{"id":261,"date":"2022-12-20T10:33:18","date_gmt":"2022-12-20T01:33:18","guid":{"rendered":"http:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/?page_id=261"},"modified":"2022-12-26T15:09:05","modified_gmt":"2022-12-26T06:09:05","slug":"symposium%e3%80%80%ef%bc%92%ef%bc%90%ef%bc%91%ef%bc%97","status":"publish","type":"page","link":"https:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/symposium%e3%80%80%ef%bc%92%ef%bc%90%ef%bc%91%ef%bc%97\/","title":{"rendered":"Symposium 2017"},"content":{"rendered":"\n

The 5th Kyoto Course on Bioinformatics for Genomic Medicine
International Symposium on Genomic Medicine \u2013 Genomics of Rare and Intractable Diseases
November 10th, 2017 Confirmed Speakers and Talk Titles<\/strong><\/p>\n\n\n\n

November 10 : Rare Diseases Symposium<\/strong><\/p>\n\n\n\n

9:00 \u2013 9:05 Opening Remarks<\/strong><\/p>\n\n\n\n

Fumihiko Matsuda (Kyoto University, Japan)<\/p>\n\n\n\n

9:05 \u2013 9:10 Welcome Remarks<\/strong><\/p>\n\n\n\n

Nagahiro Minato (Provost, Vice President, Kyoto University, Japan)<\/p>\n\n\n\n

Session 1 Chairperson: Fumihiko Matsuda & Ivo Gut<\/strong><\/p>\n\n\n\n

9:10 \u2013 9:55 The Exome and Beyond \u2013 Identifying Causes of Rare Genetic Diseases<\/strong><\/p>\n\n\n\n

Jacek Majewski (McGill University, Canada)<\/p>\n\n\n\n

9:55 \u2013 10:40 The 100,000 Genomes Project Transforming Healthcare<\/strong><\/p>\n\n\n\n

Mark J. Caulfield (Queen Mary University of London, UK)<\/p>\n\n\n\n

10:40 \u2013 11:00 Coffee break<\/em><\/strong><\/p>\n\n\n\n

11:00 \u2013 11:45 Rare Variants in Rare and Intractable Diseases<\/strong><\/p>\n\n\n\n

Naomichi Matsumoto (Yokohama City University, Japan)<\/p>\n\n\n\n

11:45 \u2013 12:30 Genomics of Complex Cerebral Small Vessel Disease<\/strong><\/p>\n\n\n\n

St\u00e9phanie Debette (University of Bordeaux, France)<\/p>\n\n\n\n

12:30 \u2013 13:30 Lunch<\/em><\/strong><\/p>\n\n\n\n

Session 2 Chairperson: Mark Lathrop & Jacek Majewski<\/strong><\/p>\n\n\n\n

13:30 \u2013 14:15 Genomics of Rare Cerebral Small Vessel Disease<\/strong><\/p>\n\n\n\n

Elisabeth Tournier-Lasserve (Paris Diderot University, France)<\/p>\n\n\n\n

14:15 \u2013 15:00 Uncovering the Metabolic Pleiotropy of Rare Disorders: The Example of Fragile X Syndrome<\/strong><\/p>\n\n\n\n

Marc-Emmanuel Dumas (Imperial College London, UK)<\/p>\n\n\n\n

15:00 \u2013 15:20 Coffee break <\/em><\/strong><\/p>\n\n\n\n

15:20 \u2013 16:05 Data Integration for Rare Diseases Facilitated by the RD-Connect Genome Phenome Platform<\/strong><\/p>\n\n\n\n

Ivo Gut (Centro Nacional de An\u00e1lisis Gen\u00f3mico, Spain)<\/p>\n\n\n\n

16:05 \u2013 16:50 Perspectives of Large-scale ALS Patient Registry Study<\/strong><\/p>\n\n\n\n

Gen Sobue (Nagoya University, Japan)<\/p>\n\n\n\n

Session 3 Short talks<\/strong><\/p>\n\n\n\n

16:50 \u2013 17:10 Collaborative Research on Analytics Platform for Rare Disease<\/strong><\/p>\n\n\n\n

Atsushi Takano (IBM Japan, Japan)<\/p>\n\n\n\n

17:10 \u2013 17:30 Application of AI technology to Identify Unknown Causal Genes of Mendelian Disorders via WGS<\/strong><\/p>\n\n\n\n

Shuji Kawaguchi (Kyoto University, Japan)<\/p>\n\n\n\n

17:30 \u2013 17:50 Development of Muscle Pathology Diagnosis Support System by Deep Learning<\/strong><\/p>\n\n\n\n

Mariko Okubo (National Center of Neurology and Psychiatry, Japan)<\/p>\n\n\n\n

17:50 \u2013 Closing Remarks<\/strong><\/p>\n\n\n\n

Mark Lathrop (McGill University, Canada)<\/p>\n","protected":false},"excerpt":{"rendered":"

The 5th Kyoto Course on Bioinformatics for Genomic MedicineInternational Symposium on Genomic Medicine \u2013 Genomics of Rare and Intractable DiseasesNovember 10th, 2017 Confirmed Speakers and Talk Titles November 10 : Rare Diseases Symposium 9:00 \u2013 9:05 Opening Remarks Fumihiko Matsuda (Kyoto University, Japan) 9:05 \u2013 9:10 Welcome Remarks Nagahiro Minato (Provost, Vice President, Kyoto University,…<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"tags":[],"class_list":["post-261","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/wp-json\/wp\/v2\/pages\/261","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/wp-json\/wp\/v2\/comments?post=261"}],"version-history":[{"count":3,"href":"https:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/wp-json\/wp\/v2\/pages\/261\/revisions"}],"predecessor-version":[{"id":378,"href":"https:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/wp-json\/wp\/v2\/pages\/261\/revisions\/378"}],"wp:attachment":[{"href":"https:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/wp-json\/wp\/v2\/media?parent=261"}],"wp:term":[{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/w3.genome.med.kyoto-u.ac.jp\/en\/wp-json\/wp\/v2\/tags?post=261"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}