Advancing Methylation Analysis with Reliable DNA Extraction

A recent study in Clinical Epigenetics (Nuttall et al., 2025) explored two ways of studying DNA methylation — an important marker that helps researchers understand how genes are turned on or off. The team compared a newer approach, enzymatic methylation sequencing (EM-seq), with the traditional bisulfite sequencing method, using a variety of real-world samples from cancer cell lines to patient plasma.

The study showed that EM-seq delivered higher-quality data and better preserved the DNA being studied. Compared to older chemical-based methods, enzymatic sequencing provided:

  • Greater DNA recovery and higher-quality sequencing libraries
  • Longer DNA fragments and less damage
  • More complete and consistent methylation coverage
  • Strong performance across challenging sample types like cfDNA and FFPE tissue

These results were achieved using high-purity DNA extracted using Omega Bio-tek’s Mag-Bind® automated purification kits. DNA from multiple sample types, including tissue, blood cells, plasma, and FFPE material, was prepared using:

All extractions were automated on the Thermo Fisher KingFisher Flex, using optimized Omega Bio-tek protocols* to ensure consistent, high-quality results across every sample.

This work also marked a major milestone, the first clinical whole-genome enzymatic methylation sequencing performed in patients with chronic lymphocytic leukemia (CLL). Researchers discovered a new link between IL-15 methylation patterns and how patients respond to a specific therapy (acalabrutinib). These findings highlight a promising new direction for detecting treatment resistance and tracking disease progression through epigenetic biomarkers.

From plasma to preserved tissue, Omega Bio-tek’s Mag-Bind® kits provide the purity, yield, and automation-ready performance needed for today’s sequencing and methylation studies. As laboratories adopt enzymatic methylation and liquid-biopsy techniques, Omega Bio-tek continues to deliver and improve reliability and throughput essential for accurate, scalable genomic research.

*Scripts are available on request from Omega Bio-tek’s Field Application Scientist Team.

https://pmc.ncbi.nlm.nih.gov/articles/PMC12495756/
Nuttall B, Karl DL, Burke K, Callahan M, Mendler K, Cingolani P, Criscione S, Naumenko S, Bibikova E, Munugalavadla V, Byrd JC, Furman RR, Brown JR, Mortlock A, Dougherty BA, Carl Barrett J, Scaltriti M, Hadfield J. Comprehensive comparison of enzymatic and bisulfite DNA methylation analysis in clinically relevant samples. Clin Epigenetics. 2025 Oct 3;17(1):156. doi: 10.1186/s13148-025-01959-0. PMID: 41044668; PMCID: PMC12495756.
Shopping Cart
Scroll to Top