September 27, 2019 - 9:00 to 17:00
Campus Biotech Geneva
The Swiss Genomics Forum I #SGF19 I organized by the Health 2030 Genome Center, will bring together researchers, clinicians, patient communities, and other stakeholder groups to meet and discuss about the future of genomics.
The following themes will be explored at the SGF2019:
- Genomics: opportunities and challenges
- Diseases: latest genomics based diagnostic and therapeutic approaches
- Personalized Health: relevance and impact of genomic medicine
- Data: legal and ethical issues around sharing patient data
- Collaboration: strategic partnerships
Background of the event:
Genomic analysis is at the forefront of research and clinical developments around the world. Leading countries in research including the USA and the UK have made substantial public and private investments in developing sequencing capacity and the necessary data analysis tools for research and clinical use.
Existing genome centers with ambitious projects have offered exceptional resources to the research and clinical communities and have led efforts to integrate genome sequencing in clinical practice.
As genome analysis becomes commonplace in research and clinics, Switzerland has much to offer in terms of scientific strength, quality of its healthcare system (including universal coverage), and detailed patient phenotyping.
In participating in our event, you will be granted 6 credits from the Swiss Society of Medical Genetics. For students, 1 ECTS with a poster/flash talk or 0.5 ECTS without.
BEFORE JULY 15 (early bird registration)
- Student fee:
- free with submission of an abstract
- without abstract CHF 30
- Others: CHF 50
FROM JULY 16 TO SEPTEMBER 10:
- Student fee: CHF 50
- Others: CHF 70
Abstract: maximum 250 words
Deadline for abstract submission and registration:
September 10, 2019
09:00 Registration & Welcome Coffee
10:00 – 10:15 Swiss Genomics Opening – Welcome Address
10:15 – 11:45 Invited keynote speakers
- Anna-Sapfo Malaspinas, University of Lausanne and SIB Swiss Institute of Bioinformatics, CH "Insights into human evolution from ancient DNA"
- Alexandre Reymond, Center for Integrative Genomics, University of Lausanne, CH "Personalized health and genome architecture: the 16p11.2 paradigm"
- Judith Zaugg, EMBL Heidelberg, DE "From epigenetics variation across individuals to disease mechanisms"
11:45 – 13:00 Lunch Break and Poster Session
13:00 – 14:30 Invited keynote speakers
- Cecilia Lindgren, University of Oxford, UK "Genomics of common disease - what is next?"
- Emmanouil Dermitzakis, University of Geneva and Health 2030 Genome Center, CH "Genetic variation in the 3D genome and its implications to disease susceptibility and cancer"
- Judy H Cho, Mount Sinai, USA "Precision Medicine Roadmap: a New York City & IBD-centric viewpoint"
14:30 – 15:00 Coffee break
15:00 – 15:30 Flash talks:
- Caterina Marconi (004) "Identification of structural variants on whole-genome sequencing data for clinical purposes"
- Sylvan Caspar (021) "Pharmacogenetics from whole genomes: at the leading edge of precision medicine using the medication safety card"
- Ambra Sartori (002) "Single-cell analysis of immune cell diversity in atherosclerotic plaques"
- Dylan Lawless (006) "Rare variants in antiviral response genes drive severe viral respiratory infections in children"
15:30 – 16:15 Panel Discussion: How Multiomics is transforming Science
16:15 – 17:00 Panel Discussion: How Multiomics is transforming Health
17:00 – 18:30 Cocktail Dinner