Fig. 6From: Single molecule counting and assessment of random molecular tagging errors with transposable giga-scale error-correcting barcodesEXB-based and random-mer-based transcriptome analysis. The ratio between random-mer and EXB-based gene expression level is shown for a 10Â ng, b 1Â ng, and c 100Â pg of input cDNA. The x-axis corresponds to the rank of the expression ratio, and is sorted independently for each sample. To emphasize the number of inflated genes, the x-axis is shown in log scale. d Technical variation between counting methods. The ratio between random-mer and EXB-based quantification coefficient of variation across technical replicates is shown for 100Â pg input. For each sample type, the coefficient of variation ratios is sorted by decreasing order. e Impact of counting methods on differential expression analysis. The number of differentially expressed genes detected with an FDR threshold of 0.05 is shown for both random-mer and EXB-based quantification methodsBack to article page