微rna基因预测的数据挖掘:类不平衡和特征数对微rna基因预测的影响

Muserref Duygu Saçar, J. Allmer
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引用次数: 23

摘要

MicroRNAs (miRNAs)是一种小的非编码rna,参与基因表达的转录后调节。它们的短(18-24)单链成熟序列涉及靶向特定基因。事实证明,实验方法是有限的,即使不是不可能,也很难通过实验建立所有的mirna及其靶标。因此,人们提出了许多预测miRNA基因和miRNA靶点的工具。这些工具中的大多数都是基于机器学习方法,并且在该领域中主要采用两类分类。不幸的是,真正的负数据是不可能获得的,目前只能获得负数据的近似值。此外,我们最近表明,现有的积极数据并非完美无缺。在这里,我们研究了班级不平衡对学习者准确率的影响,发现在最佳和最差准确率和召回值之间存在高达50%的差异。此外,我们研究了特征数量的增加,并发现了一条曲线,在召回率为0.97、精度为0.91时达到最大值,在包含超过100个特征后,性能会迅速下降。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Data mining for microrna gene prediction: On the impact of class imbalance and feature number for microrna gene prediction
MicroRNAs (miRNAs) are small, non-coding RNAs which are involved in the posttranscriptional modulation of gene expression. Their short (18-24) single stranded mature sequences are involved in targeting specific genes. It turns out that experimental methods are limited and that it is difficult, if not impossible, to establish all miRNAs and their targets experimentally. Therefore, many tools for the prediction of miRNA genes and miRNA targets have been proposed. Most of these tools are based on machine learning methods and within that area mostly two-class classification is employed. Unfortunately, truly negative data is impossible to attain and only approximations of negative data are currently available. Also, we recently showed that the available positive data is not flawless. Here we investigate the impact of class imbalance on the learner accuracy and find that there is a difference of up to 50% between the best and worst precision and recall values. In addition, we looked at increasing number of features and found a curve maximizing at 0.97 recall and 0.91 precision with quickly decaying performance after inclusion of more than 100 features.
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