EDCLoc: a prediction model for mRNA subcellular localization using improved focal loss to address multi-label class imbalance

BackgroundThe subcellular localization of mRNA plays a crucial role in gene expression regulation and various cellular processes. However, existing wet lab techniques like RNA-FISH are usually time-consuming, labor-intensive, and limited to specific tissue types. Researchers have developed several computational methods to predict mRNA subcellular localization to address this. These methods face the problem of class imbalance in multi-label classification, causing models to favor majority classes and overlook minority classes during training. Additionally, traditional feature extraction methods have high computational costs, incomplete features, and may lead to the loss of critical information. On the other hand, deep learning methods face challenges related to hardware performance and training time when handling complex sequences. They may suffer from the curse of dimensionality and overfitting problems. Therefore, there is an urgent need for more efficient and accurate prediction models.ResultsTo address these issues, we propose a multi-label classifier, EDCLoc, for predicting mRNA subcellular localization. EDCLoc reduces training pressure through a stepwise pooling strategy and applies grouped convolution blocks of varying sizes at different levels, combined with residual connections, to achieve efficient feature extraction and gradient propagation. The model employs global max pooling at the end to further reduce feature dimensions and highlight key features. To tackle class imbalance, we improved the focal loss function to enhance the model's focus on minority classes. Evaluation results show that EDCLoc outperforms existing methods in most subcellular regions. Additionally, the position weight matrix extracted by multi-scale CNN filters can match known RNA-binding protein motifs, demonstrating EDCLoc's effectiveness in capturing key sequence features.ConclusionsEDCLoc outperforms existing prediction tools in most subcellular regions and effectively mitigates class imbalance issues in multi-label classification. These advantages make EDCLoc a reliable choice for multi-label mRNA subcellular localization. The dataset and source code used in this study are available at https://github.com/DellCode233/EDCLoc.