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How AI is Transforming Rare Disease Diagnosis
Clinithink’s founder and CEO, Chris Tackaberry shares his insights on how AI is transforming rare disease diagnosis.
Chris tackaberry
Rady children institute of genomic medicine
Transforming rare disease diagnosis
Whole genome sequencing
Human phenotype ontology
Electronic medical record
Rady children
Genomic medicine
New england journal
Clinical natural language processing
Orphan drugs act
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