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Meta-analysis based on weighted ordered P-values for genomic data with heterogeneity
BACKGROUND: Meta-analysis has become increasingly popular in recent years, especially in genomic data analysis, due to the fast growth of available data and studies that target the same questions. Many methods have been developed, including classical ones such as Fisher’s combined probability test a...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4089554/ https://www.ncbi.nlm.nih.gov/pubmed/24972803 http://dx.doi.org/10.1186/1471-2105-15-226 |
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author | Li, Yihan Ghosh, Debashis |
author_facet | Li, Yihan Ghosh, Debashis |
author_sort | Li, Yihan |
collection | PubMed |
description | BACKGROUND: Meta-analysis has become increasingly popular in recent years, especially in genomic data analysis, due to the fast growth of available data and studies that target the same questions. Many methods have been developed, including classical ones such as Fisher’s combined probability test and Stouffer’s Z-test. However, not all meta-analyses have the same goal in mind. Some aim at combining information to find signals in at least one of the studies, while others hope to find more consistent signals across the studies. While many classical meta-analysis methods are developed with the former goal in mind, the latter goal has much more practicality for genomic data analysis. RESULTS: In this paper, we propose a class of meta-analysis methods based on summaries of weighted ordered p-values (WOP) that aim at detecting significance in a majority of studies. We consider weighted versions of classical procedures such as Fisher’s method and Stouffer’s method where the weight for each p-value is based on its order among the studies. In particular, we consider weights based on the binomial distribution, where the median of the p-values are weighted highest and the outlying p-values are down-weighted. We investigate the properties of our methods and demonstrate their strengths through simulations studies, comparing to existing procedures. In addition, we illustrate application of the proposed methodology by several meta-analysis of gene expression data. CONCLUSIONS: Our proposed weighted ordered p-value (WOP) methods displayed better performance compared to existing methods for testing the hypothesis that there is signal in the majority of studies. They also appeared to be much more robust in applications compared to the rth ordered p-value (rOP) method (Song and Tseng, Ann. Appl. Stat. 2014, 8(2):777–800). With the flexibility of incorporating different p-value combination methods and different weighting schemes, the weighted ordered p-values (WOP) methods have great potential in detecting consistent signal in meta-analysis with heterogeneity. |
format | Online Article Text |
id | pubmed-4089554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40895542014-07-23 Meta-analysis based on weighted ordered P-values for genomic data with heterogeneity Li, Yihan Ghosh, Debashis BMC Bioinformatics Methodology Article BACKGROUND: Meta-analysis has become increasingly popular in recent years, especially in genomic data analysis, due to the fast growth of available data and studies that target the same questions. Many methods have been developed, including classical ones such as Fisher’s combined probability test and Stouffer’s Z-test. However, not all meta-analyses have the same goal in mind. Some aim at combining information to find signals in at least one of the studies, while others hope to find more consistent signals across the studies. While many classical meta-analysis methods are developed with the former goal in mind, the latter goal has much more practicality for genomic data analysis. RESULTS: In this paper, we propose a class of meta-analysis methods based on summaries of weighted ordered p-values (WOP) that aim at detecting significance in a majority of studies. We consider weighted versions of classical procedures such as Fisher’s method and Stouffer’s method where the weight for each p-value is based on its order among the studies. In particular, we consider weights based on the binomial distribution, where the median of the p-values are weighted highest and the outlying p-values are down-weighted. We investigate the properties of our methods and demonstrate their strengths through simulations studies, comparing to existing procedures. In addition, we illustrate application of the proposed methodology by several meta-analysis of gene expression data. CONCLUSIONS: Our proposed weighted ordered p-value (WOP) methods displayed better performance compared to existing methods for testing the hypothesis that there is signal in the majority of studies. They also appeared to be much more robust in applications compared to the rth ordered p-value (rOP) method (Song and Tseng, Ann. Appl. Stat. 2014, 8(2):777–800). With the flexibility of incorporating different p-value combination methods and different weighting schemes, the weighted ordered p-values (WOP) methods have great potential in detecting consistent signal in meta-analysis with heterogeneity. BioMed Central 2014-06-28 /pmc/articles/PMC4089554/ /pubmed/24972803 http://dx.doi.org/10.1186/1471-2105-15-226 Text en Copyright © 2014 Li and Ghosh; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 | Methodology Article Li, Yihan Ghosh, Debashis Meta-analysis based on weighted ordered P-values for genomic data with heterogeneity |
title | Meta-analysis based on weighted ordered P-values for genomic data with heterogeneity |
title_full | Meta-analysis based on weighted ordered P-values for genomic data with heterogeneity |
title_fullStr | Meta-analysis based on weighted ordered P-values for genomic data with heterogeneity |
title_full_unstemmed | Meta-analysis based on weighted ordered P-values for genomic data with heterogeneity |
title_short | Meta-analysis based on weighted ordered P-values for genomic data with heterogeneity |
title_sort | meta-analysis based on weighted ordered p-values for genomic data with heterogeneity |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4089554/ https://www.ncbi.nlm.nih.gov/pubmed/24972803 http://dx.doi.org/10.1186/1471-2105-15-226 |
work_keys_str_mv | AT liyihan metaanalysisbasedonweightedorderedpvaluesforgenomicdatawithheterogeneity AT ghoshdebashis metaanalysisbasedonweightedorderedpvaluesforgenomicdatawithheterogeneity |