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MD-SVM: a novel SVM-based algorithm for the motif discovery of transcription factor binding sites

机译:MD-SVM:一种基于SVM的基于SVM的转录因子结合位点的算法

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Transcription factors (TFs) play important roles in the regulation of gene expression. They can activate or block transcription of downstream genes in a manner of binding to specific genomic sequences. Therefore, motif discovery of these binding preference patterns is of central significance in the understanding of molecular regulation mechanism. Many algorithms have been proposed for the identification of transcription factor binding sites. However, it remains a challengeable problem. Here, we proposed a novel motif discovery algorithm based on support vector machine (MD-SVM) to learn a discriminative model for TF binding sites. MD-SVM firstly obtains position weight matrix (PWM) from a set of training datasets. Then it translates the MD problem into a computational framework of multiple instance learning (MIL). It was applied to several real biological datasets. Results show that our algorithm outperforms MI-SVM in terms of both accuracy and specificity. In this paper, we modeled the TF motif discovery problem as a MIL optimization problem. The SVM algorithm was adapted to discriminate positive and negative bags of instances. Compared to other svm-based algorithms, MD-SVM show its superiority over its competitors in term of ROC AUC. Hopefully, it could be of benefit to the research community in the understanding of molecular functions of DNA functional elements and transcription factors.
机译:转录因子(TFS)在基因表达调节中起重要作用。它们可以以与特定基因组序列结合的方式激活或阻断下游基因的转录。因此,这些结合偏好模式的基序发现是对分子调控机制的理解中的情调。已经提出了许多算法用于鉴定转录因子结合位点。但是,它仍然是一个有挑战性的问题。在这里,我们提出了一种基于支持向量机(MD-SVM)的新型基序发现算法,用于学习TF结合位点的判别模型。 MD-SVM首先从一组训练数据集获得位置权重矩阵(PWM)。然后它将MD问题转换为多实例学习的计算框架(MIL)。它应用于几个真实的生物数据集。结果表明,我们的算法在精度和特异性方面优于MI-SVM。在本文中,我们将TF主题发现问题建模为MIL优化问题。 SVM算法适用于区分正面和负袋。与其他基于SVM的算法相比,MD-SVM在ROC AUC期间表现出其对竞争对手的优越性。希望,在理解DNA功能元素和转录因子的情况下,它可能有益于研究界。

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