Genomics of Rare Disease
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Wellcome Genome Campus are pleased to announce the 15th in our series of meetings on rare diseases, which will present an exciting blend of genomic science and clinical medicine. This meeting will explore how cutting-edge genomic research translates into clinical care and informs our understanding of the biology of rare disease.
The programme features the latest findings related to the genomic basis of rare diseases, providing powerful insights into human biology, disease mechanisms and therapeutic approaches. As genomic sequencing becomes more available in the hospital setting, we also examine how this is changing clinical practice.
Topics included:
- What’s new in rare disease?
- Functional genomics
- Developmental genetics
- Non-coding variants in disease
- Informatics
- Therapeutic approaches to rare disease
- Mainstreaming genomics in healthcare
Find out more here.
