A new method for diagnosing brain tumours could cut the time patients wait for treatments by weeks to hours and raise the possibility of novel types of therapy, researchers have said.

According to the Brain Tumour Charity, about 740,000 people around the world are diagnosed with a brain tumour each year, around half of which are non-cancerous. Once a brain tumour is found, a sample is taken during surgery and cells are immediately studied under a microscope by pathologists, who can often identify the type of tumour. However, genetic testing helps to make or confirm the diagnosis.

“Almost all of the samples will go for further testing anyway. But for some of them it will be absolutely crucial, because you won’t know what you’re looking at,” said Prof Matthew Loose, a co-author of the research from the University of Nottingham.

The approach is based on devices that contain membranes featuring hundreds to thousands of tiny pores, each of which has an electric current passing through it. When DNA approaches a pore it is “unzipped” into single strands; as a strand passes through the pore it disrupts the electric current.