Evidence map›Paper›PMID 41465085›Full record

ArticleGenes2025

iPro2L-Kresidual: A High-Performance Promoter Identification Model for Sequence Nonlinearity and Context Mining.

Yanjuan Li, Shicai Li, Guojun Sheng, Yu Chen

Abstract read
In one paragraph

Article in Genes, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Yanjuan LiCollege of Electrical and Information Engineering, Quzhou University, Quzhou 324000, China.
Shicai LiCollege of Computer and Control Engineering, Northeast Forestry University, Harbin 150040, China.
Guojun ShengCollege of Computer and Control Engineering, Northeast Forestry University, Harbin 150040, China.
Yu ChenCollege of Computer and Control Engineering, Northeast Forestry University, Harbin 150040, China.

Funding

National Natural Science Foundation of China 62372267National Natural Science Foundation of China 62572272Science and Technology Plan Project of Quzhou 2024K160
6 · The paper itself

Abstract

A promoter is an important non-coding DNA sequence, as it can regulate gene expression. Its abnormalities are closely associated with various diseases, such as coronary heart disease, diabetes, and tumors. Therefore, promoter identification is highly significant. Due to the insufficient nonlinear feature extraction and insufficient capture of sequence context relationships, existing single promoter identification models have a lower classification performance. To overcome these shortcomings, this paper proposed a new model called iPro2L-Kresidual. iPro2L-Kresidual integrated a residual structure with a KAN network to design a novel Kresidual module. The Kresidual module significantly enhanced the nonlinear expression capability of sequence features by using B-spline functions and residual networks. Additionally, to fully capture the sequence context relationship, iPro2L-Kresidual improved a Transformer encoder module by replacing the linear processing method with gated recurrent units, so then it can extract both local and global context features of a sequence. Furthermore, iPro2L-Kresidual designed a regularized label smoothing cross-entropy loss function to ensure training stability and prevent the model from becoming overly confident. Experimental results on 5-fold cross-validation showed that the accuracy of promoter identification and promoter strength identification, respectively, was 94.28% and 90.55%. Moreover, on an independent dataset, the prediction accuracy reached 93.13%, further demonstrating the model's strong generalization ability. This provides a novel and effective predictive model for promoter site prediction.

Indexed as

Computational BiologyData MiningPromoter Regions, GeneticSequence Analysis, DNASoftwareAlgorithmsHumansbioinformaticsdeep learningDNA promotersequence analysistwo-stage prediction

Identifiers

PMID41465085
PMCPMC12732873

What Socratic holds

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LicenceCC BY
Read underepoch 390

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.