Evidence map›Paper›PMID 31024614›Full record

ArticleFrontiers in genetics2019

Combining Sparse Group Lasso and Linear Mixed Model Improves Power to Detect Genetic Variants Underlying Quantitative Traits.

Yingjie Guo, Chenxi Wu, Maozu Guo, Quan Zou, Xiaoyan Liu, Alon Keinan

Abstract read
In one paragraph

Article in Frontiers in genetics, 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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yingjie GuoSchool of Computer Science and Technology, Harbin Institute of Technology, Harbin, China.
Chenxi WuDepartment of Mathematics, Rutgers University, Piscataway, NJ, United States.
Maozu GuoSchool of Computer Science and Technology, Harbin Institute of Technology, Harbin, China.
Quan ZouInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, China.
Xiaoyan LiuSchool of Computer Science and Technology, Harbin Institute of Technology, Harbin, China.
Alon KeinanDepartment of Computational Biology, Cornell University, Ithaca, NY, United States.

Funding

The X-factor of complex disease: From population genetics to GWAS of Chromosome XR01HG006849 · NHGRI · CORNELL UNIVERSITY · PI CLARK, ANDREW G · 2013 to 2020
$2.3M
Population Genetic Consequences of Recent Explosive Population Growth in HumansR01GM108805 · NIGMS · CORNELL UNIVERSITY · PI CLARK, ANDREW G, KEINAN, ALON · 2014 to 2017
$2.2M
NHGRI NIH HHS R01 HG006849NIGMS NIH HHS R01 GM108805
6 · The paper itself

Abstract

Genome-Wide association studies (GWAS), based on testing one single nucleotide polymorphism (SNP) at a time, have revolutionized our understanding of the genetics of complex traits. In GWAS, there is a need to consider confounding effects such as due to population structure, and take groups of SNPs into account simultaneously due to the "polygenic" attribute of complex quantitative traits. In this paper, we propose a new approach SGL-LMM that puts together sparse group lasso (SGL) and linear mixed model (LMM) for multivariate associations of quantitative traits. LMM, as has been often used in GWAS, controls for confounders, while SGL maintains sparsity of the underlying multivariate regression model. SGL-LMM first sets a fixed zero effect to learn the parameters of random effects using LMM, and then estimates fixed effects using SGL regularization. We present efficient algorithms for hyperparameter tuning and feature selection using stability selection. While controlling for confounders and constraining for sparse solutions, SGL-LMM also provides a natural framework for incorporating prior biological information into the group structure underlying the model. Results based on both simulated and real data show SGL-LMM outperforms previous approaches in terms of power to detect associations and accuracy of quantitative trait prediction.

Indexed as

genome-wide association studieslinear mixed modelquantitative traitssingle nucleotide polymorphismssparse group lasso

Identifiers

PMID31024614
PMCPMC6469383

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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.