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Removing unwanted variation in a differential methylation analysis of Illumina HumanMethylation450 array data

机译:在Illumina HumanMethylation450阵列数据的差异甲基化分析中消除不必要的变异

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Due to their relatively low-cost per sample and broad, gene-centric coverage of CpGs across the human genome, Illumina's 450k arrays are widely used in large scale differential methylation studies. However, by their very nature, large studies are particularly susceptible to the effects of unwanted variation. The effects of unwanted variation have been extensively documented in gene expression array studies and numerous methods have been developed to mitigate these effects. However, there has been much less research focused on the appropriate methodology to use for accounting for unwanted variation in methylation array studies. Here we present a novel 2-stage approach using RUV-inverse in a differential methylation analysis of 450k data and show that it outperforms existing methods.
机译:由于Illumina的450k阵列相对于每个样本而言成本相对较低,并且在整个人类基因组中覆盖了以基因为中心的广泛区域,因此被广泛用于大规模差异甲基化研究中。但是,就其本质而言,大型研究尤其容易受到不必要变化的影响。基因表达阵列研究已广泛记录了有害变异的影响,并已开发出许多方法来减轻这些影响。然而,很少有研究集中在适当的方法上,以解决甲基化阵列研究中不需要的变化。在这里,我们介绍了在450k数据的差分甲基化分析中使用RUV-inverse的新颖的2阶段方法,并表明它优于现有方法。

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