ArticleNature communications2025
Selecting fitted models under epistemic uncertainty using a stochastic process on quantile functions.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Building on models-a perspective for computational neuroscience.Cerebral cortex (New York, N.Y. : 1991) · 2025Article
- Selecting fitted models under epistemic uncertainty using a stochastic process on quantile functions.Nature communications · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Fitting models to data is an important part of the practice of science. Advances in machine learning have made it possible to fit more-and more complex-models, but have also exacerbated a problem: when multiple models fit the data equally well, which one(s) should we pick? The answer depends entirely on the modelling goal. In the scientific context, the essential goal is replicability: if a model works well to describe one experiment, it should continue to do so when that experiment is replicated tomorrow, or in another laboratory. The selection criterion must therefore be robust to the variations inherent to the replication process. In this work we develop a nonparametric method for estimating uncertainty on a model's empirical risk when replications are non-stationary, thus ensuring that a model is only rejected when another is reproducibly better. We illustrate the method with two examples: one a more classical setting, where the models are structurally distinct, and a machine learning-inspired setting, where they differ only in the value of their parameters. We show how, in this context of replicability or "epistemic uncertainty", it compares favourably to existing model selection criteria, and has more satisfactory behaviour with large experimental datasets.
Identifiers
What OpenQuestion holds
Registered trials
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.