Emerging computational tools and models for studying gut microbiota composition and function

被引:11
|
作者
Park, Seo-Young [1 ]
Ufondu, Arinzechukwu [2 ]
Lee, Kyongbum [1 ]
Jayaraman, Arul [2 ,3 ]
机构
[1] Tufts Univ, Dept Chem & Biol Engn, Medford, MA 02155 USA
[2] Texas A&M Univ, Artie McFerrin Dept Chem Engn, College Stn, TX 77843 USA
[3] Texas A&M Univ, Dept Biomed Engn, College Stn, TX 77843 USA
关键词
TIME-SERIES DATA;
D O I
10.1016/j.copbio.2020.10.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The gut microbiota and its metabolites play critical roles in human health and disease. Advances in high-throughput sequencing, mass spectrometry, and other omics assay platforms have improved our ability to generate large volumes of data exploring the temporal variations in the compositions and functions of microbial communities. To elucidate mechanisms, methods and tools are needed that can rigorously model the dependencies within time-series data. Longitudinal data are often sparse and unevenly sampled, and nontrivial challenges remain in determining statistical significance, normalization across different data types, and model validation. In this review, we highlight recent developments in models and software tools for the analysis of time series microbiome and metabolome data, as well as integration of these data.
引用
收藏
页码:301 / 311
页数:11
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