In order to identify polymorphism between KMR3 and IL50-13, we performed BLASTN analysis of 136 DEGs including 78 DEGs of qyld2.1, 25 DEGs of qyld8.2, 12 DEGs showing high fold expression and 21 reported yield related gene sequences against the scaffolds obtained by whole-genome sequencing of the restorers KMR3 (without O. rufipogon) and IL50-13 [IET21943 = RPBio4919-50-13] (with O. rufipogon). The comparison was done by considering the gene sequence corresponding to Nipponbare and its gene sequence was used to obtain the corresponding gene sequences from the scaffolds of the two restorers KMR3 and IL50-13. The orthologous genomic regions were available for all genes analysed. Further we also analyzed the effect of identified SNPs/InDels in the coding region that could affect the expression of the genes showing polymorphism and also the effect of the variants in the 2 kb upstream and downstream regions of the given genes using the SnpEff software (Wayne State University, Detroit MI USA)79. The DEGs along with their gene and chromosome names and their corresponding coordinates are given in Supplementary Table S3.
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