TY - JOUR
T1 - A test of transmission/disequilibrium for quantitative trails in pedigree data, by multiple regression
AU - George, Varghese
AU - Tiwari, Hemant K.
AU - Zhu, Xiaofeng
AU - Elston, Robert C.
N1 - Funding Information:
This study was supported in part by U.S. Public Health Service research grants GM 28353, from the National Institute of General Medical Sciences, and HL 55055, from the National Heart, Lung and Blood Institute, and by resource grant RR03655 from the National Center for Research Resources. The authors thank the reviewers for their valuable critiques, which helped us to make substantial changes and improvements to an earlier version of this report.
PY - 1999
Y1 - 1999
N2 - The transmission/disequilibrium (TD) test (TDT), proposed, by Spielman et al., for binary traits is a powerful method for detection of linkage between a marker locus and a disease locus, in the presence of allelic association. As a test for linkage disequilibrium, the TDT makes the assumption that any allelic association present is due to linkage. Allison proposed a series of TD-type tests for quantitative traits and calculated their power, assuming that the marker locus is the disease locus. All these tests assume that the observations are independent, and therefore they are applicable, as a test for linkage, only for nuclear-family data. In this report, we propose a regression-based TD-type test for linkage between a marker locus and a quantitative trait locus, using information on the parent- to-offspring transmission status of the associated allele at the marker locus. This method does not require independence of observations, thus allowing for analysis of pedigree data as well, and allows adjustment for covariates. We investigate the statistical power and validity of the test by simulating markers at various recombination fractions from the disease locus.
AB - The transmission/disequilibrium (TD) test (TDT), proposed, by Spielman et al., for binary traits is a powerful method for detection of linkage between a marker locus and a disease locus, in the presence of allelic association. As a test for linkage disequilibrium, the TDT makes the assumption that any allelic association present is due to linkage. Allison proposed a series of TD-type tests for quantitative traits and calculated their power, assuming that the marker locus is the disease locus. All these tests assume that the observations are independent, and therefore they are applicable, as a test for linkage, only for nuclear-family data. In this report, we propose a regression-based TD-type test for linkage between a marker locus and a quantitative trait locus, using information on the parent- to-offspring transmission status of the associated allele at the marker locus. This method does not require independence of observations, thus allowing for analysis of pedigree data as well, and allows adjustment for covariates. We investigate the statistical power and validity of the test by simulating markers at various recombination fractions from the disease locus.
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U2 - 10.1086/302444
DO - 10.1086/302444
M3 - Article
C2 - 10364537
AN - SCOPUS:0033364734
SN - 0002-9297
VL - 65
SP - 236
EP - 245
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 1
ER -