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Functional network composed of 1,219 genes for Schizophrenia-- a literature data mining and enrichment analysis

机译:由1,219个精神分裂症基因组成的功能网络-文献数据挖掘和富集分析

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Background: Over the past decade, numerous studies have focused on identifying genetic factors associated with schizophrenia (SCZ).Sample variations, such as size, population, race, disease status, and data processing methods resulted in selection differences. Nevertheless, no systemic study has been completed to summarize these reports and provide an objective full list of genes with a reported association to SCZ. Method: We conducted a literature data mining (LDM) of over 13,515 articles covering publications from 1958 to Feb. 2016. These articles reported multiple types of marker-disease associations between 1,219 genes and SCZ. Then we conducted a gene set enrichment analysis (GSEA) and a sub-network enrichment analysis (SNEA) to study the functional profile and validate the pathogenic significance of these genes to SCZ. Finally, we presented additional results from the systemic review, including publication date, quality scores, and authoraffiliations. Results: All of these genes have been demonstrated to present multiple mutations associating with SCZ, some of which were supported by a large number of high quality articles. Enrichment analyses showed that many psychiatric and neuropathic pathways/groups related to SCZ have been significantly enriched by these genes and that they are functionally associated with each other. Conclusion: Our results indicate that these genesmay operate as a functional biomarker network influencing the development of SCZ, and thatLDM together with GSEA and SNEA could serve as an effective approach in finding these potential target genes.
机译:背景:在过去的十年中,许多研究集中在鉴定与精神分裂症(SCZ)相关的遗传因素上,样本变化(例如大小,人口,种族,疾病状态和数据处理方法)导致选择差异。然而,还没有完成系统的研究来总结这些报道并提供客观的完整基因清单,并报道了与SCZ相关的基因。方法:我们进行了文献数据挖掘(LDM),涵盖了从1958年到2016年2月的13515篇文章。这些文章报道了1,219个基因与SCZ之间的多种标记-疾病关联。然后,我们进行了基因集富集分析(GSEA)和子网富集分析(SNEA),以研究功能概况并验证这些基因对SCZ的致病性。最后,我们介绍了系统评价的其他结果,包括发表日期,质量得分和作者隶属关系。结果:所有这些基因均已显示出与SCZ相关的多个突变,其中一些受到大量高质量文章的支持。富集分析表明,与SCZ相关的许多精神病学和神经病性途径/组已被这些基因显着富集,并且它们在功能上相互关联。结论:我们的结果表明,这些基因可能是影响SCZ发育的功能性生物标记网络,而LDM与GSEA和SNEA一起可以作为寻找这些潜在靶基因的有效方法。

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