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      PhageTerm: a tool for fast and accurate determination of phage termini and packaging mechanism using next-generation sequencing data

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          Abstract

          The worrying rise of antibiotic resistance in pathogenic bacteria is leading to a renewed interest in bacteriophages as a treatment option. Novel sequencing technologies enable description of an increasing number of phage genomes, a critical piece of information to understand their life cycle, phage-host interactions, and evolution. In this work, we demonstrate how it is possible to recover more information from sequencing data than just the phage genome. We developed a theoretical and statistical framework to determine DNA termini and phage packaging mechanisms using NGS data. Our method relies on the detection of biases in the number of reads, which are observable at natural DNA termini compared with the rest of the phage genome. We implemented our method with the creation of the software PhageTerm and validated it using a set of phages with well-established packaging mechanisms representative of the termini diversity, i.e. 5′ cos (Lambda), 3′ cos (HK97), pac (P1), headful without a pac site (T4), DTR (T7) and host fragment (Mu). In addition, we determined the termini of nine Clostridium difficile phages and six phages whose sequences were retrieved from the Sequence Read Archive. PhageTerm is freely available (https://sourceforge.net/projects/phageterm), as a Galaxy ToolShed and on a Galaxy-based server (https://galaxy.pasteur.fr).

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          Most cited references33

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          SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing.

          The lion's share of bacteria in various environments cannot be cloned in the laboratory and thus cannot be sequenced using existing technologies. A major goal of single-cell genomics is to complement gene-centric metagenomic data with whole-genome assemblies of uncultivated organisms. Assembly of single-cell data is challenging because of highly non-uniform read coverage as well as elevated levels of sequencing errors and chimeric reads. We describe SPAdes, a new assembler for both single-cell and standard (multicell) assembly, and demonstrate that it improves on the recently released E+V-SC assembler (specialized for single-cell data) and on popular assemblers Velvet and SoapDeNovo (for multicell data). SPAdes generates single-cell assemblies, providing information about genomes of uncultivatable bacteria that vastly exceeds what may be obtained via traditional metagenomics studies. SPAdes is available online ( http://bioinf.spbau.ru/spades ). It is distributed as open source software.
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            Phamerator: a bioinformatic tool for comparative bacteriophage genomics

            Background Bacteriophage genomes have mosaic architectures and are replete with small open reading frames of unknown function, presenting challenges in their annotation, comparative analysis, and representation. Results We describe here a bioinformatic tool, Phamerator, that assorts protein-coding genes into phamilies of related sequences using pairwise comparisons to generate a database of gene relationships. This database is used to generate genome maps of multiple phages that incorporate nucleotide and amino acid sequence relationships, as well as genes containing conserved domains. Phamerator also generates phamily circle representations of gene phamilies, facilitating analysis of the different evolutionary histories of individual genes that migrate through phage populations by horizontal genetic exchange. Conclusions Phamerator represents a useful tool for comparative genomic analysis and comparative representations of bacteriophage genomes.
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              Complete nucleotide sequence of bacteriophage T7 DNA and the locations of T7 genetic elements.

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                Author and article information

                Contributors
                david.bikard@pasteur.fr
                marc.monot@pasteur.fr
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                15 August 2017
                15 August 2017
                2017
                : 7
                : 8292
                Affiliations
                [1 ]Département de Microbiologie, Institut Pasteur, Laboratoire Pathogenèse des bactéries anaérobies, Paris, France
                [2 ]ISNI 0000 0000 9064 6198, GRID grid.86715.3d, Département de Microbiologie et d’infectiologie, , Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, ; Sherbrooke, QC Canada
                [3 ]Département de Microbiologie, Institut Pasteur, Groupe Biologie de Synthèse, Paris, France
                [4 ]ISNI 0000 0004 1788 6194, GRID grid.469994.f, Université Paris Diderot, , Sorbonne Paris Cité, ; Paris, France
                Author information
                http://orcid.org/0000-0003-4579-8776
                http://orcid.org/0000-0002-5729-1211
                http://orcid.org/0000-0003-0738-7335
                Article
                7910
                10.1038/s41598-017-07910-5
                5557969
                28811656
                ab5a0d0c-9638-4707-8787-0a5a82c2ec02
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 26 April 2017
                : 4 July 2017
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