PHM001
Whole Genome Sequencing

Whole Genome Sequencing (WGS) is the most advanced, precise, medical-grade DNA testing technology available today. It comprehensively decodes 3 billion DNA base pairs, covering all human genes and non-coding regions, helping you fully understand your genetic code.

World-leading Whole Genome Analysis
Analysis of 3 billion DNA sequences per individual
One test, lifelong benefits
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Unlocking the secrets of your body

Top-tier US Medical Sequencing Technology

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iOmics AI

24/7 online Q&A, with a health management expert team to develop your personal plan

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Nearly 3,000 Real-life Cases

Integration of Eastern and Western Health Management. Personalized health management plans.

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Smart Monitoring

Supports wearable and remote health monitoring systems

Who Should Consider?

Whole Genome Sequencing (WGS) is the most advanced and precise next-generation DNA testing technology. It can comprehensively decode 3 billion DNA base pairs, covering all human genes and non-coding regions, allowing you to fully understand your genetic code.

Family Planning

• Couples preparing for pregnancy
• Couples with infertility issues
• Advanced maternal age
• IVF families

Family Medical History

• Hereditary diseases
• Cancers
• Cardiovascular diseases
• Metabolic diseases

Medication Guidance

• Abnormal drug responses
• Long-term medication
• Psychiatric medication users
• Cancer treatment patients

Health Concerns

• People with chronic illnesses
• Immune system disorders
• Frequent abnormal heart rhythms
• Those with recurrent infections

Genetic Sequencing Comparison

WGS is the most comprehensive genetic test on the market, covering 100% of the genome. Can detect over 8,000 known pathogenic variants, including common cancers (breast, ovarian, prostate), diabetes, Alzheimer's, Parkinson's, congenital heart diseases, and more. Provides the most complete health risk assessment.

SNP Genotyping

~500,000 to 5m

Base Pairs Covered

Only specific known points in genes

Advantages
Ancestry analysis
Carrier screening
Athletic talent
Nutrition advice
Fast turnaround
Whole Genome Sequencing (WGS)

3 billion

Base Pairs Covered

All parts of the genome, including often-ignored regions

Advantages
Includes all SNP and WES functions
Detects 8,000+ rare genetic diseases
Drug metabolism prediction
Cancer risk
New disease associations
Whole Exome Sequencing (WES)

30 million

Base Pairs Covered

Only protein-coding regions

Advantages
Genetic disease risk
Fertility planning
Personalized medicine
Family history
Basic Genetic Counselor
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