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DeepTF: Accurate Prediction of Transcription Factor Binding Sites by Combining Multi-scale Convolution and Long Short-Term Memory Neural Network

机译:DEEPTF:通过组合多尺度卷积和长短期记忆神经网络来精确预测转录因子绑定站点

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Transcription factor binding site (TFBS), one of the DNA-protein binding sites, plays important roles in understanding regulation of gene expression and drug design. Recently, deep-learning based methods have been widely used in the prediction of TFBS. In this work, we propose a novel deep-learning model, called Combination of Multi-Scale Convolutional Network and Long Short-Term Memory Network (MCNN-LSTM), which utilizes multi-scale convolution for feature processing, and the long short-term memory network to recognize TFBS in DNA sequences. Moreover, we design a new encoding method, called multi-nucleotide one-hot (MNOH), which considers the correlation between nucleotides in adjacent positions, to further improve the prediction performance of TFBS. Stringent cross-validation and independent tests on benchmark datasets demonstrated the efficacy of MNOH and MCNN-LSTM. Based on the proposed methods, we further implement a new TFBS predictor, called DeepTF. The computational experimental results show that our predictor outperformed several existing TFBS predictors.
机译:转录因子结合位点(TFBs),DNA蛋白结合位点之一,在理解基因表达和药物设计调节方面起重要作用。最近,基于深度学习的方法已被广泛用于TFB的预测。在这项工作中,我们提出了一种新的深度学习模型,称为多尺度卷积网络和长短期内存网络(MCNN-LSTM)的组合,利用多尺度卷积来进行特征处理,以及长期短期记忆网络识别DNA序列中的TFB。此外,我们设计一种称为多核苷酸单热(MNOH)的新编码方法,其考虑了相邻位置中核苷酸之间的相关性,以进一步改善TFB的预测性能。基准数据集的严格交叉验证和独立测试证明了MNOH和MCNN-LSTM的功效。基于所提出的方法,我们进一步实施了一种新的TFBS预测因子,称为DEEPTF。计算实验结果表明,我们的预测指标优于几个现有的TFBS预测因子。

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