跳到正文
← 返回论文列表与筛选
阅读说明

本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。

DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。

引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。

关注作者按书目中的完整姓名匹配,同名和姓名变体需人工辨别。相关论文先按共享细分方向和具体方法排列,再参考通用方法与发表日期。

分类依据与纠错

AI 根据所提供的论文材料归类:摘要研究通用矩阵数据与基因组依赖结构,未明确对应面板数据或其他所列经济计量细分。

反馈分类问题

正在核对关联版本…

代码、数据与补充材料

正在核对对应版本的资源…

关注这篇论文的作者
Michael Hornstein
Roger Fan
Kerby Shedden
Shuheng Zhou

无重复矩阵型数据的均值与协方差联合估计

研究问题
当高维矩阵数据没有重复观测,且观测之间与变量之间都存在未知依赖时,如何联合估计均值和协方差并校准推断?
方法与思路
作者结合广义最小二乘与惩罚协方差或逆协方差估计,在稀疏依赖结构下联合处理未知均值,并用模拟和基因组数据说明。
材料陈述的贡献
摘要称建立一致性与收敛速率,改善均值估计效率和检验校准,并报告差异基因表达检验相对常规方法的功效提升。
阅读关注点
应核对矩阵协方差结构、稀疏性与可识别条件,以及均值和依赖估计的相互影响、检验校准及模拟比较依据。
阅读边界
仅据所给OpenAlex摘要;未提供具体结构假设、速率或功效数值,基因组应用表现不能直接推广到其他依赖数据。

原文摘要

Michael Hornsteina*, Roger Fana, Kerby Sheddena & Shuheng Zhouaba Department of Statistics, University of Michigan, Ann Arbor, MIb Department of Statistics, University of California, Riverside, CACONTACT Michael Hornstein mdhorn@umich.edu Department of Statistics, University of Michigan, Ann Arbor, MI 48109.Color versions of one or more of the figures in the article can be found online at www.tandfonline.com/r/JASA.Supplementary materials for this article are available online. Please go to www.tandfonline.com/r/JASA.ABSTRACTIt has been proposed that complex populations, such as those that arise in genomics studies, may exhibit dependencies among observations as well as among variables. This gives rise to the challenging problem of analyzing unreplicated high-dimensional data with unknown mean and dependence structures. Matrix-variate approaches that impose various forms of (inverse) covariance sparsity allow flexible dependence structures to be estimated, but cannot directly be applied when the mean and covariance matrices are estimated jointly. We present a practical method utilizing generalized least squares and penalized (inverse) covariance estimation to address this challenge. We establish consistency and obtain rates of convergence for estimating the mean parameters and covariance matrices. The advantages of our approaches are: (i) dependence graphs and covariance structures can be estimated in the presence of unknown mean structure, (ii) the mean structure becomes more efficiently estimated when accounting for the dependence structure among observations; and (iii) inferences about the mean parameters become correctly calibrated. We use simulation studies and analysis of genomic data from a twin study of ulcerative colitis to illustrate the statistical convergence and the performance of our methods in practical settings. Several lines of evidence show that the test statistics for differential gene expression produced by our methods are correctly calibrated and improve power over conventional methods. Supplementary materials for this article are available online.

笔记与分组
相关领域论文