[WEBINAR] Anchor-Based Bisulfite Sequencing (ABBS) Determines Genome-wide DNA Methylation

In this webinar, Dr. Benjamin Delatte, Group Leader, Advanced Research Lab at Active Motif discusses a newly developed and published technique, Anchor-Based Bisulfite Sequencing (ABBS) and the advantages it has for measuring DNA methylation on a genome-wide scale in comparison to traditional bisulfite based approaches.

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Check out these other popular webinars that cover additional epigenetics topics.

CUT&Tag vs ChIP-seq – From Data Generation to Analysis

In this free webinar, Dr. Sarantis Chlamydas, Ph.D., Senior Market Development Manager at Active Motif, and Amit Sinha, Ph.D., CEO of Basepair Tech discuss the best ways to generate quality data using advanced, epigenomics techniques including CUT&Tag and ChIP-Seq, and then efficiently process and interpret epigenomic data using streamlined analysis pipelines.

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Utilizing Single-cell Workflows for Clinical Multiomics Analysis

In this webinar, Dr. Rupesh Kanchi Ravi, Director of Epigenetic Services at Active Motif, discusses how newly developed single-cell workflows, such as scATAC-Seq, and scRNA-Seq can be combined to create multiomic analysis of clinical samples, representing a major advancement from previous bulk analysis approaches.

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ATAC-Seq: Mapping Open Chromatin

ATAC-Seq is a powerful technique that enables the mapping of accessible, or open, chromatin regions across the genome. The ATAC-Seq assay has been used by many researchers to investigate the role of epigenetics in many biological processes and disease states. This webinar covers the ATAC-Seq method in depth and discusses how it can be applied to epigenetics research.

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Understanding Single-Cell ATAC-Seq and its Applications

ATAC-Seq and Single-Cell ATAC-Seq (scATAC-Seq) are powerful tools for investigating the epigenetic mechanisms responsible for regulating a particular cellular response or that contribute to a disease state. This webinar will explain how these popular techniques work and discuss how they can be useful in epigenetics research.

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