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dc.contributor.authorBarratt, Jonathan
dc.date.accessioned2023-05-24T11:26:25Z
dc.date.available2023-05-24T11:26:25Z
dc.date.issued2023-01-28
dc.identifier.citationHölscher, D. L., Bouteldja, N., Joodaki, M., Russo, M. L., Lan, Y. C., Sadr, A. V., Cheng, M., Tesar, V., Stillfried, S. V., Klinkhammer, B. M., Barratt, J., Floege, J., Roberts, I. S. D., Coppo, R., Costa, I. G., Bülow, R. D., & Boor, P. (2023). Next-Generation Morphometry for pathomics-data mining in histopathology. Nature communications, 14(1), 470. https://doi.org/10.1038/s41467-023-36173-0en_US
dc.identifier.other10.1038/s41467-023-36173-0
dc.identifier.urihttp://hdl.handle.net/20.500.12904/17083
dc.description.abstractPathology diagnostics relies on the assessment of morphology by trained experts, which remains subjective and qualitative. Here we developed a framework for large-scale histomorphometry (FLASH) performing deep learning-based semantic segmentation and subsequent large-scale extraction of interpretable, quantitative, morphometric features in non-tumour kidney histology. We use two internal and three external, multi-centre cohorts to analyse over 1000 kidney biopsies and nephrectomies. By associating morphometric features with clinical parameters, we confirm previous concepts and reveal unexpected relations. We show that the extracted features are independent predictors of long-term clinical outcomes in IgA-nephropathy. We introduce single-structure morphometric analysis by applying techniques from single-cell transcriptomics, identifying distinct glomerular populations and morphometric phenotypes along a trajectory of disease progression. Our study provides a concept for Next-generation Morphometry (NGM), enabling comprehensive quantitative pathology data mining, i.e., pathomics.
dc.description.urihttps://www.nature.com/articles/s41467-023-36173-0en_US
dc.language.isoenen_US
dc.subjectBiomarkersen_US
dc.subjectKidneyen_US
dc.subjectRisk factorsen_US
dc.titleNext-generation morphometry for pathomics-data mining in histopathologyen_US
dc.typeArticleen_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
rioxxterms.versionNAen_US
rioxxterms.versionofrecordhttps://doi.org/10.1038/s41467-023-36173-0en_US
rioxxterms.typeJournal Article/Reviewen_US
refterms.panelUnspecifieden_US
html.description.abstractPathology diagnostics relies on the assessment of morphology by trained experts, which remains subjective and qualitative. Here we developed a framework for large-scale histomorphometry (FLASH) performing deep learning-based semantic segmentation and subsequent large-scale extraction of interpretable, quantitative, morphometric features in non-tumour kidney histology. We use two internal and three external, multi-centre cohorts to analyse over 1000 kidney biopsies and nephrectomies. By associating morphometric features with clinical parameters, we confirm previous concepts and reveal unexpected relations. We show that the extracted features are independent predictors of long-term clinical outcomes in IgA-nephropathy. We introduce single-structure morphometric analysis by applying techniques from single-cell transcriptomics, identifying distinct glomerular populations and morphometric phenotypes along a trajectory of disease progression. Our study provides a concept for Next-generation Morphometry (NGM), enabling comprehensive quantitative pathology data mining, i.e., pathomics.en_US
rioxxterms.funder.project94a427429a5bcfef7dd04c33360d80cden_US


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