Fig. 3From: Application of the 3′ mRNA-Seq using unique molecular identifiers in highly degraded RNA derived from formalin-fixed, paraffin-embedded tissueData comparison between the QuantSeq 3′ mRNA-Seq and TruSeq Stranded mRNA-Seq kit. A; Correlation plot. Data were normalized by log2 (TPM + 1). Each dot constitutes a gene. B; Distribution of mapped reads. The incompatible paired-end reads (15%) were not reflected in the TruSeq Stranded mRNA-Seq data. C; Number of detected genes between two platforms. D; Percentage of mapped reads distribution by RNA biotypesBack to article page