| Literature DB >> 25780273 |
Abstract
MiRNAs are small (~22nt long) non-coding RNA sequences; binds to the complementarity target sites in 3' Untranslated Region (UTR) of mRNA sequences but not restricted to other mRNA regions viz., 5' UTR and Coding sequences (CDS). Complementarity binding of miRNA to mRNA target sites either results in complete degradation of the mRNA itself or it may regulate the mRNA as an oncogene or as a tumor suppressor gene. However, the exact mechanism involved in identifying a miRNA to be associated with cancer is still unclear. Further, with the outburst in the number of miRNAs sequences recorded every year in miRBase, the gap is still widening mainly due to the laborious and economically unfavorable experimental procedures associated with the functional annotation. Motivated by the fact, we constructed a two-step support vector machine-based predictive model - miRSEQ and miRINT. However, the major pitfall during the construction of the model is the class imbalance problem. Hence, in order to overcome class imbalance problem, in the present study we empirically compare the effectiveness of two different methods viz., Synthetic Minority Oversampling Technique (SMOTE) and cost-senstive learning method. Performance measures were evaluated in terms of Precision and Recall. Based on our result, it was observed that for miRNA dataset with high class imbalance utilized for predicting association of cancer, cost-sensitive method outperformed the oversampling method.Entities:
Keywords: Cost-sensitive; SMOTE; Support Vector Machines; miRNA-mRNA interaction
Year: 2015 PMID: 25780273 PMCID: PMC4349932 DOI: 10.6026/97320630011006
Source DB: PubMed Journal: Bioinformation ISSN: 0973-2063
Figure 1Comparison of SMOTE and cost-sensitive method to overcome class imbalance in the miRNA dataset associated with cancer: A) Comparison of SMOTE and cost-sensitive method with miRSEQ classifier trained with sequence based features only; (B, C & D) Comparison of SMOTE and cost-sensitive method with miRINT trained with miRNA-mRNA interaction based features. In both the classifier, SMOTE method tends to overfit the test dataset. SMOTE and cost-sensitive methods were tested with five independent test datasets (Run 1 to 5).