Terai Goro, Komori Takashi, Asai Kiyoshi, Kin Taishin
Intec Web and Genome Informatics Corporation, Koto-ku, Tokyo, Japan, 136-0075.
RNA. 2007 Dec;13(12):2081-90. doi: 10.1261/rna.655107. Epub 2007 Oct 24.
The identification of novel miRNAs has significant biological and clinical importance. However, none of the known miRNA features alone is sufficient for accurately detecting novel miRNAs. The aim of this paper is to integrate these features in a straightforward manner for detecting miRNAs with better accuracy. Since most miRNA regions are highly conserved among vertebrates for the ability to form stable hairpin structures, we implemented a hidden Markov model that outputs multidimensional feature vectors composed of both evolutionary features and secondary structural ones. The proposed method, called miRRim, outperformed existing ones in terms of detection/prediction performance: The total number of predictions was smaller than with existing methods when the number of miRNAs detected was adjusted to be the same. Moreover, there were several candidates predicted only by our method that are clustered with the known miRNAs, suggesting that our method is able to detect novel miRNAs. Genomic coordinates of predicted miRNA can be obtained from http://mirrim.ncrna.org/.
新型微小RNA(miRNA)的鉴定具有重大的生物学和临床意义。然而,仅靠已知的miRNA特征中的任何一个都不足以准确检测新型miRNA。本文的目的是以一种直接的方式整合这些特征,以便更准确地检测miRNA。由于大多数miRNA区域在脊椎动物中因能够形成稳定的发夹结构而高度保守,我们实施了一种隐马尔可夫模型,该模型输出由进化特征和二级结构特征组成的多维特征向量。所提出的方法称为miRRim,在检测/预测性能方面优于现有方法:当检测到的miRNA数量调整为相同时,预测总数比现有方法少。此外,有几个仅由我们的方法预测的候选物与已知miRNA聚类,这表明我们的方法能够检测新型miRNA。预测的miRNA的基因组坐标可从http://mirrim.ncrna.org/获得。