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DeepARC: An Attention-based Hybrid Model for Predicting Transcription Factor Binding Sites from Positional Embedded DNA Sequence

机译:Deoperc:一种基于注意的杂种模型,用于预测定位嵌入DNA序列的转录因子结合位点

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The binding of transcription factors (TFs) to transcription factor binding sites (TFBS) plays a pivotal role in regulating gene expression and evolution. Accurately modeling the specificity of DNA and searching for TFBS helps understand the genome's function and evolution. In recent years, computational identification of TFBS has become an active field of research. Here, we propose DeepARC, an attention-based hybrid approach combining convolutional neural network (CNN) and recurrent neural network (RNN) for predicting TFBS. We employ a position-based embedding strategy to embed a DNA sequence into a matrix with distributed representation contenting the position information and then feed the distributed representations of the sequence into a CNN-BiLSTM-Attention-based framework to classify whether there is a TFBS in a sequence. Take the advantage of the attention mechanism, DeepARC can obtain more valuable information about TFBS and add interpretability to the TFBS search process. Moreover, sufficient experiments prove that DeepARC has better performance than existing predictors. The DeepARC web server is available at http://deeparc.denglab.org.
机译:转录因子(TFS)与转录因子结合位点(TFBs)的结合在调节基因表达和进化中起着枢转作用。准确地建模DNA的特异性并搜索TFB有助于了解基因组的功能和进化。近年来,TFB的计算鉴定已成为一个积极的研究领域。这里,我们提出了一种基于注意力的混合方法,将卷积神经网络(CNN)和经常性神经网络(RNN)组合用于预测TFBS的关注的混合方法。我们采用基于位置的嵌入策略嵌入的DNA序列与分布式表示contenting的位置信息,然后喂序列的分布表示为CNN-BiLSTM-基于注意机制的框架的矩阵来分类是否存在一个TFBS序列。采取注意机制的优势,Deeparc可以获得有关TFB的更有价值的信息,并为TFBS搜索过程添加解释性。此外,足够的实验证明,除了现有的预测因子,Depepcc具有更好的性能。 Deeparc Web服务器可在http://deeparc.denglab.org提供。

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