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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-7966381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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