Microarray validation: factors influencing correlation between oligonucleotide microarrays and real-time PCR

被引:415
作者
Morey, Jeanine S. [1 ]
Ryan, James C. [1 ]
Van Dolah, Frances M. [1 ]
机构
[1] NOAA, Marine Biotoxins Program, Ctr Coastal Environm Hlth & Biomol Res, Charleston, SC 29412 USA
关键词
polymerase chain reaction; microarray analysis; gene expression; nucleic acid amplification techniques; reverse transcriptase polymerase chain reaction; RNA;
D O I
10.1251/bpo126
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Quantitative real-time PCR (qPCR) is a commonly used validation tool for confirming gene expression results obtained from microarray analysis; however, microarray and qPCR data often result in disagreement. The current study assesses factors contributing to the correlation between these methods in five separate experiments employing two-color 60-mer oligonucleotide microarrays and qPCR using SYBR green. Overall, significant correlation was observed between microarray and qPCR results (rho = 0.708, p < 0.0001, n = 277) using these platforms. The contribution of factors including up- vs. down-regulation, spot intensity, rho-value, fold-change, cycle threshold (C-t), array averaging, tissue type, and tissue preparation was assessed. Filtering of microarray data for measures of quality (fold-change and rho-value) proves to be the most critical factor, with significant correlations of rho > 0.80 consistently observed when quality scores are applied.
引用
收藏
页码:175 / 193
页数:19
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