Start Smart

A Lifetime of Care in One Test！

Unlock a Healthier Future for Your Baby with Whole Genome Sequencing!

Why Start at Birth?

• Your baby’s DNA is like a roadmap to their health.

• Whole Genome Sequencing (WGS) can uncover genetic risks for rare diseases, allergies, and even how they process certain medications—right from the start!

• Early knowledge means early action, giving your baby the best chance for a happy, healthy life.

Genetic disorders can cause many health problems for kids

• About half of the cases of blindness, deafness, heart defects and severe mental disabilities in children are due to genetic disorders. These disorders also account for 40-50% of childhood deaths.

• Whole genome sequencing (WGS) is a powerful tool that can help doctors find out what's wrong in children showing symptoms that might be related to genetic issues.

Why WGS?

Early Detection: WGS can find over many rare genetic conditions that might not show up in traditional tests. This means doctors can spot problems early and start treatment sooner.

Expanded Screening: Traditional newborn screening only checks for a few conditions. WGS can screen for thousands of potential genetic issues all at once, giving a more comprehensive health check.

Personalized Care: Knowing a baby's genetic profile helps doctors tailor medical care to their specific needs, which can improve overall health.

A Gift for Life

• By screening your baby’s genome, you’re giving them the gift of a lifetime—better health, tailored care, and the chance to avoid preventable conditions.

Screen Early, Live Healthy!

Rainbow Pedi 1000 screens for 1,000+ baby diseases

by reading all their DNA, detecting rare conditions, developmental risks, and medication sensitivities early

A healthier future starts here!

Newborn & Pediatric Screening

• Brain and Nerve Problems: Autism spectrum disorder, language issues, difficulty in learning and thinking, epilepsy, developmental delays. Over 2500 genes involved.

• Metabolism Issues: Involves problems with metabolism.

• Heart Conditions: Heart defects, sudden death, heart rhythm problems. Over 2000 genes.

• Childhood Cancers: Cancers in kids.

• Allergy and Immune System Issues: Eczema, food sensitivity and frequent infections.

• Hormone Problems: Early diabetes (MODY), short height, puberty disorders. Over 1000 genes.

• Muscle Weakness: Trouble walking, climbing stairs, fall frequently and respiratory issues

For Screening of

Developmental & Language Delay, Intellectual Disability

Epilepsy, Growth and Congenital Abnormality

Whole genome sequencing looks at many types of DNA changes that might be causing health problems.

• It’s very good at finding answers for patients with complicated symptoms.

• Getting an accurate genetic diagnosis reduces misdiagnosis, helps doctors understand what to expect in the future, avoid unnecessary tests or surgeries, and take better care of patients.

For Physicians - Report Includes

• Clinically-actionable newborn and pediatric disorders

• Copy number variants equivalent to Clinical Microarray test findings (CMA)

• Fragile X

• Repeat expansions (Includes Huntington's Disease)

• Uniparental Disomy (Trio)

• Difficult-to-Detect Variants. Regions of Homozygosity

Safe, Simple, Life-Changing

WGS is a one-time test that uses a simple saliva sample

It’s safe, quick, and can provide lifelong health insights for your baby

and even your family!

• This test helps find out if your child is at risk for over 1,000 diseases that can show up early in life.

• The test follows the same method used in newborn screening (BabySeq) at Boston Children's Hospital and Harvard Medical School.

• The test looks at over 1,600 genes linked to more than 1,000 childhood diseases.

Testing Process and Reports

• Whole Genome Sequencing at 40-80x Depth

• Newest genomic and analysis technologies（30 base pairs and 20,000 genes）

• Provide a detailed analysis of hard-to-detect, disease-related genetic changes linked to complex neurological and psychiatric disorders, like autism.

• Clinical report is issued by a board-certified medical director M.D. and Ph.D. Dual degree holder).

• Genetic counseling included (Provided by Australia-registered, board-eligible genetic counselor).

Please contact our collaborating clinic, meet their physicians, and discuss if the Pedi 1000 newborn test is right for your child

Our colaborating clinic:

Venco Medical Centre

• 九龍尖沙咀彌敦道132號美麗華廣場A座16樓03室

• Unit 1603, 16/F, Mira Place Tower A, 132 Nathan Road, Tsim Sha Tsui, Kowloon.

Tel: 2882 7222