Combination of linkage evidence in complex inheritance
被引:3
|
作者:
Zhang, W
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机构:
Univ Southampton, Human Genet Res Div, Southampton Gen Hosp, Southampton SO16 6YD, Hants, EnglandUniv Southampton, Human Genet Res Div, Southampton Gen Hosp, Southampton SO16 6YD, Hants, England
Zhang, W
[1
]
Collins, A
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机构:
Univ Southampton, Human Genet Res Div, Southampton Gen Hosp, Southampton SO16 6YD, Hants, EnglandUniv Southampton, Human Genet Res Div, Southampton Gen Hosp, Southampton SO16 6YD, Hants, England
Collins, A
[1
]
Morton, NE
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机构:
Univ Southampton, Human Genet Res Div, Southampton Gen Hosp, Southampton SO16 6YD, Hants, EnglandUniv Southampton, Human Genet Res Div, Southampton Gen Hosp, Southampton SO16 6YD, Hants, England
Morton, NE
[1
]
机构:
[1] Univ Southampton, Human Genet Res Div, Southampton Gen Hosp, Southampton SO16 6YD, Hants, England
meta-analysis;
retrospective collaboration;
Self and Liang test;
D O I:
10.1159/000053367
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
The central problem of complex inheritance is to combine evidence from data that typically differ in markers, phenotypes, ascertainment, and other factors, without sacrificing the reliability that lods have given to linkage mapping for major loci. Here we evaluate 5 possible solutions on 200 replicates simulated in Genetic Analysis Workshop 10. Two methods differ from less efficient ones by distinguishing the tails of a normal distribution. Maximum likelihood scores (currently implemented only for the BETA model) and the approach of Self and Liang perform about as well as pooling samples, which is not feasible with heterogeneous data. With moderately heterogeneous data the Self and Liang method appears to be more efficient than maximum likelihood scores. Although improvements are being made in sample design and statistical analysis, the problem of combining linkage evidence from multiple data sets appears to have been solved. Allelic association presents different problems not yet addressed. Copyright (C) 2001 S. Karger AG, Basel.