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An Iterative Approach for Phylogenetic Analysis of Tumor Progression Using FISH Copy Number

机译:使用FISH拷贝数的肿瘤进展系统发育分析的迭代方法

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摘要

Copy number variants are an underlying factor in human evolution and in many diseases, especially in cancer. Tumors generally contain cells with a varying number of gene copies, and the variance in the number of gene copies follows a pattern formed by an evolutionary process. The Fluorescence in situ hybridization (FISH) provides researchers a reliable technique to measure the copy numbers of preselected genes in a group of cells. Recently, Chowdhury et al. successfully modeled the progression of tumor progression using FISH copy number to the Rectilinear Steiner Minimum Tree (RSMT) problem, and proposed both exact and heuristic algorithms to reconstruct phylogenetic trees modeling the development of cancer cell patterns. We proposed new heuristics to attack the RSMT problem, which is inspired by iterative approaches to approximate solutions to the Steiner tree in the "small phytogeny" problem [2,3]. Experimental results from both simulated and real tumor data show that our approach outperforms the previous heuristic algorithm in approximating better solutions for the RSMT problem.
机译:拷贝数变异是人类进化和许多疾病(尤其是癌症)中的潜在因素。肿瘤通常包含具有不同数量的基因拷贝的细胞,并且基因拷贝数的变化遵循由进化过程形成的模式。荧光原位杂交(FISH)为研究人员提供了一种可靠的技术,可以测量一组细胞中预选基因的拷贝数。最近,Chowdhury等人。成功地使用FISH副本数对Receilinear Steiner Minimum Tree(RSMT)问题建模了肿瘤进展的进展,并提出了精确算法和启发式算法来重建系统发育树,从而对癌细胞模式的发展进行建模。我们提出了一种新的启发式方法来解决RSMT问题,这是受“小植物遗传学”问题[2,3]中迭代方法逼近Steiner树解决方案启发的。来自模拟和真实肿瘤数据的实验结果表明,在逼近RSMT问题的更好解决方案方面,我们的方法优于以前的启发式算法。

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