SafeSEQ Testing

SafeSEQ testing can be used for the sensitive detection of single nucleotide variants (SNVs) in plasma/serum or tissue.
The high analytical sensitivity of SafeSEQ is similar to OncoBEAM performance and can reliably detect 5 mutant molecules in 10.000 wildtype molecules (0.05% MAF).

Disease Panels

Breast Cancer (BC)

Breast Cancer (BC)

AKT1, ERBB2, ESR1, KRAS, PIK3CA, TP53

Colorectal Cancer (CRC)

Colorectal Cancer (CRC)

AKT1, APC, BRAF, CTNNB1, ERBB3, FBXW7, KRAS, NRAS, PIK3CA, POLE, PPP2R1A, RNF43, SMAD4, TP53

Head and Neck Cancer (HNSCC)

Head and Neck Cancer (HNSCC)

CDKN2A, HRAS, PIK3CA, TP53

 

 

 

Single gene testing

  • TP53 stand-alone, Plasma SafeSEQ
    Hot spot regions within the TP53 gene from a single sample.
  • cKIT stand-alone, Plasma SafeSEQ
    Hot spot regions within the cKIT gene from a single sample.

SafeSEQ custom development

SafeSEQ is customizable according to your requirements (e.g. sample type, sample input, panel design, sensitivity level).
Please contact your local Sysmex Inostics sales representative or use our contact form for more information.

How can we help you?

SafeSEQ Technology

SafeSEQ Technology

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