| Discover how to extend your lab capabilities through newborn genomic research. |
| Genomic sequencing is reshaping newborn health research. Now, laboratories worldwide are evaluating how they can participate in this change. |
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Guiding the way, we’re excited to announce a new webinar, Sequencing spotlight: how to commence newborn genomic research. |
| Drawing on our 40+ year experience in newborn screening alongside key insights from our international genomic laboratory network, join us as we explore practical considerations for implementing lab-based newborn genomics. Topics include: |
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Laboratory approach (in-house sequencing vs. send-out services) |
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Genomic scope (WGS vs. targeted panels) |
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Financial considerations |
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Instrumentation, software |
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Lab infrastructure, expertise and more |
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| Whether you're taking your first steps into newborn genomic sequencing or are interested in refining your current initiatives, this session offers critical perspectives on how you can achieve your newborn research objectives. |
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| WEBINAR: log in to embark on newborn sequencing research! |
| Date: March 19 |
| Time: 10:00 AM ET | 4:00 CET |
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| Title: Sequencing spotlight: how to commence newborn genomic research |
| This webinar is for labs who are contemplating newborn genomic sequencing or would like to enhance their current genomic initiatives. Led by two experts from Revvity Omics, register now to learn how you can step into sequencing. |
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| Speakers |
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Ephrem Chin, MBA, BTech(Hon), MB(ASCP), QLC, CGMBS
VP Global OMICS Services Strategy, Technical Operations & Commercial, Revvity
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Zeq Ma
Sr. Director of Clinical Informatics,
Revvity
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