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

被引:162
作者
Oesper, Layla [1 ]
Mahmoody, Ahmad [1 ]
Raphael, Benjamin J. [1 ,2 ]
机构
[1] Brown Univ, Dept Comp Sci, Providence, RI 02912 USA
[2] Brown Univ, Ctr Computat Mol Biol, Providence, RI 02912 USA
来源
GENOME BIOLOGY | 2013年 / 14卷 / 07期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Cancer genomics; intra-tumor heterogeneity; DNA sequencing; tumor evolution; algorithms; COPY-NUMBER ALTERATIONS; CARCINOMA IN-SITU; CLONAL EVOLUTION; CANCER GENOMES; BREAST; HETEROZYGOSITY; INFORMATION; DELETION; 16Q; ARM;
D O I
10.1186/gb-2013-14-7-r80
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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/.
引用
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页数:21
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