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Fast computation of genome-metagenome interaction effects
MOTIVATION: Association studies have been widely used to search for associations between common genetic variants observations and a given phenotype. However, it is now generally accepted that genes and environment must be examined jointly when estimating phenotypic variance. In this work we consider...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329492/ https://www.ncbi.nlm.nih.gov/pubmed/32625242 http://dx.doi.org/10.1186/s13015-020-00173-2 |
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author | Guinot, Florent Szafranski, Marie Chiquet, Julien Zancarini, Anouk Le Signor, Christine Mougel, Christophe Ambroise, Christophe |
author_facet | Guinot, Florent Szafranski, Marie Chiquet, Julien Zancarini, Anouk Le Signor, Christine Mougel, Christophe Ambroise, Christophe |
author_sort | Guinot, Florent |
collection | PubMed |
description | MOTIVATION: Association studies have been widely used to search for associations between common genetic variants observations and a given phenotype. However, it is now generally accepted that genes and environment must be examined jointly when estimating phenotypic variance. In this work we consider two types of biological markers: genotypic markers, which characterize an observation in terms of inherited genetic information, and metagenomic marker which are related to the environment. Both types of markers are available in their millions and can be used to characterize any observation uniquely. OBJECTIVE: Our focus is on detecting interactions between groups of genetic and metagenomic markers in order to gain a better understanding of the complex relationship between environment and genome in the expression of a given phenotype. CONTRIBUTIONS: We propose a novel approach for efficiently detecting interactions between complementary datasets in a high-dimensional setting with a reduced computational cost. The method, named SICOMORE, reduces the dimension of the search space by selecting a subset of supervariables in the two complementary datasets. These supervariables are given by a weighted group structure defined on sets of variables at different scales. A Lasso selection is then applied on each type of supervariable to obtain a subset of potential interactions that will be explored via linear model testing. RESULTS: We compare SICOMORE with other approaches in simulations, with varying sample sizes, noise, and numbers of true interactions. SICOMORE exhibits convincing results in terms of recall, as well as competitive performances with respect to running time. The method is also used to detect interaction between genomic markers in Medicago truncatula and metagenomic markers in its rhizosphere bacterial community. SOFTWARE AVAILABILITY: An R package is available [4], along with its documentation and associated scripts, allowing the reader to reproduce the results presented in the paper. |
format | Online Article Text |
id | pubmed-7329492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73294922020-07-02 Fast computation of genome-metagenome interaction effects Guinot, Florent Szafranski, Marie Chiquet, Julien Zancarini, Anouk Le Signor, Christine Mougel, Christophe Ambroise, Christophe Algorithms Mol Biol Research MOTIVATION: Association studies have been widely used to search for associations between common genetic variants observations and a given phenotype. However, it is now generally accepted that genes and environment must be examined jointly when estimating phenotypic variance. In this work we consider two types of biological markers: genotypic markers, which characterize an observation in terms of inherited genetic information, and metagenomic marker which are related to the environment. Both types of markers are available in their millions and can be used to characterize any observation uniquely. OBJECTIVE: Our focus is on detecting interactions between groups of genetic and metagenomic markers in order to gain a better understanding of the complex relationship between environment and genome in the expression of a given phenotype. CONTRIBUTIONS: We propose a novel approach for efficiently detecting interactions between complementary datasets in a high-dimensional setting with a reduced computational cost. The method, named SICOMORE, reduces the dimension of the search space by selecting a subset of supervariables in the two complementary datasets. These supervariables are given by a weighted group structure defined on sets of variables at different scales. A Lasso selection is then applied on each type of supervariable to obtain a subset of potential interactions that will be explored via linear model testing. RESULTS: We compare SICOMORE with other approaches in simulations, with varying sample sizes, noise, and numbers of true interactions. SICOMORE exhibits convincing results in terms of recall, as well as competitive performances with respect to running time. The method is also used to detect interaction between genomic markers in Medicago truncatula and metagenomic markers in its rhizosphere bacterial community. SOFTWARE AVAILABILITY: An R package is available [4], along with its documentation and associated scripts, allowing the reader to reproduce the results presented in the paper. BioMed Central 2020-07-01 /pmc/articles/PMC7329492/ /pubmed/32625242 http://dx.doi.org/10.1186/s13015-020-00173-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Guinot, Florent Szafranski, Marie Chiquet, Julien Zancarini, Anouk Le Signor, Christine Mougel, Christophe Ambroise, Christophe Fast computation of genome-metagenome interaction effects |
title | Fast computation of genome-metagenome interaction effects |
title_full | Fast computation of genome-metagenome interaction effects |
title_fullStr | Fast computation of genome-metagenome interaction effects |
title_full_unstemmed | Fast computation of genome-metagenome interaction effects |
title_short | Fast computation of genome-metagenome interaction effects |
title_sort | fast computation of genome-metagenome interaction effects |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329492/ https://www.ncbi.nlm.nih.gov/pubmed/32625242 http://dx.doi.org/10.1186/s13015-020-00173-2 |
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