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. 2019 Aug 6;9:11372. doi: 10.1038/s41598-019-47862-6

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Comparison of amplification curves of 500 copies/reaction and 0 copies/reaction (NTC) of genomic viral RNA using Adaptive RT-PCR (blue) and standard RT-PCR (red) on a Qiagen RotorGene Q instrument for Zika (A), dengue (B), and chikungunya (C) virus. Each assay contains the same reaction mixture including all three primer and probe sets and L-DNA probes. Each amplification curve is the average of three independent runs. Individual runs are shown in Supplementary Fig. 2.