MRSLpred—a hybrid approach for predicting multi-label subcellular localization of mRNA at the genome scale

S. Choudhury, Nisha Bajiya, Sumeet Patiyal, G. Raghava
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Abstract

In the past, several methods have been developed for predicting the single-label subcellular localization of messenger RNA (mRNA). However, only limited methods are designed to predict the multi-label subcellular localization of mRNA. Furthermore, the existing methods are slow and cannot be implemented at a transcriptome scale. In this study, a fast and reliable method has been developed for predicting the multi-label subcellular localization of mRNA that can be implemented at a genome scale. Machine learning-based methods have been developed using mRNA sequence composition, where the XGBoost-based classifier achieved an average area under the receiver operator characteristic (AUROC) of 0.709 (0.668–0.732). In addition to alignment-free methods, we developed alignment-based methods using motif search techniques. Finally, a hybrid technique that combines the XGBoost model and the motif-based approach has been developed, achieving an average AUROC of 0.742 (0.708–0.816). Our method—MRSLpred—outperforms the existing state-of-the-art classifier in terms of performance and computation efficiency. A publicly accessible webserver and a standalone tool have been developed to facilitate researchers (webserver: https://webs.iiitd.edu.in/raghava/mrslpred/).
MRSLpred--在基因组尺度上预测 mRNA 多标记亚细胞定位的混合方法
过去,人们开发了多种方法来预测信使核糖核酸(mRNA)的单标记亚细胞定位。然而,用于预测多标签 mRNA 亚细胞定位的方法还很有限。此外,现有方法速度较慢,无法在转录组范围内实施。本研究开发了一种快速可靠的方法来预测 mRNA 的多标签亚细胞定位,该方法可在基因组尺度上实施。利用 mRNA 序列组成开发了基于机器学习的方法,其中基于 XGBoost 的分类器的平均接收器算子特征下面积(AUROC)达到了 0.709(0.668-0.732)。除了无配准方法外,我们还利用主题搜索技术开发了基于配准的方法。最后,我们还开发了一种混合技术,它结合了 XGBoost 模型和基于图案的方法,平均 AUROC 为 0.742(0.708-0.816)。我们的方法--MRSLpred 在性能和计算效率方面都优于现有的一流分类器。为方便研究人员使用,我们还开发了可公开访问的网络服务器和独立工具(网络服务器:https://webs.iiitd.edu.in/raghava/mrslpred/)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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