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Genome-wide prediction of vaccine targets for human herpes simplex viruses using Vaxign reverse vacc...

Genome-wide prediction of vaccine targets for human herpes simplex viruses using Vaxign reverse vacc...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3599071

Genome-wide prediction of vaccine targets for human herpes simplex viruses using Vaxign reverse vaccinology

About this item

Full title

Genome-wide prediction of vaccine targets for human herpes simplex viruses using Vaxign reverse vaccinology

Author / Creator

Publisher

England: BioMed Central

Journal title

BMC bioinformatics, 2013-03, Vol.14 Suppl 4 (Suppl 4), p.S2-S2, Article S2

Language

English

Formats

Publication information

Publisher

England: BioMed Central

More information

Scope and Contents

Contents

Herpes simplex virus (HSV) types 1 and 2 (HSV-1 and HSV-2) are the most common infectious agents of humans. No safe and effective HSV vaccines have been licensed. Reverse vaccinology is an emerging and revolutionary vaccine development strategy that starts with the prediction of vaccine targets by informatics analysis of genome sequences. Vaxign (http://www.violinet.org/vaxign) is the first web-based vaccine design program based on reverse vaccinology. In this study, we used Vaxign to analyze 52 herpesvirus genomes, including 3 HSV-1 genomes, one HSV-2 genome, 8 other human herpesvirus genomes, and 40 non-human herpesvirus genomes. The HSV-1 strain 17 genome that contains 77 proteins was used as the seed genome. The...

Alternative Titles

Full title

Genome-wide prediction of vaccine targets for human herpes simplex viruses using Vaxign reverse vaccinology

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3599071

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3599071

Other Identifiers

ISSN

1471-2105

E-ISSN

1471-2105

DOI

10.1186/1471-2105-14-S4-S2

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