Extended Activity Cliffs‐Driven Approaches on Data Splitting for the Study of Bioactivity Machine Learning Predictions

The presence of Activity Cliffs (ACs) has been known to represent a challenge for QSAR modeling. With its high data dependency, Machine Learning QSAR models will be directly influenced by the activity landscape. We propose several extended similarity and extended SALI methods to study the implications of ACs distribution on the training and test sets on the model's errors. Ununiform ACs and chemical space distribution tend to lead to worse models than the proposed uniform methods. ML modeling on AC-rich sets needs to be analyzed case-by-case. Proposed methods can be used as a tool to study the datasets, but as far as generalization, random splitting was the better-performing data splitting alternative overall.

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Publication Details

Journal
Molecular Informatics
Published
2024-11-18
DOI
https://doi.org/10.1002/minf.202400054
Citations
2
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
0.72
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article

Extended Activity Cliffs‐Driven Approaches on Data Splitting for the Study of Bioactivity Machine Learning Predictions

Ramón Alain Miranda‐Quintana, Kenneth López Pérez
2 citations
Molecular Informatics
Computational Drug Discovery Methods
0.72
article

Extended Activity Cliffs‐Driven Approaches on Data Splitting for the Study of Bioactivity Machine Learning Predictions

Ramón Alain Miranda‐Quintana, Kenneth López Pérez
article en
2 citations

Abstract

The presence of Activity Cliffs (ACs) has been known to represent a challenge for QSAR modeling. With its high data dependency, Machine Learning QSAR models will be directly influenced by the activity landscape. We propose several extended similarity and extended SALI methods to study the implications of ACs distribution on the training and test sets on the model's errors. Ununiform ACs and chemical space distribution tend to lead to worse models than the proposed uniform methods. ML modeling on AC-rich sets needs to be analyzed case-by-case. Proposed methods can be used as a tool to study the datasets, but as far as generalization, random splitting was the better-performing data splitting alternative overall.

Molecular InformaticsVol. 44(1)
University of Florida (US)
Openalex Percentile: Top 25%
Computational Drug Discovery Methods
0.72
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