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Devyser Thalassemia NGS
  • Complete one-tube analysis
  • End-to-end CE-IVD solution
  • Quick and easy implementation
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Devyser FH NGS
  • 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
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Devyser Thrombophilia
  • One single mix for testing of six relevant risk factors for thrombophilia
  • Single-tube PCR
  • Fast analysis with minimum hands-on time
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Devyser CFTR NGS
  • Full CFTR gene sequencing
  • Single-tube NGS library prep kit
  • CE-IVD
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Devyser CFTR 68
  • Detects 68 CFTR mutations
  • Allele-specific detection
  • CE-IVD
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Devyser CFTR Core
  • Detects the 36 most common mutations found in populations of European origin
  • Allele-specific detection of wild-type and variants
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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
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Devyser HFE
  • Multiplex detection of the three most important HFE mutations and the corresponding wild types
  • Single-tube PCR
  • Accurate and efficient
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Devyser CVD
  • Detects seven risk factors for cardiovascular disease
  • Single-tube PCR
  • Fast analysis with minimum hands-on time
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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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