Abstract

MicroRNAs (miRNAs) are the major class of gene-regulating molecules that bind mRNAs. They function mainly as translational repressors in mammals. Therefore, how to identify miRNAs is one of the most important problems in medical treatment. Many known pre-miRNAs have a hairpin ring structure containing more structural features, and it is difficult to identify mature miRNAs because of their short length. Therefore, most research focuses on the identification of pre-miRNAs. Most computational models rely on manual feature extraction to identify pre-miRNAs and do not consider the sequential and spatial characteristics of pre-miRNAs, resulting in a loss of information. As the number of unidentified pre-miRNAs is far greater than that of known pre-miRNAs, there is a dataset imbalance problem, which leads to a degradation of the performance of pre-miRNA identification methods. In order to overcome the limitations of existing methods, we propose a pre-miRNA identification algorithm based on a cascaded CNN-LSTM framework, called CL-PMI. We used a convolutional neural network to automatically extract features and obtain pre-miRNA spatial information. We also employed long short-term memory (LSTM) to capture time characteristics of pre-miRNAs and improve attention mechanisms for long-term dependence modeling. Focal loss was used to improve the dataset imbalance. Compared with existing methods, CL-PMI achieved better performance on all datasets. The results demonstrate that this method can effectively identify pre-miRNAs by simultaneously considering their spatial and sequential information, as well as dealing with imbalance in the datasets.

Highlights

  • MicroRNAs are ribonucleic acid molecules of about 21–23 nucleotides that are widely found in microorganisms, viruses (Pfeffer et al, 2004), and plants (Jones-Rhoades et al 2006)

  • Our method achieved the best performance in terms of SE, F-score, and positive predictive value (PPV); it did not give the highest scores on other metrics, the performance of CL-PMI was close to that of the best method

  • We proposed a new pre-miRNA identification method, called CL-MPI

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Summary

Introduction

MicroRNAs (miRNAs) are ribonucleic acid molecules of about 21–23 nucleotides that are widely found in microorganisms, viruses (Pfeffer et al, 2004), and plants (Jones-Rhoades et al 2006). They are known to regulate thousands of human genes that account for more than one-third of the genomic coding region (Bentwich et al, 2005). A study has shown that 50% of miRNAs frequently appear in tumor-associated gene regions or fragile. The pre-miRNA is digested by Dicer to form a mature miRNA (Agarwal et al, 2010). It is difficult to identify mature miRNAs owing to their short length; most previous studies have focused on identifying pre-miRNAs

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