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分类依据与纠错

AI 根据所提供的论文材料归类:摘要核心是基因组高维信号区域检测,未提供归入所列经济计量细分的直接依据。

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
Wei Zhang
Fan Wang
Fang Yao

快速信号区域检测及其全基因组关联研究应用

研究问题
当多个遗传变异的聚合效应形成信号区域时,如何同时定位多个区域,并降低全基因组区域检测的计算成本?
方法与思路
作者将高维检验与二元分割结合,加入重新搜索和区域调整,并利用动态临界值序列提高检测准确性、减少计算。
材料陈述的贡献
摘要称,方法具有理论保证,数值实验中检测表现和计算速度优于所比较方法;英国生物银行应用发现若干乳腺癌相关区域。
阅读关注点
核对动态临界值的构造、多区域搜索的错误控制、信号强度与区域间隔条件,以及新增关联区域是否经过独立验证。
阅读边界
所给为 OpenAlex 索引摘要,稿件版本未注明。摘要未说明理论限制和完整比较结果;新增区域属于关联发现,仍需进一步调查。

原文摘要

Research on the localization of the genetic basis associated with diseases or traits has been widely conducted in the last few decades. Scan methods have been developed for region-based analysis in whole-genome association studies, helping us better understand how genetics influences human diseases or traits, especially when the aggregated effects of multiple causal variants are present. In this paper, we propose a fast and effective algorithm coupling with high-dimensional test for simultaneously detecting multiple signal regions, which is distinct from existing methods using scan or knockoff statistics. The idea is to conduct binary splitting with re-search and arrangement based on a sequence of dynamic critical values to increase detection accuracy and reduce computation. Theoretical and empirical studies demonstrate that our approach enjoys favorable theoretical guarantees with fewer restrictions and exhibits superior numerical performance with faster computation. Utilizing the UK Biobank data to identify the genetic regions related to breast cancer, we confirm previous findings and meanwhile, identify a number of new regions that suggest strong associations with risk of breast cancer and deserve further investigation. Supplementary materials for this article are available online, including a standardized description of the materials available for reproducing the work.

笔记与分组
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