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Self-organizing neural network-based generative AI with embedded error inflation control enhances effective knowledge

Jörn Lötsch1, Benjamin Mayer2, Natasja de Bruin3

  • 1Institute of Clinical Pharmacology, Goethe - University, Theodor Stern Kai 7, Frankfurt am Main 60590, Germany; Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Theodor-Stern-Kai 7, Frankfurt am Main 60596, Germany; University of Helsinki, Faculty of Medicine, Helsinki 00014, Finland.

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Summary

Generative artificial intelligence (AI) method genESOM augments small preclinical datasets, enhancing knowledge extraction from limited samples. This AI approach controls errors and supports exploratory analyses, potentially reducing animal experimentation.

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And animal models and ethicsData scienceGenerative AIPreclinical research

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Area of Science:

  • Biomedical research
  • Artificial intelligence
  • Data science

Background:

  • Small sample sizes in preclinical studies limit reliable knowledge extraction and translational progress.
  • Current methods struggle to augment limited biomedical data effectively while controlling statistical errors.

Purpose of the Study:

  • To introduce genESOM, a novel generative AI method for augmenting small biomedical datasets.
  • To demonstrate genESOM's ability to control alpha-error inflation and enable safe, interpretable data augmentation.
  • To evaluate genESOM's performance against other generative models using a preclinical multiple sclerosis dataset.

Main Methods:

  • Developed genESOM, a generative AI method based on emergent self-organizing maps, separating structure learning from data synthesis.
  • Integrated error propagation mitigation via dimensionality modulation for controlled data augmentation.
  • Applied genESOM to a reduced dataset (18 mice) from a preclinical EAE multiple sclerosis study (originally 26 mice, 62 lipid mediators).

Main Results:

  • Reducing sample size from 26 to 18 mice abolished detectable group differences in statistical and machine learning analyses.
  • Augmenting the reduced dataset with genESOM-generated cases restored treatment-specific segregation and identified key lipid mediators.
  • genESOM achieved high fidelity without false positives, outperforming Gaussian mixture and conditional GAN models under similar constraints.

Conclusions:

  • genESOM offers a robust, error-controlled framework for enhancing knowledge extraction from limited preclinical data.
  • AI-driven synthetic data augmentation can support exploratory analyses and potentially reduce the need for animal experimentation.
  • genESOM demonstrates a viable strategy for overcoming data limitations in preclinical research.