Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Preparing word cloud

×

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.

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Related Resources:omictools (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

2,818 Results - per page

Show More Columns | Download Top 1000 Results

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
DBTSS: Database of Transcriptional Start Sites
 
Resource Report
Resource Website
100+ mentions
DBTSS: Database of Transcriptional Start Sites (RRID:SCR_002354) DBTSS database, data or information resource Database of transcriptional start sites (TSSs) representing exact positions in the genome based on a unique experimentally validated TSS sequencing method, TSS Seq. A major part of human adult and embryonic tissues are covered. DBTSS contains 491 million TSS tag sequences collected from a total of 20 tissues and 7 cell cultures. Also integrated is generated RNA-seq data of subcellular- fractionated RNAs and ChIP Seq data of histone modifications, RNA polymerase II and several transcriptional regulatory factors in cultured cell lines. Also included is external epigenomic data, such as chromatin map of the ENCODE project. They associated those TSS information with public and original SNV data, in order to identify single nucleotide variations (SNVs) in the regulatory regions. cdna, cdna library, transcriptional start site, transcriptome, transcriptome analysis, tss-seq, genome, adult human, embryonic, cell, rna-seq, subcellular, rna, chip seq data, histone modification, rna polymerase ii, transcriptional regulatory factor, cell line, single nucleotide variation, regulatory region, genetic valuation, transcriptional regulation, bio.tools, FASEB list is used by: Transcriptional Regulatory Element Database
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Tokyo; Tokyo; Japan
Japan Society for the Promotion of Science ;
Japanese Ministry of Education Culture Sports Science and Technology MEXT
PMID:22086958
PMID:19910371
PMID:17942421
PMID:16381981
PMID:14681363
PMID:11752328
nif-0000-02738, biotools:dbtss, OMICS_01860 https://bio.tools/dbtss SCR_002354 DBTSS: Database of Transcriptional Start Sites, DataBase of Transcriptional Start Sites 2026-08-08 12:03:53 127
MachiBase
 
Resource Report
Resource Website
1+ mentions
MachiBase (RRID:SCR_003078) MachiBase database, data or information resource Database for Drosophila melanogaster transcription profiling that allows users to search the Drosophilia genome, see sequence overviews, and look at various transcripts. The data were generated in conjunction with the recently developed high-throughput genome sequencer Illumina / Solexa using a newly developed 5'-end mRNA collection method. Approximately 25 million 25-27 nucleotide (nt) 5'-end mRNA tags from the embryos, larvae, young males, young females, old males, old females, and S2 (culture cell line) of D. melanogaster were collected. By arranging this vast amount of expression tag with other annotated data, they have built a one-stop service for Drosophila melanogaster transcription profiling. transcription profiling, genome, sequence, transcript, mrna, promoter, gene expression, development, embryo, larvae, young, male, female, old, s2, culture, cell line, expressed sequence tag, solexa is listed by: OMICtools
has parent organization: University of Tokyo; Tokyo; Japan
PMID:18842623 Free, Available for download, Freely available OMICS_01878, nif-0000-03092 SCR_003078 2026-08-08 12:03:55 1
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, database, data or information resource, service resource 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 2026-08-08 12:03:42 11
CODEHOP
 
Resource Report
Resource Website
50+ mentions
CODEHOP (RRID:SCR_002898) CODEHOP analysis service resource, data analysis service, production service resource, service resource THIS RESOURCE IS NO LONGER IN SERVICE, documented May 10, 2017. A pilot effort that has developed a centralized, web-based biospecimen locator that presents biospecimens collected and stored at participating Arizona hospitals and biospecimen banks, which are available for acquisition and use by researchers. Researchers may use this site to browse, search and request biospecimens to use in qualified studies. The development of the ABL was guided by the Arizona Biospecimen Consortium (ABC), a consortium of hospitals and medical centers in the Phoenix area, and is now being piloted by this Consortium under the direction of ABRC. You may browse by type (cells, fluid, molecular, tissue) or disease. Common data elements decided by the ABC Standards Committee, based on data elements on the National Cancer Institute''s (NCI''s) Common Biorepository Model (CBM), are displayed. These describe the minimum set of data elements that the NCI determined were most important for a researcher to see about a biospecimen. The ABL currently does not display information on whether or not clinical data is available to accompany the biospecimens. However, a requester has the ability to solicit clinical data in the request. Once a request is approved, the biospecimen provider will contact the requester to discuss the request (and the requester''s questions) before finalizing the invoice and shipment. The ABL is available to the public to browse. In order to request biospecimens from the ABL, the researcher will be required to submit the requested required information. Upon submission of the information, shipment of the requested biospecimen(s) will be dependent on the scientific and institutional review approval. Account required. Registration is open to everyone.Service to design PCR primers from protein multiple sequence alignments. NOTICE: This version of CODEHOP is no longer maintained. degenerate, primer, primer design, degenerate primer, oligonucleotide, pcr assay, gene, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Fred Hutchinson Cancer Center
PMID:20967601 THIS RESOURCE IS NO LONGER IN SERVICE biotools:codehop, OMICS_02339 https://bio.tools/codehop SCR_002898 COnsensus-DEgenerate Hybrid Oligonucleotide Primers, CODEHOP: COnsensus-DEgenerate Hybrid Oligonucleotide Primers 2026-08-08 12:03:42 75
qPrimerDepot
 
Resource Report
Resource Website
100+ mentions
qPrimerDepot (RRID:SCR_003469) qPrimerDepot database, data or information resource A database that provides quantitative real time (qRT) PCR primers for 99.96% human RefSeq sequences. For 99% of intron-bearing genes, the PCR product will cross an exon-exon border which overlaps one of the largest introns. Primers are assumed to have a uniform annealing temperature of 60C, allowing them to be used in large-scale assays. molecular probe, primer, quantitative real time pcr primer, refseq, quantitative real time pcr, FASEB list is listed by: OMICtools
has parent organization: National Cancer Institute
PMID:17068075 OMICS_02324, nif-0000-03381 SCR_003469 qPrimerDepot - A quantitative real time PCR primer database 2026-08-08 12:03:56 158
HyperTree
 
Resource Report
Resource Website
1+ mentions
HyperTree (RRID:SCR_003188) software resource, software application, source code Software application to visualize and navigate large trees in hyperbolic space. Features include: * visualize large trees with hundreds of nodes or more * rotate and drag the display in cartesian space * search and select nodes * copy clusters for pasting into other programs * color-code branches * label branches (eg, common family members) * zoom in and out * view phylogenetic trees and other hierarchical clusters, such as gene expression profile clusters * run on several platforms: Mac, Windows, Unix/Linux java is listed by: OMICtools PMID:11038340 Free, Available for download, Freely available biotools:hypertree, OMICS_04814 https://bio.tools/hypertree SCR_003188 2026-08-08 12:03:51 8
GeneFisher
 
Resource Report
Resource Website
10+ mentions
GeneFisher (RRID:SCR_003060) GeneFisher, GeneFisher2 analysis service resource, data analysis service, production service resource, service resource A web-based program for designing degenerate primers. The procedure leads to isolation of genes in a target organism using multiple alignments of related genes from different organisms. The term gene fishing refers to the technique where PCR is used to isolate a postulated but unknown target sequence from a pool of DNA. primer design, gene, degenerate primer, degenerate, primer, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Bielefeld University; North Rhine-Westphalia; Germany
PMID:8877506 Free, Freely available biotools:genefisher, OMICS_02341 https://bio.tools/genefisher SCR_003060 GeneFisher2 - Interactive PCR Primer Design 2026-08-08 12:03:42 39
SynSysNet
 
Resource Report
Resource Website
1+ mentions
SynSysNet (RRID:SCR_003180) SynSysNet database, data or information resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 19,2025. A curated database for synaptic proteins that provides adequate definitions of pre- and post-synaptic proteins, proteins present in sub-domains of the synapse, e.g. the synaptic vesicle and associated proteins, lipid rafts and postsynaptic density. In addition to data that was and will be gathered from the experiments conducted within SynSys - A European expertise Network on building the synapse, they have extracted and manually curated all relevant data on these proteins from other sources and provided an ontology for these. Novel splice forms are being identified that can be matched with proteomics data. Information on proteins, their 3D structure, binding small molecules Protein-Protein-Interactions (PPIs) and Compound-Protein-Interactions are integrated. Proteins or compounds can be searched and Interactive Networks can be visualized. The point Diseases present neurological diseases, to illustrate the role of SynSysNet in the medication. gene, synapse, protein, interaction, compound, disease, structure, model, compound, protein-drug interaction, protein-protein interaction, pathway, drug-target, small molecule, interaction network, homology, drug, drug-target interaction, compound-protein interaction, visualization, proteomics, network is listed by: OMICtools
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: KEGG
has parent organization: Charite - Universitatsmedizin Berlin; Berlin; Germany
Huntington's disease, Chorea Huntington, Epilepsy, Multiple Sclerosis, Parkinson's disease, Schizophrenia, Neurological disease European Union Seventh FPSYNSYS 242167;
DFG GRK1772;
DFG GRK1360
PMID:23143269 THIS RESOURCE IS NO LONGER IN SERVICE nlx_156893, OMICS_01914 SCR_003180 SynSysNet - Synaptic Proteins Database 2026-08-08 12:03:43 3
Hollywood
 
Resource Report
Resource Website
Hollywood (RRID:SCR_002920) Hollywood database, data or information resource Database built upon genomic annotation of splicing patterns of known genes derived from spliced alignment of complementary DNAs (cDNAs) and expressed sequence tags for human and mouse. It links features such as splice site sequence and strength, exonic splicing enhancers and silencers, conserved and non-conserved patterns of splicing, and cDNA library information for inferred alternative exons. A query tool allows searches for sets of exons with specific splicing characteristics or splicing regulatory element composition, or gives a graphical or sequence-level summary of splicing patterns for a specific gene. A graphical representation of gene splicing patterns is provided, and these patterns can alternatively be layered onto existing information in the UCSC Genome Browser. alternative splicing, exon, mrna, splicing, annotation, regulatory element, ortholog, splicing pattern, cdna is listed by: OMICtools
has parent organization: Massachusetts Institute of Technology; Massachusetts; USA;
PMID:16381932 Account required OMICS_01889, nif-0000-02972 SCR_002920 Hollywood.mit.edu, Hollywood mRNA Alternative Splicing, Hollywood.mit.edu - Alternatively spliced mRNA 2026-08-08 12:03:54 0
HomoloGene
 
Resource Report
Resource Website
100+ mentions
HomoloGene (RRID:SCR_002924) HomoloGene database, data or information resource, service resource 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 2026-08-08 12:03:42 459
MapViewer
 
Resource Report
Resource Website
100+ mentions
MapViewer (RRID:SCR_003092) Map Viewer database, data or information resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 4, 2023. Database that provides special browsing capabilities for a subset of organisms in Entrez Genomes. Map Viewer allows users to view and search an organism's complete genome, display chromosome maps, and zoom into progressively greater levels of detail, down to the sequence data for a region of interest. If multiple maps are available for a chromosome, it displays them aligned to each other based on shared marker and gene names, and, for the sequence maps, based on a common sequence coordinate system. genome, mapping, sequencing, chromosome is listed by: OMICtools
is related to: NCBI Genome
is related to: Consensus CDS
has parent organization: NCBI
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00921, nif-0000-03103 SCR_003092 Entrez Map Viewer, NCBI Map Viewer 2026-08-08 12:03:55 244
e-PCR
 
Resource Report
Resource Website
10+ mentions
e-PCR (RRID:SCR_003082) e-PCR analysis service resource, data analysis service, production service resource, service resource Web tool that identifies sequence tagged sites (STSs) within DNA sequences. Using e-PCR, you can search for sub-sequences that closely match the PCR primers and have the correct order, orientation, and spacing. The software may also be downloaded to run locally. sequence tagged site, dna sequence, reverse, forward is listed by: OMICtools
is listed by: Debian
has parent organization: NCBI
PMID:15215361
PMID:9149949
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02345 https://sources.debian.org/src/ncbi-epcr/ http://www.ncbi.nlm.nih.gov/sutils/e-pcr SCR_003082 Electronic PCR, Electronic PCR (e-PCR) 2026-08-08 12:03:50 13
Type-III-Secretion-System related database
 
Resource Report
Resource Website
Type-III-Secretion-System related database (RRID:SCR_002941) T3DB database, data or information resource Database aimed to annotate all bacterial Type III Secretion System (T3SS) related structure, effector, regulator, and auxiliary genes. type iii secretion system, gene, protein, ortholog is listed by: OMICtools
has parent organization: Chinese University of Hong Kong; Hong Kong; China
PMID:22545727 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_05160 SCR_002941 T3SS-related Database 2026-08-08 12:03:50 0
PlantProm DB
 
Resource Report
Resource Website
1+ mentions
PlantProm DB (RRID:SCR_003359) PlantProm database, data or information resource Annotated, non-redundant database of proximal promoter sequences for RNA polymerase II with experimentally determined transcription start site(s) (TSS) from various plant species. It contains 578 unrelated entries including 151, 396 and 31 promoters with experimentally verified TSS from monocot, dicot and other plants, respectively (April 2014). This DB presents the published promoter sequences with TSS(s) determined by direct experimental approaches and therefore serves as the most accurate source for development of computational promoter prediction tools. proximal promoter sequence, rna polymerase ii, transcription start site, promoter, monocot, dicot, dna sequence, taxonomy, promoter type, nucleotide frequency matrix, nucleotide composition, motif, transcription, regulatory element is listed by: OMICtools
has parent organization: University of London; London; United Kingdom
Pakistan European Union PMID:12519961 Free, Available for download, Freely available nif-0000-03308, OMICS_01875 http://www.softberry.com/berry.phtml?topic=plantprom&group=data&subgroup=plantprom http://mendel.cs.rhul.ac.uk/mendel.php?topic=plantprom SCR_003359 Plant Promoter Database, PlantProm DB 2026-08-08 12:03:43 8
PPDB: Plant Promoter Database
 
Resource Report
Resource Website
PPDB: Plant Promoter Database (RRID:SCR_003395) PPDB database, data or information resource A plant promoter database that provides information on transcription start sites (TSSs), core promoter structure and regulatory element groups (REGs) as putative and comprehensive transcriptional regulatory elements. Microarray data-based predictions have been appended as REG annotations which inform their putative physiological roles. gene, transcription start site, promoter structure, promoter, regulatory element group, homolog is listed by: OMICtools
has parent organization: Gifu University; Gifu; Japan
Japanese Ministry of Education Culture Sports Science and Technology MEXT PMID:24194597
PMID:17947329
Free, Available for download, Freely available nif-0000-03329, OMICS_01874 http://ppdb.gene.nagoya-u.ac.jp/cgi-bin/index.cgi SCR_003395 Plant Promoter Database 2026-08-08 12:03:43 0
NYCE
 
Resource Report
Resource Website
NYCE (RRID:SCR_003144) NYCE analysis service resource, data analysis service, production service resource, service resource Data analysis service that predicts subcellular location (either Nuclear, Nucleo-cytoplasmic, Cytoplasmic or Extracellular) of eukaryotic proteins using the predicted exposure value of their amino acids. subcellular localization, protein, amino acid, eukaryote is listed by: OMICtools
has parent organization: Max Delbruck Center for Molecular Medicine; Berlin; Germany
PMID:24283794 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01630 SCR_003144 2026-08-08 12:03:51 0
Babelomics
 
Resource Report
Resource Website
100+ mentions
Babelomics (RRID:SCR_002969) Babelomics analysis service resource, data analysis service, production service resource, service resource An integrative platform for the analysis of transcriptomics, proteomics and genomic data with advanced functional profiling. Version 4 of Babelomics integrates primary (normalization, calls, etc.) and secondary (signatures, predictors, associations, TDTs, clustering, etc.) analysis tools within an environment that allows relating genomic data and/or interpreting them by means of different functional enrichment or gene set methods. Such interpretation is made not only using functional definitions (GO, KEGG, Biocarta, etc.) but also regulatory information (from Transfac, Jaspar, etc.) and other levels of regulation such as miRNA-mediated interference, protein-protein interactions, text-mining module definitions and the possibility of producing de novo annotations through the Blast2GO system . Babelomics has been extensively re-engineered and now it includes the use of web services and Web 2.0 technology features, a new user interface with persistent sessions and a new extended database of gene identifiers. In this release GEPAS and Babelomics have integrated into a unique web application with many new features and improvements: * Data input: import and quality control for the most common microarray formats * Normalization and base calling: for the most common expression, tiling and SNP microarrays (Affymetrix and Agilent). * Transcriptomics: diverse analysis options that include well established as well as novel algorithms for normalization, gene selection, class prediction, clustering and time-series analysis. * Genotyping: stratification analysis, association, TDT. * Functional profiling: functional enrichment and gene set enrichment analysis with functional terms (GO, KEGG, Biocarta, etc.), regulatory (Transfac, Jaspar, miRNAs, etc.), text-mining, derived bioentities, protein-protein interaction analysis. * Integrative analysis: Different variables can be related to each other (e.g. gene expression to gnomic copy number) and the results subjected to functional analysis. Platform: Online tool platform, analysis, transcriptomics, proteomics, genomics, normalization, clustering, gene, mirna, protein, interaction, text mining, genotyping, bioentity, functional profiling, statistical analysis, functional annotation, regulatory motif, microarray, fatigo, biclustering, networkminer, gepas, gene expression, FASEB list is listed by: OMICtools
is listed by: Gene Ontology Tools
is related to: Gene Ontology
is related to: BioCarta Pathways
is related to: KEGG
is related to: TRANSFAC
is related to: JASPAR
has parent organization: CIPF Bioinformatics and Genomics Department
Spanish Ministry of Science and Innovation BIO2008-04212;
Spanish Ministry of Science and Innovation CEN-2008-1002;
Red Temtica de Investigacion Cooperativa en Cancer RD06/0020/1019;
Instituto de Salud Carlos III
PMID:20478823
PMID:18515841
PMID:16845052
PMID:14990455
PMID:15980512
PMID:17478504
Free for academic use, Account required OMICS_00748, nif-0000-30144 http://www.fatigo.org/, http://www.gepas.org/, http://babelomics3.bioinfo.cipf.es http://www.babelomics.org SCR_002969 Babelomics 4: Gene Expression and Functional Profiling Analysis Suite, Babelomics 4 2026-08-08 12:03:42 138
ResponseNet
 
Resource Report
Resource Website
1+ mentions
ResponseNet (RRID:SCR_003176) ResponseNet analysis service resource, data analysis service, production service resource, 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 2026-08-08 12:03:43 4
iLoc-Animal
 
Resource Report
Resource Website
1+ mentions
iLoc-Animal (RRID:SCR_003173) iLoc-Animal analysis service resource, data analysis service, production service resource, service resource Data analysis service for predicting subcellular localization of animal proteins with single or multiple sites. subcellular localization, animal, protein is listed by: OMICtools PMID:23370050 Free, Freely available OMICS_01623 https://pubs.rsc.org/en/content/articlelanding/2013/mb/c3mb25466f SCR_003173 iLoc-Animal: Predicting subcellular localization of animal proteins with single or multiple sites 2026-08-08 12:03:55 6
Hapmix
 
Resource Report
Resource Website
50+ mentions
Hapmix (RRID:SCR_004203) HAPMIX software resource, software application, source code Software application that uses genotyping data from SNP arrays for accurately inferring chromosomal segments of distinct continental ancestry in admixed populations, using dense genetic data. (entry from Genetic Analysis Software) gene, genetic, genomic, admixed, population, genotype, single nucleotide polymorphism, ancestry, chromosomal segment, snp array is listed by: OMICtools
is listed by: Genetic Analysis Software
has parent organization: Harvard Medical School; Massachusetts; USA
NHGRI U01-HG004168;
NHLBI R01-HL087699
PMID:19543370 Restricted nlx_22768, OMICS_02082 http://www.hsph.harvard.edu/faculty/alkes-price/software/, http://www.stats.ox.ac.uk/~myers/software.html, https://reich.hms.harvard.edu/software http://genetics.med.harvard.edu/reich/Reich_Lab/Software.html SCR_004203 2026-08-08 12:03:57 52

Can't find your Tool?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.

Can't find the RRID you're searching for? X
X
  1. RRID Portal Resources

    Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that RRID has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on RRID then you can log in from here to get additional features in RRID such as Collections, Saved Searches, and managing Resources.

  4. Searching

    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 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.