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Your Nextdoor PCP's avatar

This is an exceptionally high-signal roundup! Thank you for distilling JPM-week “noise” into directional truth. What jumped out to me is how clearly 2026 is opening with a three-layer stack: capital moving early, platform/M&A consolidation, and model deployments migrating from “R&D demo” to operational workflows. 

The most consequential theme here is translation pressure: it’s no longer enough for AI-in-bio to generate plausible candidates or elegant slides; these systems are being integrated into clinical development, diagnostics, and even care delivery (e.g., healthcare-focused LLM products rolling out alongside the conference buzz). That raises the right next questions: where are the failure modes, how do we validate “reasoning” vs. fluent text, and who is accountable when automation touches real patients? 

I also appreciated the inclusion of the regulatory/standards signals (e.g., FDA’s draft guidance endorsing Bayesian methods). Those “plumbing” shifts are often the real accelerants, because they determine what can be proven and shipped. 

This reads like early evidence that techbio is leaving its adolescence. More money, more deals, more models, now the bar becomes durable clinical value.

CGT Business Insights's avatar

Great roundup. From an advanced therapies perspective, I’m watching whether this AI wave starts touching the real bottlenecks — manufacturability, comparability, release strategy, and supply reliability — not just target ID and molecule design. The “AI + automated lab” deals are a step in that direction.

Do you see any of these platforms extending downstream into CMC/bioprocess (or is that still the missing layer)?

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