An Empirical Bayes Optimal Discovery Procedure Based on Semiparametric Hierarchical Mixture Models
Multiple testing has been widely adopted for genome-wide studies such as microarray experiments. For effective gene selection in these genome-wide studies, the optimal discovery procedure (ODP), which maximizes the number of expected true positives for each fixed number of expected false positives,...
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Online Access: | http://dx.doi.org/10.1155/2013/568480 |
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doaj-c5392fa9043a4acfb96e1c90da64e2172020-11-24T21:28:14ZengHindawi LimitedComputational and Mathematical Methods in Medicine1748-670X1748-67182013-01-01201310.1155/2013/568480568480An Empirical Bayes Optimal Discovery Procedure Based on Semiparametric Hierarchical Mixture ModelsHisashi Noma0Shigeyuki Matsui1Department of Data Science, The Institute of Statistical Mathematics, 10-3 Midori-cho, Tachikawa, Tokyo 190-8562, JapanDepartment of Data Science, The Institute of Statistical Mathematics, 10-3 Midori-cho, Tachikawa, Tokyo 190-8562, JapanMultiple testing has been widely adopted for genome-wide studies such as microarray experiments. For effective gene selection in these genome-wide studies, the optimal discovery procedure (ODP), which maximizes the number of expected true positives for each fixed number of expected false positives, was developed as a multiple testing extension of the most powerful test for a single hypothesis by Storey (Journal of the Royal Statistical Society, Series B, vol. 69, no. 3, pp. 347–368, 2007). In this paper, we develop an empirical Bayes method for implementing the ODP based on a semiparametric hierarchical mixture model using the “smoothing-by-roughening" approach. Under the semiparametric hierarchical mixture model, (i) the prior distribution can be modeled flexibly, (ii) the ODP test statistic and the posterior distribution are analytically tractable, and (iii) computations are easy to implement. In addition, we provide a significance rule based on the false discovery rate (FDR) in the empirical Bayes framework. Applications to two clinical studies are presented.http://dx.doi.org/10.1155/2013/568480 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hisashi Noma Shigeyuki Matsui |
spellingShingle |
Hisashi Noma Shigeyuki Matsui An Empirical Bayes Optimal Discovery Procedure Based on Semiparametric Hierarchical Mixture Models Computational and Mathematical Methods in Medicine |
author_facet |
Hisashi Noma Shigeyuki Matsui |
author_sort |
Hisashi Noma |
title |
An Empirical Bayes Optimal Discovery Procedure Based on Semiparametric Hierarchical Mixture Models |
title_short |
An Empirical Bayes Optimal Discovery Procedure Based on Semiparametric Hierarchical Mixture Models |
title_full |
An Empirical Bayes Optimal Discovery Procedure Based on Semiparametric Hierarchical Mixture Models |
title_fullStr |
An Empirical Bayes Optimal Discovery Procedure Based on Semiparametric Hierarchical Mixture Models |
title_full_unstemmed |
An Empirical Bayes Optimal Discovery Procedure Based on Semiparametric Hierarchical Mixture Models |
title_sort |
empirical bayes optimal discovery procedure based on semiparametric hierarchical mixture models |
publisher |
Hindawi Limited |
series |
Computational and Mathematical Methods in Medicine |
issn |
1748-670X 1748-6718 |
publishDate |
2013-01-01 |
description |
Multiple testing has been widely adopted for genome-wide studies such as microarray experiments. For effective gene selection in these genome-wide studies, the optimal discovery procedure (ODP), which maximizes the number of expected true positives for each fixed number of expected false positives, was developed as a multiple testing extension of the most powerful test for a single hypothesis by Storey (Journal of the Royal Statistical Society, Series B, vol. 69, no. 3, pp. 347–368, 2007). In this paper, we develop an empirical Bayes method for implementing the ODP based on a semiparametric hierarchical mixture model using the “smoothing-by-roughening" approach. Under the semiparametric hierarchical mixture model, (i) the prior distribution can be modeled flexibly, (ii) the ODP test statistic and the posterior distribution are analytically tractable, and (iii) computations are easy to implement. In addition, we provide a significance rule based on the false discovery rate (FDR) in the empirical Bayes framework. Applications to two clinical studies are presented. |
url |
http://dx.doi.org/10.1155/2013/568480 |
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