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:摘要主要研究通用信号定位与多重发现,变点检测只是应用例子,未提供归入宏观结构变化等细分的充分依据。

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
Asher Spector
Lucas Janson

通过贝叶斯线性规划控制信号发现与定位

研究问题
当相关性使信号位置难以精确识别时,如何输出尽量多且尽量小的不相交信号区域,同时控制错误发现?
方法与思路
作者提出 BLiP,以已有信号位置后验为输入,通过贝叶斯线性规划选择可信区域,联合处理发现数量与定位精度。
材料陈述的贡献
摘要称,BLiP 可在控制错误发现时可验证地近似最大化期望功效,并报告遗传与天文应用中的功效提升及较低追加计算成本。
阅读关注点
应核对错误发现控制所处的概率框架、后验可靠性要求、近似最优性的保证,以及功效比较如何兼顾区域大小。
阅读边界
依据 arXiv 预印本版本摘要,不能据此声称已同行评审或期刊接收,也不推断刊本变化;具体保证条件和应用比较需核对全文。

原文摘要

Scientists often must simultaneously localize and discover signals. For instance, in genetic fine-mapping, high correlations between nearby genetic variants make it hard to identify the exact locations of causal variants. So the statistical task is to output as many disjoint regions containing a signal as possible, each as small as possible, while controlling false positives. Similar problems arise in any application where signals cannot be perfectly localized, such as locating stars in astronomical surveys and changepoint detection in sequential data. Common Bayesian approaches to these problems involve computing a posterior distribution over signal locations. However, existing procedures to translate these posteriors into actual credible regions for the signals fail to capture all the information in the posterior, leading to lower power and (sometimes) inflated false discoveries. With this motivation, we introduce Bayesian Linear Programming (BLiP). Given a posterior distribution over signals, BLiP outputs credible regions for signals which verifiably nearly maximize expected power while controlling false positives. BLiP overcomes an extremely high-dimensional and nonconvex problem to verifiably nearly maximize expected power while controlling false positives. BLiP is very computationally efficient compared to the cost of computing the posterior and can wrap around nearly any Bayesian model and algorithm. Applying BLiP to existing state-of-the-art analyses of UK Biobank data (for genetic fine-mapping) and the Sloan Digital Sky Survey (for astronomical point source detection) increased power by 30-120% in just a few minutes of additional computation. BLiP is implemented in pyblip (Python) and blipr (R).

笔记与分组
相关领域论文