Differential Co-Expression Networks using RNA-seq and microarrays in Alzheimer's disease

Hyojin Kang, Junehawk Lee, S. Yu
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引用次数: 5

Abstract

Differential Co-Expression Networks (DCENs) are graphical representations of genes showing differential co-expression pattern in response to experimental conditions or genetic changes. They have been successfully applied to identify condition-specific modules and provide a picture of the dynamic changes in gene regulatory networks. DCENs analysis investigates the differences among gene interconnections by calculating the expression correlation change of each gene pair between conditions. In this study, we collected many different datasets from NCBI GEO including 25 RNA-seq and 2,102 microarray samples derived from human brain and blood in Alzheimer's disease and performed differential co-expression analyses to identify functional modules responsible for the characterization of Alzheimer's disease. The DCENs were generated using Pearson correlation coefficient and meta-analysis was conducted using rank-based method. The preliminary results show that the structural characteristics of DCENs can provide new insights into the underlying gene regulatory dynamics in Alzheimer's disease. There is low size overlap between microarray- and RNA-seq-derived DCENs however, DCENs from RNA-seq would complement ones from microarray due to the higher coverage and dynamic range of RNA-seq.
使用RNA-seq和微阵列的阿尔茨海默病差异共表达网络
差异共表达网络(dcen)是基因在实验条件或遗传变化下表现出差异共表达模式的图形表示。它们已被成功地应用于识别条件特异性模块,并提供了基因调控网络动态变化的图片。dcns分析通过计算各基因对在不同条件下的表达相关性变化来研究基因互连之间的差异。在这项研究中,我们从NCBI GEO收集了许多不同的数据集,包括来自阿尔茨海默病患者的人类大脑和血液的25个RNA-seq和2102个微阵列样本,并进行了差异共表达分析,以确定负责表征阿尔茨海默病的功能模块。采用Pearson相关系数生成dcn,采用基于秩的方法进行meta分析。初步结果表明,dcns的结构特征可以为阿尔茨海默病的潜在基因调控动力学提供新的见解。微阵列和RNA-seq衍生的dccn之间存在较小的大小重叠,但由于RNA-seq的覆盖率和动态范围更高,来自RNA-seq的dccn可以补充来自微阵列的dccn。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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