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June 15, 2001Nucleic Acids Research575 citationsOpen Access

Issues in cDNA microarray analysis: quality filtering, channel normalization, models of variations and assessment of gene effects

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GTGeorge C. Tseng

Key Points

  • This research aims to improve the accuracy of comparing gene expression levels using cDNA microarray data across different conditions.
  • Used a quality index for filtering out poor-quality genes and slides based on duplicate spots.
  • Performed calibration experiments to establish the necessity of normalization between fluorescent labels, demonstrating non-linear and slide-dependent behavior.
  • Developed a hierarchical model to assess gene effect significance in comparative experiments.
  • Identified a significant improvement in analysis accuracy after implementing the rank invariant method for selecting non-differentially expressed genes.
  • Demonstrated that calibration residuals provide valuable prior information on variance components.
  • Analyzed gene effects across two experimental groups of 125 and 4129 genes respectively, highlighting the impact of growth conditions.

Abstract

We consider the problem of comparing the gene expression levels of cells grown under two different conditions using cDNA microarray data. We use a quality index, computed from duplicate spots on the same slide, to filter out outlying spots, poor quality genes and problematical slides. We also perform calibration experiments to show that normalization between fluorescent labels is needed and that the normalization is slide dependent and non-linear. A rank invariant method is suggested to select non-differentially expressed genes and to construct normalization curves in comparative experiments. After normalization the residuals from the calibration data are used to provide prior information on variance components in the analysis of comparative experiments. Based on a hierarchical model that incorporates several levels of variations, a method for assessing the significance of gene effects in comparative experiments is presented. The analysis is demonstrated via two groups of experiments with 125 and 4129 genes, respectively, in Escherichia coli grown in glucose and acetate.

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George C. Tseng (2001) studied this question.

synapsesocial.com/papers/6a08dd8d27ceb0c2a2d60b04https://doi.org/10.1093/nar/29.12.2549
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