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What is next generation sequencing?
Next generation sequencing (NGS), massively parallel or deep sequencing are related terms that describe a DNA sequencing technology which has revolutionised genomic research. Using NGS an entire human genome can be sequenced within a single day. In contrast, the previous Sanger sequencing technology...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841808/ https://www.ncbi.nlm.nih.gov/pubmed/23986538 http://dx.doi.org/10.1136/archdischild-2013-304340 |
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author | Behjati, Sam Tarpey, Patrick S |
author_facet | Behjati, Sam Tarpey, Patrick S |
author_sort | Behjati, Sam |
collection | PubMed |
description | Next generation sequencing (NGS), massively parallel or deep sequencing are related terms that describe a DNA sequencing technology which has revolutionised genomic research. Using NGS an entire human genome can be sequenced within a single day. In contrast, the previous Sanger sequencing technology, used to decipher the human genome, required over a decade to deliver the final draft. Although in genome research NGS has mostly superseded conventional Sanger sequencing, it has not yet translated into routine clinical practice. The aim of this article is to review the potential applications of NGS in paediatrics. |
format | Online Article Text |
id | pubmed-3841808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-38418082013-11-29 What is next generation sequencing? Behjati, Sam Tarpey, Patrick S Arch Dis Child Educ Pract Ed Research in Practice Next generation sequencing (NGS), massively parallel or deep sequencing are related terms that describe a DNA sequencing technology which has revolutionised genomic research. Using NGS an entire human genome can be sequenced within a single day. In contrast, the previous Sanger sequencing technology, used to decipher the human genome, required over a decade to deliver the final draft. Although in genome research NGS has mostly superseded conventional Sanger sequencing, it has not yet translated into routine clinical practice. The aim of this article is to review the potential applications of NGS in paediatrics. BMJ Publishing Group 2013-12 2013-08-28 /pmc/articles/PMC3841808/ /pubmed/23986538 http://dx.doi.org/10.1136/archdischild-2013-304340 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Research in Practice Behjati, Sam Tarpey, Patrick S What is next generation sequencing? |
title | What is next generation sequencing? |
title_full | What is next generation sequencing? |
title_fullStr | What is next generation sequencing? |
title_full_unstemmed | What is next generation sequencing? |
title_short | What is next generation sequencing? |
title_sort | what is next generation sequencing? |
topic | Research in Practice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841808/ https://www.ncbi.nlm.nih.gov/pubmed/23986538 http://dx.doi.org/10.1136/archdischild-2013-304340 |
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