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使用像素强度校正微阵列信号饱和度的贝叶斯层次模型。

Bayesian hierarchical model for correcting signal saturation in microarrays using pixel intensities.

作者信息

Gupta Rashi, Auvinen Petri, Thomas Andrew, Arjas Elja

机构信息

Department of Mathematics and Statistics, P.O. Box 68 and Institute of Biotechnology, P.O. Box 56, University of Helsinki, FIN-00014, Helsinki, Finland.

出版信息

Stat Appl Genet Mol Biol. 2006;5:Article20. doi: 10.2202/1544-6115.1220. Epub 2006 Aug 28.

Abstract

Pixel saturation occurs when the pixel intensity exceeds the scanner upper threshold of detection and the recorded pixel intensity is then truncated at the threshold. Truncation of the pixel intensity causes the estimates of gene expression (i.e., intensity) to be biased. Microarray experiments are commonly affected by saturated pixels; as a result all higher level analyses are made on these biased gene expression estimates. In this paper, we propose a method for improving the quality of the signal for cDNA microarrays by making use of several scans at varying scanner sensitivities. For each spot, pixel level intensity readings are given as input to a Bayesian hierarchical model. The model uses the pixel intensities of the spot to provide a posterior distribution of the true expression level of the corresponding genes. The parameters of the hierarchical model are estimated jointly with these expression levels, thus performing an integrated analysis of the measurement data. The method improves in all ranges the accuracy with which intensities can be estimated and extends the dynamic range of measured gene expression at the high end. The method is generic and can be applied to data from any organism and for imaging with any scanner. Results from a real data set illustrate an improved precision in the estimation of the expression of genes compared to what can be achieved by applying standard methods and using only a single scan.

摘要

当像素强度超过扫描仪的检测上限阈值时,就会发生像素饱和,此时记录的像素强度会在该阈值处被截断。像素强度的截断会导致基因表达(即强度)的估计产生偏差。微阵列实验通常会受到饱和像素的影响;因此,所有更高层次的分析都是基于这些有偏差的基因表达估计进行的。在本文中,我们提出了一种方法,通过利用在不同扫描仪灵敏度下的多次扫描来提高cDNA微阵列信号的质量。对于每个斑点,将像素级强度读数作为输入提供给一个贝叶斯层次模型。该模型利用斑点的像素强度来提供相应基因真实表达水平的后验分布。层次模型的参数与这些表达水平一起进行估计,从而对测量数据进行综合分析。该方法在各个范围内提高了强度估计的准确性,并扩展了高端测量基因表达的动态范围。该方法具有通用性,可应用于来自任何生物体的数据以及使用任何扫描仪进行的成像。一个真实数据集的结果表明,与应用标准方法并仅使用单次扫描相比,该方法在基因表达估计方面具有更高的精度。

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