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Optical mapping as a routine tool for bacterial genome sequence finishing
BACKGROUND: In sequencing the genomes of two Xenorhabdus species, we encountered a large number of sequence repeats and assembly anomalies that stalled finishing efforts. This included a stretch of about 12 Kb that is over 99.9% identical between the plasmid and chromosome of X. nematophila. RESULTS...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2045679/ https://www.ncbi.nlm.nih.gov/pubmed/17868451 http://dx.doi.org/10.1186/1471-2164-8-321 |
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author | Latreille, Phil Norton, Stacie Goldman, Barry S Henkhaus, John Miller, Nancy Barbazuk, Brad Bode, Helge B Darby, Creg Du, Zijin Forst, Steve Gaudriault, Sophie Goodner, Brad Goodrich-Blair, Heidi Slater, Steven |
author_facet | Latreille, Phil Norton, Stacie Goldman, Barry S Henkhaus, John Miller, Nancy Barbazuk, Brad Bode, Helge B Darby, Creg Du, Zijin Forst, Steve Gaudriault, Sophie Goodner, Brad Goodrich-Blair, Heidi Slater, Steven |
author_sort | Latreille, Phil |
collection | PubMed |
description | BACKGROUND: In sequencing the genomes of two Xenorhabdus species, we encountered a large number of sequence repeats and assembly anomalies that stalled finishing efforts. This included a stretch of about 12 Kb that is over 99.9% identical between the plasmid and chromosome of X. nematophila. RESULTS: Whole genome restriction maps of the sequenced strains were produced through optical mapping technology. These maps allowed rapid resolution of sequence assembly problems, permitted closing of the genome, and allowed correction of a large inversion in a genome assembly that we had considered finished. CONCLUSION: Our experience suggests that routine use of optical mapping in bacterial genome sequence finishing is warranted. When combined with data produced through 454 sequencing, an optical map can rapidly and inexpensively generate an ordered and oriented set of contigs to produce a nearly complete genome sequence assembly. |
format | Text |
id | pubmed-2045679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-20456792007-10-31 Optical mapping as a routine tool for bacterial genome sequence finishing Latreille, Phil Norton, Stacie Goldman, Barry S Henkhaus, John Miller, Nancy Barbazuk, Brad Bode, Helge B Darby, Creg Du, Zijin Forst, Steve Gaudriault, Sophie Goodner, Brad Goodrich-Blair, Heidi Slater, Steven BMC Genomics Methodology Article BACKGROUND: In sequencing the genomes of two Xenorhabdus species, we encountered a large number of sequence repeats and assembly anomalies that stalled finishing efforts. This included a stretch of about 12 Kb that is over 99.9% identical between the plasmid and chromosome of X. nematophila. RESULTS: Whole genome restriction maps of the sequenced strains were produced through optical mapping technology. These maps allowed rapid resolution of sequence assembly problems, permitted closing of the genome, and allowed correction of a large inversion in a genome assembly that we had considered finished. CONCLUSION: Our experience suggests that routine use of optical mapping in bacterial genome sequence finishing is warranted. When combined with data produced through 454 sequencing, an optical map can rapidly and inexpensively generate an ordered and oriented set of contigs to produce a nearly complete genome sequence assembly. BioMed Central 2007-09-14 /pmc/articles/PMC2045679/ /pubmed/17868451 http://dx.doi.org/10.1186/1471-2164-8-321 Text en Copyright © 2007 Latreille et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Latreille, Phil Norton, Stacie Goldman, Barry S Henkhaus, John Miller, Nancy Barbazuk, Brad Bode, Helge B Darby, Creg Du, Zijin Forst, Steve Gaudriault, Sophie Goodner, Brad Goodrich-Blair, Heidi Slater, Steven Optical mapping as a routine tool for bacterial genome sequence finishing |
title | Optical mapping as a routine tool for bacterial genome sequence finishing |
title_full | Optical mapping as a routine tool for bacterial genome sequence finishing |
title_fullStr | Optical mapping as a routine tool for bacterial genome sequence finishing |
title_full_unstemmed | Optical mapping as a routine tool for bacterial genome sequence finishing |
title_short | Optical mapping as a routine tool for bacterial genome sequence finishing |
title_sort | optical mapping as a routine tool for bacterial genome sequence finishing |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2045679/ https://www.ncbi.nlm.nih.gov/pubmed/17868451 http://dx.doi.org/10.1186/1471-2164-8-321 |
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