Research
Research Driving the Future of Newborn Screening
Sunshine Genetics is built on scientific research, clinical collaboration, and community engagement. Together, we’re helping shape the future of genomic newborn screening in Florida.
Why This Research Matters
Sunshine Genetics is a voluntary research program studying how whole-genome sequencing can safely and responsibly expand newborn screening in Florida. By working alongside healthcare providers, researchers, and families, the program aims to better understand how genomic screening can improve early detection of medically actionable genetic conditions.
The knowledge gained through this research will help guide future newborn screening programs while ensuring families receive accurate information and appropriate support.
Florida Supports Genomic Newborn Screening
Based on a statewide public opinion survey of Florida adults
Benefits outweigh risks
Most Floridians believe genomic newborn screening provides more benefits than risks.
Leading Innovation
Floridians are proud to help lead newborn screening research for rare diseases.
Future Parents Support
Most Floridians planning to have children are interested in genomic newborn screening.
Research Participation
Most Floridians support the use of de-identified genomic screening data to advance research.
Research That Supports Better Care
Scientific Research
Whole-genome sequencing helps researchers better understand genetic conditions that may benefit from earlier detection.
Clinical Collaboration
Researchers work closely with pediatric specialists, genetic counselors, and healthcare providers across Florida.
Improving the Future
Findings from the program may help shape future approaches to newborn screening and precision medicine.
Research Partners
