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Comparison of Target Enrichment Platforms for Circulating Tumor DNA Detection

Cancer-related mortality of solid tumors remains the major cause of death worldwide. Circulating tumor DNA (ctDNA) released from cancer cells harbors specific somatic mutations. Sequencing ctDNA opens opportunities to non-invasive population screening and lays foundations for personalized therapy. I...

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Autores principales: Lam, So Ngo, Zhou, Ying Chun, Chan, Yee Man, Foo, Ching Man, Lee, Po Yi, Mok, Wing Yeung, Wong, Wing Sum, Fung, Yan Yee, Wong, Kit Yee, Huang, Jun Yuan, Chow, Chun Kin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057974/
https://www.ncbi.nlm.nih.gov/pubmed/32139724
http://dx.doi.org/10.1038/s41598-020-60375-x
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author Lam, So Ngo
Zhou, Ying Chun
Chan, Yee Man
Foo, Ching Man
Lee, Po Yi
Mok, Wing Yeung
Wong, Wing Sum
Fung, Yan Yee
Wong, Kit Yee
Huang, Jun Yuan
Chow, Chun Kin
author_facet Lam, So Ngo
Zhou, Ying Chun
Chan, Yee Man
Foo, Ching Man
Lee, Po Yi
Mok, Wing Yeung
Wong, Wing Sum
Fung, Yan Yee
Wong, Kit Yee
Huang, Jun Yuan
Chow, Chun Kin
author_sort Lam, So Ngo
collection PubMed
description Cancer-related mortality of solid tumors remains the major cause of death worldwide. Circulating tumor DNA (ctDNA) released from cancer cells harbors specific somatic mutations. Sequencing ctDNA opens opportunities to non-invasive population screening and lays foundations for personalized therapy. In this study, two commercially available platforms, Roche’s Avenio ctDNA Expanded panel and QIAgen’s QIAseq Human Comprehensive Cancer  panel were compared for (1) panel coverage of clinically relevant variants; (2) target enrichment specificity and sequencing performance; (3) the sensitivity; (4) concordance and (5) sequencing coverage using the same human blood sample with ultra-deep next-generation sequencing. Our finding suggests that Avenio detected somatic mutations in common cancers in over 70% of patients while QIAseq covered nearly 90% with a higher average number of variants per patient (Avenio: 3; QIAseq: 8 variants per patient). Both panels demonstrated similar on-target rate and percentage of reads mapped. However, Avenio had more uniform sequencing coverage across regions with different GC content. Avenio had a higher sensitivity and concordance compared with QIAseq at the same sequencing depth. This study identifies a unique niche for the application of each of the panel and allows the scientific community to make an informed decision on the technologies to meet research or application needs.
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spelling pubmed-70579742020-03-12 Comparison of Target Enrichment Platforms for Circulating Tumor DNA Detection Lam, So Ngo Zhou, Ying Chun Chan, Yee Man Foo, Ching Man Lee, Po Yi Mok, Wing Yeung Wong, Wing Sum Fung, Yan Yee Wong, Kit Yee Huang, Jun Yuan Chow, Chun Kin Sci Rep Article Cancer-related mortality of solid tumors remains the major cause of death worldwide. Circulating tumor DNA (ctDNA) released from cancer cells harbors specific somatic mutations. Sequencing ctDNA opens opportunities to non-invasive population screening and lays foundations for personalized therapy. In this study, two commercially available platforms, Roche’s Avenio ctDNA Expanded panel and QIAgen’s QIAseq Human Comprehensive Cancer  panel were compared for (1) panel coverage of clinically relevant variants; (2) target enrichment specificity and sequencing performance; (3) the sensitivity; (4) concordance and (5) sequencing coverage using the same human blood sample with ultra-deep next-generation sequencing. Our finding suggests that Avenio detected somatic mutations in common cancers in over 70% of patients while QIAseq covered nearly 90% with a higher average number of variants per patient (Avenio: 3; QIAseq: 8 variants per patient). Both panels demonstrated similar on-target rate and percentage of reads mapped. However, Avenio had more uniform sequencing coverage across regions with different GC content. Avenio had a higher sensitivity and concordance compared with QIAseq at the same sequencing depth. This study identifies a unique niche for the application of each of the panel and allows the scientific community to make an informed decision on the technologies to meet research or application needs. Nature Publishing Group UK 2020-03-05 /pmc/articles/PMC7057974/ /pubmed/32139724 http://dx.doi.org/10.1038/s41598-020-60375-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lam, So Ngo
Zhou, Ying Chun
Chan, Yee Man
Foo, Ching Man
Lee, Po Yi
Mok, Wing Yeung
Wong, Wing Sum
Fung, Yan Yee
Wong, Kit Yee
Huang, Jun Yuan
Chow, Chun Kin
Comparison of Target Enrichment Platforms for Circulating Tumor DNA Detection
title Comparison of Target Enrichment Platforms for Circulating Tumor DNA Detection
title_full Comparison of Target Enrichment Platforms for Circulating Tumor DNA Detection
title_fullStr Comparison of Target Enrichment Platforms for Circulating Tumor DNA Detection
title_full_unstemmed Comparison of Target Enrichment Platforms for Circulating Tumor DNA Detection
title_short Comparison of Target Enrichment Platforms for Circulating Tumor DNA Detection
title_sort comparison of target enrichment platforms for circulating tumor dna detection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057974/
https://www.ncbi.nlm.nih.gov/pubmed/32139724
http://dx.doi.org/10.1038/s41598-020-60375-x
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