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Detecting Perturbation in Co-Expression Modules Associated with Different Stages of HIV-1 Progression: A Multi-objective Evolutionary Approach

机译:检测与HIV-1进展不同阶段相关的共表达模块的扰动:多目标进化方法

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Investigating co-regulation pattern of a group (or cluster) of genes is widely used to explore the topological and biological properties of co-expression network in a specific phenotype condition. Recent approaches go one step beyond and look for change in co-expression patterns in a pair of phenotype conditions during a disease progression. Here we develop a novel multi-objective framework to identify co-expressed modules undergoing topological changes in two phenotype conditions during disease progression. The proposed method is demonstrated on a microarray dataset of HIV disease progression. We identify co-expression modules during propagation of HIV infection from acute to chronic stage and from acute to non-progressive stage. We also perform a comparative study to explore topological properties of the identified modules in each pair of stages. The identified modules are also enriched with significant TFs like ZNF 771, ZNF 317, FOXJ3, SMARCC1 etc. TFs in the ZNF family are coming out as common regulators of genes involved in two categories of modules.
机译:研究基因的群体(或簇)的共调控模式被广泛用于探讨在特定表型条件下共表达网络的拓扑和生物学特性。最近的方法远离疾病进展期间的一对表型条件中的共表达模式的变化。在这里,我们开发了一种新的多目标框架,以识别疾病进展期间两种表型条件下进行拓扑变化的共表达模块。在艾滋病毒疾病进展的微阵列数据集上证明了所提出的方法。我们在HIV感染从急性慢性阶段和急性到非进展阶段繁殖期间识别共表达模块。我们还进行比较研究,以探讨每对阶段中所识别模块的拓扑特性。所识别的模块也富含像ZNF 771,ZNF 317,FOXJ3,SMARCC1等在家庭ZNF转录因子被出来为参与两个类别模块的基因的共同调节剂显著的TF。

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