Recent developments in genomic technologies have enabled the genome-wide identification of regulatory elements and chromatin interactions, controlling the spatiotemporal gene expression. In this webinar, we will explore the significant involvement of non-coding genome in various human diseases, a rapidly evolving field of human genomics.
Chaired by Prof. Florence PETIT.
Welcome and Introduction
- Prof. Florence PETIT, Lille University Hospital, Lille, France
Interpreting the impact of noncoding structural variants in neurodevelopmental disorders –
- Prof. Sarah VERGULT, Ghent University, Ghent, Belgium
Finding causes of missing heritability in neurogenetic disorders: exploring the dark matter of the genome
- Dr Stefan BARAKAT, Erasmus MC, Rotterdam, Netherlands
Enhancer hijacking: A key driver of congenital disorders
- Prof. Malte SPIELMANN, Institut für Humangenetik, Lübeck, Germany
Non-coding genome in limb malformations
- Prof. Florence PETIT, Lille University Hospital, Lille, France
Discussion time
Conclusion with speakers and moderator
Participation on registration: https://events.teams.microsoft.com/event/cf3016d9-c9a4-4eb5-89fa-f6dc6f3473b6@2461c129-d44f-406d-a778-d1a3c4c1527c