Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ivády, Gergely, Madar, László, Dzsudzsák, Erika, Koczok, Katalin, Kappelmayer, János, Krulisova, Veronika, Macek, Milan, Horváth, Attila, Balogh, István
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
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
_version_ 1783301704382414848
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
work_keys_str_mv AT ivadygergely analyticalparametersandvalidationofhomopolymerdetectioninapyrosequencingbasednextgenerationsequencingsystem
AT madarlaszlo analyticalparametersandvalidationofhomopolymerdetectioninapyrosequencingbasednextgenerationsequencingsystem
AT dzsudzsakerika analyticalparametersandvalidationofhomopolymerdetectioninapyrosequencingbasednextgenerationsequencingsystem
AT koczokkatalin analyticalparametersandvalidationofhomopolymerdetectioninapyrosequencingbasednextgenerationsequencingsystem
AT kappelmayerjanos analyticalparametersandvalidationofhomopolymerdetectioninapyrosequencingbasednextgenerationsequencingsystem
AT krulisovaveronika analyticalparametersandvalidationofhomopolymerdetectioninapyrosequencingbasednextgenerationsequencingsystem
AT macekmilan analyticalparametersandvalidationofhomopolymerdetectioninapyrosequencingbasednextgenerationsequencingsystem
AT horvathattila analyticalparametersandvalidationofhomopolymerdetectioninapyrosequencingbasednextgenerationsequencingsystem
AT baloghistvan analyticalparametersandvalidationofhomopolymerdetectioninapyrosequencingbasednextgenerationsequencingsystem