A new DNA sequence entropy-based Kullback-Leibler algorithm for gene clustering.

In this study, for each gene and its exons sets, the entropy was calculated in orders one to four. Based on the relative entropy of genes and exons, Kullback-Leibler divergence was calculated. After obtaining the Kullback-Leibler distance for genes and exons sets, the results were entered as input into 7 clustering algorithms: single, complete, average, weighted, centroid, median, and K-means. To aggregate the results of clustering, the AdaBoost algorithm was used. Finally, the results of the AdaBoost algorithm were investigated by GeneMANIA prediction server to explore the results from gene annotation point of view. All calculations were performed using the MATLAB Engineering Software (2015). Following our findings on investigating the results of genes metabolic pathways based on the gene annotations, it was revealed that our proposed clustering method yielded correct, logical, and fast results. This method at the same that had not had the disadvantages of aligning allowed the genes with actual length and content to be considered and also did not require high memory for large-length sequences. We believe that the performance of the proposed method could be used with other competitive gene clustering methods to group biologically relevant set of genes. Also, the proposed method can be seen as a predictive method for those genes bearing up weak genomic annotations.
PMID: 31981184 [PubMed - as supplied by publisher]

Source: J Appl Genet - January 23, 2020 Category: Genetics & Stem Cells Authors: Dehghanzadeh H, Ghaderi-Zefrehei M, Mirhoseini SZ, Esmaeilkhaniyan S, Haruna IL, Amirpour Najafabadi H Tags: J Appl Genet Source Type: research