Skip to main content
Menu

Vanadis cfDNA Platform

With Vanadis, any laboratory, hospital, or OB group can analyze cfDNA samples in-house. Without PCR or sequencing, Vanadis empowers simplified analysis of the common chromosome abnormalities (21, 18, 13, X & Y). Welcome to a whole new way to cfDNA.

Easy: Determinations available in as soon as 72 hours

Cost-effective: Only one lab technician required to operate

Precise: Structured to minimize the failure rate

Built for all: No bioinformatics or genetic expertise required
 

For research use only. Not for use in diagnostic procedures.

revvity-core-and-sw

Featured resource

References:
  1. Conotte S., El Kenz H., De Marchin J., Jani J.C. Cell-free DNA analysis for noninvasive examination of trisomy: comparing two targeted methods. American Journal of Obstetrics & Gynecology. 2022. doi: 10.1016/j.ajog.2022.05.024
  2. Pooh R.K. et al. Clinical Validation of Fetal cfDNA Analysis Using Rolling-CircleReplication and Imaging Technology in Osaka (CRITO Study). Diagnostics 2021, 11, 1837. doi: 10.3390/diagnostics11101837
     

Revvity AI Assistant Beta