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Identification of differential modules in ankylosing spondylitis using systemic module inference and the attract method

机译:应用系统模块推断和吸引方法鉴定强直性脊柱炎中的差异模块

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摘要

The objective of the present study was to identify differential modules in ankylosing spondylitis (AS) by integrating network analysis, module inference and the attract method. To achieve this objective, four steps were conducted. The first step was disease objective network (DON) for AS, and healthy objective network (HON) inference dependent on gene expression data, protein-protein interaction networks and Spearman's correlation coefficient. In the second step, module detection was performed by utilizing a clique-merging algorithm, which comprised of exploring maximal cliques by clique algorithm and refining or merging maximal cliques with a high overlap. The third part was seed module evaluation through module pair matches by Jaccard score and module correlation density (MCD) calculation. Finally, in the fourth step, differential modules between the AS and healthy groups were identified based on a gene set enrichment analysis-analysis of variance model in the attract method. There were 5,301 nodes and 28,176 interactions both in DON and HON. A total of 20 and 21 modules were detected for the AS and healthy group, respectively. Notably, six seed modules across two groups were identified with Jaccard score ≥0.5, and these were ranked in descending order of differential MCD (ΔC). Seed module 1 had the highest ΔC of 0.077 and Jaccard score of 1.000. By accessing the attract method, one differential module between the AS group and healthy group was identified. In conclusion, the present study successfully identified one differential module for AS that may be a potential marker for AS target therapy and provide insights for future research on this disease.
机译:本研究的目的是通过整合网络分析,模块推断和吸引方法来识别强直性脊柱炎(AS)中的差异模块。为了实现这个目标,进行了四个步骤。第一步是针对AS的疾病目标网络(DON),然后根据基因表达数据,蛋白质-蛋白质相互作用网络和Spearman相关系数推断健康目标网络(HON)。在第二步中,通过使用团合并算法执行模块检测,该算法包括通过团算法探索最大团并优化或合并具有高重叠度的最大团。第三部分是通过Jaccard评分和模块相关密度(MCD)计算通过模块对匹配对种子模块进行评估。最后,在第四步中,基于吸引法中的基因集富集分析-方差模型分析,确定了AS与健康组之间的差异模块。 DON和HON中共有5,301个节点和28,176个交互。 AS和健康组分别检测到20个模块和21个模块。值得注意的是,在Jaccard得分≥0.5的情况下,确定了两组中的六个种子模块,并按差异MCD(ΔC)的降序排列。种子模块1的ΔC最高,为0.077,Jaccard得分为1.000。通过使用吸引方法,确定了AS组和健康组之间的一个差异模块。总之,本研究成功地鉴定了一种AS分化模块,它可能是AS靶标治疗的潜在标志物,并为该疾病的未来研究提供了见识。

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