DOEW02
11 August 2008 to 15 August 2008
Design of Experiments is a fundamental part of the knowledge discovery process in science and engineering, and has impact in a wide variety of fields. Long-standing principles of experimentation, such as randomisation, replication and blocking have become standards of best practice in many areas. In return, stimulus for novel research in the Design of Experiments comes from advances in technology and techniques in application fields important to science and society. These advances often result in complex experiments, for example, with large numbers of factors, many levels of randomisation, or with the aim of estimating or discriminating between nonlinear models. When these experiments cannot be designed using established methods, they motivate methodological and theoretical advances in the design of experiments. Many recent advances in the subject have come from just this synergy between application and methodology.
DEMA2008 will bring together researchers and practitioners for the interchange of new ideas on the design and analysis of experiments. The workshop will emphasise both methodology and application areas and should be of interest to scientists and engineers who use experiments, as well as to statisticians.
This workshop will be held in the final week of a month-long research programme at the Newton Institute and will provide a forum for the sharing of new ideas and advances from this programme with a wider audience. The workshop will have themes which reflect those of the research programme; in particular, new methodology for the design of genetics and proteomics studies, computer experiments and clinical trials, and sessions on more general design topics. A theme day on each of these three applied topics will be organised and participation from scientists in each field is strongly encouraged.
The cells in living organisms accomplish their functions by producing specific proteins. In order to identify the genes regulating this process high-troughput technologies have been developed over the past decade. In particular, microarray experiments for simultaneously studying the differential expression of thousands of genes are routinely used by now. Similarly, proteomics experiments analyse profiles from gas spectrometry to understand how genes are translated into proteins. In parallel with the advent of the new technologies the question of design has attracted considerable attention. The corresponding design problems are varied and often require the development of new theory or interpreting existing results in an entirely new way.
Clinical trials are experiments on living animals and humans to explore a proposed treatment for a disease and to obtain a licence for the commercial use of the treatment on non-experimental patients.
The experimental programme is often described as having several phases. Assessment of the treatment starts with healthy individuals to check the absence of adverse reactions. Experiments are then designed to determine the dosage, sometimes constrained by a need to avoid toxicity. The large Phase III trials are used to determine the advantages, if any , of the new treatment often by comparison with existing treatments. Randomization and balance over covariates are especially important in this phase.
Regulatory authorities, such as the American FDA, are rightly concerned that the designs have specified properties and are analysed in a pre-specified way. Sample size and power are two important characteristics.
However, a too rigid analytical straightjacket can conflict with the efficiency of statistical procedures if unexpected evidence becomes available during a trial. Protocols for interim analyses or changes in emphasis have to be tightly specified, in order that biases are avoided and test size and power maintained.
Particularly with human patients there is also the ethical desire to treat as many patients as possible with the better treatments. This leads to group sequential and response adaptive designs where the allocations change as responses on earlier patients become available. Controlling the properties of such trials is a complex task.
Computer experiments refers to the design and analysis of experiments on complex computer codes. An increasing number of systems are modelled via deterministic computer models, particularly where real experiments are unfeasible (too expensive, dangerous or just not possible). Examples of areas involved are engineering, environmental and climate models, geophysical models, chemical dynamics and disease models. The computer models are usually based on complex mathematics, for example, nonlinear partial differentiation equations or finite element models, with many different inputs. The output is then essentially the ouput from a solver, for example based on the finite element method. To explore and understand the models, experiments are performed where design consists of combinations of values of the input variables. As the response is deterministic, many of the standard principles of design (such as randomisation and replication) no longer apply. A new discipline of the statistical design and analysis of these experiments has developed over the last 20 years.
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Fisher Memorial Trust |
Monday 11th August 2008 | |||
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08:30 to 10:00 | No Room Required | ||
10:00 to 11:00 |
David Cox University of Oxford |
Room 1 | |
11:00 to 11:10 | No Room Required | ||
11:10 to 11:30 | No Room Required | ||
11:30 to 12:30 | Discussion Room | ||
12:30 to 13:30 | No Room Required | ||
14:00 to 14:30 | Room 1 | |
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14:30 to 15:00 |
Ching-Shui Cheng University of California, Berkeley |
Room 1 | |
15:00 to 15:30 |
Carla Vivacqua Universidade Federal do Rio Grande do Norte |
Room 1 | |
15:30 to 16:00 | No Room Required | ||
16:00 to 16:30 |
Some considerations on optimal design for non-linear mixed models |
Room 1 | |
16:30 to 17:00 |
David Woods University of Southampton |
Room 1 | |
17:00 to 17:30 |
Fetene Tekle Universiteit Maastricht |
Room 1 | |
17:30 to 18:30 | No Room Required | ||
18:45 to 19:30 | No Room Required |
Tuesday 12th August 2008 | |||
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09:30 to 10:00 |
Eric Schoen Universiteit Antwerpen |
Room 1 | |
10:00 to 10:30 |
Joachim Kunert Technische Universität Dortmund |
Room 1 | |
10:30 to 11:00 |
Luzia Trinca UNESP |
Room 1 | |
11:00 to 11:30 | No Room Required | ||
11:30 to 12:00 |
Keith Baggerly University of Texas M D Anderson Cancer Center |
Room 1 | |
12:00 to 12:30 |
Terry Speed University of California, Berkeley |
Room 1 | |
12:30 to 13:30 | No Room Required | ||
14:00 to 14:30 |
Chris Brien University of South Australia |
Room 1 | |
14:30 to 15:00 |
Kathleen Kerr University of Washington |
Room 1 | |
15:00 to 15:30 |
Rahul Mukerjee Indian Institute of Management Calcutta |
Room 1 | |
15:30 to 16:00 | No Room Required | ||
16:00 to 16:30 |
Selection of good two-color microarray designs using genetic algorithms |
Room 1 | |
16:30 to 17:00 |
Valeria Lima Passos Universiteit Maastricht |
Room 1 | |
17:00 to 17:30 |
Heiko Grossmann Queen Mary University of London |
Room 1 | |
18:45 to 19:30 | No Room Required |
Wednesday 13th August 2008 | |||
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09:30 to 10:00 |
Martina Vandebroek KU Leuven |
Room 1 | |
10:00 to 10:30 |
Bradley Jones JMP |
Room 1 | |
10:30 to 11:00 | Room 1 | |
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11:00 to 11:30 | No Room Required | ||
11:30 to 12:30 |
Rosemary Bailey Queen Mary University of London |
Room 1 | |
12:30 to 13:30 | No Room Required | ||
19:15 to 23:00 | No Room Required |
Thursday 14th August 2008 | |||
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09:30 to 10:00 |
Katrin Roth Bayer Schering Pharma AG |
Room 1 | |
10:00 to 10:30 |
Basia Bogacka Queen Mary University of London |
Room 1 | |
10:30 to 11:00 |
Stefani Biedermann University of Southampton |
Room 1 | |
11:00 to 11:30 | No Room Required | ||
11:30 to 12:00 | Room 1 | |
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12:00 to 12:30 |
Anthony Atkinson London School of Economics |
Room 1 | |
12:30 to 13:30 | No Room Required | ||
14:00 to 14:30 |
Two-stage treatment strategies based on sequential failure times |
Room 1 | |
14:30 to 15:00 |
Alessandra Giovagnoli University of Bologna |
Room 1 | |
15:00 to 15:30 |
Tim Friede University of Warwick |
Room 1 | |
15:30 to 16:00 | No Room Required | ||
16:00 to 16:30 |
An adaptive optimal design for the Emax model and its application in clinical trials |
Room 1 | |
16:30 to 17:00 |
Janet Godolphin University of Surrey |
Room 1 | |
17:00 to 17:30 |
Leslie Moore Los Alamos National Laboratory |
Room 1 | |
18:45 to 19:30 | No Room Required |
Friday 15th August 2008 | |||
---|---|---|---|
09:45 to 10:00 | Room 1 | ||
10:00 to 11:00 | Discussion Room | ||
11:00 to 11:30 | No Room Required | ||
11:30 to 12:00 | Room 1 | |
|
12:00 to 12:30 | Room 1 | |
|
12:30 to 13:30 | No Room Required | ||
14:00 to 14:30 |
Peter Qian University of Wisconsin-Madison |
Room 1 | |
14:30 to 15:00 |
Arun Kumar Ohio State University |
Room 1 | |
15:00 to 15:30 |
Daniele Romano University of Cagliari |
Room 1 | |
15:30 to 16:00 | No Room Required | ||
16:00 to 16:30 |
Multiplicative Algorithms: A class of algorithmic methods used in optimal experimental design |
Room 1 | |
16:30 to 17:00 |
Dariusz Ucinski University of Zielona Góra |
Room 1 | |
17:00 to 17:30 |
JP Morgan Virginia Polytechnic Institute and State University |
Room 1 | |
18:45 to 19:30 | No Room Required |
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