Evidence map›Paper›PMID 30705317›Full record

ArticleScientific reports2019

Joint Analysis of Multiple Phenotypes in Association Studies based on Cross-Validation Prediction Error.

Xinlan Yang, Shuanglin Zhang, Qiuying Sha

Abstract read
In one paragraph

Article in Scientific reports, 2019. 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

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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

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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.

  1. Article
  2. Article
  3. Multivariate Analysis and Modelling of multiple Brain endOphenotypes: Let's MAMBO!Computational and structural biotechnology journal · 2021
    Review
  4. Article
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.

Xinlan YangDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America.
Shuanglin ZhangDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America.
Qiuying ShaDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America. qsha@mtu.edu.

Funding

Genetic Epidemiology of COPDU01HL089897 · NHLBI · NATIONAL JEWISH HEALTH · PI CRAPO, JAMES D · 2007 to 2021
$56.9M
Genetic Epidemiology of COPDU01HL089856 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SILVERMAN, EDWIN K · 2007 to 2021
$20.7M
Statistical Methods for Rare Variant Association StudiesR15HG008209 · NHGRI · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI SHA, QIUYING · 2016 to 2016
$437k
NHGRI NIH HHS R15 HG008209NHLBI NIH HHS U01 HL089856NHLBI NIH HHS U01 HL089897
6 · The paper itself

Abstract

In genome-wide association studies (GWAS), joint analysis of multiple phenotypes could have increased statistical power over analyzing each phenotype individually to identify genetic variants that are associated with complex diseases. With this motivation, several statistical methods that jointly analyze multiple phenotypes have been developed, such as O'Brien's method, Trait-based Association Test that uses Extended Simes procedure (TATES), multivariate analysis of variance (MANOVA), and joint model of multiple phenotypes (MultiPhen). However, the performance of these methods under a wide range of scenarios is not consistent: one test may be powerful in some situations, but not in the others. Thus, one challenge in joint analysis of multiple phenotypes is to construct a test that could maintain good performance across different scenarios. In this article, we develop a novel statistical method to test associations between a genetic variant and Multiple Phenotypes based on cross-validation Prediction Error (MultP-PE). Extensive simulations are conducted to evaluate the type I error rates and to compare the power performance of MultP-PE with various existing methods. The simulation studies show that MultP-PE controls type I error rates very well and has consistently higher power than the tests we compared in all simulation scenarios. We conclude with the recommendation for the use of MultP-PE for its good performance in association studies with multiple phenotypes.

Indexed as

Computer SimulationGenome-Wide Association StudyHumansModels, GeneticPolymorphism, Single Nucleotide

Identifiers

PMID30705317
PMCPMC6355816

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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.