Chimerism monitoring after hematopoietic stem cell transplantation (HSCT) plays a key role in...
Learnings from our IVDR journey
A recent paper published by Malan et al in the Journal of the American Medical Association (JAMA)...
An expert consensus panel has recently promoted genetic testing for Familial Hypercholesterolemia...
Cystic fibrosis is one of the most common genetic disorders. The disease is caused by mutations...
The autosomal recessive inherited blood disorder, b-thalassemia, is caused by reduced or absent...
Causes Thalassemias are haemoglobinopathies characterised by an abnormal haemoglobin production...
Devyser offers an online Sequence Coverage Calculator to help plan your NGS run for optimal...
The X chromosome counting markers define non-variable sequences present on the X chromosome and an...
A short tandem repeat (STR or microsatellite) is a pattern of two or more nucleotides that are...
QF PCR analysis includes amplification, detection and analysis of chromosome-specific DNA sequences...
Library preparation
