Evidence map›Paper›PMID 19417058›Full record

ArticleBioinformatics (Oxford, England)2009

Evaluating reproducibility of differential expression discoveries in microarray studies by considering correlated molecular changes.

Min Zhang, Lin Zhang, Jinfeng Zou, Chen Yao, Hui Xiao, Qing Liu, Jing Wang, Dong Wang, Chenguang Wang, Zheng Guo

Abstract readEvaluation Study
In one paragraph

Article in Bioinformatics (Oxford, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

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43citing papers in PubMed
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3 · Its place in the literature

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43 citing papers in PubMed.

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5 · Who and what money

Authors and funding

10 authors.

Min ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Lin Zhang
Jinfeng Zou
Chen Yao
Hui Xiao
Qing Liu
Jing Wang
Dong Wang
Chenguang Wang
Zheng Guo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationAccording to current consistency metrics such as percentage of overlapping genes (POG), lists of differentially expressed genes (DEGs) detected from different microarray studies for a complex disease are often highly inconsistent. This irreproducibility problem also exists in other high-throughput post-genomic areas such as proteomics and metabolism. A complex disease is often characterized with many coordinated molecular changes, which should be considered when evaluating the reproducibility of discovery lists from different studies.

resultsWe proposed metrics percentage of overlapping genes-related (POGR) and normalized POGR (nPOGR) to evaluate the consistency between two DEG lists for a complex disease, considering correlated molecular changes rather than only counting gene overlaps between the lists. Based on microarray datasets of three diseases, we showed that though the POG scores for DEG lists from different studies for each disease are extremely low, the POGR and nPOGR scores can be rather high, suggesting that the apparently inconsistent DEG lists may be highly reproducible in the sense that they are actually significantly correlated. Observing different discovery results for a disease by the POGR and nPOGR scores will obviously reduce the uncertainty of the microarray studies. The proposed metrics could also be applicable in many other high-throughput post-genomic areas.

Indexed as

AlgorithmsComputational BiologyDatabases, GeneticGene Expression ProfilingOligonucleotide Array Sequence AnalysisReproducibility of Results

Identifiers

PMID19417058
PMCPMC2940240

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