Li Meijuan, Reilly Cavan
Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN 55455-0378, USA.
J Biomol Tech. 2008 Apr;19(2):122-8.
The quality of data from microarray analysis is highly dependent on the quality of RNA. Because of the lability of RNA, steps involved in tissue sampling, RNA purification, and RNA storage are known to potentially lead to the degradation of RNAs; therefore, assessment of RNA quality and integrity is essential. Existing methods for estimating the quality of RNA hybridized to a GeneChip either suffer from subjectivity or are inefficient in performance. To overcome these drawbacks, we propose a linear regression method for assessing RNA quality for a hybridized Genechip. In particular, our approach used the probe intensities from the .cel files that the Affymetrix software associates with each microarray. The effectiveness and the improvements of the proposed method over the existing methods are illustrated by the application of the method to the previously published 19 human Affymetrix microarray data sets for which external verification of RNA quality is available.
微阵列分析数据的质量高度依赖于RNA的质量。由于RNA的不稳定性,组织采样、RNA纯化和RNA储存过程中涉及的步骤可能会导致RNA降解;因此,评估RNA质量和完整性至关重要。现有的估计与基因芯片杂交的RNA质量的方法要么存在主观性,要么性能效率低下。为了克服这些缺点,我们提出了一种用于评估杂交基因芯片RNA质量的线性回归方法。特别是,我们的方法使用了Affymetrix软件与每个微阵列关联的.cel文件中的探针强度。通过将该方法应用于先前发表的19个人类Affymetrix微阵列数据集(这些数据集可进行RNA质量的外部验证),说明了该方法相对于现有方法的有效性和改进之处。