More than presence-absence; modelling (e)DNA concentration across time and space from qPCR survey data.

IF 0.9 Q4 STATISTICS & PROBABILITY Journal of Statistical Theory and Practice Pub Date : 2025-01-01 Epub Date: 2025-08-05 DOI:10.1007/s42519-025-00477-9
Milly Jones, Eleni Matechou, Diana Cole, Alex Diana, Jim Griffin, Sara Peixoto, Lori Lawson Handley, Andrew Buxton
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引用次数: 0

Abstract

Environmental DNA (eDNA) surveys offer a revolutionary approach to species monitoring by detecting DNA traces left by organisms in environmental samples, such as water and soil. These surveys provide a cost-effective, non-invasive, and highly sensitive alternative to traditional methods that rely on direct observation of species, especially for protected or invasive species. Quantitative PCR (qPCR) is a technique used to amplify and quantify a targeted DNA molecule, making it a popular tool for monitoring focal species. Modelling of qPCR data has so far focused on inferring species presence/absence at surveyed sites. However, qPCR output is also informative regarding DNA concentration of the species in the sample, and hence, with the appropriate modelling approach, in the environment. In this paper, we introduce a modelling framework that infers DNA concentration at surveyed sites across time and space, and as a function of covariates, from qPCR output. Our approach accounts for contamination and inhibition in lab analyses, addressing biases particularly notable at low DNA concentrations, and for the inherent stochasticity in the corresponding data. Additionally, we incorporate heteroscedasticity in qPCR output, recognizing the increased variance of qPCR data at lower DNA concentrations. We validate our model through a simulation study, comparing its performance against models that ignore contamination/inhibition and variance heterogeneity. Further, we apply the model to three case studies involving aquatic and semi-aquatic species surveys in the UK. Our findings demonstrate improved accuracy and robustness in estimating DNA concentrations, offering a refined tool for ecological monitoring and conservation efforts.

Supplementary information: The online version contains supplementary material available at 10.1007/s42519-025-00477-9.

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不仅仅是在场-缺席;(e) qPCR调查数据的DNA浓度跨越时间和空间。
环境DNA (eDNA)调查通过检测生物在环境样本(如水和土壤)中留下的DNA痕迹,为物种监测提供了一种革命性的方法。这些调查提供了一种具有成本效益、非侵入性和高灵敏度的方法,替代了依赖于直接观察物种的传统方法,特别是对受保护物种或入侵物种。定量PCR (qPCR)是一种用于扩增和量化目标DNA分子的技术,使其成为监测焦点物种的流行工具。迄今为止,qPCR数据的建模主要集中在推断调查地点的物种存在/缺失。然而,qPCR输出也提供了样品中物种DNA浓度的信息,因此,在适当的建模方法下,在环境中。在本文中,我们引入了一个建模框架,从qPCR输出推断出在被调查地点的DNA浓度跨越时间和空间,并作为协变量的函数。我们的方法解释了实验室分析中的污染和抑制,解决了在低DNA浓度下特别明显的偏差,以及相应数据中固有的随机性。此外,我们将异方差纳入qPCR输出,认识到较低DNA浓度下qPCR数据的方差增加。我们通过模拟研究验证了我们的模型,将其与忽略污染/抑制和方差异质性的模型进行了比较。此外,我们将该模型应用于涉及英国水生和半水生物种调查的三个案例研究。我们的研究结果表明,在估计DNA浓度方面提高了准确性和稳健性,为生态监测和保护工作提供了一种完善的工具。补充信息:在线版本包含补充资料,可在10.1007/s42519-025-00477-9获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Statistical Theory and Practice
Journal of Statistical Theory and Practice STATISTICS & PROBABILITY-
CiteScore
1.40
自引率
0.00%
发文量
74
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