weighted extreme learning machine
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2022 ◽  
pp. 103621
Author(s):  
Sahithi Tummalapalli ◽  
Lov Kumar ◽  
N.L. Bhanu Murthy ◽  
Aneesh Krishna

2021 ◽  
Author(s):  
JinXuan Zhai ◽  
Ji-Yong An

Abstract Background:Protein–protein interactions (PPIs) are involved in a number of cellular processes and play a key role inside cells. The prediction of PPIs is an important task towards the understanding of many bioinformatics functions and applications, such as predicting protein functions, gene-disease associations and disease-drug associations. Given that high-throughput methods are expensive and time-consuming, it is a challenging task to develop efficient and accurate computational methods for predicting PPIs .Results:In the study, a novel computational approach named WELM-SURF was developed to predict PPIs. The proposed method used Position Specific Scoring Matrix (PSSM) to capture protein evolutionary information and employed Speed Up Robot Features (SURF) to extract key features from PSSM of protein sequence. Weighted Extreme Learning Machine (WELM) is featured with short training time and great ability to execute classification efficiently by optimizing the loss function of weight matrix. Therefore, WELM classifier was used to carry out classification. The cross-validation results show that WELM-SURF obtains 97.36% and 95.12% of average accuracy on yeast and human dataset, respectively. The prediction ability of WELM-SURF was also compared with those of ELM-SRUF, SVM-SURF and other existing approaches. The comparison results further verify that WELM-SURF is obviously better than other methods.Conclusion:The experimental results proved that the WELM-SURF method is very useful for predicting PPIs and can also be applied to other bioinformatics studies of protein.


2021 ◽  
Vol 13 (3) ◽  
pp. 508
Author(s):  
Xumin Yu ◽  
Yan Feng ◽  
Yanlong Gao ◽  
Yingbiao Jia ◽  
Shaohui Mei

Due to its excellent performance in high-dimensional space, the kernel extreme learning machine has been widely used in pattern recognition and machine learning fields. In this paper, we propose a dual-weighted kernel extreme learning machine for hyperspectral imagery classification. First, diverse spatial features are extracted by guided filtering. Then, the spatial features and spectral features are composited by a weighted kernel summation form. Finally, the weighted extreme learning machine is employed for the hyperspectral imagery classification task. This dual-weighted framework guarantees that the subtle spatial features are extracted, while the importance of minority samples is emphasized. Experiments carried on three public data sets demonstrate that the proposed dual-weighted kernel extreme learning machine (DW-KELM) performs better than other kernel methods, in terms of accuracy of classification, and can achieve satisfactory results.


2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Ji-Yong An ◽  
Fan-Rong Meng ◽  
Zi-Ji Yan

Abstract Background Prediction of novel Drug–Target interactions (DTIs) plays an important role in discovering new drug candidates and finding new proteins to target. In consideration of the time-consuming and expensive of experimental methods. Therefore, it is a challenging task that how to develop efficient computational approaches for the accurate predicting potential associations between drug and target. Results In the paper, we proposed a novel computational method called WELM-SURF based on drug fingerprints and protein evolutionary information for identifying DTIs. More specifically, for exploiting protein sequence feature, Position Specific Scoring Matrix (PSSM) is applied to capturing protein evolutionary information and Speed up robot features (SURF) is employed to extract sequence key feature from PSSM. For drug fingerprints, the chemical structure of molecular substructure fingerprints was used to represent drug as feature vector. Take account of the advantage that the Weighted Extreme Learning Machine (WELM) has short training time, good generalization ability, and most importantly ability to efficiently execute classification by optimizing the loss function of weight matrix. Therefore, the WELM classifier is used to carry out classification based on extracted features for predicting DTIs. The performance of the WELM-SURF model was evaluated by experimental validations on enzyme, ion channel, GPCRs and nuclear receptor datasets by using fivefold cross-validation test. The WELM-SURF obtained average accuracies of 93.54, 90.58, 85.43 and 77.45% on enzyme, ion channels, GPCRs and nuclear receptor dataset respectively. We also compared our performance with the Extreme Learning Machine (ELM), the state-of-the-art Support Vector Machine (SVM) on enzyme and ion channels dataset and other exiting methods on four datasets. By comparing with experimental results, the performance of WELM-SURF is significantly better than that of ELM, SVM and other previous methods in the domain. Conclusion The results demonstrated that the proposed WELM-SURF model is competent for predicting DTIs with high accuracy and robustness. It is anticipated that the WELM-SURF method is a useful computational tool to facilitate widely bioinformatics studies related to DTIs prediction.


2021 ◽  
Author(s):  
An Ji Yong ◽  
Meng Fan-Rong ◽  
Yan Zi-Ji

Abstract Background: Prediction of novel Drug–Target interactions (DTIs) plays an important role in discovering new drug candidates and finding new proteins to target. In consideration of the time-consuming and expensive of experimental methods. Therefore, it is a challenging task that how to develop efficient computational approaches for the accurate predicting potential associations between drug and target. Results: In the paper, we proposed a novel computational method called WELM-SURF based on drug fingerprints and protein evolutionary information for identifying DTIs. More specifically, for exploiting protein sequence feature, Position Specific Scoring Matrix (PSSM) is applied to capturing protein evolutionary information and Speed up robot features (SURF) is employed to extract sequence key feature from PSSM. For drug fingerprints, the chemical structure of molecular substructure fingerprints was used to represent drug as feature vector. Take account of the advantage that the Weighted Extreme Learning Machine (WELM) has short training time, good generalization ability, and most importantly ability to efficiently execute classification by optimizing the loss function of weight matrix. Therefore, the WELM classifier is used to carry out classification based on extracted features for predicting DTIs. The performance of the WELM-SURF model was evaluated by experimental validations on enzyme, ion channel, GPCRs and nuclear receptor datasets by using fivefold cross-validation test. The WELM-SURF obtained average accuracies of 93.54%, 90.58%, 85.43% and 77.45% on enzyme, ion channels, GPCRs and nuclear receptor dataset respectively. We also compared our performance with the Extreme Learning Machine (ELM), the state-of-the-art Support Vector Machine (SVM) on enzyme and ion channels dataset and other exiting methods on four datasets. By comparing with experimental results, the performance of WELM-SURF is significantly better than that of ELM, SVM and other previous methods in the domain.Conclusion: The results demonstrated that the proposed WELM-SURF model is competent for predicting DTIs with high accuracy and robustness. It is anticipated that the WELM-SURF method is a useful computational tool to facilitate widely bioinformatics studies related to DTIs prediction.


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