Literature DB >> 18052911

A comparison of methods to control type I errors in microarray studies.

Jinsong Chen1, Mark J van der Laan, Martyn T Smith, Alan E Hubbard.   

Abstract

Microarray studies often need to simultaneously examine thousands of genes to determine which are differentially expressed. One main challenge in those studies is to find suitable multiple testing procedures that provide accurate control of the error rates of interest and meanwhile are most powerful, that is, they return the longest list of truly interesting genes among competitors. Many multiple testing methods have been developed recently for microarray data analysis, especially resampling based methods, such as permutation methods, the null-centered and scaled bootstrap (NCSB) method, and the quantile-transformed-bootstrap-distribution (QTBD) method. Each of these methods has its own merits and limitations. Theoretically permutation methods can fail to provide accurate control of Type I errors when the so-called subset pivotality condition is violated. The NCSB method does not suffer from that limitation, but an impractical number of bootstrap samples are often needed to get proper control of Type I errors. The newly developed QTBD method has the virtues of providing accurate control of Type I errors under few restrictions. However, the relative practical performance of the above three types of multiple testing methods remains unresolved. This paper compares the above three resampling based methods according to the control of family wise error rates (FWER) through data simulations. Results show that among the three resampling based methods, the QTBD method provides relatively accurate and powerful control in more general circumstances.

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Year:  2007        PMID: 18052911     DOI: 10.2202/1544-6115.1310

Source DB:  PubMed          Journal:  Stat Appl Genet Mol Biol        ISSN: 1544-6115


  5 in total

Review 1.  Toxicogenomic profiling of chemically exposed humans in risk assessment.

Authors:  Cliona M McHale; Luoping Zhang; Alan E Hubbard; Martyn T Smith
Journal:  Mutat Res       Date:  2010-04-09       Impact factor: 2.433

2.  Limited clinical utility of a machine learning revision prediction model based on a national hip arthroscopy registry.

Authors:  R Kyle Martin; Solvejg Wastvedt; Jeppe Lange; Ayoosh Pareek; Julian Wolfson; Bent Lund
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3.  Changes in the peripheral blood transcriptome associated with occupational benzene exposure identified by cross-comparison on two microarray platforms.

Authors:  Cliona M McHale; Luoping Zhang; Qing Lan; Guilan Li; Alan E Hubbard; Matthew S Forrest; Roel Vermeulen; Jinsong Chen; Min Shen; Stephen M Rappaport; Songnian Yin; Martyn T Smith; Nathaniel Rothman
Journal:  Genomics       Date:  2009-01-20       Impact factor: 5.736

4.  Predicting women with depressive symptoms postpartum with machine learning methods.

Authors:  Sam Andersson; Deepti R Bathula; Stavros I Iliadis; Martin Walter; Alkistis Skalkidou
Journal:  Sci Rep       Date:  2021-04-12       Impact factor: 4.379

5.  Validation of differential gene expression algorithms: application comparing fold-change estimation to hypothesis testing.

Authors:  Corey M Yanofsky; David R Bickel
Journal:  BMC Bioinformatics       Date:  2010-01-28       Impact factor: 3.169

  5 in total

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