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Bioinformatics Advance Access originally published online on July 16, 2008
Bioinformatics 2008 24(18):2057-2063; doi:10.1093/bioinformatics/btn365
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© The Author 2008. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Apparently low reproducibility of true differential expression discoveries in microarray studies

Min Zhang 1,{dagger}, Chen Yao 2,{dagger}, Zheng Guo 1,2,*, Jinfeng Zou 1,{ddagger}, Lin Zhang 2,{ddagger}, Hui Xiao 1, Dong Wang 1, Da Yang 1, Xue Gong 1, Jing Zhu 2, Yanhui Li 2 and Xia Li 1,*

1School of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150086 and 2Bioinformatics Centre and School of Life Science, University of Electronic Science and Technology of China, Chengdu 610054, China

*To whom correspondence should be addressed.


   Abstract

Motivation: Differentially expressed gene (DEG) lists detected from different microarray studies for a same disease are often highly inconsistent. Even in technical replicate tests using identical samples, DEG detection still shows very low reproducibility. It is often believed that current small microarray studies will largely introduce false discoveries.

Results: Based on a statistical model, we show that even in technical replicate tests using identical samples, it is highly likely that the selected DEG lists will be very inconsistent in the presence of small measurement variations. Therefore, the apparently low reproducibility of DEG detection from current technical replicate tests does not indicate low quality of microarray technology. We also demonstrate that heterogeneous biological variations existing in real cancer data will further reduce the overall reproducibility of DEG detection. Nevertheless, in small subsamples from both simulated and real data, the actual false discovery rate (FDR) for each DEG list tends to be low, suggesting that each separately determined list may comprise mostly true DEGs. Rather than simply counting the overlaps of the discovery lists from different studies for a complex disease, novel metrics are needed for evaluating the reproducibility of discoveries characterized with correlated molecular changes.

Contact: guoz{at}ems.hrbmu.edu.cn; lixia{at}ems.hrbmu.edu.cn

Supplementaty information: Supplementary data are available at Bioinformatics online.

{dagger}M.Zhang and C.Yao contributed equally to this work.

{ddagger}J.Zou and L.Zhang contributed equally to this work.

Associate Editor: Olga Troyanskaya


Received on April 14, 2008; revised on July 14, 2008; accepted on July 14, 2008

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