SDA: a semi-parametric differential abundance analysis method for metabolomics and proteomics data

Identifying differentially abundant features between different experimental groups is a common goal for many metabolomics and proteomics studies. However, analyzing data from mass spectrometry (MS) is difficult because the data may not be normally distributed and there is often a large fraction of z...

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Veröffentlicht in:BMC bioinformatics 2019-10, Vol.20 (1), p.501-10, Article 501
Hauptverfasser: Li, Yuntong, Fan, Teresa W M, Lane, Andrew N, Kang, Woo-Young, Arnold, Susanne M, Stromberg, Arnold J, Wang, Chi, Chen, Li
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Sprache:eng
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Zusammenfassung:Identifying differentially abundant features between different experimental groups is a common goal for many metabolomics and proteomics studies. However, analyzing data from mass spectrometry (MS) is difficult because the data may not be normally distributed and there is often a large fraction of zero values. Although several statistical methods have been proposed, they either require the data normality assumption or are inefficient. We propose a new semi-parametric differential abundance analysis (SDA) method for metabolomics and proteomics data from MS. The method considers a two-part model, a logistic regression for the zero proportion and a semi-parametric log-linear model for the possibly non-normally distributed non-zero values, to characterize data from each feature. A kernel-smoothed likelihood method is developed to estimate model coefficients and a likelihood ratio test is constructed for differential abundant analysis. The method has been implemented into an R package, SDAMS, which is available at https://www.bioconductor.org/packages/release/bioc/html/SDAMS.html . By introducing the two-part semi-parametric model, SDA is able to handle both non-normally distributed data and large fraction of zero values in a MS dataset. It also allows for adjustment of covariates. Simulations and real data analyses demonstrate that SDA outperforms existing methods.
ISSN:1471-2105
1471-2105
DOI:10.1186/s12859-019-3067-z