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Identification of Horizontally-transferred Genomic Islands and Genome Segmentation Points by Using the GC Profile Method
The nucleotide composition of genomes undergoes dramatic variations among all three kingdoms of life. GC content, an important characteristic for a genome, is related to many important functions, and therefore GC content and its distribution are routinely reported for sequenced genomes. Traditionall...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009839/ https://www.ncbi.nlm.nih.gov/pubmed/24822029 http://dx.doi.org/10.2174/1389202915999140328163125 |
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author | Zhang, Ren Ou, Hong-Yu Gao, Feng Luo, Hao |
author_facet | Zhang, Ren Ou, Hong-Yu Gao, Feng Luo, Hao |
author_sort | Zhang, Ren |
collection | PubMed |
description | The nucleotide composition of genomes undergoes dramatic variations among all three kingdoms of life. GC content, an important characteristic for a genome, is related to many important functions, and therefore GC content and its distribution are routinely reported for sequenced genomes. Traditionally, GC content distribution is assessed by computing GC contents in windows that slide along the genome. Disadvantages of this routinely used window-based method include low resolution and low sensitivity. Additionally, different window sizes result in different GC content distribution patterns within the same genome. We proposed a windowless method, the GC profile, for displaying GC content variations across the genome. Compared to the window-based method, the GC profile has the following advantages: 1) higher sensitivity, because of variation-amplifying procedures; 2) higher resolution, because boundaries between domains can be determined at one single base pair; 3) uniqueness, because the GC profile is unique for a given genome and 4) the capacity to show both global and regional GC content distributions. These characteristics are useful in identifying horizontally-transferred genomic islands and homogenous GC-content domains. Here, we review the applications of the GC profile in identifying genomic islands and genome segmentation points, and in serving as a platform to integrate with other algorithms for genome analysis. A web server generating GC profiles and implementing relevant genome segmentation algorithms is available at: www.zcurve.net. |
format | Online Article Text |
id | pubmed-4009839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-40098392014-10-01 Identification of Horizontally-transferred Genomic Islands and Genome Segmentation Points by Using the GC Profile Method Zhang, Ren Ou, Hong-Yu Gao, Feng Luo, Hao Curr Genomics Article The nucleotide composition of genomes undergoes dramatic variations among all three kingdoms of life. GC content, an important characteristic for a genome, is related to many important functions, and therefore GC content and its distribution are routinely reported for sequenced genomes. Traditionally, GC content distribution is assessed by computing GC contents in windows that slide along the genome. Disadvantages of this routinely used window-based method include low resolution and low sensitivity. Additionally, different window sizes result in different GC content distribution patterns within the same genome. We proposed a windowless method, the GC profile, for displaying GC content variations across the genome. Compared to the window-based method, the GC profile has the following advantages: 1) higher sensitivity, because of variation-amplifying procedures; 2) higher resolution, because boundaries between domains can be determined at one single base pair; 3) uniqueness, because the GC profile is unique for a given genome and 4) the capacity to show both global and regional GC content distributions. These characteristics are useful in identifying horizontally-transferred genomic islands and homogenous GC-content domains. Here, we review the applications of the GC profile in identifying genomic islands and genome segmentation points, and in serving as a platform to integrate with other algorithms for genome analysis. A web server generating GC profiles and implementing relevant genome segmentation algorithms is available at: www.zcurve.net. Bentham Science Publishers 2014-04 2014-04 /pmc/articles/PMC4009839/ /pubmed/24822029 http://dx.doi.org/10.2174/1389202915999140328163125 Text en ©2013 Bentham Science Publishers http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Zhang, Ren Ou, Hong-Yu Gao, Feng Luo, Hao Identification of Horizontally-transferred Genomic Islands and Genome Segmentation Points by Using the GC Profile Method |
title | Identification of Horizontally-transferred Genomic Islands and Genome Segmentation Points by Using the GC Profile Method |
title_full | Identification of Horizontally-transferred Genomic Islands and Genome Segmentation Points by Using the GC Profile Method |
title_fullStr | Identification of Horizontally-transferred Genomic Islands and Genome Segmentation Points by Using the GC Profile Method |
title_full_unstemmed | Identification of Horizontally-transferred Genomic Islands and Genome Segmentation Points by Using the GC Profile Method |
title_short | Identification of Horizontally-transferred Genomic Islands and Genome Segmentation Points by Using the GC Profile Method |
title_sort | identification of horizontally-transferred genomic islands and genome segmentation points by using the gc profile method |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009839/ https://www.ncbi.nlm.nih.gov/pubmed/24822029 http://dx.doi.org/10.2174/1389202915999140328163125 |
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