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Screening for interaction effects in gene expression data

Expression quantitative trait (eQTL) studies are a powerful tool for identifying genetic variants that affect levels of messenger RNA. Since gene expression is controlled by a complex network of gene-regulating factors, one way to identify these factors is to search for interaction effects between g...

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Autores principales: Castaldi, Peter J., Cho, Michael H., Liang, Liming, Silverman, Edwin K., Hersh, Craig P., Rice, Kenneth, Aschard, Hugues
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354413/
https://www.ncbi.nlm.nih.gov/pubmed/28301596
http://dx.doi.org/10.1371/journal.pone.0173847
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author Castaldi, Peter J.
Cho, Michael H.
Liang, Liming
Silverman, Edwin K.
Hersh, Craig P.
Rice, Kenneth
Aschard, Hugues
author_facet Castaldi, Peter J.
Cho, Michael H.
Liang, Liming
Silverman, Edwin K.
Hersh, Craig P.
Rice, Kenneth
Aschard, Hugues
author_sort Castaldi, Peter J.
collection PubMed
description Expression quantitative trait (eQTL) studies are a powerful tool for identifying genetic variants that affect levels of messenger RNA. Since gene expression is controlled by a complex network of gene-regulating factors, one way to identify these factors is to search for interaction effects between genetic variants and mRNA levels of transcription factors (TFs) and their respective target genes. However, identification of interaction effects in gene expression data pose a variety of methodological challenges, and it has become clear that such analyses should be conducted and interpreted with caution. Investigating the validity and interpretability of several interaction tests when screening for eQTL SNPs whose effect on the target gene expression is modified by the expression level of a transcription factor, we characterized two important methodological issues. First, we stress the scale-dependency of interaction effects and highlight that commonly applied transformation of gene expression data can induce or remove interactions, making interpretation of results more challenging. We then demonstrate that, in the setting of moderate to strong interaction effects on the order of what may be reasonably expected for eQTL studies, standard interaction screening can be biased due to heteroscedasticity induced by true interactions. Using simulation and real data analysis, we outline a set of reasonable minimum conditions and sample size requirements for reliable detection of variant-by-environment and variant-by-TF interactions using the heteroscedasticity consistent covariance-based approach.
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spelling pubmed-53544132017-04-06 Screening for interaction effects in gene expression data Castaldi, Peter J. Cho, Michael H. Liang, Liming Silverman, Edwin K. Hersh, Craig P. Rice, Kenneth Aschard, Hugues PLoS One Research Article Expression quantitative trait (eQTL) studies are a powerful tool for identifying genetic variants that affect levels of messenger RNA. Since gene expression is controlled by a complex network of gene-regulating factors, one way to identify these factors is to search for interaction effects between genetic variants and mRNA levels of transcription factors (TFs) and their respective target genes. However, identification of interaction effects in gene expression data pose a variety of methodological challenges, and it has become clear that such analyses should be conducted and interpreted with caution. Investigating the validity and interpretability of several interaction tests when screening for eQTL SNPs whose effect on the target gene expression is modified by the expression level of a transcription factor, we characterized two important methodological issues. First, we stress the scale-dependency of interaction effects and highlight that commonly applied transformation of gene expression data can induce or remove interactions, making interpretation of results more challenging. We then demonstrate that, in the setting of moderate to strong interaction effects on the order of what may be reasonably expected for eQTL studies, standard interaction screening can be biased due to heteroscedasticity induced by true interactions. Using simulation and real data analysis, we outline a set of reasonable minimum conditions and sample size requirements for reliable detection of variant-by-environment and variant-by-TF interactions using the heteroscedasticity consistent covariance-based approach. Public Library of Science 2017-03-16 /pmc/articles/PMC5354413/ /pubmed/28301596 http://dx.doi.org/10.1371/journal.pone.0173847 Text en © 2017 Castaldi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Castaldi, Peter J.
Cho, Michael H.
Liang, Liming
Silverman, Edwin K.
Hersh, Craig P.
Rice, Kenneth
Aschard, Hugues
Screening for interaction effects in gene expression data
title Screening for interaction effects in gene expression data
title_full Screening for interaction effects in gene expression data
title_fullStr Screening for interaction effects in gene expression data
title_full_unstemmed Screening for interaction effects in gene expression data
title_short Screening for interaction effects in gene expression data
title_sort screening for interaction effects in gene expression data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354413/
https://www.ncbi.nlm.nih.gov/pubmed/28301596
http://dx.doi.org/10.1371/journal.pone.0173847
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