Relevant Gene Selection and Classification of Leukemia Gene Expression Data

Author(s):  
S. Jacophine Susmi ◽  
H. Khanna Nehemiah ◽  
A. Kannan ◽  
Jabez Christopher
2007 ◽  
Vol 11 (2) ◽  
pp. 219-222 ◽  
Author(s):  
Mohd Saberi Mohamad ◽  
Sigeru Omatu ◽  
Safaai Deris ◽  
Siti Zaiton Mohd Hashim

2019 ◽  
Vol 9 (6) ◽  
pp. 1294-1300 ◽  
Author(s):  
A. Sampathkumar ◽  
P. Vivekanandan

In the field of bioinformatics research, a large volume of genetic data has been generated. Availability of higher throughput devices at lower cost has contributed to this generation of huge volumetric data. Handling such numerous data has become extremely challenging for selecting the relevant disease-causing gene. The development of microarray technology provides higher chances of cancer diagnosis, by enabling to measure the expression level of multiple genes at the same stretch. Selecting the relevant gene by using classifiers for investigation of gene expression data is a complicated process. Proper identification of gene from the gene expression datasets plays a vital role in improving the accuracy of classification. In this article, identification of the highly relevant gene from the gene expression data for cancer treatment is discussed in detail. By using modified meta-heuristic approach, known as 'parallel lion optimization' (PLOA) for selecting genes from microarray data that can classify various cancer sub-types with more accuracy. The experimental results depict that PLOA outperforms than LOA and other well-known approaches, considering the five benchmark cancer gene expression dataset. It returns 99% classification accuracy for the dataset namely Prostate, Lung, Leukemia and Central Nervous system (CNS) for top 200 genes. Prostate and Lymphoma dataset PLOA is 99.19% and 99.93% respectively. On evaluating the result with other algorithm, the higher level of accuracy in gene selection is achieved by the proposed algorithm.


2012 ◽  
Vol 43 (14) ◽  
pp. 13-18 ◽  
Author(s):  
Vibhav PrakashSingh ◽  
Singh Gaurav Arvind ◽  
Arindam G Mahapatra

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