不确定数据的贝叶斯聚类。

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Kath Nicholls, Paul D W Kirk, Chris Wallace
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引用次数: 0

摘要

聚类被广泛应用于生物信息学和许多其他领域,应用范围从探索性分析到预测。许多类型的数据都有相关的不确定性或测量误差,但很少用来为聚类提供信息。我们提出了具有不确定性的 Dirichlet Process Mixtures (DPMUnc),它是贝叶斯非参数聚类算法的扩展,利用了与数据点相关的不确定性。我们的研究表明,DPMUnc 在模拟数据上的表现优于现有方法。我们使用 GWAS 统计摘要对免疫介导疾病(IMD)进行聚类,该统计摘要具有与研究样本大小相关的不确定性。DPMUnc 将自身免疫性疾病与自身炎症性疾病区分开来,并分离出成人发病型关节炎等其他亚组。此外,我们还考虑了如何利用 DPMUnc 对使用基因特征总结的基因表达数据集进行聚类。我们首先介绍了在与发现基因特征的数据集不同的数据集上生成基因特征摘要的新程序,该程序结合了对每个个体中特征基因表达变异性的测量。我们利用三个相关的基因特征,总结了包含一系列 IMD 患者的三个公共基因表达数据集。我们发现疾病与 DPMUnc 返回的聚类之间存在关联,聚类结构在数据集中得到了复制。这项工作有两方面的意义。首先,我们证明了当数据具有相关的不确定性时,应利用这种不确定性为聚类提供信息,我们提出了一种实现这一目的的方法--DPMUnc。其次,我们提出了一种在数据集中使用基因特征的程序,而不是在最初定义基因特征的地方。我们利用相关基因特征总结了免疫介导疾病患者的基因表达数据,并使用 DPMUnc 对这些患者进行了聚类,从而展示了这一程序的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bayesian clustering with uncertain data.

Clustering is widely used in bioinformatics and many other fields, with applications from exploratory analysis to prediction. Many types of data have associated uncertainty or measurement error, but this is rarely used to inform the clustering. We present Dirichlet Process Mixtures with Uncertainty (DPMUnc), an extension of a Bayesian nonparametric clustering algorithm which makes use of the uncertainty associated with data points. We show that DPMUnc out-performs existing methods on simulated data. We cluster immune-mediated diseases (IMD) using GWAS summary statistics, which have uncertainty linked with the sample size of the study. DPMUnc separates autoimmune from autoinflammatory diseases and isolates other subgroups such as adult-onset arthritis. We additionally consider how DPMUnc can be used to cluster gene expression datasets that have been summarised using gene signatures. We first introduce a novel procedure for generating a summary of a gene signature on a dataset different to the one where it was discovered, which incorporates a measure of the variability in expression across signature genes within each individual. We summarise three public gene expression datasets containing patients with a range of IMD, using three relevant gene signatures. We find association between disease and the clusters returned by DPMUnc, with clustering structure replicated across the datasets. The significance of this work is two-fold. Firstly, we demonstrate that when data has associated uncertainty, this uncertainty should be used to inform clustering and we present a method which does this, DPMUnc. Secondly, we present a procedure for using gene signatures in datasets other than where they were originally defined. We show the value of this procedure by summarising gene expression data from patients with immune-mediated diseases using relevant gene signatures, and clustering these patients using DPMUnc.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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