285 karma · joined November 1, 2015
You either love it or hate it, depending on how well your electromagnetics class was taught.
I'm curious about what your strategy is for data collection to fuel improved algorithmic design. Are you building out experimental capacity to generate datasets in house, or is that largely farmed out to partners?
There is also one widespread approach that isn't mentioned in the article: expansion microscopy. Expansion takes the scifi-sounding approach of: what if you could make your sample physically bigger? See the Wikipedia page for more: https://en.wikipedia.org/wiki/Expansion_microscopy
For instance, Evo2 by the Arc Institute is a DNA Foundation Model that can do some really remarkable things to understand/interpret/design DNA sequences, and there are now multiple open weight models for working with biomolecules at a structural level that are equivalent to AlphaFold 3.
I'm curious if you've worked with any of those models and how they relate to NMR data and MD simulations.
And an Editorial piece (more technical than the NYT): https://www.nejm.org/doi/full/10.1056/NEJMe2505721
I agree that the modern Silicon Valley model of VC funding has been spoiled by SaaS startups, where the capital expense is smaller, the timeline to exit is shorter, and pivots are easier. It is not great for deeptech innovation because those require more capital, time, and are more technology-constrained than software. Ironically, modern VC was developed to support semiconductor startups (1970s-90s), but has drifted from that technology-heavy origin.
With all of this coming together, we should be accelerating both public and private investment in biotechnology because we're getting closer and closer to transformative therapies. But...we're failing to rise to the occasion and meet the moment.
To that end, I believe that this is the time to invest in the US biotechnology ecosystem so that we remain competitive with China. The ongoing crisis at the NIH is antithetical to this goal, as Derek Lowe's blog posts describe.
[1] https://centuryofbio.com/p/commoditization [2] https://www.wsj.com/health/pharma/the-drug-industry-is-havin...
Two examples off the top of my head: Sana recently announced islet cell transplantation without immunosuppression (press release: https://ir.sana.com/news-releases/news-release-details/sana-... ) and Vertex (ongoing trial: https://www.breakthrought1d.org/news-and-updates/vertex-laun... ).
2) Talk to people! Bounce your ideas/areas of excitement off of other people, and see what gets reflected back at you. That signal can be very helpful to see when you've stumbled across an idea or problem that might be useful to more people than just yourself, i.e. a more important area of investigation.
3) Read, read, read. And take notes on random ideas you have while reading, and things that papers missed or didn't look into. If you do this enough and take some time to reflect on it, you can start to find gaps in knowledge that could be addressed.
It is a simplified version of the introductory biology course at MIT, that doesn't _focus_ on naming/defining things in biology. Instead, it uses the lenses of genetics and biochemistry to explore how the core machinery of life works, and how we got to our current understanding. That said, there is some amount of memorization that is unavoidable.
[0] https://www.edx.org/course/introduction-to-biology-the-secre...
I really enjoyed Being Mortal by Atul Gawande (author of The Checklist Manifesto), that tells intensely personal stories about, well, the process of dying, and the increasingly prolonged tug of war between medicine and death.
One thing that may be a bit of a challenge is how quickly things change in the technology world. "Code Status" is medical lingo for the descriptor of what the patient expresses they want to have happen if their heart or breathing were to stop. Most people are full code - CPR, mechanical ventilation, etc. But patients can choose to be DNR/DNI, meaning "Do Not Resuscitate, Do Not Intubate", meaning very limited interventions would be performed.
As the tech gets better, I wonder if a more sophisticated decision tree might be needed in the future -- if XYZ happens where 30% of patients make a recovery, begin ECMO, but if ABC happens in which only 5% of patients recover, do not start ECMO.
From a study in the New England Journal of Medicine: "Conclusions: Family presence during CPR was associated with positive results on psychological variables and did not interfere with medical efforts, increase stress in the health care team, or result in medicolegal conflicts."
Full study: https://www.nejm.org/doi/full/10.1056/NEJMoa1203366
DOI for Sci-Hub: DOI: 10.1056/NEJMoa1203366
edit: slightly awkward phrasing in my original comment above. Amended: They were (and still are!) very forward thinking.
Sometimes, we have some promising leads on disease that we can begin to chase down. Most of the time, however, we have no idea where to begin, and so a shotgun basic science approach may ultimately be more fruitful. Every subfield is different and difficult to master, which is why it is so important to engage with the people who actually do the work.
I know the tone of this sounds like I'm beating a dead horse. I'm sorry.