A rapid method for microarray cross platform comparisons using gene expression signatures

被引:23
作者
Cheadle, Chris
Becker, Kevin G.
Cho-Chung, Yoon S.
Nesterova, Maria
Watkins, Tonya
Wood, William, III
Prabhu, Vinayakumar
Barnes, Kathleen C.
机构
[1] Johns Hopkins Univ, Sch Med, Div Allergy & Clin Immunol, Genom Core, Baltimore, MD 21224 USA
[2] NIA, Gene Express & Genom Unit, Intramural Res Program, NIH, Baltimore, MD 21224 USA
[3] NCI, Cellular Biochem Sect, Basic Res Lab, Ctr Canc Res,NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.mcp.2006.07.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microarray technology has become highly valuable for identifying complex changes in global gene expression patterns. The inevitable use of a variety of different platforms has compounded the difficulty of effectively comparing data between projects, laboratories, and public access databases. The need for consistent, believable results across platforms is fundamental and methods for comparing results across platforms should be as straightforward as possible. We present the results of a study comparing three major, commercially available, microarray platforms (Affymetrix, Agilent, and Illumina). Concordance estimates between platforms was based on mapping of probes to Human Gene Organization (HUGO) gene names. Appropriate data normalization procedures were applied to each dataset followed by the generation of lists of regulated genes using a common significance threshold for all three platforms. As expected, concordance measured by directly comparing genelists was relatively low (an average 22.8% for all platforms across all possible comparisons). However, when statistical tests (gene set enrichment analysis-GSEA, parametric analysis of gene enrichment-PAGE) which align genelists with continuous measures of differential gene expression were applied to the cross platform datasets using significant genelists to poll entire datasets, the relatedness of the results from all three platforms was specific, obvious, and profound. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:35 / 46
页数:12
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