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Heuristic Identification of Biological Architectures for Simulating Complex Hierarchical Genetic Interactions
Simulation plays an essential role in the development of new computational and statistical methods for the genetic analysis of complex traits. Most simulations start with a statistical model using methods such as linear or logistic regression that specify the relationship between genotype and phenot...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270828/ https://www.ncbi.nlm.nih.gov/pubmed/25395175 http://dx.doi.org/10.1002/gepi.21865 |
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author | Moore, Jason H Amos, Ryan Kiralis, Jeff Andrews, Peter C |
author_facet | Moore, Jason H Amos, Ryan Kiralis, Jeff Andrews, Peter C |
author_sort | Moore, Jason H |
collection | PubMed |
description | Simulation plays an essential role in the development of new computational and statistical methods for the genetic analysis of complex traits. Most simulations start with a statistical model using methods such as linear or logistic regression that specify the relationship between genotype and phenotype. This is appealing due to its simplicity and because these statistical methods are commonly used in genetic analysis. It is our working hypothesis that simulations need to move beyond simple statistical models to more realistically represent the biological complexity of genetic architecture. The goal of the present study was to develop a prototype genotype–phenotype simulation method and software that are capable of simulating complex genetic effects within the context of a hierarchical biology-based framework. Specifically, our goal is to simulate multilocus epistasis or gene–gene interaction where the genetic variants are organized within the framework of one or more genes, their regulatory regions and other regulatory loci. We introduce here the Heuristic Identification of Biological Architectures for simulating Complex Hierarchical Interactions (HIBACHI) method and prototype software for simulating data in this manner. This approach combines a biological hierarchy, a flexible mathematical framework, a liability threshold model for defining disease endpoints, and a heuristic search strategy for identifying high-order epistatic models of disease susceptibility. We provide several simulation examples using genetic models exhibiting independent main effects and three-way epistatic effects. |
format | Online Article Text |
id | pubmed-4270828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42708282015-02-03 Heuristic Identification of Biological Architectures for Simulating Complex Hierarchical Genetic Interactions Moore, Jason H Amos, Ryan Kiralis, Jeff Andrews, Peter C Genet Epidemiol Research Articles Simulation plays an essential role in the development of new computational and statistical methods for the genetic analysis of complex traits. Most simulations start with a statistical model using methods such as linear or logistic regression that specify the relationship between genotype and phenotype. This is appealing due to its simplicity and because these statistical methods are commonly used in genetic analysis. It is our working hypothesis that simulations need to move beyond simple statistical models to more realistically represent the biological complexity of genetic architecture. The goal of the present study was to develop a prototype genotype–phenotype simulation method and software that are capable of simulating complex genetic effects within the context of a hierarchical biology-based framework. Specifically, our goal is to simulate multilocus epistasis or gene–gene interaction where the genetic variants are organized within the framework of one or more genes, their regulatory regions and other regulatory loci. We introduce here the Heuristic Identification of Biological Architectures for simulating Complex Hierarchical Interactions (HIBACHI) method and prototype software for simulating data in this manner. This approach combines a biological hierarchy, a flexible mathematical framework, a liability threshold model for defining disease endpoints, and a heuristic search strategy for identifying high-order epistatic models of disease susceptibility. We provide several simulation examples using genetic models exhibiting independent main effects and three-way epistatic effects. BlackWell Publishing Ltd 2015-01 2014-11-13 /pmc/articles/PMC4270828/ /pubmed/25395175 http://dx.doi.org/10.1002/gepi.21865 Text en © 2015 Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Moore, Jason H Amos, Ryan Kiralis, Jeff Andrews, Peter C Heuristic Identification of Biological Architectures for Simulating Complex Hierarchical Genetic Interactions |
title | Heuristic Identification of Biological Architectures for Simulating Complex Hierarchical Genetic Interactions |
title_full | Heuristic Identification of Biological Architectures for Simulating Complex Hierarchical Genetic Interactions |
title_fullStr | Heuristic Identification of Biological Architectures for Simulating Complex Hierarchical Genetic Interactions |
title_full_unstemmed | Heuristic Identification of Biological Architectures for Simulating Complex Hierarchical Genetic Interactions |
title_short | Heuristic Identification of Biological Architectures for Simulating Complex Hierarchical Genetic Interactions |
title_sort | heuristic identification of biological architectures for simulating complex hierarchical genetic interactions |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270828/ https://www.ncbi.nlm.nih.gov/pubmed/25395175 http://dx.doi.org/10.1002/gepi.21865 |
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