Genomic Screening in Family-Based Association Testing

DSpace/Manakin Repository

Genomic Screening in Family-Based Association Testing

Citable link to this page


Title: Genomic Screening in Family-Based Association Testing
Author: Murphy, Amy; McQueen, Matthew B; Kraft, Peter; Van Steen, Kristel; Su, Jessica Ann Lasky; Lazarus, Ross; Laird, Nan M.; Lange, Christoph

Note: Order does not necessarily reflect citation order of authors.

Citation: Murphy, Amy, Matthew B. McQueen, Jessica Su, Peter Kraft, Ross Lazarus, Nan M. Laird, Christoph Lange, and Kristel Van Steen. 2005. Genomic screening in family-based association testing. BMC Genetics 6(Suppl 1):S115.
Full Text & Related Files:
Abstract: Due to the recent gains in the availability of single-nucleotide polymorphism data, genome-wide association testing has become feasible. It is hoped that this additional data may confirm the presence of disease susceptibility loci, and identify new genetic determinants of disease. However, the problem of multiple comparisons threatens to diminish any potential gains from this newly available data. To circumvent the multiple comparisons issue, we utilize a recently developed screening technique using family-based association testing. This screening methodology allows for the identification of the most promising single-nucleotide polymorphisms for testing without biasing the nominal significance level of our test statistic. We compare the results of our screening technique across univariate and multivariate family-based association tests. From our analyses, we observe that the screening technique, applied to different settings, is fairly consistent in identifying optimal markers for testing. One of the identified markers, TSC0047225, was significantly associated with both the ttth1 (p = 0.004) and ttth1-ttth4 (p = 0.004) phenotype(s). We find that both univariate- and multivariate-based screening techniques are powerful tools for detecting an association.
Published Version: doi:10.1186/1471-2156-6-S1-S115
Other Sources:
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at
Citable link to this page:
Downloads of this work:

Show full Dublin Core record

This item appears in the following Collection(s)


Search DASH

Advanced Search