The chapter explores how CRISPR CAS systems and AI models are revolutionizing gene editing, enabling precise and efficient modifications in various cells, including human cells. It discusses the development of new cast proteins like open CRISPR-1, outperforming existing ones and showcasing the potential for treating genetic diseases. Furthermore, it delves into the intersection of technology, pharmaceuticals, and gene editing, emphasizing the importance of open source tools and AI for scientific advancements.

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