TABLE 1.
Patients | SNVs detected by WES | Tumor‐informed assay | Tumor‐agnostic assay | ||
---|---|---|---|---|---|
SNVs | VAF | SNVs | VAF | ||
Pt.8 | 218 | 20 | 0.154% | 0 | 0 |
Pt.2 | 301 | 26 | 0.176% | 0 | 0 |
Pt.11 | 225 | 29 | 8.83% | 2 | 6.40% |
Abbreviations: ctDNA, circulating tumor DNA; SNV, single nucleotide variant; VAF, variant allele fraction; WES, whole‐exome sequencing.