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

Nanopore direct RNA sequencing (DRS) enables measurements of native RNA modifications. Modification-free transcripts are an important control for DRS. Additionally, it is advantageous to have canonical transcripts from multiple cell lines to better account for human transcriptome variation. Here we...

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Detalles Bibliográficos
Autores principales: McCormick, Caroline A., Akeson, Stuart, Tavakoli, Sepideh, Bloch, Dylan, Klink, Isabel N., Jain, Miten, Rouhanifard, Sara H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104151/
https://www.ncbi.nlm.nih.gov/pubmed/37066160
http://dx.doi.org/10.1101/2023.04.06.535889
Descripción
Sumario:Nanopore direct RNA sequencing (DRS) enables measurements of native RNA modifications. Modification-free transcripts are an important control for DRS. Additionally, it is advantageous to have canonical transcripts from multiple cell lines to better account for human transcriptome variation. Here we generated and analyzed Nanopore DRS datasets for five human cell lines using in vitro transcribed (IVT) RNA. We compared performance statistics amongst biological replicates. We also documented nucleotide and ionic current level variation across cell lines. These data will serve as a resource to the community for RNA modification analysis.