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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。

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分类依据与纠错

AI 根据所提供的论文材料归类:摘要主要提出通用高维似然检验,脑网络属于应用示例,尚不足以将整体方法归入所列网络或其他细分。

反馈分类问题

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代码、数据与补充材料

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关注这篇论文的作者
Yunzhang Zhu
Xiaotong Shen
Wei Pan

高维约束最大似然推断

研究问题
高维复合假设检验含有大量干扰参数时,如何降低正则化对推断的影响,并允许参数维数及检验余维随样本增长?
方法与思路
作者对受检验参数不施加正则化,对干扰参数施加控制稀疏度的零范数约束,并研究约束似然比的渐近分布。
材料陈述的贡献
摘要称,在高斯图模型与线性回归的相应条件下,似然比极限可随检验余维情况呈卡方或正态分布,扩展经典 Wilks 现象。
阅读关注点
应核对受检验参数与干扰参数的划分、稀疏约束选择、维度和余维增长条件,以及约束优化误差是否影响检验有效性。
阅读边界
仅据 OpenAlex 索引摘要,稿件版本未注明;极限分布及其适用条件未完整列出,脑网络应用不能证明对任意高维模型有效。

原文摘要

Inference in a high-dimensional situation may involve regularization of a certain form to treat overparameterization, imposing challenges to inference. The common practice of inference uses either a regularized model, as in inference after model selection, or bias-reduction known as “debias.” While the first ignores statistical uncertainty inherent in regularization, the second reduces the bias inbred in regularization at the expense of increased variance. In this article, we propose a constrained maximum likelihood method for hypothesis testing involving unspecific nuisance parameters, with a focus of alleviating the impact of regularization on inference. Particularly, for general composite hypotheses, we unregularize hypothesized parameters whereas regularizing nuisance parameters through a L0-constraint controlling the degree of sparseness. This approach is analogous to semiparametric likelihood inference in a high-dimensional situation. On this ground, for the Gaussian graphical model and linear regression, we derive conditions under which the asymptotic distribution of the constrained likelihood ratio is established, permitting parameter dimension increasing with the sample size. Interestingly, the corresponding limiting distribution is the chi-square or normal, depending on if the co-dimension of a test is finite or increases with the sample size, leading to asymptotic similar tests. This goes beyond the classical Wilks phenomenon. Numerically, we demonstrate that the proposed method performs well against it competitors in various scenarios. Finally, we apply the proposed method to infer linkages in brain network analysis based on MRI data, to contrast Alzheimer’s disease patients against healthy subjects. Supplementary materials for this article are available online.

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