Abstract

Microbes inhabit virtually all sites of the human body, yet we know very little about the role they play in our health. In recent years, there has been increasing interest in studying human-associated microbial communities, particularly since microbial dysbioses have now been implicated in a number of human diseases [1]–[3]. Dysbiosis, the disruption of the normal microbial community structure, however, is impossible to define without first establishing what “normal microbial community structure” means within the healthy human microbiome. Recent advances in sequencing technologies have made it feasible to perform large-scale studies of microbial communities, providing the tools necessary to begin to address this question [4], [5]. This led to the implementation of the Human Microbiome Project (HMP) in 2007, an initiative funded by the National Institutes of Health Roadmap for Biomedical Research and constructed as a large, genome-scale community research project [6]. Any such project must plan for data analysis, computational methods development, and the public availability of tools and data; here, we provide an overview of the corresponding bioinformatics organization, history, and results from the HMP (Figure 1).

Highlights

  • One of the Human Microbiome Project (HMP)’s major goals was the generation of a baseline catalog of the microorganisms found in and on normal human hosts, which includes defining their normal patterns of phylogeny, taxonomy, biogeography, ecology, metabolism, and function

  • The HMP has released over 100 million 16S rRNA gene reads and more than 8 Tbp of shotgun metagenomic sequences [7]

  • Deposition of nonprotected HMP data, its organization, and subsequently its public release were the mandate of the Data Analysis Coordination Center (DACC; http://hmpdacc. org), which was likewise formed early in the project

Read more

Summary

Introduction

One of the HMP’s major goals was the generation of a baseline catalog of the microorganisms found in and on normal human hosts, which includes defining their normal patterns of phylogeny, taxonomy, biogeography, ecology, metabolism, and function. HMP data generation began in earnest during the spring of 2010, at which time the largest published microbiome datasets contained approximately 1–2 million 16S rRNA gene reads using the 454 platform [14,15].

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.