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Beyond samples: A metric revealing more connections of gut microbiota between individuals

机译:超越样本:一个公制揭示了个体之间的肠道微生物群的更多联系

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Studies of gut microbiota explore their complicated connections between individuals of different characteristics by applying different metrics to abundance data obtained from fecal samples. Although classic metrics are capable to quantify differences between samples, the microbiome of fecal sample is not a good surrogate for the gut microbiome of individuals because the microbial populations of the distal colon does not adequately represent that of the entire gastrointestinal tract. To overcome the deficiency of classic metrics in which the differences can be measured between the samples analyzed, but not the corresponding populations, we propose a metric for representing composition differences in the gut microbiota of individuals. Our investigation shows this metric outperforms traditional measures for multiple scenarios. For gut microbiota in diverse geographic populations, this metric presents more explainable data variance than others, not only in regular variance analysis but also in principle component analysis and partition analysis of biologic characteristics. With time-series data, the metric further presents a strong correlation with the time interval of serial sampling. Our findings suggest that the metric is robust and powerfully detects the intrinsic variations in gut microbiota. The metric holds promise for revealing more relations between gut microbiota and human health.
机译:通过将不同的指标应用于从粪便样本获得的丰富数据,肠道微生物瘤的研究探讨了不同特征的个体之间的复杂联系。虽然经典指标能够量化样品之间的差异,但粪便样品的微生物组不是个体的肠道微生物组的良好替代因子,因为远端结肠的微生物群不充分地代表整个胃肠道的肠道。为了克服分析的样品之间可以测量差异的经典指标的缺陷,但不是相应的群体,我们提出了代表个体肠道微生物群的组成差异的度量。我们的调查显示了这种公制优于多种情景的传统措施。对于在不同地理群体中的肠道微生物群中,这种度量标准比其他度量更明显,不仅在常规方差分析中,而且在生物学特征的原则分析和分配分析中。通过时间序列数据,度量概述了与串行采样的时间间隔具有很强的相关性。我们的研究结果表明,度量稳健,有力地检测肠道微生物肿瘤的内在变化。公制持有揭示肠道微生物群和人类健康之间的更多关系。

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