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A Complete Pipeline for Isolating and Sequencing MicroRNAs, and Analyzing Them Using Open Source Tools
Published on: August 21, 2019
CL-PMI: A Precursor MicroRNA Identification Method Based on Convolutional and Long Short-Term Memory Networks
Huiqing Wang1, Yue Ma1, Chunlin Dong2
1College of Information and Computer, Taiyuan University of Technology, Taiyuan, China.
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.
Insights
Identifying pre-microRNAs (pre-miRNAs) is crucial for medical treatment. A new CL-PMI algorithm effectively identifies pre-miRNAs by analyzing spatial and sequential data, overcoming dataset imbalance issues.
Area of Science:
- Bioinformatics
- Genomics
- Computational Biology
Background:
- MicroRNAs (miRNAs) are key gene regulators, primarily acting as translational repressors in mammals.
- Identifying precursor microRNAs (pre-miRNAs) is challenging due to their short length and complex structures.
- Existing computational methods often neglect sequential and spatial characteristics, and suffer from dataset imbalance, limiting pre-miRNA identification accuracy.
Purpose of the Study:
- To develop an advanced computational method for accurate pre-miRNA identification.
- To address the limitations of existing methods, including feature extraction and dataset imbalance.
- To improve the understanding and identification of gene-regulating molecules.
Main Methods:
- Proposed a cascaded Convolutional Neural Network (CNN) and Long Short-Term Memory (LSTM) framework named CL-PMI.
- Utilized CNN for automatic spatial feature extraction and LSTM for capturing sequential characteristics.
- Incorporated attention mechanisms for long-term dependence modeling and focal loss to mitigate dataset imbalance.
Main Results:
- The CL-PMI algorithm demonstrated superior performance across all tested datasets compared to existing methods.
- The method effectively identified pre-miRNAs by integrating both spatial and sequential information.
- Focal loss successfully addressed the challenge of imbalanced datasets in pre-miRNA identification.
Conclusions:
- CL-PMI offers a robust and effective approach for pre-miRNA identification.
- The integration of CNN and LSTM, along with attention mechanisms, enhances the model's ability to capture complex pre-miRNA features.
- This study provides a significant advancement in computational methods for identifying crucial gene-regulating molecules.
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