Clinical Exome Sequencing (CES) + Mitochondrial Genome Sequencing – ONCO is an advanced genetic test designed to identify inherited and acquired genetic variations associated with cancer. It analyzes thousands of clinically relevant genes in the exome along with the complete mitochondrial genome to provide comprehensive insights into cancer risk, diagnosis, prognosis, and personalized treatment options.
Why is this Test Important?
Detects cancer-associated genetic mutations.
Identifies hereditary cancer syndromes.
Supports precision oncology and targeted therapies.
Assists in prognosis and treatment planning.
Evaluates mitochondrial DNA variations linked to cancer development.
Who Should Consider This Test?
Individuals with a personal or family history of cancer.
Patients with early-onset or rare cancers.
Individuals with multiple primary tumors.
Patients requiring targeted therapy selection.
Cases with unexplained hereditary cancer risk.
Sample Required
Peripheral Blood / DNA Sample
Benefits
✔ Comprehensive analysis of clinically significant genes ✔ Complete mitochondrial genome assessment ✔ Supports personalized cancer management ✔ Helps identify hereditary cancer predisposition ✔ Facilitates informed clinical decision-making
When is the Test Recommended?
Suspected hereditary cancer syndromes
Precision oncology evaluations
Family cancer risk assessment
Complex or undiagnosed cancer cases
Selection of targeted treatment strategies
Advanced BioCare Laboratories
Accurate genetic testing solutions for comprehensive cancer risk assessment and personalized healthcare.