Fig. 2
From: One-step diagnosis of infection and lung cancer using metagenomic sequencing
CNV pattern of BALF samples and its clinical relevance with lung cancer typing. A The frequency of each CNV type occurred in each chromosome. (B) and (C) showed the average frequency of each CNV type in subtypes of lung cancer (ie. MC, NSCLC and SCLC) and that of NSCLC (ie. ADC and SCC), respectively. The data were statistically analyzed with the use of IBM SPSS Statistics 26.0 (independent sample Mann–Whitney U test with the significance of p < 0.05). “*” represents p < 0.05; “**” represents p < 0.01; “***” represents p < 0.001. (D) The proportion of a certain CNV type of each chromosome in the same type of CNV of all chromosomes for comparison of SCC and ADC group