# DeepCE: a deep learning framework for correlation-enhanced gene regulatory network inference in single-cell RNA sequencing data

**Authors:** Qianqian Wu, Xingmiao Dai, Shiyi Lou, Siyuan Wu, Tianhai Tian

PMC · DOI: 10.1093/bioadv/vbag033 · Bioinformatics Advances · 2026-01-30

## TL;DR

DeepCE is a deep learning method that improves the accuracy of gene regulatory network inference from single-cell RNA sequencing data.

## Contribution

DeepCE introduces a novel framework combining bidirectional gated recurrent units and CNNs for enhanced GRN inference.

## Key findings

- DeepCE outperforms existing methods in GRN inference with higher AUROC and AUPR scores.
- The model effectively smooths noisy data and extracts time-lagged regulatory signals.
- Experiments on mouse and human datasets confirm its strong performance.

## Abstract

Single-cell RNA sequencing has substantially advanced our understanding of gene expression dynamics and cellular heterogeneity. In recent years, deep learning (DL) has emerged as a promising approach to infer genetic regulation. However, these methods still face challenges in representing complex regulatory mechanisms. Thus, it remains imperative to develop new algorithms to enhance both effectiveness and reliability.

We propose DeepCE, a DL framework for correlation-enhanced gene regulatory network (GRN) inference. DeepCE strengthens the extraction of dynamic regulation by integrating bidirectional gated recurrent units with convolutional neural networks (CNNs). Specifically, bidirectional gated recurrent units captures dynamic temporal dependencies, while CNNs focuses on local spatial patterns within single-cell data, enabling the model to uncover complex gene-gene interactions and generate high-quality GRNs. This framework improves the accuracy and robustness of GRN inference by smoothing noisy gene expression data, extracting time-lagged regulatory signals, and filtering out spurious correlations. Experiments conducted on mouse and human datasets demonstrate the strong performance of DeepCE. Performance evaluations show that DeepCE outperforms existing methods, achieving the highest AUROC and AUPR scores.

Codes for DeepCE are free available in the GitHub https://github.com/sxiaodai/DeepCE.

## Linked entities

- **Species:** Mus musculus (taxon 10090), Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** Mcm2 (minichromosome maintenance complex component 2) [NCBI Gene 17216] {aka BM28, CDCL1, Mcmd2, mKIAA0030}, Alg9 (ALG9 alpha-1,2-mannosyltransferase) [NCBI Gene 102580] {aka 8230402H15Rik, B430313H07Rik, Dibd1}, Cdc7 (cell division cycle 7) [NCBI Gene 12545] {aka Cdc7l1, muCdc7}, Jun (Jun proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 16476] {aka AP-1, Junc, c-jun}, Mycn (Mycn proto-oncogene, bHLH transcription factor) [NCBI Gene 18109] {aka N-myc, Nmyc, Nmyc-1, Nmyc1, bHLHe37, c-nmyc}, Mcm4 (minichromosome maintenance complex component 4) [NCBI Gene 17217] {aka 19G, Cdc21, Mcmd4, mKIAA4003, mcdc21}, Itpr3 (inositol 1,4,5-triphosphate receptor 3) [NCBI Gene 16440] {aka IP3R 3, IP3R-3, Ip3r3, Itpr-3, tf}, Cdk1 (cyclin dependent kinase 1) [NCBI Gene 12534] {aka Cdc2, Cdc2a, p34<CDC2>}
- **Diseases:** mHSC-E (MESH:D016751), L (MESH:D007926)
- **Chemicals:** DeepSEM (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** hESC — Gallus gallus (Chicken), Somatic stem cell (CVCL_JE75)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12916171/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916171/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916171/full.md

---
Source: https://tomesphere.com/paper/PMC12916171