Joint analysis of genetic and epigenetic data using a conditional autoregressive model

Abstract Background Rapidly evolving high-throughput technology has made it cost-effective to collect multilevel omic data in clinical and biological studies. Different types of omic data collected from these studies provide both shared and complementary information, and can be integrated into assoc...

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Main Authors: Xiaoxi Shen, Qing Lu
Format: Article
Language:English
Published: BMC 2018-09-01
Series:BMC Genetics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12863-018-0641-8
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spelling doaj-68cc6d75aa1f498ebfedde2f819ec0d02020-11-25T03:55:59ZengBMCBMC Genetics1471-21562018-09-0119S1515410.1186/s12863-018-0641-8Joint analysis of genetic and epigenetic data using a conditional autoregressive modelXiaoxi Shen0Qing Lu1Department of Statistics and Probability, Michigan State UniversityDepartment of Epidemiology and Biostatistics, Michigan State UniversityAbstract Background Rapidly evolving high-throughput technology has made it cost-effective to collect multilevel omic data in clinical and biological studies. Different types of omic data collected from these studies provide both shared and complementary information, and can be integrated into association analysis to enhance the power of identifying novel disease-associated biomarkers. To model the joint effect of genetic markers and DNA methylation on the phenotype of interest, we propose a joint conditional autoregressive (JCAR) model. A linear score test is used for hypothesis testing and the corresponding p value can be obtained using the Davies method. Results The JCAR model was applied to the GAW20 data from the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) study. In our application of the JCAR model, we consider a baseline model and a full model. In the baseline model, we consider 3 different scenarios: a model with only genetic information, a model with only DNA methylation information at visit 2, and a model using both genetic and DNA methylation information at visit 2. For the full model, we consider both genetic and DNA methylation information at visit 2 and visit 4. The top 10 significant genes are reported for each model. Based on the results, we found that the gene MYO3B was significant as long as the methylation information was considered in the analysis. Conclusions JCAR is a useful tool for joint association analysis of genetic and epigenetic data. It is easy to implement and is computationally efficient. It can also be extended to analyze other types of omic data.http://link.springer.com/article/10.1186/s12863-018-0641-8Joint associationsConditional autoregressive (CAR) modelLinear score test
collection DOAJ
language English
format Article
sources DOAJ
author Xiaoxi Shen
Qing Lu
spellingShingle Xiaoxi Shen
Qing Lu
Joint analysis of genetic and epigenetic data using a conditional autoregressive model
BMC Genetics
Joint associations
Conditional autoregressive (CAR) model
Linear score test
author_facet Xiaoxi Shen
Qing Lu
author_sort Xiaoxi Shen
title Joint analysis of genetic and epigenetic data using a conditional autoregressive model
title_short Joint analysis of genetic and epigenetic data using a conditional autoregressive model
title_full Joint analysis of genetic and epigenetic data using a conditional autoregressive model
title_fullStr Joint analysis of genetic and epigenetic data using a conditional autoregressive model
title_full_unstemmed Joint analysis of genetic and epigenetic data using a conditional autoregressive model
title_sort joint analysis of genetic and epigenetic data using a conditional autoregressive model
publisher BMC
series BMC Genetics
issn 1471-2156
publishDate 2018-09-01
description Abstract Background Rapidly evolving high-throughput technology has made it cost-effective to collect multilevel omic data in clinical and biological studies. Different types of omic data collected from these studies provide both shared and complementary information, and can be integrated into association analysis to enhance the power of identifying novel disease-associated biomarkers. To model the joint effect of genetic markers and DNA methylation on the phenotype of interest, we propose a joint conditional autoregressive (JCAR) model. A linear score test is used for hypothesis testing and the corresponding p value can be obtained using the Davies method. Results The JCAR model was applied to the GAW20 data from the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) study. In our application of the JCAR model, we consider a baseline model and a full model. In the baseline model, we consider 3 different scenarios: a model with only genetic information, a model with only DNA methylation information at visit 2, and a model using both genetic and DNA methylation information at visit 2. For the full model, we consider both genetic and DNA methylation information at visit 2 and visit 4. The top 10 significant genes are reported for each model. Based on the results, we found that the gene MYO3B was significant as long as the methylation information was considered in the analysis. Conclusions JCAR is a useful tool for joint association analysis of genetic and epigenetic data. It is easy to implement and is computationally efficient. It can also be extended to analyze other types of omic data.
topic Joint associations
Conditional autoregressive (CAR) model
Linear score test
url http://link.springer.com/article/10.1186/s12863-018-0641-8
work_keys_str_mv AT xiaoxishen jointanalysisofgeneticandepigeneticdatausingaconditionalautoregressivemodel
AT qinglu jointanalysisofgeneticandepigeneticdatausingaconditionalautoregressivemodel
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