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How to analyze many contingency tables simultaneously in genetic association studies

Thorsten Dickhaus 1 , Klaus Straßburger 2 , Daniel Schunk 3 , Carlos Morcillo-Suarez 4 , Thomas Illig 5 ,  and Arcadi Navarro 6
  • 1 Humboldt-University, Berlin
  • 2 German Diabetes Center, Düsseldorf
  • 3 Johannes Gutenberg-Universität Mainz and University of Zurich
  • 4 Universitat Pompeu Fabra, Barcelona
  • 5 Helmholtz Zentrum München
  • 6 ICREA and Universitat Pompeu Fabra, Barcelona

Abstract

We study exact tests for (2 x 2) and (2 x 3) contingency tables, in particular exact chi-squared tests and exact tests of Fisher type. In practice, these tests are typically carried out without randomization, leading to reproducible results but not exhausting the significance level. We discuss that this can lead to methodological and practical issues in a multiple testing framework when many tables are simultaneously under consideration as in genetic association studies.Realized randomized p-values are proposed as a solution which is especially useful for data-adaptive (plug-in) procedures. These p-values allow to estimate the proportion of true null hypotheses much more accurately than their non-randomized counterparts. Moreover, we address the problem of positively correlated p-values for association by considering techniques to reduce multiplicity by estimating the "effective number of tests" from the correlation structure.An algorithm is provided that bundles all these aspects, efficient computer implementations are made available, a small-scale simulation study is presented and two real data examples are shown.

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SAGMB publishes significant research on the application of statistical ideas to problems arising from computational biology. The range of topics includes linkage mapping, association studies, gene finding and sequence alignment, protein structure prediction, design and analysis of microarrary data, molecular evolution and phylogenetic trees, DNA topology, and data base search strategies.

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