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

BACKGROUND: 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 f...

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Autores principales: Li, Yuntong, Fan, Teresa W.M., Lane, Andrew N., Kang, Woo-Young, Arnold, Susanne M., Stromberg, Arnold J., Wang, Chi, Chen, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798423/
https://www.ncbi.nlm.nih.gov/pubmed/31623550
http://dx.doi.org/10.1186/s12859-019-3067-z
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author Li, Yuntong
Fan, Teresa W.M.
Lane, Andrew N.
Kang, Woo-Young
Arnold, Susanne M.
Stromberg, Arnold J.
Wang, Chi
Chen, Li
author_facet Li, Yuntong
Fan, Teresa W.M.
Lane, Andrew N.
Kang, Woo-Young
Arnold, Susanne M.
Stromberg, Arnold J.
Wang, Chi
Chen, Li
author_sort Li, Yuntong
collection PubMed
description BACKGROUND: 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. RESULTS: 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. CONCLUSION: 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.
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spelling pubmed-67984232019-10-21 SDA: a semi-parametric differential abundance analysis method for metabolomics and proteomics data Li, Yuntong Fan, Teresa W.M. Lane, Andrew N. Kang, Woo-Young Arnold, Susanne M. Stromberg, Arnold J. Wang, Chi Chen, Li BMC Bioinformatics Methodology Article BACKGROUND: 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. RESULTS: 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. CONCLUSION: 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. BioMed Central 2019-10-17 /pmc/articles/PMC6798423/ /pubmed/31623550 http://dx.doi.org/10.1186/s12859-019-3067-z Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Li, Yuntong
Fan, Teresa W.M.
Lane, Andrew N.
Kang, Woo-Young
Arnold, Susanne M.
Stromberg, Arnold J.
Wang, Chi
Chen, Li
SDA: a semi-parametric differential abundance analysis method for metabolomics and proteomics data
title SDA: a semi-parametric differential abundance analysis method for metabolomics and proteomics data
title_full SDA: a semi-parametric differential abundance analysis method for metabolomics and proteomics data
title_fullStr SDA: a semi-parametric differential abundance analysis method for metabolomics and proteomics data
title_full_unstemmed SDA: a semi-parametric differential abundance analysis method for metabolomics and proteomics data
title_short SDA: a semi-parametric differential abundance analysis method for metabolomics and proteomics data
title_sort sda: a semi-parametric differential abundance analysis method for metabolomics and proteomics data
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798423/
https://www.ncbi.nlm.nih.gov/pubmed/31623550
http://dx.doi.org/10.1186/s12859-019-3067-z
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