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The high temporal resolution and the asymmetric spatial activations are essential attributes of electroencephalogram (EEG) underlying emotional processes in the brain. To learn the temporal dynamics and spatial asymmetry of EEG towards accurate and generalized emotion recognition, we propose TSception, a multi-scale convolutional neural network that can classify emotions from EEG. TSception consists of dynamic temporal, asymmetric spatial, and high-level fusion layers, which learn discriminative representations in the time and channel dimensions simultaneously. The dynamic temporal layer consists of multi-scale 1D convolutional kernels whose lengths are related to the sampling rate of EEG, which learns the dynamic temporal and frequency representations of EEG. The asymmetric spatial layer takes advantage of the asymmetric EEG patterns for emotion, learning the discriminative global and hemisphere representations. The learned spatial representations will be fused by a high-level fusion layer. Using more generalized cross-validation settings, the proposed method is evaluated on two publicly available datasets DEAP and MAHNOB-HCI. The performance of the proposed network is compared with prior reported methods such as SVM, KNN, FBFgMDM, FBTSC, Unsupervised learning, DeepConvNet, ShallowConvNet, and EEGNet. TSception achieves higher classification accuracies and F1 scores than other methods in most of the experiments. The codes are available at:https://github.com/yi-ding-cs/TSception

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Learning for maximizing AUC performance is an important research problem in Machine Learning and Artificial Intelligence. Unlike traditional batch learning methods for maximizing AUC which often suffer from poor scalability, recent years have witnessed some emerging studies that attempt to maximize AUC by single-pass online learning approaches. Despite their encouraging results reported, the existing online AUC maximization algorithms often adopt simple online gradient descent approaches that fail to exploit the geometrical knowledge of the data observed during the online learning process, and thus could suffer from relatively larger regret. To address the above limitation, in this work, we explore a novel algorithm of Adaptive Online AUC Maximization (AdaOAM) which employs an adaptive gradient method that exploits the knowledge of historical gradients to perform more informative online learning. The new adaptive updating strategy of the AdaOAM is less sensitive to the parameter settings and maintains the same time complexity as previous non-adaptive counterparts. Additionally, we extend the algorithm to handle high-dimensional sparse data (SAdaOAM) and address sparsity in the solution by performing lazy gradient updating. We analyze the theoretical bounds and evaluate their empirical performance on various types of data sets. The encouraging empirical results obtained clearly highlighted the effectiveness and efficiency of the proposed algorithms.

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The glycine-binding site of the N-methyl-D-aspartate receptor (NMDAR) subunit GluN1 is a potential pharmacological target for neurodegenerative disorders. A novel combinatorial ensemble docking scheme using ligand and protein conformation ensembles and customized support vector machine (SVM)-based models to select the docked pose and to predict the docking score was generated for predicting the NMDAR GluN1-ligand binding affinity. The predicted root mean square deviation (RMSD) values in pose by SVM-Pose models were found to be in good agreement with the observed values (n = 30, r2 = 0.928–0.988,  = 0.894–0.954, RMSE = 0.002–0.412, s = 0.001–0.214), and the predicted pKi values by SVM-Score were found to be in good agreement with the observed values for the training samples (n = 24, r2 = 0.967,  = 0.899, RMSE = 0.295, s = 0.170) and test samples (n = 13, q2 = 0.894, RMSE = 0.437, s = 0.202). When subjected to various statistical validations, the developed SVM-Pose and SVM-Score models consistently met the most stringent criteria. A mock test asserted the predictivity of this novel docking scheme. Collectively, this accurate novel combinatorial ensemble docking scheme can be used to predict the NMDAR GluN1-ligand binding affinity for facilitating drug discovery.