癌症微阵列数据的基因关联分析结果受到预处理算法的影响

N. Baskaran, C. Kwoh, K. Hui
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引用次数: 1

摘要

癌症微阵列数据的基因关联分析提供了丰富的基因表达模式和癌症途径的信息,以增强对癌症诊断、预后和治疗反应性预测的潜在生物标志物的识别。然而,实现这些生物学/临床目标在很大程度上依赖于各种分析工具的功能和准确性,以挖掘这些癌症微阵列基因表达谱。目前已有多种预处理算法用于分析Affymetrix微阵列基因表达数据。以前的研究已经评估了这些算法在使用各种峰值和实验数据集准确确定基因表达方面的能力。然而,在单个癌症数据集上,这些不同的预处理算法之间检测差异表达基因的差异尚未在系统级评估中进行。在本研究中,我们评估了PLIER、GCRMA、RMA和MAS5检测差异表达基因的能力之间的可比性和差异水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outcomes of gene association analysis of cancer microarray data are impacted by pre-processing algorithms
Gene association analysis of cancer microarray data provides a wealth of information on gene expression patterns and cancer pathways to enhance the identification of potential biomarkers for cancer diagnosis, prognosis, and prediction of therapeutic responsiveness. However, achieving these biological/clinical objectives relies heavily on the functional capabilities and accuracy of the various analytical tools to mine these cancer microarray gene expression profiles. Many preprocessing algorithms exist for analyzing Affymetrix microarray gene expression data. Previous studies have evaluated these algorithms on their capabilities in accurately determining gene expression using a variety of spike-in as well as experimental data sets. However, variations in detecting differentially expressed genes between these different pre-processing algorithms on a single cancer dataset have not been done in a systems-level evaluation. In this study, we assessed the comparability and the level of variation between PLIER, GCRMA, RMA and MAS5 for their capability to detect differentially expressed genes.
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