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. 2021 May 27;29(11):1677–1689. doi: 10.1038/s41431-021-00907-9

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© The Author(s), under exclusive licence to European Society of Human Genetics 2021

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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Fig. 2 — A Ciliogenesis per control, as a percentage of the total number of cells. Cilia are indicated as either present (cilium), spot or not present (no cilium). The top bar of the graph represents the average of all controls, showing 90 ± 8% is ciliated, 7 ± 7% of the cells have a spot and 3 ± 5% is not ciliated. The error bars indicate the SD. B Cilium length of all controls in a combined violin-boxplot. The median, Q1, Q3, and range are determined using a Tukey-style boxplot. Outliers (1.5 × IQR) are indicated as dots. The number of observations per length are indicated by the width of the violinplot. The violin-boxplot on the left shows the average of all controls with a median of 3.71 ± 0.04 µm. Individual controls are shown in light gray. C The area of the IFT88 accumulations in a combined violin-boxplot as in B. The violin-boxplot on the left shows the average of all controls with a median of 0.43 ± 0.01 µm².