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Ensemble feature selection with data-driven thresholding for Alzheimer's disease biomarker discovery
BACKGROUND: Feature selection is often used to identify the important features in a dataset but can produce unstable results when applied to high-dimensional data. The stability of feature selection can be improved with the use of feature selection ensembles, which aggregate the results of multiple...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830744/ https://www.ncbi.nlm.nih.gov/pubmed/36624372 http://dx.doi.org/10.1186/s12859-022-05132-9 |
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author | Spooner, Annette Mohammadi, Gelareh Sachdev, Perminder S. Brodaty, Henry Sowmya, Arcot |
author_facet | Spooner, Annette Mohammadi, Gelareh Sachdev, Perminder S. Brodaty, Henry Sowmya, Arcot |
author_sort | Spooner, Annette |
collection | PubMed |
description | BACKGROUND: Feature selection is often used to identify the important features in a dataset but can produce unstable results when applied to high-dimensional data. The stability of feature selection can be improved with the use of feature selection ensembles, which aggregate the results of multiple base feature selectors. However, a threshold must be applied to the final aggregated feature set to separate the relevant features from the redundant ones. A fixed threshold, which is typically used, offers no guarantee that the final set of selected features contains only relevant features. This work examines a selection of data-driven thresholds to automatically identify the relevant features in an ensemble feature selector and evaluates their predictive accuracy and stability. Ensemble feature selection with data-driven thresholding is applied to two real-world studies of Alzheimer's disease. Alzheimer's disease is a progressive neurodegenerative disease with no known cure, that begins at least 2–3 decades before overt symptoms appear, presenting an opportunity for researchers to identify early biomarkers that might identify patients at risk of developing Alzheimer's disease. RESULTS: The ensemble feature selectors, combined with data-driven thresholds, produced more stable results, on the whole, than the equivalent individual feature selectors, showing an improvement in stability of up to 34%. The most successful data-driven thresholds were the robust rank aggregation threshold and the threshold algorithm threshold from the field of information retrieval. The features identified by applying these methods to datasets from Alzheimer's disease studies reflect current findings in the AD literature. CONCLUSIONS: Data-driven thresholds applied to ensemble feature selectors provide more stable, and therefore more reproducible, selections of features than individual feature selectors, without loss of performance. The use of a data-driven threshold eliminates the need to choose a fixed threshold a-priori and can select a more meaningful set of features. A reliable and compact set of features can produce more interpretable models by identifying the factors that are important in understanding a disease. |
format | Online Article Text |
id | pubmed-9830744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98307442023-01-11 Ensemble feature selection with data-driven thresholding for Alzheimer's disease biomarker discovery Spooner, Annette Mohammadi, Gelareh Sachdev, Perminder S. Brodaty, Henry Sowmya, Arcot BMC Bioinformatics Research BACKGROUND: Feature selection is often used to identify the important features in a dataset but can produce unstable results when applied to high-dimensional data. The stability of feature selection can be improved with the use of feature selection ensembles, which aggregate the results of multiple base feature selectors. However, a threshold must be applied to the final aggregated feature set to separate the relevant features from the redundant ones. A fixed threshold, which is typically used, offers no guarantee that the final set of selected features contains only relevant features. This work examines a selection of data-driven thresholds to automatically identify the relevant features in an ensemble feature selector and evaluates their predictive accuracy and stability. Ensemble feature selection with data-driven thresholding is applied to two real-world studies of Alzheimer's disease. Alzheimer's disease is a progressive neurodegenerative disease with no known cure, that begins at least 2–3 decades before overt symptoms appear, presenting an opportunity for researchers to identify early biomarkers that might identify patients at risk of developing Alzheimer's disease. RESULTS: The ensemble feature selectors, combined with data-driven thresholds, produced more stable results, on the whole, than the equivalent individual feature selectors, showing an improvement in stability of up to 34%. The most successful data-driven thresholds were the robust rank aggregation threshold and the threshold algorithm threshold from the field of information retrieval. The features identified by applying these methods to datasets from Alzheimer's disease studies reflect current findings in the AD literature. CONCLUSIONS: Data-driven thresholds applied to ensemble feature selectors provide more stable, and therefore more reproducible, selections of features than individual feature selectors, without loss of performance. The use of a data-driven threshold eliminates the need to choose a fixed threshold a-priori and can select a more meaningful set of features. A reliable and compact set of features can produce more interpretable models by identifying the factors that are important in understanding a disease. BioMed Central 2023-01-09 /pmc/articles/PMC9830744/ /pubmed/36624372 http://dx.doi.org/10.1186/s12859-022-05132-9 Text en © The Author(s) 2023 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 Spooner, Annette Mohammadi, Gelareh Sachdev, Perminder S. Brodaty, Henry Sowmya, Arcot Ensemble feature selection with data-driven thresholding for Alzheimer's disease biomarker discovery |
title | Ensemble feature selection with data-driven thresholding for Alzheimer's disease biomarker discovery |
title_full | Ensemble feature selection with data-driven thresholding for Alzheimer's disease biomarker discovery |
title_fullStr | Ensemble feature selection with data-driven thresholding for Alzheimer's disease biomarker discovery |
title_full_unstemmed | Ensemble feature selection with data-driven thresholding for Alzheimer's disease biomarker discovery |
title_short | Ensemble feature selection with data-driven thresholding for Alzheimer's disease biomarker discovery |
title_sort | ensemble feature selection with data-driven thresholding for alzheimer's disease biomarker discovery |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830744/ https://www.ncbi.nlm.nih.gov/pubmed/36624372 http://dx.doi.org/10.1186/s12859-022-05132-9 |
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