LONDON - British scientists are to map 100,000 complete DNA code sequences in a project that will make the country a world leader in genetic research on cancer and rare diseases, Prime Minister David Cameron said yesterday.
Mr Cameron announced £300 million (S$632 million) in deals to fund the mapping project, predicted to be complete by 2017.
The project will sequence the genetic codes of about 75,000 patients with cancer and rare diseases, and those of their close relatives.
Both healthy and tumour cells of the patients will be mapped, meaning about 100,000 will be sequenced in total.
"This agreement will see the UK lead the world in genetic research within years," Mr Cameron said.
Scientists hope that identifying tiny changes in the genetic code that can trigger disease will allow for personalised and more effective treatments.
An example of this kind of therapy is Herceptin, a drug which treats a breast cancer variant characterised by over-activity of the HER2 gene.
DNA samples have already been donated by a few hundred participants in a pilot, and about 10,000 are expected to have donated by the year end. Among the cancers due to be targeted are bowel, breast, leukaemia, lung, ovarian and prostate.
The Wellcome Trust charity, the Medical Research Council and Britain's National Health Service are contributing to the project, which will be overseen by Genomics England, set up by the Department of Health.
The Californian DNA sequencing company Illumina, which won a contract to provide the technology for the project, will also invest about £162 million in the project over its lifetime.
Wellcome Trust director Jeremy Farrar said genome sequencing could transform medicine.
"Twenty years from now, academics and industry will have developed therapies which will be targeted at you and specific forms of cancer," he said.
"We will look back in 20 years' time and the blockbuster chemotherapy drugs that gave you all those nasty side effects will be a thing of the past."
This article was first published on August 02, 2014.
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