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Analysis of the copy number profiles of several tumor samples from the same patient reveals the successive steps in tumorigenesis
We present a computational method, TuMult, for reconstructing the sequence of copy number changes driving carcinogenesis, based on the analysis of several tumor samples from the same patient. We demonstrate the reliability of the method with simulated data, and describe applications to three differe...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2926787/ https://www.ncbi.nlm.nih.gov/pubmed/20649963 http://dx.doi.org/10.1186/gb-2010-11-7-r76 |
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author | Letouzé, Eric Allory, Yves Bollet, Marc A Radvanyi, François Guyon, Frédéric |
author_facet | Letouzé, Eric Allory, Yves Bollet, Marc A Radvanyi, François Guyon, Frédéric |
author_sort | Letouzé, Eric |
collection | PubMed |
description | We present a computational method, TuMult, for reconstructing the sequence of copy number changes driving carcinogenesis, based on the analysis of several tumor samples from the same patient. We demonstrate the reliability of the method with simulated data, and describe applications to three different cancers, showing that TuMult is a valuable tool for the establishment of clonal relationships between tumor samples and the identification of chromosome aberrations occurring at crucial steps in cancer progression. |
format | Text |
id | pubmed-2926787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29267872010-08-24 Analysis of the copy number profiles of several tumor samples from the same patient reveals the successive steps in tumorigenesis Letouzé, Eric Allory, Yves Bollet, Marc A Radvanyi, François Guyon, Frédéric Genome Biol Method We present a computational method, TuMult, for reconstructing the sequence of copy number changes driving carcinogenesis, based on the analysis of several tumor samples from the same patient. We demonstrate the reliability of the method with simulated data, and describe applications to three different cancers, showing that TuMult is a valuable tool for the establishment of clonal relationships between tumor samples and the identification of chromosome aberrations occurring at crucial steps in cancer progression. BioMed Central 2010 2010-07-22 /pmc/articles/PMC2926787/ /pubmed/20649963 http://dx.doi.org/10.1186/gb-2010-11-7-r76 Text en Copyright ©2010 Letouzé et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Method Letouzé, Eric Allory, Yves Bollet, Marc A Radvanyi, François Guyon, Frédéric Analysis of the copy number profiles of several tumor samples from the same patient reveals the successive steps in tumorigenesis |
title | Analysis of the copy number profiles of several tumor samples from the same patient reveals the successive steps in tumorigenesis |
title_full | Analysis of the copy number profiles of several tumor samples from the same patient reveals the successive steps in tumorigenesis |
title_fullStr | Analysis of the copy number profiles of several tumor samples from the same patient reveals the successive steps in tumorigenesis |
title_full_unstemmed | Analysis of the copy number profiles of several tumor samples from the same patient reveals the successive steps in tumorigenesis |
title_short | Analysis of the copy number profiles of several tumor samples from the same patient reveals the successive steps in tumorigenesis |
title_sort | analysis of the copy number profiles of several tumor samples from the same patient reveals the successive steps in tumorigenesis |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2926787/ https://www.ncbi.nlm.nih.gov/pubmed/20649963 http://dx.doi.org/10.1186/gb-2010-11-7-r76 |
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