Direct RNA Nanopore Sequencing of Pseudomonas aeruginosa Clone C Transcriptomes

Transcription
DOI: 10.1128/jb.00418-21 Publication Date: 2021-11-15T18:03:42Z
ABSTRACT
Genome-wide gene expression of bacteria is commonly studied by high-throughput sequencing size-selected cDNA fragment libraries reverse-transcribed RNA preparations. However, the depletion rRNAs, enzymatic reverse transcription, and fragmentation, size selection, amplification during library preparation lead to inevitable losses information about initial composition pool.
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