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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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 |
work_keys_str_mv |
AT hinkwok fromconventionaltonextgenerationsequencingofepsteinbarrvirusgenomes AT alankwokshingchiang fromconventionaltonextgenerationsequencingofepsteinbarrvirusgenomes |
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