A posterior probability of linkage-based re-analysis of schizophrenia data yields evidence of linkage to chromosomes 1 and 17

被引:11
|
作者
Logue, M. W.
Brzustowicz, L. M.
Bassett, A. S.
Chow, E. W. C.
Vieland, V. J.
机构
[1] Univ Iowa, Program Publ Hlth Genet, Ctr Stat Genet Res, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Psychiat, Iowa City, IA 52242 USA
[3] Rutgers State Univ, Dept Genet, Piscataway, NJ USA
[4] Univ Med & Dent New Jersey, Dept Psychiat, New Jersey Med Sch, Newark, NJ 07103 USA
[5] Univ Toronto, Clin Genet Res Program, Ctr Addict & Mental Hlth, Toronto, ON, Canada
[6] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
关键词
schizophrenia; linkage; PPL; CAPON; NOS1AP; genome scan;
D O I
10.1159/000096035
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective: Linkage analysis using 22 Canadian pedigrees identified a promising schizophrenia candidate region on 1q23 with a maximum 2-point HLOD under a recessive model of 5.8 [Brzustowicz et al. 2000]. In the current study, we revisited this data set using a Bayesian linkage analysis technique, namely the posterior probability of linkage (PPL). Methods: The PPL has been developed as an alternative to traditional linkage analysis. It differs from both LOD scores and 'non-parametric' methods in that it directly measures the probability of linkage given the data, and incorporates prior genomic information. Results: As expected, PPL results for 1q23 supported the previously observed linkage, with an estimated multipoint PPL of 99.7%. However, the PPL supported two further results: a second peak on chromosome 1 at 1p13 with a multipoint with PPL of 70% and a chromosome 17 marker (D17S784 at 17q25) with a multipoint PPL of 44%. Conclusions: The PPL-based analysis presented has the advantage over other likelihood-based linkage methods in that it avoids maximization and produces a less complex view of the strength of evidence for linkage. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:47 / 54
页数:8
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