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A note on generalized Genome Scan Meta-Analysis statistics

BACKGROUND: Wise et al. introduced a rank-based statistical technique for meta-analysis of genome scans, the Genome Scan Meta-Analysis (GSMA) method. Levinson et al. recently described two generalizations of the GSMA statistic: (i) a weighted version of the GSMA statistic, so that different studies...

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Detalles Bibliográficos
Autores principales: Koziol, James A, Feng, Anne C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC551600/
https://www.ncbi.nlm.nih.gov/pubmed/15717930
http://dx.doi.org/10.1186/1471-2105-6-32
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author Koziol, James A
Feng, Anne C
author_facet Koziol, James A
Feng, Anne C
author_sort Koziol, James A
collection PubMed
description BACKGROUND: Wise et al. introduced a rank-based statistical technique for meta-analysis of genome scans, the Genome Scan Meta-Analysis (GSMA) method. Levinson et al. recently described two generalizations of the GSMA statistic: (i) a weighted version of the GSMA statistic, so that different studies could be ascribed different weights for analysis; and (ii) an order statistic approach, reflecting the fact that a GSMA statistic can be computed for each chromosomal region or bin width across the various genome scan studies. RESULTS: We provide an Edgeworth approximation to the null distribution of the weighted GSMA statistic, and, we examine the limiting distribution of the GSMA statistics under the order statistic formulation, and quantify the relevance of the pairwise correlations of the GSMA statistics across different bins on this limiting distribution. We also remark on aggregate criteria and multiple testing for determining significance of GSMA results. CONCLUSION: Theoretical considerations detailed herein can lead to clarification and simplification of testing criteria for generalizations of the GSMA statistic.
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spelling pubmed-5516002005-03-04 A note on generalized Genome Scan Meta-Analysis statistics Koziol, James A Feng, Anne C BMC Bioinformatics Methodology Article BACKGROUND: Wise et al. introduced a rank-based statistical technique for meta-analysis of genome scans, the Genome Scan Meta-Analysis (GSMA) method. Levinson et al. recently described two generalizations of the GSMA statistic: (i) a weighted version of the GSMA statistic, so that different studies could be ascribed different weights for analysis; and (ii) an order statistic approach, reflecting the fact that a GSMA statistic can be computed for each chromosomal region or bin width across the various genome scan studies. RESULTS: We provide an Edgeworth approximation to the null distribution of the weighted GSMA statistic, and, we examine the limiting distribution of the GSMA statistics under the order statistic formulation, and quantify the relevance of the pairwise correlations of the GSMA statistics across different bins on this limiting distribution. We also remark on aggregate criteria and multiple testing for determining significance of GSMA results. CONCLUSION: Theoretical considerations detailed herein can lead to clarification and simplification of testing criteria for generalizations of the GSMA statistic. BioMed Central 2005-02-17 /pmc/articles/PMC551600/ /pubmed/15717930 http://dx.doi.org/10.1186/1471-2105-6-32 Text en Copyright © 2005 Koziol and Feng; licensee BioMed Central Ltd.
spellingShingle Methodology Article
Koziol, James A
Feng, Anne C
A note on generalized Genome Scan Meta-Analysis statistics
title A note on generalized Genome Scan Meta-Analysis statistics
title_full A note on generalized Genome Scan Meta-Analysis statistics
title_fullStr A note on generalized Genome Scan Meta-Analysis statistics
title_full_unstemmed A note on generalized Genome Scan Meta-Analysis statistics
title_short A note on generalized Genome Scan Meta-Analysis statistics
title_sort note on generalized genome scan meta-analysis statistics
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC551600/
https://www.ncbi.nlm.nih.gov/pubmed/15717930
http://dx.doi.org/10.1186/1471-2105-6-32
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