Coverage bias in small molecule machine learning

Small molecule machine learning aims to predict chemical, biochemical, or biological properties from molecular structures, with applications such as toxicity prediction, ligand binding, and pharmacokinetics. A recent trend is developing end-to-end models that avoid explicit domain knowledge. These models assume no coverage bias in training and evaluation data, meaning the data are representative of the true distribution. However, the domain of applicability is rarely considered in such models. Here, we investigate how well large-scale datasets cover the space of known biomolecular structures. For doing so, we propose a distance measure based on solving the Maximum Common Edge Subgraph (MCES) problem, which aligns well with chemical similarity. Although this method is computationally hard, we introduce an efficient approach combining Integer Linear Programming and heuristic bounds. Our findings reveal that many widely-used datasets lack uniform coverage of biomolecular structures, limiting the predictive power of models trained on them. We propose two additional methods to assess whether training datasets diverge from known molecular distributions, potentially guiding future dataset creation to improve model performance.

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Publication Details

Journal
Nature Communications
Published
2025-01-09
DOI
https://doi.org/10.1038/s41467-024-55462-w
Citations
29
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
45.13

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article

Coverage bias in small molecule machine learning

Gunnar W. Klau, Sebastian Böcker, Fleming Kretschmer, Jan Seipp et al.
29 citations
Nature Communications
Computational Drug Discovery Methods
45.13
article

Coverage bias in small molecule machine learning

Gunnar W. Klau, Sebastian Böcker, Fleming Kretschmer, Jan Seipp, Marcus Ludwig
article en
29 citations

Abstract

Small molecule machine learning aims to predict chemical, biochemical, or biological properties from molecular structures, with applications such as toxicity prediction, ligand binding, and pharmacokinetics. A recent trend is developing end-to-end models that avoid explicit domain knowledge. These models assume no coverage bias in training and evaluation data, meaning the data are representative of the true distribution. However, the domain of applicability is rarely considered in such models. Here, we investigate how well large-scale datasets cover the space of known biomolecular structures. For doing so, we propose a distance measure based on solving the Maximum Common Edge Subgraph (MCES) problem, which aligns well with chemical similarity. Although this method is computationally hard, we introduce an efficient approach combining Integer Linear Programming and heuristic bounds. Our findings reveal that many widely-used datasets lack uniform coverage of biomolecular structures, limiting the predictive power of models trained on them. We propose two additional methods to assess whether training datasets diverge from known molecular distributions, potentially guiding future dataset creation to improve model performance.

Nature CommunicationsVol. 16(1)
Heinrich Heine University Düsseldorf (DE), Friedrich Schiller University Jena (DE)
Deutsche Forschungsgemeinschaft, Thüringer Ministerium für Wirtschaft, Wissenschaft und Digitale Gesellschaft
Openalex Percentile: Top 0%
Computational Drug Discovery Methods
45.13
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