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Spectral unmixing is a significant challenge in hyperspectral image processing. Existing unmixing methods utilize prior knowledge about the abundance distribution to solve the regularization optimization problem, where the difficulty lies in choosing appropriate prior knowledge and solving the complex regularization optimization problem. To solve these problems, we propose a hyperspectral conditional generative adversarial network (HyperGAN) method as a generic unmixing framework, based on the following assumption: the unmixing process from pixel to abundance can be regarded as a transformation of two modalities with an internal specific relationship. The proposed HyperGAN is composed of a generator and discriminator, the former completes the modal conversion from mixed hyperspectral pixel patch to the abundance of corresponding endmember of the central pixel and the latter is used to distinguish whether the distribution and structure of generated abundance are the same as the true ones. We propose hyperspectral image (HSI) Patch Transformer as the main component of the generator, which utilize adaptive attention score to capture the internal pixels correlation of the HSI patch and leverage the spatial-spectral information in a fine-grained way to achieve optimization of the unmixing process. Experiments on synthetic data and real hyperspectral data achieve impressive results compared to state-of-the-art competitors.

Publicly available collections of drug-like molecules have grown to comprise 10s of billions of possibilities in recent history due to advances in chemical synthesis. Traditional methods for identifying ``hit'' molecules from a large collection of potential drug-like candidates have relied on biophysical theory to compute approximations to the Gibbs free energy of the binding interaction between the drug to its protein target. A major drawback of the approaches is that they require exceptional computing capabilities to consider for even relatively small collections of molecules. Hyperdimensional Computing (HDC) is a recently proposed learning paradigm that is able to leverage low-precision binary vector arithmetic to build efficient representations of the data that can be obtained without the need for gradient-based optimization approaches that are required in many conventional machine learning and deep learning approaches. This algorithmic simplicity allows for acceleration in hardware that has been previously demonstrated for a range of application areas. We consider existing HDC approaches for molecular property classification and introduce two novel encoding algorithms that leverage the extended connectivity fingerprint (ECFP) algorithm. We show that HDC-based inference methods are as much as 90 times more efficient than more complex representative machine learning methods and achieve an acceleration of nearly 9 orders of magnitude as compared to inference with molecular docking. We demonstrate multiple approaches for the encoding of molecular data for HDC and examine their relative performance on a range of challenging molecular property prediction and drug-protein binding classification tasks. Our work thus motivates further investigation into molecular representation learning to develop ultra-efficient pre-screening tools.

Breast cancer is the most prevalent cancer among women worldwide, and early detection is crucial for reducing its mortality rate and improving quality of life. Dedicated breast computed tomography (CT) scanners offer better image quality than mammography and tomosynthesis in general but at higher radiation dose. To enable breast CT for cancer screening, the challenge is to minimize the radiation dose without compromising image quality, according to the ALARA principle (as low as reasonably achievable). Over the past years, deep learning has shown remarkable successes in various tasks, including low-dose CT especially few-view CT. Currently, the diffusion model presents the state of the art for CT reconstruction. To develop the first diffusion model-based breast CT reconstruction method, here we report innovations to address the large memory requirement for breast cone-beam CT reconstruction and high computational cost of the diffusion model. Specifically, in this study we transform the cutting-edge Denoising Diffusion Probabilistic Model (DDPM) into a parallel framework for sub-volume-based sparse-view breast CT image reconstruction in projection and image domains. This novel approach involves the concurrent training of two distinct DDPM models dedicated to processing projection and image data synergistically in the dual domains. Our experimental findings reveal that this method delivers competitive reconstruction performance at half to one-third of the standard radiation doses. This advancement demonstrates an exciting potential of diffusion-type models for volumetric breast reconstruction at high-resolution with much-reduced radiation dose and as such hopefully redefines breast cancer screening and diagnosis.

Located at crystal voids, interstitial anion electrons (IAEs) have diverse topologies, which may be tuned to achieve new properties. Elucidating the role of IAEs in electron-phonon coupling (EPC), and using it to design new electride superconductors, leads to the current prediction of superconducting Li8Au at high pressure. We suggest that the occurence of high-temperature superconductivity in electrides requires high-symmetry structures with hydrogen-like cages, an electron acceptor element to balance charges, and isolated IAEs coupled with medium-frequency vibrations. The uniquely designed Li8Au electride has a NaCl-type (B1) lattice, with atomic Au and cubic Li8 cages as bases. Isolated IAEs are formed at the cage centers, with extra charges taken up by Au. These octahedrally coordinated IAEs have a p-orbital-like attribute and are strongly coupled with atomic vibrations in the Li8 cages. The strong EPC in Li8Au results in a calculated Tc of 73.1 K at 250 GPa, which is the highest Tc reported to date for all the electrides. A slight substitutional Pt doping can enhance the Tc of Li8Au to exceed liquid nitrogen temperature., Comment: 7 Pages, 3 Figures

Neural Network (NN) models provide potential to speed up the drug discovery process and reduce its failure rates. The success of NN models require uncertainty quantification (UQ) as drug discovery explores chemical space beyond the training data distribution. Standard NN models do not provide uncertainty information. Methods that combine Bayesian models with NN models address this issue, but are difficult to implement and more expensive to train. Some methods require changing the NN architecture or training procedure, limiting the selection of NN models. Moreover, predictive uncertainty can come from different sources. It is important to have the ability to separately model different types of predictive uncertainty, as the model can take assorted actions depending on the source of uncertainty. In this paper, we examine UQ methods that estimate different sources of predictive uncertainty for NN models aiming at drug discovery. We use our prior knowledge on chemical compounds to design the experiments. By utilizing a visualization method we create non-overlapping and chemically diverse partitions from a collection of chemical compounds. These partitions are used as training and test set splits to explore NN model uncertainty. We demonstrate how the uncertainties estimated by the selected methods describe different sources of uncertainty under different partitions and featurization schemes and the relationship to prediction error.

For the current 3D human pose estimation task, a group of methods mainly learn the rules of 2D-3D projection from spatial and temporal correlation. However, earlier methods model the global features of the entire body joint in the time domain, but ignore the motion trajectory of individual joint. The recent work [29] considers that there are differences in motion between different joints and deals with the temporal relationship of each joint separately. However, we found that different joints show the same movement trends under some specific actions. Therefore, our proposed Fusionformer method introduces a self-trajectory module and a mutual-trajectory module based on the spatio-temporal module .After that, the global spatio-temporal features and local joint trajectory features are fused through a linear network in a parallel manner. To eliminate the influence of bad 2D poses on 3D projections, finally we also introduce a pose refinement network to balance the consistency of 3D projections. In addition, we evaluate the proposed method on two benchmark datasets (Human3.6M, MPI-INF-3DHP). Comparing our method with the baseline method poseformer, the results show an improvement of 2.4% MPJPE and 4.3% P-MPJPE on the Human3.6M dataset, respectively.

Capturing the dependencies between joints is critical in skeleton-based action recognition task. Transformer shows great potential to model the correlation of important joints. However, the existing Transformer-based methods cannot capture the correlation of different joints between frames, which the correlation is very useful since different body parts (such as the arms and legs in "long jump") between adjacent frames move together. Focus on this problem, A novel spatio-temporal tuples Transformer (STTFormer) method is proposed. The skeleton sequence is divided into several parts, and several consecutive frames contained in each part are encoded. And then a spatio-temporal tuples self-attention module is proposed to capture the relationship of different joints in consecutive frames. In addition, a feature aggregation module is introduced between non-adjacent frames to enhance the ability to distinguish similar actions. Compared with the state-of-the-art methods, our method achieves better performance on two large-scale datasets., Comment: 14 pages, 5 figures