Rainbow Genomics, established in 2016, uses whole genome sequencing, proteomics, polygenic risk scores, pharmacogenomics & nutrigenomics, to help doctors and patients to understand genetic variations, leading to improved treatment and health care outcomes.
Q1. I don’t know what causes my symptoms?
Get a diagnosis within two months
Q2. My child has unexplained disorders.
Determine the genetic cause and improve treatment outcome.
Q3. My doctor says I am at risk?
Understand your lifetime and imminent disease risks using genetics
Q4. Worry?
Learn how to monitor and prevent debilitating diseases with findings from your DNA
Obtain a diagnosis in 2 months
Know your breast, prostate and colon cancer, heart attack, stroke and diabetes lifetime risks
How likely will I have a heart attack, stroke, get lung or prostate cancer, or develop high-risk prediabetes within a few years
Which drugs and at what dosages provide the least side effect for my treatment (180 medications)
Am I deficient in absorbing brain health, heart health, and cancer prevention nutrients because of my genetics
What diet, exercise and food choices can help me lose weight effectively
DNA - Lifetime Risks
8000 Common and Rare Diseases
Proteins
Disease Onset in
A Few Years?
Heart Disease - Cancers
Better Nutrition
based on your DNA
Rainbow Genomics helps doctors to understand genetic variations, leading to improved treatment and health care outcomes.
We are a pioneer in the commercialization of genomic- and protein-based, diagnostic and preventive health care solutions to individuals.
We are committed to providing clinically-validated and evidence-based, multi-modal testing to Asian, Caucasian and mixed-race patients.
We cover a range of health issues, including hereditary disorders in both children and adults, genetic testing for medication responses, and assessing common disease risks.
We co-developed clinical applications with our institutional partners, and deploy credible clinical assessment products through highly-effective channels, to address both the domestic and medical tourism markets in Hong Kong, Japan, and the U.S.
Rainbow CEO on Expanding Precision Medicine Across Asia:
Invest HK - 香港投資推廣署
All Your DNA & 7000 Proteins
The human genome consists of 3 billion nucleotides or “letters” of DNA.
Our whole genome sequencing test analyzes all 3 billion DNA letters, providing high-quality results, often matching or exceeding those from top U.S. and European medical institutions.
We report common disease risks and health traits to help our patients prevent serious conditions and live healthier lives.
If a patient is at high risk for a common disease, our 7000-blood-protein test can predict if this disease might happen soon.
Doctors use this detailed information to better treat or prevent disease progression.
Unlike many consumer genetic tests that provide hundreds of findings that lack clinical relevance, Rainbow's whole genome sequencing provides clinically-actionable results that doctors can use to manage, treat, or prevent disorders.
We are a leader in using 7000-protein analysis to better estimate both long-term and short-term disease risks. Our current diagnostic programs combine genetic testing and protein analysis to assess the risks for heart attacks, lung cancer, diabetes, and dementia.
Through our U.S. partnerships, we use advanced multi-ethnic genetic models to predict the risk of common diseases like diabetes, stroke, and heart attacks.
We lead in combining genetic testing for rare inherited diseases with risk scores for common chronic diseases important to public health.
Unlike many genetic tests that use only a small number of genes, Rainbow analyzes the entire genome. This reduces the risk of missing important ethnic-specific genes. Many gene panels were designed using studies on Caucasian patients in the U.S. and Europe, and may not work well for Asian, mixed-race, and minority patients. Whole genome sequencing helps solve this issue.
ACMG Guidelines
We follow the latest guidelines from the American College of Medical Genetics and Genomics (ACMG) for interpreting genetic tests. Our clinical partners provide reports that are reviewed and signed by board-certified medical directors or genetic specialists.
CAP-Accredited & CLIA-Certified Laboratories
All Rainbow tests are performed at CAP (College of American Pathologists) accredited and CLIA (Clinical Laboratory Improvement Amendments) certified laboratories.
HIPAA/Patient Privacy
Patient data privacy – Rainbow follows the U.S. Health Insurance Portability and Accountability Act (HIPAA) privacy rules, established to protect the confidentiality of patients' individually identifiable health information.
Japanese Clinical Guidelines
Additional clinical interpretation provided by the Juntendo University Medical School is in compliance with Japan’s clinical testing guidelines
Operations
Operations
San Francisco
Rainbow Genomics maintains operations in the U.S. and Hong Kong.
Our English-speaking, Hong Kong-based project managers work closely with ordering physicians to collect patient samples, manage testing process, and coordinate physician report delivery.
Our partner laboratories, U.S. and Japanese medical institutions support the entire clinical testing process.
Hong Kong
Our genetic counselors and physician specialists provide multilingual (English with Japanese, Mandarin or Cantonese) genetic counseling to our patients, and consultation to physicians in local communities.
We’ve proudly partnered with doctors to improve patient care, delivering better, smarter, and more personalized treatment, making a real difference in the lives of patients!
Ownership
Rainbow Genomics is majority-owned by its management team and employees.
We maintain 100% freedom to develop high-quality and credible genetic tests for patients . We are committed to supporting physicians in local communities.