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Performance and clinical utility of a new supervised machine-learning pipeline in detecting rare ciliopathy patients based on deep phenotyping from electronic health records and semantic similarity.

Carole FaviezMarc VincentNicolas GarcelonOlivia BoyerBertrand KnebelmannLaurence HeidetSophie SaunierXiaoyi ChenAnita Burgun
Published in: Orphanet journal of rare diseases (2024)
Our pipeline reached very encouraging performance scores for pre-diagnosing ciliopathy patients. The identified patients could then undergo genetic testing. The same data-driven approach can be adapted to other rare diseases facing underdiagnosis challenges.
Keyphrases
  • end stage renal disease
  • machine learning
  • ejection fraction
  • chronic kidney disease
  • newly diagnosed
  • electronic health record
  • patient reported
  • high throughput