Technical and implementation issues in using next-generation sequencing of cancers in clinical practice.

Next-generation sequencing (NGS) of cancer genomes promises to revolutionise oncology, with the ability to design and use targeted drugs, to predict outcome and response, and to classify tumours. It is continually becoming cheaper, faster and more reliable, with the capability to identify rare yet c...

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Main Authors: Ulahannan, D, Kovac, M, Mulholland, P, Cazier, J, Tomlinson, I
Format: Journal article
Language:English
Published: 2013
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author Ulahannan, D
Kovac, M
Mulholland, P
Cazier, J
Tomlinson, I
author_facet Ulahannan, D
Kovac, M
Mulholland, P
Cazier, J
Tomlinson, I
author_sort Ulahannan, D
collection OXFORD
description Next-generation sequencing (NGS) of cancer genomes promises to revolutionise oncology, with the ability to design and use targeted drugs, to predict outcome and response, and to classify tumours. It is continually becoming cheaper, faster and more reliable, with the capability to identify rare yet clinically important somatic mutations. Technical challenges include sequencing samples of low quality and/or quantity, reliable identification of structural and copy number variation, and assessment of intratumour heterogeneity. Once these problems are overcome, the use of the data to guide clinical decision making is not straightforward, and there is a risk of premature use of molecular changes to guide patient management in the absence of supporting evidence. Paradoxically, NGS may simply move the bottleneck of personalised medicine from data acquisition to the identification of reliable biomarkers. Standardised cancer NGS data collection on an international scale would be a significant step towards optimising patient care.
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spelling oxford-uuid:d484fa0e-5992-4813-be21-ecc64a158ba92022-03-27T08:19:08ZTechnical and implementation issues in using next-generation sequencing of cancers in clinical practice.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:d484fa0e-5992-4813-be21-ecc64a158ba9EnglishSymplectic Elements at Oxford2013Ulahannan, DKovac, MMulholland, PCazier, JTomlinson, INext-generation sequencing (NGS) of cancer genomes promises to revolutionise oncology, with the ability to design and use targeted drugs, to predict outcome and response, and to classify tumours. It is continually becoming cheaper, faster and more reliable, with the capability to identify rare yet clinically important somatic mutations. Technical challenges include sequencing samples of low quality and/or quantity, reliable identification of structural and copy number variation, and assessment of intratumour heterogeneity. Once these problems are overcome, the use of the data to guide clinical decision making is not straightforward, and there is a risk of premature use of molecular changes to guide patient management in the absence of supporting evidence. Paradoxically, NGS may simply move the bottleneck of personalised medicine from data acquisition to the identification of reliable biomarkers. Standardised cancer NGS data collection on an international scale would be a significant step towards optimising patient care.
spellingShingle Ulahannan, D
Kovac, M
Mulholland, P
Cazier, J
Tomlinson, I
Technical and implementation issues in using next-generation sequencing of cancers in clinical practice.
title Technical and implementation issues in using next-generation sequencing of cancers in clinical practice.
title_full Technical and implementation issues in using next-generation sequencing of cancers in clinical practice.
title_fullStr Technical and implementation issues in using next-generation sequencing of cancers in clinical practice.
title_full_unstemmed Technical and implementation issues in using next-generation sequencing of cancers in clinical practice.
title_short Technical and implementation issues in using next-generation sequencing of cancers in clinical practice.
title_sort technical and implementation issues in using next generation sequencing of cancers in clinical practice
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