Agenda Trippelrummet, BMC in Uppsala - Nov 4

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