ArticleStatistics in medicine2015
Integrative modeling of multi-platform genomic data under the framework of mediation analysis.
Article in Statistics in medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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.
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Who cites it
9 citing papers in PubMed.
- Large-scale integration of DNA methylation and gene expression array platforms identifies bothEpigenetics · 2022Article
- A latent unknown clustering integrating multi-omics data (LUCID) with phenotypic traits.Bioinformatics (Oxford, England) · 2020Article
- Multi-SNP mediation intersection-union test.Bioinformatics (Oxford, England) · 2019Article
- Identification of trans-eQTLs using mediation analysis with multiple mediators.BMC bioinformatics · 2019Article
- Sex dimorphism in a mediatory role of the posterior midcingulate cortex in the association between anxiety and pain sensitivity.Experimental brain research · 2016Article
- Integrative genomic testing of cancer survival using semiparametric linear transformation models.Statistics in medicine · 2016Article
- Integrative Analysis of Multi-omics Data for Discovery and Functional Studies of Complex Human Diseases.Advances in genetics · 2016Review
- Exploring possible epigenetic mediation of early-life environmental exposures on adiposity and obesity development.International journal of epidemiology · 2015Review
- PON1 as a model for integration of genetic, epigenetic, and expression data on candidate susceptibility genes.Environmental epigenetics · 2015Article
Corrections and comments
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Authors and funding
1 author.
Funding
Abstract
Given the availability of genomic data, there have been emerging interests in integrating multi-platform data. Here, we propose to model genetics (single nucleotide polymorphism (SNP)), epigenetics (DNA methylation), and gene expression data as a biological process to delineate phenotypic traits under the framework of causal mediation modeling. We propose a regression model for the joint effect of SNPs, methylation, gene expression, and their nonlinear interactions on the outcome and develop a variance component score test for any arbitrary set of regression coefficients. The test statistic under the null follows a mixture of chi-square distributions, which can be approximated using a characteristic function inversion method or a perturbation procedure. We construct tests for candidate models determined by different combinations of SNPs, DNA methylation, gene expression, and interactions and further propose an omnibus test to accommodate different models. We then study three path-specific effects: the direct effect of SNPs on the outcome, the effect mediated through expression, and the effect through methylation. We characterize correspondences between the three path-specific effects and coefficients in the regression model, which are influenced by causal relations among SNPs, DNA methylation, and gene expression. We illustrate the utility of our method in two genomic studies and numerical simulation studies.
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Registered trials
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.