This liquid biopsy test analyzes key genetic alterations in 7 genes via DNA sequencing and 6 genes via RNA sequencing linked to lung cancer. It detects single nucleotide variations (SNVs), copy number variations (CNVs), insertions/deletions (InDels), and gene fusions—all from a simple blood sample.
Patients with lung cancer who cannot undergo a tissue biopsy or need a less invasive method for diagnosis, monitoring, or treatment planning.
Lung Cancer
Methodology: | NGS |
Depth of Coverage: | >2000x |
Limit of Detection: | 0.5% VAF (SNV and Indels), 0.3% VAF (Fusions) |
Sample Type: | Blood |
Container: | EDTA Vacutainer (Purple Top) |
Shipping Conditions: | Refrigerated (2- 8 ℃) |
Max Transit Time: | 72 hours |
15 Days