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Identifying Viruses from Metagenomic Data Using Deep Learning.

Quantitative Biology(2020)SCI 4区

Quantitative and Computational Biology Program | School of Mathematics and Statistics | Department of Biology | Department of Biological Sciences | Department of Computer Science | Google Inc.

Cited 277|Views5
Abstract
BACKGROUND:The recent development of metagenomic sequencing makes it possible to massively sequence microbial genomes including viral genomes without the need for laboratory culture. Existing reference-based and gene homology-based methods are not efficient in identifying unknown viruses or short viral sequences from metagenomic data.METHODS:Here we developed a reference-free and alignment-free machine learning method, DeepVirFinder, for identifying viral sequences in metagenomic data using deep learning.RESULTS:Trained based on sequences from viral RefSeq discovered before May 2015, and evaluated on those discovered after that date, DeepVirFinder outperformed the state-of-the-art method VirFinder at all contig lengths, achieving AUROC 0.93, 0.95, 0.97, and 0.98 for 300, 500, 1000, and 3000 bp sequences respectively. Enlarging the training data with additional millions of purified viral sequences from metavirome samples further improved the accuracy for identifying virus groups that are under-represented. Applying DeepVirFinder to real human gut metagenomic samples, we identified 51,138 viral sequences belonging to 175 bins in patients with colorectal carcinoma (CRC). Ten bins were found associated with the cancer status, suggesting viruses may play important roles in CRC.CONCLUSIONS:Powered by deep learning and high throughput sequencing metagenomic data, DeepVirFinder significantly improved the accuracy of viral identification and will assist the study of viruses in the era of metagenomics.
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metagenome,deep learning,virus identification,machine learning
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要点】:论文提出了一种基于深度学习的新型方法DeepVirFinder,用于从宏基因组数据中高效识别病毒序列,准确度优于现有技术,并在结直肠癌患者样本中发现了可能与癌症状态相关的病毒组。

方法】:研究采用无参考序列、无比对依赖的机器学习方法,DeepVirFinder,通过深度学习技术直接从宏基因组数据中识别病毒序列。

实验】:DeepVirFinder基于2015年5月前发现的病毒RefSeq序列进行训练,并在之后发现的病毒序列上进行评估,实验结果显示在300、500、1000和3000 bp的序列长度下,AUROC值分别达到了0.93、0.95、0.97和0.98。进一步使用来自宏病毒组样本的数百万纯净病毒序列扩充训练数据,提高了识别代表性不足的病毒组的准确性。在真实的人肠道宏基因组样本中应用DeepVirFinder,识别出了51,138个属于175个组的病毒序列,其中10个组与结直肠癌状态相关。