Abstract
Gene regulatory network (GRN) inference from gene expression data is a significant approach to understanding aspects of the biological system. Compared with generalized correlation-based methods, causality-inspired ones seem more rational to infer regulatory relationships. We propose GRINCD, a novel GRN inference framework empowered by graph representation learning and causal asymmetric learning, considering both linear and non-linear regulatory relationships. First, high-quality representation of each gene is generated using graph neural network. Then, we apply the additive noise model to predict the causal regulation of each regulator-target pair. Additionally, we design two channels and finally assemble them for robust prediction. Through comprehensive comparisons of our framework with state-of-the-art methods based on different principles on numerous datasets of diverse types and scales, the experimental results show that our framework achieves superior or comparable performance under various evaluation metrics. Our work provides a new clue for constructing GRNs, and our proposed framework GRINCD also shows potential in identifying key factors affecting cancer development.