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. 2018 Apr 18;14(4):e1007354. doi: 10.1371/journal.pgen.1007354

Fig 1. Identification of differentially decaying operons in E. coli.

Fig 1

(A-C), Differential decay in three representative E. coli operons, depicted by normalized RNA-seq coverage in steady state (black, t = 0) or at two time points (green and red) following rifampicin treatment. RNA-seq coverage was normalized by the number of uniquely mapped reads in each library. Bar graphs show average half-life calculations from three replicates with error bars representing standard deviation. (D), Ratio of steady-state mRNA abundance (blue) and mRNA half-lives (red) shown for a subset of regulated gene-pairs in which mRNA abundances and decay rates closely matched. Gene names are marked below the x-axis. Shown is the average ratio between the genes with error bars denoting standard deviation.