Evidence map›Paper›PMID 38644517›Full record

ArticleGenetic epidemiology2024

A novel application of data-consistent inversion to overcome spurious inference in genome-wide association studies.

Negar Janani, Kendra A Young, Greg Kinney, Matthew Strand, John E Hokanson, Yaning Liu, Troy Butler, Erin Austin

Abstract read
In one paragraph

Article in Genetic epidemiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Negar JananiDepartment of Mathematical and Statistical Sciences, University of Colorado Denver, Denver, Colorado, USA.ORCID 0009-0000-7308-926X
Kendra A YoungDepartment of Epidemiology, Colorado School of Public Health, Aurora, Colorado, USA.ORCID 0000-0002-8664-7635
Greg KinneyDepartment of Epidemiology, Colorado School of Public Health, Aurora, Colorado, USA.
Matthew StrandDivision of Biostatistics, National Jewish Health, Denver, Colorado, USA.
John E HokansonDepartment of Epidemiology, Colorado School of Public Health, Aurora, Colorado, USA.
Yaning LiuDepartment of Mathematical and Statistical Sciences, University of Colorado Denver, Denver, Colorado, USA.
Troy ButlerDepartment of Mathematical and Statistical Sciences, University of Colorado Denver, Denver, Colorado, USA.
Erin AustinDepartment of Mathematical and Statistical Sciences, University of Colorado Denver, Denver, Colorado, USA.

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
COPDGene NCT00608764COPDGene ProjectNational Science Foundation DMS-2208460NHLBI NIH HHS U01 HL089856NHLBI NIH HHS U01 HL089897
6 · The paper itself

Abstract

The genome-wide association studies (GWAS) typically use linear or logistic regression models to identify associations between phenotypes (traits) and genotypes (genetic variants) of interest. However, the use of regression with the additive assumption has potential limitations. First, the normality assumption of residuals is the one that is rarely seen in practice, and deviation from normality increases the Type-I error rate. Second, building a model based on such an assumption ignores genetic structures, like, dominant, recessive, and protective-risk cases. Ignoring genetic variants may result in spurious conclusions about the associations between a variant and a trait. We propose an assumption-free model built upon data-consistent inversion (DCI), which is a recently developed measure-theoretic framework utilized for uncertainty quantification. This proposed DCI-derived model builds a nonparametric distribution on model inputs that propagates to the distribution of observed data without the required normality assumption of residuals in the regression model. This characteristic enables the proposed DCI-derived model to cover all genetic variants without emphasizing on additivity of the classic-GWAS model. Simulations and a replication GWAS with data from the COPDGene demonstrate the ability of this model to control the Type-I error rate at least as well as the classic-GWAS (additive linear model) approach while having similar or greater power to discover variants in different genetic modes of transmission.

Indexed as

Genome-Wide Association StudyModels, GeneticComputer SimulationGenetic VariationGenotypeHumansModels, StatisticalPhenotypePolymorphism, Single NucleotidePulmonary Disease, Chronic ObstructiveCOPDdata‐consistent inversiongenome‐wide association studyinverse problemuncertainty quantification

Identifiers

PMID38644517
PMCPMC11938999

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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.