The INFANT Study

INFANT is a Canadian research study looking at a new kind of newborn screening using DNA, called genomic newborn screening (gNBS). This screening test looks at a baby’s DNA to find rare genetic conditions early in life. Finding these conditions early can help infants get the care and treatment they need sooner. 

The study uses the same blood sample collected for standard newborn screening and uses next-generation sequencing to screen for more than 200 conditions. Earlier identification may allow babies to receive treatment, monitoring or other care before symptoms develop.

The research will help inform the future of newborn screening in Ontario and how genomic approaches could support earlier, more targeted care for babies and children.

Learn more about the INFANT Study and how to participate.