Don’t forget…Our FAS team can be contacted online with free support advice
Use SureSeq™ CLL + CNV NGS to generate a comprehensive genomic profile, including large CNVs, SNVs and indels.
Replace multiple assays with only one!
With many of our team once being customers themselves, our scientists endeavor to create a portfolio shaped by a genuine understanding of its real-world clinical application.
Identify and resolve common FISH problems in your haematological samples with our interactive troubleshooting page.
Bookmark our events page for details on upcoming opportunities to meet. On the calendar: 9th International Workshop on Cancer Genetic & Cytogenetic Diagnostics (23-25 March), GfH and EHA.