ArticleJournal of cheminformatics2016
Filtered circular fingerprints improve either prediction or runtime performance while retaining interpretability.
Article in Journal of cheminformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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Who cites it
15 citing papers in PubMed.
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- De Novo Structure Prediction from Tandem Mass Spectra: Algorithms, Benchmarks, and Limitations.Molecules (Basel, Switzerland) · 2026Review
- Machine Learning for Toxicity Prediction Using Chemical Structures: Pillars for Success in the Real World.Chemical research in toxicology · 2025Review
- Sort & Slice: a simple and superior alternative to hash-based folding for extended-connectivity fingerprints.Journal of cheminformatics · 2024Article
- Artificial intelligence in antidiabetic drug discovery: The advances in QSAR and the prediction of α-glucosidase inhibitors.Computational and structural biotechnology journal · 2024Review
- Article
- A chemical structure and machine learning approach to assess the potential bioactivity of endogenous metabolites and their association with early-childhood hs-CRP levels.bioRxiv : the preprint server for biology · 2023Article
- Feature Selection for the Interpretation of Antioxidant Mechanisms in Plant Phenolics.Molecules (Basel, Switzerland) · 2023Article
- Hyper-Mol: Molecular Representation Learning via Fingerprint-Based Hypergraph.Computational intelligence and neuroscience · 2023Article
- Towards the prediction of non-peptidic epitopes.PLoS computational biology · 2022Article
- Should We Embed in Chemistry? A Comparison of Unsupervised Transfer Learning with PCA, UMAP, and VAE on Molecular Fingerprints.Pharmaceuticals (Basel, Switzerland) · 2021Article
- Predictive Capability of QSAR Models Based on the CompTox Zebrafish Embryo Assays: An Imbalanced Classification Problem.Molecules (Basel, Switzerland) · 2021Article
- Machine learning on drug-specific data to predict small molecule teratogenicity.Reproductive toxicology (Elmsford, N.Y.) · 2020Article
- Revealing cytotoxic substructures in molecules using deep learning.Journal of computer-aided molecular design · 2020Article
- Applications of machine learning in drug discovery and development.Nature reviews. Drug discovery · 2019Review
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2 authors.
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Abstract
backgroundEven though circular fingerprints have been first introduced more than 50 years ago, they are still widely used for building highly predictive, state-of-the-art (Q)SAR models. Historically, these structural fragments were designed to search large molecular databases. Hence, to derive a compact representation, circular fingerprint fragments are often folded to comparatively short bit-strings. However, folding fingerprints introduces bit collisions, and therefore adds noise to the encoded structural information and removes its interpretability. Both representations, folded as well as unprocessed fingerprints, are often used for (Q)SAR modeling.
resultsWe show that it can be preferable to build (Q)SAR models with circular fingerprint fragments that have been filtered by supervised feature selection, instead of applying folded or all fragments. Compared to folded fingerprints, filtered fingerprints significantly increase predictive performance and remain unambiguous and interpretable. Compared to unprocessed fingerprints, filtered fingerprints reduce the computational effort and are a more compact and less redundant feature representation. Depending on the selected learning algorithm filtering yields about equally predictive (Q)SAR models. We demonstrate the suitability of filtered fingerprints for (Q)SAR modeling by presenting our freely available web service Collision-free Filtered Circular Fingerprints that provides rationales for predictions by highlighting important structural features in the query compound (see http://coffer.informatik.uni-mainz.de).
conclusionsCircular fingerprints are potent structural features that yield highly predictive models and encode interpretable structural information. However, to not lose interpretability, circular fingerprints should not be folded when building prediction models. Our experiments show that filtering is a suitable option to reduce the high computational effort when working with all fingerprint fragments. Additionally, our experiments suggest that the area under precision recall curve is a more sensible statistic for validating (Q)SAR models for virtual screening than the area under ROC or other measures for early recognition. GRAPHICAL ABSTRACT:
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