- Product line overview
- Technical notes
- Featured kits
- Technology and application overviews
- FAQs and tips
- DNA-seq protocols
- Bioinformatics resources
- Harnessing the power of full-length transcriptome analysis for biomarker discoveries
- SMART-Seq Pro kits for biomarker detection
- Takara Bio Single-Cell Workshop, Spring 2021
- Capturing biological complexity by high-resolution single-cell genomics
- Sensitivity and scale for neuron multiomics
- Taking single-cell RNA-seq by STORM
- Pushing the limits of sensitivity for single-cell applications
- Liver metabolic function, dissecting one cell at a time
- Single-Cell Workshop at 2020 NextGen Omics Series UK
- TCR-seq methods: when to use which
- Immunogenomics to accelerate immunotherapy
- Total RNA sequencing of liquid biopsies
- MeD-Seq, a novel method to detect DNA methylation
- Automating full-length single-cell RNA-seq libraries
- Single-cell DNA-seq
- Single-cell whole transcriptome analysis
MeD-Seq, a novel method to detect DNA methylation
Next-generation sequencing (NGS) is opening new avenues for epigenetic research by uncovering mechanisms that shape cell- and disease-specific gene expression programs. Although technical challenges still exist, having NGS technologies featuring simple workflows, high-throughput capabilities, and high-quality readouts with minimal sequencing depth will help to enable further breakthroughs.
In this on-demand webinar, Dr. Wilfred van IJcken, board member at Methylomics and manager of Erasmus Center for Biomics, describes and discusses a newly developed method for genome-wide detection of DNA methylation.
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- Background on DNA methylation
- Key aspects of the novel MeD-Seq method
- Validation data of MeD-Seq
- Case study on cervical cancer after hrHPV infection
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