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Gene Regulatory Network Inference Based on Convolutional GRU

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DOI: 10.23977/acss.2025.090111 | Downloads: 17 | Views: 513

Author(s)

Siying Du 1

Affiliation(s)

1 School of Information, Yunnan Normal University, Kunming, China

Corresponding Author

Siying Du

ABSTRACT

Time-course single-cell RNA sequencing (scRNA-seq) data reflect gene expression changes over time, offering a valuable resource for exploring dynamic gene interactions and building dynamic gene regulatory networks (GRNs). However, most existing methods are typically designed for bulk RNA sequencing (bulk RNA-seq) data and cannot be directly applied to time-course scRNA-seq data. Addressing this issue, we present CGGRN, an approach based on convolutional gated recurrent unit (GRU) for inferring GRNs. CGGRN transforms time-course data into images, including raw pairwise gene images and neighborhood images, and aggregates them with time point information into a four-dimensional tensor. The tensor is then fed into the convolutional GRU to capture features for each gene pair and reconstruct the GRN. We conducted trials on four time-course scRNA-seq datasets using CGGRN, and the outcomes show that CGGRN surpasses existing models in constructing GRN.

KEYWORDS

Convolutional GRU, Gene Regulatory Network, Deep Learning

CITE THIS PAPER

Siying Du, Gene Regulatory Network Inference Based on Convolutional GRU. Advances in Computer, Signals and Systems (2025) Vol. 9: 74-78. DOI: http://dx.doi.org/10.23977/acss.2025.090111.

REFERENCES

[1] L. F. Iglesias-Martinez, W. Kolch, and T. Santra, "BGRMI: A method for inferring gene regulatory networks from time-course gene expression data and its application in breast cancer research," Scientific Reports, vol. 6, no. 1, p. 37140, 2016. 
[2] X. Zhang, J. Zhao, J.-K. Hao, X.-M. Zhao, and L. Chen, "Conditional mutual inclusive information enables accurate quantification of associations in gene regulatory networks," Nucleic acids research, vol. 43, no. 5, pp. e31-e31, 2015.
[3] E. Shapiro, T. Biezuner, and S. Linnarsson, "Single-cell sequencing-based technologies will revolutionize whole-organism science," Nature Reviews Genetics, vol. 14, no. 9, pp. 618-630, 2013.
[4] O. Stegle, S. A. Teichmann, and J. C. Marioni, "Computational and analytical challenges in single-cell transcriptomics," Nature Reviews Genetics, vol. 16, no. 3, pp. 133-145, 2015.
[5] A. Zeisel et al., "Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq," Science, vol. 347, no. 6226, pp. 1138-1142, 2015.
[6] B. Treutlein et al., "Reconstructing lineage hierarchies of the distal lung epithelium using single-cell RNA-seq," Nature, vol. 509, no. 7500, pp. 371-375, 2014.
[7] S. Islam et al., "Quantitative single-cell RNA-seq with unique molecular identifiers," Nature methods, vol. 11, no. 2, pp. 163-166, 2014.
[8] A. Sebé-Pedrós et al., "Cnidarian cell type diversity and regulation revealed by whole-organism single-cell RNA-Seq," Cell, vol. 173, no. 6, pp. 1520-1534. e20, 2018.
[9] P. W. Hook et al., "Single-cell RNA-seq of mouse dopaminergic neurons informs candidate gene selection for sporadic Parkinson disease," The American Journal of Human Genetics, vol. 102, no. 3, pp. 427-446, 2018.
[10] S. Aibar et al., "SCENIC: single-cell regulatory network inference and clustering," Nature methods, vol. 14, no. 11, pp. 1083-1086, 2017.
[11] A. Karbalayghareh, U. Braga-Neto, and E. R. Dougherty, "Intrinsically Bayesian robust classifier for single-cell gene expression time series in gene regulatory networks," in Proceedings of the 8th ACM International Conference on Bioinformatics, Computational Biology, and Health Informatics, 2017, pp. 766-767.
[12] V. A. Huynh-Thu and P. Geurts, "dynGENIE3: dynamical GENIE3 for the inference of gene networks from time series expression data," Scientific reports, vol. 8, no. 1, p. 3384, 2018.
[13] Y. Yuan and Z. Bar-Joseph, "Deep learning of gene relationships from single cell time-course expression data," Briefings in bioinformatics, vol. 22, no. 5, p. bbab142, 2021. 
[14] Y. Xu, J. Chen, A. Lyu, W. K. Cheung, and L. Zhang, "dynDeepDRIM: a dynamic deep learning model to infer direct regulatory interactions using time-course single-cell gene expression data," Briefings in Bioinformatics, vol. 23, no. 6, p. bbac424, 2022.  
[15] S. Semrau, J. E. Goldmann, M. Soumillon, T. S. Mikkelsen, R. Jaenisch, and A. Van Oudenaarden, "Dynamics of lineage commitment revealed by single-cell transcriptomics of differentiating embryonic stem cells," Nature communications, vol. 8, no. 1, p. 1096, 2017.
[16] A. M. Klein et al., "Droplet barcoding for single-cell transcriptomics applied to embryonic stem cells," Cell, vol. 161, no. 5, pp. 1187-1201, 2015.  
[17] L.-F. Chu et al., "Single-cell RNA-seq reveals novel regulators of human embryonic stem cell differentiation to definitive endoderm," Genome biology, vol. 17, pp. 1-20, 2016.
[18] S. Petropoulos et al., "Single-cell RNA-seq reveals lineage and X chromosome dynamics in human preimplantation embryos," Cell, vol. 165, no. 4, pp. 1012-1026, 2016.

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