Search for: All records

The emergence of Positron Emission Tomography (PET) imaging allows us to quantify the burden of amyloid plaques in-vivo, which is one of the hallmarks of Alzheimer’s disease (AD). However, the invasive exposure to radiation and high imaging cost significantly restrict the application of PET in characterizing the evolution of pathology burden which often requires longitudinal PET image sequences. In this regard, we propose a proof-of-concept solution to generate the complete trajectory of pathological events throughout the brain based on very limited number of PET scans. We present a novel variational autoencoder model to learn a latent population-level representation of neurodegeneration process based on the longitudinal β-amyloid measurements at each brain region and longitudinal diagnostic stages. As the propagation of pathological burdens follow the topology of brain connectome, we further cast our neural network into a supervised sequential graph VAE, where we use the brain network to guide the representation learning. Experiments show that the disentangled representation can capture disease-related dynamics of amyloid and forecast the level of amyloid depositions at future time points. 

Tremendous recent literature show that associations between different brain regions, i.e., brain connectivity, provide early symptoms of neurological disorders. Despite significant efforts made for graph neural network (GNN) techniques, their focus on graph nodes makes the state-of-the-art GNN methods not suitable for classifying brain connectivity as graphs where the objective is to characterize disease-relevant network dysfunction patterns on graph links. To address this issue, we propose Multi-resolution Edge Network (MENET) to detect disease-specific connectomic benchmarks with high discrimination power across diagnostic categories. The core of MENET is a novel graph edge-wise transform that we propose, which allows us to capture multi-resolution “connectomic” features. Using a rich set of the connectomic features, we devise a graph learning framework to jointly select discriminative edges and assign diagnostic labels for graphs. Experiments on two real datasets show that MENET accurately predicts diagnostic labels and identify brain connectivities highly associated with neurological disorders such as Alzheimer’s Disease and Attention-Deficit/Hyperactivity Disorder. 

Image-based cell counting is a fundamental yet challenging task with wide applications in biological research. In this paper, we propose a novel unified deep network framework designed to solve this problem for various cell types in both 2D and 3D images. Specifically, we first propose SAU-Net for cell counting by extending the segmentation network U-Net with a Self-Attention module. Second, we design an extension of Batch Normalization (BN) to facilitate the training process for small datasets. In addition, a new 3D benchmark dataset based on the existing mouse blastocyst (MBC) dataset is developed and released to the community. Our SAU-Net achieves state-of-the-art results on four benchmark 2D datasets - synthetic fluorescence microscopy (VGG) dataset, Modified Bone Marrow (MBM) dataset, human subcutaneous adipose tissue (ADI) dataset, and Dublin Cell Counting (DCC) dataset, and the new 3D dataset, MBC. The BN extension is validated using extensive experiments on the 2D datasets, since GPU memory constraints preclude use of 3D datasets. The source code is available at https://github.com/mzlr/sau-net.