Evidence map›Paper›PMID 40450059›Full record

ArticleScientific reports2025

Generative inpainting of incomplete Euclidean distance matrices of trajectories generated by a fractional Brownian motion.

Alexander Lobashev, Dmitry Guskov, Kirill Polovnikov

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Alexander LobashevSkolkovo Institute of Science and Technology, Moscow, Russia.
Dmitry GuskovSkolkovo Institute of Science and Technology, Moscow, Russia.
Kirill PolovnikovSkolkovo Institute of Science and Technology, Moscow, Russia. kipolovnikov@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fractional Brownian motion (fBm) exhibits both randomness and strong scale-free correlations, posing a challenge for generative artificial intelligence to replicate the underlying stochastic process. In this study, we evaluate the performance of diffusion-based inpainting methods on a specific dataset of corrupted images, which represent incomplete Euclidean distance matrices (EDMs) of fBm across various memory exponents (H). Our dataset reveals that, in the regime of low missing ratios, data imputation is unique, as the remaining partial graph is rigid, thus providing a reliable ground truth for inpainting. We find that conditional diffusion generation effectively reproduces the inherent correlations of fBm paths across different memory regimes, including sub-diffusion, Brownian motion, and super-diffusion trajectories, making it a robust tool for statistical imputation in cases with high missing ratios. Moreover, while recent studies have suggested that diffusion models memorize samples from the training dataset, our findings indicate that diffusion behaves qualitatively differently from simple database searches, allowing for generalization rather than mere memorization of the training data. As a biological application, we utilize our fBm-trained diffusion model to impute microscopy-derived distance matrices of chromosomal segments (FISH data), which are incomplete due to experimental imperfections. We demonstrate that our inpainting method outperforms standard bioinformatic methods, suggesting a novel physics-informed generative approach for the enrichment of high-throughput biological datasets.

Identifiers

PMID40450059
PMCPMC12126505

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.