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Current status of use of high throughput nucleotide sequencing in rheumatology

OBJECTIVE: Here, we assess the usage of high throughput sequencing (HTS) in rheumatic research and the availability of public HTS data of rheumatic samples. METHODS: We performed a semiautomated literature review on PubMed, consisting of an R-script and manual curation as well as a manual search on...

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Autores principales: Boegel, Sebastian, Castle, John C, Schwarting, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789458/
https://www.ncbi.nlm.nih.gov/pubmed/33408124
http://dx.doi.org/10.1136/rmdopen-2020-001324
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author Boegel, Sebastian
Castle, John C
Schwarting, Andreas
author_facet Boegel, Sebastian
Castle, John C
Schwarting, Andreas
author_sort Boegel, Sebastian
collection PubMed
description OBJECTIVE: Here, we assess the usage of high throughput sequencing (HTS) in rheumatic research and the availability of public HTS data of rheumatic samples. METHODS: We performed a semiautomated literature review on PubMed, consisting of an R-script and manual curation as well as a manual search on the Sequence Read Archive for public available HTS data. RESULTS: Of the 699 identified articles, rheumatoid arthritis (n=182 publications, 26%), systemic lupus erythematous (n=161, 23%) and osteoarthritis (n=152, 22%) are among the rheumatic diseases with the most reported use of HTS assays. The most represented assay is RNA-Seq (n=457, 65%) for the identification of biomarkers in blood or synovial tissue. We also find, that the quality of accompanying clinical characterisation of the sequenced patients differs dramatically and we propose a minimal set of clinical data necessary to accompany rheumatological-relevant HTS data. CONCLUSION: HTS allows the analysis of a broad spectrum of molecular features in many samples at the same time. It offers enormous potential in novel personalised diagnosis and treatment strategies for patients with rheumatic diseases. Being established in cancer research and in the field of Mendelian diseases, rheumatic diseases are about to become the third disease domain for HTS, especially the RNA-Seq assay. However, we need to start a discussion about reporting of clinical characterisation accompany rheumatological-relevant HTS data to make clinical meaningful use of this data.
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spelling pubmed-77894582021-01-21 Current status of use of high throughput nucleotide sequencing in rheumatology Boegel, Sebastian Castle, John C Schwarting, Andreas RMD Open Autoimmunity OBJECTIVE: Here, we assess the usage of high throughput sequencing (HTS) in rheumatic research and the availability of public HTS data of rheumatic samples. METHODS: We performed a semiautomated literature review on PubMed, consisting of an R-script and manual curation as well as a manual search on the Sequence Read Archive for public available HTS data. RESULTS: Of the 699 identified articles, rheumatoid arthritis (n=182 publications, 26%), systemic lupus erythematous (n=161, 23%) and osteoarthritis (n=152, 22%) are among the rheumatic diseases with the most reported use of HTS assays. The most represented assay is RNA-Seq (n=457, 65%) for the identification of biomarkers in blood or synovial tissue. We also find, that the quality of accompanying clinical characterisation of the sequenced patients differs dramatically and we propose a minimal set of clinical data necessary to accompany rheumatological-relevant HTS data. CONCLUSION: HTS allows the analysis of a broad spectrum of molecular features in many samples at the same time. It offers enormous potential in novel personalised diagnosis and treatment strategies for patients with rheumatic diseases. Being established in cancer research and in the field of Mendelian diseases, rheumatic diseases are about to become the third disease domain for HTS, especially the RNA-Seq assay. However, we need to start a discussion about reporting of clinical characterisation accompany rheumatological-relevant HTS data to make clinical meaningful use of this data. BMJ Publishing Group 2021-01-06 /pmc/articles/PMC7789458/ /pubmed/33408124 http://dx.doi.org/10.1136/rmdopen-2020-001324 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Autoimmunity
Boegel, Sebastian
Castle, John C
Schwarting, Andreas
Current status of use of high throughput nucleotide sequencing in rheumatology
title Current status of use of high throughput nucleotide sequencing in rheumatology
title_full Current status of use of high throughput nucleotide sequencing in rheumatology
title_fullStr Current status of use of high throughput nucleotide sequencing in rheumatology
title_full_unstemmed Current status of use of high throughput nucleotide sequencing in rheumatology
title_short Current status of use of high throughput nucleotide sequencing in rheumatology
title_sort current status of use of high throughput nucleotide sequencing in rheumatology
topic Autoimmunity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789458/
https://www.ncbi.nlm.nih.gov/pubmed/33408124
http://dx.doi.org/10.1136/rmdopen-2020-001324
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