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MIReNA: finding microRNAs with high accuracy and no learning at genome scale and from deep sequencing data.

机译:MIReNA:找到高精度的microRNA,无需在基因组规模和深度测序数据中学习。

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MOTIVATION: MicroRNAs (miRNAs) are a class of endogenes derived from a precursor (pre-miRNA) and involved in post-transcriptional regulation. Experimental identification of novel miRNAs is difficult because they are often transcribed under specific conditions and cell types. Several computational methods were developed to detect new miRNAs starting from known ones or from deep sequencing data, and to validate their pre-miRNAs. RESULTS: We present a genome-wide search algorithm, called MIReNA, that looks for miRNA sequences by exploring a multidimensional space defined by only five (physical and combinatorial) parameters characterizing acceptable pre-miRNAs. MIReNA validates pre-miRNAs with high sensitivity and specificity, and detects new miRNAs by homology from known miRNAs or from deep sequencing data. A performance comparison between MIReNA and four available predictive systems has been done. MIReNA approach is strikingly simple but it turns out to be powerful at least as much as more sophisticated algorithmic methods. MIReNA obtains better results than three known algorithms that validate pre-miRNAs. It demonstrates that machine-learning is not a necessary algorithmic approach for pre-miRNAs computational validation. In particular, machine learning algorithms can only confirm pre-miRNAs that look alike known ones, this being a limitation while exploring species with no known pre-miRNAs. The possibility to adapt the search to specific species, possibly characterized by specific properties of their miRNAs and pre-miRNAs, is a major feature of MIReNA. A parameter adjustment calibrates specificity and sensitivity in MIReNA, a key feature for predictive systems, which is not present in machine learning approaches. Comparison of MIReNA with miRDeep using deep sequencing data to predict miRNAs highlights a highly specific predictive power of MIReNA. AVAILABILITY: At the address http://www.ihes.fr/carbone/data8/.
机译:动机:MicroRNA(miRNA)是一类源自前体(pre-miRNA)的内源基因,参与转录后调控。对新的miRNA进行实验鉴定是困难的,因为它们通常在特定条件和细胞类型下转录。开发了几种计算方法来从已知的miRNA或深度测序数据中检测新的miRNA,并验证其前miRNA。结果:我们提出了一种称为MIReNA的全基因组搜索算法,该算法通过探索仅由五个可接受的前miRNA表征参数(物理和组合)定义的多维空间来寻找miRNA序列。 MIReNA以高灵敏度和特异性验证pre-miRNA,并通过同源性从已知miRNA或深度测序数据中检测新的miRNA。 MIReNA和四个可用的预测系统之间的性能比较已经完成。 MIReNA方法非常简单,但事实证明其功能至少与更复杂的算法方法一样强大。 MIReNA比三种验证pre-miRNA的已知算法获得更好的结果。它证明了机器学习不是pre-miRNAs计算验证的必要算法。特别地,机器学习算法只能确认看起来与已知的pre-miRNA相似的pre-miRNA,这在探索没有已知pre-miRNA的物种时是一个限制。 MIReNA的主要功能是使搜索适应特定物种的可能性,可能以其miRNA和pre-miRNA的特定特性为特征。参数调整可校准MIReNA的特异性和敏感性,MIReNA是预测系统的关键功能,在机器学习方法中不存在。使用深度测序数据预测miRNA的MIReNA与miRDeep的比较突出了MIReNA的高度特异性预测能力。可用性:地址为http://www.ihes.fr/carbone/data8/。

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