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Learning 3D biophysical cell properties from 2D images and cell-population statistics

Summary

A population-supervised framework infers latent biophysical quantities from single 2D red-blood-cell images and aggregates them into mean corpuscular volume, red-cell distribution width, and mean corpuscular haemoglobin, using shared local inference, a structured decoder, learned instance weighting, and device calibration. Evaluated on 390 specimens and 1,105 acquisitions across six devices, it reports Pearson correlations of 0.86–0.98 against a Sysmex analyser. The authors also formalise identifiability limits: population agreement alone does not identify single-cell properties or 3D geometry.

SourcearXiv AIAuthor: Santiago Hern\'andez-Orozco, Hector Zenil
Learning 3D biophysical cell properties from 2D images and cell-population statistics
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[Submitted on 18 Sep 2026]

Title:Learning 3D biophysical cell properties from 2D images and cell-population statistics

View a PDF of the paper titled Learning 3D biophysical cell properties from 2D images and cell-population statistics, by Santiago Hern\'andez-Orozco and 1 other authors

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Abstract:Inferring 3D cellular properties from 2D microscopy is difficult when a reference instrument reports only population statistics rather than labels for individual cells. Here we develop a population-supervised framework that maps single 2D red-cell images to latent biophysical quantities and aggregates them to mean corpuscular volume, red-cell distribution width and mean corpuscular haemoglobin. The model combines shared local inference, a biophysically structured decoder for volume and haemoglobin, learned instance weighting and device-specific calibration. We formalise conditions under which aggregate observations identify restricted instance predictors, show why population agreement does not by itself identify single-cell properties or 3D geometry, and derive the dispersion penalty induced by subset mean matching. The development dataset comprises 390 specimens and 1,105 acquisitions across six devices, with reported Pearson correlations of 0.86--0.98 against a Sysmex analyser. The framework provides a testable route from 2D images and population supervision to 3D cellular biophysics without claiming explicit 3D reconstruction.

Subjects:

Artificial Intelligence (cs.AI)

Cite as: arXiv:2609.22410 [cs.AI]

(or arXiv:2609.22410v1 [cs.AI] for this version)

https://doi.org/10.48550/arXiv.2609.22410

arXiv-issued DOI via DataCite (pending registration)

Submission history

From: Hector Zenil [view email] [v1] Fri, 18 Sep 2026 16:34:46 UTC (80 KB)

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Key points

  • Maps single 2D red-cell images to latent biophysical quantities and aggregates them to MCV, RDW, and MCH.
  • Combines shared local inference, a biophysically structured decoder for volume and haemoglobin, learned instance weighting, and device-specific calibration.
  • Formalises when aggregate observations identify restricted instance predictors and derives a dispersion penalty from subset mean matching.
  • Achieves Pearson correlations of 0.86–0.98 on 390 specimens and 1,105 acquisitions across six devices, without claiming explicit 3D reconstruction.

Highlights and analysis are generated automatically and may contain errors. Check the original source.