| Literature DB >> 35566957 |
Israr Ilyas1, Adeel Zafar1, Muhammad Talal Afzal1,2, Muhammad Faisal Javed3, Raid Alrowais4, Fadi Althoey5, Abdeliazim Mustafa Mohamed6,7, Abdullah Mohamed8, Nikolai Ivanovich Vatin9.
Abstract
The purpose of this article is to demonstrate the potential of gene expression programming (GEP) in anticipating the compressive strength of circular CFRP confined concrete columns. A new GEP model has been developed based on a credible and extensive database of 828 data points to date. Numerous analyses were carried out to evaluate and validate the presented model by comparing them with those presented previously by different researchers along with external validation comparison. In comparison to other artificial intelligence (AI) techniques, such as Artificial Neural Networks (ANN) and the adaptive neuro-fuzzy interface system (ANFIS), only GEP has the capability and robustness to provide output in the form of a simple mathematical relationship that is easy to use. The developed GEP model is also compared with linear and nonlinear regression models to evaluate the performance. Afterwards, a detailed parametric and sensitivity analysis confirms the generalized nature of the newly established model. Sensitivity analysis results indicate the performance of the model by evaluating the relative contribution of explanatory variables involved in development. Moreover, the Taylor diagram is also established to visualize how the proposed model outperformed other existing models in terms of accuracy, efficiency, and being closer to the target. Lastly, the criteria of external validation were also fulfilled by the GEP model much better than other conventional models. These findings show that the presented model effectively forecasts the confined strength of circular concrete columns significantly better than the previously established conventional regression-based models.Entities:
Keywords: CFRP; GEP; artificial intelligence; confinement; gene programming; machine learning; modelling; strength model
Year: 2022 PMID: 35566957 PMCID: PMC9100819 DOI: 10.3390/polym14091789
Source DB: PubMed Journal: Polymers (Basel) ISSN: 2073-4360 Impact factor: 4.967
Figure 1GEP Flow diagram.
Figure 2Marginal histograms for each predictor variable.
Figure 3Correlation plot based on explanatory variables.
Hyper parameters configuration incorporated for modeling.
| Sr. # | Generalized Setting | |
|---|---|---|
| 1 |
Chromosome number | 120 |
| 2 |
Gene number | 3 |
| 3 |
Size of head | 8 |
| 4 |
Genes’ linkage function | Addition |
| 5 |
Set of functions | +, /, −, ×, 3√ |
|
| ||
| 6 |
Constants per gene | 10 |
| 7 |
Data type | Floating |
| 8 |
Bound range | −10 to +10 |
|
| ||
| 9 |
Mutation: | 0.00138 |
| 10 |
Function Insertion: | 0.00206 |
| 11 |
Permutation: | 0.00476 |
| 12 |
IS Transposition: | 0.00548 |
| 13 |
RIS Transposition: | 0.00496 |
| 14 |
Inversion: | 0.00548 |
| 15 |
Gene Transposition: | 0.00157 |
| 16 |
Random Chromosomes: | 0.0026 |
| 17 |
Constant Insertion: | 0.00123 |
|
| ||
| 18 |
Uniform | 0.00755 |
| 19 |
One-Point | 0.00277 |
| 20 |
Two-Point | 0.00189 |
| 21 |
Gene | 0.00277 |
Figure 4Forecasting via GEP against actual output.
Figure 5Taylor Diagram for performance evaluation of GEP and existing models [11,12,14,15,16,20,22,79,80,81,82,83,84,85,86].
External validation assessment of AI and Regression Models.
| Sr. #. | Equation | Range | Model | Output | Reference |
|---|---|---|---|---|---|
| 1 |
|
| GEP | 0.917 | |
| MLR | 0.788 | ||||
| MNLR | 0.856 | ||||
| 2 |
|
| GEP | 0.528 | (Roy and Roy, 2008) [ |
| MLR | 0.244 | ||||
| MNLR | 0.398 | ||||
| where |
| GEP | 0.980 | ||
| MLR | 0.987 | ||||
| MNLR | 0.977 | ||||
|
|
| GEP | 0.998 | ||
| MLR | 0.997 | ||||
| MNLR | 0.988 | ||||
| 3 |
|
| GEP | 0.934 | (Golbraikh and |
| MLR | 0.965 | ||||
| MNLR | 0.952 | ||||
| 4 |
|
| GEP | 1.019 | |
| MLR | 0.980 | ||||
| MNLR | 1.014 |
Figure 6External validation based on the evaluation of proposed and exist-ing models [12,14,15,16,79,84,86].
Figure 7Parametric analysis of input variables.
Figure 8Sensitivity analysis based on the relative contribution of predictor variables.