Rare Disease Detection by Sequence Modeling with Generative Adversarial Networks
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Abstract (arXiv)
Rare diseases affecting 350 million individuals are commonly associated with delay in diagnosis or misdiagnosis. To improve those patients' outcome, rare disease detection is an important task for identifying patients with rare conditions based on longitudinal medical claims. In this paper, we present a deep learning method for detecting patients with exocrine pancreatic insufficiency (EPI) (a rare disease). The contribution includes 1) a large longitudinal study using 7 years medical claims from 1.8 million patients including 29,149 EPI patients, 2) a new deep learning model using generative adversarial networks (GANs) to boost rare disease class, and also leveraging recurrent neural networks to model patient sequence data, 3) an accurate prediction with 0.56 PR-AUC which outperformed benchmark models in terms of precision and recall.
Key facts. Cited by 3 papers in the map (data through 14 Oct 2026). First posted on arXiv 1 Jul 2019.
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Citing papers per year: 2022: 1; 2023: 1; 2024: 1.
3 papers.
- 2022A review of Generative Adversarial Networks for Electronic Health Records: applications, evaluation measures and data sourcescited by 13
- 2024Efficient Semantic Diffusion Architectures for Model Training on Synthetic Echocardiogramscited by 1
- 2023ComplicaCode: Enhancing Disease Complication Detection in Electronic Health Records through ICD Path Generationcited by 0
- 2024Efficient Semantic Diffusion Architectures for Model Training on Synthetic Echocardiograms28 Sep 2024
- 2023ComplicaCode: Enhancing Disease Complication Detection in Electronic Health Records through ICD Path Generation15 Dec 2023
- 2022A review of Generative Adversarial Networks for Electronic Health Records: applications, evaluation measures and data sources14 Mar 2022