Updates on key developments in genomics

Genomics and the trouble with 'N of 1' trials

Randomised controlled trials are a rigorous way to identify cause and effect, but when it comes to rare genomic variants, connections can be hard to detect

Finding needles in haystacks: making sense of genomic data

Sequencing the genome is just the start; interpreting the sequence is the next big challenge

Destined for fitness? The genetic influences on exercise

Studies have identified genes that can influence a person's exercise performance and response, as well as their propensity for injury

Novel 'virotherapy' shows promise for skin cancer treatment

Modified virus known as T-vec mounts dual attack on cancer cells

Sequencing cancer DNA - what are the issues?

Whole genome sequencing can reveal vast amounts about how cancer cells work, but the process of discovery is not without challenges

How to handle hospital-acquired infections with genomics

Technology used to analyse the human genome can be applied to infective agents to identify and track the outbreak

Precision in medicine in action

Genomics can help to target treatments for patients with cancer, rare inherited conditions, and infectious diseases

Unexpected genomic findings: who wants to know?

A ground-breaking survey on health professionals, researchers and the public's attitudes towards genomics raises some important questions

Gene therapy moves towards the mainstream

While still in their infancy, gene therapy techniques could hold great promise for patients with rare diseases

CRISPR: From 'silly idea' to miracle cures?

Editing a person's genome is a high-stkes proposition. Dr Alain Li Wan Po looks at the science behind it and the ethical issues at play

Detecting Down syndrome with genomics

A major US study has shown that non-invasive prenatal testing performs better than invasive methods, but what about the UK?

State of the nation: decoding the Icelandic genome

Genomic studies are focusing not just on key diseases, as with the 100,000 Genomes Project, but on whole population groups

Can the genetic 'fat map' aid obesity prevention?

New research has discovered more than 90 genetic regions that influence obesity, tripling the number of previously known regions

The 100,000 Genomes Project – sorting fact from fiction

As the first patients are set to be recruited to the main study this month: what are the truths and myths about this Project?

Step closer to mainstream precision medicine

Rare disease diagnoses made for two of the families involved in the 100,000 Genomes Project

Saving lives with genetics: newborn screening

While screening at birth targets very rare diseases, this early diagnosis can have huge benefits for the small number of affected babies

Cancer immunotherapy: genomic insights, promises and challenges

One-in-two people are likely to develop cancer, according to new research. With advances in genomics, can we improve the outcomes?

Making sense of mitochondrial disease

Updated: The UK has approved new techniques to fix problems in mitochondrial DNA. Here's how 'three-person IVF' will work

What do NHS patients want from genome sequencing?

Genetic Alliance’s report makes recommendations for the clinical use of whole genome sequencing, and the healthcare professionals that would support it

DNA sequencing and data: a combined revolution in healthcare

Advances in both genomic and digital technologies bring both opportunities and challenges for the health sector
Sample processing

Preparing NHS laboratory services for the genomic age

As efforts to embed genomics across the NHS move ahead, NHS England is consulting on proposals for a shake-up of genetics laboratory services