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Value-Added Services

Circle Premium DNA Test
The World’s Most Comprehensive DNA Test (Suitable for people of all age groups)
One Test for a Lifetime

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Introduction:

• With a simple saliva sample, uncover 500+ test reports across 20 categories, including diet and nutrition, cancer and disease risks, family planning, drug response, success/music/dance traits, skin & well-being, and personality traits, etc.

Application:

• Understand your cancer and major disease risks early with a better preparation
• Each report shows clearly your genetic needs and predispositions as well as providing personalized and actionable recommendations

Advantages:

• Non-invasive
• Discover your unique genetic profile & traits
• Guide you to lost weight in healthy way, eat smarter and train better
• A lifetime subscription of DNA updates is available, including new categories and reports

Reporting Time: Around 18 working days

Precautions:

• Avoid eating, drinking, smoking or chewing of gum 30 minutes before providing your DNA sample

Report explanation by genetics-trained health coach / genetic counsellor via phone

A Stool-based DNA test for Early Colorectal Cancer Screening- ColoClear®
(Suitable for people aged 40 or above, especially those who are at high risk for colorectal cancer & those are not suitable to undertake a colonoscopy)

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Application:

• Proven innovations in stool DNA detection technology.
• A screening test for the detection of colorectal cancer and pre-cancer cases associated DNA markers and for the presence of occult blood in human stool.

Advantages:

• Non-invasive, no side effects, easy & convenience with high accuracy rate.
• Can detect an early adenoma/tumor with a size as small as 1 cm in diameter by testing genetic materials in stool.
• Risk signal of colorectal cancer can be detected 5 years in advance resulting a prompt treatment and improvement in the survival rate.
• Sample taking is easy & convenience. Sample can be collected at home in 5 minutes.

Reporting Time: Around 10 working days

Precautions:

• Avoid eating too greasy food within 24 hours before.
• Women avoid sampling during Menstrual periods.

Report explanation by Medical staff via phone

The Total Solution for DNA Testing- Hereditary Diseases Risk Assessment
(Suitable for people of all age group, especially for family planning couple)

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Introduction:

With a screening of 2,700 genes and over 500 hereditary diseases. From cancer, development disorder to cardiac diseases, various asymptomatic genetic mutations and related health risks can be identified by this premium genetic test.

Application:

• It maps the risk of getting 500+ hereditary diseases.
• It allows you to understand all the potential threats in your future and start early prevention.
(E.g. Changing your daily diet or performing a more intensive health check-up).
• It allows family planning couples to identify each other’s hereditary diseases genetic status and can help one to understand the reproductive risk of having such hereditary diseases, thus having better management of family plan as well as reducing the risk to the lowest level.
• Result is beneficial for a lifetime. One-off blood test in a lifetime.
Reporting Time: Around 6 weeks working days
Precautions: No transfusion of blood 1 month before the test, no organ transplantation

Report explanation by Medical staff via phone

BRCA1 and BRCA2 DNA Test
(Suitable for female of all age groups, especially those with family history in breast/ ovarian cancers)

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Introduction:

• BRCA1 and BRCA2 are Human genes that produce proteins to repair damage DNA. They help to keep breast, ovaries, and other types of cells from growing and dividing too rapidly or in an uncontrolled way.
• If there is any inherited mutation from either of BRCA1 and BRCA2 genes, cells are more likely to divide and change rapidly, which can lead to developing cancer. Breast and ovarian cancers caused by gene mutations are called “hereditary breast and ovarian cancers.

Application:

• It maps the risk of getting hereditary breast & ovarian cancers.
• It allows people to start early prevention. (E.g. Changing your daily diet or performing a more intensive health check-up).
• Sharing the result with family members. If the person carriers BRCA mutation(s), her family member has 50% chance inherits the same mutation(s).
• Result is beneficial for a lifetime. One-off blood test in a lifetime.
Reporting Time: Around 7-10 working days
Precautions: No transfusion of blood 1 month before the test, no organ transplantation

Report explanation by Medical staff via phone

A genetic test for Nasopharyngeal cancer (NPC)- NP Screen Test™
(Suitable for people with family history of NPC or with symptoms of NPC)

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Introduction:

NP Screen™ is designed to specifically measure the presence of EBV DNA as an indicator of the presence of NPC through a trans-oral brush process for direct sampling.

Application:

NP Screen™ provides the only reliable and simple method for a regular screening program to help manage NPC for high and moderate risk patients. Early detection improves survival rates from 30-40% to over 90%.
Advantages: It is a simple, convenience and non-invasive test with high accuracy rate of over 99% without side effects.
Reporting Time: Around 7-10 working days

Report explanation by Medical staff via phone