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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
BaCelLo
 
Resource Report
Resource Website
10+ mentions
BaCelLo (RRID:SCR_011965) BaCelLo data analysis service, production service resource, service resource, analysis service resource A predictor for the subcellular localization of proteins in eukaryotes that is based on a decision tree of several support vector machines (SVMs). It classifies up to four localizations for Fungi and Metazoan proteins and five localizations for Plant ones. BaCelLo's predictions are balanced among different classes and all the localizations are considered as equiprobable. protein, data set, proteome is listed by: OMICtools
is listed by: SoftCite
has parent organization: University of Bologna; Bologna; Italy
PMID:16873501 OMICS_01616 SCR_011965 2026-02-13 10:56:50 45
Smart Dictionary Lookup
 
Resource Report
Resource Website
Smart Dictionary Lookup (RRID:SCR_000568) Smart Dictionary Lookup data or information resource, service resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 9, 2022. System that retrieves relevant UniProt IDs from BioThesaurus entries using a soft string matching algorithm. gene, protein uses: UniProt
uses: BioThesaurus
is listed by: OMICtools
has parent organization: University of Manchester; Manchester; United Kingdom
PMID:17698493 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01198 SCR_000568 2026-02-13 10:54:42 0
MAPPER - Multi-genome Analysis of Positions and Patterns of Elements of Regulation
 
Resource Report
Resource Website
10+ mentions
MAPPER - Multi-genome Analysis of Positions and Patterns of Elements of Regulation (RRID:SCR_003077) MAPPER, MAPPER 2, data or information resource, service resource, database A platform composed of three modules: the Database, the Search Engine, and rSNPs, for the computational identification of transcription factor binding sites (TFBSs) in multiple genomes, that combines TRANSFAC and JASPAR data with the search power of profile hidden Markov models (HMMs). The Database contains putative TFBSs found in the upstream sequences of genes from the human, mouse and D.melanogaster genomes. For each gene, they scanned the region from 10,000 base pairs upstream of the transcript start to 50 base pairs downstream of the coding sequence start against all their models. Therefore, the database contains putative binding sites in the gene promoter and in the initial introns and non-coding exons. Information displayed for each putative binding site includes the transcription factor name, its position (absolute on the chromosome, or relative to the gene), the score of the prediction, and the region of the gene the site belongs to. If the selected gene has homologs in any of the other two organisms, the program optionally displays the putative TFBSs in the homologs. The Search Engine allows the identification, visualization and selection of putative TFBSs occurring in the promoter or other regions of a gene from the human, mouse, D.melanogaster, C.elegans or S.cerevisiae genomes. In addition, it allows the user to upload a sequence to query and to build a model by supplying a multiple sequence alignment of binding sites for a transcription factor of interest. rSNPs MAPPER is designed to identify Single Nucleotide Polymorphisms (SNPs) that may have an effect on the presence of one or more TFBSs. transcription factor binding site, gene promoter, intron, non-coding exon, transcription factor, chromosome, gene, homolog, rsnp, single nucleotide polymorphism, search engine is listed by: OMICtools
has parent organization: University of Florida; Florida; USA
is parent organization of: rSNPs MAPPER
PMID:15608292
PMID:15799782
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01877, nif-0000-03101 http://bio.chip.org/mapper SCR_003077 Multi-genome Analysis of Positions and Patterns of Elements of Regulation, MAPPER 2 - Multi-genome Analysis of Positions and Patterns of Elements of Regulation, MAPPER database 2026-02-13 10:55:10 11
HomoloGene
 
Resource Report
Resource Website
100+ mentions
HomoloGene (RRID:SCR_002924) HomoloGene data or information resource, service resource, database Automated system for constructing putative homology groups from complete gene sets of wide range of eukaryotic species. Databse that provides system for automatic detection of homologs, including paralogs and orthologs, among annotated genes of sequenced eukaryotic genomes. HomoloGene processing uses proteins from input organisms to compare and sequence homologs, mapping back to corresponding DNA sequences. Reports include homology and phenotype information drawn from Online Mendelian Inheritance in Man, Mouse Genome Informatics, Zebrafish Information Network, Saccharomyces Genome Database and FlyBase. homolog, paralog, ortholog, genome, gene, protein, protein alignment, phenotype, conserved domain, homology, amino acid sequence, cell, dna, gold standard is used by: NIF Data Federation
is used by: Nowomics
is used by: MitoMiner
is listed by: OMICtools
is listed by: re3data.org
is related to: OMIM
is related to: Mouse Genome Informatics (MGI)
is related to: Zebrafish Information Network (ZFIN)
is related to: SGD
is related to: FlyBase
is related to: ProbeMatchDB 2.0
is related to: Biomine
is related to: Consensus CDS
has parent organization: NCBI
PMID:23193264 Free, Freely availalbe nif-0000-02975, r3d100010781, OMICS_01544 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=homologene
https://doi.org/10.17616/R3889F
SCR_002924 NCBI HomoloGene 2026-02-13 10:55:08 437
ResponseNet
 
Resource Report
Resource Website
1+ mentions
ResponseNet (RRID:SCR_003176) ResponseNet data analysis service, production service resource, service resource, analysis service resource WebServer that identifies high-probability signaling and regulatory paths that connect input data sets. The input includes two weighted lists of condition-related proteins and genes, such as a set of disease-associated proteins and a set of differentially expressed disease genes, and a molecular interaction network (i.e., interactome). The output is a sparse, high-probability interactome sub-network connecting the two sets that is biased toward signaling pathways. This sub-network exposes additional proteins that are potentially involved in the studied condition and their likely modes of action. Computationally, it is formulated as a minimum-cost flow optimization problem that is solved using linear programming. interactome, gene, protein, signaling pathway, signaling, regulatory, pathway, regulatory pathway, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Ben-Gurion University of the Negev; Beer-Sheva; Israel
PMID:23761447
PMID:21576238
Free, Freely available biotools:responsenet, OMICS_01562 https://bio.tools/responsenet http://netbio.bgu.ac.il/respnet/ SCR_003176 2026-02-13 10:55:11 4

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