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ViralmiR: a support-vector-machine-based method for predicting viral microRNA precursors

机译:ViraLmir:一种基于支持 - 矢量机的预测方法,用于预测病毒微小RNA前体

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Background: microRNAs (miRNAs) play a vital role in development, oncogenesis, and apoptosis by binding to mRNAs to regulate the posttranscriptional level of coding genes in mammals, plants, and insects. Recent studies have demonstrated that the expression of viral miRNAs is associated with the ability of the virus to infect a host. Identifying potential viral miRNAs from experimental sequence data is valuable for deciphering virus-host interactions. Thus far, a specific predictive model for viral miRNA identification has yet to be developed.Methods and results: Here, we present ViralmiR for identifying viral miRNA precursors on the basis of sequencing and structural information. We collected 263 experimentally validated miRNA precursors (pre-miRNAs) from 26 virus species and generated sequencing fragments from virus and human genomes as the negative dataset. Support vector machine and random forest models were established using 54 features from RNA sequences and secondary structural information. The results show that ViralmiR achieved a balanced accuracy higher than 83%, which is superior to that of previously developed tools for identifying pre-miRNAs.Conclusions: The easy-to-use ViralmiR web interface has been provided as a helpful resource for researchers to use in analyzing and deciphering virus-host interactions. The web interface of ViralmiR can be accessed at http://csb.cse.yzu.edu.tw/viralmir/.
机译:背景:MicroRNA(miRNA)通过与MRNA结合来调节哺乳动物,植物和昆虫的编码基因的后剖析水平,在发育,肿瘤发生和细胞凋亡中起着至关重要的作用。最近的研究表明,病毒miRNA的表达与病毒感染宿主的能力有关。从实验序列数据中识别潜在的病毒MiRNA对于解密病毒 - 宿主相互作用是有价值的。到目前为止,尚未开发了一种特异的病毒miRNA鉴定的预测模型。方法和结果:在这里,我们在序列和结构信息的基础上呈现病毒MIR鉴定病毒miRNA前体。我们从26个病毒物种中收集了263个实验验证的miRNA前体(前miRNA),并从病毒和人类基因组中产生测序片段作为负数据集。使用来自RNA序列和二级结构信息的54个功能建立了支持向量机和随机林模型。结果表明,Viralmir实现了高于83%的均衡精度,其优于先前开发的用于识别预先识别的工具.Conclusions:已经向研究人员提供了有用的资源提供了易于使用的病毒麦利Web界面用于分析和解密病毒 - 主机相互作用。 Viralmir的Web界面可以访问http://csb.cse.yzu.edu.tw/viralmir/。

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