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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Main Authors: Trees-Juen Chuang, Shian-Zu Wu, Yao-Ting Huang
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2013/264532
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spelling 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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