Details

No Rare Disease will go Unseen.

Join our third virtual event, dedicated solely to the advances of whole-genome sequencing and how it shines the light on rare diseases.

We will be hosting daily presentations from leading experts in the field or rare disease at:

13:00 CET/ 12:00 GMT

The broad event agenda will cover:

  • Technical feasibility of implementing whole-genome sequencing into routine clinical care
  • Clinical use cases of how whole-genome sequencing advances current standard of care
  • Discussions on the need for broadening diversity in genomics data to make genomics relevant to all

...and much more!

Date & Time
28 Nov 2022 – 30 Nov 2022
12:00 PM
Location
Online
Europe
Topic
Genetic & rare diseases
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