Evidence map›Paper›PMID 32365090›Full record

ArticlePLoS genetics2020

Simultaneous SNP selection and adjustment for population structure in high dimensional prediction models.

Sahir R Bhatnagar, Yi Yang, Tianyuan Lu, Erwin Schurr, J C Loredo-Osti, Marie Forest, Karim Oualkacha, Celia M T Greenwood

Abstract readEvaluation Study
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

8 authors.

Sahir R BhatnagarDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, Québec, Canada.ORCID 0000-0001-8956-2509
Yi YangDepartment of Mathematics and Statistics, McGill University, Montréal, Québec, Canada.
Tianyuan LuQuantitative Life Sciences, McGill University, Montréal, Québec, Canada.ORCID 0000-0002-5664-5698
Erwin SchurrDepartment of Medicine, McGill University, Montréal, Québec, Canada.ORCID 0000-0002-2640-536X
J C Loredo-OstiDepartment of Mathematics and Statistics, Memorial University, St. John's, Newfoundland and Labrador, Canada.
Marie ForestÉcole de Technologie Supérieure, Montréal, Québec, Canada.ORCID 0000-0003-0887-0572
Karim OualkachaDépartement de Mathématiques, Université du Québec à Montréal, Montréal, Québec, Canada.ORCID 0000-0002-9911-079X
Celia M T GreenwoodDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, Québec, Canada.ORCID 0000-0002-2427-5696

Funding

CIHR PJT 148620
6 · The paper itself

Abstract

Complex traits are known to be influenced by a combination of environmental factors and rare and common genetic variants. However, detection of such multivariate associations can be compromised by low statistical power and confounding by population structure. Linear mixed effects models (LMM) can account for correlations due to relatedness but have not been applicable in high-dimensional (HD) settings where the number of fixed effect predictors greatly exceeds the number of samples. False positives or false negatives can result from two-stage approaches, where the residuals estimated from a null model adjusted for the subjects' relationship structure are subsequently used as the response in a standard penalized regression model. To overcome these challenges, we develop a general penalized LMM with a single random effect called ggmix for simultaneous SNP selection and adjustment for population structure in high dimensional prediction models. We develop a blockwise coordinate descent algorithm with automatic tuning parameter selection which is highly scalable, computationally efficient and has theoretical guarantees of convergence. Through simulations and three real data examples, we show that ggmix leads to more parsimonious models compared to the two-stage approach or principal component adjustment with better prediction accuracy. Our method performs well even in the presence of highly correlated markers, and when the causal SNPs are included in the kinship matrix. ggmix can be used to construct polygenic risk scores and select instrumental variables in Mendelian randomization studies. Our algorithms are available in an R package available on CRAN (https://cran.r-project.org/package=ggmix).

Indexed as

AlgorithmsModels, GeneticPolymorphism, Single NucleotideAnimalsComputer SimulationCrosses, GeneticGenetics, PopulationGenome-Wide Association StudyHumansLeishmaniasis, CutaneousLeishmania tropicaLinear ModelsMiceMice, Inbred StrainsMultifactorial InheritanceMycobacterium bovis

Identifiers

PMID32365090
PMCPMC7224575

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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.