Epigenetics

The leading service provider for methylation studies in Europe

Epigenetic services using Micro-array and Next Generation Sequencing

We are a leading service provider for Epigenetics studies in Europe. Our wide portfolio enables you to select the most optimal method for your project. The available products range from cost-effective array-based techniques to targeted methylome sequencing methods.

All of these products are part of our ISO/IEC 17025 (L518) accreditation, which guarantees a standard high data-quality. Our dedicated methylation product specialists can help you design the most optimal research strategy. Contact us for free expert advice.

Next Level Epigenetics

With our validated applications you have the tools in hand to study different methylation loci in the most challenging samples: low quality or quantity of the available DNA is no longer hampering your project. EpiRestore™ reproducibly determines the methylation status in degraded FFPE material. Furthermore, with our SeqCap Epi procedure, we can reliably detect up to 5.5 million CpG’s with only 10 ng starting material.

We set the standard for sharply priced array and NGS methylation sequencing services.
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Reduced Representation & Whole Genome Bisulfite Sequencing

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Single cell RNA-seq

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Targeted methylation

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MethylationEPIC ‘850K’ BeadChip

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EpiRestore: restore all low integrity DNA

Epigenetics research focuses on biological or chemical influences that can change the expression of a gene. “Epi” is greek for “above or outside”, referring to the modifications such as methylation or hydroxymethylation that are attached to the DNA strands. Because the various epigenetic groups have different effects on the gene transcription, measuring these specific groups is important when explaining various (disease) phenotypes.

Choose the most optimal method for your project

 MethylationEPIC
BeadChip
EpiRestore in combination
with MethylationEPIC
SeqCap Epi using CpGiant EnrichmentWhole Genome Bisulfite Sequencing (WGBS)Reduced Representation
Bisulfite Sequencing (RRBS)
OrganismsHuman onlyHuman onlyHuman onlyAllAll
Tissue of highest abundanceAllAllAllAllAll
Methylated targets850,000 selected loci850,000 selected loci5.5 million selected lociAllMajority of loci
Validated and within ISO 17025 accreditation scopeIn progress
Applicable for FFPE samples
CostsVery budget friendlyBudget friendlyEconomical tool for a broad overview of mC lociBest option for a wide methylome viewMore economical than whole genome sequencing
BenefitsBest option for a cost-effective focused approachOnly method to study highly degraded DNALarge number of CpG sites and low input possibleUnbiased approach for methylation researchBenefits of WGBS but with reduced costs
Mostly used forEWAS studies or large cohortsAnalysis of FFPE cohorts or Guthry cards

Drug development
Low input samples
Discovery outside of published loci

In-depth analysis of selected patient samplesDiscovery research projects

Discuss your project with André

We have years of experience in the field. Talk with us about best practices and how we can help your research.

Pricing

Competitive pricing for unmatched quality

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André Wijfjes

Manager Customer Support