Inferring gene regulatory networks from single-cell transcriptomics jointly through graph neural networks and Transformer.

Yanglan Gan, Tao Liu, Guangwei Xu, Wenjing Guo, Guobing Zou
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Abstract

Inferring gene regulatory networks (GRNs) is crucial for understanding the complex regulatory relationships that govern gene expression in cells. Recently, several computational methods have been proposed for reconstructing GRNs from single-cell RNA sequencing (scRNA-seq) data. However, most of these methods primarily focus on pairwise regulatory relationships between genes, failing to leverage the global regulatory structure of GRNs, which is crucial for exploring the complex regulatory interactions between transcription factors (TFs) and their target genes. To address these limitations, we propose GTGRNS, a supervised learning framework that integrates a graph neural network with a Transformer encoder for GRN inference from scRNA-seq data. Specifically, we utilize the GraphSAGE model to integrate regulatory network topological information with gene expression features, facilitating the learning of gene representations. By leveraging the Transformer model, we further extract complex dependencies of gene pairs, which are crucial for determining regulatory levels. The comparative experiments on several benchmark datasets demonstrate the effectiveness and competitiveness of the proposed GTGRNS in the task of GRN inference.

通过图神经网络和Transformer共同推断单细胞转录组学的基因调控网络。
推断基因调控网络(grn)对于理解控制细胞中基因表达的复杂调控关系至关重要。最近,人们提出了几种计算方法来从单细胞RNA测序(scRNA-seq)数据中重建grn。然而,这些方法大多主要关注基因之间的成对调控关系,未能充分利用grn的全局调控结构,而这对于探索转录因子(tf)与其靶基因之间复杂的调控相互作用至关重要。为了解决这些限制,我们提出了GTGRNS,这是一种监督学习框架,它将图神经网络与Transformer编码器集成在一起,用于从scRNA-seq数据中推断GRN。具体而言,我们利用GraphSAGE模型将调控网络拓扑信息与基因表达特征相结合,促进基因表征的学习。通过利用Transformer模型,我们进一步提取基因对的复杂依赖,这对于确定调控水平是至关重要的。在多个基准数据集上的对比实验证明了该算法在GRN推理任务中的有效性和竞争力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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