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On Some Aspects of Variable Selection for Partial Least Squares Regression Models
Abstract
This paper tries to explore the optimum variable selection strategy for Partial Least Squares (PLS) regression using a model dataset of cytoprotection data. The compounds of the dataset were classified using K‐means clustering technique applied on standardized descriptor matrix and ten combinations of training and test sets were generated based on the obtained clusters. For a particular training set, PLS models were developed with a number of components optimized by leave‐one‐out Q2 and then the developed models were validated (externally) using the test set compounds. For each set, PLS model was initially constructed using all descriptors (variables). The variables having least standardized values of regression coefficients were deleted and the next model was developed with a reduced set of variables. These steps were performed several times until further reduction in number of variables did not improve Q2 value. In each case, statistical parameters like predictive R2 (R2pred), squared correlation coefficient between observed and predicted values with (r2) and without ($\rm{ r_0^{\rm{2}} }$) intercept and Root Mean Square Error of Prediction (RMSEP) were calculated from the test set compounds. In case of all ten sets, Q2 values steadily increase on deletion of variables while R2pred values do not show any specific trend. In no case, the highest Q2 and highest R2pred appear in the same trial, i.e., with the same combinations of variables. This suggests that from the viewpoint of external predictability, choice of variables for PLS based on Q2 value may not be optimum. Moreover, a clear separation of r2 and r02 curves in some sets suggests that such models may not be truly predictive in spite of acceptable R2pred values. Another observation is that coefficient of determination R2 for the training set is more immune to changes on deletion of variables than the validation parameters like Q2 and R2pred. Finally, a new parameter rm2 has been suggested to indicate external predictability of QSAR models.
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Cites
Golbraikh, A., & Tropsha, A. (2002) · Journal of Molecular Graphics and Modelling · doi:10.1016/s1093-3263(01)00123-1 · Cited by 3,735
Rational selection of training and test sets for the development of validated QSAR models
Golbraikh, A., Shen, M., Xiao, Z., Xiao, Y.-D., Lee, K.-H., & Tropsha, A. (2003) · Journal of Computer-Aided Molecular Design · doi:10.1023/a:1025386326946 · Cited by 712
Cited by
Roy, K., Chakraborty, P., Mitra, I., Ojha, P. K., Kar, S., & Das, R. N. (2013) · Journal of Computational Chemistry · doi:10.1002/jcc.23231 · Cited by 466
Self-citationAn evolutionary approach for modeling of shear strength of RC deep beams
Gandomi, A. H., Yun, G. J., & Alavi, A. H. (2013) · Materials and Structures · doi:10.1617/s11527-013-0039-z · Cited by 254
Amorim, A. M. B., Piochi, L. F., Gaspar, A. T., Preto, A. J., Rosário-Ferreira, N., & Moreira, I. S. (2024) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.3c00352 · Cited by 132
Najafzadeh, M., & Ghaemi, A. (2019) · Environmental Monitoring and Assessment · doi:10.1007/s10661-019-7446-8 · Cited by 128
Statistical workflow for feature selection in human metabolomics data
Antonelli, J., Claggett, B. L., Henglin, M., Kim, A., Ovsak, G., Kim, N., Deng, K., Rao, K., Tyagi, O., Watrous, J. D., et al. (2019) · Metabolites · doi:10.3390/metabo9070143 · Cited by 88
Metadata
- Authors
- Roy, P. P., & Roy, K.
- Venue
- QSAR & Combinatorial Science
- Publisher
- Wiley
- Published
- 2008-03
- Volume
- 27
- Issue
- 3
- Pages
- 302-313
- ISSN
- 1611-020X (ISSN-L)
- 1611-0218
- OpenAlex
- W2011580004
- Cited by
- 793
- References
- 2
- FWCI
- 36.24
- Type
- journal article
- Language
- en
- Open access
- closed
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