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Digital Sorting of Pure Cell Populations Enables Unambiguous Genetic Analysis of Heterogeneous Formalin-Fixed Paraffin-Embedded Tumors by Next Generation Sequencing
Precision medicine in oncology requires an accurate characterization of a tumor molecular profile for patient stratification. Though targeted deep sequencing is an effective tool to detect the presence of somatic sequence variants, a significant number of patient specimens do not meet the requiremen...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750064/ https://www.ncbi.nlm.nih.gov/pubmed/26864208 http://dx.doi.org/10.1038/srep20944 |
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author | Bolognesi, Chiara Forcato, Claudio Buson, Genny Fontana, Francesca Mangano, Chiara Doffini, Anna Sero, Valeria Lanzellotto, Rossana Signorini, Giulio Calanca, Alex Sergio, Maximilian Romano, Rita Gianni, Stefano Medoro, Gianni Giorgini, Giuseppe Morreau, Hans Barberis, Massimo Corver, Willem E. Manaresi, Nicolò |
author_facet | Bolognesi, Chiara Forcato, Claudio Buson, Genny Fontana, Francesca Mangano, Chiara Doffini, Anna Sero, Valeria Lanzellotto, Rossana Signorini, Giulio Calanca, Alex Sergio, Maximilian Romano, Rita Gianni, Stefano Medoro, Gianni Giorgini, Giuseppe Morreau, Hans Barberis, Massimo Corver, Willem E. Manaresi, Nicolò |
author_sort | Bolognesi, Chiara |
collection | PubMed |
description | Precision medicine in oncology requires an accurate characterization of a tumor molecular profile for patient stratification. Though targeted deep sequencing is an effective tool to detect the presence of somatic sequence variants, a significant number of patient specimens do not meet the requirements needed for routine clinical application. Analysis is hindered by contamination of normal cells and inherent tumor heterogeneity, compounded with challenges of dealing with minute amounts of tissue and DNA damages common in formalin-fixed paraffin-embedded (FFPE) specimens. Here we present an innovative workflow using DEPArray™ system, a microchip-based digital sorter to achieve 100%-pure, homogenous subpopulations of cells from FFPE samples. Cells are distinguished by fluorescently labeled antibodies and DNA content. The ability to address tumor heterogeneity enables unambiguous determination of true-positive sequence variants, loss-of-heterozygosity as well as copy number variants. The proposed strategy overcomes the inherent trade-offs made between sensitivity and specificity in detecting genetic variants from a mixed population, thus rescuing for analysis even the smaller clinical samples with low tumor cellularity. |
format | Online Article Text |
id | pubmed-4750064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47500642016-02-18 Digital Sorting of Pure Cell Populations Enables Unambiguous Genetic Analysis of Heterogeneous Formalin-Fixed Paraffin-Embedded Tumors by Next Generation Sequencing Bolognesi, Chiara Forcato, Claudio Buson, Genny Fontana, Francesca Mangano, Chiara Doffini, Anna Sero, Valeria Lanzellotto, Rossana Signorini, Giulio Calanca, Alex Sergio, Maximilian Romano, Rita Gianni, Stefano Medoro, Gianni Giorgini, Giuseppe Morreau, Hans Barberis, Massimo Corver, Willem E. Manaresi, Nicolò Sci Rep Article Precision medicine in oncology requires an accurate characterization of a tumor molecular profile for patient stratification. Though targeted deep sequencing is an effective tool to detect the presence of somatic sequence variants, a significant number of patient specimens do not meet the requirements needed for routine clinical application. Analysis is hindered by contamination of normal cells and inherent tumor heterogeneity, compounded with challenges of dealing with minute amounts of tissue and DNA damages common in formalin-fixed paraffin-embedded (FFPE) specimens. Here we present an innovative workflow using DEPArray™ system, a microchip-based digital sorter to achieve 100%-pure, homogenous subpopulations of cells from FFPE samples. Cells are distinguished by fluorescently labeled antibodies and DNA content. The ability to address tumor heterogeneity enables unambiguous determination of true-positive sequence variants, loss-of-heterozygosity as well as copy number variants. The proposed strategy overcomes the inherent trade-offs made between sensitivity and specificity in detecting genetic variants from a mixed population, thus rescuing for analysis even the smaller clinical samples with low tumor cellularity. Nature Publishing Group 2016-02-11 /pmc/articles/PMC4750064/ /pubmed/26864208 http://dx.doi.org/10.1038/srep20944 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Bolognesi, Chiara Forcato, Claudio Buson, Genny Fontana, Francesca Mangano, Chiara Doffini, Anna Sero, Valeria Lanzellotto, Rossana Signorini, Giulio Calanca, Alex Sergio, Maximilian Romano, Rita Gianni, Stefano Medoro, Gianni Giorgini, Giuseppe Morreau, Hans Barberis, Massimo Corver, Willem E. Manaresi, Nicolò Digital Sorting of Pure Cell Populations Enables Unambiguous Genetic Analysis of Heterogeneous Formalin-Fixed Paraffin-Embedded Tumors by Next Generation Sequencing |
title | Digital Sorting of Pure Cell Populations Enables Unambiguous Genetic Analysis of Heterogeneous Formalin-Fixed Paraffin-Embedded Tumors by Next Generation Sequencing |
title_full | Digital Sorting of Pure Cell Populations Enables Unambiguous Genetic Analysis of Heterogeneous Formalin-Fixed Paraffin-Embedded Tumors by Next Generation Sequencing |
title_fullStr | Digital Sorting of Pure Cell Populations Enables Unambiguous Genetic Analysis of Heterogeneous Formalin-Fixed Paraffin-Embedded Tumors by Next Generation Sequencing |
title_full_unstemmed | Digital Sorting of Pure Cell Populations Enables Unambiguous Genetic Analysis of Heterogeneous Formalin-Fixed Paraffin-Embedded Tumors by Next Generation Sequencing |
title_short | Digital Sorting of Pure Cell Populations Enables Unambiguous Genetic Analysis of Heterogeneous Formalin-Fixed Paraffin-Embedded Tumors by Next Generation Sequencing |
title_sort | digital sorting of pure cell populations enables unambiguous genetic analysis of heterogeneous formalin-fixed paraffin-embedded tumors by next generation sequencing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750064/ https://www.ncbi.nlm.nih.gov/pubmed/26864208 http://dx.doi.org/10.1038/srep20944 |
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