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RNA. 2007 Dec;13(12):2081-90. doi: 10.1261/rna.655107. Epub 2007 Oct 24.
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本文引用的文献

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Intronic microRNA precursors that bypass Drosha processing.绕过Drosha加工的内含子微小RNA前体。
Nature. 2007 Jul 5;448(7149):83-6. doi: 10.1038/nature05983. Epub 2007 Jun 24.
2
RNAstrand: reading direction of structured RNAs in multiple sequence alignments.RNA链:多序列比对中结构化RNA的阅读方向。
Algorithms Mol Biol. 2007 May 31;2:6. doi: 10.1186/1748-7188-2-6.
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Coordinate suppression of ERBB2 and ERBB3 by enforced expression of micro-RNA miR-125a or miR-125b.通过强制表达微小RNA miR-125a或miR-125b对ERBB2和ERBB3进行协同抑制。
J Biol Chem. 2007 Jan 12;282(2):1479-86. doi: 10.1074/jbc.M609383200. Epub 2006 Nov 16.
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A pattern-based method for the identification of MicroRNA binding sites and their corresponding heteroduplexes.一种基于模式的用于识别微小RNA结合位点及其相应异源双链体的方法。
Cell. 2006 Sep 22;126(6):1203-17. doi: 10.1016/j.cell.2006.07.031.
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Hairpins in a Haystack: recognizing microRNA precursors in comparative genomics data.大海捞针:在比较基因组学数据中识别微小RNA前体
Bioinformatics. 2006 Jul 15;22(14):e197-202. doi: 10.1093/bioinformatics/btl257.
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MicroRNAs and cell differentiation in mammalian development.微小RNA与哺乳动物发育中的细胞分化
Birth Defects Res C Embryo Today. 2006 Jun;78(2):140-9. doi: 10.1002/bdrc.20070.
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Bioinformatic discovery of microRNA precursors from human ESTs and introns.从人类EST序列和内含子中进行生物信息学方法发现微小RNA前体
BMC Genomics. 2006 Jul 3;7:164. doi: 10.1186/1471-2164-7-164.
8
Iron regulation and the cell cycle: identification of an iron-responsive element in the 3'-untranslated region of human cell division cycle 14A mRNA by a refined microarray-based screening strategy.铁调节与细胞周期:通过改进的基于微阵列的筛选策略鉴定人类细胞分裂周期14A mRNA 3'非翻译区中的铁反应元件。
J Biol Chem. 2006 Aug 11;281(32):22865-74. doi: 10.1074/jbc.M603876200. Epub 2006 Jun 7.
9
Combining multi-species genomic data for microRNA identification using a Naive Bayes classifier.使用朴素贝叶斯分类器结合多物种基因组数据进行微小RNA鉴定。
Bioinformatics. 2006 Jun 1;22(11):1325-34. doi: 10.1093/bioinformatics/btl094. Epub 2006 Mar 16.
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miRBase: microRNA sequences, targets and gene nomenclature.miRBase:微小RNA序列、靶标及基因命名法。
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miRRim:一种用于高灵敏度和特异性地寻找保守微小RNA的新型系统。

miRRim: a novel system to find conserved miRNAs with high sensitivity and specificity.

作者信息

Terai Goro, Komori Takashi, Asai Kiyoshi, Kin Taishin

机构信息

Intec Web and Genome Informatics Corporation, Koto-ku, Tokyo, Japan, 136-0075.

出版信息

RNA. 2007 Dec;13(12):2081-90. doi: 10.1261/rna.655107. Epub 2007 Oct 24.

DOI:10.1261/rna.655107
PMID:17959929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2080609/
Abstract

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/.

摘要

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。