https://www.centerwatch.com/clinical-trials/listings/NCT0511...
https://www.entandaudiologynews.com/features/ent-features/po...
265 karma · joined February 26, 2009
https://www.centerwatch.com/clinical-trials/listings/NCT0511...
https://www.entandaudiologynews.com/features/ent-features/po...
I participated in early work in optogenetics in larger brains, and Karl was my postdoc adviser. He is a deeply thoughtful and generous scientist. His book Projections unpacks some of his thinking as to how these tools may unravel and treat a panel of psychiatric conditions. The company MapLight he started is working to make these treatments a reality via ongoing clinical trials https://maplightrx.com/pipeline/
Screenshot: https://cloud.githubusercontent.com/assets/77752/5382993/9f6...
“In sum, we have identified NT (neurotensin) as a neuropeptide that signals valence in the BLA (basolateral amygdala) and showed that NT is a critical neuromodulator that orchestrates positive and negative valence assignment in amygdala neurons by extending valence-specific plasticity to behaviourally relevant timescales.”
For the adaptation, there’s a rich literature of neuroscientists in this field studying how the participant adapts to the control characteristics of the decoder, and how the decoding algorithm can be designed to adapt after seeing more data during use. Here’s one paper if you’re interested http://www.stat.columbia.edu/~liam/research/pubs/merel-fox-c...
- WPM is a difficult metric to "game", since if they make a mistake they have to select the backspace key, and then select the correct key again.
- It's a proof of concept demonstration that a human (e.g. in the BrainGate[1] clinical trial) could use this prosthetic system to communicate in text. When a human were driving the system, the keys wouldn't light up; they'd just type freely.
* optogenetic stimulation: using light-activated ion channels to modulate neural activity
* optical imaging: using genetically targeted fluorescent proteins (mainly GCaMP) to observe the activity of neurons
This article is more the second kind, and the novel aspect is that this technology couples dopamine release to calcium rises, enabling imaging of the calcium signal to be used as a proxy for the neurotransmitter's release. It's more likely to be quite useful for investigating specific scientific questions about neurotransmitter signaling than a general purpose readout for BMI.
Multielectrode arrays pick up spikes or action potentials from individual neurons directly, so you get high temporal resolution but from a sparse sample of cells. This sample turns out to be enough to do a lot of interesting things, such as controlling a mouse cursor or a robotic arm. This is already in clinical trials at a few sites, including (my lab at) Stanford.
Imaging approaches are really powerful, but the signals are often slower. This has to do with the kinetics of the proteins themselves and the signal that is being detected (calcium is slower than voltage transients). But you get to see the activity of lots of neurons. There are voltage sensitive channels that you can image, although the signal to noise ratio isn't nearly as high as yet. It's not immediately clear how this could be used for a BMI in humans, mainly because you would absolutely need optical access to the brain to image, so you'd either be opening up a window or implanting some kind of imaging sensor. The less invasive approaches you were hinting at are mostly in the first category (stimulation), where for longer wavelengths of light you wouldn't need something as invasive.
I do actually think this is disputable. As a late stage PhD candidate, I'm not sure that what I do for a living looks anything like "studying". I and my colleagues work on research problems with variable amounts of input from our advisors. We typically don't take classes after 2 years. I work 9-9 6 days a week on building experimental setups and tackling scientific questions that will be beneficial to both my employer (more papers + more grants = more overhead money for the University and more research funding for my advisor) and to my career. Yes, academia doesn't have a commercial output, but what I do isn't that dissimilar to what being a data/research scientist at a small company would do.
People (successfully) pursuing a PhD are almost by definition not "studying" anything; they're advancing the state of the art in their field. To me calling them students seems like a mechanism to depress salaries.
To be clear, I'm not trying to argue that taking this position is a bad idea, I'm just trying to better understand the opportunity and why YC research might be a better decision than a more run-of-the-mill PhD. I'm ever so slightly skeptical, but mostly just curious.
Even then, going from these messy biological details (e.g. these 20 proteins assemble into a particular form and release this neurotransmitter from this synapse when X happens) to an explanation for how the neuron works at a more algorithmic level is hard, and the field isn't there yet. Assembling and abstracting the details is hard and it's one of the goals of theoretical neuroscience. The complexity is probably a symptom of our lack of understanding, rather than the cause of it, i.e. there probably are a lot of details that we can abstract away in a simpler functional model.
I haven't read the paper, and I'm only vaguely familiar with Hawkins et al.'s HTM work. But I disagree with the claim at the end of the TR piece that these predictions are imminently testable. Thinking up a specific experiment to try and disprove theoretical ideas is often the hardest part of experimental neuroscience.
This piece he wrote shortly before he died is well worth your time. http://stanmed.stanford.edu/2015spring/before-i-go.html
If I'm reading it correctly, this article seems to suggest that the advice that pursuing work that you find fulfilling is itself responsible for lowering wages, which may be true in as much as people are willing to accept lower wages if they enjoy the work despite having better options. But what would you propose as an alternative? Pursuing work that you find less fulfilling in exchange for more money? That's not a sacrifice I'm willing to make, and I've been privileged with enough opportunity and financial security to have a choice. Of course everyone has different objective functions they're seeking to optimize, so I see why others would make different choices, which is all good by me.
I think another effect of this experiment-for-fee model would be to level the playing field for smaller labs that can't master every tool simultaneously. Whereas before a researcher would have to choose between (a) learning a new technique and buying new equipment and (b) finding an alternative way to demonstrate a result, presumably with older or less reliable methods, now they can do a very simple one-off collaboration of sorts without any of the overhead of real collaborations (esp. negotiations over authorship).
See https://github.com/djoshea/imgui/blob/master/examples/opengl...
brew install glew
brew install glfw3
cd examples/opengl_example/
make
./main