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XG-PseU:一种基于极端梯度提升的假尿嘧啶位点识别方法。

XG-PseU: an eXtreme Gradient Boosting based method for identifying pseudouridine sites.

机构信息

School of Life Sciences, and Center for Genomics and Computational Biology, North China University of Science and Technology, Tangshan, 063000, China.

Innovative Institute of Chinese Medicine and Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, 611730, China.

出版信息

Mol Genet Genomics. 2020 Jan;295(1):13-21. doi: 10.1007/s00438-019-01600-9. Epub 2019 Aug 7.

Abstract

As one of the most popular post-transcriptional modifications, pseudouridine (Ψ) participates in a series of biological processes. Therefore, the efficient detection of pseudouridine sites is very important in revealing its functions in biological processes. Although experimental techniques have been proposed for identifying Ψ sites at single-base resolution, they are still labor intensive and expensive. Recently, to fill the experimental method's gap, computational methods have been proposed for identifying Ψ sites. However, their performances are still unsatisfactory. In this paper, we proposed an eXtreme Gradient Boosting (xgboost)-based method, called XG-PseU, to identify Ψ sites based on the optimal features obtained using the forward feature selection together with increment feature selection method. Our results demonstrated that XG-PseU is superior or at least complementary to existing methods for identifying pseudouridine sites. Finally, a freely available online web server for XG-PseU was established at http://www.bioml.cn/. We wish that XG-PseU will become a useful tool for computationally identifying Ψ sites.

摘要

作为最流行的转录后修饰之一,假尿嘧啶核苷(Ψ)参与了一系列的生物过程。因此,高效地检测假尿嘧啶核苷位点对于揭示其在生物过程中的功能非常重要。尽管已经提出了一些实验技术来确定单碱基分辨率的 Ψ 位点,但这些技术仍然非常繁琐和昂贵。最近,为了弥补实验方法的不足,已经提出了一些基于计算的方法来识别 Ψ 位点。然而,它们的性能仍然不尽如人意。在本文中,我们提出了一种基于极端梯度提升(xgboost)的方法,称为 XG-PseU,该方法基于使用前向特征选择和增量特征选择方法获得的最优特征来识别 Ψ 位点。我们的结果表明,XG-PseU 在识别假尿嘧啶核苷位点方面优于或至少与现有的方法互补。最后,我们在 http://www.bioml.cn/ 上建立了一个免费的在线 XG-PseU 网络服务器。我们希望 XG-PseU 将成为一种用于计算识别 Ψ 位点的有用工具。

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