Level 3 RNAseq data, mutation maf data, and pertinent clinical data for LUAD were extracted from the TCGA dataset [14, 22]. The maftools package within the R software environment was employed for the retrieval and visualization of somatic mutations in LUAD patients [24, 25]. Visual representation in the form of horizontal histograms demonstrated a notable prevalence of mutations among LUAD patients [22].
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