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Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip

机译:在Illumina甲基化EPIC BeadChip上鉴定多态性和脱靶探针结合位点

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摘要

Genome-wide analysis of DNA methylation has now become a relatively inexpensive technique thanks to array-based methylation profiling technologies. The recently developed Illumina Infinium MethylationEPIC BeadChip interrogates methylation at over 850,000 sites across the human genome, covering 99% of RefSeq genes. This array supersedes the widely used Infinium HumanMethylation450 BeadChip, which has permitted insights into the relationship between DNA methylation and a wide range of conditions and traits. Previous research has identified issues with certain probes on both the HumanMethylation450 BeadChip and its predecessor, the Infinium HumanMethylation27 BeadChip, which were predicted to affect array performance. These issues concerned probe-binding specificity and the presence of polymorphisms at target sites. Using in silico methods, we have identified probes on the Infinium MethylationEPIC BeadChip that are predicted to (i) measure methylation at polymorphic sites and (ii) hybridise to multiple genomic regions. We intend these resources to be used for quality control procedures when analysing data derived from this platform.
机译:由于基于阵列的甲基化分析技术,DNA全甲基化的全基因组分析现已成为一种相对便宜的技术。最近开发的Illumina Infinium甲基化EPIC BeadChip可在人类基因组的超过850,000个位点询问甲基化,覆盖了RefSeq基因的99%。该阵列取代了广泛使用的Infinium HumanMethylation450 BeadChip,该芯片允许深入了解DNA甲基化与各种条件和性状之间的关系。先前的研究已经发现了有关HumanMethylation450 BeadChip及其前身Infinium HumanMethylation27 BeadChip的某些探针的问题,这些探针预计会影响阵列性能。这些问题涉及探针结合特异性和靶位点的多态性。使用计算机方法,我们已经在Infinium甲基化EPIC BeadChip芯片上鉴定出了一些探针,这些探针有望(i)在多态性位点测量甲基化,并且(ii)与多个基因组区域杂交。在分析从该平台派生的数据时,我们打算将这些资源用于质量控制程序。

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