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首页> 外文期刊>BMC research notes >Comparison of methylation patterns generated from genomic and cell-line derived DNA using the Illumina Infinium MethylationEPIC BeadChip array
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Comparison of methylation patterns generated from genomic and cell-line derived DNA using the Illumina Infinium MethylationEPIC BeadChip array

机译:使用Illumina Infin甲基化珠阵列基因组和细胞系衍生DNA产生的甲基化模式的比较

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摘要

Abstract ObjectivesGenomic DNA (gDNA) is the optimal source of DNA for methylation analysis. This study compared methylation patterns in gDNA derived from blood with cell-line derived DNA (clDNA) from the same individuals. The clDNA had been generated via an Epstein-Barr virus transformation of the participant’s lymphocytes. This analysis sought to determine whether clDNA has the potential to be utilised in lieu of finite/unavailable gDNA in methylation analyses using Illumina Infinium MethylationEPIC BeadChip arrays that assess 862,927 CpG sites.ResultsDNA samples were divided into two groups with eight gDNA and eight matched clDNA samples compared in each group (n?=?16 individuals with 32 samples in total). Methylation patterns for gDNA samples generated for both groups were compared to the clDNA equivalent samples using Partek? Genomics Suite? to assess whether the significantly different CpG sites were consistent between both groups. In total, 28,632 CpG sites with significantly different levels of methylation (p??×10?8) were common to both groups while 828,072 CpG sites assessed by the MethylationEPIC array were not significantly different in either group. This indicates that there is potential for clDNA to be used as a replacement for finite gDNA samples when absolutely necessary in DNA methylation studies.
机译:摘要目标概率DNA(GDNA)是用于甲基化分析的DNA的最佳来源。该研究与来自同一个体的细胞系衍生的DNA(CLDNA)衍生自血液中的GDNA中的甲基化模式。通过参与者的淋巴细胞的Epstein-Barr病毒转化产生CLDNA。该分析试图确定CLDNA是否具有使用Illumina Infinium甲基化珠芯片阵列中的甲基化分析中的有限/不可用的GDNA的潜力,该甲基化珠阵列评估862,927个CPG位点。分为八个GDNA和八个匹配的CLDNA样品的两组。在每组比较(n?=?16个体,总共有32个样品)。将两组产生的GDNA样品的甲基化模式与使用Partek的CldNA当量样品进行比较?基因组学套房?评估两组之间的显着不同的CPG网站是否一致。总共28,632个CpG位点,两组均常见具有明显不同水平的甲基化(P?<×10→10),而在任一组中,由甲基化阵列评估的828,072个CPG位点没有显着差异。这表明,当DNA甲基化研究中绝对必要时,CLDNA可能用作有限的GDNA样品的替代品。

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