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Convolution neural network model for predicting single guide RNA efficiency in CRISPR/Cas9 system

机译:CRISPR / CAS9系统中单引导RNA效率预测的卷积神经网络模型

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摘要

CRISPR/Cas9 is a tool which has unprecedented gene editing capabilities which if harnessed correctly can revolutionize our lives. But, the system is still in its infancy and there is scope for substantial optimization particularly in the process of guide selection. There are thousands of RNA guides which can theoretically provide gene knockouts. However, these guides do not share the same knockout efficiency. In this paper, a convolution neural network (CNN) learning model (named as DeepSgRNA) is proposed to identify & predict RNA guides for achieving better efficiency. The proposed model removes the need for any feature construction. Previously there have been attempts at automating guide selection process using machine learning (ML) with handcrafted features. The ML models have been heavily reliant on feature engineering and thus are not scalable. The hierarchical feature generation abilities of CNN's have been leveraged for this task. The model is trained on approximately 400,000 instances of sgRNA sequences from the GenomeCRISPR project dataset. A performance comparison with existing models is presented based on the Spearman correlation index. Finally, it has been seen that the proposed CNN model (DeepSgRNA) is better at predicting sgRNA guide efficiencies than all the existing models.
机译:CRISPR / CAS9是一种工具,其具有前所未有的基因编辑能力,如果正确地利用可以彻底利用,可以彻底改变我们的生活。但是,系统仍处于初期阶段,特别是在指导选择过程中具有实质性优化的范围。有成千上万的RNA指南,理论上可以提供基因敲门声。但是,这些指南不共享相同的淘汰效率。在本文中,提出了一种卷积神经网络(CNN)学习模型(名称为DeepSGRNA),以识别和预测实现更好效率的RNA指南。所提出的模型消除了对任何特征结构的需求。以前,使用手工特征的机器学习(ml),已经尝试自动化指南选择过程。 ML型号在特征工程上严重依赖,因此不可扩展。 CNN的分层特征生成能力已为此任务杠杆。该模型从Genomecrispr项目数据集接受大约400,000个SGRNA序列实例培训。根据Spearman相关索引提出了与现有模型的性能比较。最后,已经看出,所提出的CNN模型(DeepSgrna)更好地预测SGRNA引导效率而不是所有现有模型。

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