The full program can be downloaded here

8:30		welcome address
		Guillame Smits (Wellcome Trust Sanger Institute, UK)
Session 1		TECHNICAL ADVANCES
		chair : Jan Hellemans (Ghent University, Belgium)
8:40		Sequencing applications for the Illumina Genome Analyzer
		Dan Turner (Wellcome Trust Sanger Institute, UK)
9:05		Challenges for the data management and analysis of large-scale human genome sequencing
		Paul Flicek (European Bioinformatics Institute, UK)
9:30		Generating thousands of complete human genome sequences for basic and clinical research
		Stephen Lincoln (Complete Genomics, Mountain View, CA, USA)
9:55		Automated nucleic acid fractionation for Next Generation Sequencing
		Elaine Wong-Ho (Caliper Life Sciences, Hopkinton, MA, USA)
10:15		coffee break
Session 2		BIOLOGICAL APPLICATIONS
		chair : Guillame Smits (Wellcome Trust Sanger Institute, UK)
10:45		Next-generation genetics and epigenetics
		Edwin Cuppen (Hubrecht Institute, Utrecht, the Netherlands)
11:10		Plant genome de novo assembly based on next-generation sequencing data
		Heinz Himmelbauer (Center for Genomic Regulation, Barcelona, Spain)
11:35		De novo sequencing and SNP discovery using the 454 FLX sequencing platform
		Neil Hall (Center for Genomic Research, University of Liverpool, UK)
12:00		Integrating high-throughput sequencing into AFLP genome scans of non-model organisms
		Heidi Lischer (Institute of Ecology and Evolution, University of Bern, Switzerland)
12:15		Ancient DNA research without PCR : the power of single-molecule sequencing
		Michiel van Galen (Leiden University Medical Center, the Netherlands)
12:30		lunch + poster session
Session 3		TARGETED RESEQUENCING
		chair : Jo Vandesompele (Ghent University, Belgium)
14:00		Targeted Resequencing using sequence capture
		Alison Coffey (Wellcome Trust Sanger Institute, UK)
14:25		Separating wheat from chaff : molecular elucidation of genetic factors underlying mental retardation by genome partitioning and large scale NGS
		Wei Chen (BIMSB Max-Delbrück - Center for Molecular Medicine, Berlin, Germany)
14:50		Targeted capturing and subsequent next generation for the identification of causal mutations in mendelian diseases
		Delfien Syx (Ghent University, Belgium)
15:05		GS Junior : new sequencing technology for discovery in clinical research
		Marcus Droege (Roche Diagnostics, Penzberg, Germany
15:25		coffee break
Session 4		WGS MEDICAL APPLICATIONS
		chair : Gilber Vassart (Erasme University Hospital, Brussels, Belgium)
16:05		Application of next-generation sequencing in a medical setting
		Johan den Dunnen (Leinden Genome Technology Center, the Netherlands)
16:30		From genome-wide genome association to whole genome sequencing
		Ivo Gut (Centre de Genotypage, Evry, France)
16:55		Cancer transcriptome sequencing
		Martin Hirst (BC Cander Research Center, Vancouver, Canada)
17:20		awards and closure of the meeting
		Hakim El Housni (Erasme, University Hospital, Brussels, Belgium)
		Jo Vandesompele (Ghent University, Belgium)
		Guillaume Smits (Wellcome Trust Sanger Institute, UK)
17:30		drinks