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THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data

Tumor samples are typically heterogeneous, containing admixture by normal, non-cancerous cells and one or more subpopulations of cancerous cells. Whole-genome sequencing of a tumor sample yields reads from this mixture, but does not directly reveal the cell of origin for each read. We introduce THet...

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Detalles Bibliográficos
Autores principales: Oesper, Layla, Mahmoody, Ahmad, Raphael, Benjamin J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054893/
https://www.ncbi.nlm.nih.gov/pubmed/23895164
http://dx.doi.org/10.1186/gb-2013-14-7-r80
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author Oesper, Layla
Mahmoody, Ahmad
Raphael, Benjamin J
author_facet Oesper, Layla
Mahmoody, Ahmad
Raphael, Benjamin J
author_sort Oesper, Layla
collection PubMed
description Tumor samples are typically heterogeneous, containing admixture by normal, non-cancerous cells and one or more subpopulations of cancerous cells. Whole-genome sequencing of a tumor sample yields reads from this mixture, but does not directly reveal the cell of origin for each read. We introduce THetA (Tumor Heterogeneity Analysis), an algorithm that infers the most likely collection of genomes and their proportions in a sample, for the case where copy number aberrations distinguish subpopulations. THetA successfully estimates normal admixture and recovers clonal and subclonal copy number aberrations in real and simulated sequencing data. THetA is available at http://compbio.cs.brown.edu/software/.
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spelling pubmed-40548932014-06-12 THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data Oesper, Layla Mahmoody, Ahmad Raphael, Benjamin J Genome Biol Method Tumor samples are typically heterogeneous, containing admixture by normal, non-cancerous cells and one or more subpopulations of cancerous cells. Whole-genome sequencing of a tumor sample yields reads from this mixture, but does not directly reveal the cell of origin for each read. We introduce THetA (Tumor Heterogeneity Analysis), an algorithm that infers the most likely collection of genomes and their proportions in a sample, for the case where copy number aberrations distinguish subpopulations. THetA successfully estimates normal admixture and recovers clonal and subclonal copy number aberrations in real and simulated sequencing data. THetA is available at http://compbio.cs.brown.edu/software/. BioMed Central 2013 2013-07-29 /pmc/articles/PMC4054893/ /pubmed/23895164 http://dx.doi.org/10.1186/gb-2013-14-7-r80 Text en Copyright © 2013 Oesper 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
Oesper, Layla
Mahmoody, Ahmad
Raphael, Benjamin J
THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data
title THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data
title_full THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data
title_fullStr THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data
title_full_unstemmed THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data
title_short THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data
title_sort theta: inferring intra-tumor heterogeneity from high-throughput dna sequencing data
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054893/
https://www.ncbi.nlm.nih.gov/pubmed/23895164
http://dx.doi.org/10.1186/gb-2013-14-7-r80
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