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May 2, 2022

Scientists rely increasingly on models trained with machine learning to provide solutions to complex problems. But how do we know the solutions are trustworthy when the complex algorithms the models use are not easily interrogated or able to explain their decisions to humans?

That trust is especially crucial in drug discovery, for example, where machine learning is used to sort through millions of potentially toxic compounds to determine which might be safe candidates for pharmaceutical drugs.

There have been some high-profile accidents in computer science where a model could predict things quite well, but the predictions werent based on anything meaningful, says Andrew White associate professor of chemical engineering at the University of Rochester, in an interview with Chemistry World.

White and his lab have developed a new counterfactual method, described in Chemical Science, that can be used with any molecular structure-based machine learning model to better understand how the model arrived at a conclusion.

Counterfactuals can tell researchers the smallest change to the features that would alter the prediction, says lead author Geemi Wellawatte, a PhD student in Whites lab. In other words, a counterfactual is an example as close to the original, but with a different outcome.

Counterfactuals can help researchers quickly pinpoint why a model made a prediction, and whether it is valid.

The paper identifies three examples of how the new method, called MMACE (Molecular Model Agonistic Counterfactual Explanations), can be used to explain why:

The lab had to overcome some major challenges in developing MMACE. They needed a method that could be adapted for the wide array of machine-learning methods that are used in chemistry. In addition, searching for the most-similar molecule for any given scenario was also challenging because of the sheer number of possible candidate molecules.

Coauthor Aditi Seshadri in Whites lab helped solve that problem by suggesting the group adapt the STONED (Superfast traversal, optimization, novelty, exploration, and discovery) algorithm developed at the University of Toronto. STONED efficiently generates similar molecules, the fuel for counterfactual generation. Seshadri is an undergraduate researcher in Whites lab and was able to help on the project via a Rochester summer research program called Discover.

White says his team is continuing to improve MMACE, by trying other databases in their search for most similar molecules, for example, and refining the definition of molecular similarity.

The project was supported by grants from the National Science Foundation and the National Institute of General Medical Sciences of the National Institutes of Health. The University of Rochester Center for Integrated Research Computing (CIRC) provided computational resources and technical support.

Tags: Andrew White, Center for Integrated Research Computing, Department of Chemical Engineering, Hajim School of Engineering and Applied Sciences, research finding

Category: Science & Technology

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How can we be sure machine learning is accurate? - University of Rochester