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MiRKAT-MC: A Distance-Based Microbiome Kernel Association Test With Multi-Categorical Outcomes

Increasing evidence has elucidated that the microbiome plays a critical role in many human diseases. Apart from continuous and binary traits that measure the extent or presence of a disease, multi-categorical outcomes including variations/subtypes of a disease or ordinal levels of disease severity a...

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Autores principales: Jiang, Zhiwen, He, Mengyu, Chen, Jun, Zhao, Ni, Zhan, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010828/
https://www.ncbi.nlm.nih.gov/pubmed/35432465
http://dx.doi.org/10.3389/fgene.2022.841764
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author Jiang, Zhiwen
He, Mengyu
Chen, Jun
Zhao, Ni
Zhan, Xiang
author_facet Jiang, Zhiwen
He, Mengyu
Chen, Jun
Zhao, Ni
Zhan, Xiang
author_sort Jiang, Zhiwen
collection PubMed
description Increasing evidence has elucidated that the microbiome plays a critical role in many human diseases. Apart from continuous and binary traits that measure the extent or presence of a disease, multi-categorical outcomes including variations/subtypes of a disease or ordinal levels of disease severity are commonly seen in clinical studies. On top of that, studies with clustered design (i.e., family-based and longitudinal studies) are popular alternatives to population-based ones as they are able to identify characteristics on both individual and population levels and to investigate the trajectory of traits of interest over time. However, existing methods for microbiome association analysis are inadequate to handle multi-categorical outcomes, neither independent nor clustered data. We propose a microbiome kernel association test with multi-categorical outcomes (MiRKAT-MC). Our method is versatile to deal with both nominal and ordinal outcomes for independent and clustered data. In addition, it incorporates multiple ecological distances to allow for different association patterns between outcomes and microbiome compositions to be incorporated. A computationally efficient pseudo-permutation strategy is used to evaluate the statistical significance. Comprehensive simulations show that MiRKAT-MC preserves the nominal type I error and increases statistical powers under various scenarios and data types. We also apply MiRKAT-MC to real data sets with nominal and ordinal outcomes to gain biological insights. MiRKAT-MC is easy to implement, and freely available via an R package at https://github.com/Zhiwen-Owen-Jiang/MiRKATMC with a Graphical User Interface through R Shinny also available.
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spelling pubmed-90108282022-04-16 MiRKAT-MC: A Distance-Based Microbiome Kernel Association Test With Multi-Categorical Outcomes Jiang, Zhiwen He, Mengyu Chen, Jun Zhao, Ni Zhan, Xiang Front Genet Genetics Increasing evidence has elucidated that the microbiome plays a critical role in many human diseases. Apart from continuous and binary traits that measure the extent or presence of a disease, multi-categorical outcomes including variations/subtypes of a disease or ordinal levels of disease severity are commonly seen in clinical studies. On top of that, studies with clustered design (i.e., family-based and longitudinal studies) are popular alternatives to population-based ones as they are able to identify characteristics on both individual and population levels and to investigate the trajectory of traits of interest over time. However, existing methods for microbiome association analysis are inadequate to handle multi-categorical outcomes, neither independent nor clustered data. We propose a microbiome kernel association test with multi-categorical outcomes (MiRKAT-MC). Our method is versatile to deal with both nominal and ordinal outcomes for independent and clustered data. In addition, it incorporates multiple ecological distances to allow for different association patterns between outcomes and microbiome compositions to be incorporated. A computationally efficient pseudo-permutation strategy is used to evaluate the statistical significance. Comprehensive simulations show that MiRKAT-MC preserves the nominal type I error and increases statistical powers under various scenarios and data types. We also apply MiRKAT-MC to real data sets with nominal and ordinal outcomes to gain biological insights. MiRKAT-MC is easy to implement, and freely available via an R package at https://github.com/Zhiwen-Owen-Jiang/MiRKATMC with a Graphical User Interface through R Shinny also available. Frontiers Media S.A. 2022-04-01 /pmc/articles/PMC9010828/ /pubmed/35432465 http://dx.doi.org/10.3389/fgene.2022.841764 Text en Copyright © 2022 Jiang, He, Chen, Zhao and Zhan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Jiang, Zhiwen
He, Mengyu
Chen, Jun
Zhao, Ni
Zhan, Xiang
MiRKAT-MC: A Distance-Based Microbiome Kernel Association Test With Multi-Categorical Outcomes
title MiRKAT-MC: A Distance-Based Microbiome Kernel Association Test With Multi-Categorical Outcomes
title_full MiRKAT-MC: A Distance-Based Microbiome Kernel Association Test With Multi-Categorical Outcomes
title_fullStr MiRKAT-MC: A Distance-Based Microbiome Kernel Association Test With Multi-Categorical Outcomes
title_full_unstemmed MiRKAT-MC: A Distance-Based Microbiome Kernel Association Test With Multi-Categorical Outcomes
title_short MiRKAT-MC: A Distance-Based Microbiome Kernel Association Test With Multi-Categorical Outcomes
title_sort mirkat-mc: a distance-based microbiome kernel association test with multi-categorical outcomes
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010828/
https://www.ncbi.nlm.nih.gov/pubmed/35432465
http://dx.doi.org/10.3389/fgene.2022.841764
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