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Next-Generation Sequencing: From Understanding Biology to Personalized Medicine

Within just a few years, the new methods for high-throughput next-generation sequencing have generated completely novel insights into the heritability and pathophysiology of human disease. In this review, we wish to highlight the benefits of the current state-of-the-art sequencing technologies for g...

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Detalles Bibliográficos
Autores principales: Frese, Karen S., Katus, Hugo A., Meder, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009863/
https://www.ncbi.nlm.nih.gov/pubmed/24832667
http://dx.doi.org/10.3390/biology2010378
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author Frese, Karen S.
Katus, Hugo A.
Meder, Benjamin
author_facet Frese, Karen S.
Katus, Hugo A.
Meder, Benjamin
author_sort Frese, Karen S.
collection PubMed
description Within just a few years, the new methods for high-throughput next-generation sequencing have generated completely novel insights into the heritability and pathophysiology of human disease. In this review, we wish to highlight the benefits of the current state-of-the-art sequencing technologies for genetic and epigenetic research. We illustrate how these technologies help to constantly improve our understanding of genetic mechanisms in biological systems and summarize the progress made so far. This can be exemplified by the case of heritable heart muscle diseases, so-called cardiomyopathies. Here, next-generation sequencing is able to identify novel disease genes, and first clinical applications demonstrate the successful translation of this technology into personalized patient care.
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spelling pubmed-40098632014-05-07 Next-Generation Sequencing: From Understanding Biology to Personalized Medicine Frese, Karen S. Katus, Hugo A. Meder, Benjamin Biology (Basel) Review Within just a few years, the new methods for high-throughput next-generation sequencing have generated completely novel insights into the heritability and pathophysiology of human disease. In this review, we wish to highlight the benefits of the current state-of-the-art sequencing technologies for genetic and epigenetic research. We illustrate how these technologies help to constantly improve our understanding of genetic mechanisms in biological systems and summarize the progress made so far. This can be exemplified by the case of heritable heart muscle diseases, so-called cardiomyopathies. Here, next-generation sequencing is able to identify novel disease genes, and first clinical applications demonstrate the successful translation of this technology into personalized patient care. MDPI 2013-03-01 /pmc/articles/PMC4009863/ /pubmed/24832667 http://dx.doi.org/10.3390/biology2010378 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Frese, Karen S.
Katus, Hugo A.
Meder, Benjamin
Next-Generation Sequencing: From Understanding Biology to Personalized Medicine
title Next-Generation Sequencing: From Understanding Biology to Personalized Medicine
title_full Next-Generation Sequencing: From Understanding Biology to Personalized Medicine
title_fullStr Next-Generation Sequencing: From Understanding Biology to Personalized Medicine
title_full_unstemmed Next-Generation Sequencing: From Understanding Biology to Personalized Medicine
title_short Next-Generation Sequencing: From Understanding Biology to Personalized Medicine
title_sort next-generation sequencing: from understanding biology to personalized medicine
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009863/
https://www.ncbi.nlm.nih.gov/pubmed/24832667
http://dx.doi.org/10.3390/biology2010378
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