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. 2019 Dec 3;9:18246. doi: 10.1038/s41598-019-54747-1

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© The Author(s) 2019

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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The recombination breakpoints identified in 140 recombinant inbred lines (RILs) using the non-distorted polymorphic SNPs. The chromosomes are labeled as A01 to A10 and B01 to B10 and are separated by vertical lines while each horizontal line represents a single RIL. Green and red bars represent segments from NC 94022 and SunOleic 97R genotypes, respectively. Blue bars represent the heterozygous/missing call. The black and white panel at the bottom indicates the consensus 5,816 bins identified in the entire RIL population.