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Assessing Illumina technology for the high-throughput sequencing of bacteriophage genomes

Bacteriophages are the most abundant biological entities on the planet, playing crucial roles in the shaping of bacterial populations. Phages have smaller genomes than their bacterial hosts, yet there are currently fewer fully sequenced phage than bacterial genomes. We assessed the suitability of Il...

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Autores principales: Rihtman, Branko, Meaden, Sean, Clokie, Martha R.J., Koskella, Britt, Millard, Andrew D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893331/
https://www.ncbi.nlm.nih.gov/pubmed/27280068
http://dx.doi.org/10.7717/peerj.2055
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author Rihtman, Branko
Meaden, Sean
Clokie, Martha R.J.
Koskella, Britt
Millard, Andrew D.
author_facet Rihtman, Branko
Meaden, Sean
Clokie, Martha R.J.
Koskella, Britt
Millard, Andrew D.
author_sort Rihtman, Branko
collection PubMed
description Bacteriophages are the most abundant biological entities on the planet, playing crucial roles in the shaping of bacterial populations. Phages have smaller genomes than their bacterial hosts, yet there are currently fewer fully sequenced phage than bacterial genomes. We assessed the suitability of Illumina technology for high-throughput sequencing and subsequent assembly of phage genomes. In silico datasets reveal that 30× coverage is sufficient to correctly assemble the complete genome of ~98.5% of known phages, with experimental data confirming that the majority of phage genomes can be assembled at 30× coverage. Furthermore, in silico data demonstrate it is possible to co-sequence multiple phages from different hosts, without introducing assembly errors.
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spelling pubmed-48933312016-06-08 Assessing Illumina technology for the high-throughput sequencing of bacteriophage genomes Rihtman, Branko Meaden, Sean Clokie, Martha R.J. Koskella, Britt Millard, Andrew D. PeerJ Bioinformatics Bacteriophages are the most abundant biological entities on the planet, playing crucial roles in the shaping of bacterial populations. Phages have smaller genomes than their bacterial hosts, yet there are currently fewer fully sequenced phage than bacterial genomes. We assessed the suitability of Illumina technology for high-throughput sequencing and subsequent assembly of phage genomes. In silico datasets reveal that 30× coverage is sufficient to correctly assemble the complete genome of ~98.5% of known phages, with experimental data confirming that the majority of phage genomes can be assembled at 30× coverage. Furthermore, in silico data demonstrate it is possible to co-sequence multiple phages from different hosts, without introducing assembly errors. PeerJ Inc. 2016-06-01 /pmc/articles/PMC4893331/ /pubmed/27280068 http://dx.doi.org/10.7717/peerj.2055 Text en © 2016 Rihtman et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Rihtman, Branko
Meaden, Sean
Clokie, Martha R.J.
Koskella, Britt
Millard, Andrew D.
Assessing Illumina technology for the high-throughput sequencing of bacteriophage genomes
title Assessing Illumina technology for the high-throughput sequencing of bacteriophage genomes
title_full Assessing Illumina technology for the high-throughput sequencing of bacteriophage genomes
title_fullStr Assessing Illumina technology for the high-throughput sequencing of bacteriophage genomes
title_full_unstemmed Assessing Illumina technology for the high-throughput sequencing of bacteriophage genomes
title_short Assessing Illumina technology for the high-throughput sequencing of bacteriophage genomes
title_sort assessing illumina technology for the high-throughput sequencing of bacteriophage genomes
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893331/
https://www.ncbi.nlm.nih.gov/pubmed/27280068
http://dx.doi.org/10.7717/peerj.2055
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