March 25-27 2009
The 3rd Paris Workshop on Genomic Epidemiology

    Print [Word] [PDF]

Day 1 - 25. March 2009
 
Session 1: From 2nd to 3rd Generation DNA Sequencing
 
9:00-9:30 Introduction to DNA analysis Ivo Gut Evry
9:30-10:00 Cancer transcriptome sequencing Martin Hirst Vancouver
10:00-10:30 Application of 2nd Generation DNA sequencing – ChIP-seq Michel Werner Saclay
10:30-10:45 The Illumina Genome Analyzer Richard Henfrey Illumina
10:45-11:00 SOLiD 3 System, and beyond Raimo Tanzi Applied Biosystems
 
11:00-11:30 Coffee Break  
 
11:30-12:00 Integrating small RNA and epigenomic data: lessons from Arabidopsis Vincent Colot Paris
12:00-12:30 DNA methylation analysis Jörg Tost Evry
12:30-12:45 The Roche FLX system Eric Baud Roche
 
12:45-14:00 Lunch  
 
14:00-14:30 Single molecule DNA analysis Mats Nilsson Uppsala
14:30-15:00 Nanopore sequencing Hagan Bayley Oxford
15:00-15:30 Rat genetics Norbert Hübner Berlin
15:30-15:45      
15:45-16:00 Integrated Fluidic Circuits for Next-Generation Genomics Bob Jones Fluidigm
 
16:00-16:30 Coffee Break  
 
Session 2: Protein and Metabolite analysis
16:30-17:00 Discovery proteomics Hanno Langen Basel
17:00-17:30 Human Proteome Atlas Fredrik Ponten Uppsala
 

 

Day 2 - 26. March 2009
 
Session 3: Sample Collection and Storage
 
9:00-9:30 Standardisation of sample collection Tim Peakman Manchester
9:30-10:00 Helmholtz cohort project Erich Wichmann Munich
10:00-10:15 New technologies for HT-singleplex SNP Genotyping, NextGen DNA shearing and High Volume e(mulsion)PCR Niels Kruize KBiosciences
10:15-10:45 Data warehousing Alvis Brazma EBI
10:45-11:00 Some examples where nucleic acid mass spectrometry outperforms other genetic epidemiological tools Charles Cantor Sequenom
 
11:00-11:30 Coffee Break  
 
Session 4: Genetic studies of disease
 
11:30-12:00 Type 2 Diabetes Mark McCarthy Oxford
12:00-12:30 Asthma Bill Cookson London
12:30-12:45 New tools for advanced DNA methylation analysis Elizabeth Homer Qiagen
 
12:45-14:00 Lunch  
 
14:00-14:30 Alzheimer's disease Philippe Amouyel Lille
14:30-15:00 Autism Thomas Bourgeron Paris
15:00-15:30 Stem cells as a tool to study spinal motor neuron development and disease Hynek Wichterle New York
15:30-16:00 Blood pressure Patricia Munroe London
 
16:00-16:30 Coffee Break  
 
 
Session 5: Data Analysis and Interpretation
 
16:30-17:00 Following up Genomewide Association Studies: Prospects for fine-mapping and resequencing studies Gonçalo Abecassis Michigan
17:00-17:15 RNAcompete: a new method for systematic analysis of RNA-binding specificities Tim Hughes Toronto
17:15-17:30 A workflow for parallel analysis of genome-wide data sets Liisa Koivukoski Espoo
17:30-17:45 Genome-wide association study on early-onset bipolar disorder Stephane Jamain Creteil
 

 

Day 3 - 27. March 2009
 
9:00-9:30 On the use of functional gene modules
in genomics
Joaquin Dopazo Valencia
9:30-10:00 The Operon Database System Mario Foglio Evry
10:00-10:15 Multiplex PCR as a tool for human diagnostics Lotte Moens Antwerp
10:15-10:30 Matrix metalloproteinases 1 and 3 polymorphisms in the prognosis of head and neck cancer Victor Wünsch-Filho São Paulo
10:30-11:00 Statistical methods for the analysis of spectra arising from metabonomic and proteomic studies within genomic epidemiology Chris Holmes Oxford
 
11:00-11:30 Coffee Break  
 
11:30-12:00 Statistical methods II: Multi-locus association analyses Jürg Ott Beijing
12:00-12:30 Statistical methods III Simon Heath Evry
12:30-12:45 Using a Bayesian approach to combine evidence for maternal and imprinting effects from multiple studies Beate Glaser Bristol
 
12:45-14:00 Lunch  
 
14:00-14:30 Estimation of Genotype Relative Risks from Pedigree Data Dan Schaid Rochester
14:30-15:00 Statistical methods V Peter Kraft Boston
15:00-15:15 Effect of 17q variants and smoking exposure in early-onset asthma Emmanuelle Bouzigon Paris
15:15-15:45 Associated genetic variants and personalized medicine Dan Weeks Pittsburgh
15:45-16:00 Close