GAEDGRN: reconstruction of gene regulatory networks based on gravity-inspired graph autoencoders

Reconstructing high-resolution gene regulatory networks (GRNs) based on single-cell RNA sequencing data provides an opportunity to gain insight into disease pathogenesis. At present, there are a large number of GRN reconstruction methods based on graph neural networks, and they can obtain excellent performance in GRN inference by extracting network structure features. However, most of these methods fail to fully exploit the directional characteristics or even ignore them when extracting network structural features. To this end, a novel framework called GAEDGRN is proposed based on gravity-inspired graph autoencoder (GIGAE) to infer potential causal relationships between genes. Among them, GIGAE can help us capture the complex directed network topology in GRN. Additionally, due to the uneven distribution of the latent vectors generated by the graph autoencoder, a random walk-based method is used to regularize the latent vectors learnt by the encoder. Furthermore, considering that some genes in GRN usually have a significant impact on biological functions, GAEDGRN designs a gene importance score calculation method and pays attention to genes with high importance in the process of GRN reconstruction. Experimental results on seven cell types of three GRN types show that GAEDGRN achieves high accuracy and strong robustness. Moreover, a case study on human embryonic stem cells demonstrates that GAEDGRN can help identify important genes.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2025-05-01
DOI
https://doi.org/10.1093/bib/bbaf232
Citations
2
Primary Topic
Gene Regulatory Network Analysis
Type
article
Field-Weighted Citation Impact
1.61

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article

GAEDGRN: reconstruction of gene regulatory networks based on gravity-inspired graph autoencoders

Hyeonku Jin, Zhen Gao, Yansen Su, Pi-Jing Wei et al.
2 citations
Briefings in Bioinformatics
Gene Regulatory Network Analysis
1.61
article

GAEDGRN: reconstruction of gene regulatory networks based on gravity-inspired graph autoencoders

Hyeonku Jin, Zhen Gao, Yansen Su, Pi-Jing Wei, Zheng Chun-Hou
article en
2 citations

Abstract

Reconstructing high-resolution gene regulatory networks (GRNs) based on single-cell RNA sequencing data provides an opportunity to gain insight into disease pathogenesis. At present, there are a large number of GRN reconstruction methods based on graph neural networks, and they can obtain excellent performance in GRN inference by extracting network structure features. However, most of these methods fail to fully exploit the directional characteristics or even ignore them when extracting network structural features. To this end, a novel framework called GAEDGRN is proposed based on gravity-inspired graph autoencoder (GIGAE) to infer potential causal relationships between genes. Among them, GIGAE can help us capture the complex directed network topology in GRN. Additionally, due to the uneven distribution of the latent vectors generated by the graph autoencoder, a random walk-based method is used to regularize the latent vectors learnt by the encoder. Furthermore, considering that some genes in GRN usually have a significant impact on biological functions, GAEDGRN designs a gene importance score calculation method and pays attention to genes with high importance in the process of GRN reconstruction. Experimental results on seven cell types of three GRN types show that GAEDGRN achieves high accuracy and strong robustness. Moreover, a case study on human embryonic stem cells demonstrates that GAEDGRN can help identify important genes.

Briefings in BioinformaticsVol. 26(3)
Anhui University (CN)
National Natural Science Foundation of China, Anhui University, National Key Research and Development Program of China
Openalex Percentile: Top 17%
Gene Regulatory Network Analysis
1.61
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GAEDGRN: reconstruction of gene regulatory networks based on gravity-inspired graph autoencoders — Hyeonku Jin, Zhen Gao, et al. · Briefings in Bioinformatics (2025) | TGRS Research Map | TGRS