Evidence map›Paper›PMID 42387390›Full record

ArticleBMC genomics2026

pGWAS-Portal: a comprehensive online platform for integrative post-genome-wide association study analysis.

Zijun Zhu, Hailong Li, Xin Wang, Xingwang Liu, Guoyou He, Xin Zhang, Siyuan Guan, Junjie Wang, Qi Zhao, Yun Liu and 1 more

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
–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

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

11 authors.

Zijun Zhu *College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, 150081, China.
Hailong Li *College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, 150081, China.
Xin Wang *College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, 150081, China.
Xingwang LiuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, 150081, China.
Guoyou HeCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, 150081, China.
Xin ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, 150081, China.
Siyuan GuanCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, 150081, China.
Junjie WangDepartment of Medical Informatics, School of Biomedical Engineering and Informatics, Nanjing Medical University, 101 Longmian Avenue, Nanjing, Jiangsu, 211166, China.
Qi ZhaoDepartment of Cardiology, Ningbo Medical Center, LiHuiLi Hospital, Ningbo, Zhejiang, China. zq920@163.com.
Yun LiuDepartment of Medical Informatics, School of Biomedical Engineering and Informatics, Nanjing Medical University, 101 Longmian Avenue, Nanjing, Jiangsu, 211166, China. liuyun@njmu.edu.cn.
Liang ChengCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, 150081, China. liangcheng@hrbmu.edu.cn.ORCID http://orcid.org/0000-0002-6665-6710

Funding

Heilongjiang Postdoctoral Fund LBH-Q20030National Natural Science Foundation of China 62222104, 62531007, and 62172130
6 · The paper itself

Abstract

Genome-wide association study (GWAS) has revolutionized our understanding of complex traits genetics, gaining insight into the phenotypic biology, estimating their heritability, calculating genetic correlations, making clinical risk predictions, informing drug development, and inferring potential causal relationships between risk factors and health outcomes. Despite numerous algorithms and tools to explore the genetic architecture of phenotypes and investigate molecular mechanisms, the lack of an integrative and comprehensive platform for unifying these methodologies has constrained the efficiency and translational potential of post-GWAS analyses. To address this gap, we developed pGWAS-Portal, a unified one-stop platform that covers six progressive analytical modules: i) Heritability Estimate module, qualifying the contribution to trait variability; ii) Enrichment Pattern module, characterizing gene, tissue, cell type, and pathway enrichment patterns associated with phenotypic variation; iii) Cross-Trait Analysis module, integrating genetic data across multiple phenotypes; iv) Fine-Mapping module, identifying potentially causal variants within associated loci; v) Correlation and Causality module, calculating phenotypic correlations and putative causal relationships; and vi) Risk Factors Identification module, detecting potential trait-associated biological factors. Implementing over thirty well-established algorithms within a unified framework, pGWAS-Portal offers a user-friendly, freely available web server ( http://bio-computing.hrbmu.edu.cn/posgwaser ; https://bio-computing.hrbmu.edu.cn/posgwaser ) to streamline and enhance post-GWAS investigations.

Indexed as

Genome-Wide Association StudyInternetSoftwareAlgorithmsHumansPhenotypePolymorphism, Single NucleotideQuantitative Trait LociGeneticsGWASIntegrated strategyOne-stop platform

Identifiers

PMID42387390
PMCPMC13591785

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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.