{"title":"<i>pwrBRIDGE</i>: a user-friendly web application for power and sample size estimation in batch-confounded microarray studies with dependent samples.","authors":"Qing Xia, Jeffrey A Thompson, Devin C Koestler","doi":"10.1515/sagmb-2022-0003","DOIUrl":null,"url":null,"abstract":"<p><p><u>B</u>atch effect <u>R</u>eduction of m<u>I</u>croarray data with <u>D</u>ependent samples usin<u>G</u> <u>E</u>mpirical Bayes (<i>BRIDGE</i>) is a recently developed statistical method to address the issue of batch effect correction in batch-confounded microarray studies with dependent samples. The key component of the <i>BRIDGE</i> methodology is the use of samples run as technical replicates in two or more batches, \"bridging samples\", to inform batch effect correction/attenuation. While previously published results indicate a relationship between the number of bridging samples, <i>M</i>, and the statistical power of downstream statistical testing on the batch-corrected data, there is of yet no formal statistical framework or user-friendly software, for estimating <i>M</i> to achieve a specific statistical power for hypothesis tests conducted on the batch-corrected data. To fill this gap, we developed <i>pwrBRIDGE</i>, a simulation-based approach to estimate the bridging sample size, <i>M</i>, in batch-confounded longitudinal microarray studies. To illustrate the use of <i>pwrBRIDGE</i>, we consider a hypothetical, longitudinal batch-confounded study whose goal is to identify Alzheimer's disease (AD) progression-associated genes from amnestic mild cognitive impairment (aMCI) to AD in human blood after a 5-year follow-up. <i>pwrBRIDGE</i> helps researchers design and plan batch-confounded microarray studies with dependent samples to avoid over- or under-powered studies.</p>","PeriodicalId":49477,"journal":{"name":"Statistical Applications in Genetics and Molecular Biology","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2022-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550194/pdf/sagmb-21-1-sagmb-2022-0003.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Statistical Applications in Genetics and Molecular Biology","FirstCategoryId":"100","ListUrlMain":"https://doi.org/10.1515/sagmb-2022-0003","RegionNum":4,"RegionCategory":"数学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Mathematics","Score":null,"Total":0}
引用次数: 0
Abstract
Batch effect Reduction of mIcroarray data with Dependent samples usinGEmpirical Bayes (BRIDGE) is a recently developed statistical method to address the issue of batch effect correction in batch-confounded microarray studies with dependent samples. The key component of the BRIDGE methodology is the use of samples run as technical replicates in two or more batches, "bridging samples", to inform batch effect correction/attenuation. While previously published results indicate a relationship between the number of bridging samples, M, and the statistical power of downstream statistical testing on the batch-corrected data, there is of yet no formal statistical framework or user-friendly software, for estimating M to achieve a specific statistical power for hypothesis tests conducted on the batch-corrected data. To fill this gap, we developed pwrBRIDGE, a simulation-based approach to estimate the bridging sample size, M, in batch-confounded longitudinal microarray studies. To illustrate the use of pwrBRIDGE, we consider a hypothetical, longitudinal batch-confounded study whose goal is to identify Alzheimer's disease (AD) progression-associated genes from amnestic mild cognitive impairment (aMCI) to AD in human blood after a 5-year follow-up. pwrBRIDGE helps researchers design and plan batch-confounded microarray studies with dependent samples to avoid over- or under-powered studies.
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.