Updates on key developments in genomics
Are we there yet? Genome sequencing turns 20
We look back on two decades of genome sequencing and explore four areas where continued progress could provide future breakthroughs
New gene therapy hubs announced
A network of ‘innovation hubs’ are set to advance the clinical development of novel gene therapy treatments in the UK
DNA Family Secrets: the science behind the show
Now the BBC series has wrapped up, we revisit some genomics talking points and think about what may have been left out by the producers and why
NICE approves new SMA gene therapy
NHS England has made a deal on a new, life-saving treatment for the most severe form of the condition
Towards genomic equity
To advance genomics in healthcare, we must consider both the data we collect and who we collect it from. Here, bioinformatician Nana E. Mensah explains why
Haplotypes: a cut-out-and-keep guide
Although ‘haplo' means 'simple', the science can be anything but. Find out what’s hap-pening with haplotypes in our guide
Transcriptomics and mental illness
We look beyond the genome to find out how RNA can impact on the presentation of psychiatric conditions
Genomic test supports next-generation cancer drugs
Promising new cancer treatments are emerging, but how does genomics help us identify the patients who need them?
NHS to trial new multi-cancer blood test
More than 50 different types of cancer can be detected by the new test, but how will it work?
The importance of diversity in genomic datasets
We look at a recent prostate cancer study that highlights the importance of inclusivity in genomic studies
What is genomic imprinting?
We explore one type of epigenetic modification, its function in our genome and the rare conditions that have been linked to it
Filling the gaps: sequencing a chromosome
A human chromosome has been sequenced in its entirety for the first time, but why is this breakthrough important for the future of our reference genome?
Prenatal genomics - an overview
What role can genomics play before a baby is born? We break down the screening and testing options available now – from traditional methods to new technologies
Richter’s syndrome study published
A new study by GEP fellow Niamh Appleby has found potential pathways and targets for the treatment of Richter’s syndrome – an aggressive form of adult leukaemia
Genomics and the new Covid-19 variant
What do we know about the new strain of coronavirus sweeping across the UK? And how did genomics help us get there?
Key genomic technologies of 2020: treatments old and new
In the second part of our review of the year’s genomic highlights, we look at the breakthroughs that are helping patients with rare disease and cancer
Key genomic technologies of 2020: fighting Covid-19
In the first of two articles reflecting on this year, we look at how genomics became central to tackling an unprecedented global pandemic
Genetics and genomics on screen
As many people slow down for a festive break, Dr Jonathan Roberts considers presentations of genomics in five popular films
First polygenic cause found for neonatal diabetes
A new study has found the first ever polygenic cause for diabetes in children younger than six months of age
Researchers find ‘hidden’ coronavirus gene
A newly discovered gene within the genome of the SARS-CoV-2 virus could offer clues about its origins and a possible target for treatment
‘New’ de novo variants linked to developmental disorders
How do gene variants affect our health? We look at a recent study that has newly identified 28 genes associated with developmental disorders