CompensAID: An Automated Detection Tool for Reference Errors

IF 2.9 4区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS
Cytometry Part A Pub Date : 2026-03-18 Epub Date: 2026-02-23 DOI:10.1002/cyto.a.70016
Rosan Olsman, Sarah Bonte, Mattias Hofmans, Malicorne Buysse, Katrien Van der Borght, Yvan Saeys, Vincent H. J. van der Velden, Sofie Van Gassen
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引用次数: 0

Abstract

In flow cytometry, raw detector values do not directly represent fluorochrome abundances and must be mathematically unmixed using coefficients derived from single-stained reference controls. Inaccuracies in these controls, referred to as reference errors, can distort the estimated fluorochrome abundances, leading to skewed population distributions. However, as panel complexity and dataset sizes increase, manually inspecting all marker combinations for such artifacts becomes impractical. To address this challenge, we developed CompensAID, an open-source R-based tool that automatically flags marker combinations potentially affected by reference errors, thereby supporting quality control workflows in flow cytometry. Preprocessed data from both conventional and spectral flow cytometry were used to develop and validate the tool. CompensAID applies a density-based cutoff detection to automatically gate the negative and positive populations. The positive population is then divided into equally sized segments, after which the Secondary Stain Index (SSI) is computed for each segment. Marker combinations are flagged if the last segment yields an SSI value below −1. The tool's performance was evaluated against the consensus of five flow cytometry specialists. For the conventional dataset, 1761 out of 2240 marker combinations (79%) were unanimously classified as free of reference errors, while 24 marker combinations received a consensus score of three or higher, indicating that most flow cytometry specialists suspected reference errors. CompensAID successfully identified 23 out of these 24 marker combinations, achieving a sensitivity of 0.96. The single missed case involved a spillover spread error. In the spectral dataset, 1505 out of 1656 marker combinations (90%) were deemed free of reference errors. Of the 28 marker combinations suspected of reference errors, CompensAID flagged 21 marker combinations (sensitivity, 0.74). Five out of the seven missed marker combinations had SSI values close to the threshold. In both datasets, false positive findings were observed, often attributable to suboptimal gating or low event counts within the segments contributing to negative SSI values. CompensAID offers a robust approach for detecting marker combinations exhibiting signs of reference errors. While some false positives occur, the tool significantly reduces the burden of manual inspection. Its integration into quality control pipelines can enhance the reliability of flow cytometry data analysis. The R package is available at https://github.com/Olsman/CompensAID and will be made available through the Bioconductor platform.

Abstract Image

CompensAID:参考错误的自动检测工具。
在流式细胞术中,原始检测器值不能直接表示荧光色素丰度,必须使用从单染色参考对照中导出的系数在数学上不混合。这些控制的不准确性(称为参考误差)可能扭曲估计的荧光丰度,导致种群分布偏斜。然而,随着面板复杂性和数据集大小的增加,手动检查这些工件的所有标记组合变得不切实际。为了应对这一挑战,我们开发了CompensAID,这是一个基于r的开源工具,可以自动标记可能受参考错误影响的标记组合,从而支持流式细胞术中的质量控制工作流程。使用常规流式细胞术和光谱流式细胞术的预处理数据来开发和验证该工具。CompensAID应用基于密度的截止检测来自动屏蔽阴性和阳性种群。然后将阳性群体分成大小相等的片段,然后计算每个片段的次级染色指数(SSI)。如果最后一个片段的SSI值低于-1,则标记组合。该工具的性能是根据五位流式细胞术专家的共识进行评估的。对于传统数据集,2240个标记组合中有1761个(79%)被一致归类为无参考错误,而24个标记组合获得了3分或更高的共识得分,这表明大多数流式细胞术专家怀疑存在参考错误。CompensAID成功鉴定了这24个标记组合中的23个,灵敏度为0.96。唯一的遗漏案例涉及溢出传播错误。在光谱数据集中,1656个标记组合中有1505个(90%)被认为没有参考误差。在28个疑似参比错误的标记组合中,CompensAID标记了21个标记组合(敏感性,0.74)。7个缺失标记组合中有5个的SSI值接近阈值。在这两个数据集中,观察到假阳性结果,通常可归因于次优门控或导致负SSI值的片段内低事件计数。CompensAID提供了一种强大的方法来检测显示参考错误迹象的标记组合。虽然会出现一些误报,但该工具显著减少了人工检查的负担。将其集成到质量控制管道中,可以提高流式细胞术数据分析的可靠性。R包可在https://github.com/Olsman/CompensAID上获得,并将通过Bioconductor平台提供。
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
Cytometry Part A
Cytometry Part A 生物-生化研究方法
CiteScore
8.10
自引率
13.50%
发文量
183
审稿时长
4-8 weeks
期刊介绍: Cytometry Part A, the journal of quantitative single-cell analysis, features original research reports and reviews of innovative scientific studies employing quantitative single-cell measurement, separation, manipulation, and modeling techniques, as well as original articles on mechanisms of molecular and cellular functions obtained by cytometry techniques. The journal welcomes submissions from multiple research fields that fully embrace the study of the cytome: Biomedical Instrumentation Engineering Biophotonics Bioinformatics Cell Biology Computational Biology Data Science Immunology Parasitology Microbiology Neuroscience Cancer Stem Cells Tissue Regeneration.
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