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Analyzing biomarker discovery: Estimating the reproducibility of biomarker sets
Many researchers try to understand a biological condition by identifying biomarkers. This is typically done using univariate hypothesis testing over a labeled dataset, declaring a feature to be a biomarker if there is a significant statistical difference between its values for the subjects with diff...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9333302/ https://www.ncbi.nlm.nih.gov/pubmed/35901020 http://dx.doi.org/10.1371/journal.pone.0252697 |
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author | Forouzandeh, Amir Rutar, Alex Kalmady, Sunil V. Greiner, Russell |
author_facet | Forouzandeh, Amir Rutar, Alex Kalmady, Sunil V. Greiner, Russell |
author_sort | Forouzandeh, Amir |
collection | PubMed |
description | Many researchers try to understand a biological condition by identifying biomarkers. This is typically done using univariate hypothesis testing over a labeled dataset, declaring a feature to be a biomarker if there is a significant statistical difference between its values for the subjects with different outcomes. However, such sets of proposed biomarkers are often not reproducible – subsequent studies often fail to identify the same sets. Indeed, there is often only a very small overlap between the biomarkers proposed in pairs of related studies that explore the same phenotypes over the same distribution of subjects. This paper first defines the Reproducibility Score for a labeled dataset as a measure (taking values between 0 and 1) of the reproducibility of the results produced by a specified fixed biomarker discovery process for a given distribution of subjects. We then provide ways to reliably estimate this score by defining algorithms that produce an over-bound and an under-bound for this score for a given dataset and biomarker discovery process, for the case of univariate hypothesis testing on dichotomous groups. We confirm that these approximations are meaningful by providing empirical results on a large number of datasets and show that these predictions match known reproducibility results. To encourage others to apply this technique to analyze their biomarker sets, we have also created a publicly available website, https://biomarker.shinyapps.io/BiomarkerReprod/, that produces these Reproducibility Score approximations for any given dataset (with continuous or discrete features and binary class labels). |
format | Online Article Text |
id | pubmed-9333302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-93333022022-07-29 Analyzing biomarker discovery: Estimating the reproducibility of biomarker sets Forouzandeh, Amir Rutar, Alex Kalmady, Sunil V. Greiner, Russell PLoS One Research Article Many researchers try to understand a biological condition by identifying biomarkers. This is typically done using univariate hypothesis testing over a labeled dataset, declaring a feature to be a biomarker if there is a significant statistical difference between its values for the subjects with different outcomes. However, such sets of proposed biomarkers are often not reproducible – subsequent studies often fail to identify the same sets. Indeed, there is often only a very small overlap between the biomarkers proposed in pairs of related studies that explore the same phenotypes over the same distribution of subjects. This paper first defines the Reproducibility Score for a labeled dataset as a measure (taking values between 0 and 1) of the reproducibility of the results produced by a specified fixed biomarker discovery process for a given distribution of subjects. We then provide ways to reliably estimate this score by defining algorithms that produce an over-bound and an under-bound for this score for a given dataset and biomarker discovery process, for the case of univariate hypothesis testing on dichotomous groups. We confirm that these approximations are meaningful by providing empirical results on a large number of datasets and show that these predictions match known reproducibility results. To encourage others to apply this technique to analyze their biomarker sets, we have also created a publicly available website, https://biomarker.shinyapps.io/BiomarkerReprod/, that produces these Reproducibility Score approximations for any given dataset (with continuous or discrete features and binary class labels). Public Library of Science 2022-07-28 /pmc/articles/PMC9333302/ /pubmed/35901020 http://dx.doi.org/10.1371/journal.pone.0252697 Text en © 2022 Forouzandeh et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Forouzandeh, Amir Rutar, Alex Kalmady, Sunil V. Greiner, Russell Analyzing biomarker discovery: Estimating the reproducibility of biomarker sets |
title | Analyzing biomarker discovery: Estimating the reproducibility of biomarker sets |
title_full | Analyzing biomarker discovery: Estimating the reproducibility of biomarker sets |
title_fullStr | Analyzing biomarker discovery: Estimating the reproducibility of biomarker sets |
title_full_unstemmed | Analyzing biomarker discovery: Estimating the reproducibility of biomarker sets |
title_short | Analyzing biomarker discovery: Estimating the reproducibility of biomarker sets |
title_sort | analyzing biomarker discovery: estimating the reproducibility of biomarker sets |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9333302/ https://www.ncbi.nlm.nih.gov/pubmed/35901020 http://dx.doi.org/10.1371/journal.pone.0252697 |
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