Deep learning-based diagnostic system for malignant liver detection

Cancer is the second most common cause of death of human beings, whereas liver cancer is the fifth most common cause of mortality. The prevention of deadly diseases in living beings requires timely, independent, accurate, and robust detection of ailment by a computer-aided diagnostic (CAD) system. Executing such intelligent CAD requires some preliminary steps, including preprocessing, attribute analysis, and identification. In recent studies, conventional techniques have been used to develop computer-aided diagnosis algorithms. However, such traditional methods could immensely affect the structural properties of processed images with inconsistent performance due to variable shape and size of region-of-interest. Moreover, the unavailability of sufficient datasets makes the performance of the proposed methods doubtful for commercial use. To address these limitations, I propose novel methodologies in this dissertation. First, I modified a generative adversarial network to perform deblurring and contrast adjustment on computed tomography (CT) scans. Second, I designed a deep neural network with a novel loss function for fully automatic precise segmentation of liver and lesions from CT scans. Third, I developed a multi-modal deep neural network to integrate pathological data with imaging data to perform computer-aided diagnosis for malignant liver detection. The dissertation starts with background information that discusses the proposed study objectives and the workflow. Afterward, Chapter 2 reviews a general schematic for developing a computer-aided algorithm, including image acquisition techniques, preprocessing steps, feature extraction approaches, and machine learning-based prediction methods. The first study proposed in Chapter 3 discusses blurred images and their possible effects on classification. A novel multi-scale GAN network with residual image learning is proposed to deblur images. The second method in Chapter 4 addresses the issue of low-contrast CT scan images. A multi-level GAN is utilized to enhance images with well-contrast regions. Thus, the enhanced images improve the cancer diagnosis performance. Chapter 5 proposes a deep neural network for the segmentation of liver and lesions from abdominal CT scan images. A modified Unet with a novel loss function can precisely segment minute lesions. Similarly, Chapter 6 introduces a multi-modal approach for liver cancer variants diagnosis. The pathological data are integrated with CT scan images to diagnose liver cancer variants. In summary, this dissertation presents novel algorithms for preprocessing and disease detection. Furthermore, the comparative analysis validates the effectiveness of proposed methods in computer-aided diagnosis

Development Of A High Performance Mosaicing And Super-Resolution Algorithm

In this dissertation, a high-performance mosaicing and super-resolution algorithm is described. The scale invariant feature transform (SIFT)-based mosaicing algorithm builds an initial mosaic which is iteratively updated by the robust super resolution algorithm to achieve the final high-resolution mosaic. Two different types of datasets are used for testing: high altitude balloon data and unmanned aerial vehicle data. To evaluate our algorithm, five performance metrics are employed: mean square error, peak signal to noise ratio, singular value decomposition, slope of reciprocal singular value curve, and cumulative probability of blur detection. Extensive testing shows that the proposed algorithm is effective in improving the captured aerial data and the performance metrics are accurate in quantifying the evaluation of the algorithm

High-resolution fluorescence endomicroscopy for rapid evaluation of breast cancer margins

Breast cancer is a major public health problem world-wide and the second leading cause of cancer-related female deaths. Breast conserving surgery (BCS), in the form of wide local excision (WLE), allows complete tumour resection while maintaining acceptable cosmesis. It is the recommended treatment for a large number of patients with early stage disease or, in more advanced cases, following neoadjuvant chemotherapy. About 30% of patients undergoing BCS require one or more re-operative interventions, mainly due to the presence of positive margins. The standard of care for surgical margin assessment is post-operative examination of histopathological tissue sections. However, this process is invasive, introduces sampling errors and does not provide real-time assessment of the tumour status of radial margins. The objective of this thesis is to improve intra-operative assessment of margin status by performing optical biopsy in breast tissue. This thesis presents several technical and clinical developments related to confocal fluorescence endomicroscopy systems for real-time characterisation of different breast morphologies. The imaging systems discussed employ flexible fibre-bundle based imaging probes coupled to high-speed line-scan confocal microscope set-up. A preliminary study on 43 unfixed breast specimens describes the development and testing of line-scan confocal laser endomicroscope (LS-CLE) to image and classify different breast pathologies. LS-CLE is also demonstrated to assess the intra-operative tumour status of whole WLE specimens and surgical excisions with high diagnostic accuracy. A third study demonstrates the development and testing of a bespoke LS-CLE system with methylene blue (MB), an US Food and Drug Administration (FDA) approved fluorescent agent, and integration with robotic scanner to enable large-area in vivo imaging of breast cancer. The work also addresses three technical issues which limit existing fibre-bundle based fluorescence endomicroscopy systems: i) Restriction to use single fluorescence agent due to low-speed, single excitation and single fluorescence spectral band imaging systems; ii) Limited Field of view (FOV) of fibre-bundle endomicroscopes due to small size of the fibre tip and iii) Limited spatial resolution of fibre-bundle endomicroscopes due to the spacing between the individual fibres leading to fibre-pixelation effects. Details of design and development of a high-speed dual-wavelength LS-CLE system suitable for high-resolution multiplexed imaging are presented. Dual-wavelength imaging is achieved by sequentially switching between 488 nm and 660 nm laser sources for alternate frames, avoiding spectral bleed-through, and providing an effective frame rate of 60 Hz. A combination of hand-held or robotic scanning with real-time video mosaicking, is demonstrated to enable large-area imaging while still maintaining microscopic resolution. Finally, a miniaturised piezoelectric transducer-based fibre-shifting endomicroscope is developed to enhance the resolution over conventional fibre-bundle based imaging systems. The fibre-shifting endomicroscope provides a two-fold improvement in resolution and coupled to a high-speed LS-CLE scanning system, provides real-time imaging of biological samples at 30 fps. These investigations furthered the utility and applications of the fibre-bundle based fluorescence systems for rapid imaging and diagnosis of cancer margins.Open Acces

Explainable Artificial Intelligence for Image Segmentation and for Estimation of Optical Aberrations

State-of-the-art machine learning methods such as convolutional neural networks (CNNs) are frequently employed in computer vision. Despite their high performance on unseen data, CNNs are often criticized for lacking transparency — that is, providing very limited if any information about the internal decision-making process. In some applications, especially in healthcare, such transparency of algorithms is crucial for end users, as trust in diagnosis and prognosis is important not only for the satisfaction and potential adherence of patients, but also for their health. Explainable artificial intelligence (XAI) aims to open up this “black box,” often perceived as a cryptic and inconceivable algorithm, to increase understanding of the machines’ reasoning.XAI is an emerging field, and techniques for making machine learning explainable are becoming increasingly available. XAI for computer vision mainly focuses on image classification, whereas interpretability in other tasks remains challenging. Here, I examine explainability in computer vision beyond image classification, namely in semantic segmentation and 3D multitarget image regression. This thesis consists of five chapters. In Chapter 1 (Introduction), the background of artificial intelligence (AI), XAI, computer vision, and optics is presented, and the definitions of the terminology for XAI are proposed. Chapter 2 is focused on explaining the predictions of U-Net, a CNN commonly used for semantic image segmentation, and variations of this architecture. To this end, I propose the gradient-weighted class activation mapping for segmentation (Seg-Grad-CAM) method based on the well-known Grad-CAM method for explainable image classification. In Chapter 3, I present the application of deep learning to estimation of optical aberrations in microscopy biodata by identifying the present Zernike aberration modes and their amplitudes. A CNN-based approach PhaseNet can accurately estimate monochromatic aberrations in images of point light sources. I extend this method to objects of complex shapes. In Chapter 4, an approach for explainable 3D multitarget image regression is reported. First, I visualize how the model differentiates the aberration modes using the local interpretable model-agnostic explanations (LIME) method adapted for 3D image classification. Then I “explain,” using LIME modified for multitarget 3D image regression (Image-Reg-LIME), the outputs of the regression model for estimation of the amplitudes. In Chapter 5, the results are discussed in a broader context. The contribution of this thesis is the development of explainability methods for semantic segmentation and 3D multitarget image regression of optical aberrations. The research opens the door for further enhancement of AI’s transparency.:Title Page i List of Figures xi List of Tables xv 1 Introduction 1 1.1 Essential Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 1.1.1 Artificial intelligence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 1.1.2 Explainable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 1.1.3 Proposed definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 1.2 Explainable Artificial Intelligence . . . . . . . . . . . . . . . . . . . . . . . . . . 6 1.2.1 Aims and applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 1.2.2 Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 1.3 Computer Vision . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 1.3.1 Applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 1.3.2 Image classification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11 1.3.3 Image regression . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 1.3.4 Image segmentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 1.4 Optics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 1.4.1 Aberrations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 1.4.2 Zernike polynomials . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17 1.5 Thesis Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 1.5.1 Motivation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 1.5.2 Dissertation outline . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 2 Explainable Image Segmentation 23 2.1 Abstract . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23 2.2 Related Work . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24 2.3 Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26 2.3.1 CAM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26 2.3.2 Grad-CAM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27 2.3.3 U-Net . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29 2.3.4 Seg-Grad-CAM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30 2.4 Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36 2.4.1 Circles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36 2.4.2 TextureMNIST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36 2.4.3 Cityscapes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37 2.5 Results . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39 2.5.1 Circles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39 2.5.2 TextureMNIST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41 2.5.3 Cityscapes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47 2.6 Applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51 2.7 Conclusions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52 3 Estimation of Aberrations 55 3.1 Abstract . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55 3.2 Related Work . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56 3.3 Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58 3.3.1 PhaseNet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58 3.3.2 PhaseNet data generator . . . . . . . . . . . . . . . . . . . . . . . . . . . 59 3.3.3 Retrieval of noise parameters . . . . . . . . . . . . . . . . . . . . . . . . 62 3.3.4 Data generator with phantoms . . . . . . . . . . . . . . . . . . . . . . . 62 3.3.5 Restoration via deconvolution . . . . . . . . . . . . . . . . . . . . . . . . 63 3.3.6 Convolution with the “zero” synthetic PSF . . . . . . . . . . . . . . . . 63 3.4 Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64 3.4.1 Astrocytes (synthetic data) . . . . . . . . . . . . . . . . . . . . . . . . . 65 3.4.2 Fluorescent beads . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66 3.4.3 Drosophila embryo (live sample) . . . . . . . . . . . . . . . . . . . . . . 67 3.4.4 Neurons (fixed sample) . . . . . . . . . . . . . . . . . . . . . . . . . . . 68 3.5 Results . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69 3.5.1 Astrocytes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69 3.5.2 Conclusions on the results for astrocytes . . . . . . . . . . . . . . . . . . 74 3.5.3 Fluorescent beads . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75 3.5.4 Conclusions on the results for fluorescent beads . . . . . . . . . . . . . . 81 3.5.5 Drosophila embryo . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83 3.5.6 Conclusions on the results for Drosophila embryo . . . . . . . . . . . . . 87 3.5.7 Neurons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88 3.6 Conclusions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96 4 Explainable Multitarget Image Regression 99 4.1 Abstract . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99 4.2 Related Work . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100 4.3 Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 102 4.3.1 LIME . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 102 4.3.2 Superpixel algorithms . . . . . . . . . . . . . . . . . . . . . . . . . . . . 104 4.3.3 LIME for 3D image classification . . . . . . . . . . . . . . . . . . . . . . 104 4.3.4 Image-Reg-LIME: LIME for 3D image regression . . . . . . . . . . . . . 107 4.4 Results: Classification of Aberrations . . . . . . . . . . . . . . . . . . . . . . . . 109 viii TABLE OF CONTENTS 4.4.1 Transforming the regression task into classification . . . . . . . . . . . . 110 4.4.2 Data augmentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 111 4.4.3 Parameter search . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 112 4.4.4 Clustering of 3D images . . . . . . . . . . . . . . . . . . . . . . . . . . . 114 4.4.5 Explanations of classification . . . . . . . . . . . . . . . . . . . . . . . . 114 4.4.6 Conclusions on the results for classification . . . . . . . . . . . . . . . . 117 4.5 Results: Explainable Regression of Aberrations . . . . . . . . . . . . . . . . . . 118 4.5.1 Explanations with a reference value . . . . . . . . . . . . . . . . . . . . 121 4.5.2 Validation of explanations . . . . . . . . . . . . . . . . . . . . . . . . . . 122 4.6 Conclusions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 125 5 Conclusions and Outlook 127 References 12

Development and application of molecular and computational tools to image copper in cells

Copper is a trace element which is essential for many biological processes. A deficiency or excess of copper(I) ions, which is its main oxidation state of copper in cellular environment, is increasingly linked to the development of neurodegenerative diseases such as Parkinson’s and Alzheimer’s disease (PD and AD). The regulatory mechanisms for copper(I) are under active investigation and lysosomes which are best known as cellular “incinerators” have been found to play an important role in the trafficking of copper inside the cell. Therefore, it is important to develop reliable experimental methods to detect, monitor and visualise this metal in cells and to develop tools that allow to improve the data quality of microscopy recordings. This would enable the detailed exploration of cellular processes related to copper trafficking through lysosomes. The research presented in this thesis aimed to develop chemical and computational tools that can help to investigate concentration changes of copper(I) in cells (particularly in lysosomes), and it presents a preliminary case study that uses the here developed microscopy image quality enhancement tools to investigate lysosomal mobility changes upon treatment of cells with different PD or AD drugs. Chapter I first reports the synthesis of a previously reported copper(I) probe (CS3). The photophysical properties of this probe and functionality on different cell lines was tested and it was found that this copper(I) sensor predominantly localized in lipid droplets and that its photostability and quantum yield were insufficient to be applied for long term investigations of cellular copper trafficking. Therefore, based on the insights of this probe a new copper(I) selective fluorescent probe (FLCS1) was designed, synthesized, and characterized which showed superior photophysical properties (photostability, quantum yield) over CS3. The probe showed selectivity for copper(I) over other physiological relevant metals and showed strong colocalization in lysosomes in SH-SY5Y cells. This probe was then used to study and monitor lysosomal copper(I) levels via fluorescence lifetime imaging microscopy (FLIM); to the best of my knowledge this is the first copper(I) probe based on emission lifetime. Chapter II explores different computational deep learning approaches for improving the quality of recorded microscopy images. In total two existing networks were tested (fNET, CARE) and four new networks were implemented, tested, and benchmarked for their capabilities of improving the signal-to-noise ratio, upscaling the image size (GMFN, SRFBN-S, Zooming SlowMo) and interpolating image sequences (DAIN, Zooming SlowMo) in z- and t-dimension of multidimensional simulated and real-world datasets. The best performing networks of each category were then tested in combination by sequentially applying them on a low signal-to-noise ratio, low resolution, and low frame-rate image sequence. This image enhancement workstream for investigating lysosomal mobility was established. Additionally, the new frame interpolation networks were implemented in user-friendly Google Colab notebooks and were made publicly available to the scientific community on the ZeroCostDL4Mic platform. Chapter III provides a preliminary case study where the newly developed fluorescent copper(I) probe in combination with the computational enhancement algorithms was used to investigate the effects of five potential Parkinson’s disease drugs (rapamycin, digoxin, curcumin, trehalose, bafilomycin A1) on the mobility of lysosomes in live cells.Open Acces

Biological image analysis

In biological research images are extensively used to monitor growth, dynamics and changes in biological specimen, such as cells or plants. Many of these images are used solely for observation or are manually annotated by an expert. In this dissertation we discuss several methods to automate the annotating and analysis of bio-images. Two large clusters of methods have been investigated and developed. A first set of methods focuses on the automatic delineation of relevant objects in bio-images, such as individual cells in microscopic images. Since these methods should be useful for many different applications, e.g. to detect and delineate different objects (cells, plants, leafs, ...) in different types of images (different types of microscopes, regular colour photographs, ...), the methods should be easy to adjust. Therefore we developed a methodology relying on probability theory, where all required parameters can easily be estimated by a biologist, without requiring any knowledge on the techniques used in the actual software. A second cluster of investigated techniques focuses on the analysis of shapes. By defining new features that describe shapes, we are able to automatically classify shapes, retrieve similar shapes from a database and even analyse how an object deforms through time