000human2010-10-30 00:46:12http://browser.1000genomes.org/Homo_sapiens/Gene/Summary?db=core;g={{EnsemblGene}}2011-05-03 22:46:258.078.0836browser.1000genomes.orgbiogpsusersNo summary provided.pluginasu/profile/3/asuAndrew Supubliciframehuman1000 Genomes Browser1015True8.0Disease and Gene Annotations (DGA) is collaborative effort, aiming to provide a comprehensive and integrated annotation to human genome by using computable, controlled vocabulary of Disease Ontology (DO), NCBI Gene Reference Into Function (GeneRIF), and molecular interaction networks. The Disease Ontology was initially developed as part of the NUgene project starting in 2003 at Northwestern. Built on the Gene Ontology (GO) Consortium and Open Biological and Biomedical Ontologies (OBO) Foundry, DO delineates a semantically computable structure of inherited, environmental and infectious human disease that is based on a manually inspected subset of the Unified Medical Language System (UMLS) and other terms outside UMLS. The DO is organized as a directed acyclic graph (DAG). Every DO term is unique and contains textual description and external references to well-established, well-adopted terminologies that contain disease and disease related concepts such as UMLS, Medical Subject Headings (MeSH), SNOMED, OMIM and International Classification of Diseases (ICD)-9 and ICD-10. GeneRIF offers functional description to genes with high quality and frequency of update. GeneRIF is brief textual description (up to 250 characters) to gene provided by NCBI database. Every GeneRIF entry is associated a certain PubMed ID, showing biological evidences related to the description. NCBI also provides an open access to GeneRIF so that the community can contribute to GeneRIF production, which enables low mapping error of gene and high-frequent update. With intelligent electric annotation program, DGA brings them together to build a comprehensive set of disease-to-gene relationships with high disease –gene coverage and keeps the resulting knowledge current responding to update of DO and GeneRIF. Further, DGA integrates various types of molecular interaction networks so that users can investigate the relationships between disease-related genes and infer associations between diseases.annotationdiseaseofhttp://dga.nubic.northwestern.edu/pages/result.php?st=g2d&qn={{Symbol}}2012-12-08 04:12:038.062012-12-06 23:44:331063dga.nubic.northwestern.edubiogpsusersDisease and Gene Annotations (DGA) is collaborative effort that provides an integrated disease annotation for the human genomepluginwakibbe/profile/6276/wakibbeWarren KibbepubliciframehumanDisease and Gene Annotations (DGA)000None8.0Taqman gene expression assays from Applied Biosystems formerly ABIreagentshttps://www.lifetechnologies.com/order/genome-database/browse/gene-expression/gene-id/{{EntrezGene}}?referrer=BioGPS2013-12-18 02:11:418.082008-05-16 23:21:0153www.lifetechnologies.combiogpsusersTaqman gene expression assays from Life Technologiespluginasu/profile/3/asuAndrew Supubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigLife Technologies Taqman Gene Expression000human8.0Plasmid Information Database (PlasmID) is a central repository for plasmid clone collections and distribution as part of the DF/HCC DNA Resource Core based at the Harvard Institute of Proteomics (HIP). We are also the Protein Structure Initiative (PSI) Material Repository. geneticsplasmidhttp://plasmid.med.harvard.edu/PLASMID/RefseqSearchContinue.do?cdna=true&shrna=true&genomicfragment=true&tfbindsite=true&genome=true&pagesize=50&species=Homo%20sapiens&refseqType=cDNA&searchType=Gene%20ID&searchString={{EntrezGene}}2011-05-03 22:49:098.082008-12-22 17:33:26262plasmid.med.harvard.edubiogpsusersPlasmid Information Database (PlasmID) is a central repository for plasmid clone collections and distribution as part of the DF/HCC DNA...pluginasu/profile/3/asuAndrew SupubliciframehumanPlasmID000None8.0The Inparanoid program was developed at the Center for Genomics and Bioinformatics to address the need to identify orthologs. Homologs that originate from a speciation event are called orthologs and homologs that originate from a gene duplication event are called paralogs. If a duplication event predates the speciation event the parlogs are called outparalogs, and they can be present in different species. If instead an ortholog undegoes one or several duplication events, the resulting paralogs are called inparalogs, and they are co-orthologs to one or more orthologs in another species. Since an outparalog pair ought to have a more diversified function than inparalogs, it is useful to distinguish between the two. Furthermore, clustering inparalogs together allows proper identification of both one-to-one and many-to-many orthology cases. More in-depth information on this subject, the Inparanoid program and its applications has been previously published ( 1 ). The InParanoid program is available upon request to inparanoid@sbc.su.se homologinparanoidparaloghttp://inparanoid.sbc.su.se/cgi-bin/gene_search.cgi?id={{EnsemblGene}}&idtype=all&all_or_selection=all&specieslist=10&scorelimit=0.05&.submit=Submit+Query&.cgifields=specieslist&.cgifields=idtype&.cgifields=all_or_selection2009-05-05 01:07:438.072009-05-05 01:07:43438inparanoid.sbc.su.sebiogpsusersThe Inparanoid program was developed at the Center for Genomics and Bioinformatics to address the need to identify orthologs. Homologs...plugincdoherty/profile/784/cdohertyColleen Dohertypubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigInParanoid Search000None2009-12-08 17:02:05http://genechaser.stanford.edu/imgCreaterTable.php?geneId={{EntrezGene}}&qValue=0.01&isHomology=on&fold=2&rank=0&display=&orderBy=Fold&limitRec=20&cPage=1&titleIn=&typeSource=All2009-12-08 17:02:137.077.0592genechaser.stanford.edubiogpsusersNo summary provided.pluginasu/profile/3/asuAndrew Supubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigGeneChaser000None7.0Key Products & Services, Biotechnology Division: * Proteins * Antibodies * ELISA/Assay Kits * ELISpot Kits * Multiplex Assays/Arrays * Flow Cytometry Kits * mRNA Quantitation Kits * Cell Selection Kits * Cell Culture & Stem Cell Reagents * Primer Pairs * Supplemental Research Reagents * Assay Services (Analytical Testing Service and Custom Assay Development)reagentshttp://www.rndsystems.com/product_results.aspx?r=0&c=0&s=0&a=0&m=0&k={{Symbol}}&o=AND&b=False&referrer=BioGPS2009-08-03 17:02:017.062008-09-11 22:33:12138www.rndsystems.combiogpsusersKey Products & Services, Biotechnology Division: * Proteins * Antibodies * ELISA/Assay Kits * ELISpot Kits *...pluginasu/profile/3/asuAndrew Supubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigR&D Systems000None7.0US Patent and Trademark Officeliteraturepatentusptohttp://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO2&Sect2=HITOFF&p=1&u=%2Fnetahtml%2FPTO%2Fsearch-bool.html&r=0&f=S&l=50&TERM1={{Symbol}}&FIELD1=&co1=AND&TERM2=&FIELD2=&d=PTXT2009-02-05 22:39:317.062009-02-05 22:39:31330patft.uspto.govbiogpsusersUS Patent and Trademark Officepluginasu/profile/3/asuAndrew Supubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigUS Patent Full Text Database 000None7.0cancerhttp://cbio.mskcc.org/tcga-generanker/humanGeneDetails.jsp?entrez_gene_id={{EntrezGene}}2011-06-16 18:49:197.062011-06-16 03:56:28943cbio.mskcc.orgbiogpsusersGene Ranker from MSKCC ranks genes for an association with cancer using 39 gene listsplugintharding/profile/4676/thardingthardingpubliciframehumanGene Ranker: TCGA GBM 6000000None2014-04-08 02:40:53http://japantobacco.nextbio.com/c/home/home.nb?q={{Symbol}}2014-04-08 02:40:537.077.01151japantobacco.nextbio.combiogpsusersNo summary provided.pluginnaotofuruhata/profile/7715/naotofuruhatanaotofuruhatapubliciframehumanmouseratJT_NextBio