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Emergent biomarker derived from next-generation sequencing to identify pain patients requiring uncommonly high opioid doses
Next-generation sequencing (NGS) provides unrestricted access to the genome, but it produces ‘big data’ exceeding in amount and complexity the classical analytical approaches. We introduce a bioinformatics-based classifying biomarker that uses emergent properties in genetics to separate pain patient...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637232/ https://www.ncbi.nlm.nih.gov/pubmed/27139154 http://dx.doi.org/10.1038/tpj.2016.28 |
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author | Kringel, D Ultsch, A Zimmermann, M Jansen, J-P Ilias, W Freynhagen, R Griessinger, N Kopf, A Stein, C Doehring, A Resch, E Lötsch, J |
author_facet | Kringel, D Ultsch, A Zimmermann, M Jansen, J-P Ilias, W Freynhagen, R Griessinger, N Kopf, A Stein, C Doehring, A Resch, E Lötsch, J |
author_sort | Kringel, D |
collection | PubMed |
description | Next-generation sequencing (NGS) provides unrestricted access to the genome, but it produces ‘big data’ exceeding in amount and complexity the classical analytical approaches. We introduce a bioinformatics-based classifying biomarker that uses emergent properties in genetics to separate pain patients requiring extremely high opioid doses from controls. Following precisely calculated selection of the 34 most informative markers in the OPRM1, OPRK1, OPRD1 and SIGMAR1 genes, pattern of genotypes belonging to either patient group could be derived using a k-nearest neighbor (kNN) classifier that provided a diagnostic accuracy of 80.6±4%. This outperformed alternative classifiers such as reportedly functional opioid receptor gene variants or complex biomarkers obtained via multiple regression or decision tree analysis. The accumulation of several genetic variants with only minor functional influences may result in a qualitative consequence affecting complex phenotypes, pointing at emergent properties in genetics. |
format | Online Article Text |
id | pubmed-5637232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-56372322017-12-02 Emergent biomarker derived from next-generation sequencing to identify pain patients requiring uncommonly high opioid doses Kringel, D Ultsch, A Zimmermann, M Jansen, J-P Ilias, W Freynhagen, R Griessinger, N Kopf, A Stein, C Doehring, A Resch, E Lötsch, J Pharmacogenomics J Original Article Next-generation sequencing (NGS) provides unrestricted access to the genome, but it produces ‘big data’ exceeding in amount and complexity the classical analytical approaches. We introduce a bioinformatics-based classifying biomarker that uses emergent properties in genetics to separate pain patients requiring extremely high opioid doses from controls. Following precisely calculated selection of the 34 most informative markers in the OPRM1, OPRK1, OPRD1 and SIGMAR1 genes, pattern of genotypes belonging to either patient group could be derived using a k-nearest neighbor (kNN) classifier that provided a diagnostic accuracy of 80.6±4%. This outperformed alternative classifiers such as reportedly functional opioid receptor gene variants or complex biomarkers obtained via multiple regression or decision tree analysis. The accumulation of several genetic variants with only minor functional influences may result in a qualitative consequence affecting complex phenotypes, pointing at emergent properties in genetics. Nature Publishing Group 2017-10 2016-05-03 /pmc/articles/PMC5637232/ /pubmed/27139154 http://dx.doi.org/10.1038/tpj.2016.28 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Original Article Kringel, D Ultsch, A Zimmermann, M Jansen, J-P Ilias, W Freynhagen, R Griessinger, N Kopf, A Stein, C Doehring, A Resch, E Lötsch, J Emergent biomarker derived from next-generation sequencing to identify pain patients requiring uncommonly high opioid doses |
title | Emergent biomarker derived from next-generation sequencing to identify pain patients requiring uncommonly high opioid doses |
title_full | Emergent biomarker derived from next-generation sequencing to identify pain patients requiring uncommonly high opioid doses |
title_fullStr | Emergent biomarker derived from next-generation sequencing to identify pain patients requiring uncommonly high opioid doses |
title_full_unstemmed | Emergent biomarker derived from next-generation sequencing to identify pain patients requiring uncommonly high opioid doses |
title_short | Emergent biomarker derived from next-generation sequencing to identify pain patients requiring uncommonly high opioid doses |
title_sort | emergent biomarker derived from next-generation sequencing to identify pain patients requiring uncommonly high opioid doses |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637232/ https://www.ncbi.nlm.nih.gov/pubmed/27139154 http://dx.doi.org/10.1038/tpj.2016.28 |
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