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Phylogenetics Applied to Genotype/Phenotype Association and Selection Analyses with Sequence Data from Angptl4 in Humans

Genotype/phenotype association analyses (Treescan) with plasma lipid levels and functional site prediction methods (TreeSAAP and PolyPhen) were performed using sequence data for ANGPTL4 from 3,551 patients in the Dallas Heart Study. Biological assays of rare variants in phenotypic tails and results...

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Autores principales: Maxwell, Taylor J., Bendall, Matthew L., Staples, Jeffrey, Jarvis, Todd, Crandall, Keith A.
Formato: Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821009/
https://www.ncbi.nlm.nih.gov/pubmed/20162021
http://dx.doi.org/10.3390/ijms11010370
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author Maxwell, Taylor J.
Bendall, Matthew L.
Staples, Jeffrey
Jarvis, Todd
Crandall, Keith A.
author_facet Maxwell, Taylor J.
Bendall, Matthew L.
Staples, Jeffrey
Jarvis, Todd
Crandall, Keith A.
author_sort Maxwell, Taylor J.
collection PubMed
description Genotype/phenotype association analyses (Treescan) with plasma lipid levels and functional site prediction methods (TreeSAAP and PolyPhen) were performed using sequence data for ANGPTL4 from 3,551 patients in the Dallas Heart Study. Biological assays of rare variants in phenotypic tails and results from a Treescan analysis were used as “known” variants to assess the site prediction abilities of PolyPhen and TreeSAAP. The E40K variant in European Americans and the R278Q variant in African Americans were significantly associated with multiple lipid phenotypes. Combining TreeSAAP and PolyPhen performed well to predict “known” functional variants while reducing noise from false positives.
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spelling pubmed-28210092010-02-16 Phylogenetics Applied to Genotype/Phenotype Association and Selection Analyses with Sequence Data from Angptl4 in Humans Maxwell, Taylor J. Bendall, Matthew L. Staples, Jeffrey Jarvis, Todd Crandall, Keith A. Int J Mol Sci Article Genotype/phenotype association analyses (Treescan) with plasma lipid levels and functional site prediction methods (TreeSAAP and PolyPhen) were performed using sequence data for ANGPTL4 from 3,551 patients in the Dallas Heart Study. Biological assays of rare variants in phenotypic tails and results from a Treescan analysis were used as “known” variants to assess the site prediction abilities of PolyPhen and TreeSAAP. The E40K variant in European Americans and the R278Q variant in African Americans were significantly associated with multiple lipid phenotypes. Combining TreeSAAP and PolyPhen performed well to predict “known” functional variants while reducing noise from false positives. Molecular Diversity Preservation International (MDPI) 2010-01-25 /pmc/articles/PMC2821009/ /pubmed/20162021 http://dx.doi.org/10.3390/ijms11010370 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Maxwell, Taylor J.
Bendall, Matthew L.
Staples, Jeffrey
Jarvis, Todd
Crandall, Keith A.
Phylogenetics Applied to Genotype/Phenotype Association and Selection Analyses with Sequence Data from Angptl4 in Humans
title Phylogenetics Applied to Genotype/Phenotype Association and Selection Analyses with Sequence Data from Angptl4 in Humans
title_full Phylogenetics Applied to Genotype/Phenotype Association and Selection Analyses with Sequence Data from Angptl4 in Humans
title_fullStr Phylogenetics Applied to Genotype/Phenotype Association and Selection Analyses with Sequence Data from Angptl4 in Humans
title_full_unstemmed Phylogenetics Applied to Genotype/Phenotype Association and Selection Analyses with Sequence Data from Angptl4 in Humans
title_short Phylogenetics Applied to Genotype/Phenotype Association and Selection Analyses with Sequence Data from Angptl4 in Humans
title_sort phylogenetics applied to genotype/phenotype association and selection analyses with sequence data from angptl4 in humans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821009/
https://www.ncbi.nlm.nih.gov/pubmed/20162021
http://dx.doi.org/10.3390/ijms11010370
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