Evidence map›Paper›PMID 40037594›Full record

ArticleGenetics2026

Posterior estimation of longitudinal variance components from nonlongitudinal data using Bayesian Gaussian process model.

Arttu Arjas, Kalle Leppälä, Mikko J Sillanpää

Abstract read
In one paragraph

Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Arttu ArjasCentre for Wireless Communications, University of Oulu, Oulu 90014, Finland.ORCID 0000-0002-9545-0244
Kalle LeppäläThe Organismal and Evolutionary Biology Research Programme, University of Helsinki, Helsinki 00014, Finland.ORCID 0000-0002-2304-7595
Mikko J SillanpääResearch Unit of Mathematical Sciences, University of Oulu, Oulu 90014, Finland.ORCID 0000-0003-2808-2768

Funding

Research Council of Finland 346139Wellcome Trust 326291
6 · The paper itself

Abstract

Many quantitative traits can be measured from a single individual only once, making acquisition of longitudinal data impossible. In this paper, we present Gaussian process restricted Bayesian estimation, a new method tailored for estimating posterior distributions of longitudinal variance components from data where each individual contributes only 1 measurement at a single time point to the study. However, by collecting all time points together, one can think data to be longitudinal at the population level which makes it possible to estimate longitudinal variance components. The method can be also applied for reaction norm problems where it is common that a value of continuous environmental condition (e.g. temperature) is measured only once per individual. The work is based on Bayesian framework, Markov chain Monte Carlo estimation, and assuming Gaussian process-based smoothing priors for the variance components. The performance of the method is illustrated with simulated and real data sets as well as compared with a random regression model. Our method is very stable and it is flexible in handling any kind of smooth curves. Uncertainty around the variance curves is represented with 95% credible interval curves computed from the posterior distribution. The code is available at the GitHub repository https://github.com/aarjas/GP-REBE.

Indexed as

Models, GeneticQuantitative Trait, HeritableBayes TheoremComputer SimulationLongitudinal StudiesMarkov ChainsMonte Carlo MethodNormal Distributiondynamic heritabilityGaussian processMALAREML

Identifiers

PMID40037594
PMCPMC12774850

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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.