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Webinar
Sequencing spotlight: how to commence newborn genomic research
Learn how to launch newborn genomic sequencing research - covering lab setup, instrumentation, bioinformatics, data management, and scalable implementation paths.
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Genomic sequencing is rapidly reshaping the future of newborn health research. Labs around the world are asking the same question: where do we start?
This on-demand webinar brings together two of Revvity's leading experts in genomic services and clinical informatics to walk you through the practicalities when launching a newborn genomic sequencing program. Whether you're building from scratch or expanding an existing service, this session delivers a clear, actionable roadmap.
Topics include:
- Laboratory approach (in-house sequencing vs. send-out services)
- Genomic scope (WGS vs. targeted panels)
- Financial considerations
- Instrumentation, software
- Lab infrastructure, expertise and more
Speakers:
- Ephrem Chin | MBA, BTech(Hon), MB(ASCP), QLC, CGMBS, Head Global Omics Services at Revvity
- Zeq Ma | Sr. Director of Clinical Informatics at Revvity
Backed by over 300 million genomic tests performed across Revvity's global service network, this session offers real-world insight into what it takes to stand up a genomic sequencing lab and how Revvity's integrated solutions can help you get there faster.
