{"id":48658,"date":"2020-07-10T03:00:23","date_gmt":"2020-07-10T01:00:23","guid":{"rendered":"https:\/\/www.cde.ual.es\/?p=48658"},"modified":"2021-11-18T10:27:06","modified_gmt":"2021-11-18T09:27:06","slug":"h2020-shortening-the-path-to-rare-disease-diagnosis-by-using-newborn-genetic-screening-and-digital-technologies","status":"publish","type":"post","link":"https:\/\/www.cde.ual.es\/en\/h2020-shortening-the-path-to-rare-disease-diagnosis-by-using-newborn-genetic-screening-and-digital-technologies\/","title":{"rendered":"H2020. Shortening the path to Rare Disease diagnosis by using newborn genetic screening and digital technologies"},"content":{"rendered":"<p><strong>The overall objective of this call topic is to shorten the path to RD diagnosis by using newborn \/ paediatric (infants during their first weeks of life) genetic screening; and, via application of advanced digital technologies that enable rare disease diagnosis \/ identification. <\/strong>The latter might require consolidation of existing fragmented efforts.<\/p>\n<p><a href=\"https:\/\/www.cde.ual.es\/wp-content\/uploads\/2019\/04\/Bebe.jpg\"><img decoding=\"async\" class=\"wp-image-16291 aligncenter\" src=\"https:\/\/www.cde.ual.es\/wp-content\/uploads\/2019\/04\/Bebe-300x200.jpg\" alt=\"\" width=\"413\" height=\"275\" srcset=\"https:\/\/www.cde.ual.es\/wp-content\/uploads\/2019\/04\/Bebe-300x200.jpg 300w, https:\/\/www.cde.ual.es\/wp-content\/uploads\/2019\/04\/Bebe-768x513.jpg 768w, https:\/\/www.cde.ual.es\/wp-content\/uploads\/2019\/04\/Bebe.jpg 960w\" sizes=\"(max-width: 413px) 100vw, 413px\" \/><\/a><\/p>\n<h3>Specific objectives<\/h3>\n<ul>\n<li>Assessment and development of a comprehensive, strategic overview of existing converging RD resources e.g. databases, registries (such as the EU RD platform), natural history projects, platforms, reference networks, rare disease academic centers of excellence (e.g. European Reference Networks (ERNs)), and initiatives for evaluation \/ identification of potential collaboration and synergies;<\/li>\n<li>Federation of available RD databases into a RD metadata repository amenable to machine learning or other advanced digital tools;<\/li>\n<li>Co-creating a sustainable strategy for newborn genetic screening and pilot it. This could start directly after achieving objective 1;<\/li>\n<li>Based on the output of objectives 1 &amp; 2:\n<ul>\n<li>Repurposing of pre-existing diagnosis AI algorithm to identify early onset RD patients in electronic health records (EHRs). This will include at least 3 pilots in better-known rare diseases (with the understanding that solutions and algorithms developed or adapted should be amenable or made amenable to be emulated for larger sets of better-known RDs) where more robust data is available to train and test the AI algorithm(s), and \/ or;<\/li>\n<li>Design and development of new AI algorithm(s) to achieve the above goal.<\/li>\n<\/ul>\n<\/li>\n<li>Based on insights generated by objectives 1, 2 &amp; 4, either repurposing or development of a broad AI RD diagnosis \u201csymptom checker\u201d to help undiagnosed RD patients going from one health care provider (HCP) to another. In addition, exploration of further viable options to implement the symptom checker in actionable solutions for HCPs and patients.<\/li>\n<\/ul>\n<h3><span class=\"topicdescriptionkind\">Expected Impact<\/span><\/h3>\n<p>In their proposals, applicants should describe how the outputs of the project will contribute to the following impacts and include, wherever possible, baseline, targets and metrics to measure impact.<\/p>\n<h3>Deadline<\/h3>\n<p>29 September 2020 17:00:00 Brussels time<\/p>\n<h3>More information<\/h3>\n<p><a href=\"https:\/\/ec.europa.eu\/info\/funding-tenders\/opportunities\/portal\/screen\/opportunities\/topic-details\/imi2-2020-23-05;freeTextSearchKeyword=;typeCodes=0,1;statusCodes=31094502,31094501;programCode=null;programDivisionCode=null;focusAreaCode=null;crossCuttingPriorityCode=null;callCode=Default;sortQuery=openingDate;orderBy=desc;onlyTenders=false;topicListKey=topicSearchTablePageState\">Call<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The overall objective of this call topic is to shorten the path to RD diagnosis by using newborn \/ paediatric (infants during their first weeks of life) genetic screening; and, via application of advanced digital technologies that enable rare disease diagnosis \/ identification. The latter might require consolidation of existing fragmented efforts. Specific objectives Assessment [&hellip;]<\/p>\n","protected":false},"author":101012,"featured_media":16291,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_genesis_hide_title":false,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":"","footnotes":""},"categories":[366,4056,4054],"tags":[2058,2057],"class_list":{"0":"post-48658","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-eu-calls-and-awards","8":"category-glob-challenges-en","9":"category-horizon-europe","10":"tag-digital-technologies","11":"tag-newborn-genetic","12":"entry"},"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>H2020. 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