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Virome genomics: a tool for defining the human virome

High throughput, deep sequencing assays are powerful tools for gaining insights into virus–host interactions. Sequencing assays can discover novel viruses and describe the genomes of novel and known viruses. Genomic information can predict viral proteins that can be characterized, describe important...

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Detalles Bibliográficos
Autores principales: Wylie, Kristine M, Weinstock, George M, Storch, Gregory A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Ltd. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3755052/
https://www.ncbi.nlm.nih.gov/pubmed/23706900
http://dx.doi.org/10.1016/j.mib.2013.04.006
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author Wylie, Kristine M
Weinstock, George M
Storch, Gregory A
author_facet Wylie, Kristine M
Weinstock, George M
Storch, Gregory A
author_sort Wylie, Kristine M
collection PubMed
description High throughput, deep sequencing assays are powerful tools for gaining insights into virus–host interactions. Sequencing assays can discover novel viruses and describe the genomes of novel and known viruses. Genomic information can predict viral proteins that can be characterized, describe important genes in the host that control infections, and evaluate gene expression of viruses and hosts during infection. Sequencing can also describe variation and evolution of viruses during replication and transmission. This review recounts some of the major advances in the studies of virus–host interactions from the last two years, and discusses the uses of sequencing technologies relating to these studies.
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spelling pubmed-37550522014-08-01 Virome genomics: a tool for defining the human virome Wylie, Kristine M Weinstock, George M Storch, Gregory A Curr Opin Microbiol Article High throughput, deep sequencing assays are powerful tools for gaining insights into virus–host interactions. Sequencing assays can discover novel viruses and describe the genomes of novel and known viruses. Genomic information can predict viral proteins that can be characterized, describe important genes in the host that control infections, and evaluate gene expression of viruses and hosts during infection. Sequencing can also describe variation and evolution of viruses during replication and transmission. This review recounts some of the major advances in the studies of virus–host interactions from the last two years, and discusses the uses of sequencing technologies relating to these studies. The Authors. Published by Elsevier Ltd. 2013-08 2013-05-23 /pmc/articles/PMC3755052/ /pubmed/23706900 http://dx.doi.org/10.1016/j.mib.2013.04.006 Text en © 2013 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Wylie, Kristine M
Weinstock, George M
Storch, Gregory A
Virome genomics: a tool for defining the human virome
title Virome genomics: a tool for defining the human virome
title_full Virome genomics: a tool for defining the human virome
title_fullStr Virome genomics: a tool for defining the human virome
title_full_unstemmed Virome genomics: a tool for defining the human virome
title_short Virome genomics: a tool for defining the human virome
title_sort virome genomics: a tool for defining the human virome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3755052/
https://www.ncbi.nlm.nih.gov/pubmed/23706900
http://dx.doi.org/10.1016/j.mib.2013.04.006
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