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Predictiveness curves in virtual screening

Authors :
Aurélien Latouche
Matthieu Montes
Hélène Guillemain
Jean-François Zagury
Charly Empereur-Mot
Vivian Viallon
Laboratoire génomique, bioinformatique et applications (GBA)
Conservatoire National des Arts et Métiers [CNAM] (CNAM)
HESAM Université (HESAM)-HESAM Université (HESAM)
Centre d'études et de recherche en informatique et communications (CEDRIC)
Ecole Nationale Supérieure d'Informatique pour l'Industrie et l'Entreprise (ENSIIE)-Conservatoire National des Arts et Métiers [CNAM] (CNAM)
Unité Mixte de Recherche Epidémiologique et de Surveillance Transport Travail Environnement (UMRESTTE UMR T9405)
Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-Institut Français des Sciences et Technologies des Transports, de l'Aménagement et des Réseaux (IFSTTAR)
Conservatoire National des Arts et Métiers [CNAM] : EA4627
Conservatoire National des Arts et Métiers [CNAM] : EA4629
Unité Mixte de Recherche Epidémiologique et de Surveillance Transport Travail Environnement ( UMRESTTE UMR T9405 )
Université Claude Bernard Lyon 1 ( UCBL )
Université de Lyon-Université de Lyon-Institut Français des Sciences et Technologies des Transports, de l'Aménagement et des Réseaux ( IFSTTAR )
Source :
Journal of Cheminformatics, Journal of Cheminformatics, Chemistry Central Ltd. and BioMed Central, 2015, 7 (1), pp.52. ⟨10.1186/s13321-015-0100-8⟩, Journal of Cheminformatics, 2015, 7 (1), pp.52. 〈10.1186/s13321-015-0100-8〉
Publication Year :
2015
Publisher :
HAL CCSD, 2015.

Abstract

Background In the present work, we aim to transfer to the field of virtual screening the predictiveness curve, a metric that has been advocated in clinical epidemiology. The literature describes the use of predictiveness curves to evaluate the performances of biological markers to formulate diagnoses, prognoses and assess disease risks, assess the fit of risk models, and estimate the clinical utility of a model when applied to a population. Similarly, we use logistic regression models to calculate activity probabilities related to the scores that the compounds obtained in virtual screening experiments. The predictiveness curve can provide an intuitive and graphical tool to compare the predictive power of virtual screening methods. Results Similarly to ROC curves, predictiveness curves are functions of the distribution of the scores and provide a common scale for the evaluation of virtual screening methods. Contrarily to ROC curves, the dispersion of the scores is well described by predictiveness curves. This property allows the quantification of the predictive performance of virtual screening methods on a fraction of a given molecular dataset and makes the predictiveness curve an efficient tool to address the early recognition problem. To this last end, we introduce the use of the total gain and partial total gain to quantify recognition and early recognition of active compounds attributed to the variations of the scores obtained with virtual screening methods. Additionally to its usefulness in the evaluation of virtual screening methods, predictiveness curves can be used to define optimal score thresholds for the selection of compounds to be tested experimentally in a drug discovery program. We illustrate the use of predictiveness curves as a complement to ROC on the results of a virtual screening of the Directory of Useful Decoys datasets using three different methods (Surflex-dock, ICM, Autodock Vina). Conclusion The predictiveness curves cover different aspects of the predictive power of the scores, allowing a detailed evaluation of the performance of virtual screening methods. We believe predictiveness curves efficiently complete the set of tools available for the analysis of virtual screening results. Electronic supplementary material The online version of this article (doi:10.1186/s13321-015-0100-8) contains supplementary material, which is available to authorized users.

Details

Language :
English
ISSN :
17582946
Database :
OpenAIRE
Journal :
Journal of Cheminformatics, Journal of Cheminformatics, Chemistry Central Ltd. and BioMed Central, 2015, 7 (1), pp.52. ⟨10.1186/s13321-015-0100-8⟩, Journal of Cheminformatics, 2015, 7 (1), pp.52. 〈10.1186/s13321-015-0100-8〉
Accession number :
edsair.doi.dedup.....0d0d90fd8aac619e4bc9114752e7f852
Full Text :
https://doi.org/10.1186/s13321-015-0100-8⟩