Evidence map›Paper›PMID 29423954›Full record

ArticleGenetic epidemiology2018

An analytic approach for interpretable predictive models in high-dimensional data in the presence of interactions with exposures.

Sahir Rai Bhatnagar, Yi Yang, Budhachandra Khundrakpam, Alan C Evans, Mathieu Blanchette, Luigi Bouchard, Celia M T Greenwood

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Article in Genetic epidemiology, 2018. 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

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

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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

4 citing papers in PubMed.

  1. Blood transcriptome differentiates clinical clusters for asthma.The World Allergy Organization journal · 2024
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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.

Sahir Rai BhatnagarDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, QC, Canada.ORCID 0000-0001-8956-2509
Yi YangDepartment of Mathematics and Statistics, McGill University, Montréal, QC, Canada.
Budhachandra KhundrakpamMontreal Neurological Institute, McGill University, Montréal, QC, Canada.
Alan C EvansMontreal Neurological Institute, McGill University, Montréal, QC, Canada.
Mathieu BlanchetteDepartment of Computer Science, McGill University, Montréal, QC, Canada.
Luigi BouchardDepartment of Biochemistry, Université de Sherbrooke, QC, Canada.
Celia M T GreenwoodDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, QC, Canada.ORCID 0000-0002-2427-5696

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Predicting a phenotype and understanding which variables improve that prediction are two very challenging and overlapping problems in the analysis of high-dimensional (HD) data such as those arising from genomic and brain imaging studies. It is often believed that the number of truly important predictors is small relative to the total number of variables, making computational approaches to variable selection and dimension reduction extremely important. To reduce dimensionality, commonly used two-step methods first cluster the data in some way, and build models using cluster summaries to predict the phenotype. It is known that important exposure variables can alter correlation patterns between clusters of HD variables, that is, alter network properties of the variables. However, it is not well understood whether such altered clustering is informative in prediction. Here, assuming there is a binary exposure with such network-altering effects, we explore whether the use of exposure-dependent clustering relationships in dimension reduction can improve predictive modeling in a two-step framework. Hence, we propose a modeling framework called ECLUST to test this hypothesis, and evaluate its performance through extensive simulations. With ECLUST, we found improved prediction and variable selection performance compared to methods that do not consider the environment in the clustering step, or to methods that use the original data as features. We further illustrate this modeling framework through the analysis of three data sets from very different fields, each with HD data, a binary exposure, and a phenotype of interest. Our method is available in the eclust CRAN package.

Indexed as

Models, GeneticAdolescentAlgorithmsChildChild, PreschoolCluster AnalysisComputer SimulationDatabases as TopicDiseaseEpigenesis, GeneticGene Expression RegulationHumansMagnetic Resonance Imaginggene-environment interactionhigh-dimensional clusteringpenalized regressionprediction modelstopological overlap matrix

Identifiers

PMID29423954
PMCPMC6175336

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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.