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Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan.

Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan. Research Abstract Details 

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  • Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan. Abstract Text:

    iuliana ionita-lazaIuliana Ionita-Laza,matthew b mcqueenMatthew B McQueen,nan m lairdNan M Laird,christoph langeChristoph Lange,iuliana ionita-lazaIuliana Ionita-Laza,matthew b mcqueenMatthew B McQueen,nan m lairdNan M Laird,christoph langeChristoph Lange,

    For genomewide association (GWA) studies in family-based designs, we propose a novel two-stage strategy that weighs the association P values with the use of independently estimated weights. The association information contained in the family sample is partitioned into two orthogonal components--namely, the between-family information and the within-family information. The between-family component is used in the first (i.e., screening) stage to obtain a relative ranking of all the markers. The within-family component is used in the second (i.e., testing) stage in the framework of the standard family-based association test, and the resulting P values are weighted using the estimated marker ranking from the screening step. The approach is appealing, in that it ensures that all the markers are tested in the testing step and, at the same time, also uses information from the screening step. Through simulation studies, we show that testing all the markers is more powerful than testing only the most promising ones from the screening step, which was the method suggested by Van Steen et al. A comparison with a population-based approach shows that the approach achieves comparable power. In the presence of a reasonable level of population stratification, our approach is only slightly affected in terms of power and, since it is a family-based method, is completely robust to spurious effects. An application to a 100K scan in the Framingham Heart Study illustrates the practical advantages of our approach. The proposed method is of general applicability; it extends to any setting in which prior, independent ranking of hypotheses is available.

    Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan. Publishing Authors By Initials

    i ionita-lazaI Ionita-Laza,mb mcqueenMB McQueen,nm lairdNM Laird,c langeC Lange,i ionita-lazaI Ionita-Laza,mb mcqueenMB McQueen,nm lairdNM Laird,c langeC Lange,

    For similar genetic phenomena: inheritance patterns: quantitative trait, heritable research abstracts see: genetic phenomena: inheritance patterns: quantitative trait, heritable research

    PUBMED ID PMID:

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    Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: American journal of human genetics

    VOLUME: 81

    Page Numbers: 607-14

    Journal Abbreviation: Am. J. Hum. Genet.

    ISSN: 0002-9297

    DAY: 17

    MONTH: 07

    YEAR: 2007

    Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 370475

    Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan. Keywords Mesh Terms:

    KEYWORDS: Quantitative Trait, Heritable

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan. Information

    Substance Name: Genetic Markers

    Registry Number: 0

    Grant and Affiliation Information for Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan.

    AFFILIATION: Department of Biostatistics, Harvard School of Public Health, Boston, MA 02115, USA. iionita@hsph.harvard.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIMH

    GRANT: R01-MH59532

    ACRONYM: MH

    MEDLINETA: Am J Hum Genet

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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