Cancer Genetic Testing

This test uses molecular biology techniques to analyze your DNA for genetic mutations and biomarkers linked to cancer development. It helps assess inherited cancer risk, supports diagnosis, informs treatment planning, and tracks disease progression.

What’s Included in the Test:

  • Detection of key mutations (e.g., BRCA1/2) related to breast and ovarian cancer.
  • Evaluation of tumor-related gene mutations influenced by genetic and environmental factors.

Benefits:

  • Risk Assessment: Understand how family history may impact your cancer risk.
  • Early Detection: Identify genetic predispositions before symptoms arise.
  • Treatment Planning: Personalize therapeutic strategies based on genetic insights.
  • Ongoing Monitoring: Track disease progression or response to treatments.

Testing Technologies:

  • Whole Genome Sequencing (WGS)
  • Whole Exome Sequencing (WES)

Who Should Consider This Test

Individuals with a family history of cancer or known hereditary syndromes. Health-conscious individuals seeking proactive cancer risk assessment.

Sample Type

Saliva

Turnaround Time

4 weeks

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