Evidence map›Paper›PMID 42062874›Full record

ArticleBMC genomics2026

Divided-and-combined association test for pleiotropic effects with GWAS summary statistics.

Boheng Hu, Yaoyao Chen, Xueqin Zheng, Hongping Guo

Abstract read
In one paragraph

Article in BMC genomics, 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

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3 · Its place in the literature

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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

4 authors.

Boheng Hu *School of Mathematics and Statistics, Hubei Normal University, Huangshi, 435002, P.R. China.
Yaoyao Chen *School of Mathematics and Statistics, Hubei Normal University, Huangshi, 435002, P.R. China.
Xueqin ZhengSchool of Mathematics and Statistics, Hubei Normal University, Huangshi, 435002, P.R. China.
Hongping GuoSchool of Mathematics and Statistics, Hubei Normal University, Huangshi, 435002, P.R. China. guohongping@hbnu.edu.cn.

Funding

National Natural Science Foundation of China 12401344National Statistical Science Research Project of China 2024LY017
6 · The paper itself

Abstract

Many genome-wide association studies (GWAS) conducted over the past two decades have focused on testing the one-to-one association between genetic variants and complex diseases or phenotypes. Despite their considerable success, such one-to-one testing approaches are underpowered because they do not utilize information on pleiotropic effects. Currently available public GWAS summary statistics provide resources for multi-trait association testing. Quadratic statistics are widely used to detect pleiotropic effects, as they follow a chi-square or weighted chi-square distribution under the null hypothesis. Nevertheless, such methods often fail to achieve superior power. To address this limitation, this study proposes a divided-and-combined association test (DCAT) for detecting pleiotropic effects using GWAS summary statistics. DCAT constructs the covariance matrix of Z-scores by combining phenotype correlation and genotype partial correlation via the Kronecker product. It consists of a family of quadratic statistics with different covariance matrix weights and leverages the respective advantages of each statistic. The distribution of each statistic is then approximated using a location-shifted generalized gamma distribution for p-value calculation, with the resulting p-values integrated via the Cauchy combination test. Simulation results demonstrate that DCAT controls the type I error at a reasonable level and achieves the highest statistical power in most scenarios. In the real-data analysis of four cardiovascular diseases, DCAT identifies more significant genes compared with the other four representative methods.

Indexed as

Genetic PleiotropyGenome-Wide Association StudyHumansPhenotypePolymorphism, Single NucleotideAssociation analysisCauchy combination testDivided-and-combined testPleiotropic effectSummary statistics

Identifiers

PMID42062874
PMCPMC13277180

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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.