NovoFocus™ NSCLC 2.0 Test is a next generation sequencing (NGS)-based assay that analyzes 47 genes related to Non-Small Cell Lung Cancer (NSCLC) for clinically important alterations at the DNA level. These genes are known to be relevant for the diagnosis and/or treatment of various NSCLC according to National Comprehensive Cancer Network (NCCN) guideline and the medical literature.
NovoFocus™ NSCLC 2.0
Non-Small Cell Lung Cancer
14 Calendar Days
Plasma (Extracted DNA)
NovoFocus™ NSCLC 2.0 interrogates the complete coding region of 47 genes and introns of 9 genes. It can detect all four types of genomic abnormalities (SNV, InDel, CNV and fusion) and provide targeted therapy options. Besides, it analyzes pharmacogenomics and provides chemotherapy options.
Comprehensive analytical validation has been completed and the test includes rigorous quality control measures.
With leading-edge sequencing solutions and superior process efficiency, Novogene offers highly competitive prices for all our service.
Who Benefits from NovoFocus™ NSCLC 2.0?
NovoFocus™ NSCLC 2.0 is suitable for all NSCLC patients, especially for the following:
What Clinical Information Does NovoFocus™ NSCLC 2.0 Provide?
Provides the information regarding relevant biomarkers and genomic alterations to help match patients to targeted therapies.
Provides the SNP information related to efficacy and toxicity of chemotherapies.