2.4. Analysis of functional enrichment in immune-related lncRNAs with differential expression

XS Xinhai Sun
LL Liming Li
XY Xiaojie Yang
DK Dan Ke
QZ Qihong Zhong
YZ Yuanchang Zhu
LY Litao Yang
ZZ Zhenyang Zhang
JL Jiangbo Lin
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The immune score information of the TCGA samples was downloaded from ESTIMATE (ESTIMATE: Disease (mdanderson.org)). Then, all samples were classified into two groups: one with high immune scores and one with low immune scores, using the median immune score as a threshold. The differentially expressed genes (DEGs) between different immune score groups, as well as those between high- and low-risk groups, were obtained using the “limma” and “edgeR” R packages. By intersecting these DEGs, 29 immune-associated differentially expressed genes (IDEGs) (Supplementary Table S3) were obtained and used for subsequent functional enrichment. Based on these IDEGs, functional enrichment analysis was performed using the “ggplot2” and “clusterProfiler” R packages. In addition, at the genomic level, gene set enrichment analysis (GSEA) has been used to evaluate biological signatures [34]. Therefore, we used the R packages “ggplot2” and “clusterProfiler” for GSEA to determine the enrichment of signaling pathways for these IDEGs.

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