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A proximal LAVA method for genome-wide association and prediction of traits with mixed inheritance patterns
BACKGROUND: The genetic basis of phenotypic traits is highly variable and usually divided into mono-, oligo- and polygenic inheritance classes. Relatively few traits are known to be monogenic or oligogeneic. The majority of traits are considered to have a polygenic background. To what extent there a...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547073/ https://www.ncbi.nlm.nih.gov/pubmed/34702175 http://dx.doi.org/10.1186/s12859-021-04436-6 |
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author | Waldmann, Patrik |
author_facet | Waldmann, Patrik |
author_sort | Waldmann, Patrik |
collection | PubMed |
description | BACKGROUND: The genetic basis of phenotypic traits is highly variable and usually divided into mono-, oligo- and polygenic inheritance classes. Relatively few traits are known to be monogenic or oligogeneic. The majority of traits are considered to have a polygenic background. To what extent there are mixtures between these classes is unknown. The rapid advancement of genomic techniques makes it possible to directly map large amounts of genomic markers (GWAS) and predict unknown phenotypes (GWP). Most of the multi-marker methods for GWAS and GWP falls into one of two regularization frameworks. The first framework is based on [Formula: see text] -norm regularization (e.g. the LASSO) and is suitable for mono- and oligogenic traits, whereas the second framework regularize with the [Formula: see text] -norm (e.g. ridge regression; RR) and thereby is favourable for polygenic traits. A general framework for mixed inheritance is lacking. RESULTS: We have developed a proximal operator algorithm based on the recent LAVA regularization method that jointly performs [Formula: see text] - and [Formula: see text] -norm regularization. The algorithm is built on the alternating direction method of multipliers and proximal translation mapping (LAVA ADMM). When evaluated on the simulated QTLMAS2010 data, it is shown that the LAVA ADMM together with Bayesian optimization of the regularization parameters provides an efficient approach with lower test prediction mean-squared-error (65.89) than the LASSO (66.11), Ridge regression (83.41) and Elastic net (66.11). For the real pig data the test MSE of the LAVA ADMM is 0.850 compared to the LASSO, RR and EN with 0.875, 0.853 and 0.853, respectively. CONCLUSIONS: This study presents the LAVA ADMM that is capable of joint modelling of monogenic major genetic effects and polygenic minor genetic effects which can be used for both genome-wide assoiciation and prediction purposes. The statistical evaluations based on both simulated and real pig data set shows that the LAVA ADMM has better prediction properies than the LASSO, RR and EN. Julia code for the LAVA ADMM is available at: https://github.com/patwa67/LAVAADMM. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04436-6. |
format | Online Article Text |
id | pubmed-8547073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85470732021-10-26 A proximal LAVA method for genome-wide association and prediction of traits with mixed inheritance patterns Waldmann, Patrik BMC Bioinformatics Research BACKGROUND: The genetic basis of phenotypic traits is highly variable and usually divided into mono-, oligo- and polygenic inheritance classes. Relatively few traits are known to be monogenic or oligogeneic. The majority of traits are considered to have a polygenic background. To what extent there are mixtures between these classes is unknown. The rapid advancement of genomic techniques makes it possible to directly map large amounts of genomic markers (GWAS) and predict unknown phenotypes (GWP). Most of the multi-marker methods for GWAS and GWP falls into one of two regularization frameworks. The first framework is based on [Formula: see text] -norm regularization (e.g. the LASSO) and is suitable for mono- and oligogenic traits, whereas the second framework regularize with the [Formula: see text] -norm (e.g. ridge regression; RR) and thereby is favourable for polygenic traits. A general framework for mixed inheritance is lacking. RESULTS: We have developed a proximal operator algorithm based on the recent LAVA regularization method that jointly performs [Formula: see text] - and [Formula: see text] -norm regularization. The algorithm is built on the alternating direction method of multipliers and proximal translation mapping (LAVA ADMM). When evaluated on the simulated QTLMAS2010 data, it is shown that the LAVA ADMM together with Bayesian optimization of the regularization parameters provides an efficient approach with lower test prediction mean-squared-error (65.89) than the LASSO (66.11), Ridge regression (83.41) and Elastic net (66.11). For the real pig data the test MSE of the LAVA ADMM is 0.850 compared to the LASSO, RR and EN with 0.875, 0.853 and 0.853, respectively. CONCLUSIONS: This study presents the LAVA ADMM that is capable of joint modelling of monogenic major genetic effects and polygenic minor genetic effects which can be used for both genome-wide assoiciation and prediction purposes. The statistical evaluations based on both simulated and real pig data set shows that the LAVA ADMM has better prediction properies than the LASSO, RR and EN. Julia code for the LAVA ADMM is available at: https://github.com/patwa67/LAVAADMM. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04436-6. BioMed Central 2021-10-26 /pmc/articles/PMC8547073/ /pubmed/34702175 http://dx.doi.org/10.1186/s12859-021-04436-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Waldmann, Patrik A proximal LAVA method for genome-wide association and prediction of traits with mixed inheritance patterns |
title | A proximal LAVA method for genome-wide association and prediction of traits with mixed inheritance patterns |
title_full | A proximal LAVA method for genome-wide association and prediction of traits with mixed inheritance patterns |
title_fullStr | A proximal LAVA method for genome-wide association and prediction of traits with mixed inheritance patterns |
title_full_unstemmed | A proximal LAVA method for genome-wide association and prediction of traits with mixed inheritance patterns |
title_short | A proximal LAVA method for genome-wide association and prediction of traits with mixed inheritance patterns |
title_sort | proximal lava method for genome-wide association and prediction of traits with mixed inheritance patterns |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547073/ https://www.ncbi.nlm.nih.gov/pubmed/34702175 http://dx.doi.org/10.1186/s12859-021-04436-6 |
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