Evidence map›Paper›PMID 36155798›Full record

ArticleNucleic acids research2022

Geographic encoding of transcripts enabled high-accuracy and isoform-aware deep learning of RNA methylation.

Daiyun Huang, Kunqi Chen, Bowen Song, Zhen Wei, Jionglong Su, Frans Coenen, João Pedro de Magalhães, Daniel J Rigden, Jia Meng

Abstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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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

9 authors.

Daiyun HuangDepartment of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou 215123, PR China.ORCID 0000-0002-3067-7165
Kunqi ChenKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350004, PR China.ORCID 0000-0002-6025-8957
Bowen SongDepartment of Mathematical Sciences, Xi'an Jiaotong-Liverpool University, Suzhou 215123, PR China.ORCID 0000-0002-8586-0573
Zhen WeiDepartment of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou 215123, PR China.
Jionglong SuDepartment of Mathematical Sciences, Xi'an Jiaotong-Liverpool University, Suzhou 215123, PR China.
Frans CoenenDepartment of Computer Sciences, University of Liverpool, Liverpool L69 7ZB, UK.
João Pedro de MagalhãesInstitute of Life Course and Medical Sciences, University of Liverpool, Liverpool L69 7ZB, UK.ORCID 0000-0002-6363-2465
Daniel J RigdenInstitute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 7ZB, UK.
Jia MengDepartment of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou 215123, PR China.ORCID 0000-0003-3455-205X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the most pervasive epigenetic mark present on mRNA and lncRNA, N6-methyladenosine (m6A) RNA methylation regulates all stages of RNA life in various biological processes and disease mechanisms. Computational methods for deciphering RNA modification have achieved great success in recent years; nevertheless, their potential remains underexploited. One reason for this is that existing models usually consider only the sequence of transcripts, ignoring the various regions (or geography) of transcripts such as 3'UTR and intron, where the epigenetic mark forms and functions. Here, we developed three simple yet powerful encoding schemes for transcripts to capture the submolecular geographic information of RNA, which is largely independent from sequences. We show that m6A prediction models based on geographic information alone can achieve comparable performances to classic sequence-based methods. Importantly, geographic information substantially enhances the accuracy of sequence-based models, enables isoform- and tissue-specific prediction of m6A sites, and improves m6A signal detection from direct RNA sequencing data. The geographic encoding schemes we developed have exhibited strong interpretability, and are applicable to not only m6A but also N1-methyladenosine (m1A), and can serve as a general and effective complement to the widely used sequence encoding schemes in deep learning applications concerning RNA transcripts.

Indexed as

Deep LearningRNA, Long Noncoding3' Untranslated RegionsMethylationProtein IsoformsRNARNA, Messenger3' Untranslated RegionsProtein IsoformsRNARNA, Long NoncodingRNA, Messenger

Identifiers

PMID36155798
PMCPMC9561283

What Socratic holds

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Registered trials

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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.