{"id":1039002,"date":"2012-03-23T03:18:19","date_gmt":"2012-03-23T03:18:19","guid":{"rendered":"http:\/\/www.immortalitymedicine.tv\/uncategorized\/emerge-network-launches-publicly-available-database-of-phenotype-identification-algorithms.php"},"modified":"2024-08-17T16:23:12","modified_gmt":"2024-08-17T20:23:12","slug":"emerge-network-launches-publicly-available-database-of-phenotype-identification-algorithms","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/pharmacogenomics\/emerge-network-launches-publicly-available-database-of-phenotype-identification-algorithms.php","title":{"rendered":"EMERGE Network Launches Publicly Available Database of Phenotype Identification Algorithms"},"content":{"rendered":"<p><p>    By Uduak Grace    Thomas  <\/p>\n<p>    SAN FRANCISCO, Calif.  The Electronic Medical    Records and Genomics Network has launched an open resource,    dubbed the Phenotype KnowledgeBase, which offers    access to validated algorithms for identifying patients with    specific disease phenotypes based on data in their electronic    medical records.  <\/p>\n<p>    Joshua Denny, an assistant professor in the biomedical    informatics and medical departments at eMERGE participant    Vanderbilt University, described the new resource at the    American Medical Informatics Association's Summit on    Translational Bioinformatics here this week.  <\/p>\n<p>    PheKB currently includes 12 algorithms developed by members of    the eMERGE consortium, though others are welcome to contribute    their tools, Denny told BioInform.  <\/p>\n<p>    The algorithms use natural language processing techniques to    mine EMR data for patients with particular conditions of    interest to researchers, such as cataracts, Alzheimers    disease, low levels of high-density lipoprotein, type II    diabetes, among others.  <\/p>\n<p>    These algorithms make their selections using various search    criteria, such as ICD9 codes, current procedural terminology    codes, laboratories, and medications, according to the website.  <\/p>\n<p>    Scientists from the consortium have been using the algorithms    for a number of projects, including a study published last    April in which they mined data from five institutions to find    patients in each of five disease groups (BI    04\/22\/0011).  <\/p>\n<p>    Denny explained that the consortium developed the database so    that its tools could be better disseminated to other research    efforts that are also studying disease phenotypes such as the    Pharmacogenomics Research Network.  <\/p>\n<p>    Initially, the eMERGE algorithms were made available through    the consortiums Wikipedia page, but that method did not allow    the kind of interactivity the researchers were looking for,    Denny said.  <\/p>\n<p>    Through PheKB, users can share their own tools as well as any    updates that they make to existing algorithms on the website,    he said.  <\/p>\n<\/p>\n<p>Go here to read the rest:<br \/>\n<a target=\"_blank\" href=\"http:\/\/www.genomeweb.com\/informatics\/emerge-network-launches-publicly-available-database-phenotype-identification-alg\" title=\"EMERGE Network Launches Publicly Available Database of Phenotype Identification Algorithms\" rel=\"noopener\">EMERGE Network Launches Publicly Available Database of Phenotype Identification Algorithms<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> By Uduak Grace Thomas SAN FRANCISCO, Calif. The Electronic Medical Records and Genomics Network has launched an open resource, dubbed the Phenotype KnowledgeBase, which offers access to validated algorithms for identifying patients with specific disease phenotypes based on data in their electronic medical records. Joshua Denny, an assistant professor in the biomedical informatics and medical departments at eMERGE participant Vanderbilt University, described the new resource at the American Medical Informatics Association's Summit on Translational Bioinformatics here this week.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/pharmacogenomics\/emerge-network-launches-publicly-available-database-of-phenotype-identification-algorithms.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[1246862],"tags":[],"class_list":["post-1039002","post","type-post","status-publish","format-standard","hentry","category-pharmacogenomics"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/1039002"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=1039002"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/1039002\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=1039002"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=1039002"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=1039002"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}