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[微小RNA发现的计算方法]

[Computational approaches to microRNA discovery].

作者信息

Hou Yan-Yan, Ying Xiao-Min, Li Wu-Ju

机构信息

Center of Computational Biology, Beijing Institute of Basic Medical Sciences, Beijing 100850, China.

出版信息

Yi Chuan. 2008 Jun;30(6):687-96. doi: 10.3724/sp.j.1005.2008.00687.

Abstract

microRNAs (miRNAs) are endogenous non-coding RNAs of ~21 nucleotides in length discovered in recent years. They are involved in diverse pathways and play an important role in gene regulation in plants and animals. There are two main groups of approaches to miRNA discovery, which are cDNA cloning and computational identification. Since some miRNAs are expressed at a low level and the expression of many miRNAs has spatio-temporal specificity, it is difficult to find them through cDNA cloning. However, computational approaches can predict the miRNAs specifically expressed or with low abundance, which is complement to cDNA cloning. Computational approaches have hence gained wide attention. In this review, the computational approaches to miRNA discovery were summarized. According to their intrinsic characteristics, computational approaches were categorized into five classes: (1) homology search; (2) prediction based on comparative genomics; (3) scoring candidates using the sequence and structure characteristics; (4) prediction combined with targets; and (5) prediction with machine learning. The principles of each class of the approaches and their advantages and limitations in miRNA discovery were discussed. Finally, the future direction in miRNA discovery was pointed out.

摘要

微小RNA(miRNA)是近年来发现的长度约为21个核苷酸的内源性非编码RNA。它们参与多种途径,在动植物的基因调控中发挥重要作用。miRNA发现主要有两大类方法,即cDNA克隆和计算鉴定。由于一些miRNA表达水平较低,且许多miRNA的表达具有时空特异性,通过cDNA克隆很难找到它们。然而,计算方法可以预测特异性表达或低丰度的miRNA,这是对cDNA克隆的补充。因此,计算方法受到了广泛关注。在这篇综述中,总结了miRNA发现的计算方法。根据其内在特征,计算方法分为五类:(1)同源性搜索;(2)基于比较基因组学的预测;(3)利用序列和结构特征对候选物进行评分;(4)结合靶标的预测;(5)机器学习预测。讨论了每类方法的原理及其在miRNA发现中的优缺点。最后,指出了miRNA发现的未来方向。

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