The 3-day course will provide a practical introduction to analysis of next generation sequencing data from handling of raw data to applications in study of human disease. As example of analysis techniques, methods to examine whole-genome, exomic, and epigenomic sequence data will be covered in depth. We will illustrate the use of sequence data in combination with methods for mapping disease genes in genetic studies. The course provides attendees with a unique opportunity to interact closely with the world-leading researchers who serve as instructors.
Tuesday, March 29th – Thursday, March 31st, 2016
Memorial Auditorium, Kyoto University Faculty of Medicine
Yoshida Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan (Faculty of Medicine Campus) (See map here)
Introduction to human genetics, Data manipulation and variant calling (SNV, CNV), Variant annotation and disease gene annotation, Population genetics, Methods for complex analysis, Epigenomics analysis, Imputation, Mendelian randomization
Course organisers and instructors:
Guillaume Bourque (McGill U.), Koichiro Higasa (Kyoto U.) Mark Lathrop (McGill U.), Fumihiko Matsuda (Kyoto U.), Jurg Ott (Chinese Academy of Sciences & Rockefeller U.), Daniel E. Weeks (U. Pittsburgh), Ryo Yamada (Kyoto U.), plus leading researchers in computational genomics and genetics from around the world.
The course is aimed principally at advanced doctoral students or post-doctoral researchers who need to apply next-generation sequencing in medical studies. Applicants will be selected based on description of their background and future research projects to be submitted when applying the course. The number of attendees will be limited up to approximately 30.
Academic: 30,000 yen
Non-academic: 60,000 yen
February 19, 2016
We would like to express our gratitude for many applications.