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Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system
BACKGROUND: Current technologies in next-generation sequencing are offering high throughput reads at low costs, but still suffer from various sequencing errors. Although pyro- and ion semiconductor sequencing both have the advantage of delivering long and high quality reads, problems might occur whe...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822529/ https://www.ncbi.nlm.nih.gov/pubmed/29466940 http://dx.doi.org/10.1186/s12864-018-4544-x |
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author | Ivády, Gergely Madar, László Dzsudzsák, Erika Koczok, Katalin Kappelmayer, János Krulisova, Veronika Macek, Milan Horváth, Attila Balogh, István |
author_facet | Ivády, Gergely Madar, László Dzsudzsák, Erika Koczok, Katalin Kappelmayer, János Krulisova, Veronika Macek, Milan Horváth, Attila Balogh, István |
author_sort | Ivády, Gergely |
collection | PubMed |
description | BACKGROUND: Current technologies in next-generation sequencing are offering high throughput reads at low costs, but still suffer from various sequencing errors. Although pyro- and ion semiconductor sequencing both have the advantage of delivering long and high quality reads, problems might occur when sequencing homopolymer-containing regions, since the repeating identical bases are going to incorporate during the same synthesis cycle, which leads to uncertainty in base calling. The aim of this study was to evaluate the analytical performance of a pyrosequencing-based next-generation sequencing system in detecting homopolymer sequences using homopolymer-preintegrated plasmid constructs and human DNA samples originating from patients with cystic fibrosis. RESULTS: In the plasmid system average correct genotyping was 95.8% in 4-mers, 87.4% in 5-mers and 72.1% in 6-mers. Despite the experienced low genotyping accuracy in 5- and 6-mers, it was possible to generate amplicons with more than a 90% adequate detection rate in every homopolymer tract. When homopolymers in the CFTR gene were sequenced average accuracy was 89.3%, but varied in a wide range (52.2 – 99.1%). In all but one case, an optimal amplicon-sequencing primer combination could be identified. In that single case (7A tract in exon 14 (c.2046_2052)), none of the tested primer sets produced the required analytical performance. CONCLUSIONS: Our results show that pyrosequencing is the most reliable in case of 4-mers and as homopolymer length gradually increases, accuracy deteriorates. With careful primer selection, the NGS system was able to correctly genotype all but one of the homopolymers in the CFTR gene. In conclusion, we configured a plasmid test system that can be used to assess genotyping accuracy of NGS devices and developed an accurate NGS assay for the molecular diagnosis of CF using self-designed primers for amplification and sequencing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4544-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5822529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58225292018-02-26 Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system Ivády, Gergely Madar, László Dzsudzsák, Erika Koczok, Katalin Kappelmayer, János Krulisova, Veronika Macek, Milan Horváth, Attila Balogh, István BMC Genomics Research Article BACKGROUND: Current technologies in next-generation sequencing are offering high throughput reads at low costs, but still suffer from various sequencing errors. Although pyro- and ion semiconductor sequencing both have the advantage of delivering long and high quality reads, problems might occur when sequencing homopolymer-containing regions, since the repeating identical bases are going to incorporate during the same synthesis cycle, which leads to uncertainty in base calling. The aim of this study was to evaluate the analytical performance of a pyrosequencing-based next-generation sequencing system in detecting homopolymer sequences using homopolymer-preintegrated plasmid constructs and human DNA samples originating from patients with cystic fibrosis. RESULTS: In the plasmid system average correct genotyping was 95.8% in 4-mers, 87.4% in 5-mers and 72.1% in 6-mers. Despite the experienced low genotyping accuracy in 5- and 6-mers, it was possible to generate amplicons with more than a 90% adequate detection rate in every homopolymer tract. When homopolymers in the CFTR gene were sequenced average accuracy was 89.3%, but varied in a wide range (52.2 – 99.1%). In all but one case, an optimal amplicon-sequencing primer combination could be identified. In that single case (7A tract in exon 14 (c.2046_2052)), none of the tested primer sets produced the required analytical performance. CONCLUSIONS: Our results show that pyrosequencing is the most reliable in case of 4-mers and as homopolymer length gradually increases, accuracy deteriorates. With careful primer selection, the NGS system was able to correctly genotype all but one of the homopolymers in the CFTR gene. In conclusion, we configured a plasmid test system that can be used to assess genotyping accuracy of NGS devices and developed an accurate NGS assay for the molecular diagnosis of CF using self-designed primers for amplification and sequencing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4544-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-21 /pmc/articles/PMC5822529/ /pubmed/29466940 http://dx.doi.org/10.1186/s12864-018-4544-x Text en © The Author(s). 2018 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 | Research Article Ivády, Gergely Madar, László Dzsudzsák, Erika Koczok, Katalin Kappelmayer, János Krulisova, Veronika Macek, Milan Horváth, Attila Balogh, István Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system |
title | Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system |
title_full | Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system |
title_fullStr | Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system |
title_full_unstemmed | Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system |
title_short | Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system |
title_sort | analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822529/ https://www.ncbi.nlm.nih.gov/pubmed/29466940 http://dx.doi.org/10.1186/s12864-018-4544-x |
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