The -omics era has greatly expanded the repertoire of approaches available for researchers and clinicians to unravel the complexities underpinning human health: next generation sequencing (NGS) methods, advanced DNA barcoding and microfluidics, and peripheral blood mononuclear cells (PBMCs).
In this recording from the Azenta Life Sciences Breakfast Talk at ASHG 2022, Dr. Andrea O’Hara presents a workflow using the approaches mentioned above to rapidly produce a diverse set of multiomics results, including genomics, epigenomics, transcriptomics, and proteomics, from a single blood draw. This robust workflow, coupled with advanced robotics for automated sample handling and processing, enable these datatypes to be generated within days of primary sample collection, offering a rapid approach to drive greater insights into human health.
About the Presenter
Andrea O’Hara, Ph.D.
Strategic Technical Specialist, Genomics & Analytics
Azenta Life Sciences
Dr. Andrea O’Hara is a technical specialist at Azenta Life Sciences and has over 13 years of experience in next generation sequencing. She earned her Ph.D. from the University of North Carolina at Chapel Hill in genetics and molecular biology and did her postdoctoral training at the National Institutes of Health.
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