Time-course transcriptome profiling of a poxvirus using long-read full-length assay

D. ra Tombácz, István Prazsák, G. bor Torma, Zsolt Csabai, Zsolt Balázs, Norbert Moldován, B. la Dénes, Michael Snyder, Zsolt Boldogkői

Research output: Contribution to journalArticleAcademicpeer-review

3 Citations (Scopus)


Viral transcriptomes that are determined using first- and second-generation sequencing techniques are incomplete. Due to the short read length, these methods are inefficient or fail to distinguish between transcript isoforms, polycistronic RNAs, and transcriptional overlaps and readthroughs. Additionally, these approaches are insensitive for the identification of splice and transcriptional start sites (TSSs) and, in most cases, transcriptional end sites (TESs), especially in transcript isoforms with varying transcript ends, and in multi-spliced transcripts. Long-read sequencing is able to read full-length nucleic acids and can therefore be used to assemble complete transcriptome atlases. Although vaccinia virus (VACV) does not produce spliced RNAs, its transcriptome has a high diversity of TSSs and TESs, and a high degree of polycistronism that leads to enormous complexity. We applied single-molecule, real-time, and nanopore-based sequencing methods to investigate the time-lapse transcriptome patterns of VACV gene expression.
Original languageEnglish
Article number919
Issue number8
Publication statusPublished - 1 Aug 2021
Externally publishedYes


  • Gene expression
  • Long-read sequencing
  • Nanopore sequencing
  • Transcriptome profiling
  • Vaccinia virus

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