AutoGRN: An Automated Graph Neural Network Framework for Gene Regulatory Network Inference.
IEEE Journal of Biomedical and Health Informatics
|September 16, 2025
Summary
AutoGRN automatically designs optimal Graph Neural Network (GNN) architectures for gene regulatory network (GRN) inference from single-cell RNA sequencing data, improving accuracy on diverse datasets.
Area of Science:
- Computational Biology
- Bioinformatics
- Genomics
Background:
- Gene regulatory network (GRN) inference is crucial for understanding biological processes and diseases.
- Single-cell RNA sequencing (scRNA-seq) data is widely used for GRN inference but presents challenges like sparsity, noise, and heterogeneity.
- Existing Graph Neural Network (GNN) approaches struggle to generalize across diverse scRNA-seq datasets due to fixed architectures.
Purpose of the Study:
- To develop an automated framework, AutoGRN, for optimizing GNN architectures for GRN inference.
- To address the limitations of fixed GNN architectures in handling the complexities of scRNA-seq data.
- To enhance the accuracy and generalizability of GRN inference methods.
Main Methods:
- AutoGRN employs a genetic search algorithm, constrained by information entropy, to explore and identify optimal GNN architectures.
- The framework incorporates various components influencing GRN inference performance into its search space.
- The automated approach adapts GNN architectures to the specific characteristics of individual scRNA-seq datasets.
Main Results:
- AutoGRN demonstrates superior prediction accuracy compared to existing GRN inference methods.
- The proposed framework shows robust performance across multiple public scRNA-seq datasets.
- The automated architecture search effectively handles data sparsity, noise, and heterogeneity.
Conclusions:
- AutoGRN provides an effective and adaptable solution for gene regulatory network inference.
- The automated GNN architecture optimization significantly improves GRN inference accuracy and generalizability.
- This framework advances the analysis of gene interactions from complex single-cell expression data.
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