Browsing by Subject "ADR"
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Item Open Access Deepside: predicting drug side effects with deep learning(2019-09) Üner, Onur CanDrug failures due to unforeseen adverse effects at clinical trials pose health risks for the participants and cause substantial financial losses. Side effect prediction algorithms, on the other hand, have the potential to guide the drug design process. LINCS L1000 dataset provides a vast resource of gene expression profiles across different cell lines that are induced with different dosages taken at different time points. The state-of-the-art approach in the literature relies on high-quality experiments in LINCS L1000 and discard a large portion of the recorded experiments. In this study, we investigate whether more information can be extracted from this remaining set of experiments with a deep learning-based approach. We experiment with 6 different deep learning architectures that use (i) gene expression data from the LINCS L1000 project, (ii) chemical structure fingerprints of drugs, (iii) SMILES string representation of drug structure, and (iv) the atomic structure of the drug molecules. The multilayer perceptron (MLP) based model which uses chemical structures and gene expression features achieve 88% micro- AUC and 79% macro-AUC, thus offering better performance in comparison to the state-of-the-art studies on side effect prediction. We observe that the chemical structure is more predictive than the gene expression profiles despite the fact that the features are extracted with different deep learning models. Finally, the convolutional neural network-based model that uses only SMILES strings of the drugs provides 82% macro-AUC, and 88%micro-AUC improvements, better performing than the models that use gene expression and chemical structure features simultaneously.Item Open Access Does ADR listing affect the dynamics of volatility in emerging markets?(Univerzita Karlova v Praze, 2010) Umutlu, M.; Altay-Salih, A.; Akdeniz, L.This paper analyzes the time-series variation in the return volatility of non-US stocks from emerging markets that are cross-listed on US exchanges. Unlike previous studies in the cross-listing literature, return volatility is modeled using conditional heteroscedasticity models. We find that firms' exposure to risks such as local and global market betas remain unchanged after cross-listing. Moreover, we do not identify notable changes in the dynamics of the volatility of cross-listed stocks after cross-listing except for leverage effects. We further show that the mean level of conditional variance is not affected after cross-listing. Thus, our results provide counter-evidence to the belief that foreign investor participation drives volatility upward.