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Genomic testing has revolutionised cancer diagnostics, but can it improve public health prevention programmes of non-communicable diseases?
The session will explore how predictive genomics (PRS and PGx based on microarray genotyping) can be integrated with existing targeted next-generation sequencing testing to help provide maximum value to patients and healthcare systems.
Agenda:
12:00 - 12:05 Welcome and introduction. Francesco Florindi, Thermo Fisher Scientific, Belgium
12:05 - 12:25 Integrating predictive genomics in healthcare: a scenario from Finland. Olli Carpen, University of Helsinki, Finland
12:25 – 12:55 Panel discussion with the following members:
12:55 – 13:00 Q&A / Close
We have transformed human genetics with efficient workflows taking even the most difficult to obtain samples to interpreted data in just a few hours. Explore our human genetic solutions.
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For Research Use Only. Not for use in diagnostic procedures.