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:摘要聚焦基因表达实验的序贯样本量设计,中位数作为参数不足以归入经济分位数与分布效应。

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
Gilles Durrieu
Laurent Briollais

微阵列实验的序贯设计

研究问题
研究微阵列实验如何根据累积数据决定样本量,在获得足以识别不同实验条件下基因表达变化的信息时停止采样。
方法与思路
作者用稳健线性回归描述基因表达,为代表给定条件下表达中位数的截距构造序贯置信区间,并推导两类停止规则。
材料陈述的贡献
摘要称给出了连续与离散序贯方案停止变量的渐近性质及理论、数值验证,乳腺癌细胞系应用提示所需样本可更少。
阅读关注点
应核对置信区间的序贯覆盖性质、停止精度标准、多基因比较的处理,以及应用中的样本减少如何保持评估准确性。
阅读边界
依据版本未注明的 OpenAlex 索引摘要;未给出精度标准、有限样本保证或具体节省幅度,不能外推成本优势或推断刊本变化。

原文摘要

This article features online supplementary material.A critical aspect in the design of microarray studies is the determination of the sample size necessary to declare genes differentially expressed across different experimental conditions. In this article, we propose a sequential approach where the decision to stop the experiment depends on the accumulated microarray data. The study could stop whenever sufficient data have been accumulated to identify gene expression changes across several experimental conditions. The gene expression response is modeled by a robust linear regression model. We then construct a sequential confidence interval for the intercept of this model, which represents the median gene expression at a given experimental condition. We derive the stopping rule of the experiment for both continuous and discrete sequential approaches and give the asymptotic properties of the stopping variable. We demonstrate the desirable properties of our sequential approach, both theoretically and numerically. In our application to a study of hormone responsive breast cancer cell lines, we estimated the stopping variable for the sample size determination to be smaller than the actual sample size available to conduct the experiment. This means that we can obtain an accurate assessment of differential gene expression without compromising the cost and size of the study. Altogether, we anticipate that this approach could have an important contribution to microarray studies by improving the usual experimental designs and methods of analysis.

笔记与分组
相关领域论文