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Detecting marker-QTL linkage and estimating QTL gene effect and map location using a saturated genetic map.

机译:使用饱和遗传图谱检测标记物-QTL连锁并估计QTL基因效应和图谱位置。

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A simulation study was carried out on a backcross population in order to determine the effect of marker spacing, gene effect and population size on the power of marker-quantitative trait loci (QTL) linkage experiments and on the standard error of maximum likelihood estimates (MLE) of QTL gene effect and map location. Power of detecting a QTL was virtually the same for a marker spacing of 10 cM as for an infinite number of markers and was only slightly decreased for marker spacing of 20 or even 50 cM. The advantage of using interval mapping as compared to single-marker analysis was slight. "Resolving power" of a marker-QTL linkage experiment was defined as the 95% confidence interval for the QTL map location that would be obtained when scoring an infinite number of markers. It was found that reducing marker spacing below the resolving power did not add appreciably to narrowing the confidence interval. Thus, the 95% confidence interval with infinite markers sets the useful marker spacing for estimating QTL map location for a given population size and estimated gene effect.
机译:为了确定标记间隔,基因效应和种群大小对标记定量性状基因座(QTL)连锁实验的功效以及最大似然估计的标准误差(MLE)的影响,对回交群体进行了模拟研究。 )的QTL基因效应和图谱定位。对于10 cM的标记间隔,对于无限数量的标记,检测QTL的能力实际上是相同的,而对于20或什至50 cM的标记间隔,QTL的检测能力仅略有降低。与单标记分析相比,使用间隔映射的优势很小。标记-QTL连锁实验的“分辨力”定义为QTL图位置的95%置信区间,当对无数个标记进行评分时,将获得该区间。已经发现,将标记间距减小到分辨能力以下并不会明显地使置信区间变窄。因此,具有无限标记的95%置信区间设置了有用的标记间距,用于估计给定种群大小和估计的基因效应的QTL定位。

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