Multicellular, IVT-derived, unmodified human transcriptome for nanopore-direct RNA analysis.

GigaByte (Hong Kong, China) Pub Date : 2024-06-17 eCollection Date: 2024-01-01 DOI:10.46471/gigabyte.129
Caroline A McCormick, Stuart Akeson, Sepideh Tavakoli, Dylan Bloch, Isabel N Klink, Miten Jain, Sara H Rouhanifard
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引用次数: 0

Abstract

Nanopore direct RNA sequencing (DRS) enables measurements of RNA modifications. Modification-free transcripts are a practical and targeted control for DRS, providing a baseline measurement for canonical nucleotides within a matched and biologically-derived sequence context. However, these controls can be challenging to generate and carry nanopore-specific nuances that can impact analyses. We produced DRS datasets using modification-free transcripts from in vitro transcription of cDNA from six immortalized human cell lines. We characterized variation across cell lines and demonstrated how these may be interpreted. These data will serve as a versatile control and resource to the community for RNA modification analyses of human transcripts.

用于纳米孔直接 RNA 分析的多细胞、IVT 衍生、未修饰的人类转录组。
纳米孔直接 RNA 测序(DRS)可以测量 RNA 的修饰。不含修饰的转录本是 DRS 的一种实用且有针对性的对照,可在匹配的生物序列上下文中提供标准核苷酸的基线测量。然而,这些对照组的生成可能具有挑战性,而且纳米孔特有的细微差别会影响分析结果。我们使用从六个永生化人类细胞系体外转录 cDNA 的无修饰转录本制作了 DRS 数据集。我们描述了不同细胞系之间的差异,并演示了如何解释这些差异。这些数据将作为通用对照和资源提供给社区,用于人类转录本的 RNA 修饰分析。
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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来源期刊
CiteScore
2.60
自引率
0.00%
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审稿时长
5 weeks
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