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      Optimizing methods and dodging pitfalls in microbiome research

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          Abstract

          Research on the human microbiome has yielded numerous insights into health and disease, but also has resulted in a wealth of experimental artifacts. Here, we present suggestions for optimizing experimental design and avoiding known pitfalls, organized in the typical order in which studies are carried out. We first review best practices in experimental design and introduce common confounders such as age, diet, antibiotic use, pet ownership, longitudinal instability, and microbial sharing during cohousing in animal studies. Typically, samples will need to be stored, so we provide data on best practices for several sample types. We then discuss design and analysis of positive and negative controls, which should always be run with experimental samples. We introduce a convenient set of non-biological DNA sequences that can be useful as positive controls for high-volume analysis. Careful analysis of negative and positive controls is particularly important in studies of samples with low microbial biomass, where contamination can comprise most or all of a sample. Lastly, we summarize approaches to enhancing experimental robustness by careful control of multiple comparisons and to comparing discovery and validation cohorts. We hope the experimental tactics summarized here will help researchers in this exciting field advance their studies efficiently while avoiding errors.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s40168-017-0267-5) contains supplementary material, which is available to authorized users.

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample.

            The ongoing revolution in high-throughput sequencing continues to democratize the ability of small groups of investigators to map the microbial component of the biosphere. In particular, the coevolution of new sequencing platforms and new software tools allows data acquisition and analysis on an unprecedented scale. Here we report the next stage in this coevolutionary arms race, using the Illumina GAIIx platform to sequence a diverse array of 25 environmental samples and three known "mock communities" at a depth averaging 3.1 million reads per sample. We demonstrate excellent consistency in taxonomic recovery and recapture diversity patterns that were previously reported on the basis of metaanalysis of many studies from the literature (notably, the saline/nonsaline split in environmental samples and the split between host-associated and free-living communities). We also demonstrate that 2,000 Illumina single-end reads are sufficient to recapture the same relationships among samples that we observe with the full dataset. The results thus open up the possibility of conducting large-scale studies analyzing thousands of samples simultaneously to survey microbial communities at an unprecedented spatial and temporal resolution.
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              Multiple Comparisons among Means

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                Author and article information

                Contributors
                kimdk@email.chop.edu
                hofstaedtc@email.chop.edu
                zhaoc1@email.chop.edu
                matteil@email.chop.edu
                tanes@email.chop.edu
                alauder@mail.med.upenn.edu
                shescott@mail.med.upenn.edu
                cchehoud@gmail.com
                kelsen@email.chop.edu
                conradm@email.chop.edu
                collmanr@mail.med.upenn.edu
                baldassano@email.chop.edu
                bushman@mail.med.upenn.edu
                bittingerk@email.chop.edu
                Journal
                Microbiome
                Microbiome
                Microbiome
                BioMed Central (London )
                2049-2618
                5 May 2017
                5 May 2017
                2017
                : 5
                : 52
                Affiliations
                [1 ]ISNI 0000 0001 0680 8770, GRID grid.239552.a, Division of Gastroenterology, Hepatology, and Nutrition, , The Children’s Hospital of Philadelphia, ; Philadelphia, Pennsylvania 19104 USA
                [2 ]ISNI 0000 0004 1936 8972, GRID grid.25879.31, Department of Microbiology, , University of Pennsylvania, ; Philadelphia, Pennsylvania 19104 USA
                [3 ]ISNI 0000 0004 1936 8972, GRID grid.25879.31, Department of Medicine, Perelman School of Medicine, , University of Pennsylvania, ; Philadelphia, Pennsylvania 19104 USA
                Article
                267
                10.1186/s40168-017-0267-5
                5420141
                28476139
                9ce20ca6-7af6-43d9-8584-043f1d7631f4
                © The Author(s). 2017

                Open AccessThis 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.

                History
                : 24 December 2016
                : 21 April 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000060, National Institute of Allergy and Infectious Diseases;
                Award ID: P30 AI 045008
                Award ID: P30 AI 045008
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000050, National Heart, Lung, and Blood Institute;
                Award ID: R01 HL113252
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100004897, Pennsylvania Department of Health;
                Award ID: SAP # 4100068710
                Award ID: SAP # 4100068710
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100001063, Crohn's and Colitis Foundation of America;
                Award ID: Career Development Award 3276
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: 1T32DK101371-01
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2017

                metagenomics,16s rrna gene,shotgun metagenomics,environmental contamination,methods,study design,best practices

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