Explore the Future of Genomics with Oxford Nanopore
November 4, 2025 @ 12:00 – 16:15 CET
Join us for a half-day seminar at SciLifeLab Uppsala dedicated to Oxford Nanopore Technologies on November 4 at BMC, Uppsala. Discover how Oxford Nanopore enables high-accuracy, scalable sequencing across a wide range of applications, from clinical research to biodiversity studies.
Unlock the deepest level of multiomic insights on a single technology.
Date: November 4 from 12:00 to 16:16
Venue: The Triple room in Navet, BMC, SciLifeLab meeting place in Uppsala. Entrance C11, Husargatan 3.
This is a joint event hosted by Oxford Nanopore Technologies, National Genomics Infrastructure (NGI), Clinical Genomics Uppsala and Clinical Genomics Stockholm.
Program
| 12:00-13:00 | Light lunch provided by Oxford Nanopore |
| 13:00-13:05 | Welcome |
| 13:05-13:25 | Presentation of National Genomics Infrastructure (NGI) and Clinical Genomics |
| 13:25-13:45 | Information from Oxford Nanopore |
| 13:45-14:00 | Short Break |
| 14:00-14:20 | Rapid diagnostics in acute myeloid leukemia, Rebecka Östlund, Uppsala University |
| 14:20-14:40 | Long-read genome sequencing enhances diagnostics of pedriatic neurological disorders, Marlene Ek, Karolinska Institutet, Karolinska University Hospital |
| 14:40-15:10 | Coffee break |
| 15:10-15:30 | Development of STEEL-seq for analysis of single-stranded DNA breaks, Ola Söderberg, Uppsala University |
| 15:30-15:50 | A reference genome assembly and insights to male fertility in Arctic charr using ONT, Christos Palaiokostas, Swedish University of Agricultural Sciences |
| 15:50-16:10 | Long-read metagenomics in the clinical context, René Kaden, Uppsala University, Uppsala University Hospital |
| 16:10-16:15 | Closing remarks |
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