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Reproducible detection of disease-associated markers from gene expression data
BACKGROUND: Detection of disease-associated markers plays a crucial role in gene screening for biological studies. Two-sample test statistics, such as the t-statistic, are widely used to rank genes based on gene expression data. However, the resultant gene ranking is often not reproducible among dif...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991096/ https://www.ncbi.nlm.nih.gov/pubmed/27538512 http://dx.doi.org/10.1186/s12920-016-0214-5 |
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author | Omae, Katsuhiro Komori, Osamu Eguchi, Shinto |
author_facet | Omae, Katsuhiro Komori, Osamu Eguchi, Shinto |
author_sort | Omae, Katsuhiro |
collection | PubMed |
description | BACKGROUND: Detection of disease-associated markers plays a crucial role in gene screening for biological studies. Two-sample test statistics, such as the t-statistic, are widely used to rank genes based on gene expression data. However, the resultant gene ranking is often not reproducible among different data sets. Such irreproducibility may be caused by disease heterogeneity. RESULTS: When we divided data into two subsets, we found that the signs of the two t-statistics were often reversed. Focusing on such instability, we proposed a sign-sum statistic that counts the signs of the t-statistics for all possible subsets. The proposed method excludes genes affected by heterogeneity, thereby improving the reproducibility of gene ranking. We compared the sign-sum statistic with the t-statistic by a theoretical evaluation of the upper confidence limit. Through simulations and applications to real data sets, we show that the sign-sum statistic exhibits superior performance. CONCLUSION: We derive the sign-sum statistic for getting a robust gene ranking. The sign-sum statistic gives more reproducible ranking than the t-statistic. Using simulated data sets we show that the sign-sum statistic excludes hetero-type genes well. Also for the real data sets, the sign-sum statistic performs well in a viewpoint of ranking reproducibility. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12920-016-0214-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4991096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49910962016-08-20 Reproducible detection of disease-associated markers from gene expression data Omae, Katsuhiro Komori, Osamu Eguchi, Shinto BMC Med Genomics Research Article BACKGROUND: Detection of disease-associated markers plays a crucial role in gene screening for biological studies. Two-sample test statistics, such as the t-statistic, are widely used to rank genes based on gene expression data. However, the resultant gene ranking is often not reproducible among different data sets. Such irreproducibility may be caused by disease heterogeneity. RESULTS: When we divided data into two subsets, we found that the signs of the two t-statistics were often reversed. Focusing on such instability, we proposed a sign-sum statistic that counts the signs of the t-statistics for all possible subsets. The proposed method excludes genes affected by heterogeneity, thereby improving the reproducibility of gene ranking. We compared the sign-sum statistic with the t-statistic by a theoretical evaluation of the upper confidence limit. Through simulations and applications to real data sets, we show that the sign-sum statistic exhibits superior performance. CONCLUSION: We derive the sign-sum statistic for getting a robust gene ranking. The sign-sum statistic gives more reproducible ranking than the t-statistic. Using simulated data sets we show that the sign-sum statistic excludes hetero-type genes well. Also for the real data sets, the sign-sum statistic performs well in a viewpoint of ranking reproducibility. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12920-016-0214-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-18 /pmc/articles/PMC4991096/ /pubmed/27538512 http://dx.doi.org/10.1186/s12920-016-0214-5 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Research Article Omae, Katsuhiro Komori, Osamu Eguchi, Shinto Reproducible detection of disease-associated markers from gene expression data |
title | Reproducible detection of disease-associated markers from gene expression data |
title_full | Reproducible detection of disease-associated markers from gene expression data |
title_fullStr | Reproducible detection of disease-associated markers from gene expression data |
title_full_unstemmed | Reproducible detection of disease-associated markers from gene expression data |
title_short | Reproducible detection of disease-associated markers from gene expression data |
title_sort | reproducible detection of disease-associated markers from gene expression data |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991096/ https://www.ncbi.nlm.nih.gov/pubmed/27538512 http://dx.doi.org/10.1186/s12920-016-0214-5 |
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