Evidence map›Paper›PMID 42209437›Full record

ArticleBioinformatics (Oxford, England)2026

MethyNano: supervised contrastive pretraining enables robust and generalizable methylation detection from nanopore sequencing.

Jiahui Yan, Yujie Chen, Yucong Gong, Cheng Zhang, Jing Yang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 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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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jiahui YanSchool of Control and Computer Engineering, North China Electric Power University, Beijing 102206, China.ORCID 0009-0008-4246-4977
Yujie ChenSchool of Control and Computer Engineering, North China Electric Power University, Beijing 102206, China.
Yucong GongSchool of Computer Science, Key Laboratory of High Confidence Software Technologies, Peking University, Beijing 100871, China.
Cheng ZhangSchool of Computer Science, Key Laboratory of High Confidence Software Technologies, Peking University, Beijing 100871, China.
Jing YangSchool of Control and Computer Engineering, North China Electric Power University, Beijing 102206, China.

Funding

National Key Research and Development Program of China 2023YFF1205600National Key Research and Development Program of China 2024YFF1206200National Natural Science Foundation of China 62273008National Natural Science Foundation of China 62472171National Natural Science Foundation of China T2525003
6 · The paper itself

Abstract

motivation5-Methylcytosine (5mC) plays an important role in gene regulation and development. Although nanopore sequencing has enabled direct detection of 5mC, existing methods still face several limitations, including poor generalization across species and sequence contexts (CpG/CHG/CHH), as well as suboptimal integration of sequence and current signals.

resultsHere, we present MethyNano, a deep learning framework incorporating a contrastive learning strategy to detect 5mC from nanopore reads. By encouraging more discriminative and stable representations, the contrastive objective improves the model's sensitivity to rare sequence contexts and reduces its prediction uncertainty in challenging regions. Across datasets from Arabidopsis thaliana, Oryza sativa, and Homo sapiens, our model achieves superior performance on key metrics compared with other existing methods. Extensive cross-species and cross-motif experiments demonstrate the robust generalization performance of MethyNano, while dimensionality-reduction visualizations of learned features provide an intuitive view of the model's efficient representation capability. Moreover, our ablation studies show that MethyNano's architecture enables more effective integration of critical features, leading to higher predictive accuracy. AVAILABILITY AND IMPLEMENTATION: The project code is available at https://github.com/baigeHUI/MethyNano and https://doi.org/10.5281/zenodo.19858400.

Indexed as

5-MethylcytosineDeep LearningDNA MethylationNanopore SequencingSequence Analysis, DNASoftwareArabidopsisHumansOryza5-Methylcytosine

Identifiers

PMID42209437
PMCPMC13296999

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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.