Cited by 7Genetic Associations and EpidemiologyStatistical Methods and ApplicationsGenetic Mapping and Diversity in Plants and Animals

A comparison of principal component methods between multiple phenotype regression and multiple SNP regression in genetic association studies

Open access
Liu, Zhonghua, Barnett, Ian, Lin, Xihong·2020·The Annals of Applied Statistics

Abstract

Principal component analysis (PCA) is a popular method for dimension reduction in unsupervised multivariate analysis. However, existing ad hoc uses of PCA in both multivariate regression (multiple outcomes) and multiple regression (multiple predictors) lack theoretical justification. The differences in the statistical properties of PCAs in these two regression settings are not well understood. In this paper we provide theoretical results on the power of PCA in genetic association testings in both multiple phenotype and SNP-set settings. The multiple phenotype setting refers to the case when one is interested in studying the association between a single SNP and multiple phenotypes as outcomes. The SNP-set setting refers to the case when one is interested in studying the association between multiple SNPs in a SNP set and a single phenotype as the outcome. We demonstrate analytically that the properties of the PC-based analysis in these two regression settings are substantially different. We show that the lower order PCs, that is, PCs with large eigenvalues, are generally preferred and lead to a higher power in the SNP-set setting, while the higher-order PCs, that is, PCs with small eigenvalues, are generally preferred in the multiple phenotype setting. We also investigate the power of three other popular statistical methods, the Wald test, the variance component test and the minimum $p$-value test, in both multiple phenotype and SNP-set settings. We use theoretical power, simulation studies, and two real data analyses to validate our findings.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1214/19-aoas1312

Cites

26 of 26 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Liu, Z., Barnett, I., & Lin, X.
Affiliations
  • University of Hong Kong (HK)
  • University of Pennsylvania (US)
  • Harvard University (US)
Venue
The Annals of Applied Statistics
Published
2020-03-01
Volume
14
Issue
1
Pages
433-451
ISSN
  • 1932-6157 (ISSN-L)
  • 1941-7330
OpenAlex
W3017329137
Cited by
7
References
26
Citations by year
2024: 3 · 2023: 1 · 2022: 1 · 2021: 2
FWCI
0.59
Type
journal article
Language
en
Open access
Locations
  • The Annals of Applied Statistics (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • Project Euclid (Cornell University) (submittedVersion)
Funders
  • National Institutes of Health (CA134294)
  • National Heart, Lung, and Blood Institute (R01HL113338)
  • National Human Genome Research Institute (U01HG009088)
  • National Cancer Institute (U19CA203654, P01CA134294, R35CA197449)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
  • Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods and Applications
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
Keywords
principal component analysis, genetic association testing, statistical power, dimensionality reduction, Wald test, eigenvalue selection

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review