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首页> 外文期刊>The journals of gerontology.Series A. Biological sciences and medical sciences >Reproducibility, sources of variability, pooling, and sample size: important considerations for the design of high-density oligonucleotide array experiments.
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Reproducibility, sources of variability, pooling, and sample size: important considerations for the design of high-density oligonucleotide array experiments.

机译:重现性,变异性来源,合并和样本大小:设计高密度寡核苷酸阵列实验的重要考虑因素。

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We have undertaken a series of experiments to examine several issues that directly affect design of gene expression studies using Affymetrix GeneChip arrays: probe-level analysis, need for technical replication, relative contribution of various sources of variability, and utility of pooling RNA from different samples. Probe-level data were analyzed by Affymetrix MAS 5.0, and three model-based methods, PM-MM and PM-only models by dChip, and the RMA model by Bioconductor, with the latter two providing the best performance. We found that replicate chips of the same RNA have limited value in reducing total variability, and for relatively highly expressed genes in this biologically homogeneous animal model of aging, about 11% of total variation is due to day effects and the remainder is approximately equally split between sample and residual sources. We also found that pooling samples is neither advantageous nor detrimental. Finally we suggest a strategy for sample size calculations using formulas appropriate when coefficients of variation are known, target effects are expressed as fold changes, and data can be assumed to be approximately lognormally distributed.
机译:我们进行了一系列实验,研究了几个直接影响使用Affymetrix GeneChip阵列进行基因表达研究设计的问题:探针水平分析,技术复制需求,各种可变性来源的相对贡献以及从不同样品中收集RNA的实用性。探针级数据通过Affymetrix MAS 5.0和三种基于模型的方法进行了分析,dChip通过PM-MM和PM-only模型进行了分析,而Bioconductor通过RMA模型进行了分析,后两种提供了最佳性能。我们发现,相同RNA的复制芯片在降低总变异性方面价值有限,对于这种在生物学上均一的动物衰老模型中相对较高表达的基因,总变异的11%是由于日间作用,其余的大约均分在样本和残留源之间。我们还发现合并样本既无益也不有害。最后,我们提出了一种使用适当公式的样本量计算策略,该公式适用于已知变化系数,目标效应表示为倍数变化并且可以假定数据近似对数正态分布的情况。

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