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.
Authors
- Hua Jin (ORCID: https://orcid.org/0000-0001-9829-0306)
- Liqun Yu
- Changhai Qi
- Yuening Yang
- Li Mo
- Wei Song
Institutions
- Beijing Institute of Technology (CN)
- Laboratory of Molecular Genetics (PL)
- Aerospace Center Hospital (CN)
- Tsinghua University (CN)
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
Funders
- Beijing Institute of Technology
- Natural Science Foundation of Shandong Province
- Fundamental Research Funds for the Central Universities