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:摘要聚焦通用核回归与统计遗传学,二元分类本身不足以归入经济学离散选择。

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
Lorin Crawford
Kris C. Wood
Xiang Zhou
Sayan Mukherjee

带变量选择的贝叶斯近似核回归

研究问题
非线性核回归缺少类似线性回归系数的效应量时,如何为原始解释变量构造可用于变量选择的效应量类比?
方法与思路
作者利用平移不变核的随机傅里叶近似构造捕捉非线性结构的空间,再投影至原始变量,建立贝叶斯近似核回归。
材料陈述的贡献
摘要称,框架可用于非线性回归和二元分类,提供可计算的效应量类比,并在基因组预测与关联定位中展示竞争表现。
阅读关注点
应核对投影效应量的定义与解释、随机傅里叶近似误差,以及变量选择规则和两类遗传学任务的比较指标。
阅读边界
依据版本未注明的 OpenAlex 索引摘要;投影效应量不能直接解释为因果效应,摘要未说明选择错误率或具体比较结果,不能推断刊本变化。

原文摘要

Nonlinear kernel regression models are often used in statistics and machine learning because they are more accurate than linear models. Variable selection for kernel regression models is a challenge partly because, unlike the linear regression setting, there is no clear concept of an effect size for regression coefficients. In this paper, we propose a novel framework that provides an effect size analog for each explanatory variable in Bayesian kernel regression models when the kernel is shift-invariant - for example, the Gaussian kernel. We use function analytic properties of shift-invariant reproducing kernel Hilbert spaces (RKHS) to define a linear vector space that: (i) captures nonlinear structure, and (ii) can be projected onto the original explanatory variables. This projection onto the original explanatory variables serves as an analog of effect sizes. The specific function analytic property we use is that shift-invariant kernel functions can be approximated via random Fourier bases. Based on the random Fourier expansion, we propose a computationally efficient class of Bayesian approximate kernel regression (BAKR) models for both nonlinear regression and binary classification for which one can compute an analog of effect sizes. We illustrate the utility of BAKR by examining two important problems in statistical genetics: genomic selection (i.e. phenotypic prediction) and association mapping (i.e. inference of significant variants or loci). State-of-the-art methods for genomic selection and association mapping are based on kernel regression and linear models, respectively. BAKR is the first method that is competitive in both settings.

笔记与分组
相关领域论文