Evidence map›Paper›PMID 34991440›Full record

ArticleBMC bioinformatics2022

Non-parametric synergy modeling of chemical compounds with Gaussian processes.

Yuliya Shapovalova, Tom Heskes, Tjeerd Dijkstra

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Article in BMC bioinformatics, 2022. 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

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yuliya ShapovalovaRadboud University, Postbus 9010, 6500 GL, Nijmegen, The Netherlands.
Tom HeskesRadboud University, Postbus 9010, 6500 GL, Nijmegen, The Netherlands.
Tjeerd DijkstraMax Planck Institute for Developmental Biology, Max-Planck-Ring 25, 72076, Tübingen, Germany. tjeerd.dijkstra@tuebingen.mpg.de.ORCID http://orcid.org/0000-0002-4450-701X

Funding

The Dutch Research Council domain Applied and Engineered Sciences 15494
6 · The paper itself

Abstract

backgroundUnderstanding the synergetic and antagonistic effects of combinations of drugs and toxins is vital for many applications, including treatment of multifactorial diseases and ecotoxicological monitoring. Synergy is usually assessed by comparing the response of drug combinations to a predicted non-interactive response from reference (null) models. Possible choices of null models are Loewe additivity, Bliss independence and the recently rediscovered Hand model. A different approach is taken by the MuSyC model, which directly fits a generalization of the Hill model to the data. All of these models, however, fit the dose-response relationship with a parametric model.

resultsWe propose the Hand-GP model, a non-parametric model based on the combination of the Hand model with Gaussian processes. We introduce a new logarithmic squared exponential kernel for the Gaussian process which captures the logarithmic dependence of response on dose. From the monotherapeutic response and the Hand principle, we construct a null reference response and synergy is assessed from the difference between this null reference and the Gaussian process fitted response. Statistical significance of the difference is assessed from the confidence intervals of the Gaussian process fits. We evaluate performance of our model on a simulated data set from Greco, two simulated data sets of our own design and two benchmark data sets from Chou and Talalay. We compare the Hand-GP model to standard synergy models and show that our model performs better on these data sets. We also compare our model to the MuSyC model as an example of a recent method on these five data sets and on two-drug combination screens: Mott et al. anti-malarial screen and O'Neil et al. anti-cancer screen. We identify cases in which the HandGP model is preferred and cases in which the MuSyC model is preferred.

conclusionThe Hand-GP model is a flexible model to capture synergy. Its non-parametric and probabilistic nature allows it to model a wide variety of response patterns.

Indexed as

Combination therapyGaussian processesHand modelSynergy

Identifiers

PMID34991440
PMCPMC8734200

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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.