Evidence map›Paper›PMID 26489906›Full record

ArticleStatistical methods in medical research2017

Unified variable selection in semi-parametric models.

William Terry, Hongmei Zhang, Arnab Maity, Hasan Arshad, Wilfried Karmaus

Open access · greenAbstract read
In one paragraph

Article in Statistical methods in medical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 22% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Observational
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

5 authors at 3 institutions in 2 countries.

William Terry1 Department of Mathematical Sciences, University of Memphis, Memphis, USA.
Hongmei Zhang2 Division of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, University of Memphis, Memphis, USA.
Arnab Maity3 Department of Statistics, North Carolina State University, Raleigh, USA.
Hasan Arshad4 Allergy and Clinical Immunology, University of Southampton, Southampton, UK. The David Hide Asthma and Allergy Research Centre, Isle of Wight, UK.
Wilfried Karmaus2 Division of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, University of Memphis, Memphis, USA.
University of Memphis · USDavid Hide Asthma and Allergy Research Centre · GBNorth Carolina State University · US

Funding

Transgenerational epigenetic inheritance of allergy in a multigenerational cohortR01AI091905 · NIAID · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI KARMAUS, WILFRIED JJ · 2011 to 2015
$2.7M
Statistical Methods for Analysis of High-Dimensional Gene and Environment DataR00ES017744 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI MAITY, ARNAB · 2011 to 2013
$663k
Phenomics: Joint Clustering to Associate Changes in Allergy and Asthma Over TimeR21AI099367 · NIAID · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI ZHANG, HONGMEI · 2013 to 2014
$372k
NIAID NIH HHS R01 AI091905NIAID NIH HHS R21 AI099367NIEHS NIH HHS R00 ES017744
6 · The paper itself

Abstract

We propose a Bayesian variable selection method in semi-parametric models with applications to genetic and epigenetic data (e.g., single nucleotide polymorphisms and DNA methylation, respectively). The data are individually standardized to reduce heterogeneity and facilitate simultaneous selection of categorical (single nucleotide polymorphisms) and continuous (DNA methylation) variables. The Gaussian reproducing kernel is applied to the transformed data to evaluate joint effect of the variables, which may include complex interactions between, e.g., single nucleotide polymorphisms and DNA methylation. Indicator variables are introduced to the model for the purpose of variable selection. The method is demonstrated and evaluated using simulations under different scenarios. We apply the method to identify informative DNA methylation sites and single nucleotide polymorphisms in a set of genes based on their joint effect on allergic sensitization. The selected single nucleotide polymorphisms and methylation sites have the potential to serve as early markers for allergy prediction, and consequently benefit medical and clinical research to prevent allergy before its manifestation.

Indexed as

Models, GeneticModels, StatisticalBayes TheoremBiostatisticsComputer SimulationCpG IslandsDNA MethylationEpigenesis, GeneticHumansHypersensitivityMonte Carlo MethodNonlinear DynamicsNormal DistributionPolymorphism, Single NucleotideBayesian methodsDNA methylationGaussian kernelnon-linear effectsreproducing kernelsingle nucleotide polymorphismstransformationvariable selection

Identifiers

PMID26489906
PMCPMC4860150
OpenAlexW2186750688

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.