Quality Control and Robust Estimation for cDNA Microarrays With Replicates
含重复测量的 cDNA 微阵列:质量控制与稳健估计AI 解读 ↓
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。
AI 根据所提供的论文材料归类:摘要讨论基因表达测量的稳健估计与质量控制,未涉及所列经济或金融细分方向。
含重复测量的 cDNA 微阵列:质量控制与稳健估计AI 解读 ↓
正在核对关联版本…
正在核对对应版本的资源…
We consider robust estimation of gene intensities from cDNA microarray data with replicates. Several statistical methods for estimating gene intensities from microarrays have been proposed, but little work has been done on robust estimation. This is particularly relevant for experiments with replicates, because even one outlying replicate can have a disastrous effect on the estimated intensity for the gene concerned. Because of the many steps involved in the experimental process from hybridization to image analysis, cDNA microarray data often contain outliers. For example, an outlying data value could occur because of scratches or dust on the surface, imperfections in the glass, or imperfections in the array production. We develop a Bayesian hierarchical model for robust estimation of cDNA microarray intensities. Outliers are modeled explicitly using a t-distribution, and our model also addresses such classical issues as design effects, normalization, transformation, and nonconstant variance. Parameter estimation is carried out using Markov chain Monte Carlo. By identifying potential outliers, the method provides automatic quality control of replicate, array, and gene measurements. The method is applied to three publicly available gene expression datasets and compared with three other methods: ANOVA-normalized log ratios, the median log ratio, and estimation after the removal of outliers based on Dixon's test. We find that the between-replicate variability of the intensity estimates is lower for our method than for any of the others. We also address the issue of whether the background should be subtracted when estimating intensities. It has been argued that this should not be done because it increases variability, whereas the arguments for doing so are that there is a physical basis for the image background, and that not doing so will bias downward the estimated log ratios of differentially expressed genes. We show that the arguments on both sides of this debate are correct for our data, but that by using our model one can have the best of both worlds: One can subtract the background without increasing variability by much.