Quantifying the fraction of missing information for hypothesis testing in statistical and genetic studies
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Abstract: Many practical studies rely on hypothesis testing procedures applied to data sets with missing information. An important part of the analysis is to determine the impact of the missing data on the performance of the test, and this can be done by properly quantifying the relative (to complete data) amount of available information. The problem is directly motivated by applications to studies, such as linkage analyses and haplotype-based association projects, designed to identify genetic contributions to complex diseases. In the genetic studies the relative information measures are needed for the experimental design, technology comparison, interpretation of the data, and for understanding the behavior of some of the inference tools. The central difficulties in constructing such information measures arise from the multiple, and sometimes conflicting, aims in practice. For large samples, we show that a satisfactory, likelihood-based general solution exists by using appropriate forms of the relative Kullback--Leibler information, and that the proposed measures are computationally inexpensive given the maximized likelihoods with the observed data. Two measures are introduced, under the null and alternative hypothesis respectively. We exemplify the measures on data coming from mapping studies on the inflammatory bowel disease and diabetes. For small-sample problems, which appear rather frequently in practice and sometimes in disguised forms (e.g., measuring individual contributions to a large study), the robust Bayesian approach holds great promise, though the choice of a general-purpose "default prior" is a very challenging problem.
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Cites work
- scientific article; zbMATH DE number 3921704 (Why is no real title available?)
- scientific article; zbMATH DE number 107482 (Why is no real title available?)
- scientific article; zbMATH DE number 3522963 (Why is no real title available?)
- scientific article; zbMATH DE number 3567782 (Why is no real title available?)
- scientific article; zbMATH DE number 3573050 (Why is no real title available?)
- scientific article; zbMATH DE number 1086057 (Why is no real title available?)
- scientific article; zbMATH DE number 3418509 (Why is no real title available?)
- A Class of Tests for Linkage Using Affected Pedigree Members
- A Mathematical Theory of Communication
- A strong (Ross) characterization of multivariate risk aversion
- Goodness of prediction fit
- Improved minimax predictive densities under Kullback-Leibler loss
- Inference and missing data
- Maximum likelihood estimation via the ECM algorithm: A general framework
- Measuring the Relative Information in Allele-Sharing Linkage Studies
- Minimum Variance Estimation Without Regularity Assumptions
- Multipoint Linkage Analysis Using Affected Relative Pairs and Partially Informative Markers
- On the rate of convergence of the ECM algorithm
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