From Conventional to Next Generation Sequencing of Epstein-Barr Virus Genomes

Genomic sequences of Epstein–Barr virus (EBV) have been of interest because the virus is associated with cancers, such as nasopharyngeal carcinoma, and conditions such as infectious mononucleosis. The progress of whole-genome EBV sequencing has been limited by the inefficiency and cost of the first-...

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Main Authors: Hin Kwok, Alan Kwok Shing Chiang
Format: Article
Language:English
Published: MDPI AG 2016-02-01
Series:Viruses
Subjects:
Online Access:http://www.mdpi.com/1999-4915/8/3/60
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spelling doaj-7c0a493acac047b1b903bbbadc2f267c2020-11-24T22:59:41ZengMDPI AGViruses1999-49152016-02-01836010.3390/v8030060v8030060From Conventional to Next Generation Sequencing of Epstein-Barr Virus GenomesHin Kwok0Alan Kwok Shing Chiang1Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, ChinaDepartment of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, ChinaGenomic sequences of Epstein–Barr virus (EBV) have been of interest because the virus is associated with cancers, such as nasopharyngeal carcinoma, and conditions such as infectious mononucleosis. The progress of whole-genome EBV sequencing has been limited by the inefficiency and cost of the first-generation sequencing technology. With the advancement of next-generation sequencing (NGS) and target enrichment strategies, increasing number of EBV genomes has been published. These genomes were sequenced using different approaches, either with or without EBV DNA enrichment. This review provides an overview of the EBV genomes published to date, and a description of the sequencing technology and bioinformatic analyses employed in generating these sequences. We further explored ways through which the quality of sequencing data can be improved, such as using DNA oligos for capture hybridization, and longer insert size and read length in the sequencing runs. These advances will enable large-scale genomic sequencing of EBV which will facilitate a better understanding of the genetic variations of EBV in different geographic regions and discovery of potentially pathogenic variants in specific diseases.http://www.mdpi.com/1999-4915/8/3/60Epstein-Barr virusNext-generation sequencingtarget capturegenome assembly
collection DOAJ
language English
format Article
sources DOAJ
author Hin Kwok
Alan Kwok Shing Chiang
spellingShingle Hin Kwok
Alan Kwok Shing Chiang
From Conventional to Next Generation Sequencing of Epstein-Barr Virus Genomes
Viruses
Epstein-Barr virus
Next-generation sequencing
target capture
genome assembly
author_facet Hin Kwok
Alan Kwok Shing Chiang
author_sort Hin Kwok
title From Conventional to Next Generation Sequencing of Epstein-Barr Virus Genomes
title_short From Conventional to Next Generation Sequencing of Epstein-Barr Virus Genomes
title_full From Conventional to Next Generation Sequencing of Epstein-Barr Virus Genomes
title_fullStr From Conventional to Next Generation Sequencing of Epstein-Barr Virus Genomes
title_full_unstemmed From Conventional to Next Generation Sequencing of Epstein-Barr Virus Genomes
title_sort from conventional to next generation sequencing of epstein-barr virus genomes
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2016-02-01
description Genomic sequences of Epstein–Barr virus (EBV) have been of interest because the virus is associated with cancers, such as nasopharyngeal carcinoma, and conditions such as infectious mononucleosis. The progress of whole-genome EBV sequencing has been limited by the inefficiency and cost of the first-generation sequencing technology. With the advancement of next-generation sequencing (NGS) and target enrichment strategies, increasing number of EBV genomes has been published. These genomes were sequenced using different approaches, either with or without EBV DNA enrichment. This review provides an overview of the EBV genomes published to date, and a description of the sequencing technology and bioinformatic analyses employed in generating these sequences. We further explored ways through which the quality of sequencing data can be improved, such as using DNA oligos for capture hybridization, and longer insert size and read length in the sequencing runs. These advances will enable large-scale genomic sequencing of EBV which will facilitate a better understanding of the genetic variations of EBV in different geographic regions and discovery of potentially pathogenic variants in specific diseases.
topic Epstein-Barr virus
Next-generation sequencing
target capture
genome assembly
url http://www.mdpi.com/1999-4915/8/3/60
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