Evidence map›Paper›PMID 41535294›Full record

ArticleNature communications2026

Comprehensive mapping of RNA modification dynamics and crosstalk via deep learning and nanopore direct RNA-sequencing.

Han Dong, Yongsheng Gao, Zhengyi Cai, Yi Li, Xing Li, Fangqing Zhao, Jinyang Zhang

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
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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

7 authors.

Han DongState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Yongsheng GaoState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Zhengyi CaiState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Yi LiState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Xing LiState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China. li@ioz.ac.cn.ORCID http://orcid.org/0000-0003-3149-9783
Fangqing ZhaoState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China. zhfq@ioz.ac.cn.ORCID http://orcid.org/0000-0002-6216-1235
Jinyang ZhangState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China. zhangjinyang@ioz.ac.cn.ORCID http://orcid.org/0000-0002-5163-894X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the extensive studies of individual RNA modifications, the lack of methods to detect multiple modification types simultaneously has left the global epitranscriptomic landscape and its underlying crosstalk largely unexplored. Here, we present ORCA (Omni-RNA modification Characterization and Annotation), a deep learning framework that enables comprehensive mapping of RNA modification landscape using nanopore direct RNA sequencing. ORCA employs domain adversarial learning to detect and quantify a wide range of modifications by leveraging mixed stoichiometry-driven signal and sequence variability between modified and unmodified nucleotides. It also incorporates a transfer learning module for accurate annotation of modification types with minimal prior knowledge. Applying ORCA to multiple human cell lines reveals widespread, isoform-specific modification patterns, as well as intricate cooperative and competitive interactions among neighboring modification sites. This approach substantially expands the repertoire of known RNA modification sites and elucidates their spatial organization, revealing the emerging roles of RNA modifications in splicing regulation. ORCA thus provides an unbiased and generalizable framework for decoding RNA modification dynamics and their regulatory complexity across diverse biological contexts.

Indexed as

Deep LearningNanopore SequencingRNARNA Processing, Post-TranscriptionalSequence Analysis, RNAEpitranscriptomeEpitranscriptomicsHumansRNA

Identifiers

PMID41535294
PMCPMC12913617

What OpenQuestion holds

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Registered trials

None linked

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.