Table 5. The number of variants detected on ctDNA of intestinal neoplasms using both NGS panels.
Tumor origin | Intestine | Panel 1 | Panel2 |
---|---|---|---|
NGS panels' common variants, n (%) | Detected | 7 (47%) | 9 (60%) |
Not detected | 3 (20%) | 1 (7%) | |
NGS panel–related exclusive variants, n (%) | Detected | 1 (7%) | 4 (27%) |
Total variants detected by each panel | 8 (53%) | 13 (87%) | |
Total detected variants | 15 (100%) |
Abbreviations: ctDNA, circulating tumor DNA; NGS, next-generation sequencing.
Note: These are classified considering exclusive and communal ones for panel design.