使用经验贝叶斯方法(BRIDGE)减少具有依赖性样本的微阵列数据的批次效应。

IF 0.9 4区 数学 Q3 Mathematics Statistical Applications in Genetics and Molecular Biology Pub Date : 2021-12-14 DOI:10.1515/sagmb-2021-0020
Qing Xia, Jeffrey A Thompson, Devin C Koestler
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引用次数: 0

摘要

批次效应给高通量分子数据分析带来了挑战,尤其是在纵向研究中,当研究兴趣在于识别表达随时间变化的基因/特征,但时间与批次混淆时,批次效应更是问题重重。虽然有很多方法可以校正批次效应,但大多数方法都假设不同样本之间是独立的,而这一假设在纵向微阵列研究中不太可能成立。我们提出了使用经验贝叶斯降低依赖样本的微阵列数据批次效应(BRIDGE),这是一种三步参数经验贝叶斯方法,它利用在多个时间点/批次剖析的技术复制样本(即所谓的 "桥样本"),为纵向微阵列研究中批次效应的降低/减弱提供信息。我们进行了广泛的模拟研究和对真实生物数据集的分析,以对照 ComBat 和 longitudinalComBat 对 BRIDGE 的性能进行基准测试。我们的结果表明,虽然所有方法都能很好地促进时间效应的准确估计,但 BRIDGE 在消除具有桥接样本的数据集中的批次效应方面优于 ComBat 和纵向 ComBat,因此,在检测具有时间效应的基因方面,BRIDGE 的统计能力也得到了提高。无论是在模拟数据集还是真实数据集中,BRIDGE 在减少纵向微阵列研究中的批次效应方面都表现出了很强的竞争力,可以作为研究人员进行包含桥接样本的纵向微阵列研究的一种有用的预处理方法。
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Batch effect reduction of microarray data with dependent samples using an empirical Bayes approach (BRIDGE).

Batch-effects present challenges in the analysis of high-throughput molecular data and are particularly problematic in longitudinal studies when interest lies in identifying genes/features whose expression changes over time, but time is confounded with batch. While many methods to correct for batch-effects exist, most assume independence across samples; an assumption that is unlikely to hold in longitudinal microarray studies. We propose Batch effect Reduction of mIcroarray data with Dependent samples usinGEmpirical Bayes (BRIDGE), a three-step parametric empirical Bayes approach that leverages technical replicate samples profiled at multiple timepoints/batches, so-called "bridge samples", to inform batch-effect reduction/attenuation in longitudinal microarray studies. Extensive simulation studies and an analysis of a real biological data set were conducted to benchmark the performance of BRIDGE against both ComBat and longitudinalComBat. Our results demonstrate that while all methods perform well in facilitating accurate estimates of time effects, BRIDGE outperforms both ComBat and longitudinal ComBat in the removal of batch-effects in data sets with bridging samples, and perhaps as a result, was observed to have improved statistical power for detecting genes with a time effect. BRIDGE demonstrated competitive performance in batch effect reduction of confounded longitudinal microarray studies, both in simulated and a real data sets, and may serve as a useful preprocessing method for researchers conducting longitudinal microarray studies that include bridging samples.

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来源期刊
CiteScore
1.20
自引率
11.10%
发文量
8
审稿时长
6-12 weeks
期刊介绍: Statistical Applications in Genetics and Molecular Biology seeks to publish significant research on the application of statistical ideas to problems arising from computational biology. The focus of the papers should be on the relevant statistical issues but should contain a succinct description of the relevant biological problem being considered. The range of topics is wide and will include topics such as linkage mapping, association studies, gene finding and sequence alignment, protein structure prediction, design and analysis of microarray data, molecular evolution and phylogenetic trees, DNA topology, and data base search strategies. Both original research and review articles will be warmly received.
期刊最新文献
Empirically adjusted fixed-effects meta-analysis methods in genomic studies. A CNN-CBAM-BIGRU model for protein function prediction. A heavy-tailed model for analyzing miRNA-seq raw read counts. Flexible model-based non-negative matrix factorization with application to mutational signatures. Choice of baseline hazards in joint modeling of longitudinal and time-to-event cancer survival data.
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