Session 5: Human Disease- Structural Genomic Variation and Function
09:00-09:30: Wigard Kloosterman, UMC Utrecht, the Netherlands
Topic: Cause and Consequence of Complex Genomic Rearrangements
09:30-10:00: Michael Talkowski, MGH, Harvard University, USA
Topic: Sequencing Unique Human Genomes Reveals Novel loci in Autism and Predictive Phnotypes in Prenatal Diagnostics
10:00-10:30: Niels Van Der Aa, K.U.Leuven, Belgium
Topic: Single-cell Genome Sequencing Reveals Structural Variation per Cell Cycle
Chairman: Prof. Edwin Cuppen , Hubrecht Institute, the Netherlands