While there was a trend of high riskscore associated with poor prognosis for male patients, it did not reach statistical significance (p = 0.17) ( Fig. 4 C). 3.4 Enrichment analysis and pathway analysis of the high-risk and low-risk groups To investigate the possible mechanisms underlying the poor prognosis of the high-risk group, we conducted differential analysis and identified 1316 differentially expressed genes (|logFC| > 1, FDR adjusted p < 0.05) between the high-risk and low-risk groups ( Fig. 5 A).
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Disulfidptosis-related lncRNA signature reveals immune microenvironment and novel molecular subtyping of stomach adenocarcinoma.
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