SUNSHINE GENETICS
FREQUENTLY ASKED QUESTIONS (FAQs)
How is Sunshine Genetics different from standard newborn screening (NBS)?
Standard newborn screening uses a heel-prick blood sample to screen for 60 conditions in Florida. Newborn screening is part of the standard of care for all newborns born in the state of Florida. You can read more about the program here .
The Sunshine Genetics Program:
- Is an opt-in research program
- Screens a baby’s DNA, using whole genome sequencing, for over 750 rare genetic conditions
- Does not replace standard newborn screening
- If families choose not to participate, their baby will still receive routine newborn screening
Who can participate?
Enrollment has not begun, information will be coming soon. The Sunshine Genetics Program is for babies born in the State of Florida and residing in Florida.
Participation is optional, and biological parents or legal guardians must provide informed consent.
What happens if a family participates?
- A previously collected newborn heel-prick blood sample will be used
- The baby’s DNA will be analyzed for a defined list of genetic conditions
- Families are notified if a condition is suspected or if additional follow-up is needed
What kinds of genetic conditions are included?
Please review our “Gene-Conditions”tab.
Can parents choose which conditions are screened?
The study uses a predefined condition list to ensure consistency, accuracy, and research integrity. Tier 1 is not optional, but you may opt-in to Tier 2. However, our gene lists are dynamic and will evolve over time. Please refer to our “Gene-Conditions” tab for more information.
Can families withdraw consent later?
Yes. Parents may withdraw consent for future data use at any time, according to study policies.