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Major breakthrough in genome sequencing can quicken cancer diagnosis – Health Europa

A major breakthrough in genome sequencing could lead to the quicker diagnosis of cancer and rare diseases.

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Understanding human DNA sequences can inform scientists about disease and how to diagnose or treat them and a team of scientists at the School of Life Sciences, University of Nottingham, have demonstrated how to selectively sequence fragments of DNA more quickly and cost-effectively than ever before, which could have major implications in how genetic diseases are understood and diagnosed.
The new DNA scanning method allows for the selective sequencing of DNA fragments without searching through DNA…

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