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MRE-Seq is a protocol to study DNA methylation using methylation-sensitive restriction enzymes (MSREs) on genomic DNA. mRE-seq enriches unmethylated DNA and can cover 1.7 million CpG sites in the human genome. In this approach, gDNA is first digested separately with different MSREs. The library is prepared and sequenced based on size-selected restriction fragments. Deep sequencing allows for accurate detection of methylation sites in the genome. Now, CD Genomics provides you with a variety of MRE-Seq service to meet your research needs.
We currently accept DNA, cell, and tissue samples for our MRE-Seq service. Sample sources include human, animal, plant, and microbial.
1. Related experimental results raw data
2. Experimental report
3. Data analysis
4. Image and result analysis
5. Bioinformatics analysis results
6. Details in MRE-Seq Service for your writing
CD Genomics is a company that provides professional and comprehensive MRE-Seq services. We have years of experience to meet your specific project needs in using epigenomics research to add value to your research projects. CD Genomics can provide you with personalized solutions to help you thrive every step of the way around your interest in your workflow. If you would like to know more about this service, please feel free to contact us.
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