Abstract

There has been a growing interest in multitask prediction in chemoinformatics, helped by the increasing use of deep neural networks in this field. This technique is applied to multitarget data sets, where compounds have been tested against different targets, with the aim of developing models to predict a profile of biological activities for a given compound. However, multitarget data sets tend to be sparse; i.e., not all compound-target combinations have experimental values. There has been little research on the effect of missing data on the performance of multitask methods. We have used two complete data sets to simulate sparseness by removing data from the training set. Different models to remove the data were compared. These sparse sets were used to train two different multitask methods, deep neural networks and Macau, which is a Bayesian probabilistic matrix factorization technique. Results from both methods were remarkably similar and showed that the performance decrease because of missing data is at first small before accelerating after large amounts of data are removed. This work provides a first approximation to assess how much data is required to produce good performance in multitask prediction exercises.

Highlights

  • IntroductionThe target-based approach, which has dominated the field for many years, is currently giving way to a more systems-based focus, boosted by heavy investment and research in omics science

  • Drug discovery has been changing focus for the last few years

  • Multitask modelling is becoming increasingly prevalent in chemoinformatics, following the popularity of deep neural networks

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Summary

Introduction

The target-based approach, which has dominated the field for many years, is currently giving way to a more systems-based focus, boosted by heavy investment and research in omics science. In this framework, individual targets are replaced by molecular pathways with phenotypic, or cell-based, responses [1] as the optimization targets. At the same time polypharmacology, which refers to the binding of chemical compounds to more than one target, has been intensively studied [2] The aim of these approaches is to identify multiple biological effects simultaneously, to better assess the

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