FIGURE 1.

Computational description of identifying lncRNAs linked to genomic instability. We developed a somatic mutation profile. For each patient, the total number ofS somatic mutations was estimated. The numbers were then sorted in a decreasing order. Next, LUAD patients were classified into two groups, including the GU‐like group (the top 25 percent) and the GS‐like group (the last 25 percent), on the basis of the mutator phenotype. Through analyzing the lncRNA expression profiles between the two groups, lncRNAs, which had a significant correlation with genomic instability, were discovered