Bayesian mixed-effects model for the analysis of a series of FRAP images.

IF 0.8 4区 数学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Martina Feilke, Katrin Schneider, Volker J Schmid
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引用次数: 2

Abstract

The binding behavior of molecules in nuclei of living cells can be studied through the analysis of images from fluorescence recovery after photobleaching experiments. However, there is still a lack of methodology for the statistical evaluation of FRAP data, especially for the joint analysis of multiple dynamic images. We propose a hierarchical Bayesian nonlinear model with mixed-effect priors based on local compartment models in order to obtain joint parameter estimates for all nuclei as well as to account for the heterogeneity of the nuclei population. We apply our method to a series of FRAP experiments of DNA methyltransferase 1 tagged to green fluorescent protein expressed in a somatic mouse cell line and compare the results to the application of three different fixed-effects models to the same series of FRAP experiments. With the proposed model, we get estimates of the off-rates of the interactions of the molecules under study together with credible intervals, and additionally gain information about the variability between nuclei. The proposed model is superior to and more robust than the tested fixed-effects models. Therefore, it can be used for the joint analysis of data from FRAP experiments on various similar nuclei.

贝叶斯混合效应模型对一系列FRAP图像的分析。
通过对光漂白实验后荧光恢复图像的分析,可以研究活细胞细胞核内分子的结合行为。然而,对于FRAP数据的统计评价,特别是多幅动态图像的联合分析,目前还缺乏方法论。为了获得所有核的联合参数估计以及考虑核种群的异质性,我们提出了一种基于局部室模型的混合效应非线性分层贝叶斯模型。我们将该方法应用于体细胞小鼠细胞系中表达的绿色荧光蛋白标记的DNA甲基转移酶1的一系列FRAP实验,并将结果与三种不同的固定效应模型应用于同一系列FRAP实验进行了比较。利用所提出的模型,我们得到了所研究分子相互作用的偏离率和可信区间的估计值,并获得了核间变异性的信息。该模型优于已有的固定效应模型,且鲁棒性更强。因此,它可以用于各种相似核的FRAP实验数据的联合分析。
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来源期刊
Statistical Applications in Genetics and Molecular Biology
Statistical Applications in Genetics and Molecular Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-MATHEMATICAL & COMPUTATIONAL BIOLOGY
自引率
11.10%
发文量
8
期刊介绍: Statistical Applications in Genetics and Molecular Biology seeks to publish significant research on the application of statistical ideas to problems arising from computational biology. The focus of the papers should be on the relevant statistical issues but should contain a succinct description of the relevant biological problem being considered. The range of topics is wide and will include topics such as linkage mapping, association studies, gene finding and sequence alignment, protein structure prediction, design and analysis of microarray data, molecular evolution and phylogenetic trees, DNA topology, and data base search strategies. Both original research and review articles will be warmly received.
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