Fig. 6From: Impact of PNPase on the transcriptome of Rhodobacter sphaeroides and its cooperation with RNase III and RNase EMany differential 3′ ends found in the PNPase mutant can also be detected in the RNase III or RNase E mutant strain at the same genomic position. a, d, g Venn diagrams illustrating the total number of differential 3′ ends found in each mutant strain in comparison to the wild type (+: mutant enriched; −: mutant depleted) and the number differential 3′ ends which could be mapped to the same genomic position. Percentage: number of 3′ ends in respective quadrant devided by the total number of rnc/rne 32 °C/rne 42 °C enriched or depleted 3′ ends. Blue: pnp mutant; violett: rnc mutant; yellow: rne mutant at 32 °C; red: rne mutant at 42 °C. b, e, h Scatterplots depicting the intersecting analysis, every dot represents one differential 3′ end. x-axis: log2-fold change pnp mutant versus wild type; y-axis: log2-fold change rnc/rne mutant versus wild type. Feature classes harboring the observed 3′ ends are color coded. Orange: CDS; yellow: ncRNA; green: rRNA; blue: tRNA; violett: UTR. Blue lines represent a 2D density function. The histograms (grey) illustrate the distribution of intersecting 3′ end log2-fold changes of the compared strains. d, f, i Histograms display the number of intersecting 3′ ends, which are grouped in mutant enriched/depleted and feature classes. x-axis: feature class; y-axis: countBack to article page