Literature DB >> 16818002

Multiplicative background correction for spotted microarrays to improve reproducibility.

Dabao Zhang1, Min Zhang, Martin T Wells.   

Abstract

We propose a simple approach, the multiplicative background correction, to solve a perplexing problem in spotted microarray data analysis: correcting the foreground intensities for the background noise, especially for spots with genes that are weakly expressed or not at all. The conventional approach, the additive background correction, directly subtracts the background intensities from foreground intensities. When the foreground intensities marginally dominate the background intensities, the additive background correction provides unreliable estimates of the differential gene expression levels and usually presents M-A plots with fishtails or fans. Unreliable additive background correction makes it preferable to ignore the background noise, which may increase the number of false positives. Based on the more realistic multiplicative assumption instead of the conventional additive assumption, we propose to logarithmically transform the intensity readings before the background correction, with the logarithmic transformation symmetrizing the skewed intensity readings. This approach not only precludes the fishtails and fans in the M-A plots, but provides highly reproducible background-corrected intensities for both strongly and weakly expressed genes. The superiority of the multiplicative background correction to the additive one as well as the no background correction is justified by publicly available self-hybridization datasets.

Mesh:

Year:  2006        PMID: 16818002     DOI: 10.1017/S0016672306008196

Source DB:  PubMed          Journal:  Genet Res        ISSN: 0016-6723            Impact factor:   1.588


  6 in total

1.  Extreme value theory in analysis of differential expression in microarrays where either only up- or down-regulated genes are relevant or expected.

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Journal:  Genet Res (Camb)       Date:  2008-08       Impact factor: 1.588

2.  Impact of the spotted microarray preprocessing method on fold-change compression and variance stability.

Authors:  Jérôme Ambroise; Bertrand Bearzatto; Annie Robert; Bernadette Govaerts; Benoît Macq; Jean-Luc Gala
Journal:  BMC Bioinformatics       Date:  2011-10-25       Impact factor: 3.169

3.  Elucidating the identity of resistance mechanisms to prednisolone exposure in acute lymphoblastic leukemia cells through transcriptomic analysis: A computational approach.

Authors:  Emmanouil G Sifakis; George I Lambrou; Andriana Prentza; Spiros Vlahopoulos; Dimitris Koutsouris; Fotini Tzortzatou-Stathopoulou; Aristotelis A Chatziioannou
Journal:  J Clin Bioinforma       Date:  2011-12-20

4.  A multi-treatment experimental system to examine photosynthetic differentiation in the maize leaf.

Authors:  Ruairidh J H Sawers; Peng Liu; Katya Anufrikova; J T Gene Hwang; Thomas P Brutnell
Journal:  BMC Genomics       Date:  2007-01-09       Impact factor: 3.969

5.  Serum microRNA array analysis identifies miR-140-3p, miR-33b-3p and miR-671-3p as potential osteoarthritis biomarkers involved in metabolic processes.

Authors:  E Ntoumou; M Tzetis; M Braoudaki; G Lambrou; M Poulou; K Malizos; N Stefanou; L Anastasopoulou; A Tsezou
Journal:  Clin Epigenetics       Date:  2017-12-12       Impact factor: 6.551

6.  Dual Mechanisms of Metabolism and Gene Expression of the CCRF-CEM Leukemia Cells under Glucocorticoid Treatment.

Authors:  George I Lambrou; Theodoros Karakonstantakis; Spiros Vlahopoulos; Apostolos Zaravinos
Journal:  Int J Mol Sci       Date:  2021-05-31       Impact factor: 5.923

  6 in total

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