A new technology is revolutionizing the way to diagnose diseases, to predict and monitor therapies and drug treatment. The introduction of Next Generation Sequencing (NGS) technology has transformed the way scientists think about genetic information.

Attendance at the seminar is free but registration is required.


1:00 PM - 1:30 PM
Introduction
Dr. Jean-Marc Brunner, SICHH Genomics Core Facility

1:30 PM - 2:00 PM
Solutions for Clinical Genetics & Oncology Research
Dr. Andreas Keck, Illumina

2:00 PM - 2:30 PM
Prenatal screening in cases with increased nuchal translucency and/or abnormal ultrasound
Dr. Pascal Joset, Medical Genetics, Med Uni Zurich

2:30 PM - 3:00 PM
Inherited Disease Detection Research using TruSight One®
Dr. Heidi Fodstad, Molecular Genetics, CHUV Lausanne

3:00 PM - 3:30 PM
Coffee Break

3:30 PM - 4:00 PM
Validation study results using the TS One panel
in the Laboratoire de Diagnostic des Maladies Génétiques Endocriniennes clinical laboratory
Dr. Jim Acierno, Physiology, CHUV Lausanne

4:00 PM - 4:30 PM
Investigation by whole genome sequencing of severe Streptococcus pyogenes infections
Dr. Florian Tagini, Microbiology, CHUV Lausanne

4:30 PM - 5:00 PM
NGS Data Analysis solution down to variant interpretation using VariantStudio
Dr. Benjamin Farnung, Illumina

5:00 PM - 5:30 PM
NGS Data analysis using the Sophia Genetics pipeline
Dr. Bernardo Foth, Sophia Genetics SA

5:30 PM
Apero

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