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- W2952628721 abstract "Characterizing complex viral transcriptomes by conventional RNA sequencing approaches is complicated by high gene density, overlapping reading frames, and complex splicing patterns. Direct RNA sequencing (direct RNA-seq) using nanopore arrays offers an exciting alternative whereby individual polyadenylated RNAs are sequenced directly, without the recoding and amplification biases inherent to other sequencing methodologies. Here we use direct RNA-seq to profile the herpes simplex virus type 1 (HSV-1) transcriptome during productive infection of primary cells. We show how direct RNA-seq data can be used to define transcription initiation and RNA cleavage sites associated with all polyadenylated viral RNAs and demonstrate that low level read-through transcription produces a novel class of chimeric HSV-1 transcripts, including a functional mRNA encoding a fusion of the viral E3 ubiquitin ligase ICP0 and viral membrane glycoprotein L. Thus, direct RNA-seq offers a powerful method to characterize the changing transcriptional landscape of viruses with complex genomes." @default.
- W2952628721 created "2019-06-27" @default.
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- W2952628721 date "2019-02-14" @default.
- W2952628721 modified "2023-10-11" @default.
- W2952628721 title "Direct RNA sequencing on nanopore arrays redefines the transcriptional complexity of a viral pathogen" @default.
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- W2952628721 doi "https://doi.org/10.1038/s41467-019-08734-9" @default.
- W2952628721 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6376126" @default.
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