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Network-Based Integrative Analysis of Genomics Epigenomics and Transcriptomics in Autism Spectrum Disorders

机译:基于网络的自闭症谱系障碍基因组学表观基因组学和转录组学的综合分析

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摘要

Current studies suggest that autism spectrum disorders (ASDs) may be caused by many genetic factors. In fact, collectively considering multiple studies aimed at characterizing the basic pathophysiology of ASDs, a large number of genes has been proposed. Addressing the problem of molecular data interpretation using gene networks helps to explain genetic heterogeneity in terms of shared pathways. Besides, the integrative analysis of multiple omics has emerged as an approach to provide a more comprehensive view of a disease. In this work, we carry out a network-based meta-analysis of the genes reported as associated with ASDs by studies that involved genomics, epigenomics, and transcriptomics. Collectively, our analysis provides a prioritization of the large number of genes proposed to be associated with ASDs, based on genes’ relevance within the intracellular circuits, the strength of the supporting evidence of association with ASDs, and the number of different molecular alterations affecting genes. We discuss the presence of the prioritized genes in the SFARI (Simons Foundation Autism Research Initiative) database and in gene networks associated with ASDs by other investigations. Lastly, we provide the full results of our analyses to encourage further studies on common targets amenable to therapy.
机译:当前的研究表明,自闭症谱系障碍(ASD)可能是由许多遗传因素引起的。实际上,共同考虑旨在表征ASD的基本病理生理的多项研究,已经提出了许多基因。使用基因网络解决分子数据解释的问题有助于从共享途径的角度解释遗传异质性。此外,对多种组学的综合分析已成为一种提供更全面的疾病观察方法。在这项工作中,我们通过涉及基因组学,表观基因组学和转录组学的研究,对据报道与ASD相关的基因进行了基于网络的荟萃分析。总的来说,我们的分析根据细胞内回路中基因的相关性,与ASD相关的支持证据的强度以及影响基因的不同分子改变的数量,对拟与ASD相关的大量基因进行了优先排序。 。我们将通过其他调查来讨论SFARI(西蒙斯基金会自闭症研究计划)数据库和与ASD相关的基因网络中优先基因的存在。最后,我们提供了分析的全部结果,以鼓励对适合治疗的常见靶点进行进一步研究。

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