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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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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/. |
format | Online Article Text |
id | pubmed-4054893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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