Improving microRNA target prediction with gene expression profiles

被引:18
|
作者
Ovando-Vazquez, Cesare [1 ]
Lepe-Soltero, Daniel [1 ]
Abreu-Goodger, Cei [1 ]
机构
[1] IPN, Ctr Invest & Estudios Avanzados, Unidad Genom Avanzada Langebio, Guanajuato 36821, Mexico
来源
BMC GENOMICS | 2016年 / 17卷
关键词
microRNA target prediction; Support Vector Machine; Gene expression profiles; Biological context; microRNA perturbation experiments; INTEGRATIVE ANALYSIS; RNA-SEQ; TOOLS; IDENTIFICATION; REPRESSION; MIR-29B; SHOWS;
D O I
10.1186/s12864-016-2695-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Mammalian genomes encode for thousands of microRNAs, which can potentially regulate the majority of protein-coding genes. They have been implicated in development and disease, leading to great interest in understanding their function, with computational methods being widely used to predict their targets. Most computational methods rely on sequence features, thermodynamics, and conservation filters; essentially scanning the whole transcriptome to predict one set of targets for each microRNA. This has the limitation of not considering that the same microRNA could have different sets of targets, and thus different functions, when expressed in different types of cells. Results: To address this problem, we combine popular target prediction methods with expression profiles, via machine learning, to produce a new predictor: TargetExpress. Using independent data from microarrays and high-throughput sequencing, we show that TargetExpress outperforms existing methods, and that our predictions are enriched in functions that are coherent with the added expression profile and literature reports. Conclusions: Our method should be particularly useful for anyone studying the functions and targets of miRNAs in specific tissues or cells. TargetExpress is available at: http://targetexpress.ceiabreulab.org/.
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页数:13
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