Evidence map›Paper›PMID 40324005›Full record

ArticleJournal of chemical information and modeling2025

Batched Bayesian Optimization by Maximizing the Probability of Including the Optimum.

Jenna Fromer, Runzhong Wang, Mrunali Manjrekar, Austin Tripp, José Miguel Hernández-Lobato, Connor W Coley

Abstract read
In one paragraph

Article in Journal of chemical information and modeling, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jenna FromerDepartment of Chemical Engineering, MIT, Cambridge, Massachusetts 02139, United States.
Runzhong WangDepartment of Chemical Engineering, MIT, Cambridge, Massachusetts 02139, United States.
Mrunali ManjrekarDepartment of Chemical Engineering, MIT, Cambridge, Massachusetts 02139, United States.
Austin TrippDepartment of Engineering, University of Cambridge, Cambridge CB2 1CB2 1PZ, U.K.ORCID 0000-0002-0138-7740
José Miguel Hernández-LobatoDepartment of Engineering, University of Cambridge, Cambridge CB2 1CB2 1PZ, U.K.ORCID 0000-0001-7610-949X
Connor W ColeyDepartment of Chemical Engineering, MIT, Cambridge, Massachusetts 02139, United States.ORCID 0000-0002-8271-8723

Funding

Graduate Training in Computational and Systems BiologyT32GM087237 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BURGE, CHRISTOPHER B · 2009 to 2023
$4.6M
NIGMS NIH HHS T32 GM087237
6 · The paper itself

Abstract

Batched Bayesian optimization (BO) can accelerate molecular design by efficiently identifying top-performing compounds from a large chemical library. Existing acquisition strategies for batch design in BO aim to balance exploration and exploitation. This often involves optimizing nonadditive batch acquisition functions, necessitating approximation via myopic construction and/or diversity heuristics. In this work, we propose an acquisition strategy for discrete optimization that is motivated by pure exploitation, qPO (multipoint Probability of Optimality). qPO maximizes the probability that the batch includes the true optimum, which is expressed as the sum over individual acquisition scores and thereby circumvents the combinatorial challenge of optimizing a batch acquisition function. We differentiate the proposed strategy from parallel Thompson sampling and discuss how it implicitly captures diversity. Finally, we apply our method to the model-guided exploration of large chemical libraries and provide empirical evidence that it is competitive with and complements other state-of-the-art methods in batched Bayesian optimization.

Indexed as

Bayes TheoremSmall Molecule LibrariesProbabilitySmall Molecule Libraries

Identifiers

PMID40324005
PMCPMC12573218

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.