FAQs
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• Genes are made of DNA. Genes help determine how we look, like eye color and hair color, and give instructions to help our bodies function.
• Genome sequencing is a lab test that looks at all of someone’s DNA and can help find changes that cause health risks.
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• All families will meet with a doctor or genetic counselor to talk about any health problems in their family. This information can help prevent or treat some health problems.
• Half of babies, chosen at random, will have genome sequencing.
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• About 4 months after your first study visit, you will meet with a doctor or genetic counselor.
• These providers will make recommendations for you and your baby to stay as healthy as possible.
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• You will be in the study for at least 1 year.
• The study visits and surveys will take about 3 hours total.
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• There is no cost to be in the study.
• You will receive up to $150.
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Parents or guardians of any baby under 6 months old, IF:
• You speak English or Spanish.
• You are over 18 years old.
• Your baby’s doctor has already joined the study at one of our participating clinics.