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

机译:使用RNA序列和微阵列的阿尔茨海默氏病差异共表达网络

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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.
机译:差异共表达网络(DCEN)是基因的图形表示,显示了响应实验条件或遗传变化的差异共表达模式。它们已成功应用于识别条件特异性模块并提供基因调节网络动态变化的图片。 DCENs分析通过计算条件之间每个基因对的表达相关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25个RNA-seq和2102个从人脑和血液中提取的阿尔茨海默氏病微阵列样品,并进行了差异共表达分析以鉴定负责表征阿尔茨海默氏病的功能模块。使用Pearson相关系数生成DCEN,并使用基于秩的方法进行荟萃分析。初步结果表明,DCENs的结构特征可以为阿尔茨海默氏病的潜在基因调控动力学提供新的见解。来自微阵列和RNA序列的DCEN之间的大小重叠很小,但是,由于RNA-序列的覆盖范围和动态范围更高,因此来自RNA-seq的DCEN将补充来自微阵列的DCEN。

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