m6Acorr: an online tool for the correction and comparison of m6A methylation profiles

Abstract Background The analysis and comparison of RNA m6A methylation profiles have become increasingly important for understanding the post-transcriptional regulations of gene expression. However, current m6A profiles in public databases are not readily intercomparable, where heterogeneous profile...

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Main Authors: Jianwei Li, Yan Huang, Qinghua Cui, Yuan Zhou
Format: Article
Language:English
Published: BMC 2020-01-01
Series:BMC Bioinformatics
Online Access:https://doi.org/10.1186/s12859-020-3380-6
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spelling doaj-2e8b6ff650c04bbab79c3968bb795e652021-01-31T16:40:53ZengBMCBMC Bioinformatics1471-21052020-01-012111810.1186/s12859-020-3380-6m6Acorr: an online tool for the correction and comparison of m6A methylation profilesJianwei Li0Yan Huang1Qinghua Cui2Yuan Zhou3Institute of Computational Medicine, School of Artificial Intelligence, Hebei University of TechnologyInstitute of Computational Medicine, School of Artificial Intelligence, Hebei University of TechnologyDepartment of Biomedical Informatics, School of Basic Medical Sciences, Center for Noncoding RNA Medicine, Peking UniversityDepartment of Biomedical Informatics, School of Basic Medical Sciences, Center for Noncoding RNA Medicine, Peking UniversityAbstract Background The analysis and comparison of RNA m6A methylation profiles have become increasingly important for understanding the post-transcriptional regulations of gene expression. However, current m6A profiles in public databases are not readily intercomparable, where heterogeneous profiles from the same experimental report but different cell types showed unwanted high correlations. Results Several normalizing or correcting methods were tested to remove such laboratory bias. And m6Acorr, an effective pipeline for correcting m6A profiles, was presented on the basis of quantile normalization and empirical Bayes batch regression method. m6Acorr could efficiently correct laboratory bias in the simulated dataset and real m6A profiles in public databases. The preservation of biological signals was examined after correction, and m6Acorr was found to better preserve differential methylation signals, m6A regulated targets, and m6A-related biological features than alternative methods. Finally, the m6Acorr server was established. This server could eliminate the potential laboratory bias in m6A methylation profiles and perform profile–profile comparisons and functional analysis of hyper- (hypo-) methylated genes based on corrected methylation profiles. Conclusion m6Acorr was established to correct the existing laboratory bias in RNA m6A methylation profiles and perform profile comparisons on the corrected datasets. The m6Acorr server is available at http://www.rnanut.net/m6Acorr. A stand-alone version with the correction function is also available in GitHub at https://github.com/emersON106/m6Acorr.https://doi.org/10.1186/s12859-020-3380-6
collection DOAJ
language English
format Article
sources DOAJ
author Jianwei Li
Yan Huang
Qinghua Cui
Yuan Zhou
spellingShingle Jianwei Li
Yan Huang
Qinghua Cui
Yuan Zhou
m6Acorr: an online tool for the correction and comparison of m6A methylation profiles
BMC Bioinformatics
author_facet Jianwei Li
Yan Huang
Qinghua Cui
Yuan Zhou
author_sort Jianwei Li
title m6Acorr: an online tool for the correction and comparison of m6A methylation profiles
title_short m6Acorr: an online tool for the correction and comparison of m6A methylation profiles
title_full m6Acorr: an online tool for the correction and comparison of m6A methylation profiles
title_fullStr m6Acorr: an online tool for the correction and comparison of m6A methylation profiles
title_full_unstemmed m6Acorr: an online tool for the correction and comparison of m6A methylation profiles
title_sort m6acorr: an online tool for the correction and comparison of m6a methylation profiles
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2020-01-01
description Abstract Background The analysis and comparison of RNA m6A methylation profiles have become increasingly important for understanding the post-transcriptional regulations of gene expression. However, current m6A profiles in public databases are not readily intercomparable, where heterogeneous profiles from the same experimental report but different cell types showed unwanted high correlations. Results Several normalizing or correcting methods were tested to remove such laboratory bias. And m6Acorr, an effective pipeline for correcting m6A profiles, was presented on the basis of quantile normalization and empirical Bayes batch regression method. m6Acorr could efficiently correct laboratory bias in the simulated dataset and real m6A profiles in public databases. The preservation of biological signals was examined after correction, and m6Acorr was found to better preserve differential methylation signals, m6A regulated targets, and m6A-related biological features than alternative methods. Finally, the m6Acorr server was established. This server could eliminate the potential laboratory bias in m6A methylation profiles and perform profile–profile comparisons and functional analysis of hyper- (hypo-) methylated genes based on corrected methylation profiles. Conclusion m6Acorr was established to correct the existing laboratory bias in RNA m6A methylation profiles and perform profile comparisons on the corrected datasets. The m6Acorr server is available at http://www.rnanut.net/m6Acorr. A stand-alone version with the correction function is also available in GitHub at https://github.com/emersON106/m6Acorr.
url https://doi.org/10.1186/s12859-020-3380-6
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