Neljapäev, 18. juuni 2015   08:40-09:00 Registreerimine 09:00 KONVERENTSI AVAMINE Dr. Marco Kirm, Vice-Rector for Research, University of Tartu, Estonia Dr. Tõnu Esko, Estonian Genome Center, University of Tartu, Estonia 09:15-10:40 AVASESSIOON Chair: Prof. Andres Metspalu, University of Tartu, Estonia Prof. Uta Francke, Stanford University, 23andMe, US DNA is not a diagnosis: Interpreting and Communicating Sequence Variants Dr. Heiko Runz, Merck Research, US Leveraging human genetics for drug discovery 10:40-11:00 KOHVI / TEE 11:00-12:45 I SESSIOON Chair: Dr. Mait Metspalu, Estonian Biocentre, Estonia Dr. Garrett Hellenthal, UCL Genetics Institute (UGI), Department of Genetics, Evolution and Environment, UK The genetic history of the United Kingdom: the POBI project Dr. Luca Pagani, Sanger Center, UK 450 diverse high coverage whole genome sequences reveal ancient population admixture in modern human populations Prof. Boris Lenhard, Faculty of Medicine, Institute of Clinical Science, Imperial College of London, UK Promoters and long-range regulation in vertebrate development 12:45-13:55 LÕUNA 13:55-15:40 II SESSIOON Chair: Dr. Lili Milani, University of Tartu, Estonia Prof. Claes Wadelius, University of Uppsala, Sweden The secrets of GWAS are written in the reads Dr. Mia Wadelius, Department of Medical Sciences, University of Uppsala, Sweden Pharmacogenomics in the clinic - warfarin and other examples Dr. Valtteri Wirta, Science for Life Laboratory, Sweden Implementing exome and whole-genome sequencing for clinical diagnosis of inherited disorders 15:40-16:00 KOHVI / TEE 16:00-17:45 III SESSIOON Chair: Prof. Ursel Soomets, University of Tartu, Estonia Prof. Mart Saarma, Institute of Biotechnology, University of Helsinki, Finland Neurotrophic factors for neurodegenerative diseases Prof. Julian Knight, Wellcome Trust Centre for Human Genetics, Oxford, UK Understanding context specific eQTL informative for immune-related disease Dr. Andreas Pfenning, Massachusetts Institute of Technology, Computer Science and Artificial Intelligence Laboratory, US Interpreting GWAS loci through epigenomics: insights into Alzheimer’s and obesity 20:00 ÕHTUSÖÖK served at restaurant Atlantis Reede, 19. juuni 2015   09:30-11:00 IV SESSIOON Chair: Prof. Andres Metspalu, University of Tartu, Estonia Prof. Reiner Leidl, Munich School of Management, Ludwig-Maximilians University, Germany Health economics can help to improve use of genetic information in health care Prof. Jacques Beckmann, Swiss Institute of Bioinformatics, Switzerland Personalised approaches to disease and health Luc Smink, District Manager for Northern Europe, Illumina Inc, Human Genome Analysis at Scale 11:00-11:20 KOHVI / TEE 11:20-13:05 V SESSIOON Big Data Driven Medicine Chair: Prof. Jaak Vilo, University of Tartu, Estonia Dr. Ali Torkamani, Director of Genome Informatics, Scripps Translational Science Institute, US The Scripps Idiopathic Diseases in Man Initiative Prof. Peeter Ross, Tallinn Technical University, Estonia Integration of genome, health and medical data in personalised medicine Prof. Charles Auffray, European Institute for Systems Biology and Medicine Université de Lyon, France Revolutionizing healthcare and wellness management through systems medicine 13:05-14:15 LÕUNA 14:15-16:00 VI SESSIOON Neurobiology Chair: Dr. Tõnu Esko, University of Tartu, Estonia Prof. Patrick Sullivan, UNC School of Medicine, US/ Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Sweden Schizophrenia genomics: where we are & where we need to be Prof. Cynthia Bulik, UNC School of Medicine, US/Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Sweden Viewing Eating Disorders Through New Lenses: Genes & Bugs Dr. Reedik Mägi, Estonian Genome Center, University of Tartu, Estonia Genetics of obesity and beyond 16:00 KONVERENTSI LÕPETAMINE