Evidence map›Paper›PMID 36350801›Full record

ArticlePloS one2022

HCLC-FC: A novel statistical method for phenome-wide association studies.

Xiaoyu Liang, Xuewei Cao, Qiuying Sha, Shuanglin Zhang

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xiaoyu LiangDepartment of Preventive Medicine, Division of Biostatistics, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America.ORCID 0000-0001-7796-2441
Xuewei CaoDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America.ORCID 0000-0003-2136-0964
Qiuying ShaDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America.ORCID 0000-0002-9342-3269
Shuanglin ZhangDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America.ORCID 0000-0002-9478-1199

Funding

Medical Research Council MC_PC_17228Medical Research Council MC_QA137853
6 · The paper itself

Abstract

The emergence of genetic data coupled to longitudinal electronic medical records (EMRs) offers the possibility of phenome-wide association studies (PheWAS). In PheWAS, the whole phenome can be divided into numerous phenotypic categories according to the genetic architecture across phenotypes. Currently, statistical analyses for PheWAS are mainly univariate analyses, which test the association between one genetic variant and one phenotype at a time. In this article, we derived a novel and powerful multivariate method for PheWAS. The proposed method involves three steps. In the first step, we apply the bottom-up hierarchical clustering method to partition a large number of phenotypes into disjoint clusters within each phenotypic category. In the second step, the clustering linear combination method is used to combine test statistics within each category based on the phenotypic clusters and obtain p-values from each phenotypic category. In the third step, we propose a new false discovery rate (FDR) control approach. We perform extensive simulation studies to compare the performance of our method with that of other existing methods. The results show that our proposed method controls FDR very well and outperforms other methods we compared with. We also apply the proposed approach to a set of EMR-based phenotypes across more than 300,000 samples from the UK Biobank. We find that the proposed approach not only can well-control FDR at a nominal level but also successfully identify 1,244 significant SNPs that are reported to be associated with some phenotypes in the GWAS catalog. Our open-access tools and instructions on how to implement HCLC-FC are available at https://github.com/XiaoyuLiang/HCLCFC.

Indexed as

Genome-Wide Association StudyPolymorphism, Single NucleotideCluster AnalysisPhenomicsPhenotype

Identifiers

PMID36350801
PMCPMC9645610

What Socratic holds

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LicenceCC BY
Read underepoch 390

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 Socratic graph.