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Illumina HumanMethylation27 微阵列上常染色体和性连锁探针之间的序列重叠。

Sequence overlap between autosomal and sex-linked probes on the Illumina HumanMethylation27 microarray.

机构信息

Program in Genetics and Genome Biology, Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.

出版信息

Genomics. 2011 Apr;97(4):214-22. doi: 10.1016/j.ygeno.2010.12.004. Epub 2011 Jan 4.

Abstract

The Illumina Infinium HumanMethylation27 BeadChip (Illumina 27k) microarray is a high-throughput platform capable of interrogating the human DNA methylome. In a search for autosomal sex-specific DNA methylation using this microarray, we discovered autosomal CpG loci showing significant methylation differences between the sexes. However, we found that the majority of these probes cross-reacted with sequences from sex chromosomes. Moreover, we determined that 6-10% of the microarray probes are non-specific and map to highly homologous genomic sequences. Using probes targeting different CpGs that are exact duplicates of each other, we investigated the precision of these repeat measurements and concluded that the overall precision of this microarray is excellent. In addition, we identified a small number of probes targeting CpGs that include single-nucleotide polymorphisms. Overall, our findings address several technical issues associated with the Illumina 27k microarray that, once considered, will enhance the analysis and interpretation of data generated from this platform.

摘要

Illumina Infinium HumanMethylation27 BeadChip(Illumina 27k)微阵列是一种高通量平台,能够检测人类 DNA 甲基化组。在使用该微阵列寻找常染色体性别特异性 DNA 甲基化的过程中,我们发现了常染色体 CpG 位点存在显著的性别甲基化差异。然而,我们发现大多数这些探针与性染色体的序列发生交叉反应。此外,我们确定该微阵列中 6-10%的探针是非特异性的,并且映射到高度同源的基因组序列。使用靶向彼此完全重复的不同 CpG 的探针,我们研究了这些重复测量的精度,并得出结论,该微阵列的整体精度非常高。此外,我们还鉴定了少数靶向包含单核苷酸多态性的 CpG 的探针。总的来说,我们的研究结果解决了与 Illumina 27k 微阵列相关的几个技术问题,这些问题一旦被考虑,将增强对该平台生成的数据的分析和解释。

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