Lee Suman, Kim Joomyeong
Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.
MethodsX. 2015 Nov 26;3:1-7. doi: 10.1016/j.mex.2015.11.008. eCollection 2016.
We have developed an NGS-based deep bisulfite sequencing protocol for the DNA methylation analysis of genomes. This approach allows the rapid and efficient construction of NGS-ready libraries with a large number of PCR products that have been individually amplified from bisulfite-converted DNA. This approach also employs a bioinformatics strategy to sort the raw sequence reads generated from NGS platforms and subsequently to derive DNA methylation levels for individual loci. The results demonstrated that this NGS-based deep bisulfite sequencing approach provide not only DNA methylation levels but also informative DNA methylation patterns that have not been seen through other existing methods.•This protocol provides an efficient method generating NGS-ready libraries from individually amplified PCR products.•This protocol provides a bioinformatics strategy sorting NGS-derived raw sequence reads.•This protocol provides deep bisulfite sequencing results that can measure DNA methylation levels and patterns of individual loci.
我们开发了一种基于二代测序(NGS)的深度亚硫酸氢盐测序方案,用于基因组的DNA甲基化分析。这种方法能够快速、高效地构建适用于NGS的文库,文库包含大量从亚硫酸氢盐转化后的DNA中单独扩增得到的PCR产物。该方法还采用了一种生物信息学策略,对从NGS平台产生的原始序列读数进行分类,随后得出各个位点的DNA甲基化水平。结果表明,这种基于NGS的深度亚硫酸氢盐测序方法不仅能提供DNA甲基化水平,还能提供通过其他现有方法未观察到的丰富的DNA甲基化模式。
• 本方案提供了一种从单独扩增的PCR产物生成适用于NGS的文库的有效方法。
• 本方案提供了一种对NGS产生的原始序列读数进行分类的生物信息学策略。
• 本方案提供了深度亚硫酸氢盐测序结果,可测量各个位点的DNA甲基化水平和模式。