Curating the Clinical Genome Conference

This event will explore best practices for the clinical application of genomic data, focusing on variant interpretation, clinical utility, and the development of consensus-curated knowledge. Sharing data from clinical testing and aligning on common standards are essential steps toward delivering on the promise of genomic medicine.

The conference will unite global and national initiatives to promote data sharing, improve guidelines, and enhance patient care. Key themes include variant classification tools, population and newborn genome screening, non-coding and somatic variation, and the clinical use of multiplex assays of variant effect (MAVEs).

Designed for medical genomics researchers, clinicians, industry professionals, and data scientists, the programme includes expert talks, panel discussions, short oral abstracts, poster sessions, and pitch talks—offering a dynamic forum for collaboration and knowledge exchange.