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MRCNN: a deep learning model for regression of genome-wide DNA methylation

机译:MRCNN:一种深入学习模型,用于基因组宽DNA甲基化

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Background: Determination of genome-wide DNA methylation is significant for both basic research and drug development. As a key epigenetic modification, this biochemical process can modulate gene expression to influence the cell differentiation which can possibly lead to cancer. Due to the involuted biochemical mechanism of DNA methylation, obtaining a precise prediction is a considerably tough challenge. Existing approaches have yielded good predictions, but the methods either need to combine plentyof features and prerequisites or deal with only hypermethylation and hypomethylation.Results: In this paper, we propose a deep learning method for prediction of the genome-wide DNA methylation, in which the Methylation Regression is implemented by Convolutional Neural Networks (MRCNN). Through minimizing the continuous loss function, experiments show that our model is convergent and more precise than the state-of-art method (DeepCpG) according to results of the evaluation. MRCNN also achieves the discovery of de novo motifs by analysis of features from the training process.Conclusions: Genome-wide DNA methylation could be evaluated based on the corresponding local DNA sequences of target CpG loci. With the autonomous learning pattern of deep learning,MRCNN enables accurate predictions of genome-wide DNA methylation status without predefined features and discovers some de novo methylation-related motifs that match known motifs by extracting sequence patterns.
机译:背景:基因组DNA甲基化的测定对于基础研究和药物开发来说是显着的。作为关键的表观遗传修饰,这种生化过程可以调节基因表达,影响可能导致癌症的细胞分化。由于DNA甲基化的持续生物化学机制,获得精确的预测是一个很大的挑战。现有方法产生了良好的预测,但方法需要将Plyentof特征和先决条件结合或仅处理高甲基化和脱甲酰基化。结果:本文提出了一种深入学习方法,用于预测基因组宽的DNA甲基化,其中甲基化回归由卷积神经网络(MRCNN)实施。通过最小化连续损失功能,实验表明,根据评估结果,我们的模型比最先进的方法(DeptCPG)收敛和更精确。 MRCNN还通过分析来自训练过程的特征来实现DE Novo主题。结论:可以基于目标CpG基因座的相应局部DNA序列来评估基因组 - 宽DNA甲基化。利用深度学习的自主学习模式,MRCNN能够精确地预测基因组的DNA甲基化状态,而无需预定的特征,并发现通过提取序列图案来匹配已知基序的一些DE Novo甲基化相关的基序。

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