210 karma · joined November 27, 2017
(full disclosure: I am an employee who has worked with this team before internally, but I was not associated with this paper)
You misunderstood the point of the presentation. The company was a consulting firm that specialized in data science and engineering. Our clients wanted to kick the tires and see what our technical chops were before hiring us but they didn't want to let us use their proprietary and confidential data for our own tech demos.
We didn't want to just use the same open source datasets everyone else did, so we got to thinking about novel datasets we could create that might have applications for industries we sold our services to. From this, the Trainspotting project was born.
Many of us commuted via the Caltrain, which was right next to our office, and we were frequently frustrated with the unreliability (this was in ~2016 or so when car and pedestrian strikes were happening seemingly every week), so we made an app that tried to provide more accurate scheduling.
We used the official API for station:train arrival times, but we found that it was unreliable, so we wanted some ground truth data on whether a train was passing. Since our office was right next to the Castro MTV station, I had the idea to use a microphone (attached to a raspberry pi) to just listen for when the train went by. In addition to ground-truth data for validating arrival times, this gave us a chance to show off some IoT applications. It actually worked pretty well, but it had false positives (e.g. the garbage truck would set it off). So we added a camera.
We pointed it at the tracks and started streaming data off of it. At first we used very simple techniques, processing the raw stream on-device with classic computer vision algos (e.g. Haar cascades) in openCV. We discovered that the VTA, which had a track parallel to the Caltrain and was "behind" the Caltrain in our camera's shot, could cause false positives. Gradually we used more and more complex techniques like deep learning, but the raspberry pi couldn't handle it (IIRC it could only process a single frame in like 6 seconds). So we used a two-stage validation whereby the simpler, faster detectors that could run on the raw stream in real time detected a positive and then we'd send a single frame to run deep learning.
TL,DR: The whole point was to be a tech demo, not to gauge the speed. The trains were either stopping or pulling out of the station, so speed would have been useless.
We also measured networks across more than 90,000 Microsoft employees in the United States. Frankly, we expected to see them shrink significantly, given the rapid shifts in environment, daytime rhythms, and personal responsibilities. Instead, we discovered that most employees maintained their existing connections. Even more encouraging, most people’s network size increased. We had assumed that in a time of crisis, employees might strengthen networks within their own work groups in an insular way. In fact, we saw network growth not only within existing work groups but also across different groups, indicating that to adapt and thrive teams sought to build bridges.
This does not square with my lived experience. Close connections at work have stayed relatively strong, perhaps even strengthening as we shore them up with recurring 1:1s and social team meetings. Peripheral connections have gone down the toilet. Team and role homophily run rampant.I wonder what evidence they actually used to back up this statement. I suspect the effect is actually in the opposite (and more intuitive) direction, and that their finding is actually a result of the McNamara fallacy.
Drugs like LSD form non-covalent bonds with receptors. In a macro-world analogy, think of your hand sticking to a syrup-covered fork vs. a covalent bond being your hand stuck to a super-glue covered fork. Different drugs have different levels of "stickiness" (called affinity) for a particular receptor, and LSD has pretty high affinity for its target receptor, 5-HT2a, but it isn't permanently attached. In fact, affinity is defined by relative association vs. dissociation rates of drug-receptor complex.
On a microscopic level, each molecule of LSD is falling in and out of the receptor binding site stochastically. This leaves open the possibility of another drug binding to the same site (called competitive inhibition) when LSD isn't occupying the site. If another drug has a higher affinity, it will occupy the receptor more of the time. When you zoom out and consider the entire set of receptors and drugs, the sum of these individual stochastic events these effects follow characteristic patterns described by the law of mass action.
https://derangedphysiology.com/main/cicm-primary-exam/requir... is a pretty good description
*I'm simplifying parts of this somewhat.
Have you thought about supporting the people who have been laying the groundwork for the current wave of research (e.g. https://www.heffter.org/)? This new crop of research owes a lot to this group's decades long mission to bring psychedelic research back to acceptability.
[no affiliation other than knowing some of the founding board members]
Although the current focus on isolation is often described in the media as “the loneliness epidemic,” Robin Hewings, Director of Campaigns, Policy and Research for the U.K.’s Campaign to End Loneliness, warns that for a subjective, self-reported experience like loneliness, “it’s not very easy to make comparisons across time, and it’s not obvious that it’s getting worse.”
While he acknowledges that aging populations mean that there are likely to be a greater number of elderly people around who are suffering from isolation than in previous decades, he also points out that when you look at the percentages of those affected, the trends are harder to discern. “There was some work done in the late 1940s, which would seem to suggest a not dissimilar level to today. This is right at the speculative end,”
no
We're scared that you have the ability to disintermediate our control of the financial system just like you did to publishers.
>Another point is that high-middle-low effort on the D4 case. The binding assay results compared to the docking scores are shown at right. You can see that the number of potent compounds (better than 50% displacement, below that dashed line) decreases as the scores get worse; the lowest bin doesn’t have any at all. But at the same time, there are a few false-negative outliers with binding activity at pretty low scores, and at the other end of the scale, the top three bins look basically undistinguishable. So the broad strokes are there, but the details are of course smeared out a bit.
These methods can filter millions of compounds down to hundreds, but as an academic lab, it's still a herculean effort to synthesize hundreds of compounds. And out of those hundreds, you might get a couple that are active. This study is a combination hard work, yes, but also a lot of money and luck.
That being said, good for the team, and good for science. I have nothing but respect for Shoichet and Roth. Didn't ever cross paths with Irwin.
If the standard is garbage, then functionality is premium.