Evidence map›Paper›PMID 26732145›Full record

ArticleScientific reports2016

CrossNorm: a novel normalization strategy for microarray data in cancers.

Lixin Cheng, Leung-Yau Lo, Nelson L S Tang, Dong Wang, Kwong-Sak Leung

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Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

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32citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

32 citing papers in PubMed.

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  14. Platelets Purification Is a Crucial Step for Transcriptomic Analysis.International journal of molecular sciences · 2022
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Lixin ChengDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.
Leung-Yau LoDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.
Nelson L S TangDepartment of Chemical Pathology, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.
Dong WangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Kwong-Sak LeungDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Normalization is essential to get rid of biases in microarray data for their accurate analysis. Existing normalization methods for microarray gene expression data commonly assume a similar global expression pattern among samples being studied. However, scenarios of global shifts in gene expressions are dominant in cancers, making the assumption invalid. To alleviate the problem, here we propose and develop a novel normalization strategy, Cross Normalization (CrossNorm), for microarray data with unbalanced transcript levels among samples. Conventional procedures, such as RMA and LOESS, arbitrarily flatten the difference between case and control groups leading to biased gene expression estimates. Noticeably, applying these methods under the strategy of CrossNorm, which makes use of the overall statistics of the original signals, the results showed significantly improved robustness and accuracy in estimating transcript level dynamics for a series of publicly available datasets, including titration experiment, simulated data, spike-in data and several real-life microarray datasets across various types of cancers. The results have important implications for the past and the future cancer studies based on microarray samples with non-negligible difference. Moreover, the strategy can also be applied to other sorts of high-throughput data as long as the experiments have global expression variations between conditions.

Indexed as

Computational BiologyComputer SimulationDatasets as TopicGene Expression ProfilingHumansNeoplasmsOligonucleotide Array Sequence AnalysisReproducibility of Results

Identifiers

PMID26732145
PMCPMC4702063

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