利用 TEA-GCN 构建集合基因功能网络,从未获授权的转录组数据中捕捉组织/条件特异性共表达

Peng Ken Lim, Ruoxi Wang, Jenet Princy Antony Velankanni, Marek Mutwil
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引用次数: 0

摘要

从公共转录组数据集生成的基因共表达网络(GCN)可以阐明基因之间的共调控和共功能关系,使GCN成为预测基因功能的重要工具。然而,目前的 GCN 构建方法对数据质量很敏感,而且所发现的基因间关系的可解释性仍然很困难。为了解决这个问题,我们提出了一种新方法:两层集合聚合(TEA-)GCN。TEA-GCN 利用对大型转录组数据集的无监督分区和三个相关系数,通过两步聚合过程生成集合 GCN。我们的研究表明,TEA-GCN 在发现基因间正确的功能关系方面优于目前三种模式物种的最先进技术,而且不仅能捕捉条件/组织特异性基因共表达,还能通过使用自然语言处理(NLP)来解释它们。此外,我们还发现 TEA-GCN 在识别转录因子及其激活靶标之间的关系方面表现尤为突出,这使它在推断基因调控网络方面非常有效。TEA-GCN可在https://github.com/pengkenlim/TEA-GCN。
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Constructing Ensemble Gene Functional Networks Capturing Tissue/condition-specific Co-expression from Unlabled Transcriptomic Data with TEA-GCN
Gene co-expression networks (GCNs) generated from public transcriptomic datasets can elucidate the co-regulatory and co-functional relationships between genes, making GCNs an important tool to predict gene functions. However, current GCN construction methods are sensitive to the quality of the data, and the interpretability of the identified relationships between genes is still difficult. To address this, we present a novel method: Two-Tier Ensemble Aggregation (TEA-) GCN. TEA-GCN utilizes unsupervised partitioning of big transcriptomic datasets and three correlation coefficients to generate ensemble GCNs in a two-step aggregation process. We show that TEA-GCN outperforms in finding correct functional relationships between genes over the current state-of-the-art across three model species, and is able to not only capture condition/tissue-specific gene co-expression but explain them through the use of natural language processing (NLP). In addition, we found TEA-GCN to be especially performant in identifying relationships between transcription factors and their activation targets, making it effective in inferring gene regulatory networks. TEA-GCN is available at https://github.com/pengkenlim/TEA-GCN.
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