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Could federated data analysis be the catalyst accelerating the introduction of newborn genome screening for the detection of genetic disease?

Figure 1. An overview of how federated data analysis can be incorporated into an undiagnosed disease program targeting newborns to help enable secure data access across research laboratories and clinics worldwide. (A) The steps involved in diagnosing a rare disease in an affected newborn; (B) A summary of how federated data analysis is performed and the benefits that can be gained.

Rare Disease and Orphan Drugs Journal
ISSN 2771-2893 (Online)
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https://www.portico.org/publishers/oae/