An Entropy-Based Directed Random Walk for Cancer Classification Using Gene Expression Data Based on Bi-Random Walk on Two Separated Networks
The integration of microarray technologies and machine learning methods has become popular in predicting the pathological condition of diseases and discovering risk genes. Traditional microarray analysis considers pathways as a simple gene set, treating all genes in the pathway identically while ig...
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my.uthm.eprints.100722023-10-11T03:23:42Z http://eprints.uthm.edu.my/10072/ An Entropy-Based Directed Random Walk for Cancer Classification Using Gene Expression Data Based on Bi-Random Walk on Two Separated Networks Xin Hui Tay, Xin Hui Tay Kasim, Shahreen Tole Sutikno, Tole Sutikno Md Fudzee, Mohd Farhan Hassan, Rohayanti Emelia Akashah Patah Akhir, Emelia Akashah Patah Akhir Aziz, Norshakirah Choon Sen Seah, Choon Sen Seah T Technology (General) The integration of microarray technologies and machine learning methods has become popular in predicting the pathological condition of diseases and discovering risk genes. Traditional microarray analysis considers pathways as a simple gene set, treating all genes in the pathway identically while ignoring the pathway network’s structure information. This study proposed an entropy-based directed random walk (e-DRW) method to infer pathway activities. Two enhancements from the conventional DRW were conducted, which are (1) to increase the coverage of human pathway information by constructing two inputting networks for pathway activity inference, and (2) to enhance the gene-weighting method in DRW by incorporating correlation coefficient values and t-test statistic scores. To test the objectives, gene expression datasets were used as input datasets while the pathway datasets were used as reference datasets to build two directed graphs. The withindataset experiments indicated that e-DRW method demonstrated robust and superior performance in terms of classification accuracy and robustness of the predicted risk-active pathways compared to the other methods. In conclusion, the results revealed that e-DRW not only improved the prediction performance, but also effectively extracted topologically important pathways and genes that were specifically related to the corresponding cancer types. Mdpi 2023 Article PeerReviewed text en http://eprints.uthm.edu.my/10072/1/J16097_fc692a6f023a80413e40b199966c0376.pdf Xin Hui Tay, Xin Hui Tay and Kasim, Shahreen and Tole Sutikno, Tole Sutikno and Md Fudzee, Mohd Farhan and Hassan, Rohayanti and Emelia Akashah Patah Akhir, Emelia Akashah Patah Akhir and Aziz, Norshakirah and Choon Sen Seah, Choon Sen Seah (2023) An Entropy-Based Directed Random Walk for Cancer Classification Using Gene Expression Data Based on Bi-Random Walk on Two Separated Networks. Genes, 14 (574). pp. 1-13. https://doi.org/10.3390/genes14030574 |
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T Technology (General) Xin Hui Tay, Xin Hui Tay Kasim, Shahreen Tole Sutikno, Tole Sutikno Md Fudzee, Mohd Farhan Hassan, Rohayanti Emelia Akashah Patah Akhir, Emelia Akashah Patah Akhir Aziz, Norshakirah Choon Sen Seah, Choon Sen Seah An Entropy-Based Directed Random Walk for Cancer Classification Using Gene Expression Data Based on Bi-Random Walk on Two Separated Networks |
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The integration of microarray technologies and machine learning methods has become popular in predicting the pathological condition of diseases and discovering risk genes. Traditional microarray analysis considers pathways as a simple gene set, treating all genes in the pathway
identically while ignoring the pathway network’s structure information. This study proposed an entropy-based directed random walk (e-DRW) method to infer pathway activities. Two enhancements from the conventional DRW were conducted, which are (1) to increase the coverage of human pathway information by constructing two inputting networks for pathway activity inference, and (2) to enhance the gene-weighting method in DRW by incorporating correlation coefficient values and t-test statistic scores. To test the objectives, gene expression datasets were used as input datasets while the pathway datasets were used as reference datasets to build two directed graphs. The withindataset experiments indicated that e-DRW method demonstrated robust and superior performance in terms of classification accuracy and robustness of the predicted risk-active pathways compared to the other methods. In conclusion, the results revealed that e-DRW not only improved the prediction
performance, but also effectively extracted topologically important pathways and genes that were specifically related to the corresponding cancer types. |
format |
Article |
author |
Xin Hui Tay, Xin Hui Tay Kasim, Shahreen Tole Sutikno, Tole Sutikno Md Fudzee, Mohd Farhan Hassan, Rohayanti Emelia Akashah Patah Akhir, Emelia Akashah Patah Akhir Aziz, Norshakirah Choon Sen Seah, Choon Sen Seah |
author_facet |
Xin Hui Tay, Xin Hui Tay Kasim, Shahreen Tole Sutikno, Tole Sutikno Md Fudzee, Mohd Farhan Hassan, Rohayanti Emelia Akashah Patah Akhir, Emelia Akashah Patah Akhir Aziz, Norshakirah Choon Sen Seah, Choon Sen Seah |
author_sort |
Xin Hui Tay, Xin Hui Tay |
title |
An Entropy-Based Directed Random Walk for Cancer
Classification Using Gene Expression Data Based on
Bi-Random Walk on Two Separated Networks |
title_short |
An Entropy-Based Directed Random Walk for Cancer
Classification Using Gene Expression Data Based on
Bi-Random Walk on Two Separated Networks |
title_full |
An Entropy-Based Directed Random Walk for Cancer
Classification Using Gene Expression Data Based on
Bi-Random Walk on Two Separated Networks |
title_fullStr |
An Entropy-Based Directed Random Walk for Cancer
Classification Using Gene Expression Data Based on
Bi-Random Walk on Two Separated Networks |
title_full_unstemmed |
An Entropy-Based Directed Random Walk for Cancer
Classification Using Gene Expression Data Based on
Bi-Random Walk on Two Separated Networks |
title_sort |
entropy-based directed random walk for cancer
classification using gene expression data based on
bi-random walk on two separated networks |
publisher |
Mdpi |
publishDate |
2023 |
url |
http://eprints.uthm.edu.my/10072/1/J16097_fc692a6f023a80413e40b199966c0376.pdf http://eprints.uthm.edu.my/10072/ https://doi.org/10.3390/genes14030574 |
_version_ |
1779440619024809984 |
score |
13.211869 |