A lasting legacy
Meet the next generation of genomic scientists who are benefiting from our founder's generosity
DECIPHER: Fuelling Rare Disease Research
More than 15 years ago, a hospital doctor realised that bringing people’s genetic data together could provide answers for families affected by rare diseases. With the help of the Sanger Institute, the DECIPHER project has been helping families ever since
Connecting With Science
Staff at the Wellcome Genome Campus are supported to connect people with their science - find out more
Day in the life: Software Developer – making research happen
Meet the people building software to enable high-throughput genomics at the Sanger Institute.
Sanger’s super-sized sequencing scales new heights
We're celebrating: we've just read the same amount of DNA in one year as we achieved in the previous 25 years combined. This dizzying speed offers unprecedented possibilities to unlock new understanding in health and disease
More than just malaria
Researchers can change children's futures in many more ways than just helping to beat a killer disease...
Getting smart about artificial intelligence
Sanger researchers are harnessing the power of AI to extract new knowledge from the ever increasing flood of genomic data. The findings could transform medicine and biological understanding.
Science in a conflict zone: Investigating cholera in Yemen
In addition to the civil war, Yemen is experiencing the worst epidemic of cholera ever recorded. We spoke to Ankur Rakesh, a volunteer doctor with Médecins Sans Frontières (MSF) / Doctors Without Borders, who travelled to Yemen in July 2017 to study the genomics of this highly infectious and deadly disease
A new deal on data – articulating the contract between science and people
Now is the time for scientists to strike a deal everyone that benefits society as well as research, argue Anna Middleton, Vivienne Parry and Julian Borra
