Support the future of rare disease diagnostics
Your donation helps unlock life-saving answers hidden in our DNA—bringing hope to newborns and families affected by rare genetic conditions. By supporting whole genome sequencing research, you're fueling breakthroughs in early detection and diagnosis, often before symptoms appear. Together, we’re transforming newborn screening and building a future where no child’s condition goes undetected—and every genome tells a story of hope.
Disclaimer: Versailles Boutique is a small business and not a registered 501(c)(3) nonprofit organization. As such, donations made through this page are not tax-deductible under U.S. law. All contributions will be forwarded in full to a local research institute to support their groundbreaking work in whole genome sequencing research, with a focus on newborn screening and rare disease diagnostics. We deeply appreciate your generosity and commitment to advancing genomic medicine. If you have any questions about your donation or how funds are allocated, feel free to contact me directly.
How your contribution makes a difference
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Accelerates Research: Funds cutting-edge studies to validate whole genome sequencing as a reliable tool in early diagnostics.
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Improves Technology: Supports development of faster, more accurate sequencing methods tailored for newborns.
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Expands Data Analysis: Enables advanced bioinformatics to interpret complex genetic data and identify rare conditions.
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Enhances Clinical Integration: Helps hospitals and labs incorporate genome sequencing into routine newborn screening programs.
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Empowers Families: Provides resources and support for families navigating rare disease diagnoses.
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Trains Experts: Invests in education for genetic counselors, pediatricians, and researchers to improve care and communication.
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