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. 2021 Sep 25;20:380. doi: 10.1186/s12936-021-03894-w

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© The Author(s) 2021

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. 3 — PD-LAMP specificity in 10% blood. A A 2% agarose gel from LAMP reactions in blood containing malarial strains P. falciparum and P. vivax alongside controls Chikungunya and dengue virus (III) at 6 × 10⁴ parasites/µL blood after a 60-min LAMP reaction. Only malaria samples amplified, demonstrated by the DNA banding pattern in the gel. B Diffusion coefficients from smartphone PD analysis, where malaria samples showed a significant difference from Chikungunya virus, dengue virus (III) and NTC (One-way ANOVA Dunnett’s post-hoc test). NTC represents blood without spiked pathogens (N = 3)