ReadCurrent:基于 VDCNN 的快速准确纳米孔选择性测序工具。

IF 6.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Kechen Fan, Mengfan Li, Jiarong Zhang, Zihan Xie, Daguang Jiang, Xiaochen Bo, Dongsheng Zhao, Shenghui Shi, Ming Ni
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引用次数: 0

摘要

通过纳米孔选择性测序技术,可以利用计算方法而不是实验方法(如靶向多聚酶链反应或杂交捕获)对感兴趣的DNA进行靶向测序。与序列比对策略相比,深度学习(DL)模型在对目标 DNA 和非目标 DNA 进行分类方面具有很大的速度优势。然而,这些基于深度学习的工具准确性相对较低,阻碍了它们在纳米孔选择性测序中的应用。在此,我们介绍一种基于 DL 的工具 ReadCurrent,它以电流作为输入,用于纳米孔选择性测序。ReadCurrent 采用了改进的深度卷积神经网络(VDCNN)架构,与传统的 VDCNN 相比,训练计算成本大大降低,推理速度更快。我们在人类、酵母、细菌和病毒等 10 个纳米孔测序数据集上评估了 ReadCurrent 的性能。我们发现,ReadCurrent 的平均分类准确率达到 98.57%,优于其他四种基于 DL 的选择性测序方法。在从人类 DNA 中选择性测序微生物 DNA 的实验验证中,ReadCurrent 实现了 2.85 的富集比,高于 MinKNOW 使用序列比对策略实现的 2.7 的富集比。总之,ReadCurrent 可以快速、高精度地对目标 DNA 和非目标 DNA 进行分类,为纳米孔选择性测序提供了另一种工具箱。ReadCurrent 可在 https://github.com/Ming-Ni-Group/ReadCurrent 上获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ReadCurrent: a VDCNN-based tool for fast and accurate nanopore selective sequencing.

Nanopore selective sequencing allows the targeted sequencing of DNA of interest using computational approaches rather than experimental methods such as targeted multiplex polymerase chain reaction or hybridization capture. Compared to sequence-alignment strategies, deep learning (DL) models for classifying target and nontarget DNA provide large speed advantages. However, the relatively low accuracy of these DL-based tools hinders their application in nanopore selective sequencing. Here, we present a DL-based tool named ReadCurrent for nanopore selective sequencing, which takes electric currents as inputs. ReadCurrent employs a modified very deep convolutional neural network (VDCNN) architecture, enabling significantly lower computational costs for training and quicker inference compared to conventional VDCNN. We evaluated the performance of ReadCurrent across 10 nanopore sequencing datasets spanning human, yeasts, bacteria, and viruses. We observed that ReadCurrent achieved a mean accuracy of 98.57% for classification, outperforming four other DL-based selective sequencing methods. In experimental validation that selectively sequenced microbial DNA from human DNA, ReadCurrent achieved an enrichment ratio of 2.85, which was higher than the 2.7 ratio achieved by MinKNOW using the sequence-alignment strategy. In summary, ReadCurrent can rapidly classify target and nontarget DNA with high accuracy, providing an alternative in the toolbox for nanopore selective sequencing. ReadCurrent is available at https://github.com/Ming-Ni-Group/ReadCurrent.

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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
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