Determining the order of every base in an organism's genome. Differs from genotyping, which only looks at a specific subset of genetic variants.
Genomic variation focusing on antibiotic resistance of Haemophilus influenzae has been categorised on a global scale...
The latest event from PET brought together professionals and patient voices to explore how best to improve access to genetic and genomic testing for rare disease...
Genomics could have a transformative impact for newborn screening, explains Amanda Pichini...
A rare eye cancer, which may have otherwise been missed, has been detected in a newborn baby enrolled in a whole genome sequencing study...
An advanced DNA sequencing tool can identify previously undetectable genetic mutations in human tissue with high accuracy...
A world-first gene therapy has successfully been used to restore the immune system of a teenager with a rare genetic condition...
Genetic Alliance UK has been reviewing the 168-page document to understand what the Plan means for the 3.5 million people living with genetic, rare, and undiagnosed conditions in the UK...
Genomics has the potential to reshape the NHS into a more proactive, cost-efficient, and patient-responsive system, writes Zeenat Beebeejaun. But it can only do so if built on a foundation of trust, transparency, and fairness...
The UK Government hopes to offer whole genome sequencing for all newborns in England within the next ten years, building upon the work of the Generation Study...
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