PULASki: Learning inter-rater variability using statistical distances to improve probabilistic segmentation
Soumick Chatterjee1, Franziska Gaidzik2, Alessandro Sciarra3
1Data and Knowledge Engineering Group, Faculty of Computer Science, Otto von Guericke University Magdeburg, Germany; Genomics Research Centre, Human Technopole, Milan, Italy.
Abstract:
In the domain of medical imaging, many supervised learning based methods for segmentation face several challenges such as high variability in annotations from multiple experts, paucity of labelled data and class imbalanced datasets. These issues may result in segmentations that lack the requisite precision for clinical analysis and can be misleadingly overconfident without associated uncertainty quantification. This work proposes the PULASki method as a computationally efficient generative tool for biomedical image segmentation that accurately captures variability in expert annotations, even in small datasets. This approach makes use of an improved loss function based on statistical distances in a conditional variational autoencoder structure (Probabilistic UNet) , which improves learning of the conditional decoder compared to the standard cross-entropy particularly in class imbalanced problems. The proposed method was analysed for two structurally different segmentation tasks (intracranial vessel and multiple sclerosis (MS) lesion) and compare our results to four well-established baselines in terms of quantitative metrics and qualitative output. These experiments involve class-imbalanced datasets characterised by challenging features, including suboptimal signal-to-noise ratios and high ambiguity. Empirical results demonstrate the PULASKi method outperforms all baselines at the 5% significance level. Our experiments are also of the first to present a comparative study of the computationally feasible segmentation of complex geometries using 3D patches and the traditional use of 2D slices. The generated segmentations are shown to be much more anatomically plausible than in the 2D case, particularly for the vessel task. Our method can also be applied to a wide range of multi-label segmentation tasks and is useful for downstream tasks such as hemodynamic modelling (computational fluid dynamics and data assimilation), clinical decision making, and treatment planning.
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