PSO-CFDP:一种基于粒子群优化的癌症亚型自动密度峰值聚类方法

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY
Human Heredity Pub Date : 2019-08-14 DOI:10.1159/000501481
Xuhui Zhu, J. Shang, Y. Sun, Feng Li, Jin-Xing Liu, Shasha Yuan
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引用次数: 5

摘要

癌症分型对于癌症患者的预测、诊断和精确治疗具有重要意义。许多聚类方法已经被提出用于癌症亚型。2014年,一种名为密度峰快速搜索和查找聚类(CFDP)的聚类算法被提出并发表在《科学》杂志上,该算法已被应用于癌症亚型,并取得了引人注目的结果。然而,CFDP需要手动设置两个关键参数(聚类中心和截止距离),而它们的最优值很难确定。为了克服这一限制,本文提出了一种称为PSO-CFDP的自动聚类方法,该方法通过多次运行改进的粒子群优化算法来自动确定聚类中心和截止距离。在四个基准数据集和两个真实的癌症基因表达数据集上进行了使用PSO-CFDP以及LR-CFDP、STClu、CH-CCFDAC和CFDP的实验。结果表明,PSO-CFDP可以在可控的时间/成本内自动确定聚类中心和截止距离,从而提高癌症分型的准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PSO-CFDP: A Particle Swarm Optimization-Based Automatic Density Peaks Clustering Method for Cancer Subtyping
Cancer subtyping is of great importance for the prediction, diagnosis, and precise treatment of cancer patients. Many clustering methods have been proposed for cancer subtyping. In 2014, a clustering algorithm named Clustering by Fast Search and Find of Density Peaks (CFDP) was proposed and published in Science, which has been applied to cancer subtyping and achieved attractive results. However, CFDP requires to set two key parameters (cluster centers and cutoff distance) manually, while their optimal values are difficult to be determined. To overcome this limitation, an automatic clustering method named PSO-CFDP is proposed in this paper, in which cluster centers and cutoff distance are automatically determined by running an improved particle swarm optimization (PSO) algorithm multiple times. Experiments using PSO-CFDP, as well as LR-CFDP, STClu, CH-CCFDAC, and CFDP, were performed on four benchmark datasets and two real cancer gene expression datasets. The results show that PSO-CFDP can determine cluster centers and cutoff distance automatically within controllable time/cost and, therefore, improve the accuracy of cancer subtyping.
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来源期刊
Human Heredity
Human Heredity 生物-遗传学
CiteScore
2.50
自引率
0.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: Gathering original research reports and short communications from all over the world, ''Human Heredity'' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all ''Human Heredity'' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
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