Evidence map›Paper›PMID 41000441›Full record

ArticleBioinformatics and biology insights2025

Understanding the Impact of Individual Nucleotide on Oxford Nanopore Current Signals With Interpretable Prediction Models.

Yenan Wang, Zhixing Wu, Jia Meng

Abstract read
In one paragraph

Article in Bioinformatics and biology insights, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

3 authors.

Yenan WangDepartment of Biosciences and Bioinformatics, Center for Intelligent RNA Therapeutics, Suzhou Key Laboratory of Cancer Biology and Chronic Disease, School of Science, Suzhou, China.
Zhixing WuDepartment of Biosciences and Bioinformatics, Center for Intelligent RNA Therapeutics, Suzhou Key Laboratory of Cancer Biology and Chronic Disease, School of Science, Suzhou, China.ORCID https://orcid.org/0009-0007-6479-8591
Jia MengDepartment of Biosciences and Bioinformatics, Center for Intelligent RNA Therapeutics, Suzhou Key Laboratory of Cancer Biology and Chronic Disease, School of Science, Suzhou, China.ORCID https://orcid.org/0000-0003-3455-205X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxford nanopore sequencing enabled real-time, long-read analysis of DNA by detecting ionic current signals associated with K-mer sequences. Although many studies analyzed sequence and modification detection, our understanding of how multiple nucleotides of the K-mer sequence determine nanopore signals together is still limited. In this study, we seek to unveil the positional impact of individual nucleotide through interpretable prediction models. Multiple machine learning models were trained and optimized. To increase model interpretability and explore underlying mechanisms, the tool of SHapley Additive exPlanations was applied to make an assessment of both nucleotides and positions. Our results show that previously unseen Oxford nanopore signals were accurately predicted, and results were consistent on two different modes (R

Indexed as

current signalDNAmachine learningOxford nanoporepredictionsequencing

Identifiers

PMID41000441
PMCPMC12457769

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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 OpenQuestion graph.