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DirectRMDB: a database of post-transcriptional RNA modifications unveiled from direct RNA sequencing technology
With advanced technologies to map RNA modifications, our understanding of them has been revolutionized, and they are seen to be far more widespread and important than previously thought. Current next-generation sequencing (NGS)-based modification profiling methods are blind to RNA modifications and...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825532/ https://www.ncbi.nlm.nih.gov/pubmed/36382409 http://dx.doi.org/10.1093/nar/gkac1061 |
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author | Zhang, Yuxin Jiang, Jie Ma, Jiongming Wei, Zhen Wang, Yue Song, Bowen Meng, Jia Jia, Guifang de Magalhães, João Pedro Rigden, Daniel J Hang, Daiyun Chen, Kunqi |
author_facet | Zhang, Yuxin Jiang, Jie Ma, Jiongming Wei, Zhen Wang, Yue Song, Bowen Meng, Jia Jia, Guifang de Magalhães, João Pedro Rigden, Daniel J Hang, Daiyun Chen, Kunqi |
author_sort | Zhang, Yuxin |
collection | PubMed |
description | With advanced technologies to map RNA modifications, our understanding of them has been revolutionized, and they are seen to be far more widespread and important than previously thought. Current next-generation sequencing (NGS)-based modification profiling methods are blind to RNA modifications and thus require selective chemical treatment or antibody immunoprecipitation methods for particular modification types. They also face the problem of short read length, isoform ambiguities, biases and artifacts. Direct RNA sequencing (DRS) technologies, commercialized by Oxford Nanopore Technologies (ONT), enable the direct interrogation of any given modification present in individual transcripts and promise to address the limitations of previous NGS-based methods. Here, we present the first ONT-based database of quantitative RNA modification profiles, DirectRMDB, which includes 16 types of modification and a total of 904,712 modification sites in 25 species identified from 39 independent studies. In addition to standard functions adopted by existing databases, such as gene annotations and post-transcriptional association analysis, we provide a fresh view of RNA modifications, which enables exploration of the epitranscriptome in an isoform-specific manner. The DirectRMDB database is freely available at: http://www.rnamd.org/directRMDB/. |
format | Online Article Text |
id | pubmed-9825532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98255322023-01-10 DirectRMDB: a database of post-transcriptional RNA modifications unveiled from direct RNA sequencing technology Zhang, Yuxin Jiang, Jie Ma, Jiongming Wei, Zhen Wang, Yue Song, Bowen Meng, Jia Jia, Guifang de Magalhães, João Pedro Rigden, Daniel J Hang, Daiyun Chen, Kunqi Nucleic Acids Res Database Issue With advanced technologies to map RNA modifications, our understanding of them has been revolutionized, and they are seen to be far more widespread and important than previously thought. Current next-generation sequencing (NGS)-based modification profiling methods are blind to RNA modifications and thus require selective chemical treatment or antibody immunoprecipitation methods for particular modification types. They also face the problem of short read length, isoform ambiguities, biases and artifacts. Direct RNA sequencing (DRS) technologies, commercialized by Oxford Nanopore Technologies (ONT), enable the direct interrogation of any given modification present in individual transcripts and promise to address the limitations of previous NGS-based methods. Here, we present the first ONT-based database of quantitative RNA modification profiles, DirectRMDB, which includes 16 types of modification and a total of 904,712 modification sites in 25 species identified from 39 independent studies. In addition to standard functions adopted by existing databases, such as gene annotations and post-transcriptional association analysis, we provide a fresh view of RNA modifications, which enables exploration of the epitranscriptome in an isoform-specific manner. The DirectRMDB database is freely available at: http://www.rnamd.org/directRMDB/. Oxford University Press 2022-11-16 /pmc/articles/PMC9825532/ /pubmed/36382409 http://dx.doi.org/10.1093/nar/gkac1061 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Database Issue Zhang, Yuxin Jiang, Jie Ma, Jiongming Wei, Zhen Wang, Yue Song, Bowen Meng, Jia Jia, Guifang de Magalhães, João Pedro Rigden, Daniel J Hang, Daiyun Chen, Kunqi DirectRMDB: a database of post-transcriptional RNA modifications unveiled from direct RNA sequencing technology |
title | DirectRMDB: a database of post-transcriptional RNA modifications unveiled from direct RNA sequencing technology |
title_full | DirectRMDB: a database of post-transcriptional RNA modifications unveiled from direct RNA sequencing technology |
title_fullStr | DirectRMDB: a database of post-transcriptional RNA modifications unveiled from direct RNA sequencing technology |
title_full_unstemmed | DirectRMDB: a database of post-transcriptional RNA modifications unveiled from direct RNA sequencing technology |
title_short | DirectRMDB: a database of post-transcriptional RNA modifications unveiled from direct RNA sequencing technology |
title_sort | directrmdb: a database of post-transcriptional rna modifications unveiled from direct rna sequencing technology |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825532/ https://www.ncbi.nlm.nih.gov/pubmed/36382409 http://dx.doi.org/10.1093/nar/gkac1061 |
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