Cargando…
Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform
BACKGROUND: ‘Next-generation’ (NGS) sequencing has wide application in medical genetics, including the detection of somatic variation in cancer. The Ion Torrent-based (IONT) platform is among NGS technologies employed in clinical, research and diagnostic settings. However, identifying mutations from...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753459/ https://www.ncbi.nlm.nih.gov/pubmed/29301485 http://dx.doi.org/10.1186/s12859-017-1991-3 |
_version_ | 1783290274056765440 |
---|---|
author | Deshpande, Aditya Lang, Wenhua McDowell, Tina Sivakumar, Smruthy Zhang, Jiexin Wang, Jing San Lucas, F. Anthony Fowler, Jerry Kadara, Humam Scheet, Paul |
author_facet | Deshpande, Aditya Lang, Wenhua McDowell, Tina Sivakumar, Smruthy Zhang, Jiexin Wang, Jing San Lucas, F. Anthony Fowler, Jerry Kadara, Humam Scheet, Paul |
author_sort | Deshpande, Aditya |
collection | PubMed |
description | BACKGROUND: ‘Next-generation’ (NGS) sequencing has wide application in medical genetics, including the detection of somatic variation in cancer. The Ion Torrent-based (IONT) platform is among NGS technologies employed in clinical, research and diagnostic settings. However, identifying mutations from IONT deep sequencing with high confidence has remained a challenge. We compared various computational variant-calling methods to derive a variant identification pipeline that may improve the molecular diagnostic and research utility of IONT. RESULTS: Using IONT, we surveyed variants from the 409-gene Comprehensive Cancer Panel in whole-section tumors, intra-tumoral biopsies and matched normal samples obtained from frozen tissues and blood from four early-stage non-small cell lung cancer (NSCLC) patients. We used MuTect, Varscan2, IONT’s proprietary Ion Reporter, and a simple subtraction we called “Poor Man’s Caller.” Together these produced calls at 637 loci across all samples. Visual validation of 434 called variants was performed, and performance of the methods assessed individually and in combination. Of the subset of inspected putative variant calls (n=223) in genomic regions that were not intronic or intergenic, 68 variants (30%) were deemed valid after visual inspection. Among the individual methods, the Ion Reporter method offered perhaps the most reasonable tradeoffs. Ion Reporter captured 83% of all discovered variants; 50% of its variants were visually validated. Aggregating results from multiple packages offered varied improvements in performance. CONCLUSIONS: Overall, Ion Reporter offered the most attractive performance among the individual callers. This study suggests combined strategies to maximize sensitivity and positive predictive value in variant calling using IONT deep sequencing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1991-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5753459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57534592018-01-05 Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform Deshpande, Aditya Lang, Wenhua McDowell, Tina Sivakumar, Smruthy Zhang, Jiexin Wang, Jing San Lucas, F. Anthony Fowler, Jerry Kadara, Humam Scheet, Paul BMC Bioinformatics Methodology Article BACKGROUND: ‘Next-generation’ (NGS) sequencing has wide application in medical genetics, including the detection of somatic variation in cancer. The Ion Torrent-based (IONT) platform is among NGS technologies employed in clinical, research and diagnostic settings. However, identifying mutations from IONT deep sequencing with high confidence has remained a challenge. We compared various computational variant-calling methods to derive a variant identification pipeline that may improve the molecular diagnostic and research utility of IONT. RESULTS: Using IONT, we surveyed variants from the 409-gene Comprehensive Cancer Panel in whole-section tumors, intra-tumoral biopsies and matched normal samples obtained from frozen tissues and blood from four early-stage non-small cell lung cancer (NSCLC) patients. We used MuTect, Varscan2, IONT’s proprietary Ion Reporter, and a simple subtraction we called “Poor Man’s Caller.” Together these produced calls at 637 loci across all samples. Visual validation of 434 called variants was performed, and performance of the methods assessed individually and in combination. Of the subset of inspected putative variant calls (n=223) in genomic regions that were not intronic or intergenic, 68 variants (30%) were deemed valid after visual inspection. Among the individual methods, the Ion Reporter method offered perhaps the most reasonable tradeoffs. Ion Reporter captured 83% of all discovered variants; 50% of its variants were visually validated. Aggregating results from multiple packages offered varied improvements in performance. CONCLUSIONS: Overall, Ion Reporter offered the most attractive performance among the individual callers. This study suggests combined strategies to maximize sensitivity and positive predictive value in variant calling using IONT deep sequencing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1991-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-04 /pmc/articles/PMC5753459/ /pubmed/29301485 http://dx.doi.org/10.1186/s12859-017-1991-3 Text en © The Author(s) 2017 Open Access This 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 | Methodology Article Deshpande, Aditya Lang, Wenhua McDowell, Tina Sivakumar, Smruthy Zhang, Jiexin Wang, Jing San Lucas, F. Anthony Fowler, Jerry Kadara, Humam Scheet, Paul Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform |
title | Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform |
title_full | Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform |
title_fullStr | Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform |
title_full_unstemmed | Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform |
title_short | Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform |
title_sort | strategies for identification of somatic variants using the ion torrent deep targeted sequencing platform |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753459/ https://www.ncbi.nlm.nih.gov/pubmed/29301485 http://dx.doi.org/10.1186/s12859-017-1991-3 |
work_keys_str_mv | AT deshpandeaditya strategiesforidentificationofsomaticvariantsusingtheiontorrentdeeptargetedsequencingplatform AT langwenhua strategiesforidentificationofsomaticvariantsusingtheiontorrentdeeptargetedsequencingplatform AT mcdowelltina strategiesforidentificationofsomaticvariantsusingtheiontorrentdeeptargetedsequencingplatform AT sivakumarsmruthy strategiesforidentificationofsomaticvariantsusingtheiontorrentdeeptargetedsequencingplatform AT zhangjiexin strategiesforidentificationofsomaticvariantsusingtheiontorrentdeeptargetedsequencingplatform AT wangjing strategiesforidentificationofsomaticvariantsusingtheiontorrentdeeptargetedsequencingplatform AT sanlucasfanthony strategiesforidentificationofsomaticvariantsusingtheiontorrentdeeptargetedsequencingplatform AT fowlerjerry strategiesforidentificationofsomaticvariantsusingtheiontorrentdeeptargetedsequencingplatform AT kadarahumam strategiesforidentificationofsomaticvariantsusingtheiontorrentdeeptargetedsequencingplatform AT scheetpaul strategiesforidentificationofsomaticvariantsusingtheiontorrentdeeptargetedsequencingplatform |