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AI 根据所提供的论文材料归类:摘要研究多维统计图模型和癌症数据,未提供经济网络或因果干扰方面的直接证据。

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稀疏多维图模型的统一贝叶斯框架

研究问题
研究如何利用多轴数据结构,估计每个维度变量之间的条件依赖,并兼容不同类型图结构的组合。
方法与思路
以各维度精度矩阵的矩阵分解构造图模型,通过似然边缘化设计部分折叠 Gibbs 后验抽样方案。
材料陈述的贡献
摘要称框架可统一处理有向图、无向可分解图及其组合,并以模拟、卵巢癌蛋白组和癌症死亡数据展示。
阅读关注点
应核对不同图类型的适用范围、矩阵分解与稀疏先验设定,以及抽样效率和模拟优势的比较标准。
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索引材料混有作者信息与补充材料提示;摘要未详述技术条件和优势数值,不能将条件依赖解释为因果关系。

原文摘要

Yang Niab, Francesco C. Stingoac* & Veerabhadran Baladandayuthapaniaa Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TXb Department of Statistics and Data Sciences, The University of Texas at Austin, Austin, TXc Dipartimento di Statistica, Informatica, Applicazioni “G.Parenti,” University of Florence, Florence, ItalyCONTACT Francesco C. Stingo fstingo@mdanderson.org Dipartimento di Statistica, Informatica, Applicazioni “G.Parenti,” University of Florence, 50134 Florence, ItalySupplementary materials for this article are available online. Please go to www.tandfonline.com/r/JASA.ABSTRACTMulti-dimensional data constituted by measurements along multiple axes have emerged across many scientific areas such as genomics and cancer surveillance. A common objective is to investigate the conditional dependencies among the variables along each axes taking into account multi-dimensional structure of the data. Traditional multivariate approaches are unsuitable for such highly structured data due to inefficiency, loss of power, and lack of interpretability. In this article, we propose a novel class of multi-dimensional graphical models based on matrix decompositions of the precision matrices along each dimension. Our approach is a unified framework applicable to both directed and undirected decomposable graphs as well as arbitrary combinations of these. Exploiting the marginalization of the likelihood, we develop efficient posterior sampling schemes based on partially collapsed Gibbs samplers. Empirically, through simulation studies, we show the superior performance of our approach in comparison with those of benchmark and state-of-the-art methods. We illustrate our approaches using two datasets: ovarian cancer proteomics and U.S. cancer mortality. Supplementary materials for this article are available online.

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