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DeepSplice: Deep classification of novel splice junctions revealed by RNA-seq

机译:DeepSplice:RNA-seq揭示的新型剪接连接的深度分类

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Alternative splicing (AS) is a regulated process that enables the production of multiple mRNA transcripts from a single multi-exon gene. The availability of large-scale RNA-seq datasets has made it possible to predict splice junctions, as well as splice sites through spliced alignment to the reference genome. This greatly enhances the capability to decipher gene structures and explore the diversity of splicing variants. However, existing ab initio aligners are vulnerable to false positive spliced alignments as a result of sequence errors and random sequence matches. These spurious alignments can lead to a significant set of false positive splice junction predictions, confusing downstream analyses of splice variant detection and abundance estimation. In this work, we illustrate that splice junction sequence characteristics can be ascertained from experimental data with deep learning techniques. We employ deep convolutional neural networks for a novel splice junction classification tool named DeepSplice that (i) outperforms state-of-the-art methods for predicting splice sites, (ii) shows high computational efficiency and (iii) can be applied to self-defined training data by users.
机译:选择性剪接(AS)是一种受调控的过程,可从单个多外显子基因产生多个mRNA转录本。大规模RNA-seq数据集的可用性使预测剪接点以及通过与参考基因组的剪接比对预测剪接位点成为可能。这大大增强了解密基因结构和探索剪接变体多样性的能力。然而,由于序列错误和随机序列匹配,现有的从头算式比对器容易受到假阳性剪接比对的影响。这些虚假的对齐方式可能导致大量假阳性的拼接结预测,从而使下游的拼接变异检测和丰度估计分析混乱。在这项工作中,我们说明了可以使用深度学习技术从实验数据确定剪接点序列特征。我们将深度卷积神经网络用于名为DeepSplice的新型剪接点分类工具,该工具(i)优于最新的预测剪接位点的方法,(ii)显示出很高的计算效率,并且(iii)可以应用于自用户定义的培训数据。

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