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Flyer
Vanadis NIPT system - Flyer for Patients
Explains the fundamentals of Vanadis NIPT, including how the test works, the conditions tested, the time it can be performed, and the benefits of the screening test.
Flyer
The future of newborn sequencing research
Communicates the key strengths and components of our newborn sequencing workflow. Built for flexibility, discover our end-to-end sequencing workflow – all offered from one partner.
Brochure
Vanadis NIPT system
Outlines differentiating features of the Vanadis NIPT system, inclusive of minimal hands-on time, walkaway automation, high precision and no PCR or sequencing. Empowering any laboratory to conduct NIPT in-house.
Brochure
Vanadis cfDNA platform
Highlights the defining features behind the Vanadis cfDNA platform, including its ease of use, full automation, high precision and no PCR or sequencing required. Now any lab can conduct cfDNA analysis in-house.
Flyer
Vanadis cfDNA platform - Flyer for Laboratories
Flyer that hightlights the Vanadis cfDNA platform, built for all laboratories.
Flyer
Vanadis NIPT system - Flyer for Providers
Communicates the key strengths and features behind the Vanadis NIPT system, inclusive of high precision, no sequencing, no PCR, improved detection rate, minimal invasive procedures and no-call results.
Brochure
Newborn sequencing research for laboratories
Highlights the defining features behind our newborn sequencing workflow. Provides a list of instrumentation, software components and key features, in addition to offering a host of starting points on how laboratories can commence.
Literature - Publication Review
60 second spotlight: prenatal screening for autosomal trisomies
Quick summary of a prospective 2-center study of 862 twin pregnancies. Compared no-call rate and performance against 16,382 singleton pregnancies.
Flyer
Evoya Software Security
This flyer provides information on the security aspects of Evoya newborn screening software
Infographic
Newborn sequencing research with Revvity
Infographic highlights Revvity's newborn sequencing workflow, featuring 390+ genes, for advancing genomic research while simplifying laboratory processes.
Flyer
Official gene panel flyer
Summary of Revvity NGS gene panel used for newborn DNA sequencing research in the laboratory.
Flyer
Newborn Health - Working with Revvity
Revvity's comprehensive solutions and services for newborn health betterment.
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