Evidence map›Paper›PMID 41663212›Full record

ReviewRNA biology2026

Advanced deep learning strategies in nanopore RNA sequencing.

Crystal Ling, Benjamin Lebeau, Kwoh Chee Keong, Melissa Fullwood

Abstract readReview
In one paragraph

Review in RNA biology, 2026. 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

4 authors.

Crystal LingSchool of Biological Sciences, Nanyang Technological University, Singapore.ORCID 0000-0002-3487-8036
Benjamin LebeauSchool of Biological Sciences, Nanyang Technological University, Singapore.ORCID 0000-0003-1218-2983
Kwoh Chee KeongCollege of Computing and Data Science, Nanyang Technological University, Singapore.
Melissa FullwoodSchool of Biological Sciences, Nanyang Technological University, Singapore.ORCID 0000-0003-0321-7865

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epitranscriptome comprises chemical modifications found on RNA molecules that play essential roles in co- and post-transcriptional gene regulation. Dysregulation of these modifications has been implicated in various diseases, fuelling interest in evaluating them as emerging biomarkers and therapeutic targets. Nanopore direct RNA sequencing provides a powerful platform for profiling diverse RNA modifications at single-molecule resolution, but the complexity of the signals requires advanced computational approaches for interpretation. Artificial intelligence, particularly deep learning (DL), has become central to this effort. While classical DL architectures such as convolutional and recurrent neural networks have been widely applied, more recent approaches employ specialized learning frameworks and ensemble strategies to address challenges of data scarcity, noise, and biological variability while providing higher resolution output. In this review, we summarize these developments and highlight future multidisciplinary opportunities at the intersection of artificial intelligence and biology for characterizing the epitranscriptome obtained with direct RNA nanopore sequencing.

Indexed as

Deep LearningNanopore SequencingSequence Analysis, RNAComputational BiologyEpitranscriptomeEpitranscriptomicsHumansDeep learningdirect RNA sequencingepitranscriptomenanopore sequencingRNA modifications

Identifiers

PMID41663212
PMCPMC12915787

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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 Socratic graph.