Evidence map›Paper›PMID 28511641›Full record

ArticleBMC genetics2017

Network-based regularization for high dimensional SNP data in the case-control study of Type 2 diabetes.

Jie Ren, Tao He, Ye Li, Sai Liu, Yinhao Du, Yu Jiang, Cen Wu

Abstract read
In one paragraph

Article in BMC genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  12. Gene-Environment Interaction: A Variable Selection Perspective.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
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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

7 authors.

Jie RenDepartment of Statistics, Kansas State University, 1116 Mid-Campus Drive N., 66506, Manhattan, KS, USA.
Tao HeDepartment of Mathematics, San Francisco State University, San Francisco, CA, USA.
Ye LiDepartment of Biostatistics, Yale University, New Haven, CT, USA.
Sai LiuDivision of Nephrology, School of Medicine, Stanford University, Palo Alto, CA, USA.
Yinhao DuDepartment of Statistics, Kansas State University, 1116 Mid-Campus Drive N., 66506, Manhattan, KS, USA.
Yu JiangDivision of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, University of Memphis, Memphis, TN, USA.
Cen WuDepartment of Statistics, Kansas State University, 1116 Mid-Campus Drive N., 66506, Manhattan, KS, USA. wucen@ksu.edu.ORCID 0000-0002-5172-141X

Funding

Genes and Environment Initiatives in Type 2 DiabetesU01HG004399 · NHGRI · HARVARD SCHOOL OF PUBLIC HEALTH · PI HU, FRANK B · 2007 to 2008
$1.2M
NHGRI NIH HHS U01 HG004399
6 · The paper itself

Abstract

backgroundOver the past decades, the prevalence of type 2 diabetes mellitus (T2D) has been steadily increasing around the world. Despite large efforts devoted to better understand the genetic basis of the disease, the identified susceptibility loci can only account for a small portion of the T2D heritability. Some of the existing approaches proposed for the high dimensional genetic data from the T2D case-control study are limited by analyzing a few number of SNPs at a time from a large pool of SNPs, by ignoring the correlations among SNPs and by adopting inefficient selection techniques.

methodsWe propose a network constrained regularization method to select important SNPs by taking the linkage disequilibrium into account. To accomodate the case control study, an iteratively reweighted least square algorithm has been developed within the coordinate descent framework where optimization of the regularized logistic loss function is performed with respect to one parameter at a time and iteratively cycle through all the parameters until convergence.

resultsIn this article, a novel approach is developed to identify important SNPs more effectively through incorporating the interconnections among them in the regularized selection. A coordinate descent based iteratively reweighed least squares (IRLS) algorithm has been proposed.

conclusionsBoth the simulation study and the analysis of the Nurses's Health Study, a case-control study of type 2 diabetes data with high dimensional SNP measurements, demonstrate the advantage of the network based approach over the competing alternatives.

Indexed as

AlgorithmsGene Regulatory NetworksPolymorphism, Single NucleotideCase-Control StudiesComputer SimulationDiabetes Mellitus, Type 2HumansLinkage DisequilibriumCase–control association studyNetwork-based regularizationRegularized logistic regressionType 2 diabetesVariable selection

Identifiers

PMID28511641
PMCPMC5434559

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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.