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关注这篇论文的作者
Soham Ghosh

带图马蹄先验的多元变系数BART模型

研究问题
摘要称,研究如何同时建模多个相关结果的非线性、异质且结果特定的回归效应,以及结果间具有科学意义的残差依赖,避免现有方法在树结构共享与均值结构简化之间的取舍。
方法与思路
作者提出multiVCBART:系数矩阵每个元素由独立BART集成表示,使预测效应随修饰变量非线性变化;对精度矩阵施加Graphical Horseshoe先验刻画稀疏残差条件依赖;并设计将多元高斯似然化为标量伪响应更新的采样器,解耦树回拟合与图马蹄步骤。
材料陈述的贡献
摘要称其贡献包括:提出联合建模灵活结果特定系数曲面与稀疏残差精度矩阵的框架;给出首个联合估计残差依赖的多元BART后验收缩率,证明对光滑性与结构稀疏性的近极小极大自适应;在稀疏高维数据上优于现有多元树模型与贝叶斯SUR竞争者;并在药物敏感性数据重分析中识别生物标志物信号与残差药理网络。
阅读关注点
阅读全文时应核对:变系数BART集成的具体先验与识别约束;Graphical Horseshoe刻画残差依赖的假设;采样器解耦的推导与计算复杂度;后验收缩率所需条件与稀疏性设定;模拟与实证比较的数据、基线、评价指标及可复现性。
阅读边界
仅凭摘要无法判断定理条件、模拟设计、基线公平性与实证结论的稳健性;摘要未说明样本量、超参数选择与敏感性分析。该文为arXiv预印本,未经同行评审验证,不能据此声称已被期刊接收。

原文摘要

Modern multivariate regression problems involve several related outcomes whose regression effects are not only nonlinear, heterogeneous, and outcome-specific, but also where the residual dependence among outcomes is scientifically meaningful. Existing multivariate Bayesian tree-based methods typically address only part of this problem: some impose substantial sharing of tree architecture across outcomes, which is overly restrictive when responses depend on distinct predictors or effect modifiers, while others accommodate residual dependence but retain simpler mean structures. This paper develops multiVCBART, a multivariate varying-coefficient Bayesian additive regression tree framework that jointly models flexible outcome-specific coefficient surfaces and a sparse residual precision matrix. Each entry of the coefficient matrix $B(x)$ is represented by an independent BART ensemble, allowing predictor effects to vary nonlinearly with modifiers $x$ across outcomes, while a Graphical Horseshoe prior on the precision matrix $Ω$ captures parsimonious residual conditional dependence. To permit efficient computation, we introduce a sampler that reduces the multivariate Gaussian likelihood to a sequence of scalar pseudo-response updates, decoupling the tree backfitting from the Graphical Horseshoe step. Theoretically, we establish the first posterior contraction rates for a multivariate BART model with jointly estimated residual dependence, proving near-minimax adaptation to underlying smoothness and structural sparsity. Empirically, multiVCBART outperforms existing multivariate tree models and Bayesian SUR competitors on sparse, high-dimensional datasets. Finally, in a re-analysis of the Genomics of Drug Sensitivity in Cancer dataset, our method identifies distinct biomarker signals and recovers a coherent residual pharmacologic network.

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