DEG identification and PageMan analysis

YY YanLing Yin
TY TianHui Yang
SL Shuang Li
XL Xiaoning Li
WW Wei Wang
SF ShuGao Fan
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DEGs in the transcriptome data were identified through the utilization of the DESeq2 package (v1.22.1) within the R programming environment. Raw read counts were used as input data for the analysis. DEGs were identified using criteria where the absolute value of log2 (fold change (FC)) ≥ 1, and the false discovery rate (FDR) < 0.05.

Enrichment analysis of the DEGs was performed using the PageMan software (v3.0.0), which is a commonly used tool for functional analysis of large-scale omics data in plants. The log2 (FC) of NaCl vs. CK and that of NaCl+MeJA vs. CK were input into PageMan, and the significantly enriched BINs were identified using the Wilcoxon statistical test with default parameters provided by PageMan.

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