Literature DB >> 33521327

Generalized Structured Component Analysis in candidate gene association studies: applications and limitations.

Paul A Thompson1, Dorothy V M Bishop1, Else Eising2, Simon E Fisher2,3, Dianne F Newbury4.   

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. Copyright:
© 2020 Thompson PA et al.

Entities:  

Keywords:  GSCA; Structural equation modelling; developmental language disorder; genetics; power analysis; simulation

Year:  2020        PMID: 33521327      PMCID: PMC7818107          DOI: 10.12688/wellcomeopenres.15396.2

Source DB:  PubMed          Journal:  Wellcome Open Res        ISSN: 2398-502X


  25 in total

1.  Characterization of single-nucleotide polymorphisms in coding regions of human genes.

Authors:  M Cargill; D Altshuler; J Ireland; P Sklar; K Ardlie; N Patil; N Shaw; C R Lane; E P Lim; N Kalyanaraman; J Nemesh; L Ziaugra; L Friedland; A Rolfe; J Warrington; R Lipshutz; G Q Daley; E S Lander
Journal:  Nat Genet       Date:  1999-07       Impact factor: 38.330

2.  Pathway-based association study of multiple candidate genes and multiple traits using structural equation models.

Authors:  Hela Romdhani; Heungsun Hwang; Gilles Paradis; Marie-Helene Roy-Gagnon; Aurelie Labbe
Journal:  Genet Epidemiol       Date:  2014-12-30       Impact factor: 2.135

3.  A genomewide scan identifies two novel loci involved in specific language impairment.

Authors: 
Journal:  Am J Hum Genet       Date:  2002-01-04       Impact factor: 11.025

4.  Sample Size Requirements for Structural Equation Models: An Evaluation of Power, Bias, and Solution Propriety.

Authors:  Erika J Wolf; Kelly M Harrington; Shaunna L Clark; Mark W Miller
Journal:  Educ Psychol Meas       Date:  2013-12       Impact factor: 2.821

5.  Next-generation genotype imputation service and methods.

Authors:  Sayantan Das; Lukas Forer; Sebastian Schönherr; Carlo Sidore; Adam E Locke; Alan Kwong; Scott I Vrieze; Emily Y Chew; Shawn Levy; Matt McGue; David Schlessinger; Dwight Stambolian; Po-Ru Loh; William G Iacono; Anand Swaroop; Laura J Scott; Francesco Cucca; Florian Kronenberg; Michael Boehnke; Gonçalo R Abecasis; Christian Fuchsberger
Journal:  Nat Genet       Date:  2016-08-29       Impact factor: 38.330

Review 6.  Detecting gene-gene interactions that underlie human diseases.

Authors:  Heather J Cordell
Journal:  Nat Rev Genet       Date:  2009-06       Impact factor: 53.242

7.  Genome-wide screening for DNA variants associated with reading and language traits.

Authors:  A Gialluisi; D F Newbury; E G Wilcutt; R K Olson; J C DeFries; W M Brandler; B F Pennington; S D Smith; T S Scerri; N H Simpson; M Luciano; D M Evans; T C Bates; J F Stein; J B Talcott; A P Monaco; S Paracchini; C Francks; S E Fisher
Journal:  Genes Brain Behav       Date:  2014-08-29       Impact factor: 3.449

8.  Generalized Structured Component Analysis in candidate gene association studies: applications and limitations.

Authors:  Paul A Thompson; Dorothy V M Bishop; Else Eising; Simon E Fisher; Dianne F Newbury
Journal:  Wellcome Open Res       Date:  2020-10-08

9.  Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.

Authors:  R Nudel; N H Simpson; G Baird; A O'Hare; G Conti-Ramsden; P F Bolton; E R Hennessy; S M Ring; G Davey Smith; C Francks; S Paracchini; A P Monaco; S E Fisher; D F Newbury
Journal:  Genes Brain Behav       Date:  2014-03-24       Impact factor: 3.449

10.  Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis.

Authors:  Dianne F Newbury; Nuala H Simpson; Paul A Thompson; Dorothy V M Bishop
Journal:  Wellcome Open Res       Date:  2018-02-12
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  2 in total

1.  Generalized Structured Component Analysis in candidate gene association studies: applications and limitations.

Authors:  Paul A Thompson; Dorothy V M Bishop; Else Eising; Simon E Fisher; Dianne F Newbury
Journal:  Wellcome Open Res       Date:  2020-10-08

2.  Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis.

Authors:  Dianne F Newbury; Nuala H Simpson; Paul A Thompson; Dorothy V M Bishop
Journal:  Wellcome Open Res       Date:  2020-09-07
  2 in total

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