Our core mission is to make clinically actionable genomics solutions available and accessible to all families. Enabling early diagnosis of clinical conditions for proactive management and providing families peace of mind.
We are commited to empowering families with advanced pediatric genetic insights, fostering confidence, inclusivity, and peace of mind to help every child thrive with personalized health care.
We are dedicated to supporting families with understanding and care, offering a comforting andc empathetic experience as they navigate their child's health journey.
We empower parents with clear, actionable insights and personalized genetic health information, enabling them to make informed decisions and advocate confidently for their child's well-being.
We are committed to serving all families, embracing diverse backgrounds, cultures, and identities to ensure every parent feels valued, respected, and included.
We strive for excellence in pediatric genetic screening, using state-of-the-art technology and evidence-based practices to provide the most accurate and reliable insights for proactive health management.
Fore and its network of partners are committed to advancing personalized healthcare by delivering the highest quality service. Together, they provide expertise in sequencing, analysis, genetic counseling, clinical planning, security, and privacy.
Fore has assembled a team of professionals and partners to help improve the lives of children and make healthcare more proactive.
Fore Genomics, established by a group of life science executives, seeks to translate genomic research advances into clinical applications.
Our team of professionals and partners aims to bridge the gap between genomic potential and preventive health, providing families with personalized healthcare solutions to proactively improve children's lives.