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Strategy for Intercorrelation Identification between Metabolome and Microbiome

机译:代谢物和微生物组之间的互相关鉴定策略

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摘要

Accumulating evidence points to the strong and complicated associations between the metabolome and the microbiome, which play diverse roles in physiology and pathology. Various correlation analysis approaches were applied to identify microbe-metabolite associations. Given the strengths and weaknesses of the existing methods and considering the characteristics of different types of omics data, we designed a special strategy, called Generalized coRrelation analysis for Metabolome and Microbiome (GRaMM), for the intercorrelation discovery between the metabolome and microbiome. GRaMM can properly deal with two types of omics data, the effect of confounders, and both linear and nonlinear correlations by integrating several complementary methods such as the classical linear regression, the emerging maximum information coefficient (MIC), the metabolic confounding effect elimination (MCEE), and the centered log-ratio transformation (CLR). GRaMM contains four sequential computational steps: (1) metabolic and microbial data preprocessing, (2) linear/nonlinear type identification, (3) data correction and correlation detection, and (4) p value correction. The performances of GRaMM, including the accuracy, sensitivity, specificity, false positive rate, applicability, and effects of preprocessing and confounder adjustment steps, were evaluated and compared with three other methods in multiple simulated and real-world datasets. To our knowledge, GRaMM is the first strategy designed for the intercorrelation analysis between metabolites and microbes. The Matlab function and an R package were developed and are freely available for academic use (comply with GNU GPL.V3 license).
机译:累积证据点指向代谢物和微生物组之间的强烈和复杂的关联,这在生理和病理学中起着不同的作用。应用各种相关性分析方法来鉴定微生物 - 代谢物关联。鉴于现有方法的优点和缺点并考虑不同类型的常规数据的特征,我们设计了一种特殊的策略,称为代谢物和微生物组(克的微生物组(Gramm)的广义相关分析,用于代谢物和微生物组之间的相互腐败发现。通过整合诸如经典线性回归的若干互补方法,新出现的最大信息系数(MIC),代谢混杂效应消除(MCEE) )和中心的记录比转换(CLR)。格式包含四个顺序计算步骤:(1)代谢和微生物数据预处理,(2)线性/非线性型识别,(3)数据校正和相关检测,(4)P值校正。重新进行的表演,包括精度,灵敏度,特异性,假阳性率,适用性和对预处理和混淆调整步骤的影响,并与多个模拟和现实世界数据集中的其他三种方法进行比较。为了我们的知识,格式是第一种专为代谢物和微生物之间的互连分析而设计的策略。 MATLAB功能和R包装是开发的,可自由用于学术用途(符合GNU GPL.v3许可证)。

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  • 来源
    《Analytical chemistry》 |2019年第22期|共9页
  • 作者单位

    Shanghai Jiao Tong Univ Affiliated Peoples Hosp 6 Shanghai Key Lab Diabet Mellitus Shanghai 200233 Peoples R China;

    Shanghai Jiao Tong Univ Affiliated Peoples Hosp 6 Shanghai Key Lab Diabet Mellitus Shanghai 200233 Peoples R China;

    Univ Hawaii Canc Ctr 701 Ilalo St Honolulu HI 96813 USA;

    Univ Hawaii Canc Ctr 701 Ilalo St Honolulu HI 96813 USA;

    Shanghai Jiao Tong Univ Affiliated Peoples Hosp 6 Shanghai Key Lab Diabet Mellitus Shanghai 200233 Peoples R China;

    Shanghai Jiao Tong Univ Affiliated Peoples Hosp 6 Shanghai Key Lab Diabet Mellitus Shanghai 200233 Peoples R China;

    Shanghai Jiao Tong Univ Affiliated Peoples Hosp 6 Shanghai Key Lab Diabet Mellitus Shanghai 200233 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
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