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Biology subjects

Kuru, H. I.

Publications and source records attributed to Kuru, H. I..

2 recordsLinked to original sources

PRER: A Patient Representation with Pairwise Relative Expression of Proteins on Biological Networks

Changes in protein and gene expression levels are often used as features to predictive models such as survival prediction. A common strategy to aggregate information on individual proteins is to integrate the expression information with biological networks. We propose a novel patient representation in this work where we integrate proteins expression levels with the protein-protein interaction (PPI) networks. Patient representation with PRER (Pairwise Relative Expressions with Random walks) uses the neighborhood of a protein to capture the dysregulation patterns in protein abundance. Specifically, PRER computes a feature vector for a patient by comparing the source proteins protein expression level with other proteins levels in its neighborhood. This neighborhood of the source protein is derived using a biased random-walk strategy on the network. We test PRERs performance through a survival prediction task in 10 different cancers using random forest survival models. PRER representation yields a statistically significant predictive performance in 9 out of 10 cancer types when compared to a representation based on individual protein expression. We also identify important proteins that are not important in the models trained with the expression values but emerge as predictive in models trained with PRER features. The set of identified relations provides a valuable collection of biomarkers with high prognostic value. PRER representation can be used for other complex diseases and prediction tasks that use molecular expression profiles as input. PRER is freely available at: https://github.com/hikuru/PRER

systems biology

MatchMaker: A Deep Learning Framework for Drug Synergy Prediction

Drug combination therapies have been a viable strategy for the treatment of complex diseases such as cancer due to increased efficacy and reduced side effects. However, experimentally validating all possible combinations for synergistic interaction even with high-throughout screens is intractable due to vast combinatorial search space. Computational techniques can reduce the number of combinations to be evaluated experimentally by prioritizing promising candidates. We present MatchMaker that predicts drug synergy scores using drug chemical structure information and gene expression profiles of cell lines in a deep learning framework. For the first time, our model utilizes the largest known drug combination dataset to date, DrugComb. We compare the performance of MatchMaker with the state-of-the-art models and observe up to ~ 20% correlation and ~ 40% mean squared error (MSE) improvements over the next best method. We investigate the cell types and drug pairs that are relatively harder to predict and present novel candidate pairs. MatchMaker is built and available at https://github.com/tastanlab/matchmaker

bioinformatics