Evidence map›Paper›PMID 42777013›Full record

ArticlePLoS genetics2026

Univariate-guided sparse regression for Biobank-scale high-dimensional omics data.

Joshua Richland, Tuomo Kiiskinen, William Wang, Wenhui Sophia Lu, Balasubramanian Narasimhan, Trevor Hastie, Manuel Rivas, Robert Tibshirani

Abstract read
In one paragraph

Article in PLoS genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. CuGen: A GPU-accelerated framework for large-scale genomics.medRxiv : the preprint server for health sciences · 2026
    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

8 authors.

Joshua RichlandDepartment of Statistics, Stanford University, Stanford, California, United States of America.ORCID https://orcid.org/0009-0000-4744-1813
Tuomo KiiskinenDepartment of Biomedical Data Science, Stanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0002-6306-8227
William WangDepartment of Computer Science, Stanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0002-3186-3453
Wenhui Sophia LuDepartment of Statistics, Stanford University, Stanford, California, United States of America.
Balasubramanian NarasimhanDepartment of Statistics, Stanford University, Stanford, California, United States of America.
Trevor HastieDepartment of Statistics, Stanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0002-0164-3142
Manuel RivasDepartment of Biomedical Data Science, Stanford University, Stanford, California, United States of America.
Robert TibshiraniDepartment of Statistics, Stanford University, Stanford, California, United States of America.

Funding

New Statistical Methods for Medical Signals and ImagesR01GM134483 · NIGMS · STANFORD UNIVERSITY · PI Iain M Johnstone · 2019 to 2026
$3.9M
SOFTWARE FOR LARGE-SCALE INFERENCE OF THE GENETICS OF LIFESTYLE MEASURES, BIOMARKERS, AND COMMON AND RARE DISEASESR01HG010140 · NHGRI · STANFORD UNIVERSITY · PI KUNDAJE, ANSHUL, MONTGOMERY, STEPHEN · 2018 to 2022
$2.0M
NHGRI NIH HHS R01 HG010140NIGMS NIH HHS R01 GM134483
6 · The paper itself

Abstract

We present a scalable framework for computing polygenic risk scores (PRS) in high-dimensional genomic settings using the recently introduced Univariate-Guided Sparse Regression (uniLasso). UniLasso is a two-stage penalized regression procedure that leverages univariate coefficients and magnitudes to stabilize feature selection and produce sparse predictive models. Building on its theoretical and empirical advantages, we adapt uniLasso for application to the UK Biobank, a population-based repository comprising over one million genetic variants measured on hundreds of thousands of individuals from the United Kingdom. We further extend the framework to incorporate external summary statistics via uniLasso ES (external scores). These signals guide the regression toward variants with prior evidence of association by informing penalty weights and sign constraints. Both uniLasso ES and uniLasso ultimately fit multivariate models using individual-level target data; the external statistics guide, rather than replace, this fitting. Our results demonstrate that uniLasso attains predictive performance comparable to standard Lasso while selecting substantially fewer variants, yielding sparser and potentially more interpretable models. Moreover, it remains competitive with other PRS estimation methods, such as PRS-CS and lassosum2.

Indexed as

Biological Specimen BanksGenomicsMultifactorial InheritanceGenetic Risk ScoreGenome-Wide Association StudyHumansModels, GeneticPolymorphism, Single NucleotideRegression AnalysisUK BiobankUnited Kingdom

Identifiers

PMID42777013
PMCPMC13623159

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.