01 How should low VAF variants be interpreted?
Patients
NCCN guidelines strongly recommend broad-panel Next-Generation Sequencing (NGS) to identify actionable genomic alterations in advanced, metastatic, or high-risk cancers, particularly for NSCLC, breast, and gastrointestinal tumors
02 What does “ctDNA not detected” mean clinically?
Clinicians
NCCN guidelines strongly recommend broad-panel Next-Generation Sequencing (NGS) to identify actionable genomic alterations in advanced, metastatic, or high-risk cancers, particularly for NSCLC, breast, and gastrointestinal tumors
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