What is this test?
Chronic diseases stem from an interaction between genes and the environment. Genes determine how susceptible we are to a disease. These tests are designed to identify 67 genes associated with chronic diseases and 24 genes linked to various types of cancer. They enable a quick and precise assessment of our genetic risks for developing a disease, providing evidence for the early detection and treatment of the disease.
What is it for?
                        Why is it needed?
- 
                                Screening for diseases
Knowing our genetic predispositions allows for the development of more personalized and tailored preventive measures including lifestyle modifications, routine health check-ups, and targeted screening for specific conditions. They are crucial for the early detection and treatment of diseases.
 - 
                                Personalized health management
Everyone can craft a health management plan covering diet, exercise, and the use of medications tailored to their own genetic makeup, to reduce health risks and live a longer life.
 
Specifications
Parameters  | Standards  | 
|---|---|
Enrichment method  | Multiplex PCR  | 
Compatible sequencers  | Illumina and MGI  | 
Number of genes  | 247  | 
Number of variants  | 277  | 
Variant type  | SNP  | 
Number of amplicons  | 275  | 
Length of amplicons  | 200-300 bp  | 
Number of pools  | 1  | 
Sample input amount  | 10-100 ng  | 
Sample types  | Oral swabs, saliva, blood, and DNA  | 
Library preparation time  | 4.5 hours  | 
Hands-on time  | < 1 hour  | 
Type of sequencing  | PE150  | 
Target designed rate  | 100%  | 
Coverage  | 100%  | 
> 0.2× mean depth (uniformity)  | > 90%  | 
On-target rate  | > 90%  | 
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