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孙女设计中遗传标记与数量性状基因座间连锁的限制最大似然分析。

Restricted maximum likelihood analysis of linkage between genetic markers and quantitative trait loci for a granddaughter design.

作者信息

Van Arendonk J A, Tier B, Bink M C, Bovenhuis H

机构信息

Wageningen Institute of Animal Sciences, Wageningen Agricultural University, The Netherlands.

出版信息

J Dairy Sci. 1998 Sep;81 Suppl 2:76-84. doi: 10.3168/jds.s0022-0302(98)70156-0.

Abstract

A REML for the estimation of location and variance of a single quantitative trait locus, together with polygenic and residual variance, is described for the analysis of a granddaughter design. The method is based on a mixed linear model that includes the allelic effects of the quantitative trait locus, which are assumed to be normally distributed. Information from four marker loci situated on a single chromosome was available to derive the covariances at the linked quantitative trait locus. A derivative-free algorithm is described that makes use of the specific structure of the granddaughter design. The procedure has been applied to simulated data for a granddaughter design with 50 grandsire families of 40 sires each. Error variance was 60, and total additive genetic variance equaled 40; the quantitative trait locus explained either 10 or 25% of the latter variance. The size of the marker bracket containing the quantitative trait locus was either 10 or 30 cM. The power of detecting the quantitative trait locus ranged from 19 to 99%. Estimates of total genetic variance and variance explained by the quantitative trait locus were found to be empirically unbiased. A small bias was found in location estimates, especially when markers were not fully informative. The accuracy of parameter estimates was greatly improved by the use of information from individual daughters.

摘要

本文描述了一种用于估计单个数量性状位点的位置和方差以及多基因方差和残差方差的REML方法,用于孙女设计的分析。该方法基于一个混合线性模型,该模型包括数量性状位点的等位基因效应,假设其呈正态分布。利用位于一条染色体上的四个标记位点的信息来推导连锁数量性状位点处的协方差。描述了一种无导数算法,该算法利用了孙女设计的特定结构。该程序已应用于具有50个祖父系家族、每个家族有40个父系的孙女设计的模拟数据。误差方差为60,总加性遗传方差等于40;数量性状位点解释了后者方差的10%或25%。包含数量性状位点的标记区间大小为10或30厘摩。检测数量性状位点的功效范围为19%至99%。发现总遗传方差和数量性状位点解释的方差估计在经验上是无偏的。在位置估计中发现了小的偏差,特别是当标记信息不完全时。通过使用来自单个女儿的信息,参数估计的准确性得到了极大提高。

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