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Updated: Mar 11, 2026

MS2-Affinity Purification Coupled with RNA Sequencing in Gram-Positive Bacteria
Published on: February 23, 2021
Analyzing Prokaryotic RNA-Seq Data: A Case Study Identifying Holo-Fur Regulated Genes in Campylobacter jejuni
Sophie Bérubé1, James Butcher1, Alain Stintzi2
1Ottawa Institute of Systems Biology, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, 451 Smyth Road, Ottawa, ON, Canada, K1H 8M5.
Abstract:
In recent years, RNA-seq has become an important method in the process of measuring gene expression in various cells and organisms. This chapter will detail all the bioinformatic steps that should be undertaken to determine differentially expressed genes from a typical RNA-seq experiment. Each step will be clearly explained in "non-bioinformatic" terminology so that readers embarking on RNA-seq analysis will be able to understand the rationale and reasoning behind each step. Moreover, the exact command lines used to process the data will be presented along with a description of the various flags and commands.
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