Description
(395 genes Mutation, Copy Number variations
and Fusion analysis with TMB)
Tissue, NA, Fasting or Non Fasting: As suggested by doctor
Sample Required:
FFPE tissue block at room temperature OR fresh tissue in DCGL Preservative Solution at 2–8°C; tumour content >10%.
Test Time:
Biopsy-dependent. Report in 8–12 working days.
Test Normal Range:
No fixed normal range.
What is the Test?
A highly comprehensive NGS panel evaluating **395 genes** for **mutations, CNVs, fusions, and tumour mutation burden (TMB)**. It provides deeper tumour profiling compared to standard panels and is useful in planning targeted or immunotherapy.
Test Procedure:
Tissue undergoes multi-layered genomic sequencing, including mutation calling, CNV analysis, fusion detection and TMB calculation.
When to Take the Test:
When a more detailed understanding of tumour genetics is required, especially to guide immunotherapy.
Who Should Take This Test:
Patients needing extensive genomic information to help determine personalised treatment strategies.
Precautions for Exceptional Cases (Pregnancy, etc.):
Ensure tumour adequacy; pregnant individuals should inform their physician.
