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High-throughput sequencing insights into T-cell receptor repertoire diversity in aging
Decline in T-cell generation leading to T-cell receptor repertoire contraction is a cornerstone of immune system aging, and consequent disorders. High-throughput sequencing enables in-depth immune repertoire characterization, but blood samples are too small to capture its total diversity. New comput...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652363/ https://www.ncbi.nlm.nih.gov/pubmed/26582264 http://dx.doi.org/10.1186/s13073-015-0242-3 |
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author | Goronzy, Jörg J. Qi, Qian Olshen, Richard A. Weyand, Cornelia M. |
author_facet | Goronzy, Jörg J. Qi, Qian Olshen, Richard A. Weyand, Cornelia M. |
author_sort | Goronzy, Jörg J. |
collection | PubMed |
description | Decline in T-cell generation leading to T-cell receptor repertoire contraction is a cornerstone of immune system aging, and consequent disorders. High-throughput sequencing enables in-depth immune repertoire characterization, but blood samples are too small to capture its total diversity. New computational models could enable accurate estimation of this diversity. |
format | Online Article Text |
id | pubmed-4652363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46523632015-11-20 High-throughput sequencing insights into T-cell receptor repertoire diversity in aging Goronzy, Jörg J. Qi, Qian Olshen, Richard A. Weyand, Cornelia M. Genome Med Comment Decline in T-cell generation leading to T-cell receptor repertoire contraction is a cornerstone of immune system aging, and consequent disorders. High-throughput sequencing enables in-depth immune repertoire characterization, but blood samples are too small to capture its total diversity. New computational models could enable accurate estimation of this diversity. BioMed Central 2015-11-19 /pmc/articles/PMC4652363/ /pubmed/26582264 http://dx.doi.org/10.1186/s13073-015-0242-3 Text en © Goronzy et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Comment Goronzy, Jörg J. Qi, Qian Olshen, Richard A. Weyand, Cornelia M. High-throughput sequencing insights into T-cell receptor repertoire diversity in aging |
title | High-throughput sequencing insights into T-cell receptor repertoire diversity in aging |
title_full | High-throughput sequencing insights into T-cell receptor repertoire diversity in aging |
title_fullStr | High-throughput sequencing insights into T-cell receptor repertoire diversity in aging |
title_full_unstemmed | High-throughput sequencing insights into T-cell receptor repertoire diversity in aging |
title_short | High-throughput sequencing insights into T-cell receptor repertoire diversity in aging |
title_sort | high-throughput sequencing insights into t-cell receptor repertoire diversity in aging |
topic | Comment |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652363/ https://www.ncbi.nlm.nih.gov/pubmed/26582264 http://dx.doi.org/10.1186/s13073-015-0242-3 |
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