Distribution Matching : Semi-Supervised Feature Selection for Biased Labelled Data

In the context of data science and machine learning, feature selection is a widely used technique that focuses on reducing the dimensionality of a dataset. It is commonly used to improve model accuracy by preventing data redundancy and over-fitting, but can also be beneficial in applications such as data compression. The majority of feature selection techniques rely on labelled data. In many real-world scenarios, however, data is only partially labelled and thus requires so-called semi-supervised techniques, which can utilise both labelled and unlabelled data. While unlabelled data is often obtainable in abundance, labelled datasets are smaller and potentially biased. This thesis presents a method called distribution matching, which offers a way to do feature selection in a semi-supervised setup. Distribution matching is a wrapper method, which trains models to select features that best affect model accuracy. It addresses the problem of biased labelled data directly by incorporating unlabelled data into a cost function which approximates expected loss on unseen data. In experiments, the method is shown to successfully minimise the expected loss transparently on a synthetic dataset. Additionally, a comparison with related methods is performed on a more complex EMNIST dataset

Explainable cardiac pathology classification on cine MRI with motion characterization by semi-supervised learning of apparent flow

We propose a method to classify cardiac pathology based on a novel approach to extract image derived features to characterize the shape and motion of the heart. An original semi-supervised learning procedure, which makes efficient use of a large amount of non-segmented images and a small amount of images segmented manually by experts, is developed to generate pixel-wise apparent flow between two time points of a 2D+t cine MRI image sequence. Combining the apparent flow maps and cardiac segmentation masks, we obtain a local apparent flow corresponding to the 2D motion of myocardium and ventricular cavities. This leads to the generation of time series of the radius and thickness of myocardial segments to represent cardiac motion. These time series of motion features are reliable and explainable characteristics of pathological cardiac motion. Furthermore, they are combined with shape-related features to classify cardiac pathologies. Using only nine feature values as input, we propose an explainable, simple and flexible model for pathology classification. On ACDC training set and testing set, the model achieves 95% and 94% respectively as classification accuracy. Its performance is hence comparable to that of the state-of-the-art. Comparison with various other models is performed to outline some advantages of our model