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Single-copy detection of somatic variants from solid and liquid biopsy

Accurate detection of somatic variants, against a background of wild-type molecules, is essential for clinical decision making in oncology. Existing approaches, such as allele-specific real-time PCR, are typically limited to a single target gene and lack sensitivity. Alternatively, next-generation s...

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Autores principales: Silva, Ana-Luisa, Powalowska, Paulina Klaudyna, Stolarek, Magdalena, Gray, Eleanor Ruth, Palmer, Rebecca Natalie, Herman, Bram, Frayling, Cameron Alexander, Balmforth, Barnaby William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966381/
https://www.ncbi.nlm.nih.gov/pubmed/33727644
http://dx.doi.org/10.1038/s41598-021-85545-3
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author Silva, Ana-Luisa
Powalowska, Paulina Klaudyna
Stolarek, Magdalena
Gray, Eleanor Ruth
Palmer, Rebecca Natalie
Herman, Bram
Frayling, Cameron Alexander
Balmforth, Barnaby William
author_facet Silva, Ana-Luisa
Powalowska, Paulina Klaudyna
Stolarek, Magdalena
Gray, Eleanor Ruth
Palmer, Rebecca Natalie
Herman, Bram
Frayling, Cameron Alexander
Balmforth, Barnaby William
author_sort Silva, Ana-Luisa
collection PubMed
description Accurate detection of somatic variants, against a background of wild-type molecules, is essential for clinical decision making in oncology. Existing approaches, such as allele-specific real-time PCR, are typically limited to a single target gene and lack sensitivity. Alternatively, next-generation sequencing methods suffer from slow turnaround time, high costs, and are complex to implement, typically limiting them to single-site use. Here, we report a method, which we term Allele-Specific PYrophosphorolysis Reaction (ASPYRE), for high sensitivity detection of panels of somatic variants. ASPYRE has a simple workflow and is compatible with standard molecular biology reagents and real-time PCR instruments. We show that ASPYRE has single molecule sensitivity and is tolerant of DNA extracted from plasma and formalin fixed paraffin embedded (FFPE) samples. We also demonstrate two multiplex panels, including one for detection of 47 EGFR variants. ASPYRE presents an effective and accessible method that simplifies highly sensitive and multiplexed detection of somatic variants.
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spelling pubmed-79663812021-03-19 Single-copy detection of somatic variants from solid and liquid biopsy Silva, Ana-Luisa Powalowska, Paulina Klaudyna Stolarek, Magdalena Gray, Eleanor Ruth Palmer, Rebecca Natalie Herman, Bram Frayling, Cameron Alexander Balmforth, Barnaby William Sci Rep Article Accurate detection of somatic variants, against a background of wild-type molecules, is essential for clinical decision making in oncology. Existing approaches, such as allele-specific real-time PCR, are typically limited to a single target gene and lack sensitivity. Alternatively, next-generation sequencing methods suffer from slow turnaround time, high costs, and are complex to implement, typically limiting them to single-site use. Here, we report a method, which we term Allele-Specific PYrophosphorolysis Reaction (ASPYRE), for high sensitivity detection of panels of somatic variants. ASPYRE has a simple workflow and is compatible with standard molecular biology reagents and real-time PCR instruments. We show that ASPYRE has single molecule sensitivity and is tolerant of DNA extracted from plasma and formalin fixed paraffin embedded (FFPE) samples. We also demonstrate two multiplex panels, including one for detection of 47 EGFR variants. ASPYRE presents an effective and accessible method that simplifies highly sensitive and multiplexed detection of somatic variants. Nature Publishing Group UK 2021-03-16 /pmc/articles/PMC7966381/ /pubmed/33727644 http://dx.doi.org/10.1038/s41598-021-85545-3 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Silva, Ana-Luisa
Powalowska, Paulina Klaudyna
Stolarek, Magdalena
Gray, Eleanor Ruth
Palmer, Rebecca Natalie
Herman, Bram
Frayling, Cameron Alexander
Balmforth, Barnaby William
Single-copy detection of somatic variants from solid and liquid biopsy
title Single-copy detection of somatic variants from solid and liquid biopsy
title_full Single-copy detection of somatic variants from solid and liquid biopsy
title_fullStr Single-copy detection of somatic variants from solid and liquid biopsy
title_full_unstemmed Single-copy detection of somatic variants from solid and liquid biopsy
title_short Single-copy detection of somatic variants from solid and liquid biopsy
title_sort single-copy detection of somatic variants from solid and liquid biopsy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966381/
https://www.ncbi.nlm.nih.gov/pubmed/33727644
http://dx.doi.org/10.1038/s41598-021-85545-3
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