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Insights
Thalassemias

Challenges in Thalassemia diagnosis

Thalassemia is typically caused by sequence variants in the HBA1, HBA2 or HBB genes.
Case study
Transplantation

A new NGS-based method for chimerism monitoring

New, highly sensitive and precise methods for mixed chimerism analytics
Technology
Thalassemias

NGS testing in clinical practice - what to expect

Staffing requirements, breadth of assay technologies, assessing the impact on workflows
Product update
Transplantation

Devyser launches first NGS-based test for mixed chimerism

Devyser Chimerism is an NGS library kit which enables both screening and monitoring using a single reaction mix.
Whitepaper
Oncology

Easily identify BRCA1 and BRCA2 genetic mutations

Read more about simple identification of both BRCA1 and BRCA2 genes in the whitepaper
Insights
Rapid aneuploidy analysis

Principles of QF-PCR

QF PCR analysis includes amplification, detection and analysis of chromosome-specific DNA sequences known as genetic markers or small tandem repeats (STRs).
Insights
Rapid aneuploidy analysis

STR markers

A short tandem repeat (STR or microsatellite) is a pattern of two or more nucleotides that are repeated directly adjacent to each other.
Insights
Rapid aneuploidy analysis

X-chromosome counting markers

The Devyser QF-PCR kits includes several X-chromosome counting markers for reliable detection of Turner syndrome.
Insights
Thalassemias

Changing needs for thalassemia testing and how it will impact clinical labs

What you need to know about thalassemia prevalence and the implications for clinical laboratories.
Tips and tricks
Thalassemias

Sequence planning

Devyser offers an online Sequence Coverage Calculator to help plan your NGS run for optimal results.
Insights
Thalassemias

About Thalassemia

Thalassemias are haemoglobinopathies characterised by an abnormal haemoglobin production that can lead to anaemia and destruction of red blood cells.
Insights
Rapid aneuploidy analysis

Thrombophilia an important factor in thrombosis risk

Every year world thrombosis day is held on October 13 to bring awareness to the potential risks of developing thrombisis.
Insights
Oncology

NGS identification of both male and female cancer risks

Do you know a man who has participated at least once in “Movember”?
Insights
Oncology

CRISPR Helps BRCA1 Researchers Determine Functional And Non-Functional Mutations

BRCA1 variants may generally be divided into three categories: benign variants, which cause no clinical concern; deleterious variants
Insights
Thalassemias

CRISPR-Cas9 presents new possibilities for Thalassemia treatment.

The autosomal recessive inherited blood disorder, b-thalassemia, is caused by reduced or absent synthesis of the beta chains of hemoglobin due to mutations
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