Dogme: A nextflow pipeline for reprocessing nanopore RNA and DNA modifications.

Elnaz Abdollahzadeh, Ali Mortazavi
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Abstract

Motivation: The Oxford Nanopore Technologies (ONT) platform allows for the direct detection of RNA and DNA modifications from unamplified nucleic acids, which is a significant advantage over other platforms. However, the rapid updates to ONT basecalling models and the evolving landscape of computational tools for modification detection bring about challenges for reproducible and standardized analyses. To address these challenges, we developed Dogme, which is a Nextflowbased workflow that automates the processing of ONT data, including basecalling, alignment, modification detection, and transcript quantification. Dogme automates the reprocessing of ONT POD5 files by integrating basecalling using Dorado, read mapping using minimap2 and subsequent analysis steps such as running modkit. The pipeline supports three major types of ONT sequencing data - direct RNA (dRNA), complementary DNA (cDNA), and genomic DNA (gDNA) - enabling comprehensive analyses across different library preparations. Dogme facilitates detection of diverse RNA modifications supported by Dorado such as N6-methyladenosine (m6A), 5-methylcytosine (m5C), inosine, pseudouridine, 2'-Omethylation (Nm) and DNA methylation, while concurrently quantifying full-length transcript isoforms LR-Kallisto for transcript quantification for dRNA and cDNA.

Results: We applied Dogme to three separate mouse C2C12 myoblast replicates using direct RNA sequencing on MinION flow cells. We detected an average of 147,879 m6A, 86,673 m5C, 21,242 inosine, 24,540 pseudouridine, and 83,841 2'- O-methylation sites per replicate with 96,581 m6A, 43,446 m5C, 8,825 inosine, 10,048 pseudouridine, and 30,157 2'-O- methylation sites detected in all three biological replicates. The pipeline produced reproducible modification profiles and transcript expression levels across replicates, demonstrating its utility for integrative long-read transcriptomic and epigenomic analyses.

Availability: Dogme is implemented in Nextflow and is freely available under the MIT license at https://github.com/mortazavilab/dogme , with documentation provided for installation and usage.

道格姆:纳米孔RNA和DNA修饰再处理的下一个流程。
动机:牛津纳米孔技术(ONT)平台允许从未扩增的核酸中直接检测RNA和DNA修饰,这是其他平台的显著优势。然而,ONT基调用模型的快速更新和用于修饰检测的计算工具的不断发展,为可重复性和标准化分析带来了挑战。为了应对这些挑战,我们开发了Dogme,这是一个基于nextflow的工作流程,可以自动处理ONT数据,包括基调用、比对、修改检测和转录本量化。Dogme通过集成使用Dorado的基础调用、使用minimap2的读取映射以及随后的分析步骤(如运行modkit),实现了ONT POD5文件的自动再处理。该管道支持三种主要类型的ONT测序数据-直接RNA (dRNA),互补DNA (cDNA)和基因组DNA (gDNA) -能够跨不同文库制备进行全面分析。Dogme可以检测Dorado支持的多种RNA修饰,如n6 -甲基腺苷(m6A)、5-甲基胞嘧啶(m5C)、肌苷、假尿嘧啶、2'-甲基化(Nm)和DNA甲基化,同时定量全长转录异构体LR-Kallisto,用于定量dRNA和cDNA的转录物。结果:我们将Dogme应用于3个独立的小鼠C2C12成肌细胞复制,对MinION流细胞进行直接RNA测序。每个重复平均检测到147,879个m6A、86,673个m5C、21,242个肌苷、24,540个假尿苷和83,841个2'- o -甲基化位点,其中在所有三个生物重复中检测到96,581个m6A、43,446个m5C、8,825个肌苷、10,048个假尿苷和30,157个2'- o -甲基化位点。该管道产生了可重复的修饰谱和转录物表达水平,证明了其在综合长读转录组学和表观基因组学分析中的实用性。可用性:Dogme在Nextflow中实现,在MIT许可下可在https://github.com/mortazavilab/dogme免费获得,并提供安装和使用文档。
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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