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!