A controlled in silico benchmark for GNN prediction of tissue dynamics

Abstract Graph Neural Networks (GNNs) are promising tools for predicting tissue dynamics, but choosing the right architecture remains difficult because experimental datasets are limited, noisy, and system-specific. We introduce a controlled in silico benchmark for comparing GNN architectures on a vertex-model task: predicting relaxed cell–cell interface lengths after a cell neighbor exchange. Because simulated data provide known ground truth, we can vary tissue geometry, mechanics, perturbation complexity, dataset size, and input features independently. Provably Powerful Graph Networks (PPGN) and Principal Neighborhood Aggregation (PNA) were most sample-efficient when pre-event edge lengths were provided, whereas performance dropped sharply with topology alone. We also revealed a predict-or-copy strategy, whereby predictions far from the exchange copied pre-event lengths instead of predicting long-range changes. Prediction was harder in disordered tissues, suggesting hexagonality as a simple indicator of difficulty. These results provide a reproducible testbed for diagnosing feature dependence, copying behavior, and geometric consistency in tissue-remodeling prediction.

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Publication Details

Journal
npj Systems Biology and Applications
Published
2026-08-13
DOI
https://doi.org/10.1038/s41540-026-00804-1
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00

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article

A controlled in silico benchmark for GNN prediction of tissue dynamics

Matej Krajnc, Siqi Miao, Hadar Serviansky, Tomer Stern et al.
npj Systems Biology and Applications
Single-cell and spatial transcriptomics
article

A controlled in silico benchmark for GNN prediction of tissue dynamics

Matej Krajnc, Siqi Miao, Hadar Serviansky, Tomer Stern, Adnan Hafeez, Troy Comi, Pan Li
article en

Abstract

Abstract Graph Neural Networks (GNNs) are promising tools for predicting tissue dynamics, but choosing the right architecture remains difficult because experimental datasets are limited, noisy, and system-specific. We introduce a controlled in silico benchmark for comparing GNN architectures on a vertex-model task: predicting relaxed cell–cell interface lengths after a cell neighbor exchange. Because simulated data provide known ground truth, we can vary tissue geometry, mechanics, perturbation complexity, dataset size, and input features independently. Provably Powerful Graph Networks (PPGN) and Principal Neighborhood Aggregation (PNA) were most sample-efficient when pre-event edge lengths were provided, whereas performance dropped sharply with topology alone. We also revealed a predict-or-copy strategy, whereby predictions far from the exchange copied pre-event lengths instead of predicting long-range changes. Prediction was harder in disordered tissues, suggesting hexagonality as a simple indicator of difficulty. These results provide a reproducible testbed for diagnosing feature dependence, copying behavior, and geometric consistency in tissue-remodeling prediction.

npj Systems Biology and Applications
Georgia Institute of Technology (US), Princeton University (US), University of Michigan (US), Jožef Stefan Institute (SI), Weizmann Institute of Science (IL)
National Science Foundation, Nvidia, Javna Agencija za Raziskovalno Dejavnost RS, Russian Science Foundation, National Institutes of Health, National Institute of General Medical Sciences
Openalex Percentile: Top 16%
Single-cell and spatial transcriptomics
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