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Luca, D.* ; Ringquist, S.* ; Klei, L.* ; Lee, AB.* ; Gieger, C. ; Wichmann, H.-E. ; Schreiber, S.* ; Krawczak, M.* ; Lu, Y.* ; Styche, A.* ; Devlin, B.* ; Roeder, K.* ; Trucco, M.*

On the use of general control samples for genome-wide association studies: Genetic matching highlights causal variants.

Am. J. Hum. Genet. 82, 453-463 (2008)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
Resources being amassed for genome-wide association (GWA) studies include "control databases" genotyped with a large-scale SNP array. How to use these databases effectively is an open question. We develop a method to match, by genetic ancestry, controls to affected individuals (cases). The impact of this method, especially for heterogeneous human populations, is to reduce the false-positive rate, inflate other spuriously small p values, and have little impact on the p values associated with true positive loci. Thus, it highlights true positives by downplaying false positives. We perform a GWA by matching Americans with type 1 diabetes (T1D) to controls from Germany. Despite the complex study design, these analyses identify numerous loci known to confer risk for T1D.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
ISSN (print) / ISBN 0002-9297
e-ISSN 1537-6605
Quellenangaben Volume: 82, Issue: 2, Pages: 453-463 Article Number: , Supplement: ,
Publisher Elsevier
Publishing Place New York, NY
Non-patent literature Publications
Reviewing status Peer reviewed