Literature DB >> 23889143

An optimal test with maximum average power while controlling FDR with application to RNA-seq data.

Yaqing Si1, Peng Liu.   

Abstract

The recent RNA-seq technology is an attractive method to study gene expression. One of the most important goals in RNA-seq data analysis is to detect genes differentially expressed across treatments. Although several statistical methods have been published, there are no theoretical justifications for whether these methods are optimal or how to search for the optimal test. Furthermore, most proposed tests are designed for testing whether the mean expression levels are exactly the same or not across treatments, whereas sometimes, biologists are interested in detecting genes with expression changes larger than a certain threshold. Another issue with current methods is that the false discovery rate (FDR) control is not well studied. In this manuscript, we propose a test to address all the above issues. Under model assumptions, we derive an optimal test that achieves the maximum of average power among those that control FDR at the same level. We also provide an approximated version, the approximated most average powerful (AMAP) test, for practical implementation. The proposed method allows for testing null hypotheses that are much more general than the ones most previous studies have considered, and it leads to a natural way of controlling the FDR. Through simulation studies, we show that our test has a higher power than other methods, including the widely-used edgeR, DESeq, and baySeq methods, as well as better FDR control than two other FDR control procedures commonly used in practice. For demonstration, we also apply the proposed method to a real RNA-seq dataset obtained from maize.
© 2013, The International Biometric Society.

Entities:  

Keywords:  Empirical Bayes; FDR control; Gene expression; Maximum average power; RNA-seq

Mesh:

Year:  2013        PMID: 23889143     DOI: 10.1111/biom.12036

Source DB:  PubMed          Journal:  Biometrics        ISSN: 0006-341X            Impact factor:   2.571


  7 in total

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2.  Leptomonas seymouri: Adaptations to the Dixenous Life Cycle Analyzed by Genome Sequencing, Transcriptome Profiling and Co-infection with Leishmania donovani.

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3.  ShrinkBayes: a versatile R-package for analysis of count-based sequencing data in complex study designs.

Authors:  Mark A van de Wiel; Maarten Neerincx; Tineke E Buffart; Daoud Sie; Henk M W Verheul
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4.  RNA-Seq Count Data Modelling by Grey Relational Analysis and Nonparametric Gaussian Process.

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Journal:  PLoS One       Date:  2016-10-26       Impact factor: 3.240

5.  Selective Histone Deacetylase 6 Inhibition Normalizes B Cell Activation and Germinal Center Formation in a Model of Systemic Lupus Erythematosus.

Authors:  Jingjing Ren; Michelle D Catalina; Kristin Eden; Xiaofeng Liao; Kaitlin A Read; Xin Luo; Ryan P McMillan; Matthew W Hulver; Matthew Jarpe; Prathyusha Bachali; Amrie C Grammer; Peter E Lipsky; Christopher M Reilly
Journal:  Front Immunol       Date:  2019-10-25       Impact factor: 7.561

6.  Dispersion estimation and its effect on test performance in RNA-seq data analysis: a simulation-based comparison of methods.

Authors:  William Michael Landau; Peng Liu
Journal:  PLoS One       Date:  2013-12-09       Impact factor: 3.240

7.  NBLDA: negative binomial linear discriminant analysis for RNA-Seq data.

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Journal:  BMC Bioinformatics       Date:  2016-09-13       Impact factor: 3.169

  7 in total

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