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Deep cell phenotyping and spatial analysis of multiplexed imaging with TRACERx-PHLEX.

Authors :
Magness, Alastair
Colliver, Emma
Enfield, Katey S. S.
Lee, Claudia
Shimato, Masako
Daly, Emer
Moore, David A.
Sivakumar, Monica
Valand, Karishma
Levi, Dina
Hiley, Crispin T.
Hobson, Philip S.
van Maldegem, Febe
Reading, James L.
Quezada, Sergio A.
Downward, Julian
Sahai, Erik
Swanton, Charles
Angelova, Mihaela
Source :
Nature Communications; 6/15/2024, Vol. 15 Issue 1, p1-20, 20p
Publication Year :
2024

Abstract

The growing scale and dimensionality of multiplexed imaging require reproducible and comprehensive yet user-friendly computational pipelines. TRACERx-PHLEX performs deep learning-based cell segmentation (deep-imcyto), automated cell-type annotation (TYPEx) and interpretable spatial analysis (Spatial-PHLEX) as three independent but interoperable modules. PHLEX generates single-cell identities, cell densities within tissue compartments, marker positivity calls and spatial metrics such as cellular barrier scores, along with summary graphs and spatial visualisations. PHLEX was developed using imaging mass cytometry (IMC) in the TRACERx study, validated using published Co-detection by indexing (CODEX), IMC and orthogonal data and benchmarked against state-of-the-art approaches. We evaluated its use on different tissue types, tissue fixation conditions, image sizes and antibody panels. As PHLEX is an automated and containerised Nextflow pipeline, manual assessment, programming skills or pathology expertise are not essential. PHLEX offers an end-to-end solution in a growing field of highly multiplexed data and provides clinically relevant insights. Imaging dozens of proteins in situ and at large scales increases the complexity of data analysis. Here, the authors develop an end-to-end solution for multiplexed image analysis that facilitates data interpretation for clinically relevant insights. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
15
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
177992249
Full Text :
https://doi.org/10.1038/s41467-024-48870-5