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      On Two Novel Parameters for Validation of Predictive QSAR Models

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          Abstract

          Validation is a crucial aspect of quantitative structure–activity relationship (QSAR) modeling. The present paper shows that traditionally used validation parameters (leave-one-out Q 2 for internal validation and predictive R 2 for external validation) may be supplemented with two novel parameters r m 2 and R p 2 for a stricter test of validation. The parameter r m 2 (overall) penalizes a model for large differences between observed and predicted values of the compounds of the whole set (considering both training and test sets) while the parameter R p 2 penalizes model R 2 for large differences between determination coefficient of nonrandom model and square of mean correlation coefficient of random models in case of a randomization test. Two other variants of r m 2 parameter, r m 2 (LOO) and r m 2 (test), penalize a model more strictly than Q 2 and R 2 pred respectively. Three different data sets of moderate to large size have been used to develop multiple models in order to indicate the suitability of the novel parameters in QSAR studies. The results show that in many cases the developed models could satisfy the requirements of conventional parameters (Q 2 and R 2 pred) but fail to achieve the required values for the novel parameters r m 2 and R p 2. Moreover, these parameters also help in identifying the best models from among a set of comparable models. Thus, a test for these two parameters is suggested to be a more stringent requirement than the traditional validation parameters to decide acceptability of a predictive QSAR model, especially when a regulatory decision is involved.

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          The problem of overfitting.

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            Beware of q2!

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              The Importance of Being Earnest: Validation is the Absolute Essential for Successful Application and Interpretation of QSPR Models

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                Author and article information

                Journal
                Molecules
                Molecules
                molecules
                Molecules
                Molecular Diversity Preservation International
                1420-3049
                29 April 2009
                May 2009
                : 14
                : 5
                : 1660-1701
                Affiliations
                Drug Theoretics and Cheminformatics Lab, Division of Medicinal and Pharmaceutical Chemistry, Department of Pharmaceutical Technology, Jadavpur University, Kolkata 700 032, India; E-mails: partha_chemju@ 123456yahoo.co.in (P-P.R.), somnath_juph@ 123456yahoo.co.in (S.P.), indranimitra06@ 123456gmail.com (I.M.)
                Author notes
                [* ]Author to whom correspondence should be addressed; E-mail: kunalroy_in@ 123456yahoo.com or kroy@ 123456pharma.jdvu.ac.in ; Fax: +91-33-2837 1078.
                Author information
                https://orcid.org/0000-0003-4486-8074
                Article
                molecules-14-01660
                10.3390/molecules14051660
                6254296
                19471190
                9100efab-9371-4c3f-813b-c68823aaee68
                © 2009 by the authors;

                licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/3.0/).

                History
                : 16 April 2009
                : 24 April 2009
                : 28 April 2009
                Categories
                Article

                qsar,validation,internal validation,external validation,randomization

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