In this work, we present a method for synthetic CT (sCT) generation from zero-echo-time (ZTE) MRI aimed at structural and quantitative accuracies of the image, with a particular focus on the accurate bone density value prediction. We propose a loss function that favors a spatially sparse region in the image. We harness the ability of a multi-task network to produce correlated outputs as a framework to enable localisation of region of interest (RoI) via classification, emphasize regression of values within RoI and still retain the overall accuracy via global regression. The network is optimized by a composite loss function that combines a dedicated loss from each task. We demonstrate how the multi-task network with RoI focused loss offers an advantage over other configurations of the network to achieve higher accuracy of performance. This is relevant to sCT where failure to accurately estimate high Hounsfield Unit values of bone could lead to impaired accuracy in clinical applications. We compare the dose calculation maps from the proposed sCT and the real CT in a radiation therapy treatment planning setup.
We consider the problem of automatically prescribing oblique planes (short axis, 4 chamber and 2 chamber views) in Cardiac Magnetic Resonance Imaging (MRI). A concern with technologist-driven acquisitions of these planes is the quality and time taken for the total examination. We propose an automated solution incorporating anatomical features external to the cardiac region. The solution uses support vector machine regression models wherein complexity and feature selection are optimized using multi-objective genetic algorithms. Additionally, we examine the robustness of our approach by training our models on images with additive Rician-Gaussian mixtures at varying Signal to Noise (SNR) levels. Our approach has shown promising results, with an angular deviation of less than 15 degrees on 90% cases across oblique planes, measured in terms of average 6-fold cross validation performance -- this is generally within acceptable bounds of variation as specified by clinicians.