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A comparison of methods for interpreting random forest models of genetic association in the presence of non-additive interactions
BACKGROUND: Non-additive interactions among genes are frequently associated with a number of phenotypes, including known complex diseases such as Alzheimer’s, diabetes, and cardiovascular disease. Detecting interactions requires careful selection of analytical methods, and some machine learning algo...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847145/ https://www.ncbi.nlm.nih.gov/pubmed/33514397 http://dx.doi.org/10.1186/s13040-021-00243-0 |
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author | Orlenko, Alena Moore, Jason H. |
author_facet | Orlenko, Alena Moore, Jason H. |
author_sort | Orlenko, Alena |
collection | PubMed |
description | BACKGROUND: Non-additive interactions among genes are frequently associated with a number of phenotypes, including known complex diseases such as Alzheimer’s, diabetes, and cardiovascular disease. Detecting interactions requires careful selection of analytical methods, and some machine learning algorithms are unable or underpowered to detect or model feature interactions that exhibit non-additivity. The Random Forest method is often employed in these efforts due to its ability to detect and model non-additive interactions. In addition, Random Forest has the built-in ability to estimate feature importance scores, a characteristic that allows the model to be interpreted with the order and effect size of the feature association with the outcome. This characteristic is very important for epidemiological and clinical studies where results of predictive modeling could be used to define the future direction of the research efforts. An alternative way to interpret the model is with a permutation feature importance metric which employs a permutation approach to calculate a feature contribution coefficient in units of the decrease in the model’s performance and with the Shapely additive explanations which employ cooperative game theory approach. Currently, it is unclear which Random Forest feature importance metric provides a superior estimation of the true informative contribution of features in genetic association analysis. RESULTS: To address this issue, and to improve interpretability of Random Forest predictions, we compared different methods for feature importance estimation in real and simulated datasets with non-additive interactions. As a result, we detected a discrepancy between the metrics for the real-world datasets and further established that the permutation feature importance metric provides more precise feature importance rank estimation for the simulated datasets with non-additive interactions. CONCLUSIONS: By analyzing both real and simulated data, we established that the permutation feature importance metric provides more precise feature importance rank estimation in the presence of non-additive interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13040-021-00243-0. |
format | Online Article Text |
id | pubmed-7847145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78471452021-02-01 A comparison of methods for interpreting random forest models of genetic association in the presence of non-additive interactions Orlenko, Alena Moore, Jason H. BioData Min Research BACKGROUND: Non-additive interactions among genes are frequently associated with a number of phenotypes, including known complex diseases such as Alzheimer’s, diabetes, and cardiovascular disease. Detecting interactions requires careful selection of analytical methods, and some machine learning algorithms are unable or underpowered to detect or model feature interactions that exhibit non-additivity. The Random Forest method is often employed in these efforts due to its ability to detect and model non-additive interactions. In addition, Random Forest has the built-in ability to estimate feature importance scores, a characteristic that allows the model to be interpreted with the order and effect size of the feature association with the outcome. This characteristic is very important for epidemiological and clinical studies where results of predictive modeling could be used to define the future direction of the research efforts. An alternative way to interpret the model is with a permutation feature importance metric which employs a permutation approach to calculate a feature contribution coefficient in units of the decrease in the model’s performance and with the Shapely additive explanations which employ cooperative game theory approach. Currently, it is unclear which Random Forest feature importance metric provides a superior estimation of the true informative contribution of features in genetic association analysis. RESULTS: To address this issue, and to improve interpretability of Random Forest predictions, we compared different methods for feature importance estimation in real and simulated datasets with non-additive interactions. As a result, we detected a discrepancy between the metrics for the real-world datasets and further established that the permutation feature importance metric provides more precise feature importance rank estimation for the simulated datasets with non-additive interactions. CONCLUSIONS: By analyzing both real and simulated data, we established that the permutation feature importance metric provides more precise feature importance rank estimation in the presence of non-additive interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13040-021-00243-0. BioMed Central 2021-01-29 /pmc/articles/PMC7847145/ /pubmed/33514397 http://dx.doi.org/10.1186/s13040-021-00243-0 Text en © The Author(s) 2021 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 Orlenko, Alena Moore, Jason H. A comparison of methods for interpreting random forest models of genetic association in the presence of non-additive interactions |
title | A comparison of methods for interpreting random forest models of genetic association in the presence of non-additive interactions |
title_full | A comparison of methods for interpreting random forest models of genetic association in the presence of non-additive interactions |
title_fullStr | A comparison of methods for interpreting random forest models of genetic association in the presence of non-additive interactions |
title_full_unstemmed | A comparison of methods for interpreting random forest models of genetic association in the presence of non-additive interactions |
title_short | A comparison of methods for interpreting random forest models of genetic association in the presence of non-additive interactions |
title_sort | comparison of methods for interpreting random forest models of genetic association in the presence of non-additive interactions |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847145/ https://www.ncbi.nlm.nih.gov/pubmed/33514397 http://dx.doi.org/10.1186/s13040-021-00243-0 |
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