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

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

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

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

New, highly sensitive and precise methods for mixed chimerism analytics

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

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

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

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

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

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

Cystic Fibrosis is one of the most common genetic disorders.

Read more about simple identification of both BRCA1 and BRCA2 genes in the whitepaper

An expert consensus panel has recently promoted genetic testing for Familial Hypercholesterolemia (FH) as a standard of care for patients with probable FH

In this study, the Devyser BRCA test was used to analyse 227 patient DNA samples.