Evidence map›Paper›PMID 24987464›Full record

ArticleJournal of cheminformatics2014

Using beta binomials to estimate classification uncertainty for ensemble models.

Robert D Clark, Wenkel Liang, Adam C Lee, Michael S Lawless, Robert Fraczkiewicz, Marvin Waldman

Abstract read
In one paragraph

Article in Journal of cheminformatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Tales from the war on error: the art and science of curating QSAR data.Journal of computer-aided molecular design · 2015
    Article
  10. Article
  11. How accurately can we predict the melting points of drug-like compounds?Journal of chemical information and modeling · 2014
    Article
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.

Robert D ClarkDepartment of Life Sciences, Simulations Plus, Inc., 45205 10th Street West, Lancaster, CA 93534, USA.
Wenkel LiangDepartment of Life Sciences, Simulations Plus, Inc., 45205 10th Street West, Lancaster, CA 93534, USA.
Adam C LeeDepartment of Life Sciences, Simulations Plus, Inc., 45205 10th Street West, Lancaster, CA 93534, USA.
Michael S LawlessDepartment of Life Sciences, Simulations Plus, Inc., 45205 10th Street West, Lancaster, CA 93534, USA.
Robert FraczkiewiczDepartment of Life Sciences, Simulations Plus, Inc., 45205 10th Street West, Lancaster, CA 93534, USA.
Marvin WaldmanDepartment of Life Sciences, Simulations Plus, Inc., 45205 10th Street West, Lancaster, CA 93534, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundQuantitative structure-activity (QSAR) models have enormous potential for reducing drug discovery and development costs as well as the need for animal testing. Great strides have been made in estimating their overall reliability, but to fully realize that potential, researchers and regulators need to know how confident they can be in individual predictions.

resultsSubmodels in an ensemble model which have been trained on different subsets of a shared training pool represent multiple samples of the model space, and the degree of agreement among them contains information on the reliability of ensemble predictions. For artificial neural network ensembles (ANNEs) using two different methods for determining ensemble classification - one using vote tallies and the other averaging individual network outputs - we have found that the distribution of predictions across positive vote tallies can be reasonably well-modeled as a beta binomial distribution, as can the distribution of errors. Together, these two distributions can be used to estimate the probability that a given predictive classification will be in error. Large data sets comprised of logP, Ames mutagenicity, and CYP2D6 inhibition data are used to illustrate and validate the method. The distributions of predictions and errors for the training pool accurately predicted the distribution of predictions and errors for large external validation sets, even when the number of positive and negative examples in the training pool were not balanced. Moreover, the likelihood of a given compound being prospectively misclassified as a function of the degree of consensus between networks in the ensemble could in most cases be estimated accurately from the fitted beta binomial distributions for the training pool.

conclusionsConfidence in an individual predictive classification by an ensemble model can be accurately assessed by examining the distributions of predictions and errors as a function of the degree of agreement among the constituent submodels. Further, ensemble uncertainty estimation can often be improved by adjusting the voting or classification threshold based on the parameters of the error distribution. Finally, the profiles for models whose predictive uncertainty estimates are not reliable provide clues to that effect without the need for comparison to an external test set.

Indexed as

ANNEArtificial neural network ensembleClassificationConfidenceError estimationPredictive valueQSARUncertainty

Identifiers

PMID24987464
PMCPMC4076254

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Registered trials

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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.