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The challenge of detecting genotype-by-methylation interaction: GAW20
BACKGROUND: GAW20 working group 5 brought together researchers who contributed 7 papers with the aim of evaluating methods to detect genetic by epigenetic interactions. GAW20 distributed real data from the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) study, including single-nucleotide p...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157121/ https://www.ncbi.nlm.nih.gov/pubmed/30255819 http://dx.doi.org/10.1186/s12863-018-0650-7 |
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author | de Andrade, Mariza Warwick Daw, E. Kraja, Aldi T. Fisher, Virginia Wang, Lan Hu, Ke Li, Jing Romanescu, Razvan Veenstra, Jenna Sun, Rui Weng, Haoyi Zhou, Wenda |
author_facet | de Andrade, Mariza Warwick Daw, E. Kraja, Aldi T. Fisher, Virginia Wang, Lan Hu, Ke Li, Jing Romanescu, Razvan Veenstra, Jenna Sun, Rui Weng, Haoyi Zhou, Wenda |
author_sort | de Andrade, Mariza |
collection | PubMed |
description | BACKGROUND: GAW20 working group 5 brought together researchers who contributed 7 papers with the aim of evaluating methods to detect genetic by epigenetic interactions. GAW20 distributed real data from the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) study, including single-nucleotide polymorphism (SNP) markers, methylation (cytosine-phosphate-guanine [CpG]) markers, and phenotype information on up to 995 individuals. In addition, a simulated data set based on the real data was provided. RESULTS: The 7 contributed papers analyzed these data sets with a number of different statistical methods, including generalized linear mixed models, mediation analysis, machine learning, W-test, and sparsity-inducing regularized regression. These methods generally appeared to perform well. Several papers confirmed a number of causative SNPs in either the large number of simulation sets or the real data on chromosome 11. Findings were also reported for different SNPs, CpG sites, and SNP–CpG site interaction pairs. CONCLUSIONS: In the simulation (200 replications), power appeared generally good for large interaction effects, but smaller effects will require larger studies or consortium collaboration for realizing a sufficient power. |
format | Online Article Text |
id | pubmed-6157121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61571212018-10-01 The challenge of detecting genotype-by-methylation interaction: GAW20 de Andrade, Mariza Warwick Daw, E. Kraja, Aldi T. Fisher, Virginia Wang, Lan Hu, Ke Li, Jing Romanescu, Razvan Veenstra, Jenna Sun, Rui Weng, Haoyi Zhou, Wenda BMC Genet Proceedings BACKGROUND: GAW20 working group 5 brought together researchers who contributed 7 papers with the aim of evaluating methods to detect genetic by epigenetic interactions. GAW20 distributed real data from the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) study, including single-nucleotide polymorphism (SNP) markers, methylation (cytosine-phosphate-guanine [CpG]) markers, and phenotype information on up to 995 individuals. In addition, a simulated data set based on the real data was provided. RESULTS: The 7 contributed papers analyzed these data sets with a number of different statistical methods, including generalized linear mixed models, mediation analysis, machine learning, W-test, and sparsity-inducing regularized regression. These methods generally appeared to perform well. Several papers confirmed a number of causative SNPs in either the large number of simulation sets or the real data on chromosome 11. Findings were also reported for different SNPs, CpG sites, and SNP–CpG site interaction pairs. CONCLUSIONS: In the simulation (200 replications), power appeared generally good for large interaction effects, but smaller effects will require larger studies or consortium collaboration for realizing a sufficient power. BioMed Central 2018-09-17 /pmc/articles/PMC6157121/ /pubmed/30255819 http://dx.doi.org/10.1186/s12863-018-0650-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Proceedings de Andrade, Mariza Warwick Daw, E. Kraja, Aldi T. Fisher, Virginia Wang, Lan Hu, Ke Li, Jing Romanescu, Razvan Veenstra, Jenna Sun, Rui Weng, Haoyi Zhou, Wenda The challenge of detecting genotype-by-methylation interaction: GAW20 |
title | The challenge of detecting genotype-by-methylation interaction: GAW20 |
title_full | The challenge of detecting genotype-by-methylation interaction: GAW20 |
title_fullStr | The challenge of detecting genotype-by-methylation interaction: GAW20 |
title_full_unstemmed | The challenge of detecting genotype-by-methylation interaction: GAW20 |
title_short | The challenge of detecting genotype-by-methylation interaction: GAW20 |
title_sort | challenge of detecting genotype-by-methylation interaction: gaw20 |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157121/ https://www.ncbi.nlm.nih.gov/pubmed/30255819 http://dx.doi.org/10.1186/s12863-018-0650-7 |
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