通过基因网络透视遗传学研究。

ArXiv Pub Date : 2024-10-30
Marc Subirana-Granés, Jill Hoffman, Haoyu Zhang, Christina Akirtava, Sutanu Nandi, Kevin Fotso, Milton Pividori
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引用次数: 0

摘要

了解复杂性状的遗传基础是基因组学领域的一项长期挑战。全基因组关联研究(GWAS)发现了成千上万个变异与性状的关联,但这些变异大多位于非编码区,因此与生物功能的联系难以捉摸。虽然转录组关联研究(TWAS)等传统方法通过将遗传变异与基因表达联系起来加深了我们的理解,但它们往往忽略了基因与基因之间的相互作用。在此,我们回顾了目前整合不同分子数据的方法,利用机器学习方法根据共表达和功能关系识别基因模块。这些整合方法(如 PhenoPLIER)结合了 TWAS 和药物诱导转录图谱,可有效捕捉具有生物学意义的基因网络。这种整合提供了对疾病过程的特定背景理解,同时突出了核心和外围基因。这些见解为新的治疗目标铺平了道路,并提高了个性化医疗中基因研究的可解释性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic studies through the lens of gene networks.

Understanding the genetic basis of complex traits is a longstanding challenge in the field of genomics. Genome-wide association studies (GWAS) have identified thousands of variant-trait associations, but most of these variants are located in non-coding regions, making the link to biological function elusive. While traditional approaches, such as transcriptome-wide association studies (TWAS), have advanced our understanding by linking genetic variants to gene expression, they often overlook gene-gene interactions. Here, we review current approaches to integrate different molecular data, leveraging machine learning methods to identify gene modules based on co-expression and functional relationships. These integrative approaches, like PhenoPLIER, combine TWAS and drug-induced transcriptional profiles to effectively capture biologically meaningful gene networks. This integration provides a context-specific understanding of disease processes while highlighting both core and peripheral genes. These insights pave the way for novel therapeutic targets and enhance the interpretability of genetic studies in personalized medicine.

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