A Novel Framework for the Identification and Analysis of Duplicons between Human and Chimpanzee
Human and other primate genomes consist of many segmental duplications (SDs) due to fixation of copy number variations (CNVs). Structure of these duplications within the human genome has been shown to be a complex mosaic composed of juxtaposed subunits (called duplicons). These duplicons are difficu...
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doaj-fe9bee093b6549d3b286bb34a58b2d3f2020-11-25T00:36:25ZengHindawi LimitedBioMed Research International2314-61332314-61412013-01-01201310.1155/2013/264532264532A Novel Framework for the Identification and Analysis of Duplicons between Human and ChimpanzeeTrees-Juen Chuang0Shian-Zu Wu1Yao-Ting Huang2Genomics Research Center, Academia Sinica, Taipei, TaiwanDepartment of Computer Science and Information Engineering, National Chung Cheng University, No.168 University Road Chiayi, TaiwanDepartment of Computer Science and Information Engineering, National Chung Cheng University, No.168 University Road Chiayi, TaiwanHuman and other primate genomes consist of many segmental duplications (SDs) due to fixation of copy number variations (CNVs). Structure of these duplications within the human genome has been shown to be a complex mosaic composed of juxtaposed subunits (called duplicons). These duplicons are difficult to be uncovered from the mosaic repeat structure. In addition, the distribution and evolution of duplicons among primates are still poorly investigated. In this paper, we develop a statistical framework for discovering duplicons via integration of a Hidden Markov Model (HMM) and a permutation test. Our comparative analysis indicates that the mosaic structure of duplicons is common in CNV/SD regions of both human and chimpanzee genomes, and a subset of core duplicons is shared by the majority of CNVs/SDs. Phylogenetic analyses using duplicons suggested that most CNVs/SDs share common duplication ancestry. Many human/chimpanzee duplicons flank both ends of CNVs, which may be hotspots of nonallelic homologous recombination.http://dx.doi.org/10.1155/2013/264532 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Trees-Juen Chuang Shian-Zu Wu Yao-Ting Huang |
spellingShingle |
Trees-Juen Chuang Shian-Zu Wu Yao-Ting Huang A Novel Framework for the Identification and Analysis of Duplicons between Human and Chimpanzee BioMed Research International |
author_facet |
Trees-Juen Chuang Shian-Zu Wu Yao-Ting Huang |
author_sort |
Trees-Juen Chuang |
title |
A Novel Framework for the Identification and Analysis of Duplicons between Human and Chimpanzee |
title_short |
A Novel Framework for the Identification and Analysis of Duplicons between Human and Chimpanzee |
title_full |
A Novel Framework for the Identification and Analysis of Duplicons between Human and Chimpanzee |
title_fullStr |
A Novel Framework for the Identification and Analysis of Duplicons between Human and Chimpanzee |
title_full_unstemmed |
A Novel Framework for the Identification and Analysis of Duplicons between Human and Chimpanzee |
title_sort |
novel framework for the identification and analysis of duplicons between human and chimpanzee |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2013-01-01 |
description |
Human and other primate genomes consist of many segmental
duplications (SDs) due to fixation of copy number variations (CNVs). Structure of these duplications within the human genome has been shown to be a complex mosaic composed of juxtaposed subunits (called duplicons). These duplicons are difficult to be uncovered from the mosaic repeat structure. In addition, the distribution and evolution of duplicons among primates are still poorly investigated. In this paper, we develop a statistical framework for discovering duplicons via integration of a Hidden Markov Model (HMM) and a permutation test. Our comparative analysis indicates that the mosaic structure of duplicons is common in CNV/SD regions of both human and chimpanzee genomes, and a subset of core duplicons is shared by the majority of CNVs/SDs. Phylogenetic analyses using duplicons suggested that most CNVs/SDs share common duplication ancestry. Many human/chimpanzee duplicons flank both ends of CNVs, which may be hotspots of nonallelic homologous recombination. |
url |
http://dx.doi.org/10.1155/2013/264532 |
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