Evidence map›Paper›PMID 41469552›Full record

ArticleBMC bioinformatics2025

DCPR: a deep learning framework for circadian phase reconstruction.

Xiao Han, Xiaochen Cen, Zhijin Li, Xiaobo Zhou, Zhiwei Ji

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Xiao HanCollege of Artificial Intelligence, Nanjing Agricultural University, No. 666 Binjiang Avenue, Nanjing, 211800, Jiangsu, China.
Xiaochen CenCollege of Artificial Intelligence, Nanjing Agricultural University, No. 666 Binjiang Avenue, Nanjing, 211800, Jiangsu, China.
Zhijin LiDepartment of Neurosurgery, Division of Life Science and Medicine, The First Affiliated Hospital of USTC (Anhui Provincial Hospital), University of Science and Technology of China, Hefei, 230036, Anhui, China.
Xiaobo ZhouSchool of Biomedical Informatics, The University of Texas Health Science Center at Houston, 7000 Fannin Street, Houston, TX, 77030, USA.
Zhiwei JiCollege of Artificial Intelligence, Nanjing Agricultural University, No. 666 Binjiang Avenue, Nanjing, 211800, Jiangsu, China. Zhiwei.Ji@njau.edu.cn.

Funding

Agricultural Science and Technology Innovation Foundation of Jiangsu Province CX (23) 3125
6 · The paper itself

Abstract

backgroundThe circadian clock is an evolutionarily conserved system that orchestrates 24-h physiological rhythms through transcriptional and translational feedback loops. Mounting evidence suggests a bidirectional relationship between circadian rhythm alteration and disease progression, positioning the circadian clock as a potential therapeutic target. Due to the scarcity of high-resolution temporal omics data, it remains very challenging to elucidate the underlying regulatory mechanisms of the circadian system. As a practical alternative, public untimed transcriptomic datasets offer the potential to infer gene expression oscillations retrospectively. However, existing computational approaches for circadian phase estimation often suffer from limited predictive accuracy, reducing their ability to reliably reconstruct rhythmic gene expression patterns.

resultsTo overcome these limitations, we develop DCPR, an unsupervised deep learning framework designed to accurately reconstruct the circadian phase from untimed transcriptomic data. Through comprehensive analyses of both simulated and real data, DCPR consistently overperforms existing methods in circadian phase estimation. Additional validations using knowledgebase mining and ex vivo experimental data further support DCPR's efficacy in reconstructing the oscillatory pattern of gene expression and detecting circadian variation.

conclusionsOur study demonstrates that DCPR is a highly versatile tool for systematically identifying transcriptional rhythms from untimed expression data. This tool will facilitate therapeutics discovery for circadian-related behavioral and pathological disorders.

Indexed as

Circadian ClocksCircadian RhythmComputational BiologyDeep LearningAnimalsGene Expression ProfilingHumansTranscriptomeAlzheimer’s diseaseCircadian rhythmCircadian variationGene expressionPhase reconstruction

Identifiers

PMID41469552
PMCPMC12866578

What Socratic holds

Textmetadata
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Registered trials

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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 Socratic graph.