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. 2020 May 13;19:181. doi: 10.1186/s12936-020-03249-x

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 1 — Distribution of fold-changes of samples from whole-blood (a) or dried blood spots (b) as measured by the plasmepsin 2–pfmdr1 TaqMan qPCR assay. Tick marks underneath the bar graphs indicate individual sample status for the breakpoint PCR assay (BP, top line), with blue indicating no breakpoint detected and red containing the breakpoint, or exo-E415G SNP (EXO, bottom line), where yellow represents the wildtype E amino acid and green is the mutant G amino acid. Bars are coloured by their predicted plasmepsin 2 copy number of either 1, 2, 3, or 4+ (green, yellow, orange, and red, respectively)