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Drug discovery is a complicated, time-consuming and expensive process. The cost for each new molecular entity (NME) is estimated at $1.8 billion. Furthermore, for a new drug to be FDA approved it often takes nearly a decade and approximately 20 new drugs being approved by the US Food and Drug Administration (FDA) each year. Accurately predicting drug-target interactions (DTIs) by computational methods is an important area of drug research, which brings about a broad prospect for fast and low-risk drug development. By accurate prediction of drugs and targets interactions scientists can scale-down huge experimental space and reduce the costs and help to faster drug development as well as predicting the side effects and potential function of new drugs. Many approaches have been taken by researchers to solve DTI problem and enhance the accuracy of methods. State-of-the-art approaches are based on various techniques, such as deep learning methods-like stacked auto-encoder-, matrix factorization, network inference, and ensemble methods. In this work, we have taken a new approach based on node embedding in a heterogeneous interaction network to obtain the representation of each node in the interaction network and then use a binary classifier such as logistic regression to solve this prominent problem in the pharmaceutical industry. Most introduced network-based methods use a homogeneous network of interactions as their input data whereas in the real word problem there exist other informative networks to help to enhance the prediction and by considering the homogeneous networks we lose some precious network information. Hence, in this work, we have tried to work on the heterogeneous network and have improved the accuracy of methods in comparison to baseline methods. [ABSTRACT FROM AUTHOR]

Since EEG signals encode an individual's intent of executing an action, scientists have extensively focused on this topic. Motor Imagery (MI) signals have been used by researchers to assistance disabled persons, for autonomous driving and even control devices such as wheelchairs. Therefore, accurate decoding of these signals is essential to develop a Brain–Computer interface (BCI) systems. Due to dynamic nature, low signal-to-noise ratio and complexity of EEG signals, EEG decoding is not simple task. Extracting temporal and spatial features from EEG is accessible via Convolution neural network (CNN). However, enhanced CNN models are required to learn the dynamic correlations existing in MI signals. It is found that good features are extracted via CNN in both deep and shallow models, which indicate that various levels related features can be mined. In this case, spatial patterns from multi-scaled data in different frequency bands are learnt at first and then the temporal and frequency band information from projected signals is extracted. Here, to make use of neural activity phenomena, the feature extraction process employed is based on Multi-scale FBCSP (MSFBCSP). In CNN, the envelope of each spatially filtered signal is extracted in time dimension by performing Hilbert transform. However, to access common morphologies, the convolutional operation across time is performed first and then another convolution layer across channels in the frequency band is used to represent the carried information in a more compact form. Moreover, Bayesian approach is used for mapping hyperparameters to a probability of score on the objective function. The prominent feature of the proposed network is the high capacity of preserving and utilizing the information encoded in frequency bands. Our proposed method significantly improves the efficiency of current classification method in specific dataset of the physionet. According to empirical evaluations, strong robustness and high decoding classification are two distinctive characteristics of our proposed work. [ABSTRACT FROM AUTHOR]