MRE-Seq Service

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.  

Specific MRE-Seq Service Approaches We Offer

Services Advantages

Our Capabilities

Workflow

Workflow

Sample Requirements

We currently accept DNA, cell, and tissue samples for our MRE-Seq service. Sample sources include human, animal, plant, and microbial.

Service Process

Service Process

Deliverables

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

Our Features

  • CD Genomics has established a proven epigenomics sequencing platform for a variety of applications. We'll help you design the right MRE-Seq service to aid your scientific research.
  • CD Genomicsis a leading epigenomics sequencing technology company offering a trusted suite of services and solutions, especially with our extensive experience in MRE-Seq service.

Why Choose Us?

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.

! For research purposes only, not intended for clinical diagnosis or individual assessments.
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