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Loeffler 4.0: Diagnostic Metagenomics

A new world of possibilities for “virus discovery” was opened up with high-throughput sequencing becoming available in the last decade. While scientifically metagenomic analysis was established before the start of the era of high-throughput sequencing, the availability of the first second-generation...

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Detalles Bibliográficos
Autores principales: Höper, Dirk, Wylezich, Claudia, Beer, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112322/
https://www.ncbi.nlm.nih.gov/pubmed/29029726
http://dx.doi.org/10.1016/bs.aivir.2017.08.001
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author Höper, Dirk
Wylezich, Claudia
Beer, Martin
author_facet Höper, Dirk
Wylezich, Claudia
Beer, Martin
author_sort Höper, Dirk
collection PubMed
description A new world of possibilities for “virus discovery” was opened up with high-throughput sequencing becoming available in the last decade. While scientifically metagenomic analysis was established before the start of the era of high-throughput sequencing, the availability of the first second-generation sequencers was the kick-off for diagnosticians to use sequencing for the detection of novel pathogens. Today, diagnostic metagenomics is becoming the standard procedure for the detection and genetic characterization of new viruses or novel virus variants. Here, we provide an overview about technical considerations of high-throughput sequencing-based diagnostic metagenomics together with selected examples of “virus discovery” for animal diseases or zoonoses and metagenomics for food safety or basic veterinary research.
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spelling pubmed-71123222020-04-02 Loeffler 4.0: Diagnostic Metagenomics Höper, Dirk Wylezich, Claudia Beer, Martin Adv Virus Res Article A new world of possibilities for “virus discovery” was opened up with high-throughput sequencing becoming available in the last decade. While scientifically metagenomic analysis was established before the start of the era of high-throughput sequencing, the availability of the first second-generation sequencers was the kick-off for diagnosticians to use sequencing for the detection of novel pathogens. Today, diagnostic metagenomics is becoming the standard procedure for the detection and genetic characterization of new viruses or novel virus variants. Here, we provide an overview about technical considerations of high-throughput sequencing-based diagnostic metagenomics together with selected examples of “virus discovery” for animal diseases or zoonoses and metagenomics for food safety or basic veterinary research. Elsevier Inc. 2017 2017-09-21 /pmc/articles/PMC7112322/ /pubmed/29029726 http://dx.doi.org/10.1016/bs.aivir.2017.08.001 Text en Copyright © 2017 Elsevier Inc. All rights reserved. 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
Höper, Dirk
Wylezich, Claudia
Beer, Martin
Loeffler 4.0: Diagnostic Metagenomics
title Loeffler 4.0: Diagnostic Metagenomics
title_full Loeffler 4.0: Diagnostic Metagenomics
title_fullStr Loeffler 4.0: Diagnostic Metagenomics
title_full_unstemmed Loeffler 4.0: Diagnostic Metagenomics
title_short Loeffler 4.0: Diagnostic Metagenomics
title_sort loeffler 4.0: diagnostic metagenomics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112322/
https://www.ncbi.nlm.nih.gov/pubmed/29029726
http://dx.doi.org/10.1016/bs.aivir.2017.08.001
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