McCormick Caroline A, Akeson Stuart, Tavakoli Sepideh, Bloch Dylan, Klink Isabel N, Jain Miten, Rouhanifard Sara H
Department of Bioengineering, Northeastern University, Boston, MA, 02115, United States.
Department of Physics, Northeastern University, Boston, MA, 02115, United States.
bioRxiv. 2024 May 28:2023.04.06.535889. doi: 10.1101/2023.04.06.535889.
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 analysis. We produced DRS datasets using modification-free transcripts from transcription (IVT) 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 analysis of human transcripts.
纳米孔直接RNA测序(DRS)能够对RNA修饰进行测量。无修饰转录本是DRS实用且有针对性的对照,可为匹配的生物学来源序列背景中的标准核苷酸提供基线测量。然而,这些对照的生成可能具有挑战性,并且带有可能影响分析的纳米孔特异性细微差别。我们使用来自六种永生化人类细胞系的cDNA体外转录(IVT)产生的无修饰转录本生成了DRS数据集。我们对细胞系间的差异进行了表征,并展示了如何对这些差异进行解读。这些数据将作为一种通用对照和资源供学界用于人类转录本的RNA修饰分析。