A major breakthrough in genome sequencing could lead to the quicker diagnosis of cancer and rare diseases. 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 [ ]
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Saturday 16 January 2021
healtheuropa - 1 month ago
Major breakthrough in genome sequencing can quicken cancer diagnosis
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