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Thousands of patients participate in research studies to sequence their genes
Step 1
Patients are surveyed to understand their detailed health history and asked to upload their data.
Step 2
DNA and survey data is stored in biobanks along with health history records.
Step 3
Data scientists compare populations and their DNA to determine the likelihood of a disease.
Step 4
Government agencies review the results.
Step 5
The polygenic risks core is certified and published.
Step 6
Your health, guided by genetics.
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