کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2058628 | 1543967 | 2016 | 7 صفحه PDF | دانلود رایگان |
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.
Figure optionsDownload as PowerPoint slide
Journal: MethodsX - Volume 3, 2016, Pages 1–7