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极端不一致同胞对检测寡基因疾病位点的有效性。

Effectiveness of extreme discordant sib pairs to detect oligogenic disease loci.

作者信息

Rogus J J, Harrington D P, Jorgenson E, Xu X

机构信息

Program for Population Genetics, Harvard School of Public Health, Boston, Massachusetts 02115, USA.

出版信息

Genet Epidemiol. 1997;14(6):879-84. doi: 10.1002/(SICI)1098-2272(1997)14:6<879::AID-GEPI53>3.0.CO;2-J.

Abstract

A method for the genomic screening of quantitative traits using extreme discordant sib pairs (EDSPs) has recently been described by Risch and Zhang [1995; 1996]. For many models relevant to common, genetically complex diseases, EDSPs are the most powerful siblings for detecting linkage. Thus, if such siblings can be identified and collected, powerful studies with reasonable genotyping budgets can be conducted. Using a subset of the GAW10 data, we have simulated a genomic screen using EDSPs. From the 4,780 total families in the first 20 replicates of 239 families, there were 100, 104, 155, 107, and 180 EDSP families for Q1, Q2, Q3, Q4, and Q5, respectively. EDSP data were analyzed for each trait using a modified version of MAPMAKER/SIBS capable of handling extreme discordant sib pairs. Four regions, one for Q1, one for Q2, and two for Q4, were able to exceed a threshold for linkage corresponding to a 0.001 pointwise significance level. In three cases, maximum lod score (MLS) peaks occurred within 3.8 cM of a major gene. In the fourth case, the MLS peak occurred 28.4 cM from a major gene. Omission of parents and an alternative definition of EDSP were also investigated.

摘要

最近,里施和张[1995年;1996年]描述了一种使用极端不一致同胞对(EDSPs)进行数量性状基因组筛查的方法。对于许多与常见的、遗传复杂疾病相关的模型,EDSPs是检测连锁关系最有效的同胞对。因此,如果能够识别并收集这样的同胞对,就可以在合理的基因分型预算下开展有力的研究。我们使用GAW10数据的一个子集,模拟了使用EDSPs进行的基因组筛查。在前239个家庭的20次重复中的4780个总家庭中,Q1、Q2、Q3、Q4和Q5分别有100、104、155、107和180个EDSP家庭。使用能够处理极端不一致同胞对的MAPMAKER/SIBS的修改版本,对每个性状的EDSP数据进行了分析。四个区域,一个对应Q1,一个对应Q2,两个对应Q4,能够超过对应于0.001逐点显著性水平的连锁阈值。在三种情况下,最大似然比分数(MLS)峰值出现在一个主基因的3.8厘摩范围内。在第四种情况下,MLS峰值出现在距一个主基因28.4厘摩处。还研究了省略父母以及EDSP的另一种定义。

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