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Devyser Chimerism NGS

 

Devyser Chimerism NGS utilizes NGS technology for very early detection of graft rejection and disease relapse in hematopoietic stem cell transplanted patients.

 

For further information on the Devyser Chimerism NGS Kit, click here.

To download the Devyser Chimerism NGS Kit handbook, click here.

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Devyser Thalassemia NGS

 

With the Devyser Thalassemia kit you can detect all mutations in HBA1, HBA2 and HBB using a single, one-tube NGS assay. The assay detects single nucleotide polymorphisms (SNVs), indels and CNVs. The extremely simple procedure makes it an excellent choice for any lab, whether you are running advanced second level genetic testing or large scale mutation screening. The fast, simple and robust NGS workflow replaces complex multi-step protocols and eliminates the need for maintaining multiple thalassemia assays in your lab.

 

For further information on the Devyser Thalassemia NGS Kit, click here.

To download the Devyser Thalassemia NGS Kit handbook, click here.

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Devyser BRCA NGS

 

Devyser BRCA NGS utilizes NGS technology and proprietary multiplex PCR primer chemistry to provides full and uniform coverage of BRCA1 and BRCA2, covering all exons and exon/intron junctions. The kit uses overlapping primer design to ascertain superior INDEL coverage and downstream CNV analysis. It can be used to detect both germline and somatic mutations.

 

For further information on the Devyser BRCA NGS Kit, click here.

To download the Devyser BRCA NGS Kit handbook, click here.

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Devyser HBOC NGS

 

Devyser HBOC NGS utilizes NGS technology for targeted sequencing of 12 genes relevant for hereditary breast and ovarian cancers (HBOC).

 

It can be used as a follow-up after negative BRCA testing, or combined with Devyser BRCA NGS Kit for analysis of 14 genes in total  

 

For further information on the Devyser HBOC NGS Kit, click here.

To download the Devyser HBOC NGS Kit handbook, click here.

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