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- Reading the Effect of Tea Leaves…and Beating Genetic Fatalism in Breast Cancer
- Tet1 Enzyme Based Enrichment Method for Methylome Sequencing: TamC-Seq
- Introducing Aba-seq for Enzyme Based High-Res Mapping of Mammalian Hydroxymethylomes
- Methylome Data in Lethal Prostate Cancer Supports Personalized Medicine
- New Years Resolution, Reflection on Cancer Research
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- Bill Graham on Sirtuin3 Reprograms Mitochondrial Epigenetic Pathways: How Diet Affects Age
- Doug on Will the Long History of Breast Cancer Research Culminate with Epigenetics Based Personalized Medicine?
- Canada Joins the International Human Epigenome Consortium – Q&A with Tomi Pastinen of Génome Québec | Epigenetics Experts Blog on Q&A with BLUEPRINT’s Henk Stunnenberg on the New Leukemia, Blood Epigenome Project
- Doug on Oxidative Bisulfite Sequencing (oxBS-Seq) A Brilliant Advance for Epigenetics
- The Epigenetics of Real-Life Stress and Serotonin | Epigenetics Experts Blog on Situational Stress Makes Short-Term Epigenetic Changes
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Tag Archives: DNA
There is exciting news regarding a new method to detect 5-hmC quantitatively at high resolution – using any sequencing platform. The new method, termed oxidative bisulfite sequencing (oxBS-Seq) , was applied to explore the 5-hmC mark’s potential functional role in epigenetic plasticity. First author Michael J. Booth, along with collaborators from the Wolf Reik lab at the Babraham Institute, and Shankar Balasubramanian lab at Cambridge University, have reported their work in Science Magazine. In brief, this method uses potassium perruthenate (KRuO4) oxidation to convert 5hmC to 5fC (formylcytosine), and is followed up by conventional bisulfite conversion. Through this process C and 5-hmC sites convert to Uracil, whereas 5-mC does not. OxBS-Seq data is then subtracted from BS-Seq data. The group … Continue reading
