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  Generalized Structured Component Analysis in candidate gene association studies: Applications and limitations [version 2; peer review: 3 approved]

Thompson, P. A., Bishop, D. V. M., Eising, E., Fisher, S. E., & Newbury, D. F. (2020). Generalized Structured Component Analysis in candidate gene association studies: Applications and limitations [version 2; peer review: 3 approved]. Wellcome Open Research, 4: 142. doi:10.12688/wellcomeopenres.15396.2.

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2021
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© 2020 Thompson PA et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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 Creators:
Thompson, Paul A.1, Author
Bishop, Dorothy V. M.1, Author
Eising, Else2, Author           
Fisher, Simon E.2, 3, Author           
Newbury, Dianne F.4, Author
Affiliations:
1University of Oxford, Oxford, UK, ou_persistent22              
2Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, ou_792549              
3Donders Institute for Brain, Cognition and Behaviour, External Organizations, ou_55236              
4Oxford Brookes University, Oxford, UK, ou_persistent22              

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 Abstract: Background: Generalized Structured Component Analysis (GSCA) is a component-based alternative to traditional covariance-based structural equation modelling. This method has previously been applied to test for association between candidate genes and clinical phenotypes, contrasting with traditional genetic association analyses that adopt univariate testing of many individual single nucleotide polymorphisms (SNPs) with correction for multiple testing.
Methods: We first evaluate the ability of the GSCA method to replicate two previous findings from a genetics association study of developmental language disorders. We then present the results of a simulation study to test the validity of the GSCA method under more restrictive data conditions, using smaller sample sizes and larger numbers of SNPs than have previously been investigated. Finally, we compare GSCA performance against univariate association analysis conducted using PLINK v1.9.
Results: Results from simulations show that power to detect effects depends not just on sample size, but also on the ratio of SNPs with effect to number of SNPs tested within a gene. Inclusion of many SNPs in a model dilutes true effects.
Conclusions: We propose that GSCA is a useful method for replication studies, when candidate SNPs have been identified, but should not be used for exploratory analysis.

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Language(s): eng - English
 Dates: 2020-10-08
 Publication Status: Published online
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.12688/wellcomeopenres.15396.2
 Degree: -

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Title: Wellcome Open Research
Source Genre: Journal
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Publ. Info: UK : F1000Research
Pages: - Volume / Issue: 4 Sequence Number: 142 Start / End Page: - Identifier: Other: 2398-502X
CoNE: https://pure.mpg.de/cone/journals/resource/2398-502X