マーカーレス腫瘍位置決めを目的とした深層学習に基づく患者固有標的輪郭予測モデルの開発

京都大学新制・課程博士博士(人間健康科学)甲第24542号人健博第113号新制||人健||8(附属図書館)京都大学大学院医学研究科人間健康科学系専攻(主査)教授 中尾 恵, 教授 杉本 直三, 教授 黒田 知宏学位規則第4条第1項該当Doctor of Human Health SciencesKyoto UniversityDFA

A scalable parallel finite element framework for growing geometries. Application to metal additive manufacturing

This work introduces an innovative parallel, fully-distributed finite element framework for growing geometries and its application to metal additive manufacturing. It is well-known that virtual part design and qualification in additive manufacturing requires highly-accurate multiscale and multiphysics analyses. Only high performance computing tools are able to handle such complexity in time frames compatible with time-to-market. However, efficiency, without loss of accuracy, has rarely held the centre stage in the numerical community. Here, in contrast, the framework is designed to adequately exploit the resources of high-end distributed-memory machines. It is grounded on three building blocks: (1) Hierarchical adaptive mesh refinement with octree-based meshes; (2) a parallel strategy to model the growth of the geometry; (3) state-of-the-art parallel iterative linear solvers. Computational experiments consider the heat transfer analysis at the part scale of the printing process by powder-bed technologies. After verification against a 3D benchmark, a strong-scaling analysis assesses performance and identifies major sources of parallel overhead. A third numerical example examines the efficiency and robustness of (2) in a curved 3D shape. Unprecedented parallelism and scalability were achieved in this work. Hence, this framework contributes to take on higher complexity and/or accuracy, not only of part-scale simulations of metal or polymer additive manufacturing, but also in welding, sedimentation, atherosclerosis, or any other physical problem where the physical domain of interest grows in time

Automating the Reconstruction of Neuron Morphological Models: the Rivulet Algorithm Suite

The automatic reconstruction of single neuron cells is essential to enable large-scale data-driven investigations in computational neuroscience. The problem remains an open challenge due to various imaging artefacts that are caused by the fundamental limits of light microscopic imaging. Few previous methods were able to generate satisfactory neuron reconstruction models automatically without human intervention. The manual tracing of neuron models is labour heavy and time-consuming, making the collection of large-scale neuron morphology database one of the major bottlenecks in morphological neuroscience. This thesis presents a suite of algorithms that are developed to target the challenge of automatically reconstructing neuron morphological models with minimum human intervention. We first propose the Rivulet algorithm that iteratively backtracks the neuron fibres from the termini points back to the soma centre. By refining many details of the Rivulet algorithm, we later propose the Rivulet2 algorithm which not only eliminates a few hyper-parameters but also improves the robustness against noisy images. A soma surface reconstruction method was also proposed to make the neuron models biologically plausible around the soma body. The tracing algorithms, including Rivulet and Rivulet2, normally need one or more hyper-parameters for segmenting the neuron body out of the noisy background. To make this pipeline fully automatic, we propose to use 2.5D neural network to train a model to enhance the curvilinear structures of the neuron fibres. The trained neural networks can quickly highlight the fibres of interests and suppress the noise points in the background for the neuron tracing algorithms. We evaluated the proposed methods in the data released by both the DIADEM and the BigNeuron challenge. The experimental results show that our proposed tracing algorithms achieve the state-of-the-art results

Seasonal Arctic sea ice forecasting with probabilistic deep learning

Anthropogenic warming has led to an unprecedented year-round reduction in Arctic sea ice extent. This has far-reaching consequences for indigenous and local communities, polar ecosystems, and global climate, motivating the need for accurate seasonal sea ice forecasts. While physics-based dynamical models can successfully forecast sea ice concentration several weeks ahead, they struggle to outperform simple statistical benchmarks at longer lead times. We present a probabilistic, deep learning sea ice forecasting system, IceNet. The system has been trained on climate simulations and observational data to forecast the next 6 months of monthly-averaged sea ice concentration maps. We show that IceNet advances the range of accurate sea ice forecasts, outperforming a state-of-the-art dynamical model in seasonal forecasts of summer sea ice, particularly for extreme sea ice events. This step-change in sea ice forecasting ability brings us closer to conservation tools that mitigate risks associated with rapid sea ice loss

Méthodes multi-organes rapides avec a priori de forme pour la localisation et la segmentation en imagerie médicale 3D

With the ubiquity of imaging in medical applications (diagnostic, treatment follow-up, surgery planning. . . ), image processing algorithms have become of primary importance. Algorithms help clinicians extract critical information more quickly and more reliably from increasingly large and complex acquisitions. In this context, anatomy localization and segmentation is a crucial component in modern clinical workflows. Due to particularly high requirements in terms of robustness, accuracy and speed, designing such tools remains a challengingtask.In this work, we propose a complete pipeline for the segmentation of multiple organs in medical images. The method is generic, it can be applied to varying numbers of organs, on different imaging modalities. Our approach consists of three components: (i) an automatic localization algorithm, (ii) an automatic segmentation algorithm, (iii) a framework for interactive corrections. We present these components as a coherent processing chain, although each block could easily be used independently of the others. To fulfill clinical requirements, we focus on robust and efficient solutions. Our anatomy localization method is based on a cascade of Random Regression Forests (Cuingnet et al., 2012). One key originality of our work is the use of shape priors for each organ (thanks to probabilistic atlases). Combined with the evaluation of the trained regression forests, they result in shape-consistent confidence maps for each organ instead of simple bounding boxes. Our segmentation method extends the implicit template deformation framework of Mory et al. (2012) to multiple organs. The proposed formulation builds on the versatility of the original approach and introduces new non-overlapping constraintsand contrast-invariant forces. This makes our approach a fully automatic, robust and efficient method for the coherent segmentation of multiple structures. In the case of imperfect segmentation results, it is crucial to enable clinicians to correct them easily. We show that our automatic segmentation framework can be extended with simple user-driven constraints to allow for intuitive interactive corrections. We believe that this final component is key towards the applicability of our pipeline in actual clinical routine.Each of our algorithmic components has been evaluated on large clinical databases. We illustrate their use on CT, MRI and US data and present a user study gathering the feedback of medical imaging experts. The results demonstrate the interest in our method and its potential for clinical use.Avec l’utilisation de plus en plus répandue de l’imagerie dans la pratique médicale (diagnostic, suivi, planification d’intervention, etc.), le développement d’algorithmes d’analyse d’images est devenu primordial. Ces algorithmes permettent aux cliniciens d’analyser et d’interpréter plus facilement et plus rapidement des données de plus en plus complexes. Dans ce contexte, la localisation et la segmentation de structures anatomiques sont devenues des composants critiques dans les processus cliniques modernes. La conception de tels outils pour répondre aux exigences de robustesse, précision et rapidité demeure cependant un réel défi technique.Ce travail propose une méthode complète pour la segmentation de plusieurs organes dans des images médicales. Cette méthode, générique et pouvant être appliquée à un nombre varié de structures et dans différentes modalités d’imagerie, est constituée de trois composants : (i) un algorithme de localisation automatique, (ii) un algorithme de segmentation, (iii) un outil de correction interactive. Ces différentes parties peuvent s’enchaîner aisément pour former un outil complet et cohérent, mais peuvent aussi bien être utilisées indépendemment. L’accent a été mis sur des méthodes robustes et efficaces afin de répondre aux exigences cliniques. Notre méthode de localisation s’appuie sur une cascade de régression par forêts aléatoires (Cuingnet et al., 2012). Elle introduit l’utilisation d’informations a priori de forme, spécifiques à chaque organe (grâce à des atlas probabilistes) pour des résultats plus cohérents avec la réalité anatomique. Notre méthode de segmentation étend la méthode de segmentation par modèle implicite (Mory et al., 2012) à plusieurs modèles. La formulation proposée permet d’obtenir des déformations cohérentes, notamment en introduisant des contraintes de non recouvrement entre les modèles déformés. En s’appuyant sur des forces images polyvalentes, l’approche proposée se montre robuste et performante pour la segmentation de multiples structures. Toute méthode automatique n’est cependant jamais parfaite. Afin que le clinicien garde la main sur le résultat final, nous proposons d’enrichir la formulation précédente avec des contraintes fournies par l’utilisateur. Une optimisation localisée permet d’obtenir un outil facile à utiliser et au comportement intuitif. Ce dernier composant est crucial pour que notre outil soit réellement utilisable en pratique. Chacun de ces trois composants a été évalué sur plusieurs grandes bases de données cliniques (en tomodensitométrie, imagerie par résonance magnétique et ultrasons). Une étude avec des utilisateurs nous a aussi permis de recueillir des retours positifs de plusieurs experts en imagerie médicale. Les différents résultats présentés dans ce manuscrit montrent l’intérêt de notre méthode et son potentiel pour une utilisation clinique

Nonrigid reconstruction of 3D breast surfaces with a low-cost RGBD camera for surgical planning and aesthetic evaluation

Accounting for 26% of all new cancer cases worldwide, breast cancer remains the most common form of cancer in women. Although early breast cancer has a favourable long-term prognosis, roughly a third of patients suffer from a suboptimal aesthetic outcome despite breast conserving cancer treatment. Clinical-quality 3D modelling of the breast surface therefore assumes an increasingly important role in advancing treatment planning, prediction and evaluation of breast cosmesis. Yet, existing 3D torso scanners are expensive and either infrastructure-heavy or subject to motion artefacts. In this paper we employ a single consumer-grade RGBD camera with an ICP-based registration approach to jointly align all points from a sequence of depth images non-rigidly. Subtle body deformation due to postural sway and respiration is successfully mitigated leading to a higher geometric accuracy through regularised locally affine transformations. We present results from 6 clinical cases where our method compares well with the gold standard and outperforms a previous approach. We show that our method produces better reconstructions qualitatively by visual assessment and quantitatively by consistently obtaining lower landmark error scores and yielding more accurate breast volume estimates