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. 2016 Apr 23;17:299. doi: 10.1186/s12864-016-2619-0

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© Olsson et al. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.

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Fig. 1 — a The genomic location of the two CNVs and b the comparison of results obtained using quantitative PCR (qPCR) and droplet digital PCR (ddPCR) for assays in each (CNV_14.3: Assay-CNV-East; CNV_16.1: Assay-CNV-759 and Assay-CNV-E). Regression analysis showed Assay-CNV-East reported reasonably similar results (r ² = 0.72), whilst concordance was lower for Assay-CNV-759 (r ² = 0.64) and Assay-CNV-E (r ² = 0.44). In each assay it can be seen ddPCR reports tighter clustering at higher qPCR values