IVOct 5, 2023Code
How Good Are Synthetic Medical Images? An Empirical Study with Lung UltrasoundMenghan Yu, Sourabh Kulhare, Courosh Mehanian et al.
Acquiring large quantities of data and annotations is known to be effective for developing high-performing deep learning models, but is difficult and expensive to do in the healthcare context. Adding synthetic training data using generative models offers a low-cost method to deal effectively with the data scarcity challenge, and can also address data imbalance and patient privacy issues. In this study, we propose a comprehensive framework that fits seamlessly into model development workflows for medical image analysis. We demonstrate, with datasets of varying size, (i) the benefits of generative models as a data augmentation method; (ii) how adversarial methods can protect patient privacy via data substitution; (iii) novel performance metrics for these use cases by testing models on real holdout data. We show that training with both synthetic and real data outperforms training with real data alone, and that models trained solely with synthetic data approach their real-only counterparts. Code is available at https://github.com/Global-Health-Labs/US-DCGAN.
LGAug 5, 2019
Fully-automated patient-level malaria assessment on field-prepared thin blood film microscopy images, including Supplementary InformationCharles B. Delahunt, Mayoore S. Jaiswal, Matthew P. Horning et al.
Malaria is a life-threatening disease affecting millions. Microscopy-based assessment of thin blood films is a standard method to (i) determine malaria species and (ii) quantitate high-parasitemia infections. Full automation of malaria microscopy by machine learning (ML) is a challenging task because field-prepared slides vary widely in quality and presentation, and artifacts often heavily outnumber relatively rare parasites. In this work, we describe a complete, fully-automated framework for thin film malaria analysis that applies ML methods, including convolutional neural nets (CNNs), trained on a large and diverse dataset of field-prepared thin blood films. Quantitation and species identification results are close to sufficiently accurate for the concrete needs of drug resistance monitoring and clinical use-cases on field-prepared samples. We focus our methods and our performance metrics on the field use-case requirements. We discuss key issues and important metrics for the application of ML methods to malaria microscopy.