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首页> 外文期刊>Computational and Structural Biotechnology Journal >Identifying the minimum amplicon sequence depth to adequately predict classes in eDNA-based marine biomonitoring using supervised machine learning
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Identifying the minimum amplicon sequence depth to adequately predict classes in eDNA-based marine biomonitoring using supervised machine learning

机译:使用监督机器学习确定基于EDNA的海洋生物制剂的充分预测类别的最小扩增子序列深度

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Environmental DNA metabarcoding is a powerful approach for use in biomonitoring and impact assessments. Amplicon-based eDNA sequence data are characteristically highly divergent in sequencing depth (total reads per sample) as influenced inter alia by the number of samples simultaneously analyzed per sequencing run. The random forest (RF) machine learning algorithm has been successfully employed to accurately classify unknown samples into monitoring categories. To employ RF to eDNA data, and avoid sequencing-depth artifacts, sequence data across samples are normalized using rarefaction, a process that inherently loses information. The aim of this study was to inform future sampling designs in terms of the relationship between sampling depth and RF accuracy. We analyzed three published and one new bacterial amplicon datasets, using a RF, based initially on the maximal rarefied data available (minimum mean of??30,000 reads across all datasets) to give our baseline performance. We then evaluated the RF classification success based on increasingly rarefied datasets. We found that extreme to moderate rarefaction (50–5000 sequences per sample) was sufficient to achieve prediction performance commensurate to the full data, depending on the classification task. We did not find that the number of classification classes, data balance across classes, or the total number of sequences or samples, were associated with predictive accuracy. We identified the ability of the training data to adequately characterize the classes being mapped as the most important criterion and discuss how this finding can inform future sampling design for eDNA based biomonitoring to reduce costs and computation time.
机译:环境DNA Metabarcoding是一种用于生物监测和影响评估的强大方法。基于扩增子的EDNA序列数据在测序深度(每个样品的总读数)中是特性高度发散的,因为通过每个测序运行同时分析的样品的数量尤其影响。随机森林(RF)机器学习算法已成功用于将未知样本准确地分类为监测类别。为了使用RF到EDNA数据,避免测序深度伪像,使用稀疏标准化样本的序列数据,该过程固有地失去信息。本研究的目的是在采样深度和RF精度之间的关系方面通知未来的采样设计。我们分析了三个已发表的和一个新的细菌扩增子数据集,最初基于最大稀土数据(最小均值?& 30,000遍布所有数据集的读数)以提供我们的基准性能。然后,我们基于越来越稀薄的数据集评估了RF分类成功。我们发现极致的稀疏(每个样本的50-5000个序列)足以实现对完整数据的预测性能,具体取决于分类任务。我们没有发现分类类数,类跨类的数据余额或序列或样本总数,与预测精度相关联。我们确定了培训数据以充分表征所映射为最重要的标准的课程的能力,并讨论该发现如何为未来的基于EDNA的生物监测方式通知未来的采样设计,以降低成本和计算时间。

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