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. 2023 Nov 21;4(11):101281. doi: 10.1016/j.xcrm.2023.101281

Figure 2.

Figure 2

Detection of the cancer genes using different types of variations

(A) Overview of the plasma multi-omics variation atlas (including 30 patients with STAD, 23 patients with CRC, and 18 HDs).

(B) cfDNA copy number and cfRNA abundance for TP53. HD, healthy donor; CRC, colorectal cancer; STAD, stomach adenocarcinoma. The dotted lines represent 95% specificity defined by HDs.

(C) Detection capacity for each cancer gene, combing different variations derived from cfDNA (cfWGS and cfMeDIP-seq) and total cfRNA-seq data. Frequently altered genes are defined by a greater than 75% detection ratio.

(D) Distribution of variation types among all genes that are frequently altered.

(E) Altered genes with top detection ratios ranked by cfRNA and cfDNA, respectively.