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Comprehensive statistical inference of the clonal structure of cancer from multiple biopsies

A comprehensive characterization of tumor genetic heterogeneity is critical for understanding how cancers evolve and escape treatment. Although many algorithms have been developed for capturing tumor heterogeneity, they are designed for analyzing either a single type of genomic aberration or individ...

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Autores principales: Liu, Jie, Halloran, John T., Bilmes, Jeffrey A., Daza, Riza M., Lee, Choli, Mahen, Elisabeth M., Prunkard, Donna, Song, Chaozhong, Blau, Sibel, Dorschner, Michael O., Gadi, Vijayakrishna K., Shendure, Jay, Blau, C. Anthony, Noble, William S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717219/
https://www.ncbi.nlm.nih.gov/pubmed/29208983
http://dx.doi.org/10.1038/s41598-017-16813-4
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author Liu, Jie
Halloran, John T.
Bilmes, Jeffrey A.
Daza, Riza M.
Lee, Choli
Mahen, Elisabeth M.
Prunkard, Donna
Song, Chaozhong
Blau, Sibel
Dorschner, Michael O.
Gadi, Vijayakrishna K.
Shendure, Jay
Blau, C. Anthony
Noble, William S.
author_facet Liu, Jie
Halloran, John T.
Bilmes, Jeffrey A.
Daza, Riza M.
Lee, Choli
Mahen, Elisabeth M.
Prunkard, Donna
Song, Chaozhong
Blau, Sibel
Dorschner, Michael O.
Gadi, Vijayakrishna K.
Shendure, Jay
Blau, C. Anthony
Noble, William S.
author_sort Liu, Jie
collection PubMed
description A comprehensive characterization of tumor genetic heterogeneity is critical for understanding how cancers evolve and escape treatment. Although many algorithms have been developed for capturing tumor heterogeneity, they are designed for analyzing either a single type of genomic aberration or individual biopsies. Here we present THEMIS (Tumor Heterogeneity Extensible Modeling via an Integrative System), which allows for the joint analysis of different types of genomic aberrations from multiple biopsies taken from the same patient, using a dynamic graphical model. Simulation experiments demonstrate higher accuracy of THEMIS over its ancestor, TITAN. The heterogeneity analysis results from THEMIS are validated with single cell DNA sequencing from a clinical tumor biopsy. When THEMIS is used to analyze tumor heterogeneity among multiple biopsies from the same patient, it helps to reveal the mutation accumulation history, track cancer progression, and identify the mutations related to treatment resistance. We implement our model via an extensible modeling platform, which makes our approach open, reproducible, and easy for others to extend.
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spelling pubmed-57172192017-12-08 Comprehensive statistical inference of the clonal structure of cancer from multiple biopsies Liu, Jie Halloran, John T. Bilmes, Jeffrey A. Daza, Riza M. Lee, Choli Mahen, Elisabeth M. Prunkard, Donna Song, Chaozhong Blau, Sibel Dorschner, Michael O. Gadi, Vijayakrishna K. Shendure, Jay Blau, C. Anthony Noble, William S. Sci Rep Article A comprehensive characterization of tumor genetic heterogeneity is critical for understanding how cancers evolve and escape treatment. Although many algorithms have been developed for capturing tumor heterogeneity, they are designed for analyzing either a single type of genomic aberration or individual biopsies. Here we present THEMIS (Tumor Heterogeneity Extensible Modeling via an Integrative System), which allows for the joint analysis of different types of genomic aberrations from multiple biopsies taken from the same patient, using a dynamic graphical model. Simulation experiments demonstrate higher accuracy of THEMIS over its ancestor, TITAN. The heterogeneity analysis results from THEMIS are validated with single cell DNA sequencing from a clinical tumor biopsy. When THEMIS is used to analyze tumor heterogeneity among multiple biopsies from the same patient, it helps to reveal the mutation accumulation history, track cancer progression, and identify the mutations related to treatment resistance. We implement our model via an extensible modeling platform, which makes our approach open, reproducible, and easy for others to extend. Nature Publishing Group UK 2017-12-05 /pmc/articles/PMC5717219/ /pubmed/29208983 http://dx.doi.org/10.1038/s41598-017-16813-4 Text en © The Author(s) 2017 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
Liu, Jie
Halloran, John T.
Bilmes, Jeffrey A.
Daza, Riza M.
Lee, Choli
Mahen, Elisabeth M.
Prunkard, Donna
Song, Chaozhong
Blau, Sibel
Dorschner, Michael O.
Gadi, Vijayakrishna K.
Shendure, Jay
Blau, C. Anthony
Noble, William S.
Comprehensive statistical inference of the clonal structure of cancer from multiple biopsies
title Comprehensive statistical inference of the clonal structure of cancer from multiple biopsies
title_full Comprehensive statistical inference of the clonal structure of cancer from multiple biopsies
title_fullStr Comprehensive statistical inference of the clonal structure of cancer from multiple biopsies
title_full_unstemmed Comprehensive statistical inference of the clonal structure of cancer from multiple biopsies
title_short Comprehensive statistical inference of the clonal structure of cancer from multiple biopsies
title_sort comprehensive statistical inference of the clonal structure of cancer from multiple biopsies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717219/
https://www.ncbi.nlm.nih.gov/pubmed/29208983
http://dx.doi.org/10.1038/s41598-017-16813-4
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