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AI 根据所提供的论文材料归类:摘要研究一般回归变量选择与遗传精细定位,没有明确经济结构或因果识别框架,遗传效应措辞不足以支持所列领域分类。

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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
Gao Wang
Abhishek Sarkar
Peter Carbonetto
Matthew Stephens

回归变量选择的新方法及其在遗传精细定位中的应用

研究问题
在线性回归的高度相关协变量与稀疏可检测效应场景中,如何量化应选择哪些变量的不确定性,并将其用于遗传精细定位?
方法与思路
作者将稀疏系数写为单效应向量之和,构建 SuSiE 模型,并用 IBSS 拟合;算法优化后验的变分近似,输出每次选择的变量分布。
材料陈述的贡献
摘要称,该近似后验可生成变量可信集合;数值实验在遗传精细定位任务中优于既有方法,并以影响人类细胞系可变剪接的变异为例。
阅读关注点
应核对单效应数量与先验设定、变分优化的性质、可信集合的构造与校准,以及高度相关变量下的表现和一般回归应用的限制。
阅读边界
仅据所给 Crossref 摘要;性能优势限于作者报告的任务,未提供比较细节,可信集合也不能自动解释为因果变量识别或频率学覆盖保证。

原文摘要

Summary We introduce a simple new approach to variable selection in linear regression, with a particular focus on quantifying uncertainty in which variables should be selected. The approach is based on a new model—the ‘sum of single effects’ model, called ‘SuSiE’—which comes from writing the sparse vector of regression coefficients as a sum of ‘single-effect’ vectors, each with one non-zero element. We also introduce a corresponding new fitting procedure—iterative Bayesian stepwise selection (IBSS)—which is a Bayesian analogue of stepwise selection methods. IBSS shares the computational simplicity and speed of traditional stepwise methods but, instead of selecting a single variable at each step, IBSS computes a distribution on variables that captures uncertainty in which variable to select. We provide a formal justification of this intuitive algorithm by showing that it optimizes a variational approximation to the posterior distribution under SuSiE. Further, this approximate posterior distribution naturally yields convenient novel summaries of uncertainty in variable selection, providing a credible set of variables for each selection. Our methods are particularly well suited to settings where variables are highly correlated and detectable effects are sparse, both of which are characteristics of genetic fine mapping applications. We demonstrate through numerical experiments that our methods outperform existing methods for this task, and we illustrate their application to fine mapping genetic variants influencing alternative splicing in human cell lines. We also discuss the potential and challenges for applying these methods to generic variable-selection problems.

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