds ;
Howard Hughes Medical Institute ;
BBSRC BB/L024136/1;
Wellcome Trust 108433/Z/15/Z
PMID:24288371
PMID:19920124
Acknowledgement requested, Available via FTP biotools:pfam, OMICS_01696, r3d100012850, nlx_72111 https://bio.tools/pfam, https://doi.org/10.17616/R3QV4F http://pfam.sanger.ac.uk/ SCR_004726 Pfam Database, Protein Families Database, PFAM, Pfam protein families database 2026-09-03 05:01:26 17424
NEWT
 
Resource Report
Resource Website
10+ mentions
NEWT (RRID:SCR_004477) NEWT data or information resource, database NEWT is the taxonomy database maintained by the UniProt group. It integrates taxonomy data compiled in the NCBI database and data specific to the UniProt Knowledgebase. Browse by hierarchy, List all, or Complete proteomes. Organisms are classified in a hierarchical tree structure. Our taxonomy database contains every node (taxon) of the tree. UniProtKB taxonomy data is manually curated: next to manually verified organism names, we provide a selection of external links, organism strains and viral host information. Species with protein sequences stored in the UniProt Knowledgebase are named according to UniProt nomenclature. We endeavour to maintain a list of manually curated species names for which protein sequence data is available. In particular, we have adopted a systematic convention for naming viral and bacterial strains and isolates. Links to external sites are chosen by the UniProt taxonomy team and show pictures and various scientific data of interest (taxonomy, biology, physiology,...). archaea, bacteria, eukaryota, viruses, cellular organism, sequence, viroid, gold standard, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: NCBI Taxonomy
has parent organization: UniProt
PMID:12824428 nlx_46189, biotools:newt https://bio.tools/newt http://www.ebi.ac.uk/newt/ SCR_004477 UniProtKB taxonomy database, UniProt Taxonomy Database, UniProt Taxonomy 2026-09-03 05:01:22 23
Ancestrymap
 
Resource Report
Resource Website
10+ mentions
Ancestrymap (RRID:SCR_004353) ANCESTRYMAP software application, software resource, source code Software application that finds skews in ancestry that are potentially associated with disease genes in recently mixed populations like African Americans. It can be downloaded for either UNIX or Linux. disease gene, ancestry, gene, genomic, unix, linux, admixture mapping, admixture, genome, linkage disequilibrium, population is listed by: OMICtools
is listed by: Genetic Analysis Software
is listed by: bio.tools
has parent organization: Harvard Medical School; Massachusetts; USA
Burroughs Wellcome Fund ;
NHGRI K-01 HG002758-01
PMID:15088269 Restricted nlx_39116, biotools:ancestrymap, OMICS_02083 https://reich.hms.harvard.edu/software, https://bio.tools/ancestrymap http://genepath.med.harvard.edu/~reich/Software.htm, http://genetics.med.harvard.edu/reich/Reich_Lab/Software.html SCR_004353 2026-09-03 05:01:55 12
Selectome: a Database of Positive Selection
 
Resource Report
Resource Website
1+ mentions
Selectome: a Database of Positive Selection (RRID:SCR_004542) data or information resource, database Database of positive selection based on a rigorous branch-site specific likelihood test. Positive selection is detected using CODEML on all branches of animal gene trees. duplication, events, gene, animal, positive selection, speciation, p-value, speciation, duplication, selectome, phylogenetic, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: University of Lausanne; Lausanne; Switzerland
PMID:24225318 nif-0000-03451, biotools:selectome https://bio.tools/selectome SCR_004542 Selectome 2026-09-03 05:01:46 9
Homologous Sequences in Ensembl Animal Genomes
 
Resource Report
Resource Website
1+ mentions
Homologous Sequences in Ensembl Animal Genomes (RRID:SCR_008356) HOMOLENS data or information resource, database Database of homologous genes from Ensembl organisms, structured under ACNUC sequence database management system. It allows to select sets of homologous genes among species, and to visualize multiple alignments and phylogenetic trees. It is possible to search for orthologous genes in a wide range of taxons. HOMOLENS is particularly useful for comparative sequence analysis, phylogeny and molecular evolution studies. More generally, HOMOLENS gives an overall view of what is known about a peculiar gene family. Note that HOMOLENS is split into two databases on this server: HOMOLENS contains the protein sequences while HOMOLENSDNA contains the nucleotide sequences. Protein sequences of HOMOLENS have been generated by translating the CDS of HOMOLENSDNA and using associated cross-references to generate the annotations. ensembl, evolution, gene, alignment, comparative, homologous, molecular, nucleotide, organism, phylogenetic, phylogeny, protein, sequence, specie, structure, taxon, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: Claude Bernard University Lyon 1; Lyon; France
biotools:homolens, nif-0000-25424 https://bio.tools/homolens SCR_008356 2026-09-03 05:03:05 3
Regulatory Sequence Analysis Tools
 
Resource Report
Resource Website
100+ mentions
Regulatory Sequence Analysis Tools (RRID:SCR_008560) data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on February 28,2023. Retrieve-ensembl-seq is included in the software suite regulatory sequence analysis tools (RSAT), allowing instant submission of retrieved sequences to further analysis tools. AVAILABILITY: retrieve-ensembl-seq is integrated in the RSAT suite: http://rsat.ulb.ac.be/rsat. Web site: http://rsat.ulb.ac.be/rsat/retrieve-ensembl-seq_form.cgi. Web services: http://rsat.ulb.ac.be/rsat/web_services/RSATWS.wsdl. Stand-alone distribution: freely available under an academic licence to download from the RSAT web site. The complete manual, a convenient tutorial and demos are available from the RSAT website. Additional help can be found on the RSAT public forum. bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
is related to: Yeast Search for Transcriptional Regulators And Consensus Tracking
DOI:10.1093/nar/gkv362 THIS RESOURCE IS NO LONGER IN SERVICE biotools:rsat, nif-0000-31437, OMICS_08097 https://bio.tools/rsat https://sources.debian.org/src/rsat/ SCR_008560 RSAT 2026-09-03 05:02:55 108
Single Nucleotide Polymorphism Spectral Decomposition (SNPSpD)
 
Resource Report
Resource Website
10+ mentions
Single Nucleotide Polymorphism Spectral Decomposition (SNPSpD) (RRID:SCR_008621) SNPSpD analysis service resource, data analysis service, production service resource, service resource SNPSpD is a method of correcting for non-independance of single nucleotide polymorphisms (SNPs) in linkage disequilibrium (LD) with each other, on the basis of the spectral decomposition (SpD) of matrices of LD between SNP''s. Additionally, output from SNPSpD includes eigenvalues, principal-component coefficients, and factor loadings after varimax rotation, enabling the selection of a subset of SNPs that optimize the information in a genomic region. bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: Queensland Institute of Medical Research
National Health and MRC Australia 241916 PMID:14997420 biotools:snpspd, nif-0000-31985 https://bio.tools/snpspd http://genepi.qimr.edu.au/general/daleN/SNPSp SCR_008621 Single Nucleotide Polymorphism Spectral Decomposition 2026-09-03 05:02:56 18
Webproanalyst
 
Resource Report
Resource Website
Webproanalyst (RRID:SCR_008348) analysis service resource, data analysis service, production service resource, service resource WebProAnalyst provides web-accessible analysis for scanning the quantitative structure-activity relationships in protein families. It searches for a sequence region, whose substitutions are correlated with variations in the activities of a homologous protein set, the so-called activity modulating sites. WebProAnalyst allows users to search for the key physicochemical characteristics of the sites that affect the changes in protein activities. It enables the building of multiple linear regression and neural networks models that relate these characteristics to protein activities. WebProAnalyst implements multiple linear regression analysis, back propagation neural networks and the Structure-Activity Correlation/Determination Coefficient (SACC/SADC). A back propagation neural network is implemented as a two-layered network, one layer as input, the other as output (Rumelhart et al, 1986). WebProAnalyst uses alignment of amino acid sequences and data on protein activity (pK, Km, ED50, among others). The input data are the numerical values for the physicochemical characteristics of a site in the multiple alignment given by a slide window. The output data are the predicted activity values. The current version of WebProAnalyst handles a single activity for a single protein. The SACC/SADC may be defined as an estimate of the strongest multiple correlation between the physicochemical characteristics of a site in a multiple alignment and protein activities. The SACC/SADC coefficient makes possible the calculation of the possible highest correlation achievable for the quantitative relationship between the physicochemical properties of sites and protein activities. The SACC/SADC is a convenient means for an arrangement of positions by their functional significance. WebProAnalyst outputs a list of multiple alignment positions, the respective correlation values, also regression analysis parameters for the relationships between the amino acid physicochemical characteristics at these positions and the protein activity values. family, functional, activity, alignment, amino acid, homologous, modulating site, neural, physicochemical, propagation, protein, quantitative, region, relationship, scan, sequence, structure, substitution, variation, bio.tools is listed by: bio.tools
is listed by: Debian
nif-0000-25212, biotools:webproanalyst https://bio.tools/webproanalyst SCR_008348 Webproanalyst 2026-09-03 05:03:08 0
GeneSeeker
 
Resource Report
Resource Website
1+ mentions
GeneSeeker (RRID:SCR_008347) data or information resource, database The GeneSeeker allows you to search across different databases simultaneously, given a known human genetic location and expression/phenotypic pattern. The GeneSeeker returns any found gene names which are located on the specified location and expressed in the specified tissue. To search for more expression location in one search, just enter them in the textbox for the expression location and separate them with logical operators (and, or, not). You can specify as many tissues as you want, the program starts 20 queries simultaneously, and then waits for a query to finish before starting another query, to keep server loads to a minimum. You can also search only for expression, just leave the cytogenetic location fields blank, and do the query. If you only want to look for one cytogenetic location, only fill in the first location field, and the GeneSeeker will search with only this one. Housekeeping genes , found in Swissprot can be excluded, or genes that are to be excluded can be specified. Human chromosome localizations are translated with an oxford-grid to mouse chromosome localizations, and then submitted to the Mgd. Sponsors: GeneSeeker is a service provided by the Centre for Molecular and Biomolecular Informatics (CMBI). expression, federated database, gene, genetic, biomolecular, chromosome, cytogenetic, database, human, localization, location, molecular, pattern, phenotypic, tissue, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: Radboud University; Nijmegen; The Netherlands
biotools:geneseeker, nif-0000-25211 https://bio.tools/geneseeker SCR_008347 GeneSeeker 2026-09-03 05:03:04 5
DNAtraffic
 
Resource Report
Resource Website
DNAtraffic (RRID:SCR_008886) DNAtraffic data or information resource, database DNAtraffic database is dedicated to be an unique comprehensive and richly annotated database of genome dynamics during the cell life. DNAtraffic contains extensive data on the nomenclature, ontology, structure and function of proteins related to control of the DNA integrity mechanisms such as chromatin remodeling, DNA repair and damage response pathways from eight model organisms commonly used in the DNA-related study: Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorhabditis elegans, Saccharomyces cerevisiae, Schizosaccharomyces pombe, Escherichia coli and Arabidopsis thaliana. DNAtraffic contains comprehensive information on diseases related to the assembled human proteins. Database is richly annotated in the systemic information on the nomenclature, chemistry and structure of the DNA damage and drugs targeting nucleic acids and/or proteins involved in the maintenance of genome stability. One of the DNAtraffic database aim is to create the first platform of the combinatorial complexity of DNA metabolism pathway analysis. Database includes illustrations of pathway, damage, protein and drug. Since DNAtraffic is designed to cover a broad spectrum of scientific disciplines it has to be extensively linked to numerous external data sources. Database represents the result of the manual annotation work aimed at making the DNAtraffic database much more useful for a wide range of systems biology applications. DNAtraffic database is freely available and can be queried by the name of DNA network process, DNA damage, protein, disease, and drug. dna, cell cycle, genome, nomenclature, ontology, structure, function, protein, chromatin remodeling, dna repair, damage response pathway, pathway, damage, drug, annotation, disease, dna network process, dna damage, gene sequence, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: Polish Academy of Sciences Warsaw; Warsaw; Poland
Norwegian Financial Mechanism PNRF-143-AI-1/07;
Polish Ministry of Science and Higher Education N N301 165835
PMID:22110027 Free biotools:dnatraffic, nlx_151312 https://bio.tools/dnatraffic SCR_008886 DNAtraffic database 2026-09-03 05:02:50 0
SPIKE
 
Resource Report
Resource Website
100+ mentions
SPIKE (RRID:SCR_010466) SPIKE data or information resource, database, service resource Database of curated human signaling pathways with an associated interactive software tool for analysis and dynamic visualization of pathways. Individual pathway maps can be viewed and downloaded; the entire database may be browsed, or launched via a map viewer tool that allows dynamic visualization of the database and save networks in XGMML format that can be viewed in all generic XGMML viewers. Map Topics * Cell cycle progress and check points * DNA damage response * Programmed cell death related processes * Stress-activated transcription factors * Mitogen-activated protein kinase pathways * Immune response signaling * HEarSpike: hearing related pathways visualization, analysis, cellular, signaling pathway, regulatory network, function, genomic, proteomic, cell cycle, dna damage, cell death, stress, transcription factor, mitogen, protein kinase, pathway, immune response, signaling, hearing, dna damage response, programmed cell death, development, ear, bio.tools, FASEB list is listed by: bio.tools
is listed by: Debian
is related to: ConsensusPathDB
has parent organization: Tel Aviv University; Ramat Aviv; Israel
Cancer A-T Children's Project ;
Wolfson Foundation ;
European Union FP7 ;
Israel Science Foundation
PMID:21097778
PMID:18289391
biotools:spike, nlx_157705 https://bio.tools/spike SCR_010466 Signaling Pathway Integrated Knowledge Engine 2026-09-03 05:03:19 131
NEBcutter
 
Resource Report
Resource Website
100+ mentions
NEBcutter (RRID:SCR_010664) analysis service resource, data analysis service, production service resource, service resource This tool will take a DNA sequence and find the large, non-overlapping open reading frames using the E.coli genetic code and the sites for all Type II and commercially available Type III restriction enzymes that cut the sequence just once. By default, only enzymes available from NEB are used, but other sets may be chosen. Just enter your sequence and submit. Further options will appear with the output. The maximum size of the input file is 1 MByte, and the maximum sequence length is 300 KBases. NEBcutter produces a variety of outputs including restriction enzyme maps, theoretical digests and links into the restriction enzyme database, REBASE (http://rebase.neb.com/rebase/rebase.html). Importantly, its table of recognition sites is updated daily from REBASE and it marks all sites that are potentially affected by DNA methylation (Dam, Dcm, etc.). Many options exist to choose the enzymes used for digestion, including all known specificities, subsets of those that are commercially available or sets of enzymes that produce compatible termini. bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
has parent organization: New England Biolabs
PMID:12824395 biotools:nebcutter, nlx_71778 https://bio.tools/nebcutter SCR_010664 2026-09-03 05:03:03 151
omiRas
 
Resource Report
Resource Website
10+ mentions
omiRas (RRID:SCR_010833) omiRas analysis service resource, data analysis service, production service resource, service resource A web server for the annotation, comparison and visualization of interaction networks of non-coding RNAs derived from small RNA-Sequencing experiments of two different conditions. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:23946503 biotools:omiras, OMICS_00383 https://bio.tools/omiras SCR_010833 2026-09-03 05:03:02 14

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    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    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 NIF 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.