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. 2019 Aug 22;9:12265. doi: 10.1038/s41598-019-48478-6

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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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(A) The column diagram of DEGs for QCL5019 vs. QCL8006_1 and QCL5019 vs. QCL8006_2. X axis represents pairwise and Y axis means number of screened DEGs. Blue bar denotes down-regulated genes and red bar for the up-regulated. (B) The intersection heatmap of DEGs for QCL5019 vs. QCL8006_1 and QCL5019 vs. QCL8006_2. Gradient color barcode at the right top indicates log2 (FC) value (FC, Fold change of expression in triple recessive mutant vs waxy parent). Each row represents a DEG and each column represents one condition pairwise. DEGs with similar fold change value are clustered both at row and column level.