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The bit about virtual cells being more like GWAS than AlphaFold is underappreciated. When you're working with transcriptomic perturbation data, the relationship between disease state and treatment isnt a clean foldable protein structure problem its noisy, probabilistic, and heavily context-dependent. The expectation that we'd just get another AlphaFold moment for cells misses how fundamentaly different the data challenge is when you're dealing with complex systems rather than single-molecule structures.

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