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Hereditary cancer risk screening using NGS.

Testing uses a whole blood sample of at least 5 mL, with results available in 12 working days.

Why Is Hereditary Cancer Screening Important?

Cancer Risk Can Be Genetic

Identify genetic mutations associated with increased cancer risk

Understand patterns of cancer inheritance in the family

Plan better prevention and monitoring

Genetic counselling can help people understand testing and results.

Who Should Consider Hereditary Cancer Screening?

Testing may be considered especially for those who:

01

Have a strong family history of cancer

• Have several family members with the same or related cancers

• Had cancer at a relatively young age

02

Were recently diagnosed with cancer

• Need genetic information to support treatment strategies

03

Have a family member with a cancer-related gene mutation

04

Want to learn about cancer risk proactively

• To help plan prevention and early detection

About Hereditary Cancer Screening

This screening assesses hereditary cancer risk. Gene panel and cancer coverage details have not been verified for this offering.

Specific Cancer Panel Options

Panel-specific gene and cancer coverage has not been verified. Contact NGI to confirm available testing options.

Testing Information

Obtain informed consent and provide genetic counselling. Positive findings may require confirmation.

Personalized Prevention

Test results can help doctors develop

Prevention strategies

Early detection schedules

Risk monitoring

Considerations for specific treatments

How Is Hereditary Cancer Screening Performed?

1

Consultation

Discuss your health and family cancer history with a healthcare professional.

2

Sample Collection

Collect at least 5 mL of whole blood.

3

Genetic Analysis

The sample is analyzed using Next-Generation Sequencing (NGS) technology.

4

Results Consultation

Discuss the results with a healthcare professional to determine appropriate prevention, early detection, or follow-up steps.