Abstract:Computed tomography (CT) has been used worldwide for decades as one of the most important non-invasive tests in assisting diagnosis. However, the ionizing nature of X-ray exposure raises concerns about potential health risks such as cancer. The desire for lower radiation dose has driven researchers to improve the reconstruction quality, especially by removing noise and artifacts. Although previous studies on low-dose computed tomography (LDCT) denoising have demonstrated the potential of learning-based methods, most of them were developed on the simulated data collected using Radon transform. However, the real-world scenario significantly differs from the simulation domain, and the joint optimization of denoising with the modern CT image reconstruction pipeline is still missing. In this paper, for the commercially available third-generation multi-slice spiral CT scanners, we propose a two-stage method that better exploits the complete reconstruction pipeline for LDCT denoising across different domains. Our method makes good use of the high redundancy of both the multi-slice projections and the volumetric reconstructions while avoiding the collapse of information in conventional cascaded frameworks. The dedicated design also provides a clearer interpretation of the workflow. Through extensive evaluations, we demonstrate its superior performance against state-of-the-art methods.
Abstract:We present a novel methodology for control of neural circuits based on deep reinforcement learning. Our approach achieves aimed behavior by generating external continuous stimulation of existing neural circuits (neuromodulation control) or modulations of neural circuits architecture (connectome control). Both forms of control are challenging due to nonlinear and recurrent complexity of neural activity. To infer candidate control policies, our approach maps neural circuits and their connectome into a grid-world like setting and infers the actions needed to achieve aimed behavior. The actions are inferred by adaptation of deep Q-learning methods known for their robust performance in navigating grid-worlds. We apply our approach to the model of \textit{C. elegans} which simulates the full somatic nervous system with muscles and body. Our framework successfully infers neuropeptidic currents and synaptic architectures for control of chemotaxis. Our findings are consistent with in vivo measurements and provide additional insights into neural control of chemotaxis. We further demonstrate the generality and scalability of our methods by inferring chemotactic neural circuits from scratch.