ModiDeC: a multi-RNA modification classifier for direct nanopore sequencing

RNA modifications play a crucial role in various cellular functions. Here, we present ModiDeC, a deep-learning-based classifier able to identify and distinguish multiple RNA modifications (N6-methyladenosine, inosine, pseudouridine, 2'-O-methylguanosine, and N1-methyladenosine) using direct RNA sequencing. Alongside ModiDeC, we provide an extensive database of in vitro-transcribed and synthetic sequences generated with both the new RNA004 chemistry and the old RNA002 kit. We show that RNA modifications can be accurately recognized and distinguished across different sequence motifs using synthetic data as well as in HEK293T cells and human blood samples. ModiDeC comes with a graphical user interface and an Epi2ME pipeline that allows easy customization and adaptation to specific research questions, such as learning and classifying additional RNA modifications and further sequence motifs. The reproducibility across samples, together with the low rate of false positives, underscores the potential of ModiDeC as a powerful tool for advancing the analysis of the epitranscriptome and RNA modification.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-07-19
DOI
https://doi.org/10.1093/nar/gkaf673
Citations
9
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
7.25

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article

ModiDeC: a multi-RNA modification classifier for direct nanopore sequencing

Mark Helm, Marko Jörg, Susanne Gerber, Stefan Mündnich et al.
9 citations
Nucleic Acids Research
RNA modifications and cancer
7.25
article

ModiDeC: a multi-RNA modification classifier for direct nanopore sequencing

Mark Helm, Marko Jörg, Susanne Gerber, Stefan Mündnich, Kristina Friedland, Anna Wierczeiko, Tamer Butto, Stefan Pastore, Nicolò Alagna, Johannes Friedrich, Johannes Miedema, Lioba Lehmann, L Walz
article en
9 citations

Abstract

RNA modifications play a crucial role in various cellular functions. Here, we present ModiDeC, a deep-learning-based classifier able to identify and distinguish multiple RNA modifications (N6-methyladenosine, inosine, pseudouridine, 2'-O-methylguanosine, and N1-methyladenosine) using direct RNA sequencing. Alongside ModiDeC, we provide an extensive database of in vitro-transcribed and synthetic sequences generated with both the new RNA004 chemistry and the old RNA002 kit. We show that RNA modifications can be accurately recognized and distinguished across different sequence motifs using synthetic data as well as in HEK293T cells and human blood samples. ModiDeC comes with a graphical user interface and an Epi2ME pipeline that allows easy customization and adaptation to specific research questions, such as learning and classifying additional RNA modifications and further sequence motifs. The reproducibility across samples, together with the low rate of false positives, underscores the potential of ModiDeC as a powerful tool for advancing the analysis of the epitranscriptome and RNA modification.

Nucleic Acids ResearchVol. 53(14)
Johannes Gutenberg University Mainz (DE), University Medical Center of the Johannes Gutenberg University Mainz (DE), Quantitative BioSciences (US)
Deutsche Forschungsgemeinschaft, Johannes Gutenberg-Universität Mainz, Boehringer Ingelheim Stiftung
Openalex Percentile: Top 2%
RNA modifications and cancer
7.25
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