Evidence map›Paper›PMID 41716221›Full record

ArticleBioinformatics advances2026

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

Qianqian Wu, Xingmiao Dai, Shiyi Lou, Siyuan Wu, Tianhai Tian

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Article in Bioinformatics advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Qianqian WuSchool of Mathematics, Hefei University of Technology, Hefei, Anhui 230009, China.ORCID https://orcid.org/0000-0002-7450-9550
Xingmiao DaiSchool of Mathematics, Hefei University of Technology, Hefei, Anhui 230009, China.
Shiyi LouSchool of Mathematics, Hefei University of Technology, Hefei, Anhui 230009, China.
Siyuan WuComputational BioMedicine Lab, College of Science and Engineering, James Cook University, Townsville, QLD 4188, Australia.ORCID https://orcid.org/0000-0003-2871-5473
Tianhai TianSchool of Mathematics, Monash University, Melbourne, Wellington Road, Melbourne, VIC 3800, Australia.ORCID https://orcid.org/0000-0001-6191-0209

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: 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. Results: 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. Availability and implementation: Codes for DeepCE are free available in the GitHub https://github.com/sxiaodai/DeepCE.

Identifiers

PMID41716221
PMCPMC12916171

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.