BatchFLEX: feature-level equalization of X-batch

Motivation Integrative analysis of heterogeneous expression data remains challenging due to variations in platform, RNA quality, sample processing, and other unknown technical effects. Selecting the approach for removing unwanted batch effects can be a time-consuming and tedious process, especially...

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Published inBioinformatics (Oxford, England) Vol. 40; no. 10
Main Authors Davis, Joshua T, Obermayer, Alyssa N, Soupir, Alex C, Hesterberg, Rebecca S, Duong, Thac, Yang, Ching-Yao, Dao, Ken Phong, Manley, Brandon J, Grass, G Daniel, Avram, Dorina, Rodriguez, Paulo C, Fridley, Brooke L, Yu, Xiaoqing, Teng, Mingxiang, Wang, Xuefeng, Shaw, Timothy I
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.10.2024
Oxford Publishing Limited (England)
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Summary:Motivation Integrative analysis of heterogeneous expression data remains challenging due to variations in platform, RNA quality, sample processing, and other unknown technical effects. Selecting the approach for removing unwanted batch effects can be a time-consuming and tedious process, especially for more biologically focused investigators. Results Here, we present BatchFLEX, a Shiny app that can facilitate visualization and correction of batch effects using several established methods. BatchFLEX can visualize the variance contribution of a factor before and after correction. As an example, we have analyzed ImmGen microarray data and enhanced its expression signals that distinguishes each immune cell type. Moreover, our analysis revealed the impact of the batch correction in altering the gene expression rank and single-sample GSEA pathway scores in immune cell types, highlighting the importance of real-time assessment of the batch correction for optimal downstream analysis. Availability and implementation Our tool is available through Github https://github.com/shawlab-moffitt/BATCH-FLEX-ShinyApp with an online example on Shiny.io https://shawlab-moffitt.shinyapps.io/batch_flex/.
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Joshua T Davis and Alyssa N Obermayer equal contribution.
ISSN:1367-4811
1367-4803
1367-4811
DOI:10.1093/bioinformatics/btae587