Cargando…

Examination of previously identified associations within the Genetic Analysis Workshop 19 data

We investigate the possible replication of “known” associated single-nucleotide polymorphisms (SNPs) with blood pressure and expression phenotypes. Previous studies have provided a list of 95 SNPs thought to be associated with blood pressure phenotypes, of which 44 were present in the Genetic Analys...

Descripción completa

Detalles Bibliográficos
Autores principales: Howey, Richard A. J., Eu-ahsunthornwattana, Jakris, Darlay, Rebecca, Cordell, Heather J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133475/
https://www.ncbi.nlm.nih.gov/pubmed/27980618
http://dx.doi.org/10.1186/s12919-016-0012-2
_version_ 1782471269503991808
author Howey, Richard A. J.
Eu-ahsunthornwattana, Jakris
Darlay, Rebecca
Cordell, Heather J.
author_facet Howey, Richard A. J.
Eu-ahsunthornwattana, Jakris
Darlay, Rebecca
Cordell, Heather J.
author_sort Howey, Richard A. J.
collection PubMed
description We investigate the possible replication of “known” associated single-nucleotide polymorphisms (SNPs) with blood pressure and expression phenotypes. Previous studies have provided a list of 95 SNPs thought to be associated with blood pressure phenotypes, of which 44 were present in the Genetic Analysis Workshop 19 (GAW19) family-imputed genome-wide association studies (GWAS) data and 4 in the GAW19 unrelateds sequence data. Using only the real (not simulated) GAW19 data, we show through the use of statistical tests that account for family relatedness, using FaST-LMM (Factored Spectrally Transformed Linear Mixed Model), that none of our candidate SNPs yields a significant p value. Furthermore, a study of epistasis, aiming to detect statistical interactions between loci with respect to their association with transcription levels has provided a list of 30 associated interacting SNP pairs, of which 13 are present in the GAW19 family GWAS and expression data. We show for this set of results, using the program GEMMA (genome-wide efficient mixed-model analysis) to account for family relatedness, that there is evidence of replication within the real GAW19 data. Two individual SNP pairs reach significance, and the set of remaining results give a combined p value of 0.017 that at least 1 of these remaining SNP pairs interacts to influence an expression phenotype.
format Online
Article
Text
id pubmed-5133475
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-51334752016-12-15 Examination of previously identified associations within the Genetic Analysis Workshop 19 data Howey, Richard A. J. Eu-ahsunthornwattana, Jakris Darlay, Rebecca Cordell, Heather J. BMC Proc Proceedings We investigate the possible replication of “known” associated single-nucleotide polymorphisms (SNPs) with blood pressure and expression phenotypes. Previous studies have provided a list of 95 SNPs thought to be associated with blood pressure phenotypes, of which 44 were present in the Genetic Analysis Workshop 19 (GAW19) family-imputed genome-wide association studies (GWAS) data and 4 in the GAW19 unrelateds sequence data. Using only the real (not simulated) GAW19 data, we show through the use of statistical tests that account for family relatedness, using FaST-LMM (Factored Spectrally Transformed Linear Mixed Model), that none of our candidate SNPs yields a significant p value. Furthermore, a study of epistasis, aiming to detect statistical interactions between loci with respect to their association with transcription levels has provided a list of 30 associated interacting SNP pairs, of which 13 are present in the GAW19 family GWAS and expression data. We show for this set of results, using the program GEMMA (genome-wide efficient mixed-model analysis) to account for family relatedness, that there is evidence of replication within the real GAW19 data. Two individual SNP pairs reach significance, and the set of remaining results give a combined p value of 0.017 that at least 1 of these remaining SNP pairs interacts to influence an expression phenotype. BioMed Central 2016-10-18 /pmc/articles/PMC5133475/ /pubmed/27980618 http://dx.doi.org/10.1186/s12919-016-0012-2 Text en © The Author(s). 2016 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
Howey, Richard A. J.
Eu-ahsunthornwattana, Jakris
Darlay, Rebecca
Cordell, Heather J.
Examination of previously identified associations within the Genetic Analysis Workshop 19 data
title Examination of previously identified associations within the Genetic Analysis Workshop 19 data
title_full Examination of previously identified associations within the Genetic Analysis Workshop 19 data
title_fullStr Examination of previously identified associations within the Genetic Analysis Workshop 19 data
title_full_unstemmed Examination of previously identified associations within the Genetic Analysis Workshop 19 data
title_short Examination of previously identified associations within the Genetic Analysis Workshop 19 data
title_sort examination of previously identified associations within the genetic analysis workshop 19 data
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133475/
https://www.ncbi.nlm.nih.gov/pubmed/27980618
http://dx.doi.org/10.1186/s12919-016-0012-2
work_keys_str_mv AT howeyrichardaj examinationofpreviouslyidentifiedassociationswithinthegeneticanalysisworkshop19data
AT euahsunthornwattanajakris examinationofpreviouslyidentifiedassociationswithinthegeneticanalysisworkshop19data
AT darlayrebecca examinationofpreviouslyidentifiedassociationswithinthegeneticanalysisworkshop19data
AT cordellheatherj examinationofpreviouslyidentifiedassociationswithinthegeneticanalysisworkshop19data