Learn Image Object Co-segmentation with Multi-scale Feature Fusion

© 2019 IEEE. Image object co-segmentation aims to segment common objects in a group of images. This paper proposes a novel neural network, which extracts multi-scale convolutional features at multiple layers via a modified VGG network and fuses them both within and across images as the intra-image and the inter-image features. Then these two kinds of features are further fused at each scale as the multi-scale co-features of common objects, and finally the multi-scale co-features are summed up and upsampled to obtain the co-segmentation results. To simplify the network and reduce the rapidly rising resource cost along with the inputs, the reduced input size, less downsampling and dilation convolution are adopted in the proposed model. Experimental results on the public dataset demonstrate that the proposed model achieves a comparable performance to the state-of-The-Art co-segmentation methods while the computation cost has been effectively reduced

Graph learning and its applications : a thesis presented in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Computer Science, Massey University, Albany, Auckland, New Zealand

Since graph features consider the correlations between two data points to provide high-order information, i.e., more complex correlations than the low-order information which considers the correlations in the individual data, they have attracted much attention in real applications. The key of graph feature extraction is the graph construction. Previous study has demonstrated that the quality of the graph usually determines the effectiveness of the graph feature. However, the graph is usually constructed from the original data which often contain noise and redundancy. To address the above issue, graph learning is designed to iteratively adjust the graph and model parameters so that improving the quality of the graph and outputting optimal model parameters. As a result, graph learning has become a very popular research topic in traditional machine learning and deep learning. Although previous graph learning methods have been applied in many fields by adding a graph regularization to the objective function, they still have some issues to be addressed. This thesis focuses on the study of graph learning aiming to overcome the drawbacks in previous methods for different applications. We list the proposed methods as follows. • We propose a traditional graph learning method under supervised learning to consider the robustness and the interpretability of graph learning. Specifically, we propose utilizing self-paced learning to assign important samples with large weights, conducting feature selection to remove redundant features, and learning a graph matrix from the low dimensional data of the original data to preserve the local structure of the data. As a consequence, both important samples and useful features are used to select support vectors in the SVM framework. • We propose a traditional graph learning method under semi-supervised learning to explore parameter-free fusion of graph learning. Specifically, we first employ the discrete wavelet transform and Pearson correlation coefficient to obtain multiple fully connected Functional Connectivity brain Networks (FCNs) for every subject, and then learn a sparsely connected FCN for every subject. Finally, the ℓ1-SVM is employed to learn the important features and conduct disease diagnosis. • We propose a deep graph learning method to consider graph fusion of graph learning. Specifically, we first employ the Simple Linear Iterative Clustering (SLIC) method to obtain multi-scale features for every image, and then design a new graph fusion method to fine-tune features of every scale. As a result, the multi-scale feature fine-tuning, graph learning, and feature learning are embedded into a unified framework. All proposed methods are evaluated on real-world data sets, by comparing to state-of-the-art methods. Experimental results demonstrate that our methods outperformed all comparison methods

Texture and Colour in Image Analysis

Research in colour and texture has experienced major changes in the last few years. This book presents some recent advances in the field, specifically in the theory and applications of colour texture analysis. This volume also features benchmarks, comparative evaluations and reviews

Content-aware approach for improving biomedical image analysis: an interdisciplinary study series

Biomedicine is a highly interdisciplinary research area at the interface of sciences, anatomy, physiology, and medicine. In the last decade, biomedical studies have been greatly enhanced by the introduction of new technologies and techniques for automated quantitative imaging, thus considerably advancing the possibility to investigate biological phenomena through image analysis. However, the effectiveness of this interdisciplinary approach is bounded by the limited knowledge that a biologist and a computer scientist, by professional training, have of each other’s fields. The possible solution to make up for both these lacks lies in training biologists to make them interdisciplinary researchers able to develop dedicated image processing and analysis tools by exploiting a content-aware approach. The aim of this Thesis is to show the effectiveness of a content-aware approach to automated quantitative imaging, by its application to different biomedical studies, with the secondary desirable purpose of motivating researchers to invest in interdisciplinarity. Such content-aware approach has been applied firstly to the phenomization of tumour cell response to stress by confocal fluorescent imaging, and secondly, to the texture analysis of trabecular bone microarchitecture in micro-CT scans. Third, this approach served the characterization of new 3-D multicellular spheroids of human stem cells, and the investigation of the role of the Nogo-A protein in tooth innervation. Finally, the content-aware approach also prompted to the development of two novel methods for local image analysis and colocalization quantification. In conclusion, the content-aware approach has proved its benefit through building new approaches that have improved the quality of image analysis, strengthening the statistical significance to allow unveiling biological phenomena. Hopefully, this Thesis will contribute to inspire researchers to striving hard for pursuing interdisciplinarity

Immunohistochemical and electrophysiological investigation of E/I balance alterations in animal models of frontotemporal dementia

Behavioural variant frontotemporal dementia (bvFTD) is a neurodegenerative disease characterised by changes in behaviour. Apathy, behavioural disinhibition and stereotyped behaviours are the first symptoms to appear and all have a basis in reward and pleasure deficits. The ventral striatum and ventral regions of the globus pallidus are involved in reward and pleasure. It is therefore reasonable to suggest alterations in these regions may underpin bvFTD. One postulated contributory factor is alteration in E/I balance in striatal regions. GABAergic interneurons play a role in E/I balance, acting as local inhibitory brakes, they are therefore a rational target for research investigating early biological predictors of bvFTD. To investigate this, we will carry out immunohistochemical staining for GABAergic interneurons (parvalbumin and neuronal nitric oxide synthase) in striatal regions of brains taken from CHMP2B mice, a validated animal model of bvFTD. We hypothesise that there will be fewer GABAergic interneurons in the striatum which may lead to ‘reward-seeking’ behaviour in bvFTD. This will also enable us to investigate any preclinical alterations in interneuron expression within this region. Results will be analysed using a mixed ANOVA and if significant, post hoc t-tests will be used. The second part of our study will involve extracellular recordings from CHMP2B mouse brains using a multi-electrode array (MEA). This will enable us to determine if there are alterations in local field potentials (LFP) in preclinical and symptomatic animals. We will also be able to see if neuromodulators such as serotonin and dopamine effect LFPs after bath application. We will develop slice preparations to preserve pathways between the ventral tegmental area and the ventral pallidum, an output structure of the striatum, and the dorsal raphe nucleus and the VP. Using the MEA we will stimulate an endogenous release of dopamine and serotonin using the slice preparations as described above. This will enable us to see if there are any changes in LFPs after endogenous release of neuromodulators. We hypothesise there will be an increase in LFPs due to loss of GABAergic interneurons