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一种用于检测显示数量性状基因座(QTL)活性的染色体片段的多标记模型。

A multi-marker model for detecting chromosomal segments displaying QTL activity.

作者信息

Rodolphe F, Lefort M

机构信息

INRA, Centre de Recherches de Jouy en Josas, Laboratoire de Biométrie, France.

出版信息

Genetics. 1993 Aug;134(4):1277-88. doi: 10.1093/genetics/134.4.1277.

DOI:10.1093/genetics/134.4.1277
PMID:8375662
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1205595/
Abstract

A statistical method is presented for detecting quantitative trait loci (QTLs), based on the linear model. Unlike methods able to detect a few well separated QTLs and to estimate their effects and positions, this method considers the genome as a whole and enables the detection of chromosomal segments involved in the differences between two homozygous lines, and their backcross, doubled haploid, or F2 progenies, for a quantitative trait. Genetic markers must be codominant, but missing markers are accepted, provided they are missing independently from the experiment. Asymptotic properties, which are of practical use, are developed. This method does not rely on strong genetic hypotheses, and thus does not permit any precise genetic analysis of the trait under study, but it does assess which regions of the genome are involved, whatever the complexity of the genetic determinism (number, effects and interactions among QTLs). Simultaneous use of several methods, including this one, should lead to better efficiency in QTL detection.

摘要

提出了一种基于线性模型检测数量性状基因座(QTL)的统计方法。与能够检测少数几个分离良好的QTL并估计其效应和位置的方法不同,该方法将基因组作为一个整体来考虑,能够检测涉及两个纯合品系及其回交、加倍单倍体或F2后代之间数量性状差异的染色体片段。遗传标记必须是共显性的,但缺失的标记也被接受,前提是它们的缺失与实验无关。还推导了具有实际应用价值的渐近性质。该方法不依赖于强遗传假设,因此不允许对所研究的性状进行任何精确的遗传分析,但它确实能评估基因组的哪些区域涉及其中,无论遗传决定因素(QTL的数量、效应和相互作用)的复杂性如何。同时使用几种方法,包括这种方法,应该会提高QTL检测的效率。

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本文引用的文献

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Molecular-marker-facilitated investigations of quantitative-trait loci in maize. I. Numbers, genomic distribution and types of gene action.分子标记辅助的玉米数量性状基因座研究。I. 数量、基因组分布及基因作用类型
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On the use of the moments method of estimation to obtain approximate maximum likelihood estimates of linkage between a genetic marker and a quantitative locus.
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