TY - JOUR
T1 - Power comparison of parametric and nonparametric linkage tests in small pedigrees
AU - Sham, Pak Chung
AU - Lin, Ming Wei
AU - Zhao, Jing Hua
AU - Curtis, David
N1 - Funding Information:
This work was supported by Wellcome Trust grant 055379, Medical Research Council grant G9700821, and National Institutes of Health grant EY-12562. M.-W.L. was supported by the Ministry of Education, Taiwan, Republic of China. We are grateful to an anonymous referee, for valuable comments that resulted in substantial revision of the Discussion section.
PY - 2000
Y1 - 2000
N2 - When the mode of inheritance of a disease is unknown, the LOD-score method of linkage analysis must take into account uncertainties in model parameters. We have previously proposed a parametric linkage test called 'MFLOD,' which does not require specification of disease model parameters. In the present study, we introduce two new model-free parametric linkage tests, known as 'MLOD' and 'MALOD.' These tests are defined, respectively, as the LOD score and the admixture LOD score, maximized (subject to the same constraints as MFLOD) over disease-model parameters. We compared the power of these three parametric linkage tests and that of two nonparametric linkage tests, NP(all) and NPL(pairs), which are implemented in GENEHUNTER. With the use of small pedigrees and a fully informative marker, we found the powers of MLOD, NPL(all), and NPL(pairs) to be almost equivalent to each other and not far below that of a LOD-score analysis performed under the assumption the correct genetic parameters. Thus, linkage analysis is not much hindered by uncertain mode of inheritance. The results also suggest that both parametric and nonparametric methods are suitable for linkage analysis of complex disorders in small pedigrees. However, whether these results apply to large pedigrees remains to be answered.
AB - When the mode of inheritance of a disease is unknown, the LOD-score method of linkage analysis must take into account uncertainties in model parameters. We have previously proposed a parametric linkage test called 'MFLOD,' which does not require specification of disease model parameters. In the present study, we introduce two new model-free parametric linkage tests, known as 'MLOD' and 'MALOD.' These tests are defined, respectively, as the LOD score and the admixture LOD score, maximized (subject to the same constraints as MFLOD) over disease-model parameters. We compared the power of these three parametric linkage tests and that of two nonparametric linkage tests, NP(all) and NPL(pairs), which are implemented in GENEHUNTER. With the use of small pedigrees and a fully informative marker, we found the powers of MLOD, NPL(all), and NPL(pairs) to be almost equivalent to each other and not far below that of a LOD-score analysis performed under the assumption the correct genetic parameters. Thus, linkage analysis is not much hindered by uncertain mode of inheritance. The results also suggest that both parametric and nonparametric methods are suitable for linkage analysis of complex disorders in small pedigrees. However, whether these results apply to large pedigrees remains to be answered.
UR - http://www.scopus.com/inward/record.url?scp=0033911219&partnerID=8YFLogxK
U2 - 10.1086/302888
DO - 10.1086/302888
M3 - Article
C2 - 10762550
AN - SCOPUS:0033911219
SN - 0002-9297
VL - 66
SP - 1661
EP - 1668
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 5
ER -