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      Inexpensive Multiplexed Library Preparation for Megabase-Sized Genomes

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          Abstract

          Whole-genome sequencing has become an indispensible tool of modern biology. However, the cost of sample preparation relative to the cost of sequencing remains high, especially for small genomes where the former is dominant. Here we present a protocol for rapid and inexpensive preparation of hundreds of multiplexed genomic libraries for Illumina sequencing. By carrying out the Nextera tagmentation reaction in small volumes, replacing costly reagents with cheaper equivalents, and omitting unnecessary steps, we achieve a cost of library preparation of $8 per sample, approximately 6 times cheaper than the standard Nextera XT protocol. Furthermore, our procedure takes less than 5 hours for 96 samples. Several hundred samples can then be pooled on the same HiSeq lane via custom barcodes. Our method will be useful for re-sequencing of microbial or viral genomes, including those from evolution experiments, genetic screens, and environmental samples, as well as for other sequencing applications including large amplicon, open chromosome, artificial chromosomes, and RNA sequencing.

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          Most cited references11

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          Community structure and metabolism through reconstruction of microbial genomes from the environment.

          Microbial communities are vital in the functioning of all ecosystems; however, most microorganisms are uncultivated, and their roles in natural systems are unclear. Here, using random shotgun sequencing of DNA from a natural acidophilic biofilm, we report reconstruction of near-complete genomes of Leptospirillum group II and Ferroplasma type II, and partial recovery of three other genomes. This was possible because the biofilm was dominated by a small number of species populations and the frequency of genomic rearrangements and gene insertions or deletions was relatively low. Because each sequence read came from a different individual, we could determine that single-nucleotide polymorphisms are the predominant form of heterogeneity at the strain level. The Leptospirillum group II genome had remarkably few nucleotide polymorphisms, despite the existence of low-abundance variants. The Ferroplasma type II genome seems to be a composite from three ancestral strains that have undergone homologous recombination to form a large population of mosaic genomes. Analysis of the gene complement for each organism revealed the pathways for carbon and nitrogen fixation and energy generation, and provided insights into survival strategies in an extreme environment.
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            Transforming clinical microbiology with bacterial genome sequencing.

            Whole-genome sequencing of bacteria has recently emerged as a cost-effective and convenient approach for addressing many microbiological questions. Here, we review the current status of clinical microbiology and how it has already begun to be transformed by using next-generation sequencing. We focus on three essential tasks: identifying the species of an isolate, testing its properties, such as resistance to antibiotics and virulence, and monitoring the emergence and spread of bacterial pathogens. We predict that the application of next-generation sequencing will soon be sufficiently fast, accurate and cheap to be used in routine clinical microbiology practice, where it could replace many complex current techniques with a single, more efficient workflow.
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              Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition

              We characterize and extend a highly efficient method for constructing shotgun fragment libraries in which transposase catalyzes in vitro DNA fragmentation and adaptor incorporation simultaneously. We apply this method to sequencing a human genome and find that coverage biases are comparable to those of conventional protocols. We also extend its capabilities by developing protocols for sub-nanogram library construction, exome capture from 50 ng of input DNA, PCR-free and colony PCR library construction, and 96-plex sample indexing.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                22 May 2015
                2015
                : 10
                : 5
                : e0128036
                Affiliations
                [1 ]Department of Systems Biology, Harvard Medical School, Boston, Massachusetts, United States of America
                [2 ]Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts, United States of America
                [3 ]FAS Center for Systems Biology, Harvard University, Cambridge, Massachusetts, United States of America
                [4 ]Department of Physics, Harvard University, Cambridge, Massachusetts, United States of America
                [5 ]Faculty of Biology and Department of Computer Science, Technion-Israel Institute of Technology, Haifa, Israel
                University of Illinois at Chicago, UNITED STATES
                Author notes

                Competing Interests: This study was partially funding by Hoffman-LaRoche (RK). There are no further declarations relating to employment, consultancy, patents, products in development, or marketed products. This does not alter the authors' adherence to PLOS ONE policies on sharing data and materials. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

                Conceived and designed the experiments: MB SK TL HC MMD RK. Performed the experiments: MB SK TL HC. Analyzed the data: MB SK TL HC. Contributed reagents/materials/analysis tools: MMD RK. Wrote the paper: MB SK TL HC MMD RK.

                Article
                PONE-D-14-58256
                10.1371/journal.pone.0128036
                4441430
                26000737
                9df73f82-8c0c-44d0-a071-cc231d976953
                Copyright @ 2015

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

                History
                : 29 December 2014
                : 21 April 2015
                Page count
                Figures: 5, Tables: 0, Pages: 15
                Funding
                This work was supported by the National Science Foundation Mathematical Sciences Postdoctoral Research Fellowship DMS-0903013 (to MB, http://www.nsf.gov/), Career Award at the Scientific Interface from the Burroughs Wellcome Foundation (to SK, http://www.bwfund.org/), the James S. McDonnell Foundation (to MMD, https://www.jsmf.org/), the Alfred P. Sloan Foundation (to MMD, http://www.sloan.org/), PHY 1313638 from the US National Science Foundation (to MMD, http://www.nsf.gov/), US National Institutes of Health grant R01-GM081617 (to RK) and R01-GM104239 (to MMD, http://www.nih.gov/), European Research Council FP7 ERC Grant 281891 (to RK, http://erc.europa.eu/), and Hoffman-LaRoche (to RK, http://www.rocheusa.com/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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