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How do you find a single typo in a person’s DNA that causes a rare disease? It is like finding a needle in a 9-billion-piece haystack.
Enter AlphaGenome Atlas: a new AI-powered database charting the molecular impact of every possible genetic variant.
Scientists are already using it to look into unsolved rare diseases, map rare mutations linked to complex traits, and more.
🔗 Find out how by tapping the link → https://goo.gle/4ihF2LZ



