Tsz Pan Tong, Aoran Wang, George Panagopoulos, Jun Pang
Gene regulation is central to understanding cellular processes and development, potentially leading to the discovery of new treatments for diseases and personalized medicine. Inferring gene regulatory networks (GRNs) from single-cell RNA sequencing (scRNA-seq) data presents significant challenges due to its high dimensionality and complexity. Existing tree-based models, such as GENIE3 and GRNBOOST2, demonstrated scalability and explainability in GRN inference, but they cannot distinguish regulation types nor effectively capture continuous cellular dynamics. In this paper, we introduce scKAN, a novel model that employs a Kolmogorov-Arnold network (KAN) with explainable AI to infer GRNs from scRNA-seq data. By modeling gene expression as differentiable functions matching the smooth nature of cellular dynamics, scKAN can accurately and precisely detect activation and inhibition regulations through explainable AI and geometric tools. We conducted extensive experiments on the BEELINE benchmark, and scKAN surpasses and improves the leading signed GRN inference models ranging from 5.40\% to 28.37\% in AUROC and from 1.97\% to 40.45\% in AUPRC. These results highlight the potential of scKAN in capturing the underlying biological processes in gene regulation without prior knowledge of the graph structure.
Quantitative mode stability for the wave equation on the Kerr-Newman spacetime
Risk-Aware Objective-Based Forecasting in Inertia Management
Chainalysis: Geography of Cryptocurrency 2023
Periodicity in Cryptocurrency Volatility and Liquidity
Impact of Geometric Uncertainty on the Computation of Abdominal Aortic Aneurysm Wall Strain
Simulation-based Bayesian inference with ameliorative learned summary statistics -- Part I