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. 2016 Jun 13;17:451. doi: 10.1186/s12864-016-2802-3

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© The Author(s). 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. 3 — Cranberry linkage map marker density/depth and genome-wide patterns of segregation distortion. Segregation distortion is plotted as a function of Chi-squared value (y axis) for monogenic marker segregation ratios against marker position on each of the twelve LGs of the integrated map. Uniparental markers for P₁ (female is heterozygote) are indicated with pink, uniparental markers for P₂ (male is heterozygote) are displayed in light blue, whereas biparental markers (both parents heterozygotes) are shown in gold dots. Dots with red halo indicate markers with Chi-squared values significant at p-values ≤ 0.10. Genetic distances are displayed in cM on the x axis. MD label on the y axis refers to marker density across the linkage group