The NBV Genomics event is organised yearly by the NBV workgroup Genomics. This years event is centered around the theme:
Diagnostics and Genomics - Testing for Health
Download the programme flyer here.
PROGRAM | |
09:30-10:00 | Reception - Registration |
10:00-10:10 | Session 1: Introduction, NBV Genomics and Diagnostics |
DIAGNOSTICS & INNOVATION | |
10:10-10:50 | Session 2: Dàmi Rebergen - Cuclomics Real-time cfDNA sequencing technology for monitoring/detection of cancer through analysis of circulating tumor DNA from liquid biopsies as well as AI-driven methylation tumor classification technology |
10:50-11:30 | Session 3: Edwin Cuppen - Hartwig Medical Foundation Experiences with the next generation of next generation sequencers: Ultima Genomics and Roche Axelios |
11:30-12:10 | Session 4: Björn Menten - Ghent University Revolutionizing Human Genetic: Advances in Sequencing Technologies for Rare Disorders |
12:10-13:00 | Lunch & Sponsor Booths |
MEDICAL DIAGNOSTICS &HEALTH | |
13:00-13:40 | Session 5: Wietse Mulder, founder and former CEO of GenDx An entrepreneurial journey in the IVD market and beyond: from academic start-up to securing legacy through transferring company to strategic partner |
13:40-14:20 | Session 6: Eddy de Boer - UMCG-Bionano ONT Long-Read Sequencing and optical genome mapping as First-Tier Diagnostics Tests: Evaluating their Feasibility as All-in-One Genomic Solutions |
14:20-15:00 | Session 7: Tjakko van Ham - Erasmus MC Improving diagnostics for genetic disease using RNA |
15:00-15:30 | Coffee Break |
PUBLIC HEALTH DIAGNOSTICS | |
15:30-16:10 | Session 8: Sandra Heil - RIVM public health and genomics Genomics from a public health perspective |
16:10-16:50 | Session 9: Bart Keijser - TNO, ACTA Oral systems Biology: elucidating the interaction between microbial communities and host physiology of the human mouth |
16:50-17:00 | Session 10: NBV Genomics - Closure |
Dinner and Networking | |
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