Fig. 6From: Elimination of PCR duplicates in RNA-seq and small RNA-seq using unique molecular identifiersFraction of PCR duplicates across genes for (a) a series of UMI RNA-seq and small RNA-seq libraries made with different amount of starting materials, and (b) a series of UMI small RNA-seq libraries all made with 5 μg of total mouse testis RNA and with an increasing number of PCR cyclesBack to article page