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Guide
Example Report for PG-seq Core Panel
This report is an example of the output from utilizing the software associated with the PG-seq Core Panel.
Application Note
Embryo Identification, tracking and contamination monitoring using Mitochondrial SNVs.
Embryo Identification, tracking and contamination monitoring using Mitochondrial SNVs.
Flyer
Improving sample tracking in PGT-A.
Learn how when combined with the innovative Cap2™ tubes from Azenta® Life Sciences, the PG-Seq™ Rapid v2 kit provides an efficient and error-minimizing solution for PGT-A.
Flyer
End to end solution for PGT-A
This flyer showcases Revvity's end to end solution for PGTA.
Technical Note
Introducing AlphaLISA SureFire® Biotin Free: A Versatile Immunoassay Platform for Biotin-Rich Samples.
Featuring homogeneous detection of cell-based proteins, this note shows you how to utilize an innovative system optimized for biotin-rich media while maintaining unmatched assay performance and versatility.
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
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.
Brochure
PlGF 1-2-3™ brochure for pre-eclampsia
PlGF 1-2-3 brochure for pre-eclampsia screening in the 1st trimester.
Flyer
Newborn Health - Working with Revvity
Revvity's comprehensive solutions and services for newborn health betterment.
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
The future of NGS software
A modular NGS software suite with LIMS, DNA analysis, and interpretation tools, designed to enhance genomic research workflows.
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