TY - JOUR
T1 - Exploring the role of environmental factors in association and linkage studies
AU - Seillier-Moiseiwitsch, Françoise
AU - Ramaswami, Anand
AU - Tripputi, Mark
AU - Pankow, James
AU - Newman, Beth
PY - 1999
Y1 - 1999
N2 - We analyzed some simulated data to assess the success of statistical methodologies to establish the role of the environmental factors (EF) and to identify associated and linked markers. We considered five replicates for each of the four studies, and, with the knowledge of the generating model, concentrated our analyses on chromosomes (CH) 1, 3, and 5. To determine the influence of EF and associated markers on the affection status (AS), we utilized chi-square tests for independence and recursive partitioning (via the CART software). To identify linked markers, we scanned the relevant chromosomes with nonparametric multipoint linkage (NPL) and transmission/disequilibrium tests. These analyses were performed on the whole data set as well as on subsets of individuals and families defined by exposure to EF. CART correctly selected the associated marker (D1G024) and EFI for Study (ST) 1 and did not generate trees for the other studies. NPL identified the relevant regions on CH3 and CH5 but failed to do so for CHI, except in ST4. Stratifying families by exposure to EF1 did not consistently incpease sensitivity of NPL to the relevant CH3 markers, but did help characterize the genetic heterogeneity and identify linked families.
AB - We analyzed some simulated data to assess the success of statistical methodologies to establish the role of the environmental factors (EF) and to identify associated and linked markers. We considered five replicates for each of the four studies, and, with the knowledge of the generating model, concentrated our analyses on chromosomes (CH) 1, 3, and 5. To determine the influence of EF and associated markers on the affection status (AS), we utilized chi-square tests for independence and recursive partitioning (via the CART software). To identify linked markers, we scanned the relevant chromosomes with nonparametric multipoint linkage (NPL) and transmission/disequilibrium tests. These analyses were performed on the whole data set as well as on subsets of individuals and families defined by exposure to EF. CART correctly selected the associated marker (D1G024) and EFI for Study (ST) 1 and did not generate trees for the other studies. NPL identified the relevant regions on CH3 and CH5 but failed to do so for CHI, except in ST4. Stratifying families by exposure to EF1 did not consistently incpease sensitivity of NPL to the relevant CH3 markers, but did help characterize the genetic heterogeneity and identify linked families.
KW - Nonparametric multipoint linkage
KW - Recursive partitioning
KW - Transmission/disequilibrium test
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U2 - 10.1002/gepi.13701707117
DO - 10.1002/gepi.13701707117
M3 - Article
C2 - 10597519
AN - SCOPUS:0032710201
SN - 0741-0395
VL - 17
SP - S715-S720
JO - Genetic epidemiology
JF - Genetic epidemiology
IS - SUPPL. 1
ER -