RESTORE: Robust intEnSiTy nORmalization mEthod for Multiplexed Imaging
Young Hwan ChangiD, Koei ChiniD, Guillaume ThibaultiD, Jennifer R. EngiD, Erik A. BurlingameiD, Joe W. GrayiD
Abstract
Recent advances in multiplexed imaging technologies promise to improve the understanding of the functional states of individual cells and the interactions between the cells in tissues. This often requires compilation of results from multiple samples. However, quantitative integration of information between samples is complicated by variations in staining intensity and background fluorescence that obscure biological variations. Failure to remove these unwanted artefacts will complicate downstream analysis and diminish the value of multiplexed imaging for clinical applications. Here, to compensate for unwanted variations, we automatically identify negative control cells for each marker within the same tissue and use their expression levels to infer background signal level. The intensity profile is normalized by the inferred level of the negative control cells to remove between-sample variation. Using a tissue microarray data and a pair of longitudinal biopsies sample, we demonstrated that the proposed approach can remove unwanted variations effectively and shows robust performance.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 31
- FWCI
- 2.50
- Field percentile
- top 10%
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Quantifying and correcting slide-to-slide variation in multiplexed immunofluorescence images
Coleman R. Harris, Eliot T. McKinley, … Simon Vandekar·BioinformaticsPeer-reviewed·Dec 31, 2021
- UniFORM: Towards Universal Immunofluorescence Normalization for Multiplex Tissue Imaging
Kunlun Wang, Kaoutar Ait-Ahmad, … Young Hwan Chang·Cell Reports MethodsPeer-reviewed·Sep 1, 2025
- Semi-automated background removal limits loss of data and normalises the images for downstream analysis of imaging mass cytometry data
M. E. Ijsselsteijn, A. Somarakis, … N. F. C. C. de Miranda·bioRxiv·Nov 26, 2020
- IMC-Denoise: a content aware denoising pipeline to enhance Imaging Mass Cytometry
Peng Lu, Karolyn A. Oetjen, … Daniel L.J. Thorek·Nature CommunicationsPeer-reviewed·Mar 23, 2023
- bgnorm: A Generative Statistical Framework for Background Correction, Normalisation, and Quality Control in Multiplex Spatial Proteomics
Malvika Kharbanda, Rafael Tubelleza, … Dharmesh Dinesh Bhuva·bioRxiv·Aug 11, 2026
- A Platform-Independent Framework for Phenotyping of Multiplex Tissue Imaging Data
Mansooreh Ahmadian, Christian Rickert, … Kimberly Rae Jordan·PLoS Computational BiologyPeer-reviewed·Sep 21, 2023