Transform your cytogenetics workflow

Transform your cytogenetics workflow

Rich Shippy, Director of Product Marketing , illumina
Topic: Reproductive & Genetic Health

Learn how to seamlessly integrate next-generation sequencing and array applications all on a single system for your cytogenetic research. The NextSeq 550 allows laboratories to comprehensively analyze SNVs and CNVs, thereby significantly increasing the chances of detecting cytogenetic abnormalities. With the addition of BeadChip array scanning for Cytogenomics and Karyomapping applications, the NextSeq 550 System can now deliver unparalleled flexibility for your research.

Watch the webinar to discover how the new BeadChip array scanning capability will help simplify your workflow and accelerate your next breakthrough.



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