Statistical Analysis of Microbiome Data with R PDF Download

Author: Yinglin Xia
Publisher: Springer
ISBN: 9811315345
Category : Computers
Languages : en
Pages : 518

View

Book Description
This unique book addresses the statistical modelling and analysis of microbiome data using cutting-edge R software. It includes real-world data from the authors’ research and from the public domain, and discusses the implementation of R for data analysis step by step. The data and R computer programs are publicly available, allowing readers to replicate the model development and data analysis presented in each chapter, so that these new methods can be readily applied in their own research. The book also discusses recent developments in statistical modelling and data analysis in microbiome research, as well as the latest advances in next-generation sequencing and big data in methodological development and applications. This timely book will greatly benefit all readers involved in microbiome, ecology and microarray data analyses, as well as other fields of research.

Author: Somnath Datta
Publisher: Springer Nature
ISBN: 3030733513
Category : Medical
Languages : en
Pages : 349

View

Book Description
Microbiome research has focused on microorganisms that live within the human body and their effects on health. During the last few years, the quantification of microbiome composition in different environments has been facilitated by the advent of high throughput sequencing technologies. The statistical challenges include computational difficulties due to the high volume of data; normalization and quantification of metabolic abundances, relative taxa and bacterial genes; high-dimensionality; multivariate analysis; the inherently compositional nature of the data; and the proper utilization of complementary phylogenetic information. This has resulted in an explosion of statistical approaches aimed at tackling the unique opportunities and challenges presented by microbiome data. This book provides a comprehensive overview of the state of the art in statistical and informatics technologies for microbiome research. In addition to reviewing demonstrably successful cutting-edge methods, particular emphasis is placed on examples in R that rely on available statistical packages for microbiome data. With its wide-ranging approach, the book benefits not only trained statisticians in academia and industry involved in microbiome research, but also other scientists working in microbiomics and in related fields.

Author: Yinglin Xia
Publisher: Springer Nature
ISBN: 3031213912
Category : Science
Languages : en
Pages : 717

View

Book Description
This unique book addresses the bioinformatic and statistical modelling and also the analysis of microbiome data using cutting-edge QIIME 2 and R software. It covers core analysis topics in both bioinformatics and statistics, which provides a complete workflow for microbiome data analysis: from raw sequencing reads to community analysis and statistical hypothesis testing. It includes real-world data from the authors’ research and from the public domain, and discusses the implementation of QIIME 2 and R for data analysis step-by-step. The data as well as QIIME 2 and R computer programs are publicly available, allowing readers to replicate the model development and data analysis presented in each chapter so that these new methods can be readily applied in their own research. Bioinformatic and Statistical Analysis of Microbiome Data is an ideal book for advanced graduate students and researchers in the clinical, biomedical, agricultural, and environmental fields, as well as those studying bioinformatics, statistics, and big data analysis.

Author: Yinglin Xia
Publisher: American Chemical Society
ISBN: 0841299161
Category : Science
Languages : en
Pages : 229

View

Book Description
Compared with other research fields, both microbiome and metabolomics data are complicated and have some unique characteristics, respectively. Thus, choosing an appropriate statistical test or method is a very important step in the analysis of microbiome and metabolomics data. However, this is still a difficult task for those biomedical researchers without a statistical background and for those biostatisticians who do not have research experiences in these fields. Graduate students studying microbiome and metabolomics; statisticians, working on microbiome and metabolomics projects, either for their own research, or for their collaborative research for experimental design, grant application, and data analysis; and researchers who investigate biomedical and biochemical projects with the microbiome, metabolome, and multi-omics data analysis will benefit from reading this work.

Author: Yinglin Xia
Publisher: CRC Press
ISBN: 1040045669
Category : Mathematics
Languages : en
Pages : 457

View

Book Description
This unique book officially defines microbiome statistics as a specific new field of statistics and addresses the statistical analysis of correlation, association, interaction, and composition in microbiome research. It also defines the study of the microbiome as a hypothesis-driven experimental science and describes two microbiome research themes and six unique characteristics of microbiome data, as well as investigating challenges for statistical analysis of microbiome data using the standard statistical methods. This book is useful for researchers of biostatistics, ecology, and data analysts. Presents a thorough overview of statistical methods in microbiome statistics of parametric and nonparametric correlation, association, interaction, and composition adopted from classical statistics and ecology and specifically designed for microbiome research. Performs step-by-step statistical analysis of correlation, association, interaction, and composition in microbiome data. Discusses the issues of statistical analysis of microbiome data: high dimensionality, compositionality, sparsity, overdispersion, zero-inflation, and heterogeneity. Investigates statistical methods on multiple comparisons and multiple hypothesis testing and applications to microbiome data. Introduces a series of exploratory tools to visualize composition and correlation of microbial taxa by barplot, heatmap, and correlation plot. Employs the Kruskal–Wallis rank-sum test to perform model selection for further multi-omics data integration. Offers R code and the datasets from the authors’ real microbiome research and publicly available data for the analysis used. Remarks on the advantages and disadvantages of each of the methods used.

Author: Weijia Fu
Publisher:
ISBN:
Category :
Languages : en
Pages : 39

View

Book Description
Progress in high throughput sequencing has facilitated the conduct of large scale microbiome profiling studies which have already begun to elucidate the role of microbes in many disorders and clinical outcomes. Despite the many successes, statistical analysis of data from these studies continues to pose a challenge. In the thesis, we proposed methods to study two specific challenges: batch effects and integrative analysis of microbiome and other omics data. Both issues are increasingly relevant problems. As studies get larger, batching becomes inevitable and integrative analysis is imperative for gaining clues as to the mechanisms underlying discovered associations. The thesis is composed of two projects. In the first project, we compared six existing batch correction methods for microarray data when applied to microbiome data. Two real microbiome data sets were used to evaluate the performance using data visualization and several evaluation metrics. Our results suggest that an empirical bayes approach (ComBat), when applied appropriately, can outperform other methods. In the second project, we proposed a robust microbiome regression-based kernel association test (MiRKAT-R) to screen a large number of genomic markers for association with microbiome profiles. This approach utilizes a recently developed robust kernel machine test. We further propose to incorporate an omnibus test that simultaneously considers different models so as to allow for different relationships between the individual markers and microbiome composition. Systematic simulations and applications to real data show that the MiRKAT-R improves both type I error control and power.

Author: Robert G. Beiko
Publisher:
ISBN: 9781493987283
Category : Microbiology
Languages : en
Pages : 324

View

Book Description

Author: Gibraan Rahman
Publisher:
ISBN:
Category :
Languages : en
Pages : 0

View

Book Description
Next-generation sequencing (NGS) has effected an explosion of research into the relationship between genetic information and a variety of biological conditions. One of the most exciting areas of study is how the trillions of microbial species that we share this Earth with affect our health. However, the process of extracting useful biological insights from this breadth of data is far from trivial. There are numerous statistical and computational considerations in addition to the already complex and messy biological problems. In this thesis, I describe my work on developing and implementing software to tackle the complex world of statistical microbiome analysis. In the first part of this thesis, we review the applications and challenges of performing dimensionality reduction on microbiome data comprising thousands of microbial taxa. When dealing with this high dimensionality, it is imperative to be able to get an overview of the community structure in a lower dimensional space that can be both visualized and interpreted. We review the statistical considerations for dimensionality reduction and the existing tools and algorithms that can and cannot address them. This includes discussions about sparsity, compositionality, and phylogenetic signal. We also make recommendations about tools and algorithms to consider for different use-cases. In the second part of this thesis, we present a new software, Evident, designed to assist researchers with statistical analysis of microbiome effect sizes and power analysis. Effect sizes of statistical tests are not widely reported in microbiome datasets, limiting the interpretability of community differences such as alpha and beta diversity. As more large microbiome studies are produced, researchers have the opportunity to mine existing datasets to get a sense of the effect size for different biological conditions. These, in turn, can be used to perform power analysis prior to designing an experiment, allowing researchers to better allocate resources. We show how Evident is scalable to dozens of datasets and provides easy calculation and exploration of effect sizes and power analysis from existing data. In the third part of this thesis, we describe a novel investigation into the joint microbiome and metabolome axis in colorectal cancer. In most cases of sporadic colorectal cancers (CRC), tumorigenesis is a multistep process driven by genomic alterations in concert with dietary influences. In addition, mounting evidence has implicated the gut microbiome as an effector in the development and progression of CRC. While large meta-analyses have provided mechanistic insight into disease progression in CRC patients, study heterogeneity has limited causal associations. To address this limitation, multi-omics studies on genetically controlled cohorts of mice were performed to distinguish genetic and dietary influences. Diet was identified as the major driver of microbial and metabolomic differences, with reductions in alpha diversity and widespread changes in cecal metabolites seen in HFD-fed mice. Similarly, the levels of non-classic amino acid conjugated forms of the bile acid cholic acid (AA-CAs) increased with HFD. We show that these AA-CAs signal through the nuclear receptor FXR and membrane receptor TGR5 to functionally impact intestinal stem cell growth. In addition, the poor intestinal permeability of these AA-CAs supports their localization in the gut. Moreover, two cryptic microbial strains, Ileibacterium valens and Ruminococcus gnavus, were shown to have the capacity to synthesize these AA-CAs. This multi-omics dataset from CRC mouse models supports diet-induced shifts in the microbiome and metabolome in disease progression with potential utility in directing future diagnostic and therapeutic developments. In the fourth chapter, we demonstrate a new framework for performing differential abundance analysis using customized statistical modeling. As we learn more and more about the relationship between the microbiome and biological conditions, experimental protocols are becoming more and more complex. For example, meta-analyses, interventions, longitudinal studies, etc. are being used to better understand the dynamic nature of the microbiome. However, statistical methods to analyze these relationships are lacking--especially in the field of differential abundance. Finding biomarkers associated with conditions of interest must be performed with statistical care when dealing with these kinds of experimental designs. We present BIRDMAn, a software package integrating probabilistic programming with Stan to build custom models for analyzing microbiome data. We show that, on both simulated and real datasets, BIRDMAn is able to extract novel biological signals that are missed by existing methods. These chapters, taken together, advance our knowledge of statistical analysis of microbiome data and provide tools and references for researchers looking to perform analysis on their own data.

Author: Achal Dhariwal
Publisher:
ISBN:
Category :
Languages : en
Pages :

View

Book Description
"The advancements in next-generation sequencing technologies have revolutionized microbiome research by allowing culture-independent high-throughput profiling of the genetic contents of microbial communities. Nowadays, 16S rRNA based marker gene sequencing is widely used to characterize the taxonomic composition and phylogenetic diversity of complex microbial communities. However, statistical, visual and functional analysis of such data possess great challenges. In addition, many aspects of the current approaches can be improved to get a better understanding of communities. The proper analysis of the resulting large and complicated datasets remains a key bottleneck in current microbiome studies. Over the last decade, powerful computational pipelines and standard protocols have been developed to support efficient raw data processing and annotation of microbiome data. The focus has now shifted towards downstream statistical analysis and functional interpretation. To address this bottleneck, we have developed MicrobiomeAnalyst, a user-friendly web-based tool that incorporates recent progresses in statistics and interactive visualization techniques, coupled with novel knowledge bases, to facilitate comprehensive analysis of common data sets generated from microbiome studies. MicrobiomeAnalyst contains four major components, including i) a module for community diversity profiling, comparative analysis and functional prediction of 16S rRNA marker gene data; ii) a module for exploratory data analysis, functional profiling and metabolic network visualization for shotgun metagenomics or metatranscriptomics data; iii) a module to help users to interpret their taxa of interest via enrichment analysis against ~300 taxon sets manually collected from recent literature and public databases; and iv) a module to allow users to visually explore their data sets within the context of compatible public data (meta-analysis) for pattern discovery and biological insights. The tool is freely accessible at http://www.microbiomeanalyst.ca. " --

Author: Lingjing Jiang
Publisher:
ISBN:
Category :
Languages : en
Pages : 101

View

Book Description
The microbiome is inherently dynamic, driven by interactions among microbes, with the host, and with the environment. At any point in life, human microbiome can be dramatically altered, either transiently or long term, by diseases, medical interventions or even daily routines. Since the human microbiome is highly dynamic and personalized, longitudinal microbiome studies that sample human-associated microbial communities repeatedly over time provide valuable information for researchers to observe both inter- and intra-individual variability, or to measure changes in response to an intervention in real time. Despite this increasing need in longitudinal data analysis, statistical methods for analyzing sparse longitudinal microbiome data and longitudinal multi-omics data still lag behind. In this dissertation, we describe our efforts in developing two novel statistical methods, Bayesian functional principal components analysis (SFPCA) for sparse longitudinal data analysis, and multivariate sparse functional principal components analysis (mSFPCA) for longitudinal microbiome multi-omics data analysis. Beyond longitudinal data analysis, we are also interested in utilizing statistical techniques for addressing the "reproducibility crisis" in microbiome research, especially in the indispensable task of feature selection. Instead of developing "the best" feature selection method, we focus on discovering a reproducible criterion called Stability for evaluating feature selection methods in order to yield reproducible results in microbiome analysis. To set an appropriate motivation and context for our work, Chapter 1 reviews the importance of longitudinal studies in human microbiome research, and presents the crucial need of developing novel statistical methods to meet the new challenges in longitudinal microbiome data analysis, and of producing reproducible results in microbiome feature selection. Chapter 2 introduces Bayesian SFPCA, a flexible Bayesian approach to SFPCA that enables efficient model selection and graphical model diagnostics for valid longitudinal microbiome applications. Chapter 3 presents mSFPCA, an extension of Bayesian SFPCA from modeling a univariate temporal outcome to simultaneously characterizing multiple temporal measurements, and inferring their temporal associations based on mutual information estimation. Chapter 4 proposes to use reproducibility criterion such as Stability instead of popular model prediction metric such as mean squared error (MSE) to quantify the reproducibility of identified microbial features.