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Modelling of zero-inflation improves inference of metagenomic gene count data

机译:零膨胀的建模改善了偏见基因计数数据的推断

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摘要

Metagenomics enables the study of gene abundances in complex mixtures of microorganisms and has become a standard methodology for the analysis of the human microbiome. However, gene abundance data is inherently noisy and contains high levels of biological and technical variability as well as an excess of zeros due to non-detected genes. This makes the statistical analysis challenging. In this study, we present a new hierarchical Bayesian model for inference of metagenomic gene abundance data. The model uses a zero-inflated overdispersed Poisson distribution which is able to simultaneously capture the high gene-specific variability as well as zero observations in the data. By analysis of three comprehensive datasets, we show that zero-inflation is common in metagenomic data from the human gut and, if not correctly modelled, it can lead to substantial reductions in statistical power. We also show, by using resampled metagenomic data, that our model has, compared to other methods, a higher and more stable performance for detecting differentially abundant genes. We conclude that proper modelling of the gene-specific variability, including the excess of zeros, is necessary to accurately describe gene abundances in metagenomic data. The proposed model will thus pave the way for new biological insights into the structure of microbial communities.
机译:Metagenomics能够在微生物的复杂混合物中研究基因丰富,并已成为分析人微生物组的标准方法。然而,基因丰富数据本质上是嘈杂的,并且由于未检测到的基因,含有高水平的生物和技术性变异性以及过量的零。这使得统计分析具有挑战性。在这项研究中,我们提出了一种新的等级贝叶斯模型,用于推断偏见基因丰富数据。该模型使用零充气的过度分散的泊松分布,该泊松分布能够同时捕获高基因特异性可变性以及数据中的零观察。通过分析三个综合数据集,我们表明零充通量在来自人体肠道的偏移数据中常见,如果没有正确建模,它可能导致统计能力的大量减少。我们还通过使用重采采样的Metagenomic数据来显示我们的模型与其他方法相比,对检测差异丰富的基因进行更高且更稳定的性能。我们得出结论,需要适当的基因特异性变异性,包括过量的零,以准确地描述偏心组数据中的基因丰富。因此,拟议的模型将为新的生物洞察铺平进入微生物社区结构的方式。

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