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Max Baur, University of Bonn
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Nuala Sheehan, University of Leicester
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Elizabeth A Thompson, University of Washington
About:
The aim of this workshop was to gather together a sufficiently expert group with interests ranging across diverse areas of genetic epidemiological application in order to focus on the computational and methodological issues that are common to family studies, genetic association studies and the analyses of complex traits. One objective was to assess existing methods of analysis of large and complex datasets, to consider appropriate adaptation of these methods and to investigate the potential for new methods which address common problematic features of all these datasets. Another was to actively encourage young researchers into this field by providing the opportunity to become acquainted with the main research issues in the area and to make vital contacts with the leading people and their groups in an informal small group setting.
Speakers
David Clayton, University of Cambridge | Genome-Wide Association Studies; Experiences of the WTCCC |
Duncan Thomas, University of Southern California | Complex Biological Pathways |
Francoise Clerget Darpoux, INSERM & Paris-Sud University | Multifactorial Diseases: A Gap Between Association Information and the Understanding of the Pathogenic Process |
Laura Almasy, Southwest Foundation for Biomedical Research | Quantitative Risk Factors for Identifying Genes in Complex Diseases |
Elizabeth A Thompson, University of Washington | Assessing the Significance of Linkage Signals |
David Balding, Imperial College London | Population Structure and Genetic Associations |
Peter Holmans, University of Wales College of Medicine | Use of Covariates in Model-Free Linkage and Association |
Sarah Lewis, University of Bristol | Some Practical Examples Illustrating the Use of Mendelian Randomisation |
Tim Bishop, Cancer Research UK | Challenges to Understanding Disease Aetiology with Family Studies |
Wally Gilks, University of Leeds | DNA is not a Straight Line |
Dawn Teare, University of Sheffield | Study of a Candidate Copy Number Polymorphism in Asthma Families |
Juni Palmgren, Karolinska Institute | The GeneStat Web Portal |
Vanessa Didelez, University College London | Causal Inference for Genetic Epidemiology Using Mendelian Randomisation |
Alun Thomas, University of Utah | Towards Linkage Analysis with Markers in Linkage Disequilibrium by Graphical Modelling |
John Whittaker, London School of Hygiene and Tropical Medicine | Baysian Meta-Analysis of Genetic Association Studies |
Heather Cordell, Newcastle University | Testing and Estimation of Genotype and Haplotype Effects in Family-Based Analysis of Quantitative Traits with Missing Genotype Data |
Simon Heath, National Genotyping Centre | Detection/Reconstruction of Family Relationships Using Genotype Data from Whole Genome Arrays |
Elja Arjas, University of Helsinki | Estimating Genealogies from Marker Data: a Bayesian Approach |
Cornelia Van Duijn, Erasmus University Medical Centre | Splitting Complex Pedigrees for Linkage Analysis |
Thore Egeland, Ullevål University Hospital | Adjusting for Relatedness Among Founders in Linkage Analysis |
Konstantin Strauch, Philipps University Marburg | A Close View of the Possible Triangle |