Evidence map›Paper›PMID 37027223›Full record

ArticleBioinformatics (Oxford, England)2023

Summary statistics-based association test for identifying the pleiotropic effects with set of genetic variants.

Deliang Bu, Xiao Wang, Qizhai Li

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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.

Deliang BuSchool of Statistics, Capital University of Economics and Business, Beijing, China.ORCID 0000-0001-9939-5708
Xiao WangSchool of Mathematics and Statistics, Qingdao University, Qingdao, China.
Qizhai LiLSC, NCMIS, Academy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationTraditional genome-wide association study focuses on testing one-to-one relationship between genetic variants and complex human diseases or traits. While its success in the past decade, this one-to-one paradigm lacks efficiency because it does not utilize the information of intrinsic genetic structure and pleiotropic effects. Due to privacy reasons, only summary statistics of current genome-wide association study data are publicly available. Existing summary statistics-based association tests do not consider covariates for regression model, while adjusting for covariates including population stratification factors is a routine issue.

resultsIn this work, we first derive the correlation coefficients between summary Wald statistics obtained from linear regression model with covariates. Then, a new test is proposed by integrating three-level information including the intrinsic genetic structure, pleiotropy, and the potential information combinations. Extensive simulations demonstrate that the proposed test outperforms three other existing methods under most of the considered scenarios. Real data analysis of polyunsaturated fatty acids further shows that the proposed test can identify more genes than the compared existing methods. AVAILABILITY AND IMPLEMENTATION: Code is available at https://github.com/bschilder/ThreeWayTest.

Indexed as

Genome-Wide Association StudyPolymorphism, Single NucleotideHumansLinear ModelsPhenotype

Identifiers

PMID37027223
PMCPMC10115469

What OpenQuestion holds

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LicenceCC BY
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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.