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Devyser Thalassemia NGS

Complete one-tube analysis

End-to-end CE-IVD solution

Quick and easy implementation

Comprehensive gene panel for Familial hypercholesterolemia (FH)

Identify 12 SNPs in polygenic FH & the 6 SNPs to predict statin response

Single-tube workflow for fast results

Devyser Thrombophilia

One single mix for testing of six relevant risk factors for thrombophilia

Single-tube PCR

Fast analysis with minimum hands-on time

Devyser CFTR NGS

Full CFTR gene sequencing

Single-tube NGS library prep kit

Devyser CFTR 68

Detects 68 CFTR mutations

Allele-specific detection

Devyser CFTR Core

Detects the 36 most common mutations found in populations of European origin

Allele-specific detection of wild-type and variants

Devyser CFTR Italia

Designed for the Italian population

Detects the normal and mutant alleles at 31 loci of the CFTR gene

Includes ID markers for sample identity confirmation

Multiplex detection of the three most important HFE mutations and the corresponding wild types

Single-tube PCR

Accurate and efficient

Detects seven risk factors for cardiovascular disease

Single-tube PCR

Fast analysis with minimum hands-on time

Hereditary

Devyser offers a broad panel of allele-specific and NGS-based test kits for hereditary diseases.

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Devyser’s test kits are used to detect genetic variants associated with a wide variety of genetic disorders including thalassemia, cystic fibrosis, familial hypercholesterolemia and thrombophilia. Results may be used by clinicians to guide patient treatment and management.

Related articles

Whitepaper: NGS: Changing the game in CFTR analysis

Booklet: Devyser Thalassemia

Whitepaper: Familial hypercholesterolemia: Genetic diagnosis and cascade testing using NGS

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