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?
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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.
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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 |
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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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