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Last year, a ten-month-old baby in the US was the first person in the world to have their rare genetic disease effectively cured through the use of CRISPR gene editing technology. But the rollout of CRISPR across a wide range of genetic conditions has been hampered by its inconsistency, and its potential to cause harm to healthy genes. Now a team of Melbourne scientists have used AI to develop a fast and accurate way to keep CRISPR in line.

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