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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:结合多尺度卷积和长短期记忆神经网络准确预测转录因子结合位点。

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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)是DNA-蛋白质结合位点之一,在理解基因表达调控和药物设计中起着重要作用。最近,基于深度学习的方法已广泛用于TFBS的预测中。在这项工作中,我们提出了一种新颖的深度学习模型,称为多尺度卷积网络与长短期记忆网络(MCNN-LSTM)的组合,该模型利用多尺度卷积进行特征处理,并采用长短期记忆网络识别DNA序列中的TFBS。此外,我们设计了一种新的编码方法,称为多核苷酸单发(MNOH),它考虑了相邻位置核苷酸之间的相关性,以进一步提高TFBS的预测性能。严格的交叉验证和对基准数据集的独立测试证明了MNOH和MCNN-LSTM的功效。基于提出的方法,我们进一步实现了一个新的TFBS预测器,称为DeepTF。计算实验结果表明,我们的预测器优于几种现有的TFBS预测器。

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