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基于模拟的古代和现代宏基因组数据对宏基因组分类器进行基准测试。

Benchmarking Metagenomic Classifiers on Simulated Ancient and Modern Metagenomic Data.

作者信息

Pusadkar Vaidehi, Azad Rajeev K

机构信息

Department of Biological Sciences, University of North Texas, Denton, TX 76203, USA.

BioDiscovery Institute, University of North Texas, Denton, TX 76203, USA.

出版信息

Microorganisms. 2023 Oct 2;11(10):2478. doi: 10.3390/microorganisms11102478.

Abstract

Taxonomic profiling of ancient metagenomic samples is challenging due to the accumulation of specific damage patterns on DNA over time. Although a number of methods for metagenome profiling have been developed, most of them have been assessed on modern metagenomes or simulated metagenomes mimicking modern metagenomes. Further, a comparative assessment of metagenome profilers on simulated metagenomes representing a spectrum of degradation depth, from the extremity of ancient (most degraded) to current or modern (not degraded) metagenomes, has not yet been performed. To understand the strengths and weaknesses of different metagenome profilers, we performed their comprehensive evaluation on simulated metagenomes representing human dental calculus microbiome, with the level of DNA damage successively raised to mimic modern to ancient metagenomes. All classes of profilers, namely, DNA-to-DNA, DNA-to-protein, and DNA-to-marker comparison-based profilers were evaluated on metagenomes with varying levels of damage simulating deamination, fragmentation, and contamination. Our results revealed that, compared to deamination and fragmentation, human and environmental contamination of ancient DNA (with modern DNA) has the most pronounced effect on the performance of each profiler. Further, the DNA-to-DNA (e.g., Kraken2, Bracken) and DNA-to-marker (e.g., MetaPhlAn4) based profiling approaches showed complementary strengths, which can be leveraged to elevate the state-of-the-art of ancient metagenome profiling.

摘要

由于DNA上特定损伤模式会随时间积累,对古代宏基因组样本进行分类分析具有挑战性。尽管已经开发了许多宏基因组分析方法,但大多数方法是在现代宏基因组或模拟现代宏基因组的模拟宏基因组上进行评估的。此外,尚未对代表从古代(降解程度最高)到当前或现代(未降解)宏基因组的一系列降解深度的模拟宏基因组上的宏基因组分析器进行比较评估。为了了解不同宏基因组分析器的优缺点,我们在代表人类牙菌斑微生物组的模拟宏基因组上对它们进行了全面评估,依次提高DNA损伤水平以模拟从现代到古代的宏基因组。在模拟脱氨基、片段化和污染的不同损伤水平的宏基因组上,对所有类型的分析器,即基于DNA与DNA、DNA与蛋白质以及DNA与标记物比较的分析器进行了评估。我们的结果表明,与脱氨基和片段化相比,古代DNA(与现代DNA)的人类和环境污染对每个分析器的性能影响最为显著。此外,基于DNA与DNA(如Kraken2、Bracken)和DNA与标记物(如MetaPhlAn4)的分析方法显示出互补的优势,可用于提升古代宏基因组分析的技术水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5a9/10609333/d063f0cab783/microorganisms-11-02478-g001.jpg

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