Evidence map›Paper›PMID 37418505›Full record

ArticlePLoS genetics2023

A flexible empirical Bayes approach to multivariate multiple regression, and its improved accuracy in predicting multi-tissue gene expression from genotypes.

Fabio Morgante, Peter Carbonetto, Gao Wang, Yuxin Zou, Abhishek Sarkar, Matthew Stephens

Abstract read
In one paragraph

Article in PLoS genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Covariate-moderated Empirical Bayes Matrix Factorization.Advances in neural information processing systems · 2025
    Article
  4. Article
  5. Quantitative omnigenic model discovers interpretable genome-wide associations.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. 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.

Fabio MorganteCenter for Human Genetics, Clemson University, Greenwood, South Carolina, United States of America.ORCID 0000-0003-3285-1988
Peter CarbonettoDepartment of Human Genetics, University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0003-1144-6780
Gao WangDepartment of Human Genetics, University of Chicago, Chicago, Illinois, United States of America.
Yuxin ZouDepartment of Statistics, University of Chicago, Chicago, Illinois, United States of America.
Abhishek SarkarDepartment of Human Genetics, University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0002-4636-9255
Matthew StephensDepartment of Human Genetics, University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0001-5397-9257

Funding

Statistical Methods for Gene Regulatory Analysis From Single Cell Genomics DataP20GM139769 · NIGMS · CLEMSON UNIVERSITY · PI ANHOLT, ROBERT R. H, ARNO, GAVIN · 2021 to 2025
$10.8M
Genome analysis: statistical methods and applicationsR01HG002585 · NHGRI · UNIVERSITY OF WASHINGTON · PI MATTHEW STEPHENS · 2002 to 2026
$8.4M
Multiomics data integration methods to discover putative causal variants, genes and patient heterogeneity for Alzheimers diseaseR01AG076901 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Gao Wang · 2023 to 2026
$2.4M
Understanding and using gene-by-context interactions in human complex trait geneticsR35GM146868 · NIGMS · CLEMSON UNIVERSITY · PI Fabio Morgante · 2022 to 2026
$1.9M
NHGRI NIH HHS R01 HG002585NIA NIH HHS R01 AG076901NIGMS NIH HHS P20 GM139769NIGMS NIH HHS R35 GM146868
6 · The paper itself

Abstract

Predicting phenotypes from genotypes is a fundamental task in quantitative genetics. With technological advances, it is now possible to measure multiple phenotypes in large samples. Multiple phenotypes can share their genetic component; therefore, modeling these phenotypes jointly may improve prediction accuracy by leveraging effects that are shared across phenotypes. However, effects can be shared across phenotypes in a variety of ways, so computationally efficient statistical methods are needed that can accurately and flexibly capture patterns of effect sharing. Here, we describe new Bayesian multivariate, multiple regression methods that, by using flexible priors, are able to model and adapt to different patterns of effect sharing and specificity across phenotypes. Simulation results show that these new methods are fast and improve prediction accuracy compared with existing methods in a wide range of settings where effects are shared. Further, in settings where effects are not shared, our methods still perform competitively with state-of-the-art methods. In real data analyses of expression data in the Genotype Tissue Expression (GTEx) project, our methods improve prediction performance on average for all tissues, with the greatest gains in tissues where effects are strongly shared, and in the tissues with smaller sample sizes. While we use gene expression prediction to illustrate our methods, the methods are generally applicable to any multi-phenotype applications, including prediction of polygenic scores and breeding values. Thus, our methods have the potential to provide improvements across fields and organisms.

Indexed as

Models, GeneticPolymorphism, Single NucleotideBayes TheoremComputer SimulationGene ExpressionGenotypePhenotype

Identifiers

PMID37418505
PMCPMC10355440

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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.