Nordic Precision Medicine Forum 2025 (NPMF 25)
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Healthcare in the Nordics benefits from access to leading research, technologies and standards of care. Yet challenges remain, such as small population sizes, a difficulty in starting new clinical trials and a lack of funding for international research projects. The Forum provides a platform to overcome such barriers and find ways to further advance precision medicine.
Join Oxford Nanopore's workshop on Monday 28 April at 15:45 - 17:15, more details on this below!
Please visit our booth if you are able to attend the event.
Speakers
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Jakob Ørtvig, Oxford Nanopore Technologies)
Pitt Niehusmann, Department of Pathology and Division for Cancer Medicine, Oslo University HospitalOxford Nanopore long-read sequencing technology is creating new opportunities for exploring the genome in greater detail. In this talk, I will present research insights from the implementation of whole genome sequencing and adaptive sampling workflows at the genomic sequencing core facility at Aarhus University Hospital. These approaches are being used to investigate complex genomic features across a range of conditions, including rare diseases and cancer. Our work aims to support a deeper understanding and evaluate the potential of long-read sequencing for future clinical applications.
Oxford Nanopore long-read sequencing technology is creating new opportunities for exploring the genome in greater detail. In this talk, I will present research insights from the implementation of whole genome sequencing and adaptive sampling workflows at the genomic sequencing core facility at Aarhus University Hospital. These approaches are being used to investigate complex genomic features across a range of conditions, including rare diseases and cancer. Our work aims to support a deeper understanding and evaluate the potential of long-read sequencing for future clinical applications.
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Ole Halfdan Larsen, Department of Molecular Medicine, Aarhus University Hospital, Denmark
