Evidence map›Paper›PMID 32804302›Full record

ArticleBehavior genetics2020

Modeling the Dependence Structure in Genome Wide Association Studies of Binary Phenotypes in Family Data.

Souvik Seal, Jeffrey A Boatman, Matt McGue, Saonli Basu

Abstract read
In one paragraph

Article in Behavior genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

4 authors.

Souvik SealDivision of Biostatistics, University of Minnesota, Minneapolis, MN, USA. sealx017@umn.edu.ORCID 0000-0003-3268-610X
Jeffrey A BoatmanDivision of Biostatistics, University of Minnesota, Minneapolis, MN, USA.
Matt McGueDepartment of Psychology, University of Minnesota, Minneapolis, MN, USA.
Saonli BasuDivision of Biostatistics, University of Minnesota, Minneapolis, MN, USA.

Funding

Statistical Methods for detection of genome-wide GxE interactions in longitudinalR01DA033958 · NIDA · UNIVERSITY OF MINNESOTA · PI BASU, SAONLI · 2013 to 2016
$1.1M
Improved Heritability Estimation by Spatial Mapping of Genetic RelationshipsR21DA046188 · NIDA · UNIVERSITY OF MINNESOTA · PI BASU, SAONLI · 2018 to 2019
$398k
NIDA NIH HHS R01 DA033958NIDA NIH HHS R21 DA046188
6 · The paper itself

Abstract

Genome-wide association studies (GWASs) are a popular tool for detecting association between genetic variants or single nucleotide polymorphisms (SNPs) and complex traits. Family data introduce complexity due to the non-independence of the family members. Methods for non-independent data are well established, but when the GWAS contains distinct family types, explicit modeling of between-family-type differences in the dependence structure comes at the cost of significantly increased computational burden. The situation is exacerbated with binary traits. In this paper, we perform several simulation studies to compare multiple candidate methods to perform single SNP association analysis with binary traits. We consider generalized estimating equations (GEE), generalized linear mixed models (GLMMs), or generalized least square (GLS) approaches. We study the influence of different working correlation structures for GEE on the GWAS findings and also the performance of different analysis method(s) to conduct a GWAS with binary trait data in families. We discuss the merits of each approach with attention to their applicability in a GWAS. We also compare the performances of the methods on the alcoholism data from the Minnesota Center for Twin and Family Research (MCTFR) study.

Indexed as

Computational BiologyComputer SimulationData AnalysisFamilyGenome-Wide Association StudyHumansLeast-Squares AnalysisLinear ModelsModels, GeneticModels, StatisticalMultifactorial InheritancePolymorphism, Single NucleotideQuantitative Trait LociFamily dataGeneralized estimating equationGeneralized least squaresGeneralized linear mixed effect modelGenome-wide scanPopulation-based association analysis

Identifiers

PMID32804302
PMCPMC7581561

What Socratic holds

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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 Socratic graph.