Systematic comparison of tools used for m6A mapping from nanopore direct RNA sequencing

Direct RNA sequencing using nanopore platform can be used to detect N6-methyladenosine (m6A) modifications on mRNAs. Here the authors systematically compare tools used for m6A detection from nanopore direct sequencing.

Bibliographic Details
Main Authors: Zhen-Dong Zhong, Ying-Yuan Xie, Hong-Xuan Chen, Ye-Lin Lan, Xue-Hong Liu, Jing-Yun Ji, Fu Wu, Lingmei Jin, Jiekai Chen, Daniel W. Mak, Zhang Zhang, Guan-Zheng Luo
Format: Article
Language:English
Published: Nature Portfolio 2023-04-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-023-37596-5
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author Zhen-Dong Zhong
Ying-Yuan Xie
Hong-Xuan Chen
Ye-Lin Lan
Xue-Hong Liu
Jing-Yun Ji
Fu Wu
Lingmei Jin
Jiekai Chen
Daniel W. Mak
Zhang Zhang
Guan-Zheng Luo
author_facet Zhen-Dong Zhong
Ying-Yuan Xie
Hong-Xuan Chen
Ye-Lin Lan
Xue-Hong Liu
Jing-Yun Ji
Fu Wu
Lingmei Jin
Jiekai Chen
Daniel W. Mak
Zhang Zhang
Guan-Zheng Luo
author_sort Zhen-Dong Zhong
collection DOAJ
description Direct RNA sequencing using nanopore platform can be used to detect N6-methyladenosine (m6A) modifications on mRNAs. Here the authors systematically compare tools used for m6A detection from nanopore direct sequencing.
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spelling doaj.art-da7983b5010a43419a87347461c7e37b2023-04-09T11:20:28ZengNature PortfolioNature Communications2041-17232023-04-0114111410.1038/s41467-023-37596-5Systematic comparison of tools used for m6A mapping from nanopore direct RNA sequencingZhen-Dong Zhong0Ying-Yuan Xie1Hong-Xuan Chen2Ye-Lin Lan3Xue-Hong Liu4Jing-Yun Ji5Fu Wu6Lingmei Jin7Jiekai Chen8Daniel W. Mak9Zhang Zhang10Guan-Zheng Luo11MOE Key Laboratory of Gene Function and Regulation, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen UniversityMOE Key Laboratory of Gene Function and Regulation, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen UniversityMOE Key Laboratory of Gene Function and Regulation, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen UniversityMOE Key Laboratory of Gene Function and Regulation, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen UniversityMOE Key Laboratory of Gene Function and Regulation, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen UniversityMOE Key Laboratory of Gene Function and Regulation, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen UniversityMOE Key Laboratory of Gene Function and Regulation, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen UniversityCAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of SciencesCAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of SciencesSchool of Biomedical Sciences, LKS Faculty of Medicine, The University of Hong KongMOE Key Laboratory of Gene Function and Regulation, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen UniversityMOE Key Laboratory of Gene Function and Regulation, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen UniversityDirect RNA sequencing using nanopore platform can be used to detect N6-methyladenosine (m6A) modifications on mRNAs. Here the authors systematically compare tools used for m6A detection from nanopore direct sequencing.https://doi.org/10.1038/s41467-023-37596-5
spellingShingle Zhen-Dong Zhong
Ying-Yuan Xie
Hong-Xuan Chen
Ye-Lin Lan
Xue-Hong Liu
Jing-Yun Ji
Fu Wu
Lingmei Jin
Jiekai Chen
Daniel W. Mak
Zhang Zhang
Guan-Zheng Luo
Systematic comparison of tools used for m6A mapping from nanopore direct RNA sequencing
Nature Communications
title Systematic comparison of tools used for m6A mapping from nanopore direct RNA sequencing
title_full Systematic comparison of tools used for m6A mapping from nanopore direct RNA sequencing
title_fullStr Systematic comparison of tools used for m6A mapping from nanopore direct RNA sequencing
title_full_unstemmed Systematic comparison of tools used for m6A mapping from nanopore direct RNA sequencing
title_short Systematic comparison of tools used for m6A mapping from nanopore direct RNA sequencing
title_sort systematic comparison of tools used for m6a mapping from nanopore direct rna sequencing
url https://doi.org/10.1038/s41467-023-37596-5
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