Nanopore-m6A-finder, a novel m6A site caller for Nanopore DRS data

Introduction: A detection methods based on second-generation sequencing, Nanopore direct RNA sequencing (DRS) offers the unique advantage of capturing native modifications. Methods: A prediction computational framework that employs the XGBoost model in the mRNA exonic region and a hard-voting ensemble of XGBoost and random forest models in the poly(A) region. Results and discussion: A site annotation in GLORI v2.0, demonstrating the good performance of our method in the region possessing a stretch of continuous A-sequences. Moreover, our method predicted that m6A might exist in the human HEK293 poly(A) region, suggesting a possibly conserved phenomenon of a modified poly(A) tail beyond the previously reported T. brucei variant surface glycoprotein (VSG) transcripts. Together, these results established NP-mFinder as a robust and versatile tool for transcriptome-wide m6A profiling with DRS data at single-read resolution.

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Publication Details

Journal
Frontiers in Genetics
Published
2026-04-21
DOI
https://doi.org/10.3389/fgene.2026.1770769
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.00

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article

Nanopore-m6A-finder, a novel m6A site caller for Nanopore DRS data

Hua Jin, Liqun Yu, Changhai Qi, Yuening Yang et al.
Frontiers in Genetics
RNA modifications and cancer
article

Nanopore-m6A-finder, a novel m6A site caller for Nanopore DRS data

Hua Jin, Liqun Yu, Changhai Qi, Yuening Yang, Li Mo, Wei Song
article en

Abstract

Introduction: A detection methods based on second-generation sequencing, Nanopore direct RNA sequencing (DRS) offers the unique advantage of capturing native modifications. Methods: A prediction computational framework that employs the XGBoost model in the mRNA exonic region and a hard-voting ensemble of XGBoost and random forest models in the poly(A) region. Results and discussion: A site annotation in GLORI v2.0, demonstrating the good performance of our method in the region possessing a stretch of continuous A-sequences. Moreover, our method predicted that m6A might exist in the human HEK293 poly(A) region, suggesting a possibly conserved phenomenon of a modified poly(A) tail beyond the previously reported T. brucei variant surface glycoprotein (VSG) transcripts. Together, these results established NP-mFinder as a robust and versatile tool for transcriptome-wide m6A profiling with DRS data at single-read resolution.

Frontiers in GeneticsVol. 17
Beijing Institute of Technology (CN), Laboratory of Molecular Genetics (PL), Aerospace Center Hospital (CN), Tsinghua University (CN)
Beijing Institute of Technology, Natural Science Foundation of Shandong Province, Fundamental Research Funds for the Central Universities
Life in Land
Openalex Percentile: Top 20%
RNA modifications and cancer
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