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Comparison of somatic variant detection algorithms using Ion Torrent targeted deep sequencing data

BACKGROUND: The application of next-generation sequencing in cancer has revealed the genomic landscape of many tumour types and is nowadays routinely used in research and clinical settings. Multiple algorithms have been developed to detect somatic variation from sequencing data using either paired t...

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Autores principales: Wang, Qing, Kotoula, Vassiliki, Hsu, Pei-Chen, Papadopoulou, Kyriaki, Ho, Joshua W. K., Fountzilas, George, Giannoulatou, Eleni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929331/
https://www.ncbi.nlm.nih.gov/pubmed/31874647
http://dx.doi.org/10.1186/s12920-019-0636-y
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author Wang, Qing
Kotoula, Vassiliki
Hsu, Pei-Chen
Papadopoulou, Kyriaki
Ho, Joshua W. K.
Fountzilas, George
Giannoulatou, Eleni
author_facet Wang, Qing
Kotoula, Vassiliki
Hsu, Pei-Chen
Papadopoulou, Kyriaki
Ho, Joshua W. K.
Fountzilas, George
Giannoulatou, Eleni
author_sort Wang, Qing
collection PubMed
description BACKGROUND: The application of next-generation sequencing in cancer has revealed the genomic landscape of many tumour types and is nowadays routinely used in research and clinical settings. Multiple algorithms have been developed to detect somatic variation from sequencing data using either paired tumour-blood or tumour-only samples. Most of these methods have been developed and evaluated for the identification of somatic variation using Illumina sequencing datasets of moderate coverage. However, a comprehensive evaluation of somatic variant detection algorithms on Ion Torrent targeted deep sequencing data has not been performed. METHODS: We have applied three somatic detection algorithms, Torrent Variant Caller, MuTect2 and VarScan2, on a large cohort of ovarian cancer patients comprising of 208 paired tumour-blood samples and 253 tumour-only samples sequenced deeply on Ion Torrent Proton platform across 330 amplicons. Subsequently, the concordance and performance of the three somatic variant callers were assessed. RESULTS: We have observed low concordance across the algorithms with only 0.5% of SNV and 0.02% of INDEL calls in common across all three methods. The intersection of all methods showed better performance when assessed using correlation with known mutational signatures, overlap with COSMIC variation and by examining the variant characteristics. The Torrent Variant Caller also performed well with the advantage of not eliminating a high number of variants that could lead to high type II error. CONCLUSIONS: Our results suggest that caution should be taken when applying state-of-the-art somatic variant algorithms to Ion Torrent targeted deep sequencing data. Better quality control procedures and strategies that combine results from multiple methods should ensure that higher accuracy is achieved. This is essential to ensure that results from bioinformatics pipelines using Ion Torrent deep sequencing can be robustly applied in cancer research and in the clinic.
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spelling pubmed-69293312019-12-30 Comparison of somatic variant detection algorithms using Ion Torrent targeted deep sequencing data Wang, Qing Kotoula, Vassiliki Hsu, Pei-Chen Papadopoulou, Kyriaki Ho, Joshua W. K. Fountzilas, George Giannoulatou, Eleni BMC Med Genomics Research BACKGROUND: The application of next-generation sequencing in cancer has revealed the genomic landscape of many tumour types and is nowadays routinely used in research and clinical settings. Multiple algorithms have been developed to detect somatic variation from sequencing data using either paired tumour-blood or tumour-only samples. Most of these methods have been developed and evaluated for the identification of somatic variation using Illumina sequencing datasets of moderate coverage. However, a comprehensive evaluation of somatic variant detection algorithms on Ion Torrent targeted deep sequencing data has not been performed. METHODS: We have applied three somatic detection algorithms, Torrent Variant Caller, MuTect2 and VarScan2, on a large cohort of ovarian cancer patients comprising of 208 paired tumour-blood samples and 253 tumour-only samples sequenced deeply on Ion Torrent Proton platform across 330 amplicons. Subsequently, the concordance and performance of the three somatic variant callers were assessed. RESULTS: We have observed low concordance across the algorithms with only 0.5% of SNV and 0.02% of INDEL calls in common across all three methods. The intersection of all methods showed better performance when assessed using correlation with known mutational signatures, overlap with COSMIC variation and by examining the variant characteristics. The Torrent Variant Caller also performed well with the advantage of not eliminating a high number of variants that could lead to high type II error. CONCLUSIONS: Our results suggest that caution should be taken when applying state-of-the-art somatic variant algorithms to Ion Torrent targeted deep sequencing data. Better quality control procedures and strategies that combine results from multiple methods should ensure that higher accuracy is achieved. This is essential to ensure that results from bioinformatics pipelines using Ion Torrent deep sequencing can be robustly applied in cancer research and in the clinic. BioMed Central 2019-12-24 /pmc/articles/PMC6929331/ /pubmed/31874647 http://dx.doi.org/10.1186/s12920-019-0636-y Text en © The Author(s). 2019 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
Wang, Qing
Kotoula, Vassiliki
Hsu, Pei-Chen
Papadopoulou, Kyriaki
Ho, Joshua W. K.
Fountzilas, George
Giannoulatou, Eleni
Comparison of somatic variant detection algorithms using Ion Torrent targeted deep sequencing data
title Comparison of somatic variant detection algorithms using Ion Torrent targeted deep sequencing data
title_full Comparison of somatic variant detection algorithms using Ion Torrent targeted deep sequencing data
title_fullStr Comparison of somatic variant detection algorithms using Ion Torrent targeted deep sequencing data
title_full_unstemmed Comparison of somatic variant detection algorithms using Ion Torrent targeted deep sequencing data
title_short Comparison of somatic variant detection algorithms using Ion Torrent targeted deep sequencing data
title_sort comparison of somatic variant detection algorithms using ion torrent targeted deep sequencing data
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929331/
https://www.ncbi.nlm.nih.gov/pubmed/31874647
http://dx.doi.org/10.1186/s12920-019-0636-y
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