Ψ-co-mAFiA: Concurrent detection of pseudouridine and m6A in single RNA molecules.

IF 5.4
Adrian Chan, Isabel S Naarmann-de Vries, Christoph Dieterich
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引用次数: 0

Abstract

>: The development of third-generation sequencing technologies enables the detection of RNA modifications at single-molecule resolution. Specifically for direct RNA sequencing (dRNA-Seq) on the ONT platform, we have previously developed an m6A detection algorithm called mAFiA. Here, we present the updated method, now covering all 18 DRACH m6A contexts as well as the identification of pseudouridine sites (Ψ). Our modification level predictions compare favorably with orthogonal methods and respond to knockdown or knock out of writer proteins. The simultaneous detection of multiple modifications on a single RNA molecule opens up the possibility to study cross-modification interactions.

Availability: Ψ-co-mAFiA is available at https://github.com/dieterich-lab/psi-co-mAFiA and licensed under GPLv3.0. An archived version of the software is available on Zenodo at https://doi.org/10.5281/zenodo.16797676.

Supplementary information: Supplementary data are available at Bioinformatics online.

Ψ-co-mAFiA:伪尿嘧啶和m6A在单个RNA分子中的同时检测。
b>:第三代测序技术的发展使单分子分辨率的RNA修饰检测成为可能。针对ONT平台上的直接RNA测序(RNA- seq),我们之前开发了一种名为mAFiA的m6A检测算法。在这里,我们提出了更新的方法,现在涵盖了所有18个DRACH m6A上下文以及假尿嘧啶位点的识别(Ψ)。我们的修饰水平预测与正交方法比较有利,并对写蛋白的敲低或敲出作出反应。同时检测单个RNA分子上的多种修饰为研究交叉修饰相互作用开辟了可能性。可用性:Ψ-co-mAFiA可从https://github.com/dieterich-lab/psi-co-mAFiA获得,并在GPLv3.0下获得许可。该软件的存档版本可在Zenodo上获得:https://doi.org/10.5281/zenodo.16797676.Supplementary information:补充数据可在Bioinformatics在线获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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