Department of Computer Science and Engineering, Tezpur University, Tezpur, Assam, India.
J Biosci. 2020;45.
A gene co-expression network (CEN) is of biological interest, since co-expressed genes share common functions and biological processes or pathways. Finding relationships among modules can reveal inter-modular preservation, and similarity in transcriptome, functional, and biological behaviors among modules of the same or two different datasets. There is no method which explores the one-to-one relationships and one-to-many relationships among modules extracted from control and disease samples based on both topological and semantic similarity using both microarray and RNA seq data. In this work, we propose a novel fusion measure to detect mapping between modules from two sets of co-expressed modules extracted from control and disease stages of Alzheimer's disease (AD) and Parkinson's disease (PD) datasets. Our measure considers both topological and biological information of a module and is an estimation of four parameters, namely, semantic similarity, eigengene correlation, degree difference, and the number of common genes. We analyze the consensus modules shared between both control and disease stages in terms of their association with diseases. We also validate the close associations between human and chimpanzee modules and compare with the state-ofthe- art method. Additionally, we propose two novel observations on the relationships between modules for further analysis.
基因共表达网络(CEN)具有生物学意义,因为共表达的基因具有共同的功能和生物过程或途径。发现模块之间的关系可以揭示模块之间的模块间保存和转录组、功能和生物学行为的相似性,这些模块来自相同或两个不同数据集。目前还没有一种方法可以利用微阵列和 RNA-seq 数据,根据拓扑和语义相似性,探索从对照和疾病样本中提取的模块之间的一对一关系和一对多关系。在这项工作中,我们提出了一种新的融合度量标准,用于检测从阿尔茨海默病(AD)和帕金森病(PD)数据集的对照和疾病阶段提取的两组共表达模块之间的模块之间的映射。我们的度量标准同时考虑了模块的拓扑和生物学信息,是对四个参数的估计,即语义相似性、特征基因相关性、度差和共同基因数。我们根据与疾病的关联,分析了在两个对照和疾病阶段之间共享的共识模块。我们还验证了人类和黑猩猩模块之间的密切关联,并与最先进的方法进行了比较。此外,我们还提出了两个关于模块之间关系的新观察结果,以进行进一步分析。