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Article: Evaluation of metabolite-microbe correlation detection methods

TitleEvaluation of metabolite-microbe correlation detection methods
Authors
KeywordsCorrelation analysis
Metabolome
Microbiome
Issue Date2019
Citation
Analytical Biochemistry, 2019, v. 567, p. 106-111 How to Cite?
AbstractDifferent correlation detection methods have been specifically designed for the microbiome data analysis considering the compositional data structure and different sequencing depths. Along with the speedy development of omics studies, there is an increasing interest in discovering the biological associations between microbes and host metabolites. This raises the need of finding proper statistical methods that facilitate the correlation analysis across different omics studies. Here, we comprehensively evaluated six different correlation methods, i.e., Pearson correlation, Spearman correlation, Sparse Correlations for Compositional data (SparCC), Correlation inference for Compositional data through Lasso (CCLasso), Mutual Information Coefficient (MIC), and Cosine similarity methods, for the correlations detection between microbes and metabolites. Three simulated and two real-world data sets (from public databases and our lab) were used to examine the performance of each method regarding its specificity, sensitivity, similarity, accuracy, and stability with different sparsity. Our results indicate that although each method has its own pros and cons in different scenarios, Spearman correlation and MIC outperform the others with their overall performances. A strategic guidance was also proposed for the correlation analysis between microbe and metabolite.
Persistent Identifierhttp://hdl.handle.net/10722/342584
ISSN
2023 Impact Factor: 2.6
2023 SCImago Journal Rankings: 0.493
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYou, Yijun-
dc.contributor.authorLiang, Dandan-
dc.contributor.authorWei, Runmin-
dc.contributor.authorLi, Mengci-
dc.contributor.authorLi, Yitao-
dc.contributor.authorWang, Jingye-
dc.contributor.authorWang, Xiaoyan-
dc.contributor.authorZheng, Xiaojiao-
dc.contributor.authorJia, Wei-
dc.contributor.authorChen, Tianlu-
dc.date.accessioned2024-04-17T07:04:50Z-
dc.date.available2024-04-17T07:04:50Z-
dc.date.issued2019-
dc.identifier.citationAnalytical Biochemistry, 2019, v. 567, p. 106-111-
dc.identifier.issn0003-2697-
dc.identifier.urihttp://hdl.handle.net/10722/342584-
dc.description.abstractDifferent correlation detection methods have been specifically designed for the microbiome data analysis considering the compositional data structure and different sequencing depths. Along with the speedy development of omics studies, there is an increasing interest in discovering the biological associations between microbes and host metabolites. This raises the need of finding proper statistical methods that facilitate the correlation analysis across different omics studies. Here, we comprehensively evaluated six different correlation methods, i.e., Pearson correlation, Spearman correlation, Sparse Correlations for Compositional data (SparCC), Correlation inference for Compositional data through Lasso (CCLasso), Mutual Information Coefficient (MIC), and Cosine similarity methods, for the correlations detection between microbes and metabolites. Three simulated and two real-world data sets (from public databases and our lab) were used to examine the performance of each method regarding its specificity, sensitivity, similarity, accuracy, and stability with different sparsity. Our results indicate that although each method has its own pros and cons in different scenarios, Spearman correlation and MIC outperform the others with their overall performances. A strategic guidance was also proposed for the correlation analysis between microbe and metabolite.-
dc.languageeng-
dc.relation.ispartofAnalytical Biochemistry-
dc.subjectCorrelation analysis-
dc.subjectMetabolome-
dc.subjectMicrobiome-
dc.titleEvaluation of metabolite-microbe correlation detection methods-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.ab.2018.12.008-
dc.identifier.pmid30557528-
dc.identifier.scopuseid_2-s2.0-85058979530-
dc.identifier.volume567-
dc.identifier.spage106-
dc.identifier.epage111-
dc.identifier.eissn1096-0309-
dc.identifier.isiWOS:000456353600015-

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