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Rapid Genome Mapping in Nanochannel Arrays for Highly Complete and Accurate De Novo Sequence Assembly of the Complex Aegilops tauschii Genome

Next-generation sequencing (NGS) technologies have enabled high-throughput and low-cost generation of sequence data; however, de novo genome assembly remains a great challenge, particularly for large genomes. NGS short reads are often insufficient to create large contigs that span repeat sequences a...

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Autores principales: Hastie, Alex R., Dong, Lingli, Smith, Alexis, Finklestein, Jeff, Lam, Ernest T., Huo, Naxin, Cao, Han, Kwok, Pui-Yan, Deal, Karin R., Dvorak, Jan, Luo, Ming-Cheng, Gu, Yong, Xiao, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566107/
https://www.ncbi.nlm.nih.gov/pubmed/23405223
http://dx.doi.org/10.1371/journal.pone.0055864
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author Hastie, Alex R.
Dong, Lingli
Smith, Alexis
Finklestein, Jeff
Lam, Ernest T.
Huo, Naxin
Cao, Han
Kwok, Pui-Yan
Deal, Karin R.
Dvorak, Jan
Luo, Ming-Cheng
Gu, Yong
Xiao, Ming
author_facet Hastie, Alex R.
Dong, Lingli
Smith, Alexis
Finklestein, Jeff
Lam, Ernest T.
Huo, Naxin
Cao, Han
Kwok, Pui-Yan
Deal, Karin R.
Dvorak, Jan
Luo, Ming-Cheng
Gu, Yong
Xiao, Ming
author_sort Hastie, Alex R.
collection PubMed
description Next-generation sequencing (NGS) technologies have enabled high-throughput and low-cost generation of sequence data; however, de novo genome assembly remains a great challenge, particularly for large genomes. NGS short reads are often insufficient to create large contigs that span repeat sequences and to facilitate unambiguous assembly. Plant genomes are notorious for containing high quantities of repetitive elements, which combined with huge genome sizes, makes accurate assembly of these large and complex genomes intractable thus far. Using two-color genome mapping of tiling bacterial artificial chromosomes (BAC) clones on nanochannel arrays, we completed high-confidence assembly of a 2.1-Mb, highly repetitive region in the large and complex genome of Aegilops tauschii, the D-genome donor of hexaploid wheat (Triticum aestivum). Genome mapping is based on direct visualization of sequence motifs on single DNA molecules hundreds of kilobases in length. With the genome map as a scaffold, we anchored unplaced sequence contigs, validated the initial draft assembly, and resolved instances of misassembly, some involving contigs <2 kb long, to dramatically improve the assembly from 75% to 95% complete.
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spelling pubmed-35661072013-02-12 Rapid Genome Mapping in Nanochannel Arrays for Highly Complete and Accurate De Novo Sequence Assembly of the Complex Aegilops tauschii Genome Hastie, Alex R. Dong, Lingli Smith, Alexis Finklestein, Jeff Lam, Ernest T. Huo, Naxin Cao, Han Kwok, Pui-Yan Deal, Karin R. Dvorak, Jan Luo, Ming-Cheng Gu, Yong Xiao, Ming PLoS One Research Article Next-generation sequencing (NGS) technologies have enabled high-throughput and low-cost generation of sequence data; however, de novo genome assembly remains a great challenge, particularly for large genomes. NGS short reads are often insufficient to create large contigs that span repeat sequences and to facilitate unambiguous assembly. Plant genomes are notorious for containing high quantities of repetitive elements, which combined with huge genome sizes, makes accurate assembly of these large and complex genomes intractable thus far. Using two-color genome mapping of tiling bacterial artificial chromosomes (BAC) clones on nanochannel arrays, we completed high-confidence assembly of a 2.1-Mb, highly repetitive region in the large and complex genome of Aegilops tauschii, the D-genome donor of hexaploid wheat (Triticum aestivum). Genome mapping is based on direct visualization of sequence motifs on single DNA molecules hundreds of kilobases in length. With the genome map as a scaffold, we anchored unplaced sequence contigs, validated the initial draft assembly, and resolved instances of misassembly, some involving contigs <2 kb long, to dramatically improve the assembly from 75% to 95% complete. Public Library of Science 2013-02-06 /pmc/articles/PMC3566107/ /pubmed/23405223 http://dx.doi.org/10.1371/journal.pone.0055864 Text en © 2013 Hastie 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hastie, Alex R.
Dong, Lingli
Smith, Alexis
Finklestein, Jeff
Lam, Ernest T.
Huo, Naxin
Cao, Han
Kwok, Pui-Yan
Deal, Karin R.
Dvorak, Jan
Luo, Ming-Cheng
Gu, Yong
Xiao, Ming
Rapid Genome Mapping in Nanochannel Arrays for Highly Complete and Accurate De Novo Sequence Assembly of the Complex Aegilops tauschii Genome
title Rapid Genome Mapping in Nanochannel Arrays for Highly Complete and Accurate De Novo Sequence Assembly of the Complex Aegilops tauschii Genome
title_full Rapid Genome Mapping in Nanochannel Arrays for Highly Complete and Accurate De Novo Sequence Assembly of the Complex Aegilops tauschii Genome
title_fullStr Rapid Genome Mapping in Nanochannel Arrays for Highly Complete and Accurate De Novo Sequence Assembly of the Complex Aegilops tauschii Genome
title_full_unstemmed Rapid Genome Mapping in Nanochannel Arrays for Highly Complete and Accurate De Novo Sequence Assembly of the Complex Aegilops tauschii Genome
title_short Rapid Genome Mapping in Nanochannel Arrays for Highly Complete and Accurate De Novo Sequence Assembly of the Complex Aegilops tauschii Genome
title_sort rapid genome mapping in nanochannel arrays for highly complete and accurate de novo sequence assembly of the complex aegilops tauschii genome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566107/
https://www.ncbi.nlm.nih.gov/pubmed/23405223
http://dx.doi.org/10.1371/journal.pone.0055864
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