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Prioritized subset analysis: improving power in genome-wide association studies.

Prioritized subset analysis: improving power in genome-wide association studies. Research Abstract Details 

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  • Prioritized subset analysis: improving power in genome-wide association studies. Abstract Text:

    chun liChun Li,mingyao liMingyao Li,ethan m langeEthan M Lange,richard m watanabeRichard M Watanabe,chun liChun Li,mingyao liMingyao Li,ethan m langeEthan M Lange,richard m watanabeRichard M Watanabe,

    BACKGROUND: Genome-wide association studies (GWAS) are now feasible for studying the genetics underlying complex diseases. For many diseases, a list of candidate genes or regions exists and incorporation of such information into data analyses can potentially improve the power to detect disease variants. Traditional approaches for assessing the overall statistical significance of GWAS results ignore such information by inherently treating all markers equally. METHODS: We propose the prioritized subset analysis (PSA), in which a prioritized subset of markers is pre-selected from candidate regions, and the false discovery rate (FDR) procedure is carried out in the prioritized subset and its complementary subset, respectively. RESULTS: The PSA is more powerful than the whole-genome single-step FDR adjustment for a range of alternative models. The degree of power improvement depends on the fraction of associated SNPs in the prioritized subset and their nominal power, with higher fraction of associated SNPs and higher nominal power leading to more power improvement. The power improvement can be substantial; for disease loci not included in the prioritized subset, the power loss is almost negligible. CONCLUSION: The PSA has the flexibility of allowing investigators to combine prior information from a variety of sources, and will be a useful tool for GWAS.

    Prioritized subset analysis: improving power in genome-wide association studies. Publishing Authors By Initials

    c liC Li,m liM Li,em langeEM Lange,rm watanabeRM Watanabe,c liC Li,m liM Li,em langeEM Lange,rm watanabeRM Watanabe,

    For similar genetic phenomena: variation (genetics): polymorphism, genetic: polymorphism, single nucleotide research abstracts see: genetic phenomena: variation (genetics): polymorphism, genetic: polymorphism, single nucleotide research

    PUBMED ID PMID:

    MEDLINE DATE:

    Prioritized subset analysis: improving power in genome-wide association studies. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Human heredity

    VOLUME: 65

    Page Numbers: 129-41

    Journal Abbreviation: Hum. Hered.

    ISSN: 1423-0062

    DAY: 12

    MONTH: 10

    YEAR: 2007

    Prioritized subset analysis: improving power in genome-wide association studies. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 200525

    Prioritized subset analysis: improving power in genome-wide association studies. Keywords Mesh Terms:

    KEYWORDS: Polymorphism, Single Nucleotide

    MESH TERMS: methods

    Chemical & Substance for Abstract: Prioritized subset analysis: improving power in genome-wide association studies. Information

    Substance Name: Genetic Markers

    Registry Number: 0

    Grant and Affiliation Information for Prioritized subset analysis: improving power in genome-wide association studies.

    AFFILIATION: Department of Biostatistics, Center for Human Genetics Research, Vanderbilt University School of Medicine, Nashville, TN 37232, USA. chun.li@vanderbilt.edu

    Country: Switzerland

    Switzerland Research PublicationSwitzerland Research Publication

    AGENCY: United States NIDDK

    GRANT: R01 DK066368-03

    ACRONYM: DK

    MEDLINETA: Hum Hered

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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