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Global repeat discovery and estimation of genomic copy number in a large, complex genome using a high-throughput 454 sequence survey

BACKGROUND: Extensive computational and database tools are available to mine genomic and genetic databases for model organisms, but little genomic data is available for many species of ecological or agricultural significance, especially those with large genomes. Genome surveys using conventional seq...

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Autores principales: Swaminathan, Kankshita, Varala, Kranthi, Hudson, Matthew E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894642/
https://www.ncbi.nlm.nih.gov/pubmed/17524145
http://dx.doi.org/10.1186/1471-2164-8-132
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author Swaminathan, Kankshita
Varala, Kranthi
Hudson, Matthew E
author_facet Swaminathan, Kankshita
Varala, Kranthi
Hudson, Matthew E
author_sort Swaminathan, Kankshita
collection PubMed
description BACKGROUND: Extensive computational and database tools are available to mine genomic and genetic databases for model organisms, but little genomic data is available for many species of ecological or agricultural significance, especially those with large genomes. Genome surveys using conventional sequencing techniques are powerful, particularly for detecting sequences present in many copies per genome. However these methods are time-consuming and have potential drawbacks. High throughput 454 sequencing provides an alternative method by which much information can be gained quickly and cheaply from high-coverage surveys of genomic DNA. RESULTS: We sequenced 78 million base-pairs of randomly sheared soybean DNA which passed our quality criteria. Computational analysis of the survey sequences provided global information on the abundant repetitive sequences in soybean. The sequence was used to determine the copy number across regions of large genomic clones or contigs and discover higher-order structures within satellite repeats. We have created an annotated, online database of sequences present in multiple copies in the soybean genome. The low bias of pyrosequencing against repeat sequences is demonstrated by the overall composition of the survey data, which matches well with past estimates of repetitive DNA content obtained by DNA re-association kinetics (Cot analysis). CONCLUSION: This approach provides a potential aid to conventional or shotgun genome assembly, by allowing rapid assessment of copy number in any clone or clone-end sequence. In addition, we show that partial sequencing can provide access to partial protein-coding sequences.
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spelling pubmed-18946422007-06-19 Global repeat discovery and estimation of genomic copy number in a large, complex genome using a high-throughput 454 sequence survey Swaminathan, Kankshita Varala, Kranthi Hudson, Matthew E BMC Genomics Research Article BACKGROUND: Extensive computational and database tools are available to mine genomic and genetic databases for model organisms, but little genomic data is available for many species of ecological or agricultural significance, especially those with large genomes. Genome surveys using conventional sequencing techniques are powerful, particularly for detecting sequences present in many copies per genome. However these methods are time-consuming and have potential drawbacks. High throughput 454 sequencing provides an alternative method by which much information can be gained quickly and cheaply from high-coverage surveys of genomic DNA. RESULTS: We sequenced 78 million base-pairs of randomly sheared soybean DNA which passed our quality criteria. Computational analysis of the survey sequences provided global information on the abundant repetitive sequences in soybean. The sequence was used to determine the copy number across regions of large genomic clones or contigs and discover higher-order structures within satellite repeats. We have created an annotated, online database of sequences present in multiple copies in the soybean genome. The low bias of pyrosequencing against repeat sequences is demonstrated by the overall composition of the survey data, which matches well with past estimates of repetitive DNA content obtained by DNA re-association kinetics (Cot analysis). CONCLUSION: This approach provides a potential aid to conventional or shotgun genome assembly, by allowing rapid assessment of copy number in any clone or clone-end sequence. In addition, we show that partial sequencing can provide access to partial protein-coding sequences. BioMed Central 2007-05-24 /pmc/articles/PMC1894642/ /pubmed/17524145 http://dx.doi.org/10.1186/1471-2164-8-132 Text en Copyright © 2007 Swaminathan et al; licensee BioMed Central Ltd. https://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 (https://creativecommons.org/licenses/by/2.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Swaminathan, Kankshita
Varala, Kranthi
Hudson, Matthew E
Global repeat discovery and estimation of genomic copy number in a large, complex genome using a high-throughput 454 sequence survey
title Global repeat discovery and estimation of genomic copy number in a large, complex genome using a high-throughput 454 sequence survey
title_full Global repeat discovery and estimation of genomic copy number in a large, complex genome using a high-throughput 454 sequence survey
title_fullStr Global repeat discovery and estimation of genomic copy number in a large, complex genome using a high-throughput 454 sequence survey
title_full_unstemmed Global repeat discovery and estimation of genomic copy number in a large, complex genome using a high-throughput 454 sequence survey
title_short Global repeat discovery and estimation of genomic copy number in a large, complex genome using a high-throughput 454 sequence survey
title_sort global repeat discovery and estimation of genomic copy number in a large, complex genome using a high-throughput 454 sequence survey
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894642/
https://www.ncbi.nlm.nih.gov/pubmed/17524145
http://dx.doi.org/10.1186/1471-2164-8-132
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