DESeq2-MultiBatch: batch correction for multi-factorial RNA-seq experiments.

IF 1.9 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Genome Pub Date : 2026-01-01 DOI:10.1139/gen-2025-0049
Julien Roy, Adrian S Monthony, Davoud Torkamaneh
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引用次数: 0

Abstract

RNA sequencing experiments frequently encounter batch effects that can significantly distort biological interpretations, particularly in complex, multi-factorial studies where biological variables interact with experimental batch conditions. Existing batch correction tools primarily address technical variability and often neglect these critical interaction effects, resulting in incomplete adjustments. To address this gap, we introduce DESeq2-MultiBatch, a novel, lightweight batch correction method implemented entirely within the DESeq2 analytical framework. Unlike conventional approaches, DESeq2-MultiBatch directly leverages DESeq2's internal model estimates to correct raw gene count data from experimental batch effects, including interactions with biological variables. Here, we demonstrate that DESeq2-MultiBatch effectively remove batch-related variability while retaining the effects of other factors, allowing the method to be used as a robust, practical solution for improving exploratory data visualization and downstream analyses in multi-factorial RNA-seq studies.

DESeq2-MultiBatch:多因子RNA-seq实验的批量校正。
RNA测序实验经常会遇到批效应,这可能会严重扭曲生物学解释,特别是在复杂的多因素研究中,生物变量与实验批条件相互作用。现有的批量校正工具主要处理技术可变性,经常忽略这些关键的相互作用,导致调整不完整。为了解决这一差距,我们引入了DESeq2- multibatch,这是一种完全在DESeq2分析框架内实现的新型轻量级批处理校正方法。与传统方法不同,DESeq2- multibatch直接利用DESeq2的内部模型估计来纠正来自实验批效应的原始基因计数数据,包括与生物变量的相互作用。在这里,我们证明了DESeq2-MultiBatch有效地消除了批次相关的可变性,同时保留了其他因素的影响,使该方法成为一种强大的、实用的解决方案,可用于改善多因子RNA-seq研究中的探索性数据可视化和下游分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genome
Genome 生物-生物工程与应用微生物
CiteScore
5.30
自引率
3.20%
发文量
42
审稿时长
6-12 weeks
期刊介绍: Genome is a monthly journal, established in 1959, that publishes original research articles, reviews, mini-reviews, current opinions, and commentaries. Areas of interest include general genetics and genomics, cytogenetics, molecular and evolutionary genetics, developmental genetics, population genetics, phylogenomics, molecular identification, as well as emerging areas such as ecological, comparative, and functional genomics.
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