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. 2021 Jan 11;11:389. doi: 10.1038/s41598-020-79698-w

Figure 6.

Figure 6

Established VCN genomic DNA standards showed uniform performance and accuracy when evaluated by independent laboratory. Genomic DNA extracted from developed VCN standard cell lines was evaluated by an independent laboratory using the RRE duplex assay for VCN determination by qPCR and ddPCR. The qPCR results represent a mean of four independent qPCR runs performed by two independent operators at NIST laboratory on two different qPCR instruments and using two different DNA inputs, with four replicates run for each condition (in total 32 qPCR data points for each tested VCN standard). The ddPCR results are concordant with the qPCR assay results and each data point represents a mean of two independent ddPCR runs performed on Bio-Rad QX200 instrument by two independent operators and using two different DNA inputs (in total 16 ddPCR data points for each tested VCN standard). The error bars are the sample standard deviations for the means of the data sets, with N = 32 for qPCR and N = 16 for the ddPCR results.