OSCA: a tool for omic-data-based complex trait analysis

The rapid increase of omic data has greatly facilitated the investigation of associations between omic profiles such as DNA methylation (DNAm) and complex traits in large cohorts. Here, we propose a mixed-linear-model-based method called MOMENT that tests for association between a DNAm probe and tra...

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Published in:Genome Biology Vol. 20; no. 1; p. 107
Main Authors: Zhang, Futao, Chen, Wenhan, Zhu, Zhihong, Zhang, Qian, Nabais, Marta F, Qi, Ting, Deary, Ian J, Wray, Naomi R, Visscher, Peter M, McRae, Allan F, Yang, Jian
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Published: England BioMed Central 28-05-2019
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Abstract The rapid increase of omic data has greatly facilitated the investigation of associations between omic profiles such as DNA methylation (DNAm) and complex traits in large cohorts. Here, we propose a mixed-linear-model-based method called MOMENT that tests for association between a DNAm probe and trait with all other distal probes fitted in multiple random-effect components to account for unobserved confounders. We demonstrate by simulations that MOMENT shows a lower false positive rate and more robustness than existing methods. MOMENT has been implemented in a versatile software package called OSCA together with a number of other implementations for omic-data-based analyses.
AbstractList The rapid increase of omic data has greatly facilitated the investigation of associations between omic profiles such as DNA methylation (DNAm) and complex traits in large cohorts. Here, we propose a mixed-linear-model-based method called MOMENT that tests for association between a DNAm probe and trait with all other distal probes fitted in multiple random-effect components to account for unobserved confounders. We demonstrate by simulations that MOMENT shows a lower false positive rate and more robustness than existing methods. MOMENT has been implemented in a versatile software package called OSCA together with a number of other implementations for omic-data-based analyses.
Abstract The rapid increase of omic data has greatly facilitated the investigation of associations between omic profiles such as DNA methylation (DNAm) and complex traits in large cohorts. Here, we propose a mixed-linear-model-based method called MOMENT that tests for association between a DNAm probe and trait with all other distal probes fitted in multiple random-effect components to account for unobserved confounders. We demonstrate by simulations that MOMENT shows a lower false positive rate and more robustness than existing methods. MOMENT has been implemented in a versatile software package called OSCA together with a number of other implementations for omic-data-based analyses.
ArticleNumber 107
Author Deary, Ian J
McRae, Allan F
Nabais, Marta F
Visscher, Peter M
Yang, Jian
Wray, Naomi R
Zhu, Zhihong
Qi, Ting
Zhang, Qian
Zhang, Futao
Chen, Wenhan
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  surname: Zhang
  fullname: Zhang, Futao
  organization: Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, 4072, Australia
– sequence: 2
  givenname: Wenhan
  surname: Chen
  fullname: Chen, Wenhan
  organization: Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, 4072, Australia
– sequence: 3
  givenname: Zhihong
  surname: Zhu
  fullname: Zhu, Zhihong
  organization: Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, 4072, Australia
– sequence: 4
  givenname: Qian
  surname: Zhang
  fullname: Zhang, Qian
  organization: Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, 4072, Australia
– sequence: 5
  givenname: Marta F
  surname: Nabais
  fullname: Nabais, Marta F
  organization: University of Exeter Medical School, Devon, EX2 5DW, UK
– sequence: 6
  givenname: Ting
  surname: Qi
  fullname: Qi, Ting
  organization: Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, 4072, Australia
– sequence: 7
  givenname: Ian J
  surname: Deary
  fullname: Deary, Ian J
  organization: Centre for Cognitive Ageing and Cognitive Epidemiology, Department of Psychology, University of Edinburgh, 7 George Square, Edinburgh, EH8 9JZ, UK
– sequence: 8
  givenname: Naomi R
  surname: Wray
  fullname: Wray, Naomi R
  organization: Queensland Brain Institute, The University of Queensland, Brisbane, Queensland, 4072, Australia
– sequence: 9
  givenname: Peter M
  surname: Visscher
  fullname: Visscher, Peter M
  organization: Queensland Brain Institute, The University of Queensland, Brisbane, Queensland, 4072, Australia
– sequence: 10
  givenname: Allan F
  surname: McRae
  fullname: McRae, Allan F
  organization: Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, 4072, Australia
– sequence: 11
  givenname: Jian
  orcidid: 0000-0003-2001-2474
  surname: Yang
  fullname: Yang, Jian
  email: jian.yang.qt@gmail.com, jian.yang.qt@gmail.com, jian.yang.qt@gmail.com
  organization: Institute for Advanced Research, Wenzhou Medical University, Wenzhou, 325027, Zhejiang, China. jian.yang.qt@gmail.com
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31138268$$D View this record in MEDLINE/PubMed
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Snippet The rapid increase of omic data has greatly facilitated the investigation of associations between omic profiles such as DNA methylation (DNAm) and complex...
Abstract The rapid increase of omic data has greatly facilitated the investigation of associations between omic profiles such as DNA methylation (DNAm) and...
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StartPage 107
SubjectTerms Age
Aged
Computer Simulation
Data analysis
Deoxyribonucleic acid
DNA
DNA Methylation
DNA probes
Gene expression
Genetic Techniques
Genotype & phenotype
Humans
Linear Models
Metabolomics - methods
Method
Phenotype
Software
Studies
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Title OSCA: a tool for omic-data-based complex trait analysis
URI https://www.ncbi.nlm.nih.gov/pubmed/31138268
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